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Susceptibility Differences (susceptibility + difference)
Selected AbstractsUsing forward calculations of the magnetic field perturbation due to a realistic vascular model to explore the BOLD effectNMR IN BIOMEDICINE, Issue 6 2008José P. Marques Abstract This paper assesses the reliability of the infinite cylinder model used previously in the literature to simulate blood oxygenation level dependent (BOLD) signal changes. A three-dimensional finite element method was applied to a realistic model of the cortical vasculature, and the results compared with those generated from a simple model of the vasculature as a set of independent, randomly oriented, infinite cylinders. The realistic model is based on scanning electron microscopy measurements of the terminal vascular bed in the superficial cortex of the rat. Good agreement is found between the two models with regard to the extravascular R2* and R2 dependence on the cerebral blood volume and blood oxygenation fraction. Using the realistic model, it is also possible to gain further understanding of the relative importance of intravascular and extravascular BOLD contrast. A simple parameterisation of the dependence of the relaxation rates on relative cerebral blood volume and blood,tissue susceptibility difference was carried out, allowing discussion of the variation in the form of the haemodynamic response with field strength. Copyright © 2007 John Wiley & Sons, Ltd. [source] Suppression of background gradients in (B0 gradient-based) NMR diffusion experimentsCONCEPTS IN MAGNETIC RESONANCE, Issue 5 2007Gang Zheng Abstract Artifacts arising from background gradients are very common in NMR diffusion (i.e., PGSE) experiments involving B0 gradients because of the unavoidable magnetic susceptibility differences and B0 inhomogeneity within and around the sample. This article presents the general methodology to develop PGSE sequences with background gradient suppression. Most of the available methods which can be used for the suppression of the effects of background gradients are discussed. And two newly developed methods are presented in detail: frequency analysis of spin-dephasing, which assumes the artifacts due to background gradients come from the resonance between the spin-dephasing caused by applied gradients and background gradients, and asymmetric bipolar stimulated-echo-based PGSE, which can suppress the effects of nonconstant background gradients. © 2007 Wiley Periodicals, Inc.Concepts Magn Reson Part A 30A: 261,277, 2007. [source] Aging and decision making: Differences in susceptibility to the risky-choice framing effect between older and younger adults in JapanJAPANESE PSYCHOLOGICAL RESEARCH, Issue 3 2010SATOSHI WATANABE Abstract This study investigates the characteristics of the risky-choice framing effect among older adults (more than 65 years of age) in comparison to younger adults. Data from a questionnaire survey with randomly sampled participants from voter lists in two cities in northern Japan were reanalyzed. Wang's (1996) definition of the risky-choice framing effect was applied for analyzing data. The younger group showed a typical risky-choice framing effect, while the older group failed to show any framing effect. Both age groups in the positive frame showed an increasingly higher risk-aversive tendency corresponding to the monotonically increased number of human lives at risk. The modified value function was proposed to explain the susceptibility differences in the framing effect between the two groups. The socioemotional selectivity theory and the decision mode were applied for explaining the shape of the modified value function of the older group. [source] Testing Genetic Susceptibility Loci for Alcoholic Heart Muscle DiseaseALCOHOLISM, Issue 10 2001Olli A. Kajander Background: Although many heavy alcohol users have subclinical alcoholic heart muscle disease, only a very few develop severe dilated cardiomyopathy. Therefore, and because cardiac abnormalities correlate only weakly with the duration or quantity of drinking, individual susceptibility differences may exist. In this work we examined whether common gene variants previously associated with cardiac hypertrophy or altered alcohol metabolism could modify the effects of alcohol on the heart. Methods: We studied 700 middle-aged male victims of sudden death who underwent a medicolegal autopsy. In addition to routine postmortem examination, the weights and the cavity and wall dimensions of the left and right ventricle were measured. Coronary artery stenoses were determined from a silicone rubber cast of the arteries. Alcohol consumption and cardiovascular risk factors were assessed by a structured interview of the spouse. The following gene polymorphisms were determined by using polymerase chain reaction restriction fragment length polymorphism and solid-phase minisequencing techniques: angiotensin converting enzyme I/D, angiotensin II type 1 receptor 1166A/C, aldosterone synthase ,344C/T, alcohol dehydrogenases 2 and 3, acetaldehyde dehydrogenase 2, and cytochrome P-450 2E1 Dra I, Pst I, Rsa I, and Msp I. Results: The most consistent effects of alcohol (p < 0.05) were a higher total heart weight and a larger right ventricle size with increasing daily drinking. However, these and other effects of alcohol were statistically fully independent of the studied genotypes. Conclusions: The gene polymorphisms selected for and analyzed in our study are unlikely to modify the effects of alcohol on the heart. Other unknown factors determine the individual susceptibility to alcoholic heart muscle disease. [source] Susceptibility gradient mapping (SGM): A new postprocessing method for positive contrast generation applied to superparamagnetic iron oxide particle (SPIO)-labeled cellsMAGNETIC RESONANCE IN MEDICINE, Issue 3 2008Hannes Dahnke Abstract Local susceptibility gradients result in a dephasing of the precessing magnetic moments and thus in a fast decay of the NMR signals. In particular, cells labeled with superparamagnetic iron oxide particles (SPIOs) induce hypointensities, making the in vivo detection of labeled cells from such a negative image contrast difficult. In this work, a new method is proposed to selectively turn this negative contrast into a positive contrast. The proposed method calculates the susceptibility gradient and visualizes it