Calcium Pyrophosphate
Chondrocalcinosis
Microscopy, Polarization
Crystallization
Scleral Diseases
Calcium Phosphates
Synovial Fluid
Phosphate Transport Proteins
Gout
Pyrophosphatases
Uric Acid
Tetramisole
Joint Diseases
Osteoarthritis
Durapatite
Thiamine Pyrophosphate
Cartilage, Articular
Arthritis
Hydroxyapatites
Technetium Tc 99m Pyrophosphate
Calcium Signaling
Phosphoribosyl Pyrophosphate
Dental Caries
Fluorides
Fluoridation
Fluorosis, Dental
Toothpastes
Cariostatic Agents
Transduction mechanisms of porcine chondrocyte inorganic pyrophosphate elaboration. (1/116)
OBJECTIVE: To investigate cellular signaling mechanisms that influence chondrocyte production of inorganic pyrophosphate (PPi), which promotes calcium pyrophosphate dihydrate (CPPD) crystal deposition. METHODS: Articular chondrocyte and cartilage cultures were stimulated with protein kinase C (PKC) activator and adenyl cyclase activator. Generation of extracellular PPi was measured. RESULTS: Adenyl cyclase activation resulted in diminished pyrophosphate generation. PKC activation stimulated pyrophosphate elaboration. CONCLUSION: Two signaling pathways, cAMP and PKC, modulate generation of extracellular pyrophosphate by cartilage and chondrocytes. They are novel targets for potentially diminishing extracellular pyrophosphate elaboration that leads to CPPD crystal deposition. (+info)Myelopathy due to calcification of the cervical ligamenta flava: a report of two cases in West Indian patients. (2/116)
Two cases of cervical myelopathy due to calcification of the ligamenta flava (CLF) are described for the first time in black patients from the French West Indies. A pre-operative CT scan differentiated the diagnosis from one of ossification of the ligamenta flava. Microanalysis on the operatively excised specimen in one patient revealed a mixture of calcium pyrophosphate dihydrate crystals and hydroxypatite crystals. Poor outcome in one patient contrasting with excellent recovery in the other one, who had undergone posterior decompressive laminectomy, emphasizes the importance of surgery in the management of CLF. (+info)Most calcium pyrophosphate crystals appear as non-birefringent. (3/116)
OBJECTIVE: To determine the proportion of calcium pyrophosphate dihydrate (CPPD) crystals that appear as non-birefringent when observed under the polarised light microscope. METHODS: Two observers examined independently 10 synovial fluid samples obtained during an episode of arthritis attributable to CPPD crystals. Ten synovial fluid samples from patients with acute gout were used as a reference. The examination was performed after placing a fluid sample in a Niebauer haemocytometric chamber; a crystal count was done first under ordinary light, then in the area corresponding to a 0.1 ml, under polarised light RESULTS: The percentages of birefringence appreciated for CPPD were 18% (confidence intervals (CI) 12, 24) for observer 1, and 17% (CI 10, 24) for observer 2 (difference NS). The percentages of birefringence for monosodium urate were 127% (CI 103, 151) for observer 1 and 107% (CI 100, 114) for observer 2 (difference NS). Percentages above 100% indicate that crystals missed under ordinary light became apparent under polarised light. CONCLUSION: Only about one fifth of all CPPD crystals identified by bright field microscopy show birefringence when the same synovial fluid sample is observed under polarised light. If a search for CPPD crystals is conducted under polarised light, the majority of the crystals will be missed. Ordinary light allows a better rate of CPPD crystal detection but observation under polarised light of crystals showing birefringence is required for definitive CPPD crystal identification. (+info)Extracellular signal-regulated kinase 1/extracellular signal-regulated kinase 2 mitogen-activated protein kinase signaling and activation of activator protein 1 and nuclear factor kappaB transcription factors play central roles in interleukin-8 expression stimulated by monosodium urate monohydrate and calcium pyrophosphate crystals in monocytic cells. (4/116)
OBJECTIVE: Monosodium urate monohydrate (MSU) and calcium pyrophosphate dihydrate (CPPD) crystals cause acute gout and pseudogout, respectively. Because acute gout and pseudogout appear to be dependent on interleukin-8 (IL-8)-induced neutrophil ingress, this study was undertaken to define and compare how MSU and CPPD crystals stimulate IL-8 messenger RNA (mRNA) expression in mononuclear phagocytes. METHODS: MSU and CPPD crystal-induced mitogen-activated protein kinase (MAPK) signal transduction and IL-8 transcriptional activation were studied in human monocytic cells, using the THP-1 cell line. RESULTS: MSU and CPPD crystals (0.5 mg/ml) induced activation of c-Jun N-terminal kinase, extracellular signal-regulated kinase 1 (ERK-1)/ERK-2, and p38 MAPK pathways in THP-1 cells. Activation of the ERK-1/ERK-2 pathway was essential for MSU and CPPD crystal-induced IL-8 mRNA expression, whereas the p38 pathway played a greater role in IL-8 mRNA expression in response to CPPD crystals in comparison with MSU crystals. Both crystals induced the binding of nuclear factor kappaB (NF-kappaB), including the NF-kappaB complex c-Rel/RelA, and activator protein 1 (AP-1, including N-terminal phosphorylated c-Jun) to the IL-8 promoter. Both crystals induced transcriptional activation of the IL-8 promoter, which was dependent on activation of c-Rel/RelA and AP-1. Activation of the NF-IL-6 transcription factor played a lesser role. Finally, crystal-induced IL-8 promoter activation was mediated by activation of the ERK-1/ERK-2 pathway, as demonstrated by transfection of dominant-negative raf-1. CONCLUSION: These results indicate that ERK-1/ ERK-2 signaling and transcriptional activation through AP-1 and NF-kappaB are essential for the induction of IL-8 expression in mononuclear phagocytes in response to CPPD and MSU crystals. (+info)Calcification of the cervical ligamentum flavum--case report. (5/116)
A 52-year-old male presented with calcification of the cervical ligamentum flavum manifesting as hypesthesia of the bilateral middle, ring, and little fingers and ulnar halves of both forearms, as well as motor weakness in the bilateral upper extremities and gait disturbance. Cervical x-ray tomography detected a round calcified mass on the posterior wall of the cervical canal at the C-5 level. Computed tomography showed the round, nodular calcified mass more clearly. Magnetic resonance imaging showed an epidural low intensity mass compressing and distorting the cervical cord at the C-5 level on both T1- and T2-weighted images. Administration of gadolinium-diethylenetriaminepenta-acetic acid caused marginal enhancement of the mass. The lesion was eventually removed by posterior laminectomy. The mass was composed of a very hard crystal-like calcified deposition in the ligamentum flavum. X-ray diffraction analysis of the histological specimen showed calcium pyrophosphate dihydrate (CPPD) and hydroxyapatite in the crystal-like substance, confirming that CPPD is responsible for calcification of the cervical ligamentum flavum. (+info)Deposition of calcium pyrophosphate in tissue after revision arthroplasty of the hip. (6/116)
We reviewed histologically the incidence and pathogenesis of the deposition of calcium pyrophosphate dihydrate (CPPD) crystals in the pseudocapsule, femoral and acetabular membranes and periprosthetic tissue at revision of 789 cases of failed total hip replacement. In 13, periprosthetic tissues were found to have deposits of CPPD crystals in areas of cartilaginous metaplasia; four also showed evidence of localised deposition of amyloid. None of the patients had a history of chondrocalcinosis in the hip or other joints. Cartilaginous metaplasia and other changes in periprosthetic tissues may predispose to the deposition of CPPD and associated localised amyloid. (+info)Retro-odontoid massive calcium pyrophosphate crystal deposition--case report. (7/116)
