Neuroticism polygenic risk score predicts 20-year burden of depressive symptoms for Whites but not Blacks.

Journal of medical research and innovation Pub Date : 2020-01-01 Epub Date: 2019-08-26
Shervin Assari, Arash Javanbakht, Mohammed Saqib, Hamid Helmi, Mohsen Bazargan, Jennifer A Smith
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Abstract

Background: Black-White differences are reported in social, psychological, behavioral, medical, and biological correlates of depression. This study was conducted to compare Black and White older adults for the association between neuroticism polygenic risk score (N-PRS) and chronicity of depressive symptoms over 20 years.

Methods: Data came from the Health and Retirement Study (HRS), 1990 - 2012, a nationally representative sample of Americans above age 50. Current analysis followed 9,249 individuals (7,924 Whites and 1,325 Blacks) for up to 22 years. Depressive symptoms were measured every two years between 1992 and 2012 using the 8-item Center for Epidemiological Studies-Depression Scale (CES-D-8). The independent variable was N-PRS. The dependent variable was average depressive symptoms between 1992 and 2012. Linear regression was used for data analysis.

Results: In the pooled sample, higher N-PRS was associated with higher average depressive symptoms over the 20-year follow up period [b=0.01, 95%CI=0.00 to 0.04], net of all covariates. We also found an interaction between race and N-PRS [b=-0.02, 95%CI=-0.03 to 0.00], suggesting a stronger effect of N-PRS on 20-year average depressive symptoms for Whites than Blacks. Based on our race-specific linear regression models, higher N-PRS was associated with higher depressive symptoms from 1992 to 2012 for Whites [b=0.01, 95%CI=0.01 to 0.02] but not Blacks [b=0.00, 95%CI=-0.02 to 0.02].

Conclusion: Black and White older adults may differ in the salience of the existing N-PRS for depressive symptoms, which better reflects the burden of depression for Whites than Blacks. This may be because the existing PRSs are derived from mostly or exclusively White samples, limiting their applicability in other race groups. Racial variation in psychosocial, clinical, and biological correlates of depression needs further research.

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神经质多基因风险评分可预测白人而非黑人 20 年的抑郁症状负担。
背景:据报道,黑人和白人在抑郁症的社会、心理、行为、医学和生物学相关性方面存在差异。本研究比较了黑人和白人老年人神经质多基因风险评分(N-PRS)与 20 年抑郁症状慢性化之间的关系:数据来自 1990 - 2012 年的健康与退休研究(HRS),这是一项针对 50 岁以上美国人的全国代表性抽样调查。本次分析对 9,249 人(7,924 名白人和 1,325 名黑人)进行了长达 22 年的跟踪调查。在 1992 年至 2012 年期间,每两年使用 8 项流行病学研究中心抑郁量表 (CES-D-8) 测量一次抑郁症状。自变量为 N-PRS。因变量为 1992 年至 2012 年间的平均抑郁症状。数据分析采用线性回归法:在汇总样本中,扣除所有协变量后,较高的 N-PRS 与 20 年随访期间较高的平均抑郁症状相关[b=0.01,95%CI=0.00 至 0.04]。我们还发现种族与 N-PRS 之间存在交互作用 [b=-0.02,95%CI=-0.03 至 0.00],这表明 N-PRS 对白人 20 年平均抑郁症状的影响比对黑人更大。根据我们的种族特异性线性回归模型,从1992年到2012年,白人[b=0.01,95%CI=0.01至0.02]而黑人[b=0.00,95%CI=-0.02至0.02]较高的N-PRS与较高的抑郁症状相关:黑人和白人老年人在抑郁症状现有 N-PRS 的显著性方面可能存在差异,该 N-PRS 比黑人更能反映白人的抑郁负担。这可能是因为现有的 PRS 主要或完全来自白人样本,限制了其在其他种族群体中的适用性。抑郁症的社会心理、临床和生物学相关因素的种族差异还需要进一步研究。
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