American Native Continental Ancestry Group
European Continental Ancestry Group
African Continental Ancestry Group
Asian Continental Ancestry Group
Oceanic Ancestry Group
European Union
Polymorphism, Single Nucleotide
Genetics, Population
Genome-Wide Association Study
Genotype
Haplotypes
Gene Frequency
Gene Pool
Genetic Predisposition to Disease
African Americans
Indians, South American
Genetic Loci
Linkage Disequilibrium
Ethnic Groups
Alleles
Trinidad and Tobago
Genome, Human
Genetic Markers
Heart rate and subsequent blood pressure in young adults: the CARDIA study. (1/13036)
The objective of the present study was to examine the hypothesis that baseline heart rate (HR) predicts subsequent blood pressure (BP) independently of baseline BP. In the multicenter longitudinal Coronary Artery Risk Development in Young Adults study of black and white men and women initially aged 18 to 30 years, we studied 4762 participants who were not current users of antihypertensive drugs and had no history of heart problems at the baseline examination (1985-1986). In each race-sex subgroup, we estimated the effect of baseline HR on BP 2, 5, 7, and 10 years later by use of repeated measures regression analysis, adjusting for baseline BP, age, education, body fatness, physical fitness, fasting insulin, parental hypertension, cigarette smoking, alcohol consumption, oral contraceptive use, and change of body mass index from baseline. The association between baseline HR and subsequent systolic BP (SBP) was explained by multivariable adjustment. However, HR was an independent predictor of subsequent diastolic BP (DBP) regardless of initial BP and other confounders in white men, white women, and black men (0.7 mm Hg increase per 10 bpm). We incorporated the part of the association that was already present at baseline by not adjusting for baseline DBP: the mean increase in subsequent DBP was 1.3 mm Hg per 10 bpm in white men, white women, and black men. A high HR may be considered a risk factor for subsequent high DBP in young persons. (+info)Obstetric and neonatal outcome following chronic hypertension in pregnancy among different ethnic groups. (2/13036)
We retrospectively studied pre-eclampsia rate and obstetric outcome in a cohort of 436 pregnancies amongst 318 women of different ethnic backgrounds attending an antenatal hypertension clinic from 1980-1997, identifying 152 women (213 pregnancies) with chronic essential hypertension. The ethnic breakdown was: White, 64 (30.0%) pregnancies in 48 (31.5%) women; Black/Afro-Caribbean, 79 (37.1%) pregnancies in 56 (36.8%) women; and Indo-Asians, 70 (32.3%) pregnancies in 48 (31.6%) women. The prevalences of pre-eclampsia in White, Black and Indo-Asian women were 17.2%, 12.7% and 18.6%, respectively (p = 0.58). Pregnancies of Indo-Asian women were of shorter gestation, and babies in this group also had lower birth weight and ponderal index compared to those of White and Black women (all p < 0.05). The proportions of overall perinatal mortality were 1.6% for Whites (1/64), 3.8% for Blacks (3/79) and 10.0% for Indo-Asians (7/70), suggesting increased risk in the Indo-Asian group. Indo-Asian women with chronic essential hypertension need careful antenatal care and observation during pregnancy. (+info)Associations of anti-beta2-glycoprotein I autoantibodies with HLA class II alleles in three ethnic groups. (3/13036)
OBJECTIVE: To determine any HLA associations with anti-beta2-glycoprotein I (anti-beta2GPI) antibodies in a large, retrospectively studied, multiethnic group of 262 patients with primary antiphospholipid antibody syndrome (APS), systemic lupus erythematosus (SLE), or another connective tissue disease. METHODS: Anti-beta2GPI antibodies were detected in sera using an enzyme-linked immunosorbent assay. HLA class II alleles (DRB1, DQA1, and DQB1) were determined by DNA oligotyping. RESULTS: The HLA-DQB1*0302 (DQ8) allele, typically carried on HLA-DR4 haplotypes, was associated with anti-beta2GPI when compared with both anti-beta2GPI-negative SLE patients and ethnically matched normal controls, especially in Mexican Americans and, to a lesser extent, in whites. Similarly, when ethnic groups were combined, HLA-DQB1*0302, as well as HLA-DQB1*03 alleles overall (DQB1*0301, *0302, and *0303), were strongly correlated with anti-beta2GPI antibodies. The HLA-DR6 (DR13) haplotype DRB1*1302; DQB1*0604/5 was also significantly increased, primarily in blacks. HLA-DR7 was not significantly increased in any of these 3 ethnic groups, and HLA-DR53 (DRB4*0101) was increased in Mexican Americans only. CONCLUSION: Certain HLA class II haplotypes genetically influence the expression of antibodies to beta2GPI, an important autoimmune response in the APS, but there are variations in HLA associations among different ethnic groups. (+info)Prevalence of hepatitis B surface antigen and antibody in white and black patients with diabetes mellitus. (4/13036)