An 86-year-old male presented with progressive myelopathy due to retro-odontoid massive deposits of calcium pyrophosphate dihydrate (CPPD) crystals. Magnetic resonance imaging revealed a non-enhanced isointense extradural mass on the T1-weighted image and heterogeneously intense mass on the T2-weighted image. Computed tomography showed typical punctate and linear calcifications within the mass. The mass was resected via a lateral approach resulting in marked improvement of the symptoms. Histological examination revealed birefringent rhomboid crystals consistent with CPPD. CPPD deposition should be considered in the differential diagnosis of retro-odontoid extradural mass because surgical therapy is beneficial even for elderly patients. (+info)Inhibition of TNF-alpha-induced neutrophil apoptosis by crystals of calcium pyrophosphate dihydrate is mediated by the extracellular signal-regulated kinase and phosphatidylinositol 3-kinase/Akt pathways up-stream of caspase 3. (8/116)
The role of protein kinases in the inhibition of TNF-alpha associated apoptosis of human neutrophils by crystals of calcium pyrophosphate dihydrate (CPPD) (25 mg/ml) was investigated. We monitored the activities of the p44 extracellular signal-regulated kinase 1 (ERK1) and p42 ERK2 mitogen-activated protein (MAP) kinases and phosphatidylinositol 3-kinase (PI3-K)-regulated protein kinase B (Akt) in neutrophils incubated with TNF-alpha and CPPD crystals, separately and in combination, in parallel with the endogenous caspase 3 activity and DNA fragmentation. CPPD crystals were observed to induce a robust and transient activation of ERK1, ERK2, and Akt, whereas TNF-alpha produced only a modest and delayed activation of Akt. In the presence of TNF-alpha, Akt activity was enhanced, and CPPD crystal-induced activation of ERK1 and ERK2 was more sustained than with CPPD crystals alone, but TNF-alpha itself reduced the basal phosphotransferase activities of these MAP kinases. Preincubation with the MAP kinase kinase (MEK1) inhibitors PD98059 (20 ng/ml) and U0126 (250 nM), or the PI3-K inhibitors wortmannin (100 nM) and LY294002 (50 microM) repressed the activation of ERK1, ERK2, and Akt in association with CPPD crystal incubation, in the absence or presence of TNF-alpha. Furthermore, the inhibition of the Mek1/Mek2-->ERK1/ERK2 or PI3-K/Akt pathways reversed CPPD crystal-associated suppression of TNF-alpha-induced caspase 3 activation and neutrophil apoptosis. Together, these results indicate that CPPD crystals function to induce acute inflammatory responses through ERK1/ERK2 and PI3-K/Akt-mediated stimulation of neutrophil activation and repression of apoptosis. (+info)Calcium pyrophosphate is a mineral compound made up of calcium and pyrophosphate ions. In the body, it can form crystals that deposit in joints, causing a type of arthritis known as calcium pyrophosphate deposition (CPPD) disease or pseudogout. CPPD disease is characterized by sudden attacks of joint pain and swelling, often in the knee or wrist. The condition is more common in older adults and can also occur in people with underlying medical conditions such as hyperparathyroidism, hemochromatosis, and hypophosphatasia. Calcium pyrophosphate crystals may also be found in the fluid around the heart (pericardial fluid) or in other tissues, but they do not always cause symptoms.
Chondrocalcinosis is a medical condition characterized by the deposition of calcium pyrophosphate dihydrate crystals in the fibrous cartilage (also known as chondral or articular cartilage) and/or the joint cavity (synovial fluid). This cartilage is present in various parts of the body, including the ears, nose, respiratory tract, and connective tissues such as those found in joints.
Calcium pyrophosphate dihydrate crystals are normally present in small amounts within the body; however, an overabundance of these crystals can lead to chondrocalcinosis. The condition is often associated with osteoarthritis and can affect people of all ages but is more common in older adults.
Chondrocalcinosis may not always cause symptoms, but when it does, they can include joint pain, stiffness, swelling, and warmth. These symptoms are similar to those seen in other forms of arthritis, making chondrocalcinosis difficult to diagnose based on symptoms alone. Diagnosis typically involves imaging techniques such as X-rays or ultrasounds, as well as joint fluid analysis to identify the presence of calcium pyrophosphate dihydrate crystals.
Treatment for chondrocalcinosis is generally focused on managing symptoms and addressing any underlying conditions that may contribute to the development or progression of the disease. This can include medications such as nonsteroidal anti-inflammatory drugs (NSAIDs) to reduce pain and inflammation, joint aspiration to remove excess fluid and crystals from the affected area, and physical therapy to maintain joint mobility and strength. In some cases, surgery may be necessary to repair or replace damaged joints.
Diphosphates, also known as pyrophosphates, are chemical compounds that contain two phosphate groups joined together by an oxygen atom. The general formula for a diphosphate is P~PO3~2-, where ~ represents a bond. Diphosphates play important roles in various biological processes, such as energy metabolism and cell signaling. In the context of nutrition, diphosphates can be found in some foods, including milk and certain vegetables.
Polarized light microscopy is a type of microscopy that uses polarized light to enhance contrast and reveal unique optical properties in specimens. In this technique, a polarizing filter is placed under the light source, which polarizes the light as it passes through. The specimen is then illuminated with this linearly polarized light. As the light travels through the specimen, its plane of polarization may be altered due to birefringence, a property of certain materials that causes the light to split into two separate rays with different refractive indices.
A second polarizing filter, called an analyzer, is placed in the light path between the objective and the eyepiece. The orientation of this filter can be adjusted to either allow or block the transmission of light through the microscope. When the polarizer and analyzer are aligned perpendicularly, no light will pass through if the specimen does not exhibit birefringence. However, if the specimen has birefringent properties, it will cause the plane of polarization to rotate, allowing some light to pass through the analyzer and create a contrasting image.
Polarized light microscopy is particularly useful for observing structures in minerals, crystals, and certain biological materials like collagen fibers, muscle proteins, and starch granules. It can also be used to study stress patterns in plastics and other synthetic materials.
Crystallization is a process in which a substance transitions from a liquid or dissolved state to a solid state, forming a crystal lattice. In the medical context, crystallization can refer to the formation of crystals within the body, which can occur under certain conditions such as changes in pH, temperature, or concentration of solutes. These crystals can deposit in various tissues and organs, leading to the formation of crystal-induced diseases or disorders.
For example, in patients with gout, uric acid crystals can accumulate in joints, causing inflammation, pain, and swelling. Similarly, in nephrolithiasis (kidney stones), minerals in the urine can crystallize and form stones that can obstruct the urinary tract. Crystallization can also occur in other medical contexts, such as in the formation of dental calculus or plaque, and in the development of cataracts in the eye.
