MTHFR C677T、MTHFR A1298C、MTRR A66G and MTR A2756G polymorphisms and male infertility risk: a systematic review and meta-analysis.


Journal

Reproductive biology and endocrinology : RB&E
ISSN: 1477-7827
Titre abrégé: Reprod Biol Endocrinol
Pays: England
ID NLM: 101153627

Informations de publication

Date de publication:
30 Oct 2024
Historique:
received: 21 06 2023
accepted: 23 10 2024
medline: 31 10 2024
pubmed: 31 10 2024
entrez: 31 10 2024
Statut: epublish

Résumé

Epidemiological studies have reported that polymorphisms of folate-metabolizing genes have a significant impact on male infertility. However, the results of published studies have come to different conclusions. To determine an association between folate-metabolizing gene polymorphisms and the risk of male infertility. The meta-analysis was conducted according to the PRISMA 2020 statement. The protocol was registered with PROSPERO (CRD42023412251). Studies were searched from PubMed, Google Scholar, Embase, Scopus, and the Cochrane Library up to 24st October2023. Articles that satisfied the inclusion criteria were evaluated for their quality using the Newcastle-Ottawa Scale. Data were extracted from the eligible studies and were analyzed for pooled up odds ratio (OR) with 95% confidence interval (CI). Meta-analysis was conducted using STATA 12. Forty-six case-control studies were included in the meta-analysis which comprised 20,639 participants. The pooled analysis revealed that the MTHFR C677T polymorphism was significantly associated with male infertility and abnormospermia.Three-fifths of the model showed there was a significant association between the MTR A2756G polymorphism and male infertility. Both MTHFR A1298C and MTRR A66G polymorphisms were not significantly associated with male fertility. Furthermore, subgroup analysis revealed a significant association between the MTHFR C677T polymorphism and male fertility in Asian countries. This meta-analysis suggests that the MTHFR C677T and MTR A2756G polymorphisms may be a potential risk factor for male infertility.

Sections du résumé

BACKGROUND BACKGROUND
Epidemiological studies have reported that polymorphisms of folate-metabolizing genes have a significant impact on male infertility. However, the results of published studies have come to different conclusions.
OBJECTIVE OBJECTIVE
To determine an association between folate-metabolizing gene polymorphisms and the risk of male infertility.
METHODS METHODS
The meta-analysis was conducted according to the PRISMA 2020 statement. The protocol was registered with PROSPERO (CRD42023412251). Studies were searched from PubMed, Google Scholar, Embase, Scopus, and the Cochrane Library up to 24st October2023. Articles that satisfied the inclusion criteria were evaluated for their quality using the Newcastle-Ottawa Scale. Data were extracted from the eligible studies and were analyzed for pooled up odds ratio (OR) with 95% confidence interval (CI). Meta-analysis was conducted using STATA 12.
RESULTS RESULTS
Forty-six case-control studies were included in the meta-analysis which comprised 20,639 participants. The pooled analysis revealed that the MTHFR C677T polymorphism was significantly associated with male infertility and abnormospermia.Three-fifths of the model showed there was a significant association between the MTR A2756G polymorphism and male infertility. Both MTHFR A1298C and MTRR A66G polymorphisms were not significantly associated with male fertility. Furthermore, subgroup analysis revealed a significant association between the MTHFR C677T polymorphism and male fertility in Asian countries.
CONCLUSION CONCLUSIONS
This meta-analysis suggests that the MTHFR C677T and MTR A2756G polymorphisms may be a potential risk factor for male infertility.

Identifiants

pubmed: 39478547
doi: 10.1186/s12958-024-01306-7
pii: 10.1186/s12958-024-01306-7
doi:

Substances chimiques

Methylenetetrahydrofolate Reductase (NADPH2) EC 1.5.1.20
MTHFR protein, human EC 1.5.1.20
5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase EC 2.1.1.13
methionine synthase reductase EC 1.18.1.-
Ferredoxin-NADP Reductase EC 1.18.1.2
MTR protein, human EC 2.1.1.13.

Types de publication

Systematic Review Meta-Analysis Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

133

Informations de copyright

© 2024. The Author(s).

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Auteurs

Feng Li (F)

Hainan General Hospital (Hainan Affiliated Hospital of Hainan Medical University), Haikou, Hainan Province, 570311, China.

Ju-Ju Qi (JJ)

The First Hospital of Shijiazhuang, Shijiazhuang, Heibei Province, 050011, China.

Li-Xin Li (LX)

The First Hospital of Shijiazhuang, Shijiazhuang, Heibei Province, 050011, China.

Teng-Fei Yan (TF)

Baoding No.1, Central Hospital, Baoding, Hebei Province, 071000, China. ytfdeyouxiang@126.com.

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