Visually evoked cyclovergence and extended listing's law.
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Cyclovergence is a simultaneously occurring cyclorotation of the two eyes in opposite directions. Cyclovergence can be elicited visually by opposite cyclorotation of the two eyes' images. It also can occur in conjunction with horizontal vergence and vertical version in a stereotyped manner as described by the extended Listing's law (or L2). We manipulated L2-related and visually evoked cyclovergence independently, using stereoscopic images of three-dimensional (3D) scenes. During pursuit in the midsagittal plane, cyclovergence followed L2. The amount of L2-related cyclovergence during pursuit varied between subjects. Each pursuit trial was repeated three times. Two of the three trials had additional image rotation to visually evoke cyclovergence. We could separate the L2-related and visual components of cyclovergence by subtraction of the cyclovergence response in matched trials that differed only in the image rotation that was applied during pursuit. This indicates that visual and L2-related contributions to cyclovergence add linearly, suggesting the presence of two independent systems. Visually evoked cyclovergence gains were characteristic for a given subject, little affected by visual stimulus parameters, and usually low (0.1-0.5) when a static target was fixated. Gain and phase lag of the visually evoked cyclovergence during vertical pursuit was comparable with that during fixation of a static target. The binocular orientations are in better agreement to orientations predicted by L2 then would be predicted by nulling of the cyclodisparities. On the basis of our results, we suggest that visually driven and L2-related cyclovergence are independent of each other and superimpose linearly. (+info)
Effects of controlled breathing, mental activity and mental stress with or without verbalization on heart rate variability.
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OBJECTIVES: To assess whether talking or reading (silently or aloud) could affect heart rate variability (HRV) and to what extent these changes require a simultaneous recording of respiratory activity to be correctly interpreted. BACKGROUND: Sympathetic predominance in the power spectrum obtained from short- and long-term HRV recordings predicts a poor prognosis in a number of cardiac diseases. Heart rate variability is often recorded without measuring respiration; slow breaths might artefactually increase low frequency power in RR interval (RR) and falsely mimic sympathetic activation. METHODS: In 12 healthy volunteers we evaluated the effect of free talking and reading, silently and aloud, on respiration, RR and blood pressure (BP). We also compared spontaneous breathing to controlled breathing and mental arithmetic, silent or aloud. The power in the so called low- (LF) and high-frequency (HF) bands in RR and BP was obtained from autoregressive power spectrum analysis. RESULTS: Compared with spontaneous breathing, reading silently increased the speed of breathing (p < 0.05), decreased mean RR and RR variability and increased BP. Reading aloud, free talking and mental arithmetic aloud shifted the respiratory frequency into the LF band, thus increasing LF% and decreasing HF% to a similar degree in both RR and respiration, with decrease in mean RR but with minor differences in crude RR variability. CONCLUSIONS: Simple mental and verbal activities markedly affect HRV through changes in respiratory frequency. This possibility should be taken into account when analyzing HRV without simultaneous acquisition and analysis of respiration. (+info)
Exploiting rate-related hysteresis in repolarization alternans to improve risk stratification for ventricular tachycardia.
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OBJECTIVES: We sought to study the effect of heart rate acceleration and deceleration on the ability of repolarization alternans (RPA) to stratify ventricular tachycardia (VT) risk. BACKGROUND: Heart rate fluctuations alter arrhythmic propensity, yet it is unclear whether fluctuations, as well as absolute rate, dynamically increase VT risk. We hypothesized that repolarization heterogeneity reflected by RPA would exhibit hysteresis during rising and falling heart rate, which may reflect arrhythmic propensity. METHODS: The RPA magnitude (absolute voltage of alternation [V(alt)] and T-wave alternans ratio [TWAR]) and temporal distribution were determined from the electrocardiogram (ECG) in 60 patients during paced heart rate acceleration from 100 to 150 beats/min, then deceleration to 100 beats/min at electrophysiologic study (EPS). The V(alt) and TWAR thresholds were varied prospectively to generate receiver-operating characteristics (ROC) for the prediction of inducible VT at EPS. RESULTS: Thirty-six patients were induced into VT and 24 were not. Hysteresis of RPA was seen. The V(alt) reached steady-state within 60 beats of each rate transition and was higher in deceleration than in acceleration at matched heart rates. In induced patients, V(alt) rose then fell with heart rate. In noninduced patients, V(alt) was insensitive to acceleration, but rose on initial deceleration. The RPA distributed later within repolarization in induced patients but, on deceleration, moved earlier in both groups. By ROC analysis, V(alt) = 2.6 microV in late repolarization at 120 beats/min provided optimal sensitivity and specificity for VT in acceleration (87.5% and 88.7%, respectively) versus deceleration (80% and 62.5%, respectively; p = 0.004, chi-square test). CONCLUSIONS: 1) Physiologic fluctuations in heart rate may affect the clinical utility of RPA for VT risk stratification; and 2) repolarization dispersion measured by RPA is more exaggerated during deceleration than acceleration at matched heart rates (rate hysteresis). (+info)
Methods and limits of digital image compression of retinal images for telemedicine.