Scleral diseases refer to conditions that affect the sclera, which is the tough, white outer coating of the eye. The sclera helps to maintain the shape of the eye and provides protection for the internal structures. Scleral diseases can cause inflammation, degeneration, or thinning of the sclera, leading to potential vision loss or other complications. Some examples of scleral diseases include:
1. Scleritis: an inflammatory condition that causes pain, redness, and sensitivity in the affected area of the sclera. It can be associated with autoimmune disorders, infections, or trauma.
2. Episcleritis: a less severe form of inflammation that affects only the episclera, a thin layer of tissue overlying the sclera. Symptoms include redness and mild discomfort but typically no pain.
3. Pinguecula: a yellowish, raised deposit of protein and fat that forms on the conjunctiva, the clear membrane covering the sclera. While not a disease itself, a pinguecula can cause irritation or discomfort and may progress to a more severe condition called a pterygium.
4. Pterygium: a fleshy growth that extends from the conjunctiva onto the cornea, potentially obstructing vision. It is often associated with prolonged sun exposure and can be removed surgically if it becomes problematic.
5. Scleral thinning or melting: a rare but serious condition where the sclera degenerates or liquefies, leading to potential perforation of the eye. This can occur due to autoimmune disorders, infections, or as a complication of certain surgical procedures.
6. Ocular histoplasmosis syndrome (OHS): a condition caused by the Histoplasma capsulatum fungus, which can lead to scarring and vision loss if it involves the macula, the central part of the retina responsible for sharp, detailed vision.
It is essential to consult an ophthalmologist or eye care professional if you experience any symptoms related to scleral diseases to receive proper diagnosis and treatment.
Calcium phosphates are a group of minerals that are important components of bones and teeth. They are also found in some foods and are used in dietary supplements and medical applications. Chemically, calcium phosphates are salts of calcium and phosphoric acid, and they exist in various forms, including hydroxyapatite, which is the primary mineral component of bone tissue. Other forms of calcium phosphates include monocalcium phosphate, dicalcium phosphate, and tricalcium phosphate, which are used as food additives and dietary supplements. Calcium phosphates are important for maintaining strong bones and teeth, and they also play a role in various physiological processes, such as nerve impulse transmission and muscle contraction.
Synovial fluid is a viscous, clear, and straw-colored fluid found in the cavities of synovial joints, bursae, and tendon sheaths. It is produced by the synovial membrane, which lines the inner surface of the capsule surrounding these structures.
The primary function of synovial fluid is to reduce friction between articulating surfaces, providing lubrication for smooth and painless movement. It also acts as a shock absorber, protecting the joints from external forces during physical activities. Synovial fluid contains nutrients that nourish the articular cartilage, hyaluronic acid, which provides its viscoelastic properties, and lubricin, a protein responsible for boundary lubrication.
Abnormalities in synovial fluid composition or volume can indicate joint-related disorders, such as osteoarthritis, rheumatoid arthritis, gout, infection, or trauma. Analysis of synovial fluid is often used diagnostically to determine the underlying cause of joint pain, inflammation, or dysfunction.
Phosphate transport proteins are membrane-bound proteins responsible for the active transport of phosphate ions across cell membranes. They play a crucial role in maintaining appropriate phosphate concentrations within cells and between intracellular compartments, which is essential for various biological processes such as energy metabolism, signal transduction, and bone formation.
These proteins utilize the energy derived from ATP hydrolysis or other sources to move phosphate ions against their concentration gradient, thereby facilitating cellular uptake of phosphate even when extracellular concentrations are low. Phosphate transport proteins can be classified based on their structure, function, and localization into different types, including sodium-dependent and sodium-independent transporters, secondary active transporters, and channels.
Dysregulation of phosphate transport proteins has been implicated in several pathological conditions, such as renal Fanconi syndrome, tumoral calcinosis, and hypophosphatemic rickets. Therefore, understanding the molecular mechanisms underlying phosphate transport protein function is essential for developing targeted therapies to treat these disorders.
Gout is a type of inflammatory arthritis that occurs when urate crystals accumulate in and around the joints, causing sudden attacks of severe pain, swelling, redness, and tenderness. Urate crystals can form when there are high levels of uric acid in the blood. Uric acid is a waste product that is produced when the body breaks down purines, substances that are found naturally in certain foods, such as steak, organ meats, and seafood. Other foods also promote higher levels of uric acid, such as alcoholic beverages, especially beer, and drinks sweetened with fruit sugar (fructose).
Normally, uric acid dissolves in the blood and passes through the kidneys and out of the body in urine. But sometimes either the body produces too much uric acid or the kidneys excrete too little uric acid. When this happens, uric acid can build up, forming sharp, needle-like urate crystals in a joint or surrounding tissue that cause pain, inflammation and swelling.
Gout most commonly affects the big toe but can also occur in any joint in the body. The symptoms of gout are often acute, occurring suddenly without warning and frequently at night. The attacks are characterized by a rapid onset of pain, swelling, warmth, and redness in the affected joint. An attack of gout can be so painful that it wakes you up from sleep.
Over time, gout can cause permanent damage to the joints and surrounding tissue, resulting in chronic arthritis. If left untreated, gout also can lead to an accumulation of uric acid crystals in the kidneys, which can result in kidney stones.
Pyrophosphatases are enzymes that catalyze the hydrolysis or cleavage of pyrophosphate (PPi) into two inorganic phosphate (Pi) molecules. This reaction is essential for many biochemical processes, such as energy metabolism and biosynthesis pathways, where pyrophosphate is generated as a byproduct. By removing the pyrophosphate, pyrophosphatases help drive these reactions forward and maintain the thermodynamic equilibrium.
There are several types of pyrophosphatases found in various organisms and cellular compartments, including:
1. Inorganic Pyrophosphatase (PPiase): This enzyme is widely distributed across all kingdoms of life and is responsible for hydrolyzing inorganic pyrophosphate into two phosphates. It plays a crucial role in maintaining the cellular energy balance by ensuring that the reverse reaction, the formation of pyrophosphate from two phosphates, does not occur spontaneously.
2. Nucleotide Pyrophosphatases: These enzymes hydrolyze the pyrophosphate bond in nucleoside triphosphates (NTPs) and deoxynucleoside triphosphates (dNTPs), converting them into nucleoside monophosphates (NMPs) or deoxynucleoside monophosphates (dNMPs). This reaction is important for regulating the levels of NTPs and dNTPs in cells, which are necessary for DNA and RNA synthesis.
3. ATPases and GTPases: These enzymes belong to a larger family of P-loop NTPases that use the energy released from pyrophosphate bond hydrolysis to perform mechanical work or transport ions across membranes. Examples include the F1F0-ATP synthase, which synthesizes ATP using a proton gradient, and various molecular motors like myosin, kinesin, and dynein, which move along cytoskeletal filaments.
Overall, pyrophosphatases are essential for maintaining cellular homeostasis by regulating the levels of nucleotides and providing energy for various cellular processes.
Uric acid is a chemical compound that is formed when the body breaks down purines, which are substances that are found naturally in certain foods such as steak, organ meats and seafood, as well as in our own cells. After purines are broken down, they turn into uric acid and then get excreted from the body in the urine.
However, if there is too much uric acid in the body, it can lead to a condition called hyperuricemia. High levels of uric acid can cause gout, which is a type of arthritis that causes painful swelling and inflammation in the joints, especially in the big toe. Uric acid can also form crystals that can collect in the kidneys and lead to kidney stones.
