Age-dependent patterns of schizophrenia genetic risk affect cognition

被引:2
|
作者
Kuo, Susan S. [1 ,2 ,3 ]
Musket, Christie W. [1 ]
Rupert, Petra E. [1 ]
Almasy, Laura [4 ]
Gur, Ruben C. [5 ]
Prasad, Konasale M. [6 ,7 ,8 ]
Roalf, David R. [5 ]
Gur, Raquel E. [5 ]
Nimgaonkar, Vishwajit L. [6 ,8 ,9 ]
Pogue-Geile, Michael F. [1 ,6 ]
机构
[1] Univ Pittsburgh, Dept Psychol, Pittsburgh, PA 15260 USA
[2] Broad Inst MIT & Harvard, Stanley Ctr Psychiat Genet, Cambridge, MA 02142 USA
[3] Harvard Med Sch, Ctr Genom Med, Massachusetts Gen Hosp, Boston, MA USA
[4] Univ Penn, Dept Genet, Philadelphia, PA USA
[5] Univ Penn, Dept Psychiat, Philadelphia, PA 19104 USA
[6] Univ Pittsburgh, Dept Psychiat, Philadelphia, PA USA
[7] Univ Pittsburgh, Dept Bioengn, Philadelphia, PA USA
[8] Vet Affairs Pittsburgh Healthcare Syst, Pittsburgh, PA USA
[9] Univ Pittsburgh, Dept Human Genet, Pittsburgh, PA USA
基金
美国国家卫生研究院; 加拿大健康研究院;
关键词
Psychiatric genetics; Developmental risk; Psychosis; Clinical high risk; Age of onset; Heritability; POLYGENIC RISK; TWIN; OVERLAP; NEUROCOGNITION; METAANALYSIS; CHILDHOOD; PSYCHOSIS; DEFICITS; ABILITY; HEALTH;
D O I
10.1016/j.schres.2022.05.012
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Cognition shares substantial genetic overlap with schizophrenia, yet it remains unclear whether such genetic effects become significant during developmental periods of elevated risk for schizophrenia, such as the peak age of onset. We introduce an investigative framework integrating epidemiological, developmental, and genetic approaches to determine whether genetic effects shared between schizophrenia and cognition are significant across periods of differing risk for schizophrenia onset, and whether these effects are shared with depression. 771 European-American participants, including 636 (ages 15-84 years) from families with at least two first-degree relatives with schizophrenia and 135 unrelated controls, were divided into three age-risk groups based on ages relative to epidemiological age of onset patterns for schizophrenia: Pre-Peak (before peak age-of-onset: 15 to 22 years), Post-Peak (after peak age-of-onset: 23-42 years), and Plateau (during plateau of age-of-onset: over 42 years). For general cognition and 11 specific cognitive traits, we estimated genetic correlations with schizophrenia and with depression within each age-risk group. Genetic effects shared between deficits in general cognition and schizophrenia were nonsignificant before peak age of onset, yet were high and significant after peak age of onset and during the plateau of onset. These age-dependent genetic effects were largely consistent across specific cognitive traits and not transdiagnostically shared with depression. Schizophrenia genetic effects appear to influence cognitive traits in an age-dependent manner, supporting late developmental and perhaps neurodegenerative models that hypothesize increased expression of schizophrenia risk genes during and after the peak age of risk. Our findings underscore the utility of cognitive traits for tracking schizophrenia genetic effects across the lifespan.
引用
收藏
页码:39 / 48
页数:10
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