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Paraoxonase single nucleotide variants show associations with polycystic ovary syndrome: a meta-analysis.


ABSTRACT: BACKGROUND:Etiology of polycystic ovary syndrome (PCOS) is attributed to genetic and environmental factors. One environmental factor is oxidative stress. Paraoxonase 1 (PON1) is an antioxidant high-density lipoprotein-associated enzyme encoded by the PON1 gene. The PON1 gene has been implicated in the risk for PCOS, the influence of which appears to come from single nucleotide variants (SNVs) at multiple genetic loci. However, association study reports have been inconsistent which compels a meta-analysis to obtain more precise estimates. METHODS:From 12 publications, extracted genotype data were used in two genetic procedures. First, linkage disequilibrium (LD) was used to group eight PON SNVs into three: LD1, LD2 and LD3. Second, frequencies of the variant (var), wild-type (wt) and heterozygous (het) genotypes were used for genetic modeling (allele-genotype for LD1 and standard for LD2 and LD3). Risk associations were expressed in terms of pooled odds ratios (ORs), 95% confidence intervals (CIs) and Pa-values. Evidence was considered strong when significance was high (Pa?

SUBMITTER: Kunjantarachot A 

PROVIDER: S-EPMC7678182 | biostudies-literature | 2020 Nov

REPOSITORIES: biostudies-literature

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Paraoxonase single nucleotide variants show associations with polycystic ovary syndrome: a meta-analysis.

Kunjantarachot Anthicha A   Pabalan Noel N   Jarjanazi Hamdi H   Christofolini Denise Maria DM   Montagna Erik E   Barbosa Caio Parente CP   Bianco Bianca B  

Reproductive biology and endocrinology : RB&E 20201120 1


<h4>Background</h4>Etiology of polycystic ovary syndrome (PCOS) is attributed to genetic and environmental factors. One environmental factor is oxidative stress. Paraoxonase 1 (PON1) is an antioxidant high-density lipoprotein-associated enzyme encoded by the PON1 gene. The PON1 gene has been implicated in the risk for PCOS, the influence of which appears to come from single nucleotide variants (SNVs) at multiple genetic loci. However, association study reports have been inconsistent which compel  ...[more]

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