It's important for individuals with gout or recurrent kidney stones to monitor their uric acid levels and follow a treatment plan prescribed by their healthcare provider, which may include medications to lower uric acid levels and dietary modifications.
Tetramisole is an anthelmintic drug, which is used to treat infections caused by certain parasitic worms. It is an equimolar mixture of two stereoisomers, levamisole and dexamisole. Levamisole is the active ingredient that has antiparasitic properties.
Levamisole works by paralyzing the worms in the gut, which leads to their expulsion from the body. It is used to treat a variety of parasitic worm infestations, including roundworm, hookworm, and whipworm infections. In addition to its anthelmintic properties, levamisole has also been found to have immunomodulatory effects and has been used off-label in the treatment of some cancers and autoimmune disorders.
It is important to note that tetramisole/levamisole should only be used under the supervision of a healthcare provider, as it can have serious side effects if not used properly.
Calcinosis is a medical condition characterized by the abnormal deposit of calcium salts in various tissues of the body, commonly under the skin or in the muscles and tendons. These calcium deposits can form hard lumps or nodules that can cause pain, inflammation, and restricted mobility. Calcinosis can occur as a complication of other medical conditions, such as autoimmune disorders, kidney disease, and hypercalcemia (high levels of calcium in the blood). In some cases, the cause of calcinosis may be unknown. Treatment for calcinosis depends on the underlying cause and may include medications to manage calcium levels, physical therapy, and surgical removal of large deposits.
Joint diseases is a broad term that refers to various conditions affecting the joints, including but not limited to:
1. Osteoarthritis (OA): A degenerative joint disease characterized by the breakdown of cartilage and underlying bone, leading to pain, stiffness, and potential loss of function.
2. Rheumatoid Arthritis (RA): An autoimmune disorder causing inflammation in the synovial membrane lining the joints, resulting in swelling, pain, and joint damage if left untreated.
3. Infectious Arthritis: Joint inflammation caused by bacterial, viral, or fungal infections that spread through the bloodstream or directly enter the joint space.
4. Gout: A type of arthritis resulting from the buildup of uric acid crystals in the joints, typically affecting the big toe and characterized by sudden attacks of severe pain, redness, and swelling.
5. Psoriatic Arthritis (PsA): An inflammatory joint disease associated with psoriasis, causing symptoms such as pain, stiffness, and swelling in the joints and surrounding tissues.
6. Juvenile Idiopathic Arthritis (JIA): A group of chronic arthritis conditions affecting children, characterized by joint inflammation, pain, and stiffness.
7. Ankylosing Spondylitis: A form of arthritis primarily affecting the spine, causing inflammation, pain, and potential fusion of spinal vertebrae.
8. Bursitis: Inflammation of the fluid-filled sacs (bursae) that cushion joints, leading to pain and swelling.
9. Tendinitis: Inflammation or degeneration of tendons, which connect muscles to bones, often resulting in pain and stiffness near joints.
These conditions can impact the function and mobility of affected joints, causing discomfort and limiting daily activities. Proper diagnosis and treatment are essential for managing joint diseases and preserving joint health.
Osteoarthritis (OA) is a type of joint disease that is characterized by the breakdown and eventual loss of cartilage - the tissue that cushions the ends of bones where they meet in the joints. This breakdown can cause the bones to rub against each other, causing pain, stiffness, and loss of mobility. OA can occur in any joint, but it most commonly affects the hands, knees, hips, and spine. It is often associated with aging and can be caused or worsened by obesity, injury, or overuse.
The medical definition of osteoarthritis is: "a degenerative, non-inflammatory joint disease characterized by the loss of articular cartilage, bone remodeling, and the formation of osteophytes (bone spurs). It is often associated with pain, stiffness, and decreased range of motion in the affected joint."
Dura Mater: The tough, outer membrane that covers the brain and spinal cord.
Hydroxyapatite: A naturally occurring mineral form of calcium apatite, also known as dahllite, with the formula Ca5(PO4)3(OH), is the primary mineral component of biological apatites found in bones and teeth.
Therefore, "Durapatite" isn't a recognized medical term, but it seems like it might be a combination of "dura mater" and "hydroxyapatite." If you meant to ask about a material used in medical or dental applications that combines properties of both dura mater and hydroxyapatite, please provide more context.
The knee joint, also known as the tibiofemoral joint, is the largest and one of the most complex joints in the human body. It is a synovial joint that connects the thighbone (femur) to the shinbone (tibia). The patella (kneecap), which is a sesamoid bone, is located in front of the knee joint and helps in the extension of the leg.
The knee joint is made up of three articulations: the femorotibial joint between the femur and tibia, the femoropatellar joint between the femur and patella, and the tibiofibular joint between the tibia and fibula. These articulations are surrounded by a fibrous capsule that encloses the synovial membrane, which secretes synovial fluid to lubricate the joint.
The knee joint is stabilized by several ligaments, including the medial and lateral collateral ligaments, which provide stability to the sides of the joint, and the anterior and posterior cruciate ligaments, which prevent excessive forward and backward movement of the tibia relative to the femur. The menisci, which are C-shaped fibrocartilaginous structures located between the femoral condyles and tibial plateaus, also help to stabilize the joint by absorbing shock and distributing weight evenly across the articular surfaces.
The knee joint allows for flexion, extension, and a small amount of rotation, making it essential for activities such as walking, running, jumping, and sitting.
Thiamine pyrophosphate (TPP) is the active form of thiamine (vitamin B1) that plays a crucial role as a cofactor in various enzymatic reactions, particularly in carbohydrate metabolism. TPP is essential for the functioning of three key enzymes: pyruvate dehydrogenase, alpha-ketoglutarate dehydrogenase, and transketolase. These enzymes are involved in critical processes such as the conversion of pyruvate to acetyl-CoA, the oxidative decarboxylation of alpha-ketoglutarate in the Krebs cycle, and the pentose phosphate pathway, which is important for generating reducing equivalents (NADPH) and ribose sugars for nucleotide synthesis. A deficiency in thiamine or TPP can lead to severe neurological disorders, including beriberi and Wernicke-Korsakoff syndrome, which are often observed in alcoholics due to poor nutrition and impaired thiamine absorption.
Articular cartilage is the smooth, white tissue that covers the ends of bones where they come together to form joints. It provides a cushion between bones and allows for smooth movement by reducing friction. Articular cartilage also absorbs shock and distributes loads evenly across the joint, protecting the bones from damage. It is avascular, meaning it does not have its own blood supply, and relies on the surrounding synovial fluid for nutrients. Over time, articular cartilage can wear down or become damaged due to injury or disease, leading to conditions such as osteoarthritis.
Arthritis is a medical condition characterized by inflammation in one or more joints, leading to symptoms such as pain, stiffness, swelling, and reduced range of motion. There are many different types of arthritis, including osteoarthritis, rheumatoid arthritis, psoriatic arthritis, gout, and lupus, among others.
Osteoarthritis is the most common form of arthritis and is caused by wear and tear on the joints over time. Rheumatoid arthritis, on the other hand, is an autoimmune disorder in which the body's immune system mistakenly attacks the joint lining, causing inflammation and damage.
Arthritis can affect people of all ages, including children, although it is more common in older adults. Treatment for arthritis may include medications to manage pain and reduce inflammation, physical therapy, exercise, and in some cases, surgery.