The prevalence of hepatitis B surface antigen (HBSAg) and antibody (anti-HBS) was determined in 531 white and 519 black diabetic outpatients and in appropriate white and black control populations. There was no difference between the prevalence of either HBSAg or anti-HBS in either the white or black diabetics and that in the white and black controls. These findings make it unlikely that the vast majority of patients with diabetes mellitus have either an increased susceptibility to infection by the hepatitis B virus or an impaired ability to clear the virus once they are infected. (+info)Biochemical indices of osteomalacia in pregnant Asian immigrants in Britain. (5/13036)
Serum calcium, phosphate and alkaline phosphatase, and urinary calcium excretion were examined during the second trimester of uncomplicated normal pregnancy in Asian immigrants to Britain and in local Caucasians. The mean serum calcium was significantly lower in Asians than in Caucasians, and the mean serum alkaline phosphatase was significantly higher in Asians. The geometric mean of the urinary calcium excretion was highly significantly lower in Asians than in Caucasians. The variances of the serum calcium, serum alkaline phosphatase, and urine calcium excretion did not differ significantly in the two populations. This indicates that there is a shift in values of immigrant Asians as a group compared with Caucasians. A comparison with figures obtained on normal nonpregnant persons of both suggests that the shift is not an inherent feature of the Asian population. (+info)Racial differences in the outcome of left ventricular dysfunction. (6/13036)
BACKGROUND: Population-based studies have found that black patients with congestive heart failure have a higher mortality rate than whites with the same condition. This finding has been attributed to differences in the severity, causes, and management of heart failure, the prevalence of coexisting conditions, and socioeconomic factors. Although these factors probably account for some of the higher mortality due to congestive heart failure among blacks, we hypothesized that racial differences in the natural history of left ventricular dysfunction might also have a role. METHODS: Using data from the Studies of Left Ventricular Dysfunction (SOLVD) prevention and treatment trials, in which all patients received standardized therapy and follow-up, we conducted a retrospective analysis of the outcomes of asymptomatic and symptomatic left ventricular systolic dysfunction among black and white participants. The mean (+/-SD) follow-up was 34.2+/-14.0 months in the prevention trial and 32.3+/-14.8 months in the treatment trial among the black and white participants. RESULTS: The overall mortality rates in the prevention trial were 8.1 per 100 person-years for blacks and 5.1 per 100 person years for whites. In the treatment trial, the rates were 16.7 per 100 person-years and 13.4 per 100 person-years, respectively. After adjustment for age, coexisting conditions, severity and causes of heart failure, and use of medications, blacks had a higher risk of death from all causes in both the SOLVD prevention trial (relative risk, 1.36; 95 percent confidence interval, 1.06 to 1.74; P=0.02) and the treatment trial (relative risk, 1.25; 95 percent confidence interval, 1.04 to 1.50; P=0.02). In both trials blacks were also at higher risk for death due to pump failure and for the combined end point of death from any cause or hospitalization for heart failure, our two predefined indicators of the progression of left ventricular systolic dysfunction. CONCLUSIONS: Blacks with mild-to-moderate left ventricular systolic dysfunction appear to be at higher risk for progression of heart failure and death from any cause than similarly treated whites. These results suggest that there may be racial differences in the outcome of asymptomatic and symptomatic left ventricular systolic dysfunction. (+info)The effect of race and sex on physicians' recommendations for cardiac catheterization. (7/13036)
