Ya-Li Hao, Chun-Miao Liu, Na Wang, Rong-Miao Zhou, Ya-Nan Wei, Xiao-Shuang Bai, Xi Huang
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Compared with CC genotype, a significant association of CT genotype (p = 0.019), TT genotype (p < 0.001) and combined CT + TT genotype (p < 0.001) with reduced risk of PCOS was observed. The result of linkage disequilibrium analysis showed that these two SNPs are in complete linkage disequilibrium (r<sup>2</sup> = 1). For rs7176005 SNP, compared with CC genotype, CT, TT and CT + TT genotypes reduced the risk of PCOS. The age, BMI-adjusted OR were 0.650 (95% CI = 0.460-0.917), 0.158 (95% CI = 0.066-0.376) and 0.545(95% CI = 0.391-0.759), respectively.</p><p><strong>Conclusions: </strong>These findings highlight a significant association between CYP19 gene polymorphisms and PCOS susceptibility, implying potential protective effects of T and A alleles. Of course, the major limitation of this study is the sample size of the case-control study. Larger cohort studies are needed to confirm these findings and investigate the underlying causes.</p>","PeriodicalId":8915,"journal":{"name":"BMC Medical Genomics","volume":"18 1","pages":"43"},"PeriodicalIF":2.1000,"publicationDate":"2025-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11892123/pdf/","citationCount":"0","resultStr":"{\"title\":\"Association of CYP19 gene SNPs (rs7176005 and rs6493497) with polycystic ovary syndrome susceptibility in Northern Chinese women.\",\"authors\":\"Ya-Li Hao, Chun-Miao Liu, Na Wang, Rong-Miao Zhou, Ya-Nan Wei, Xiao-Shuang Bai, Xi Huang\",\"doi\":\"10.1186/s12920-025-02115-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>The objective of this study was to elucidate the relationship between two single nucleotide polymorphisms (SNPs) rs7176005 and rs6493497 in CYP19 gene and the risk of polycystic ovary syndrome (PCOS) in Northern Chinese women.</p><p><strong>Methods: </strong>In this case-control study, a total of 340 women with PCOS and 340 matched healthy controls were recruited. 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引用次数: 0
摘要
目的:探讨CYP19基因rs7176005和rs6493497两个单核苷酸多态性与中国北方女性多囊卵巢综合征(PCOS)发病风险的关系。方法:在本病例对照研究中,共招募340名PCOS女性和340名匹配的健康对照者。采用聚合酶链反应连接酶检测反应(PCR-LDR)方法对CYP19基因外显子1 5′侧区rs7176005和rs6493497两个snp位点进行了分析。结果:我们观察到rs7176005和rs6493497与PCOS风险降低显著相关。与CC基因型相比,CT基因型(p = 0.019)、TT基因型(p = 2 = 1)显著相关。对于rs7176005 SNP,与CC基因型相比,CT、TT和CT + TT基因型降低了PCOS的风险。年龄、bmi调整OR分别为0.650 (95% CI = 0.460-0.917)、0.158 (95% CI = 0.066-0.376)和0.545(95% CI = 0.391-0.759)。结论:这些发现突出了CYP19基因多态性与PCOS易感性之间的显著关联,提示T和a等位基因可能具有保护作用。当然,本研究的主要局限性在于病例对照研究的样本量。需要更大规模的队列研究来证实这些发现并调查潜在原因。
Association of CYP19 gene SNPs (rs7176005 and rs6493497) with polycystic ovary syndrome susceptibility in Northern Chinese women.
Purpose: The objective of this study was to elucidate the relationship between two single nucleotide polymorphisms (SNPs) rs7176005 and rs6493497 in CYP19 gene and the risk of polycystic ovary syndrome (PCOS) in Northern Chinese women.
Methods: In this case-control study, a total of 340 women with PCOS and 340 matched healthy controls were recruited. Polymerase chain reaction ligase detection reaction (PCR-LDR) method was used to investigate two SNPs (rs7176005 and rs6493497) in the 5'-flanking region of CYP19 gene exon 1.
Results: We observed a significant association of rs7176005 and rs6493497 with reduced risk of PCOS. Compared with CC genotype, a significant association of CT genotype (p = 0.019), TT genotype (p < 0.001) and combined CT + TT genotype (p < 0.001) with reduced risk of PCOS was observed. The result of linkage disequilibrium analysis showed that these two SNPs are in complete linkage disequilibrium (r2 = 1). For rs7176005 SNP, compared with CC genotype, CT, TT and CT + TT genotypes reduced the risk of PCOS. The age, BMI-adjusted OR were 0.650 (95% CI = 0.460-0.917), 0.158 (95% CI = 0.066-0.376) and 0.545(95% CI = 0.391-0.759), respectively.
Conclusions: These findings highlight a significant association between CYP19 gene polymorphisms and PCOS susceptibility, implying potential protective effects of T and A alleles. Of course, the major limitation of this study is the sample size of the case-control study. Larger cohort studies are needed to confirm these findings and investigate the underlying causes.
期刊介绍:
BMC Medical Genomics is an open access journal publishing original peer-reviewed research articles in all aspects of functional genomics, genome structure, genome-scale population genetics, epigenomics, proteomics, systems analysis, and pharmacogenomics in relation to human health and disease.