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Published in: Reproductive Biology and Endocrinology 1/2019

Open Access 01-12-2019 | Research

Effects of FSHR polymorphisms on premature ovarian insufficiency in human beings: a meta-analysis

Authors: Wenling Huang, Ying Cao, Lei Shi

Published in: Reproductive Biology and Endocrinology | Issue 1/2019

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Abstract

Background

Whether follicle-stimulating hormone receptor (FSHR) polymorphisms are implicated in premature ovarian insufficiency (POI) remains controversial. Thus, we performed this study to explore correlation between FSHR polymorphisms and POI in human beings.

Methods

Literature retrieve was conducted in PubMed, Medline, Embase and CNKI. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated.

Results

Sixteen studies were enrolled for analyses. No significant relationship with POI was found for rs6165 and rs6166 polymorphisms in overall analyses. Further subgroup analyses revealed that rs6166 polymorphism was significantly associated with the risk of POI in Asians with both FEM and REM. Nevertheless, we failed to detect any significant associations with POI for other ethnicities.

Conclusions

Our findings indicated that FSHR rs6166 polymorphism may serve as a potential genetic biomarker of POI in Asians, but not in other ethnicities.
Literature
2.
go back to reference Laven JS. Primary ovarian insufficiency. Semin Reprod Med. 2016;34:230–4.CrossRef Laven JS. Primary ovarian insufficiency. Semin Reprod Med. 2016;34:230–4.CrossRef
3.
go back to reference Yonkers KA, Simoni MK. Premenstrual disorders. Am J Obstet Gynecol. 2018;218:68–74.CrossRef Yonkers KA, Simoni MK. Premenstrual disorders. Am J Obstet Gynecol. 2018;218:68–74.CrossRef
4.
go back to reference Ferrarini E, Russo L, Fruzzetti F, et al. Clinical characteristics and genetic analysis in women with premature ovarian insufficiency. Maturitas. 2013;74:61–7.CrossRef Ferrarini E, Russo L, Fruzzetti F, et al. Clinical characteristics and genetic analysis in women with premature ovarian insufficiency. Maturitas. 2013;74:61–7.CrossRef
5.
go back to reference Rossetti R, Ferrari I, Bonomi M, et al. Genetics of primary ovarian insufficiency. Clin Genet. 2017;9:183–98.CrossRef Rossetti R, Ferrari I, Bonomi M, et al. Genetics of primary ovarian insufficiency. Clin Genet. 2017;9:183–98.CrossRef
7.
go back to reference Meduri G, Bachelot A, Cocca MP, et al. Molecular pathology of the FSH receptor: new insights into FSH physiology. Mol Cell Endocrinol. 2008;282:130–42.CrossRef Meduri G, Bachelot A, Cocca MP, et al. Molecular pathology of the FSH receptor: new insights into FSH physiology. Mol Cell Endocrinol. 2008;282:130–42.CrossRef
8.
go back to reference Trevisan CM, Peluso C, Cordts EB, et al. Ala307Thr and Asn680Ser polymorphisms of FSHR gene in human reproduction outcomes. Cell Physiol Biochem. 2014;34:1527–35.CrossRef Trevisan CM, Peluso C, Cordts EB, et al. Ala307Thr and Asn680Ser polymorphisms of FSHR gene in human reproduction outcomes. Cell Physiol Biochem. 2014;34:1527–35.CrossRef
9.
go back to reference Borgbo T, Jeppesen JV, Lindgren I, et al. Effect of the FSH receptor single nucleotide polymorphisms (FSHR 307/680) on the follicular fluid hormone profile and the granulosa cell gene expression in human small antral follicles. Mol Hum Reprod. 2015;21:255–61.CrossRef Borgbo T, Jeppesen JV, Lindgren I, et al. Effect of the FSH receptor single nucleotide polymorphisms (FSHR 307/680) on the follicular fluid hormone profile and the granulosa cell gene expression in human small antral follicles. Mol Hum Reprod. 2015;21:255–61.CrossRef
10.
go back to reference La Marca A, Papaleo E, Alviggi C, et al. The combination of genetic variants of the FSHB and FSHR genes affects serum FSH in women of reproductive age. Hum Reprod. 2013;28:1369–74.CrossRef La Marca A, Papaleo E, Alviggi C, et al. The combination of genetic variants of the FSHB and FSHR genes affects serum FSH in women of reproductive age. Hum Reprod. 2013;28:1369–74.CrossRef
11.
go back to reference Moher D, Liberati A, Tetzlaff J, et al. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Ann Intern Med. 2009;151:264–9.CrossRef Moher D, Liberati A, Tetzlaff J, et al. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Ann Intern Med. 2009;151:264–9.CrossRef
12.
go back to reference Stang A. Critical evaluation of the Newcastle-Ottawa scale for the assessment of the quality of nonrandomized studies in meta-analyses. Eur J Epidemiol. 2010;25:603–5.CrossRef Stang A. Critical evaluation of the Newcastle-Ottawa scale for the assessment of the quality of nonrandomized studies in meta-analyses. Eur J Epidemiol. 2010;25:603–5.CrossRef
13.
go back to reference Xie X, Shi X, Liu M. The roles of TLR gene polymorphisms in atherosclerosis: a systematic review and meta-analysis of 35,317 subjects. Scand J Immunol. 2017;86:50–8.CrossRef Xie X, Shi X, Liu M. The roles of TLR gene polymorphisms in atherosclerosis: a systematic review and meta-analysis of 35,317 subjects. Scand J Immunol. 2017;86:50–8.CrossRef
14.
go back to reference Shi X, Xie X, Jia Y, et al. Associations of insulin receptor and insulin receptor substrates genetic polymorphisms with polycystic ovary syndrome: a systematic review and meta-analysis. J Obstet Gynaecol Res. 2016;42:844–54.CrossRef Shi X, Xie X, Jia Y, et al. Associations of insulin receptor and insulin receptor substrates genetic polymorphisms with polycystic ovary syndrome: a systematic review and meta-analysis. J Obstet Gynaecol Res. 2016;42:844–54.CrossRef
15.
go back to reference Xie X, Shi X, Xun X, et al. Endothelial nitric oxide synthase gene single nucleotide polymorphisms and the risk of hypertension: a meta-analysis involving 63,258 subjects. Clin Exp Hypertens. 2017;39:175–82.CrossRef Xie X, Shi X, Xun X, et al. Endothelial nitric oxide synthase gene single nucleotide polymorphisms and the risk of hypertension: a meta-analysis involving 63,258 subjects. Clin Exp Hypertens. 2017;39:175–82.CrossRef
Metadata
Title
Effects of FSHR polymorphisms on premature ovarian insufficiency in human beings: a meta-analysis
Authors
Wenling Huang
Ying Cao
Lei Shi
Publication date
01-12-2019
Publisher
BioMed Central
Published in
Reproductive Biology and Endocrinology / Issue 1/2019
Electronic ISSN: 1477-7827
DOI
https://doi.org/10.1186/s12958-019-0528-1

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