BACKGROUND: Epidemiologic studies have reported differences in the use of cardiovascular procedures according to the race and sex of the patient. Whether the differences stem from differences in the recommendations of physicians remains uncertain. METHODS: We developed a computerized survey instrument to assess physicians' recommendations for managing chest pain. Actors portrayed patients with particular characteristics in scripted interviews about their symptoms. A total of 720 physicians at two national meetings of organizations of primary care physicians participated in the survey. Each physician viewed a recorded interview and was given other data about a hypothetical patient. He or she then made recommendations about that patient's care. We used multivariate logistic-regression analysis to assess the effects of the race and sex of the patients on treatment recommendations, while controlling for the physicians' assessment of the probability of coronary artery disease as well as for the age of the patient, the level of coronary risk, the type of chest pain, and the results of an exercise stress test. RESULTS: The physicians' mean (+/-SD) estimates of the probability of coronary artery disease were lower for women (probability, 64.1+/-19.3 percent, vs. 69.2+/-18.2 percent for men; P<0.001), younger patients (63.8+/-19.5 percent for patients who were 55 years old, vs. 69.5+/-17.9 percent for patients who were 70 years old; P<0.001), and patients with nonanginal pain (58.3+/-19.0 percent, vs. 64.4+/-18.3 percent for patients with possible angina and 77.1+/-14.0 percent for those with definite angina; P=0.001). Logistic-regression analysis indicated that women (odds ratio, 0.60; 95 percent confidence interval, 0.4 to 0.9; P=0.02) and blacks (odds ratio, 0.60; 95 percent confidence interval, 0.4 to 0.9; P=0.02) were less likely to be referred for cardiac catheterization than men and whites, respectively. Analysis of race-sex interactions showed that black women were significantly less likely to be referred for catheterization than white men (odds ratio, 0.4; 95 percent confidence interval, 0.2 to 0.7; P=0.004). CONCLUSIONS: Our findings suggest that the race and sex of a patient independently influence how physicians manage chest pain. (+info)Genetic polymorphism and interethnic variability of plasma paroxonase activity. (8/13036)
A method for determining plasma paroxonase activity using an auto-analyser is described. Frequency distributions for British and Indian subjects show bimodality. A study of 40 British families confirms the presence of a genetic polymorphism with regard to plasma paroxonase activity. Two phenotypes can be defined, controlled by two alleles at one autosomal locus. The frequency of the low activity phenotype is less in the Indian population than in the British population. Malay, Chinese, and African subjects fail to show obvious bimodality. (+info)Explanation: Genetic predisposition to disease is influenced by multiple factors, including the presence of inherited genetic mutations or variations, environmental factors, and lifestyle choices. The likelihood of developing a particular disease can be increased by inherited genetic mutations that affect the functioning of specific genes or biological pathways. For example, inherited mutations in the BRCA1 and BRCA2 genes increase the risk of developing breast and ovarian cancer.
The expression of genetic predisposition to disease can vary widely, and not all individuals with a genetic predisposition will develop the disease. Additionally, many factors can influence the likelihood of developing a particular disease, such as environmental exposures, lifestyle choices, and other health conditions.
Inheritance patterns: Genetic predisposition to disease can be inherited in an autosomal dominant, autosomal recessive, or multifactorial pattern, depending on the specific disease and the genetic mutations involved. Autosomal dominant inheritance means that a single copy of the mutated gene is enough to cause the disease, while autosomal recessive inheritance requires two copies of the mutated gene. Multifactorial inheritance involves multiple genes and environmental factors contributing to the development of the disease.
Examples of diseases with a known genetic predisposition:
1. Huntington's disease: An autosomal dominant disorder caused by an expansion of a CAG repeat in the Huntingtin gene, leading to progressive neurodegeneration and cognitive decline.
2. Cystic fibrosis: An autosomal recessive disorder caused by mutations in the CFTR gene, leading to respiratory and digestive problems.
3. BRCA1/2-related breast and ovarian cancer: An inherited increased risk of developing breast and ovarian cancer due to mutations in the BRCA1 or BRCA2 genes.
4. Sickle cell anemia: An autosomal recessive disorder caused by a point mutation in the HBB gene, leading to defective hemoglobin production and red blood cell sickling.
