Mallet Jasmina, Le Strat Yann, Dubertret Caroline, Gorwood Philip
APHP, Department of Psychiatry, Universitary Hospital Louis Mourier, 92700 Colombes, France.
Université de Paris, Institute of Psychiatry and Neuroscience of Paris (IPNP), INSERM U1266, Paris F-75014, France.
J Clin Med. 2020 Jan 25;9(2):341. doi: 10.3390/jcm9020341.
Schizophrenia is a multifactorial disease associated with widespread cognitive impairment. Although cognitive deficits are one of the factors most strongly associated with functional impairment in schizophrenia (SZ), current treatment strategies hardly tackle these impairments. To develop more efficient treatment strategies in patients, a better understanding of their pathogenesis is needed. Recent progress in genetics, driven by large genome-wide association studies (GWAS) and the use of polygenic risk scores (PRS), has provided new insights about the genetic architecture of complex human traits, including cognition and SZ. Here, we review the recent findings examining the genetic links between SZ and cognitive functions in population-based samples as well as in participants with SZ. The performed meta-analysis showed a negative correlation between the polygenetic risk score of schizophrenia and global cognition ( < 0.001) when the samples rely on general and healthy participants, while no significant correlation was detected when the three studies devoted to schizophrenia patients were meta-analysed ( > 0.05). Our review and meta-analysis therefore argues against universal pleiotropy for schizophrenia alleles and cognition, since cognition in SZ patients would be underpinned by the same genetic factors than in the general population, and substantially independent of common variant liability to the disorder.
精神分裂症是一种与广泛认知障碍相关的多因素疾病。尽管认知缺陷是精神分裂症(SZ)中与功能障碍关联最紧密的因素之一,但目前的治疗策略几乎无法解决这些障碍。为了为患者制定更有效的治疗策略,需要更好地了解其发病机制。由大规模全基因组关联研究(GWAS)和多基因风险评分(PRS)的使用推动的遗传学最新进展,为包括认知和SZ在内的复杂人类特征的遗传结构提供了新的见解。在这里,我们回顾了最近在基于人群的样本以及SZ患者中研究SZ与认知功能之间遗传联系的发现。进行的荟萃分析表明,当样本为普通健康参与者时,精神分裂症的多基因风险评分与整体认知之间呈负相关(<0.001),而对三项针对精神分裂症患者的研究进行荟萃分析时未检测到显著相关性(>0.05)。因此,我们的综述和荟萃分析反对精神分裂症等位基因与认知的普遍多效性,因为SZ患者的认知与普通人群一样,由相同的遗传因素支撑,并且基本上独立于该疾病的常见变异易感性。