Candidate Genes for Age at Menarche Are Associated With Uterine Leiomyoma - Sorbonne Université
Journal Articles Frontiers in Genetics Year : 2021

Candidate Genes for Age at Menarche Are Associated With Uterine Leiomyoma

Abstract

Age at menarche (AAM) is an important marker of the pubertal development and function of the hypothalamic-pituitary-ovarian system. It was reported as a possible factor for a risk of uterine leiomyoma (UL). However, while more than 350 loci for AAM have been determined by genome-wide association studies (GWASs) to date, no studies of these loci for their association with UL have been conducted so far. In this study, we analyzed 52 candidate loci for AAM for possible association with UL in a sample of 569 patients and 981 controls. The results of the study suggested that 23 out of the 52 studied polymorphisms had association with UL. Locus rs7759938 LIN28B was individually associated with the disease according to the dominant model. Twenty loci were associated with UL within 11 most significant models of intergenic interactions. Nine loci involved in 16 most significant models of interactions between single-nucleotide polymorphism (SNP), induced abortions, and chronic endometritis were associated with UL. Among the 23 loci associated with UL, 16 manifested association also with either AAM (7 SNPs) or height and/or body mass index (BMI) (13 SNPs). The above 23 SNPs and 514 SNPs linked to them have non-synonymous, regulatory, and expression quantitative trait locus (eQTL) significance for 35 genes, which play roles in the pathways related to development of the female reproductive organs and hormone-mediated signaling [false discovery rate (FDR) ≤ 0.05]. This is the first study reporting associations of candidate genes for AAM with UL.
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Dates and versions

hal-03148523 , version 1 (22-02-2021)

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Irina Ponomarenko, Evgeny Reshetnikov, Alexey Polonikov, Irina Verzilina, Inna Sorokina, et al.. Candidate Genes for Age at Menarche Are Associated With Uterine Leiomyoma. Frontiers in Genetics, 2021, 11, pp.512940. ⟨10.3389/fgene.2020.512940⟩. ⟨hal-03148523⟩
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