The genetic and environmental etiology of novel frequency-driven regional parcellations of abnormal white matter

IF 1.6 3区 医学 Q3 GENETICS & HEREDITY
Shu-Ju Lin, Nathan A. Gillespie, Randy Notestine, Anthony C. Gamst, Anna M. Chen, Linda K. McEvoy, Matthew S. Panizzon, Jeremy A. Elman, Stephen J. Glatt, Donald J. Hagler Jr, Michael C. Neale, Carol E. Franz, William S. Kremen, Christine Fennema-Notestine
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Abstract

The prevalence of white matter disease increases with age and is associated with cerebrovascular disease, cognitive decline, and risk for dementia. MRI measures of abnormal signal in the white matter (AWM) provide estimates of damage, however, regional patterns of AWM may be differentially influenced by genetic or environmental factors. With our data-driven regional parcellation approach, we created a probability distribution atlas using Vietnam Era Twin Study of Aging (VETSA) data (n = 475, mean age 67.6 years) and applied a watershed algorithm to define separate regional parcellations. We report biometrical twin modeling for five anatomically distinct regions: (1) Posterior, (2) Superior frontal and parietal, (3) Anterior and inferior frontal with deep areas, (4) Occipital, and (5) Anterior periventricular. We tested competing multivariate hypotheses to identify unique influences and to explain sources of covariance among the parcellations. Family aggregation could be entirely explained by additive genetic influences, with additive genetic variance (heritability) ranging from 0.69 to 0.79. Most genetic correlations between parcellations ranged from moderate to high (rg = 0.57–0.85), although two were small (rg = 0.35–0.39), consistent with varying degrees of unique genetic influences. This proof-of-principle investigation demonstrated the value of our novel, data-driven parcellations, with identifiable genetic and environmental differences, for future exploration.

新频率驱动的区域性异常白质小片的遗传和环境病因。
白质疾病的发病率随着年龄的增长而增加,并与脑血管疾病、认知能力下降和痴呆症风险有关。磁共振成像测量白质中的异常信号(AWM)可估算出损伤程度,但AWM的区域模式可能会受到遗传或环境因素的不同影响。通过数据驱动的区域划分方法,我们利用越南老龄化双胞胎研究(VETSA)数据(n = 475,平均年龄 67.6 岁)创建了概率分布图谱,并应用分水岭算法定义了独立的区域划分。我们报告了五个解剖学上不同区域的生物计量双胞胎模型:(1)后部,(2)额叶上部和顶叶,(3)额叶前部和下部及深部,(4)枕叶,以及(5)前脑室周围。我们测试了相互竞争的多元假设,以确定独特的影响因素,并解释各区系之间的协方差来源。家族聚集性完全可以用加性遗传影响来解释,加性遗传变异(遗传率)在 0.69 至 0.79 之间。大多数旁系之间的遗传相关性介于中度到高度之间(rg = 0.57-0.85),但有两个旁系之间的遗传相关性较小(rg = 0.35-0.39),这与不同程度的独特遗传影响是一致的。这项原理验证调查证明了我们新颖的、数据驱动的、具有可识别的遗传和环境差异的旁系结构在未来探索中的价值。
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来源期刊
CiteScore
5.90
自引率
7.10%
发文量
40
审稿时长
4-8 weeks
期刊介绍: Neuropsychiatric Genetics, Part B of the American Journal of Medical Genetics (AJMG) , provides a forum for experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. It is a resource for novel genetics studies of the heritable nature of psychiatric and other nervous system disorders, characterized at the molecular, cellular or behavior levels. Neuropsychiatric Genetics publishes eight times per year.
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