Hydroxyapatite is a calcium phosphate mineral that makes up about 70% of the inorganic component of bone and teeth in humans and other animals. It has the chemical formula Ca10(PO4)6(OH)2. Hydroxyapatite is a naturally occurring mineral form of calcium apatite, with the idealized crystal structure consisting of alternating calcium and phosphate layers.
In addition to its natural occurrence in bone and teeth, hydroxyapatite has various medical applications due to its biocompatibility and osteoconductive properties. It is used as a coating on orthopedic implants to promote bone growth and integration with the implant, and it is also used in dental and oral healthcare products for remineralization of tooth enamel. Furthermore, hydroxyapatite has been studied for its potential use in drug delivery systems, tissue engineering, and other biomedical applications.
Technetium Tc 99m Pyrophosphate (Tc-99m PYP) is a radiopharmaceutical agent used in nuclear medicine imaging, specifically myocardial perfusion imaging. It is a complex of technetium-99m, a metastable isotope of technetium, with pyrophosphate, a molecule that accumulates in damaged heart muscle tissue.
When injected into the patient's bloodstream, Tc-99m PYP is taken up by the heart muscle in proportion to its blood flow and the degree of damage or scarring (fibrosis). This allows for the detection and evaluation of conditions such as myocardial infarction (heart attack), cardiomyopathy, and heart transplant rejection.
The imaging procedure involves the injection of Tc-99m PYP, followed by the acquisition of images using a gamma camera, which detects the gamma rays emitted by the technetium-99m isotope. The resulting images provide information about the distribution and extent of heart muscle damage, helping physicians to make informed decisions regarding diagnosis and treatment planning.
Calcium signaling is the process by which cells regulate various functions through changes in intracellular calcium ion concentrations. Calcium ions (Ca^2+^) are crucial second messengers that play a critical role in many cellular processes, including muscle contraction, neurotransmitter release, gene expression, and programmed cell death (apoptosis).
Intracellular calcium levels are tightly regulated by a complex network of channels, pumps, and exchangers located on the plasma membrane and intracellular organelles such as the endoplasmic reticulum (ER) and mitochondria. These proteins control the influx, efflux, and storage of calcium ions within the cell.
Calcium signaling is initiated when an external signal, such as a hormone or neurotransmitter, binds to a specific receptor on the plasma membrane. This interaction triggers the opening of ion channels, allowing extracellular Ca^2+^ to flow into the cytoplasm. In some cases, this influx of calcium ions is sufficient to activate downstream targets directly. However, in most instances, the increase in intracellular Ca^2+^ serves as a trigger for the release of additional calcium from internal stores, such as the ER.
The release of calcium from the ER is mediated by ryanodine receptors (RyRs) and inositol trisphosphate receptors (IP3Rs), which are activated by specific second messengers generated in response to the initial external signal. The activation of these channels leads to a rapid increase in cytoplasmic Ca^2+^, creating a transient intracellular calcium signal known as a "calcium spark" or "calcium puff."
These localized increases in calcium concentration can then propagate throughout the cell as waves of elevated calcium, allowing for the spatial and temporal coordination of various cellular responses. The duration and amplitude of these calcium signals are finely tuned by the interplay between calcium-binding proteins, pumps, and exchangers, ensuring that appropriate responses are elicited in a controlled manner.
Dysregulation of intracellular calcium signaling has been implicated in numerous pathological conditions, including neurodegenerative diseases, cardiovascular disorders, and cancer. Therefore, understanding the molecular mechanisms governing calcium homeostasis and signaling is crucial for the development of novel therapeutic strategies targeting these diseases.
Polyisoprenyl phosphates are a type of organic compound that play a crucial role in the biosynthesis of various essential biomolecules in cells. They are formed by the addition of isoprene units, which are five-carbon molecules with a branched structure, to a phosphate group.
In medical terms, polyisoprenyl phosphates are primarily known for their role as intermediates in the biosynthesis of dolichols and farnesylated proteins. Dolichols are long-chain isoprenoids that function as lipid carriers in the synthesis of glycoproteins, which are proteins that contain carbohydrate groups attached to them. Farnesylated proteins, on the other hand, are proteins that have been modified with a farnesyl group, which is a 15-carbon isoprenoid. This modification plays a role in the localization and function of certain proteins within the cell.
Abnormalities in the biosynthesis of polyisoprenyl phosphates and their downstream products have been implicated in various diseases, including cancer, neurological disorders, and genetic syndromes. Therefore, understanding the biology and regulation of these compounds is an active area of research with potential therapeutic implications.
Phosphoribosyl Pyrophosphate (PRPP) is defined as a key intracellular nucleotide metabolite that plays an essential role in the biosynthesis of purine and pyrimidine nucleotides, which are the building blocks of DNA and RNA. PRPP is synthesized from ribose 5-phosphate and ATP by the enzyme PRPP synthase. It contributes a phosphoribosyl group in the conversion of purines and pyrimidines to their corresponding nucleotides, which are critical for various cellular processes such as DNA replication, repair, and gene expression. Abnormal levels of PRPP have been implicated in several genetic disorders, including Lesch-Nyhan syndrome and PRPP synthetase superactivity.
Dental caries, also known as tooth decay or cavities, refers to the damage or breakdown of the hard tissues of the teeth (enamel, dentin, and cementum) due to the activity of acid-producing bacteria. These bacteria ferment sugars from food and drinks, producing acids that dissolve and weaken the tooth structure, leading to cavities.
The process of dental caries development involves several stages:
1. Demineralization: The acidic environment created by bacterial activity causes minerals (calcium and phosphate) to be lost from the tooth surface, making it weaker and more susceptible to decay.
2. Formation of a white spot lesion: As demineralization progresses, a chalky white area appears on the tooth surface, indicating early caries development.
3. Cavity formation: If left untreated, the demineralization process continues, leading to the breakdown and loss of tooth structure, resulting in a cavity or hole in the tooth.
4. Infection and pulp involvement: As the decay progresses deeper into the tooth, it can reach the dental pulp (the soft tissue containing nerves and blood vessels), causing infection, inflammation, and potentially leading to toothache, abscess, or even tooth loss.
Preventing dental caries involves maintaining good oral hygiene, reducing sugar intake, using fluoride toothpaste and mouthwash, and having regular dental check-ups and cleanings. Early detection and treatment of dental caries can help prevent further progression and more severe complications.
Fluorides are ionic compounds that contain the fluoride anion (F-). In the context of dental and public health, fluorides are commonly used in preventive measures to help reduce tooth decay. They can be found in various forms such as sodium fluoride, stannous fluoride, and calcium fluoride. When these compounds come into contact with saliva, they release fluoride ions that can be absorbed by tooth enamel. This process helps to strengthen the enamel and make it more resistant to acid attacks caused by bacteria in the mouth, which can lead to dental caries or cavities. Fluorides can be topically applied through products like toothpaste, mouth rinses, and fluoride varnishes, or systemically ingested through fluoridated water, salt, or supplements.
Fluoridation is the process of adding fluoride to a public water supply to reduce tooth decay. The level of fluoride that is typically added to the water is regulated and maintained at around 0.7-1.2 parts per million (ppm), which has been shown to be effective in reducing dental caries while minimizing the risk of fluorosis, a cosmetic condition caused by excessive fluoride intake during tooth development.
