Cross-Ancestry Polygenic Prediction of Bipolar Disorder and Obsessive-Compulsive Disorder in India.

Bharath Holla, Suhas Ganesh, Jayant Mahadevan, Reeteka Sud, Meghana Janardhanan, Srinivas Balachander, Swarna Buddha Nayok, Pavithra Jayasankar, Manuel Mattheisen, Nora Strom, Patrick F Sullivan, Hailiang Huang, Peter P Zandi, Janardhan Y C Reddy, Vivek Benegal, Sanjeev Jain, Meera Purushottam, Biju Viswanath
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Abstract

Most genetic studies of psychiatric disorders have been conducted predominantly in populations of European ancestry, limiting evidence for the transferability of polygenic scores (PGS) to other populations. This cross-sectional study evaluated the predictive performance of European-derived PGS for bipolar disorder (BD) and obsessive-compulsive disorder (OCD) in an Indian sample. Participants (N = 2531) included individuals with BD (N = 463), OCD (N = 554), and controls (N = 1514) recruited from hospital- and community-based samples. Genotyping was performed using the Illumina Global Screening Array. PGS were derived from the summary statistics of European-ancestry genome-wide association studies using two Bayesian methods, PRS-CS-auto and SBayesRC. Principal component analyses demonstrated genetic overlap of the study population with other South Asian populations. BD PGS showed significant predictive performance, explaining approximately 6%-7% of liability-scale variance with PGS-only AUCs of ~0.71. OCD PGS showed lower but significant predictive performance, explaining ~2%-3% of variance with AUCs of approximately 0.59. Bayesian approaches showed better predictive performance than conventional clumping-and-thresholding. These findings demonstrate that European-derived psychiatric PGS can retain predictive information in an Indian population, although performance differed between disorders. The application of Bayesian PGS methods in this Indian cohort supports their utility for cross-ancestry prediction, while reinforcing the need for larger genomic studies in South Asian and other underrepresented populations.

印度双相情感障碍和强迫症的跨祖先多基因预测。
大多数精神疾病的遗传研究主要是在欧洲血统的人群中进行的,这限制了多基因评分(PGS)可转移到其他人群的证据。本横断面研究评估了欧洲衍生的PGS对印度样本双相情感障碍(BD)和强迫症(OCD)的预测性能。参与者(N = 2531)包括从医院和社区样本中招募的双相障碍(N = 463)、强迫症(N = 554)和对照组(N = 1514)。使用Illumina Global Screening Array进行基因分型。PGS来源于欧洲人祖先全基因组关联研究的汇总统计,采用两种贝叶斯方法,PRS-CS-auto和SBayesRC。主成分分析表明,研究人群与其他南亚人群遗传重叠。BD PGS表现出显著的预测性能,解释了约6%-7%的责任量表方差,仅PGS的auc为~0.71。OCD PGS表现出较低但显著的预测性能,解释了2%-3%的方差,auc约为0.59。贝叶斯方法比传统的聚类阈值方法表现出更好的预测性能。这些发现表明,欧洲衍生的精神病学PGS可以在印度人群中保留预测信息,尽管不同疾病的表现不同。贝叶斯PGS方法在印度队列中的应用支持了其跨祖先预测的实用性,同时加强了在南亚和其他代表性不足的人群中进行更大规模基因组研究的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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