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新型频率驱动的异常白质区域划分的遗传和环境病因学。

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

作者信息

Lin Shu-Ju, Gillespie Nathan A, Notestine Randy, Gamst Anthony C, Chen Anna M, McEvoy Linda K, Panizzon Matthew S, Elman Jeremy A, Glatt Stephen J, Hagler Donald J, Neale Michael C, Franz Carol E, Kremen William S, Fennema-Notestine Christine

机构信息

Department of Psychiatry, University of California, San Diego, La Jolla, California, USA.

Center for Behavior Genetics of Aging, University of California, San Diego, La Jolla, California, USA.

出版信息

Am J Med Genet B Neuropsychiatr Genet. 2025 Jan;198(1):e33004. doi: 10.1002/ajmg.b.33004. Epub 2024 Aug 16.

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 (r = 0.57-0.85), although two were small (r = 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.

摘要

白质疾病的患病率随年龄增长而增加,且与脑血管疾病、认知衰退及痴呆风险相关。磁共振成像(MRI)对白质异常信号(AWM)的测量可提供损伤评估,然而,AWM的区域模式可能受到遗传或环境因素的不同影响。利用我们数据驱动的区域分割方法,我们使用越南战争时期双生子衰老研究(VETSA)数据(n = 475,平均年龄67.6岁)创建了一个概率分布图集,并应用分水岭算法定义单独的区域分割。我们报告了五个解剖学上不同区域的双生子生物统计学建模:(1)后部,(2)额上回和顶叶,(3)额前回和额下回深部区域,(4)枕叶,以及(5)脑室周围前部。我们测试了相互竞争的多变量假设,以确定独特影响并解释分割区域之间的协方差来源。家族聚集可完全由加性遗传影响解释,加性遗传方差(遗传率)范围为0.69至0.79。分割区域之间的大多数遗传相关性从中度到高度不等(r = 0.57 - 0.85),尽管有两个较小(r = 0.35 - 0.39),这与不同程度的独特遗传影响一致。这项原理验证研究证明了我们新颖的数据驱动分割方法的价值,其具有可识别的遗传和环境差异,可供未来探索。

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