Fluoridation can also refer to the process of applying fluoride to the teeth through other means, such as topical fluoride applications in dental offices or the use of fluoride toothpaste. However, community water fluoridation is the most common and cost-effective method of delivering fluoride to a large population.
The practice of water fluoridation has been endorsed by numerous public health organizations, including the World Health Organization (WHO), the Centers for Disease Control and Prevention (CDC), and the American Dental Association (ADA). Despite some controversy surrounding the practice, extensive research has consistently shown that community water fluoridation is a safe and effective way to prevent tooth decay and improve oral health.
Dental fluorosis is a developmental disturbance of dental enamel caused by excessive exposure to fluoride during tooth development. It is characterized by hypomineralization of the enamel, resulting in various appearances ranging from barely noticeable white spots to brown staining and pitting of the teeth. The severity depends on the amount, duration, and timing of fluoride intake, as well as individual susceptibility. Mild dental fluorosis is typically asymptomatic but can affect the appearance of teeth, while severe cases may cause tooth sensitivity and increased susceptibility to tooth decay.
I'm sorry for any confusion, but "toothpastes" is the plural form of "toothpaste," which is not a medical condition or procedure that requires a definition. However, I can provide you with some information about toothpaste.
Toothpaste is a dental hygiene product used to clean and maintain the health of teeth and gums. It generally contains mild abrasives, flavoring, and fluoride to help remove plaque, prevent tooth decay, and freshen breath. There are various types of toothpastes available on the market, including those formulated for sensitive teeth, whitening, gum health, and tartar control. It is essential to choose a toothpaste that meets your specific dental needs and has the American Dental Association (ADA) Seal of Acceptance, ensuring its safety and effectiveness.
Cariostatic agents are substances or medications that are used to prevent or inhibit the development and progression of dental caries, also known as tooth decay or cavities. These agents work by reducing the ability of bacteria in the mouth to produce acid, which can erode the enamel and dentin of the teeth and lead to cavities.
There are several types of cariostatic agents that are commonly used in dental care, including:
1. Fluorides: These are the most widely used and well-studied cariostatic agents. They work by promoting the remineralization of tooth enamel and making it more resistant to acid attacks. Fluoride can be found in toothpaste, mouthwashes, gels, varnishes, and fluoridated water supplies.
2. Antimicrobial agents: These substances work by reducing the population of bacteria in the mouth that contribute to tooth decay. Examples include chlorhexidine, triclosan, and xylitol.
3. Casein phosphopeptide-amorphous calcium phosphate (CPP-ACP): This is a complex protein that has been shown to help remineralize tooth enamel and reduce the risk of dental caries. It can be found in some toothpastes and mouthwashes.
4. Silver diamine fluoride: This is a topical fluoride compound that contains silver ions, which have antimicrobial properties. It has been shown to be effective in preventing and arresting dental caries, particularly in high-risk populations such as young children and older adults with dry mouth.
It's important to note that while cariostatic agents can help reduce the risk of tooth decay, they are not a substitute for good oral hygiene practices such as brushing twice a day, flossing daily, and visiting the dentist regularly.
I'm not aware of a medical definition for "DMF Index." The abbreviation "DMF" could potentially stand for many things, as it is used in various contexts across different fields. In the field of dentistry, DMF stands for Decayed, Missing, and Filled teeth/surfaces, which is a method for measuring dental caries or tooth decay. However, there is no standard medical definition for "DMF Index." If you could provide more context or specify the field of study or practice, I would be happy to help further!
Calcium pyrophosphate
Calcium pyrophosphate dihydrate crystal deposition disease
Nicola Dalbeth
ACDC (medicine)
Birefringence
Neodymium(III) phosphate
ANKH
Mineralogy
Chondrocalcinosis
Synovial fluid
Pyrophosphate
Crystal arthropathy
ADCY2
Arthrocentesis
Hypophosphatasia
Rhomboid
Pyrophosphoric acid
Milwaukee shoulder syndrome
Gobihadros
Arthritis
Joint
Rail transport in Nauru
CILP
2021 in archosaur paleontology
Glyptotherium
Condenser (optics)
Anakinra
Monoarthritis
Technetium-99m
NOD-like receptor
Calcium pyrophosphate - Wikipedia
Diseases associated with calcium pyrophosphate deposition disease
Calcium Pyrophosphate Deposition (CPPD) Disease: Practice Essentials, Etiology, Epidemiology
Calcium Pyrophosphate Deposition (CPPD) Disease Clinical Presentation: History, Physical Examination, Complications
Pathology Outlines - Calcium pyrophosphate crystal deposition disease
Craniocervical Junction Calcium Pyrophosphate Deposition Causing Hypoglossal Nerve Palsy. - International Association for the...
Patterns of radiographic abnormalities associated with basic calcium phosphate and calcium pyrophosphate dihydrate crystal...
Ferric Pyrophosphate manufacturer in India | Mineral Active Manufacturer | Global Calcium
Calcium Pyrophosphate (CPP) Arthritis - Bone, Joint, and Muscle Disorders - MSD Manual Consumer Version
Calcium Pyrophosphate Deposition (CPPD) - The Rheumatology Lab
Pseudogout - Calcium Pyrophosphate Deposition
Imaging in Calcium Pyrophosphate Deposition Disease: Overview, Radiography, Computed Tomography
Repositório Institucional da Universidade de Aveiro: Influence of Mg-doping, calcium pyrophosphate impurities and cooling rate...
Fever with acute arthritis in calcium pyrophosphate dihydrate deposition disease: a missed explanation for altered mental...
Evaluation of Calcium Pyrophosphate Dihydrate Deposition Disease by Ultrasound<...
Diagnosis and Treatment of Calcium Pyrophosphate Deposition (CPPD) Disease: A Review. | Read by QxMD
Periarticular calcium pyrophosphate deposition disease in a young patient: a case report - Health, Sports & Rehabilitation...
Evaluation of crystals in formalin-fixed, paraffin-embedded tissue sections for the differential diagnosis of pseudogout, gout,...
Bone Mineral Density News, Research
Effect of EHDP on calcium accumulation and technetium-99m pyrophosphate uptake in experimental myocardial infarction<...
GAIN OF FUNCTION ANKH VARIANTS CAUSE BOTH FAMILIAL AND SPORADIC CALCIUM PYROPHOSPHATE DIHYDRATE CHONDROCALCINOSIS - Nuffield...
Ultrasound imaging for the rheumatologist. XXV. Sonographic assessment of the knee in patients with gout and calcium...
Gout is caused by monosodium urate monohydrate crystals; pseudogout is caused by calcium pyrophosphate (CPP) crystals and is...
Pseudogout: Calcium Pyrophosphate Deposition (CPPD) Like gout, pseudogout is caused by a build-up of microscopic crystals in a...