5. Type 1 diabetes: An autoimmune disease caused by a combination of genetic and environmental factors, including multiple genes in the HLA complex.
Understanding the genetic basis of disease can help with early detection, prevention, and treatment. For example, genetic testing can identify individuals who are at risk for certain diseases, allowing for earlier intervention and preventive measures. Additionally, understanding the genetic basis of a disease can inform the development of targeted therapies and personalized medicine."
Spanish West Indies
Mauritians
Race and ethnicity in Latin America
Race, Evolution, and Behavior
Universal Decimal Classification
Genetic history of the Iberian Peninsula
Other White
List of MeSH codes (M01)
English Americans
Stonehenge
Australians
Genetic history of Europe
Human genetic clustering
Southeast Asia
Demographics of Mauritius
Genealogical DNA test
Race and genetics
Human genetic variation
Blond
South Slavs
Genetic studies on Bosniaks
Y Chromosome Haplotype Reference Database
International English
Anglo-Saxon settlement of Britain
Enrique Iglesias
Haole
Ethnic origins of people in Canada
Knovíz culture
Mary Rose
Jōmon people
KF Skënderbeu Korçë
Marine mammal
Boston
Grover Cleveland
Nicki Minaj
Genetic studies on Serbs
Henry Hastings Sibley
John Ross (Cherokee chief)
Genealogy
Macanese people
Hobart
Tai peoples
List of ancient Germanic peoples
Bergen County, New Jersey
Luso-Asians
History of the nude in art
List of accidents and incidents involving military aircraft before 1925
White Horse Stone
Românul
Dogu'a Tembien
Huns
Baháʼí Faith in North America
New England
List of unsolved deaths
Kingston, Ontario
Demographics of Mexico
Joseph Hewes
The Bahamas
Lottery
Browsing Regional Committee for Europe: 46th session by Subject "European Continental Ancestry Group"
Browsing Regional Committee for Europe: 46th session by Subject
Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families
STRANGE FRUIT | Pandaemonium
Individual Differences in Boys' and Girls' Timing and Tempo of Puberty: Modeling Development With Nonlinear Growth Models -...
Published Research | School of Social Work
DeCS
Mercapturic acids derived from the toxicants acrolein and crotonaldehyde in the urine of cigarette smokers from five ethnic...
Internal Medicine - Research output - Mayo Clinic
Electrocardiograms in Healthy North American Children in the Digital Age - Fingerprint
- Albert Einstein College of...
Published Research | School of Social Work
"Large-scale association analysis identifies new lung cancer susceptibi" by James D McKay, Rayjean J Hung et al.
Alfred and Gail Engelberg Department of Family Medicine and Community Health - Publications & Research Outputs - Icahn...
Francis, L.<...
Further evidence of an engagement-achievement paradox among U.S. high school students - Fingerprint
- Rutgers, The State...
Effects of moderate to vigorous intensity cycling on appetite, ad libitum energy intake and appetite-related hormones in...
Department of Surgery - Research output
- Research Profiles at Washington University School of Medicine
Trends in prevalence of short sleep duration and trouble sleeping among US adults, 2005-2018 - Fingerprint - HSC
Role of Vitamin D Receptor Activation in Racial Disparities in Kidney Disease Outcomes<...
Changing pattern of esophageal cancer incidence in New Mexico<...
Implicit Bias Predicts Liking of Ingroup Members Who Are Comfortable With Intergroup Interaction<...
Predicting intentions to continue exclusive breastfeeding for 6 months: A comparison among racial/ethnic groups<...
Painting the human tree of life | Discover Magazine
DeCS 2011 - December 22, 2011 version
Genomic diversity and admixture differs for Stone-Age Scandinavian foragers and farmers. | Center for Academic Research and...
Pesquisa | Portal Regional da BVS
Chronic widespread pain is associated with slower cognitive processing speed in middle-aged and older European men. - Nuffield...
Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease. A meta-analysis....
Multiple novel prostate cancer susceptibility signals identified by fine-mapping of known risk loci among Europeans. - Nuffield...