in a parametric map directly from a regular gradient-echo image dataset. The susceptibility gradient map is determined in a postprocessing step, requiring no dedicated pulse sequences or adaptation of the sequence before and during image acquisition. Phantom experiments demonstrated that local susceptibility differences can be quantified. In vivo experiments showed the feasibility of the method for tracking of SPIO-labeled cells. The method bears the potential also for usage in other applications, including the detection of contrast agents and interventional devices as well as metal implants. Magn Reson Med 60:595,603, 2008. © 2007 Wiley-Liss, Inc. [source] Quantitative lung perfusion mapping at 0.2 T using FAIR True-FISP MRIMAGNETIC RESONANCE IN MEDICINE, Issue 5 2006Petros Martirosian Abstract Perfusion measurements in lung tissue using arterial spin labeling (ASL) techniques are hampered by strong microscopic field gradients induced by susceptibility differences between the alveolar air and the lung parenchyma. A true fast imaging with steady precession (True-FISP) sequence was adapted for applications in flow-sensitive alternating inversion recovery (FAIR) lung perfusion imaging at 0.2 Tesla and 1.5 Tesla. Conditions of microscopic static field distribution were assessed in four healthy volunteers at both field strengths using multiecho gradient-echo sequences. The full width at half maximum (FWHM) values of the frequency distribution for 180,277 Hz at 1.5 Tesla were more than threefold higher compared to 39,109 Hz at 0.2 Tesla. The influence of microscopic field inhomogeneities on the True-FISP signal yield was simulated numerically. Conditions allowed for the development of a FAIR True-FISP sequence for lung perfusion measurement at 0.2 Tesla, whereas at 1.5 Tesla microscopic field inhomogeneities appeared too distinct. Perfusion measurements of lung tissue were performed on eight healthy volunteers and two patients at 0.2 Tesla using the optimized FAIR True-FISP sequence. The average perfusion rates in peripheral lung regions in transverse, sagittal, and coronal slices of the left/right lung were 418/400, 398/416, and 370/368 ml/100 g/min, respectively. This work suggests that FAIR True-FISP sequences can be considered appropriate for noninvasive lung perfusion examinations at low field strength. Magn Reson Med, 2006. © 2006 Wiley-Liss, Inc. [source] Standardized T2* map of normal human heart in vivo to correct T2* segmental artefactsNMR IN BIOMEDICINE, Issue 6 2007Vincenzo Positano Abstract A segmental, multislice, multi-echo T2* MRI approach could be useful in heart iron-overloaded patients to account for heterogeneous iron distribution, demonstrated by histological studies. However, segmental T2* assessment in heart can be affected by the presence of geometrical and susceptibility artefacts, which can act on different segments in different ways. The aim of this study was to assess T2* value distribution in the left ventricle and to develop a correction procedure to compensate for artefactual variations in segmental analysis. MRI was performed in four groups of 22 subjects each: healthy subjects (I), controls (II) (thalassemia intermedia patients without iron overload), thalassemia major patients with mild (III) and heavy (IV) iron overload. Three short-axis views (basal, median, and apical) of the left ventricle were obtained and analyzed using custom-written, previously validated software. The myocardium was automatically segmented into a 16-segment standardized heart model, and the mean T2* value for each segment was calculated. Punctual distribution of T2* over the myocardium was assessed, and T2* inhomogeneity maps for the three slices were obtained. In group I, no significant variation in the mean T2* among slices was found. T2* showed a characteristic circumferential variation in all three slices. The effect of susceptibility differences induced by cardiac veins was evident, together with low-scale variations induced by geometrical artefacts. Using the mean segmental deviations as correction factors, an artefact correction map was developed and used to normalize segmental data. The correction procedure was validated on group II. Group IV showed no significant presence of segmental artefacts, confirming the hypothesis that susceptibility artefacts are additive in nature and become negligible for high levels of iron overload. Group III showed a greater variability with respect to normal subjects. The correction map failed to compensate for these variations if both additive and percentage-based corrections were applied. This may reinforce the hypothesis that true inhomogeneity in iron deposition exists. Copyright © 2007 John Wiley & Sons, Ltd. [source] Magnetic-field-induced vertigo: A theoretical and experimental investigationBIOELECTROMAGNETICS, Issue 5 2007P.M. Glover Abstract Vertigo-like sensations or apparent perception of movement are reported by some subjects and operators in and around high field whole body magnetic resonance body scanners. Induced currents (which modulate the firing rate of the vestibular hair cell), magneto-hydrodynamics (MDH), and tissue magnetic susceptibility differences have all been proposed as possible mechanisms for this effect. In this article, we examine the theory underlying each of these mechanisms and explore resulting predictions. Experimental evidence is summarised in the following findings: 30% of subjects display a postural sway response at a field-gradient product of 1 T2m,1; a determining factor for experience of vertigo is the total unipolar integrated field change over a period greater than 1 s; the perception of dizziness is not necessarily related to a high value of the rate of change of magnetic field; eight of ten subjects reported sensations ranging from mild to severe when exposed to a magnetic field change of the order of 4.7 T in 1.9 s; no subjects reported any response when exposed to 50 ms pulses of dB/dt of 2 Ts,1 amplitude. The experimental evidence supports the hypothesis that magnetic-field related vertigo results from both magnetic susceptibility differences between vestibular organs and surrounding fluid, and induced currents acting on the vestibular hair cells. Both mechanisms are consistent with theoretical predictions. Bioelectromagnetics 28:349,361, 2007. © 2007 Wiley-Liss, Inc. 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