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Canakinumab (Ilaris) - Medical Clinical Policy Bulletins | Aetna
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Pseudoxanthoma elasticum: MedlinePlus Genetics
CPPD30
- Crystals of the tetrahydrate can be prepared by reacting sodium pyrophosphate, Na4P2O7 with calcium nitrate, Ca(NO3)2, at carefully controlled pH and temperature: Na4P2O7(aq)+2 Ca(NO3)2(aq)→ Ca2P2O7·4 H2O + 4 NaNO3 The dihydrate, sometimes termed CPPD, can be formed by the reaction of pyrophosphoric acid with calcium chloride:[citation needed] CaCl2 + H4P2O7(aq) → Ca2P2O7·2 H2O + HCl. (wikipedia.org)
- Calcium pyrophosphate deposition (CPPD) disease is a metabolic arthropathy caused by the deposition of calcium pyrophosphate dihydrate in and around joints, especially in articular cartilage and fibrocartilage (see the images below). (medscape.com)
- Although the exact mechanism for the development of CPPD remains unknown, increased adenosine triphosphate breakdown with resultant increased inorganic pyrophosphate in the joints results from aging, genetic factors, or both. (medscape.com)
- Therefore, inorganic pyrophosphate can bind calcium, leading to CPPD deposition in the cartilage and synovium. (medscape.com)
- Radiographs and synovial fluids from 66 knees representing 59 patients with symptomatic osteoarthritis were evaluated to determine the pattern of radiographic abnormalities associated with basic calcium phosphate (BCP), calcium pyrophosphate dihydrate (CPPD), or both crystals together. (bmj.com)
- In CPPD, calcium pyrophosphate (CPP) crystals form in the blood and settle in joint Crystal deposits trigger an inflammatory attack in the joint. (rheumlab.org)
- Phosphate-to-pyrophosphate ratios less than 3 result in CPPD formation. (medscape.com)
- Formation of CPPD crystals requires levels of pyrophosphate 10-40 times normal serum levels. (medscape.com)
- Calcium pyrophosphate dihydrate (CPPD) deposition disease is a relatively common condition primarily affecting the elderly. (qxmd.com)
- Objective: Our aim was to characterize the ultrasonographic features of patients with calcium pyrophosphate dihydrate (CPPD) deposition disease, and compare X-ray and ultrasound in evaluating CPPD deposition disease. (tmu.edu.tw)
- Diagnosis and Treatment of Calcium Pyrophosphate Deposition (CPPD) Disease: A Review. (qxmd.com)
- Calcium Pyrophosphate Dihydrate (CPPD) crystal-related arthropathies are a common cause of acute and chronic arthritis caused by the deposition of calcium pyrophosphate crystals in joints and soft tissues, resulting in inflammation and joint damage. (qxmd.com)
- Calcium pyrophosphate deposition disease (CPPD) is an arthropathy that affects the synovium and periarticular tissues. (jhsrm.org)
- Only two H&E-stained sections showed scant calcium pyrophosphate dihydrate (CPPD) crystals in pseudogout. (nih.gov)
- However, polarizing microscopy of sections stained with NAES method allowed demonstration of CPPD crystals with positive birefringence in pseudogout, MSU crystals with negative birefringence in gout, and calcium hydroxyapatite crystals without birefringence in tumoral calcinosis. (nih.gov)
- The knee is a frequent target for gout and calcium pyrophosphate dihydrate (CPPD) disease with involvement of both articular and peri-articular structures. (unimib.it)
- pseudogout is caused by calcium pyrophosphate dehydrate crystals (CPPD). (vesflot.ru)
- Pseudogout's medical name is calcium pyrophosphate deposition (CPPD) disease. (vesflot.ru)
- Calcium pyrophosphate deposition (CPPD)also known as "pseudogout" is a type of arthritis. (vesflot.ru)
- In CPPD, calcium pyrophosphate (CPP) crystals form in the blood. (vesflot.ru)
- Pseudogout is also called calcium pyrophosphate deposition or CPPD. (vesflot.ru)
- Pseudogout is caused by the deposition of calcium pyrophosphate dihydrate (CPPD) crystals in the joints. (vesflot.ru)
- Gout and pseudogout (also called calcium pyrophosphate deposition disease, or CPPD) are forms of arthritis which cause sudden and extremely painful attacks. (vesflot.ru)
- In pseudogout, or CPPD, crystals of pyrophosphate dihydrate form in your joints causing pain. (vesflot.ru)
- Calcium Pyrophosphate Deposition (CPPD) also known as Pseudogout, is a joint problem caused by crystals of calcium salt called Pyrophosphate that are deposited. (vesflot.ru)
- Pseudogout: Calcium Pyrophosphate Deposition (CPPD) Like gout, pseudogout is caused by a build-up of microscopic crystals in a joint and can lead to sudden. (vsmira.ru)
- Gout symptoms can be confused with another type of arthritis called calcium pyrophosphate deposition (CPPD) , formerly called pseudogout. (arthritis.org)
- However, the crystals that irritate the joint in CPPD are calcium phosphate crystals, not the uric acid crystals that cause gout. (arthritis.org)
- Modality: X-Ray Diagnosis: CPPD Key Points: Calcium pyrophosphate dihydrate disease (CPPD). (radrounds.com)
- However, hydroxyapatite (HA) ( calcific tendonitis ) or calcium pyrophosphate (CPPD) ( pseudogout ), though rare in this location, were also possibilities. (medscape.com)
Gout12
- Deposition of dihydrate crystals in cartilage are responsible for the severe joint pain in cases of calcium pyrophosphate deposition disease (pseudo gout) whose symptoms are similar to those of gout. (wikipedia.org)
- Calcium pyrophosphate (CPP) arthritis (previously called pseudogout) is a disorder caused by deposits of calcium pyrophosphate dihydrate crystals in the joint cartilage, leading to intermittent attacks of painful joint inflammation similar to gout or a chronic arthritis similar to rheumatoid arthritis. (msdmanuals.com)
- Pseudogout involves acute, gout-like, inflammatory attacks that occur secondary to calcium pyrophosphate dihydrate crystal deposition within joints. (vesflot.ru)
- Gout and pseudogout are crystal arthropathies · Crystals of urate (in gout) and calcium pyrophosphate (in pseudogout) are precipitated in joints · Neutrophils. (vesflot.ru)
- Pseudogout refers to gout-like attacks, characterized by acute localized pain and swelling, that occur in patients with calcium crystal deposits in the. (vesflot.ru)
- Pseudogout (SOO-doe-gout) is a form of arthritis caused by calcium pyrophosphate crystal deposits in a joint, most commonly the knee. (vesflot.ru)
- Gout and pseudogout-calcium pyrophosphate deposition disease. (vesflot.ru)
- The buildup of crystals in gout is triggered by elevated levels of uric acid, while pseudogout is caused by a buildup of calcium pyrophosphate dihydrate. (vesflot.ru)
- Gout also causes joint pain and swelling, but is caused by a buildup of uric acid instead of calcium crystals. (vesflot.ru)
- Differentiate between gout and pyrophosphate deposition disease. (continuingeducation.net)
- While gout is caused by crystals formed from uric acid, pseudogout is the result of calcium crystals. (hss.edu)
- Both are forms of inflammatory arthritis, but gout joint inflammation is caused by uric acid crystals, while pseudogout joint inflammation is caused by crystals formed from calcium pyrophosphate dihydrate. (hss.edu)
Disease16
- Moeen S, Qureshi MB, Ud Din N. Calcium pyrophosphate crystal deposition disease. (pathologyoutlines.com)
- Ferric pyrophosphate is an iron replacement product intended for the treatment of iron loss or iron deficiency in patients with chronic kidney disease and pregnant ladies. (globalcalcium.com)
- Calcium pyrophosphate deposition disease (CPDD) is a type of arthritis caused by the deposition of calcium pyrophosphate crystals. (medscape.com)
