Genome-wide association study (GWAS) identified PCOS susceptibility variants and replicates reported risk variants

被引:3
|
作者
Sharma, Priya [1 ]
Senapati, Sabyasachi [2 ]
Goyal, Lajya Devi [3 ]
Kaur, Balpreet [3 ]
Kamra, Pooja [4 ]
Khetarpal, Preeti [1 ]
机构
[1] Cent Univ Punjab, Sch Hlth Sci, Dept Human Genet & Mol Med, Lab Reprod & Dev Disorders, Bathinda 151401, India
[2] Cent Univ Punjab, Sch Hlth Sci, Dept Human Genet & Mol Med, Lab Immunogen, Bathinda 151401, India
[3] AIIMS, Dept Obstet & Gynaecol, Bathinda 151001, India
[4] Kamra Hosp, Dept Obstet & Gynaecol, Malout 152107, India
关键词
Genetics; GWAS; PCOS; Phenotype; Replication; POLYCYSTIC-OVARY-SYNDROME; OBESITY; LOCI;
D O I
10.1007/s00404-024-07400-w
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
BackgroundGenetic predisposition and environmental factors are considered risk factors for polycystic ovary syndrome (PCOS). Genome-wide association studies (GWAS) have been reported from various subpopulations to evaluate SNPs associated with PCOS risk. No PCOS-associated GWAS study has been reported from India so far.PurposeThe current study was conducted to identify the PCOS-susceptible loci among the North Indian population and to validate the significant loci reported by previous GWAS studies.MethodsA total of 272 participants with 134 PCOS patients and 138 age-matched healthy controls were recruited. Genomic DNA was isolated and genotyped by using Infinium Global Screening Array v3.0 microchip considering HWE 10e-5 statistically significant.ResultsA total of fifteen markers have been identified as candidate PCOS risk factors. Only two SNPs, namely rs17186366 and rs11171739 have been identified through replication analysis while comparing the previously reported PCOS GWAS data. In-silico analysis was performed to study the functional impact of identified significant genes for gene ontology, pathways related to gene set, and cluster analysis to determine protein-protein interaction among genes or gene products.ConclusionThe study suggests that multiple variants play an important role in PCOS pathogenesis and emphasizes the importance of further genetic studies among Indian subpopulations. The study also validates two previously reported SNPs in the Indian population.What this study adds to clinical workStudy summarizes the importance of candidate gene markers validated by replication and in-silico functional study, significantly involved in PCOS pathogenesis in the studied population. These markers can be used in the future as diagnostic markers for clinical phenotype identification.ConclusionThe study suggests that multiple variants play an important role in PCOS pathogenesis and emphasizes the importance of further genetic studies among Indian subpopulations. The study also validates two previously reported SNPs in the Indian population.What this study adds to clinical workStudy summarizes the importance of candidate gene markers validated by replication and in-silico functional study, significantly involved in PCOS pathogenesis in the studied population. These markers can be used in the future as diagnostic markers for clinical phenotype identification.ConclusionThe study suggests that multiple variants play an important role in PCOS pathogenesis and emphasizes the importance of further genetic studies among Indian subpopulations. The study also validates two previously reported SNPs in the Indian population.What this study adds to clinical workStudy summarizes the importance of candidate gene markers validated by replication and in-silico functional study, significantly involved in PCOS pathogenesis in the studied population. These markers can be used in the future as diagnostic markers for clinical phenotype identification.
引用
收藏
页码:2009 / 2019
页数:11
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