rs11676014 - IL1A - IL1B
Magnitude 2.8 · 1 study on file
Reported associations
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Genome-wide association study of primary dysmenorrhea in the Taiwan Biobank validates associations near the NGF and IL1 gene loci. - Journal of human genetics (2022) · Lee CC, Lee MG, Huang IH, Tan J, McCaw ZR, Su KY, Hsu TC, Huang RYJ, Kuo PH, Chen SC · PubMed 35351958
Using the Taiwan Biobank, we aimed to identify traits and genetic variations that could predispose Han Chinese women to primary dysmenorrhea. Cases of primary dysmenorrhea included those who self-reported "frequent dysmenorrhea" in a dysmenorrhea-related Taiwan Biobank questionnaire, and those who have been diagnosed with severe dysmenorrhea by a physician. Controls were those without self-reported dysmenorrhea. Customized Axiom-Taiwan Biobank Array Plates were used to perform whole-genome genotyping, PLINK was used to perform association tests, and HaploReg was used to conduct functional annotations of SNPs and bioinformatic analyses. The GWAS analysis included 1186 cases and 24,020 controls. We identified 53 SNPs that achieved genome-wide significance (P < 5 × 10 , which cluster
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Lifestyle context
Concrete actions anchored to the cited research. We do not prescribe, we describe.
Discuss with your doctor
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dysmenorrhea prevention and treatment options Moderate
Genetic predisposition to dysmenorrhea warrants proactive discussion of management strategies with healthcare provider
Screening
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menstrual pain severity and dysmenorrhea symptoms Moderate
IL1A-IL1B genetic variants are associated with increased primary dysmenorrhea risk through inflammatory pathways
Maintain a symptom diary tracking pain severity, duration, and impact on daily activities during each menstrual cycle