Psychiatric and Neurodevelopmental Genetics Unit, Department of Psychiatry and Center for Human Genetic Research, Massachusetts General Hospital, Boston, MA.
Department of Psychiatry, Harvard Medical School, Boston, MA.
Schizophr Bull. 2017 Jul 1;43(4):788-800. doi: 10.1093/schbul/sbw146.
Schizophrenia is characterized by neuropsychological deficits across many cognitive domains. Cognitive phenotypes with high heritability and genetic overlap with schizophrenia liability can help elucidate the mechanisms leading from genes to psychopathology. We performed a meta-analysis of 170 published twin and family heritability studies of >800 000 nonpsychiatric and schizophrenia subjects to accurately estimate heritability across many neuropsychological tests and cognitive domains. The proportion of total variance of each phenotype due to additive genetic effects (A), shared environment (C), and unshared environment and error (E), was calculated by averaging A, C, and E estimates across studies and weighting by sample size. Heritability ranged across phenotypes, likely due to differences in genetic and environmental effects, with the highest heritability for General Cognitive Ability (32%-67%), Verbal Ability (43%-72%), Visuospatial Ability (20%-80%), and Attention/Processing Speed (28%-74%), while the lowest heritability was observed for Executive Function (20%-40%). These results confirm that many cognitive phenotypes are under strong genetic influences. Heritability estimates were comparable in nonpsychiatric and schizophrenia samples, suggesting that environmental factors and illness-related moderators (eg, medication) do not substantially decrease heritability in schizophrenia samples, and that genetic studies in schizophrenia samples are informative for elucidating the genetic basis of cognitive deficits. Substantial genetic overlap between cognitive phenotypes and schizophrenia liability (average rg = -.58) in twin studies supports partially shared genetic etiology. It will be important to conduct comparative studies in well-powered samples to determine whether the same or different genes and genetic variants influence cognition in schizophrenia patients and the general population.
精神分裂症的特点是在许多认知领域存在神经认知缺陷。具有高遗传性和与精神分裂症易感性遗传重叠的认知表型,可以帮助阐明从基因到精神病理学的机制。我们对 170 项已发表的关于>80 万非精神病和精神分裂症受试者的双胞胎和家庭遗传研究进行了荟萃分析,以准确估计许多神经心理学测试和认知领域的遗传率。通过在研究之间平均 A、C 和 E 估计值并按样本量加权,可以计算出每个表型的总方差中由于加性遗传效应(A)、共享环境(C)和非共享环境和误差(E)引起的比例。表型的遗传率各不相同,这可能是由于遗传和环境效应的差异所致,其中一般认知能力(32%-67%)、言语能力(43%-72%)、视空间能力(20%-80%)和注意力/处理速度(28%-74%)的遗传率最高,而执行功能的遗传率最低(20%-40%)。这些结果证实,许多认知表型受到强烈的遗传影响。非精神病和精神分裂症样本的遗传率估计值相当,这表明环境因素和与疾病相关的调节剂(例如,药物)不会在精神分裂症样本中大大降低遗传率,并且精神分裂症样本中的遗传研究对于阐明认知缺陷的遗传基础是有信息的。双胞胎研究中认知表型和精神分裂症易感性(平均 rg = -.58)之间存在大量遗传重叠,支持部分共享遗传病因。在有足够效力的样本中进行比较研究,以确定相同或不同的基因和遗传变异是否会影响精神分裂症患者和普通人群的认知,这将是很重要的。