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遗传对重性抑郁障碍、双相情感障碍和精神分裂症谱系障碍患者跨诊断症状维度的贡献。

Genetic contributions to transdiagnostic symptom dimensions in patients with major depressive disorder, bipolar disorder, and schizophrenia spectrum disorders.

机构信息

Institute of Human Genetics, University of Bonn, School of Medicine & University Hospital Bonn, Bonn, Germany.

Department of Psychiatry and Psychotherapy, University of Marburg, Marburg, Germany; Center for Mind, Brain and Behavior, University of Marburg, Marburg, Germany.

出版信息

Schizophr Res. 2023 Feb;252:161-171. doi: 10.1016/j.schres.2023.01.002. Epub 2023 Jan 16.

Abstract

Major depressive disorder (MDD), bipolar disorder (BD), and schizophrenia spectrum disorders (SZ) exhibit considerable phenotypic and genetic overlap. However, the contribution of genetic factors to their shared psychopathological symptom dimensions remains unclear. The present exploratory study investigated genetic contributions to the symptom dimensions "Depression", "Negative syndrome", "Positive formal thought disorder", "Paranoid-hallucinatory syndrome", and "Increased appetite" in a transdiagnostic subset of the German FOR2107 cohort (n = 1042 patients with MDD, BD, or SZ). As replication cohort, a subset of the German/Austrian PsyCourse study (n = 816 patients with MDD, BD, or SZ) was employed. First, the relationship between symptom dimensions and common variants associated with MDD, BD, and SZ was investigated via polygenic risk score (PRS) association analyses, with disorder-specific PRS as predictors and symptom dimensions as outcomes. In the FOR2107 study sample, PRS for BD and SZ were positively associated with "Positive formal thought disorder", the PRS for SZ was positively associated with "Paranoid-hallucinatory syndrome", and the PRS for BD was negatively associated with "Depression". The effects of PRS for SZ were replicated in PsyCourse. No significant associations were observed for the MDD PRS. Second, genome-wide association studies (GWAS) were performed for the five symptom dimensions. No genome-wide significant associations and no replicable suggestive associations (p < 1e-6 in the GWAS) were identified. In summary, our results suggest that, similar to diagnostic categories, transdiagnostic psychiatric symptom dimensions are attributable to polygenic contributions with small effect sizes. Further studies in larger thoroughly phenotyped psychiatric cohorts are required to elucidate the genetic factors that shape psychopathological symptom dimensions.

摘要

重度抑郁症(MDD)、双相情感障碍(BD)和精神分裂症谱系障碍(SZ)表现出相当大的表型和遗传重叠。然而,遗传因素对其共同的精神病理学症状维度的贡献仍不清楚。本探索性研究调查了遗传因素对德国 FOR2107 队列中跨诊断亚组(n=1042 例 MDD、BD 或 SZ 患者)的“抑郁”、“阴性综合征”、“阳性形式思维障碍”、“偏执-幻觉综合征”和“食欲增加”症状维度的贡献。作为复制队列,采用德国/奥地利 PsyCourse 研究的一个亚组(n=1042 例 MDD、BD 或 SZ 患者)。首先,通过多基因风险评分(PRS)关联分析研究了症状维度与与 MDD、BD 和 SZ 相关的常见变异体之间的关系,以疾病特异性 PRS 为预测因子,以症状维度为结果。在 FOR2107 研究样本中,BD 和 SZ 的 PRS 与“阳性形式思维障碍”呈正相关,SZ 的 PRS 与“偏执-幻觉综合征”呈正相关,BD 的 PRS 与“抑郁”呈负相关。SZ 的 PRS 效应在 PsyCourse 中得到了复制。MDD 的 PRS 没有观察到显著的关联。其次,对五个症状维度进行了全基因组关联研究(GWAS)。未发现全基因组显著关联和可复制的提示性关联(GWAS 中 p<1e-6)。总之,我们的结果表明,与诊断类别相似,跨诊断精神病理学症状维度归因于具有小效应大小的多基因贡献。需要在更大、更彻底表型化的精神科队列中进行进一步研究,以阐明塑造精神病理学症状维度的遗传因素。

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