Pesquisa | Prevenção e Controle de Câncer
Genetic ancestry3
- Our results highlight the need to move away from discrete genetic ancestry clusters towards the continuum of genetic ancestries when considering PGSs. (bvsalud.org)
- Although methods to infer genetic ancestry have historically relied upon genome-wide markers, the adaptation to targeted clinical sequencing panels presents an opportunity to incorporate ancestry inference into routine diagnostic workflows. (bvsalud.org)
- Genotypic data were obtained from the PRACTICAL consortium for 6253 men with African genetic ancestry. (nih.gov)
Whites1
- Among racial groups, whites underwent the largest majority of operations (86.2%), followed by black (6.9%) and Hispanic (2.8%) races. (elsevierpure.com)
Populations9
- Here, using a large and diverse Los Angeles biobank5 (ATLAS, n = 36,778) along with the UK Biobank6 (UKBB, n = 487,409), we show that PGS accuracy decreases individual-to-individual along the continuum of genetic ancestries7 in all considered populations, even within traditionally labelled 'homogeneous' genetic ancestries. (bvsalud.org)
- Accurate ancestry inference is critical for identifying genetic contributors of cancer disparities among populations. (bvsalud.org)
- We show that global ancestral contributions and admixture of continental populations can be quantitatively inferred using markers captured by the MSK-IMPACT clinical panel. (bvsalud.org)
- African descent populations in the United States have high rates of type 2 diabetes and are incorrectly represented as a single group. (cdc.gov)
- prevalence is higher in African descent populations, 14%, compared with White populations of European descent (White populations), 9% (1). (cdc.gov)
- Additionally, African descent populations are represented as a single group, despite being comprised of African American (91%), Afro-Caribbean (4.7%), and African (3.7%) people (2,3). (cdc.gov)
- His team studies interethnic differences in the distribution of genetic and environmental risk factors, with particular emphasis on populations of African ancestry. (nih.gov)
- CRGGH continues to use genomic data generated in African populations to refine and fine-map loci identified in European and Asian populations for multiple traits including glucose, uric acid, bilirubin, CRP and serum lipids. (nih.gov)
- Dr. Rotimi and his group have contributed with over 50 publications to describing the prevalence and understanding the etiology of diabetes and related traits in African ancestry populations. (nih.gov)
Ethnicity1
- Rates of pathogenic/likely pathogenic germline variants (PVs) and downstream counseling were compared across ancestry groups (mutually exclusive groups based on self-reported race/ethnicity and Ashkenazi Jewish [AJ] heritage) using nonparametric tests and multivariable logistic regression models. (bvsalud.org)
Racial Groups1
- Persons having origins in any of the white racial groups of Europe, the Middle East, or North Africa. (nih.gov)
Datasets1
- To understand the role of CNVs across human diseases, we examine the CNV genomic landscape of 100,028 unrelated individuals of European ancestry, using SNP and CGH array datasets. (nih.gov)
Genome-wide1
- Here 14,803 cases and 12,262 controls of European descent were genotyped on the OncoArray and combined with existing data for an aggregated genome-wide association study (GWAS) analysis of lung cancer in 29,266 cases and 56,450 controls. (psjhealth.org)
Interpretation1
- GD is significantly correlated with PGS estimates themselves for 82 of 84 traits, further emphasizing the importance of incorporating the continuum of genetic ancestries in PGS interpretation. (bvsalud.org)
Groupings2
- Polygenic scores (PGSs) have limited portability across different groupings of individuals (for example, by genetic ancestries and/or social determinants of health), preventing their equitable use1-3. (bvsalud.org)
- By cross-referencing our data set with 1000 Genomes, we identified significant associations between continental and calibration groupings. (nih.gov)
Individuals3
- Individuals whose ancestral origins are in the continent of Europe. (nih.gov)
- notably, the closest GD decile of individuals with Hispanic Latino American ancestries show similar PGS performance to the furthest GD decile of individuals with European ancestries. (bvsalud.org)
- SIGNIFICANCE: We performed a comprehensive analysis of ancestral associations with somatic mutations in a real-world pan-cancer cohort, including >5,000 non-European individuals. (bvsalud.org)
Ethnic group1
- An ethnic group of putative Caucasoid origin. (bvsalud.org)
Subjects1
- Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations. (nih.gov)
Ancestral1
- It is thought that Native Americans infected by subtype E and Pacific Islanders, including those infected by subtype D in the Japanese archipelago, originated from a common ancestral genetic stock in continental Asia. (cdc.gov)
Descent3
- Type 2 diabetes disproportionately affects African descent groups, yet contributing factors are often overlooked. (cdc.gov)
- To ensure early type 2 diabetes detection, heterogeneity within African descent groups must be recognized, and more reliable testing strategies must be identified. (cdc.gov)
- 6.5% for type 2 diabetes) may perform suboptimally in evaluating glycemic status among African descent groups. (cdc.gov)
Adenocarcinoma1
- Age-adjusted incidence rates for both adenocarcinoma or squamous cell carcinoma were compared among ethnic groups in 5-yr intervals. (elsevierpure.com)
African6
- Despite the comparable overall prevalence of driver alterations by ancestry group, the proportion of patients with clinically actionable alterations was lower for African (30%) compared with European (33%) ancestry. (bvsalud.org)
- CRGGH published the first GWAS for blood pressure (BP) in AA using data from the Howard University Family Study, a population-based sample of ~2,000 related and unrelated African Americans from the Washington, DC area that was collected by Dr. Rotimi and his group. (nih.gov)
- Performance of African-ancestry-specific polygenic hazard score varies according to local ancestry in 8q24. (nih.gov)
- We previously developed an African-ancestry-specific polygenic hazard score (PHS46+African) that substantially improved prostate cancer risk stratification in men with African ancestry. (nih.gov)
- Herein, we used principal component (PC) analysis to uncover subpopulations of men with African ancestry for whom the utility of PHS46+African may differ. (nih.gov)
- Further research to improve the clinical utility of polygenic risk scores (or models) is needed to improve health outcomes for men of African ancestry. (nih.gov)
Results1
- HbA 1c results were compared with other ethnic groups or validated against the oral glucose tolerance test (OGTT), fasting plasma glucose (FPG), or previous diagnosis. (cdc.gov)
Race2
- In the total sample as well as in all sex-by-race groups, VAT and SAT were negatively related to BMD, after adjustment for lean body mass (LBM) and several covariates. (syr.edu)
- Race and sex interactions were not significant, indicating that the relationships were similar across race and sex groups. (syr.edu)
Persons1
- Observation of a population for a sufficient number of persons over a sufficient number of years to generate incidence or mortality rates subsequent to the selection of the study group. (lookformedical.com)
Disease2
- As sickle cell disease originates in areas where malaria is prevalent, it is found in equatorial Africa, parts of southern Europe, southern Turkey, parts of the Middle East and in much of central India. (kenanmalik.com)
- These groups may or may not be exposed to factors hypothesized to influence the probability of the occurrence of a particular disease or other outcome. (lookformedical.com)
Glucose1
- A heterogeneous group of disorders characterized by HYPERGLYCEMIA and GLUCOSE INTOLERANCE. (lookformedical.com)
WHITE1
- Note that OMB category WHITE is available for the United States population groups. (nih.gov)
Performance1
- The model consists of 46 SNPs identified in Europeans and 3 SNPs from 8q24 shown to improve model performance in Africans. (nih.gov)
Associations1
- In a pan-cancer cohort of 45,157 patients, we observed differences by ancestry in the frequency of somatic alterations, recapitulating known associations and revealing novel associations. (bvsalud.org)
Health care1
- HN - 2023 BX - Accessibility of Primary Care BX - Accessible Primary Care FX - Primary Health Care MH - Acute Aortic Syndrome UI - D000094683 MN - C14.907.109.70 MS - A group of aortic diseases presented with acute chest pain. (nih.gov)
Parts1
- This group, also called Europoid, centers around the Mediterranean Sea but includes other parts of Europe. (nih.gov)
Journal1
- European Journal of Epidemiology. (wustl.edu)
Strategies1
- Future research should focus on preventative strategies for ethnic groups at high risk for PTB. (elsevier.com)
Population1
- Thus, we conducted a molecular epidemiology HHV-8 survey of the Buryat population, a major indigenous group in southern Siberia, to gain new insights into the origins, possibly common, of HHV-8 subtypes D and E. (cdc.gov)
Type1
- In all minority groups, squamous cell carcinoma remained the predominant type. (elsevierpure.com)