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DOI 10.1038/s41598-020-59228-4

Медицинская библиотека · Scientific reports · 2020

Genotype-independent association between vitamin D deficiency and polycystic ovarian syndrome in Lahore, Pakistan.

Lone Nasira M, Riaz Saba, Eusaph Amna Z, Mein Charles A, Wozniak Eva L, Xenakis Theodoros, Wu Zhenqiang, Younis Sidra, Jolliffe David A, Junaid Kashaf, Martineau Adrian R

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

Both vitamin D deficiency and single nucleotide polymorphisms (SNPs) in the gene encoding the vitamin D receptor (VDR) have been widely reported to associate with susceptibility to polycystic ovarian syndrome (PCOS). A case-control study was conducted to study the influence of vitamin D status and genotpye for 24 SNPs in four genes in the vitamin D pathway (VDR, DBP, CYP27B1, CYP24A1) on PCOS. Statistical analyses were conducted to identify phenotypic and genotypic factors associated with risk of PCOS and to test for interactions between genotype and vitamin D status. PCOS was independently associated with lower age, higher body mass index, lower waist-hip ratio, vitamin D deficiency (serum 25-hydroxyvitamin D concentration <10 ng/mL), lack of outdoor exercise, increased fasting glucose and a family history of PCOS in at least one first degree relative. No statistically significant association was observed between the genotype of any SNP investigated and risk of PCOS, either as a main effect or in interaction with vitamin D status. We report a strong and independent association between vitamin D deficiency and risk of PCOS in Pakistan, that was not modified by genetic variation in the vitamin D pathway.

Для цитирования: Lone Nasira M, Riaz Saba, Eusaph Amna Z, Mein Charles A, Wozniak Eva L, Xenakis Theodoros, Wu Zhenqiang, Younis Sidra, Jolliffe David A, Junaid Kashaf, Martineau Adrian R. Genotype-independent association between vitamin D deficiency and polycystic ovarian syndrome in Lahore, Pakistan.. Scientific reports. 2020. DOI: 10.1038/s41598-020-59228-4.

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