Genetic Determinants of Premature Menopause in A Mashhad Population Cohort
نویسندگان
1 Department of Medical Genetics and Molecular Medicine, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
2 Department of Medical Genetics and Molecular Medicine, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
3 Department of Medical Genetics and Molecular Medicine, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
4 Department of Medical Genetics and Molecular Medicine, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
5 Metabolic Syndrome Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
6 International UNESCO Center for Health-Related Basic Sciences and Human Nutrition, Mashhad University of Medical Sciences, Mashhad, Iran
7 Department of Genetics, Faculty of Biological science, Shahid Beheshti University,Tehran, Iran
8 Student Research Committee, Mashhad University of Medical Sciences, Mashhad, Iran
9 Student Research Committee, Mashhad University of Medical Sciences, Mashhad, Iran.
10 Student Research Committee, Mashhad University of Medical Sciences, Mashhad, Iran
doi
10.22074/ijfs.2020.134688چکیده
Background: Premature menopause is characterized by amenorrhea before age of 40 years, markedly raised serumluteinizing hormone (LH) level, follicle-stimulating hormone (FSH) level and reduced serum level of estradiol.Genome-wide analysis suggested several loci associated with premature menopause. Here, we aimed to analyze associationof variants at the MCM8, FNDC4, PRRC2A, TLK1, ZNF346 and TMEM150B gene loci with prematuremenopause.Materials and Methods: In this cross-sectional study, a total of 117 women with premature menopause were comparedto 183 healthy women. Anthropometric indices were measured in all participants: height, weight, body mass index(BMI), waist circumference (WC) and wrist circumference. Eight single-nucleotide polymorphisms (SNPs) of theindicated genes (rs16991615, rs244715, rs451417, rs1046089, rs7246479, rs4806660, rs10183486 and rs2303369)were identified from the literature. Genotyping was performed using tetra-ARMS polymerase chain reaction (PCR)and ASO-PCR methods.Results: T allele of the rs16991615, rs1046089, rs7246479 and rs10183486, C allele of rs244715, rs451417 andrs4806660 as well as TT genotype of rs2303369 were associated with an increased risk of premature menopause,likely causing susceptibility to primary ovarian insufficiency (POI) in comparison with C allele. We also found anassociation between the rs16991615 SNP with premature menopause. Frequency of the minor allele in cases wasincreased for all SNPs in comparison with controls. All minor alleles, except for rs2303369, showed a statisticallysignificant increased odds ratio (OR). However, after Bonferroni correction for multiple testing, none of the P valueswere remained significant.Conclusion: The selected polymorphisms in MCM8, FNDC4, PRRC2A, TLK1, ZNF346 and TMEM150B genesmay potentially affect susceptibility to premature menopause, although replication of the results in larger cohort couldclarify this.
