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Common Variant rs9939609 in Gene FTO Confers Risk to Polycystic Ovary Syndrome

BACKGROUND: Fat mass and obesity-associated gene (FTO) has been associated with obesity, especially the common variant rs9939609. Polycystic ovary syndrome (PCOS) is a complex endocrine-metabolic disorder and over 50% of patients are overweight/obese. Thus FTO is a potential candidate gene for PCOS...

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Autores principales: Li, Tao, Wu, Keliang, You, Li, Xing, Xiuye, Wang, Peng, Cui, Linlin, Liu, Hongbin, Cui, Yuqian, Bian, Yuehong, Ning, Yunna, Zhao, Han, Tang, Rong, Chen, Zi-Jiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3698074/
https://www.ncbi.nlm.nih.gov/pubmed/23840863
http://dx.doi.org/10.1371/journal.pone.0066250
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author Li, Tao
Wu, Keliang
You, Li
Xing, Xiuye
Wang, Peng
Cui, Linlin
Liu, Hongbin
Cui, Yuqian
Bian, Yuehong
Ning, Yunna
Zhao, Han
Tang, Rong
Chen, Zi-Jiang
author_facet Li, Tao
Wu, Keliang
You, Li
Xing, Xiuye
Wang, Peng
Cui, Linlin
Liu, Hongbin
Cui, Yuqian
Bian, Yuehong
Ning, Yunna
Zhao, Han
Tang, Rong
Chen, Zi-Jiang
author_sort Li, Tao
collection PubMed
description BACKGROUND: Fat mass and obesity-associated gene (FTO) has been associated with obesity, especially the common variant rs9939609. Polycystic ovary syndrome (PCOS) is a complex endocrine-metabolic disorder and over 50% of patients are overweight/obese. Thus FTO is a potential candidate gene for PCOS but their relationship is confusing and remains to be clarified in different population with a large sample size. METHOD: This study was performed adopting a two-stage design by genotyping SNP rs9939609. The first set comprise of 741 PCOS and 704 control subjects, with data from our previous GWAS. The second phase of replication study was performed among another independent group of 2858 PCOS and 2358 control subjects using TaqMan-MGB probe assay. All subjects are from Han Chinese. RESULTS: The less meaningful association of FTO rs9939609 and PCOS discovered in GWAS (P = 2.47E-03), was further confirmed in the replication study (P = 1.86E-09). Using meta-analysis, the P-meta value has reached 6.89E-12, over-exceeding the genome-wide association level of 5.00E-8. By combination, the P value was 1.26E-11 and after BMI adjustment it remained significant(P = 1.82E-06). To further elucidate whether this association is resulted from obesity or PCOS per se, the samples were divided into two groups–obese and non-obese PCOS, and the results were still positive in obese group (P obese = 5.81E-05, OR = 1.55), as well as in non-obese PCOS group (P non-obese = 7.06E-04, OR = 1.28). CONCLUSION: Variant rs9939609 in FTO is associated with PCOS in Chinese women, not only in obese PCOS subjects, but also in non-obese cases.
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spelling pubmed-36980742013-07-09 Common Variant rs9939609 in Gene FTO Confers Risk to Polycystic Ovary Syndrome Li, Tao Wu, Keliang You, Li Xing, Xiuye Wang, Peng Cui, Linlin Liu, Hongbin Cui, Yuqian Bian, Yuehong Ning, Yunna Zhao, Han Tang, Rong Chen, Zi-Jiang PLoS One Research Article BACKGROUND: Fat mass and obesity-associated gene (FTO) has been associated with obesity, especially the common variant rs9939609. Polycystic ovary syndrome (PCOS) is a complex endocrine-metabolic disorder and over 50% of patients are overweight/obese. Thus FTO is a potential candidate gene for PCOS but their relationship is confusing and remains to be clarified in different population with a large sample size. METHOD: This study was performed adopting a two-stage design by genotyping SNP rs9939609. The first set comprise of 741 PCOS and 704 control subjects, with data from our previous GWAS. The second phase of replication study was performed among another independent group of 2858 PCOS and 2358 control subjects using TaqMan-MGB probe assay. All subjects are from Han Chinese. RESULTS: The less meaningful association of FTO rs9939609 and PCOS discovered in GWAS (P = 2.47E-03), was further confirmed in the replication study (P = 1.86E-09). Using meta-analysis, the P-meta value has reached 6.89E-12, over-exceeding the genome-wide association level of 5.00E-8. By combination, the P value was 1.26E-11 and after BMI adjustment it remained significant(P = 1.82E-06). To further elucidate whether this association is resulted from obesity or PCOS per se, the samples were divided into two groups–obese and non-obese PCOS, and the results were still positive in obese group (P obese = 5.81E-05, OR = 1.55), as well as in non-obese PCOS group (P non-obese = 7.06E-04, OR = 1.28). CONCLUSION: Variant rs9939609 in FTO is associated with PCOS in Chinese women, not only in obese PCOS subjects, but also in non-obese cases. Public Library of Science 2013-07-01 /pmc/articles/PMC3698074/ /pubmed/23840863 http://dx.doi.org/10.1371/journal.pone.0066250 Text en © 2013 Li et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Li, Tao
Wu, Keliang
You, Li
Xing, Xiuye
Wang, Peng
Cui, Linlin
Liu, Hongbin
Cui, Yuqian
Bian, Yuehong
Ning, Yunna
Zhao, Han
Tang, Rong
Chen, Zi-Jiang
Common Variant rs9939609 in Gene FTO Confers Risk to Polycystic Ovary Syndrome
title Common Variant rs9939609 in Gene FTO Confers Risk to Polycystic Ovary Syndrome
title_full Common Variant rs9939609 in Gene FTO Confers Risk to Polycystic Ovary Syndrome
title_fullStr Common Variant rs9939609 in Gene FTO Confers Risk to Polycystic Ovary Syndrome
title_full_unstemmed Common Variant rs9939609 in Gene FTO Confers Risk to Polycystic Ovary Syndrome
title_short Common Variant rs9939609 in Gene FTO Confers Risk to Polycystic Ovary Syndrome
title_sort common variant rs9939609 in gene fto confers risk to polycystic ovary syndrome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3698074/
https://www.ncbi.nlm.nih.gov/pubmed/23840863
http://dx.doi.org/10.1371/journal.pone.0066250
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