Department of Family Medicine, Madigan Army Medical Center Tacoma, WA, USA ; Department of Psychiatry, Maryland Psychiatric Research Center, University of Maryland School of Medicine Baltimore, MD, USA.
Department of Psychiatry, Maryland Psychiatric Research Center, University of Maryland School of Medicine Baltimore, MD, USA ; Department of Physics, University of Maryland Baltimore, MD, USA ; South Texas Diabetes and Obesity Institute, University of Texas Health Science Center at San Antonio San Antonio, TX, USA.
Front Genet. 2015 Feb 13;6:26. doi: 10.3389/fgene.2015.00026. eCollection 2015.
Obesity is a chronic metabolic disorder that may also lead to reduced white matter integrity, potentially due to shared genetic risk factors. Genetic correlation analyses were conducted in a large cohort of Mexican American families in San Antonio (N = 761, 58% females, ages 18-81 years; 41.3 ± 14.5) from the Genetics of Brain Structure and Function Study. Shared genetic variance was calculated between measures of adiposity [(body mass index (BMI; kg/m(2)) and waist circumference (WC; in)] and whole-brain and regional measurements of cerebral white matter integrity (fractional anisotropy). Whole-brain average and regional fractional anisotropy values for 10 major white matter tracts were calculated from high angular resolution diffusion tensor imaging data (DTI; 1.7 × 1.7 × 3 mm; 55 directions). Additive genetic factors explained intersubject variance in BMI (heritability, h (2) = 0.58), WC (h (2) = 0.57), and FA (h (2) = 0.49). FA shared significant portions of genetic variance with BMI in the genu (ρG = -0.25), body (ρG = -0.30), and splenium (ρG = -0.26) of the corpus callosum, internal capsule (ρG = -0.29), and thalamic radiation (ρG = -0.31) (all p's = 0.043). The strongest evidence of shared variance was between BMI/WC and FA in the superior fronto-occipital fasciculus (ρG = -0.39, p = 0.020; ρG = -0.39, p = 0.030), which highlights region-specific variation in neural correlates of obesity. This may suggest that increase in obesity and reduced white matter integrity share common genetic risk factors.
肥胖是一种慢性代谢紊乱疾病,也可能导致白质完整性降低,这可能是由于存在共同的遗传风险因素。在圣安东尼奥的一个大型墨西哥裔美国家庭队列(N=761,女性占 58%,年龄 18-81 岁;平均年龄 41.3±14.5 岁)中进行了遗传相关性分析,该研究来自大脑结构和功能遗传学研究。在体脂测量值(身体质量指数(BMI;kg/m2)和腰围(WC;in))和全脑及大脑白质完整性的区域测量值(各向异性分数)之间计算了共同遗传方差。使用高角度分辨率弥散张量成像数据(DTI;1.7×1.7×3mm;55 个方向)计算了 10 条主要白质束的全脑平均和区域各向异性分数值。BMI(遗传力,h2=0.58)、WC(h2=0.57)和 FA(h2=0.49)的个体间差异可由加性遗传因素解释。FA 与胼胝体的膝部(ρG=-0.25)、体部(ρG=-0.30)和压部(ρG=-0.26)、内囊(ρG=-0.29)和丘脑辐射(ρG=-0.31)之间存在显著的遗传方差共享部分(ρG=-0.25,p=0.043)。在胼胝体上额枕束(ρG=-0.39,p=0.020;ρG=-0.39,p=0.030)中,BMI/WC 和 FA 之间存在共同方差的最强证据,这突出了肥胖的神经相关性存在区域特异性差异。这可能表明肥胖增加和白质完整性降低存在共同的遗传风险因素。