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PURPOSE: To investigate image compression of digital retinal images and the effect of various levels of compression on the quality of the images. METHODS: JPEG (Joint Photographic Experts Group) and Wavelet image compression techniques were applied in five different levels to 11 eyes with subtle retinal abnormalities and to 4 normal eyes. Image quality was assessed by four different methods: calculation of the root mean square (RMS) error between the original and compressed image, determining the level of arteriole branching, identification of retinal abnormalities by experienced observers, and a subjective assessment of overall image quality. To verify the techniques used and findings, a second set of retinal images was assessed by calculation of RMS error and overall image quality. RESULTS: Plots and tabulations of the data as a function of the final image size showed that when the original image size of 1.5 MB was reduced to 29 KB using JPEG compression, there was no serious degradation in quality. The smallest Wavelet compressed images in this study (15 KB) were generally still of acceptable quality. CONCLUSIONS: For situations where digital image transmission time and costs should be minimized, Wavelet image compression to 15 KB is recommended, although there is a slight cost of computational time. Where computational time should be minimized, and to remain compatible with other imaging systems, the use of JPEG compression to 29 KB is an excellent alternative. (+info)
Reconstruction of electroncephalogram brain maps by incorporating the blind source separation concept.
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Electroencephalogram (EEG) brain maps provide useful and reliable neurodiagnostic information. Accurate reconstruction of the data requires an efficient separation of the electrode signals. Although autoregressive (AR) spectrum estimation highly refines the signals, it cannot remove the effect of adjacent electrode signals. This report describes an efficient blind signal separation (BSS) method. The algorithm identifies the coefficients of an adaptive FIR filter by minimization of a cost function in terms of the corresponding fourth-order cumulants. Applying this method, the quality of the results is far superior to the traditional methods. (+info)
Polymerization of rod-like macromolecular monomers studied by stopped-flow, multiangle light scattering: set-up, data processing, and application to fibrin formation.
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Many biological supramolecular structures are formed by polymerization of macromolecular monomers. Light scattering techniques can provide structural information from such systems, if suitable procedures are used to collect the data and then to extract the relevant parameters. We present an experimental set-up in which a commercial multiangle laser light scattering photometer is linked to a stopped-flow mixer, allowing, in principle, the time-resolved extrapolation of the weight-average molecular weight M(w) and of the z-average square radius of gyration (z) of the polymers from Zimm-like plots. However, if elongated structures are formed as the polymerization proceeds, curved plots rapidly arise, from which M(w) and (z) cannot be recovered by linear fitting. To verify the correctness of a polynomial fitting procedure, polydisperse collections of rod-like or worm-like particles of different lengths, generated at various stages during bifunctional polycondensations of rod-like macromolecular monomers, were considered. Then, the angular dependence of their time-averaged scattered intensity was calculated in the Rayleigh-Gans-Debye approximation, with random and systematic noise also added to the data. For relatively narrow size distributions, a third-degree polynomial fitting gave satisfactory results across a broad range of conversion degrees, yielding M(w) and (z) values within 2% and no greater than 10-20%, respectively, of the calculated values. When more broad size distributions were analyzed, the procedure still performed well for semiflexible polymers, but started to seriously underestimate both M(w) and (z) when rigid rod-like particles were analyzed, even at relatively low conversion degrees. The data were also analyzed in the framework of the Casassa approximation, from which the mass per unit length of the polymers can be derived. These procedures were applied to a set of data taken on the early stages of the thrombin-catalyzed polymerization of fibrinogen, a rod-like macromolecule approximately 50 nm long. The polymers, grown in the absence of Ca(2+) by rate-limiting amounts of thrombin, appeared to be characterized by a much broader size distribution than the one expected for a classical Flory bifunctional polycondensation, and they seem to behave as relatively flexible worm-like double-stranded chains. Evidence for the formation of fibrinogen-fibrin monomer complexes is also inferred from the time dependence of the mass/length ratio. However, our data are also compatible with the presence of limited amounts of single-stranded structures in the very early stages, either as a secondary, less populated pathway, or as transient intermediates to the classical double-stranded fibrils. (+info)
Orientation formed by a spot's trajectory: a two-dimensional population approach in primary visual cortex.
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There exist a large number of visual illusions indicating that perception differs from pure representation of physical input. For example, a spot of light can be characterized by its position, but it does not contribute any information about orientation. However, when moved fast enough, a continuous streak along its trajectory is perceived that helps to determine the orientation of the movement path. The question arises whether the processing of the trajectory and its orientation are simultaneously represented in the primary visual cortex. Here I show that decoding neural population activity within a two-dimensional parameter space represents both (1) physical input given by the actual position of the moving spot and (2) orientation. This latter parameter has no physical counterpart in the stimulus but must be actively formed by spatiotemporal integration of the spot's trajectory. (+info)
SAGEmap: a public gene expression resource.
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We have constructed a public gene expression data repository and online data access and analysis, WWW and FTP sites for serial analysis of gene expression (SAGE) data. The WWW and FTP components of this resource, SAGEmap, are located at http://www.ncbi.nlm.nih. gov/sage and ftp://ncbi.nlm.nih.gov/pub/sage, respectively. We herein describe SAGE data submission procedures, the construction and characteristics of SAGE tags to gene assignments, the derivation and use of a novel statistical test designed specifically for differential-type analyses of SAGE data, and the organization and use of this resource. (+info)