Association of polygenic liabilities for schizophrenia and bipolar disorder with educational attainment and cognitive aging.

IF 5.8 1区 医学 Q1 PSYCHIATRY
Chi-Shin Wu, Chia-Lin Hsu, Mei-Chen Lin, Mei-Hsin Su, Yen-Feng Lin, Chia-Yen Chen, Po-Chang Hsiao, Yi-Jiun Pan, Pei-Chun Chen, Yen-Tsung Huang, Shi-Heng Wang
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Abstract

To elucidate the specific and shared genetic background of schizophrenia (SCZ) and bipolar disorder (BPD), this study explored the association of polygenic liabilities for SCZ and BPD with educational attainment and cognitive aging. Among 106,806 unrelated community participants from the Taiwan Biobank, we calculated the polygenic risk score (PRS) for SCZ (PRSSCZ) and BPD (PRSBPD), shared PRS between SCZ and BPD (PRSSCZ+BPD), and SCZ-specific PRS (PRSSCZvsBPD). Based on the sign-concordance of the susceptibility variants with SCZ/BPD, PRSSCZ was split into PRSSCZ_concordant/PRSSCZ_discordant, and PRSBPD was split into PRSBPD_concordant/PRSBPD_discordant. Ordinal logistic regression models were used to estimate the association with educational attainment. Linear regression models were used to estimate the associations with cognitive aging (n = 27,005), measured by the Mini-Mental State Examination (MMSE), and with MMSE change (n = 6194 with mean follow-up duration of 3.9 y) in individuals aged≥ 60 years. PRSSCZ, PRSBPD, and PRSSCZ+BPD were positively associated with educational attainment, whereas PRSSCZvsBPD was negatively associated with educational attainment. PRSSCZ was negatively associated with MMSE, while PRSBPD was positively associated with MMSE. The concordant and discordant parts of polygenic liabilities have contrasting association, PRSSCZ_concordant and PRSBPD_concordant mainly determined these effects mentioned above. PRSSCZvsBPD predicted decreases in the MMSE scores. Using a large collection of community samples, this study provided evidence for the contrasting effects of polygenic architecture in SCZ and BPD on educational attainment and cognitive aging and suggested that SCZ and BPD were not genetically homogeneous.

精神分裂症和双相情感障碍的多基因责任与教育程度和认知老化的关系。
为了阐明精神分裂症(SCZ)和躁郁症(BPD)的特定和共有遗传背景,本研究探讨了SCZ和BPD的多基因责任与教育程度和认知老化的关联。在来自台湾生物库的 106,806 位无亲属关系的社区参与者中,我们计算了 SCZ(PRSSCZ)和 BPD(PRSBPD)的多基因风险评分(PRS)、SCZ 和 BPD 的共享风险评分(PRSSCZ+BPD)以及 SCZ 的特异性风险评分(PRSSCZvsBPD)。根据易感性变异与 SCZ/BPD 的符号一致性,PRSSCZ 被分为 PRSSCZ_concordant/PRSSCZ_discordant 两类,PRSBPD 被分为 PRSBPD_concordant/PRSBPD_discordant 两类。采用顺序逻辑回归模型来估计与教育程度的关系。线性回归模型用于估计与认知老化(n = 27 005)(通过小型精神状态检查(MMSE)测量)以及与 MMSE 变化(n = 6194,平均随访时间为 3.9 年)(年龄≥ 60 岁)的相关性。PRSSCZ、PRSBPD和PRSSCZ+BPD与受教育程度呈正相关,而PRSSCZvsBPD与受教育程度呈负相关。PRSSCZ 与 MMSE 呈负相关,而 PRSBPD 与 MMSE 呈正相关。多基因负债的一致和不一致部分具有相反的关联,PRSSCZ_一致和 PRSBPD_一致主要决定了上述效应。PRSSCZvsBPD 预测了 MMSE 分数的下降。本研究通过收集大量社区样本,为 SCZ 和 BPD 的多基因结构对教育程度和认知老化的不同影响提供了证据,并表明 SCZ 和 BPD 在基因上并不一致。
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来源期刊
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
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