- Calcium pyrophosphate deposition disease (CPDD) is divided into several varieties, primarily pseudogout and chondrocalcinosis. (medscape.com)
- Periarticular metacarpophalangeal and interphalangeal joint calcification may be a component of that form of calcium pyrophosphate deposition disease (CPDD). (medscape.com)
- These cysts are not specific for calcium pyrophosphate deposition disease. (medscape.com)
- Pseudorheumatoid calcium pyrophosphate deposition disease (CPDD) has a polyarticular character. (medscape.com)
- Crumbling-type erosions of calcium pyrophosphate deposition disease in the metacarpophalangeal and proximal and distal interphalangeal joints. (medscape.com)
- The skeletal and clinical distribution pattern of nonerosive components of primary calcium pyrophosphate deposition disease (CPDD) are shown in the table below. (medscape.com)
- Fever with acute arthritis in calcium pyrophosphate dihydrate deposition disease: a missed explanation for altered mental status in elderly patients? (qxmd.com)
- The presented case highlights the importance of imaging examinations and aspirate analysis using optical microscopy in establishing the positive diagnosis of calcium pyrophosphate deposition disease. (jhsrm.org)
- Researchers will present the first-ever study of fractures and calcium pyrophosphate deposition disease at ACR Convergence 2023, the American College of Rheumatology's annual meeting. (news-medical.net)
- Secondary hyperparathyroidism develops when there are conditions like chronic kidney disease , which can lead to low calcium, high phosphate, and low vitamin D levels. (osmosis.org)
- Pseudogout, or calcium pyrophosphate deposition disease (CPDD), is a form of inflammatory arthritis caused by crystals that form in the joints. (hss.edu)
- Calcium pyrophosphate disease and polymyalgia reumatica: association or coincidence? (bvsalud.org)
- Comment on "Ultrasound shoulder assessment of calcium pyrophosphate disease with suspected polymyalgia rheumatica" Ottaviani et al. (bvsalud.org)
Arthritis3
- Synovial calcium pyrophosphate crystals, seen on polarizing microscopy, characterize pseudogout, an acute goutlike arthritis. (medscape.com)
- Pseudogout is a type of inflammation of joints (arthritis) that is caused by deposits of crystals, called calcium pyrophosphate, in and around the joints. (vesflot.ru)
- Pseudogout is a type of inflammatory arthritis that causes joint inflammation due to the body depositing calcium pyrophosphate crystals in the joint and. (vesflot.ru)
Deposition of calcium1
- Pyrophosphate helps control deposition of calcium and other minerals in the body. (medlineplus.gov)
Ferric pyrophosphate3
- The usage of ferric pyrophosphate is based on the strong complex formation between the two species. (globalcalcium.com)
- The Increase in solubility for ferric pyrophosphate is attributed to the formation of soluble complexes between Fe (III) and pyrophosphate ions. (globalcalcium.com)
- Ferric pyrophosphate is a widely used iron source in food fortification and in nutritional supplements, due to its white color, which is very uncommon for Fe salts. (globalcalcium.com)
Inorganic pyrophosphate1
- The ANKH protein is involved in transport of inorganic pyrophosphate (PPi), which regulates calcification, bone mineralization, and bone resorption. (medscape.com)
Articular1
- This can be recognized grossly as a calcified sheet reflecting over the articular surface and as concretions of calcium pyrophosphate exuded beyond the subchondral articular surface. (medscape.com)
Phosphate2
- Patterns of radiographic abnormalities associated with basic calcium phosphate and calcium pyrophosphate dihydrate crystal deposition in the knee. (bmj.com)
- Alpha and beta-tricalcium phosphates are allotropic phases which play a very important role as bone graft substitutes, namely in calcium phosphate cements. (ua.pt)
Pseudogout is caused1
- pseudogout is caused by calcium pyrophosphate (CPP) crystals and is more accurately termed calcium. (vesflot.ru)
Calcification1
- These findings suggests that calcification inhibitors, and possibly other calcium-blocking agents, may alter the sensitivity of Tc-99m PYP myocardial scintigraphy, but the specific effects of each calcium antagonist must be evaluated. (elsevierpure.com)
Crystal3
- Although many metabolic and endocrine diseases have been reported to predispose to calcium pyrophosphate dihydrate crystal deposition, the validity of many of these associations remains unclear. (nih.gov)
- Calcium Pyrophosphate Crystal Size and characteristics. (uclahealth.org)
- Calcium pyrophosphate crystal deposition in a cohort of 57 patients with Gitelman syndrome. (cdc.gov)
Known as calcium1
- Also known as calcium pyrophosphate. (vesflot.ru)
Hydroxyapatite2
- The role of calcium pyrophosphate impurities derived from a certain calcium-deficiency, hydroxyapatite impurities derived from calcium excess, and various ionic substitutions on thermal stability of these phases was not yet fully disclosed. (ua.pt)
- the atypical location of a single calcium pyrophosphate deposition in the supraspinatus tendon, a tendon that is usually correlated with hydroxyapatite deposition. (jhsrm.org)
Extracellular2
- Now, the majority of the extracellular calcium, the calcium in the blood and interstitium , is split almost equally between two groups - calcium that is diffusible and calcium that is not diffusible. (osmosis.org)
- Changes in the body 's levels of extracellular calcium are detected by a surface receptor in parathyroid cells that's called the calcium-sensing receptor. (osmosis.org)
Salt1
- Calcium pyrophosphate (Ca2P2O7) is a chemical compound, an insoluble calcium salt containing the pyrophosphate anion. (wikipedia.org)
Accumulation2
- Pseudoxanthoma elasticum (PXE) is a progressive disorder that is characterized by the accumulation of deposits of calcium and other minerals (mineralization) in elastic fibers. (medlineplus.gov)
- Alternatively, a lack of functioning MRP6 may impair the transport of a substance that would normally prevent mineralization, leading to the abnormal accumulation of calcium and other minerals characteristic of PXE. (medlineplus.gov)
Neutrophils1
- Gram stain demonstrated the presence of few, thin, gram-negative bacilli with pyrophosphate calcium crystals and neutrophils ( Figure ). (cdc.gov)
Citrate1
- DB are visualized in unfixed, unstained, whole mount EM preparations due to their calcium content or by staining platelets with lead citrate and uranyl acetate. (medscape.com)
Regulates1
- Hyperparathyroidism is a condition in which the parathyroid glands produce too much parathyroid hormone (PTH), which regulates calcium levels in the blood. (osmosis.org)
Adenosine1
- ATP can be broken down into other molecules, including adenosine monophosphate (AMP) and pyrophosphate. (medlineplus.gov)
Deposits1
- However, calcium deposits in a joint may not cause symptoms. (msdmanuals.com)
Serum1
- Events that affect serum calcium levels also may precipitate attacks of pseudogout. (medscape.com)
Parathyroid hormone1
- Parathyroid hormone comes from the parathyroid glands which are buried within the thyroid gland , and their main job is to keep blood calcium levels stable. (osmosis.org)
Hypercalcemia2
- Hyperparathyroidism In hypercalcemia, the level of calcium in blood is too high. (msdmanuals.com)
- It is characterized by excess PTH that leads to high blood calcium levels ( hypercalcemia ), bone mass loss, kidney stones , and other health problems, such as psychiatric issues. (osmosis.org)
Form1
- If someone develops pseudogout, they form and react to calcium pyrophosphate (CPP). (vesflot.ru)