A mutant single nucleotide polymorphism of follicle-stimulating hormone receptor is associated with a lower risk of endometriosis
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⤵ 9 in-corpus citations
AI-generated summary
This study investigated a specific single nucleotide polymorphism in the follicle-stimulating hormone receptor and found it associated with a reduced risk of developing endometriosis.
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Abstract
Six hundred thirty-seven Taiwanese Chinese women including 300 patients with endometriosis and 337 controls without endometriosis were enrolled to investigate the association between nonsynonymous single nucleotide polymorphism of the FSH receptor gene and the risk of endometriosis. For the A/G polymorphism of FSH receptor gene (Asn680Ser), a univariate analysis for women with endometriosis demonstrated that both the GG genotype (680Ser/Ser) and GA genotype (680Ser/Asn) were associated with a significantly lower risk of endometriosis.
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Cited by (9)
- Epidemiologic Factors Associated with Endometriosis in East Asia 2019
- Associations between a single nucleotide polymorphism of stress-induced phosphoprotein 1 and endometriosis/adenomyosis 2018
- The Impact of FSHR Gene Polymorphisms Ala307Thr and Asn680Ser in the Endometriosis Development 2018
- A review of the risk factors, genetics and treatment of endometriosis in Chinese women: a comparative update 2018
- LH (Trp8Arg/Ile15Thr), LHR (insLQ) and FSHR (Asn680Ser) polymorphisms genotypic prevalence in women with endometriosis and infertility 2015
- Follicle-stimulating hormone receptor gene polymorphisms in women with endometriosis 2014
- Understanding the role of epigenomic, genomic and genetic alterations in the development of endometriosis (review) 2014
- TP53 gene polymorphisms at codons 11, 72, and 248 and association with endometriosis in a Brazilian population 2014
- Functional analyses of endometriosis-related polymorphisms in the estrogen synthesis and metabolism-related genes 2012
Source provenance
- europepmc
- last seen: 2026-10-14T06:08:39.101224+00:00
- openalex
- last seen: 2026-06-10T17:14:06.276822+00:00
- pubmed
- last seen: 2026-10-08T21:07:58.051504+00:00
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