Genotypephenotype correlations of PCOS susceptibility SNPs identified by GWAS in a large cohort of Han Chinese women

被引:93
作者
Cui, Linlin [1 ,2 ,3 ,4 ]
Zhao, Han [1 ,2 ,3 ,4 ]
Zhang, Bo [5 ]
Qu, Zhongyu [6 ]
Liu, Jiayin [7 ]
Liang, Xiaoyan [8 ]
Zhao, Xiaoming [9 ]
Zhao, Junli [10 ]
Sun, Yingpu [11 ]
Wang, Peng [1 ,2 ,3 ,4 ]
Li, Tao [1 ,2 ,3 ,4 ]
Shi, Yuhua [1 ,2 ,3 ,4 ]
Chen, Zi-Jiang [1 ,2 ,3 ,4 ]
机构
[1] Shandong Univ, Prov Hosp, Ctr Reprod Med, Jinan 250021, Peoples R China
[2] Natl Res Ctr Assisted Reprod Technol & Reprod Gen, Jinan 250021, Peoples R China
[3] Minist Educ, Key Lab Reprod Endocrinol, Jinan 250021, Peoples R China
[4] Shandong Prov Key Lab Reprod Med, Jinan 250021, Peoples R China
[5] Maternal & Child Hlth Hosp Guangxi Zhuang Autonom, Reprod Med Ctr, Nanning 530003, Peoples R China
[6] Shandong Univ, Prov Hosp, Dept Ultrasonog, Jinan 250100, Peoples R China
[7] Nanjing Med Univ, Affiliated Hosp 1, Dept Reprod Med, Nanjing 210129, Jiangsu, Peoples R China
[8] Sun Yat Sen Univ, Affiliated Hosp 6, Dept Reprod Med, Guangzhou 510080, Guangdong, Peoples R China
[9] Shanghai Jiao Tong Univ, Renji Hosp, Ctr Reprod Med, Shanghai 200127, Peoples R China
[10] Ningxia Med Univ, Affiliated Hosp, Ctr Reprod Med, Yinchuan 750003, Peoples R China
[11] Zhengzhou Univ, Affiliated Hosp 1, Ctr Reprod Med, Zhengzhou 450052, Peoples R China
基金
中国国家自然科学基金;
关键词
PCOS; phenotype; THADA; DENND1A; POLYCYSTIC-OVARY-SYNDROME; GENOME-WIDE ASSOCIATION; CHROMOSOME; 2P16.3; LOCI; 2P21; REPLICATION; PHENOTYPES; HIRSUTISM; VARIANTS; DENND1A;
D O I
10.1093/humrep/des424
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Are there any correlations between the phenotypes of polycystic ovary syndrome (PCOS) and the genotypes of the PCOS susceptibility single nucleotide polymorphisms (SNPs) in THADA, DENND1A and LHCGR? The PCOS susceptibility genes, THADA and DENND1A, carry risk alleles that are associated with endocrine and metabolic disturbances in patients with PCOS. PCOS is a heterogeneous endocrinopathy characterized by oligo-anovulation, hyperandrogenism and polycystic ovaries. In a previous genome-wide association study, the SNP variants rs13429458, rs12478601, rs2479106, rs10818854 and rs13405728 in the THADA, DENND1A and LHCGR genes were identified as being independently associated with PCOS. The aim of this study was to identify any additional correlations between the phenotypes of PCOS and genotypes of the five SNPs described in the previous study. In the present cross-sectional study, a total of 1731 PCOS patients and 4964 controls were enrolled. Patients were diagnosed according to Rotterdam criteria. Clinical information was collected from the patients and controls. Endocrine and metabolic parameters were evaluated for phenotypegenotype correlation analyses. Using a recessive model, the AA group for rs13429458 in THADA was associated with increased luteinizing hormone (LH) (P 0.01) and testosterone (T) (P 0.02) levels in subjects with PCOS; the LH/follicle-stimulating hormone ratio was also higher in the AA group (P 0.01). Also using a recessive model, the CC genotype of rs12478601, also in THADA, was associated with increased levels of low-density lipoprotein (P 0.02). Using a dominant model, the GG AG group for rs2479106 in DENND1A was associated with elevated serum insulin levels 2 h after a glucose load in the patients with PCOS (P 0.02). All of the comparisons were adjusted for age and BMI. The relatively younger age of the participants may represent a considerable bias when evaluating metabolic alterations as a function of different genotypes, as significant metabolic disturbances may emerge later in life. Furthermore, the sample sizes of several sub-genotype groups were relatively small; to some extent this limited the statistical power of the analysis. The PCOS susceptibility genes, THADA and DENND1A, carry risk alleles that are associated with endocrine and metabolic disturbances in PCOS patients of Han Chinese descent. The findings have shown genuine heterogeneity, stratified on the basis of both clinical findings and genotypes. Replication of these results is expected in other ethnic groups. This research was supported by the National Basic Research Program of China (973 program) (2010CB945002, 2012CB944700), the National Natural Science Foundation of China (81000238, 81070461, 81000236, 30973170), the Graduate Independent Innovation Foundation of Shandong University (GIIFSDU) (21300070613242, 21300070613246), the Science Research Foundation item of no-earnings health vocation (201002013) and the National Key Technology Research and Development Program (2011BAI17B00). There are no competing interests.
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页码:538 / 544
页数:7
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