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Age at natural menopause genetic risk score in relation to age at natural menopause and primary open-angle glaucoma in a US-based sample
- Source :
- Menopause, Menopause, Lippincott, Williams & Wilkins, 2017, 24 (2), pp.150-156. ⟨10.1097/GME.0000000000000741⟩, Menopause (New York, N.Y.), vol 24, iss 2, Menopause (New York, N.y.)
- Publication Year :
- 2017
- Publisher :
- HAL CCSD, 2017.
-
Abstract
- Supplemental Digital Content is available in the text<br />Objective: Several attributes of female reproductive history, including age at natural menopause (ANM), have been related to primary open-angle glaucoma (POAG). We assembled 18 previously reported common genetic variants that predict ANM to determine their association with ANM or POAG. Methods: Using data from the Nurses’ Health Study (7,143 women), we validated the ANM weighted genetic risk score in relation to self-reported ANM. Subsequently, to assess the relation with POAG, we used data from 2,160 female POAG cases and 29,110 controls in the National Eye Institute Glaucoma Human Genetics Collaboration Heritable Overall Operational Database (NEIGHBORHOOD), which consists of 8 datasets with imputed genotypes to 5.6+ million markers. Associations with POAG were assessed in each dataset, and site-specific results were meta-analyzed using the inverse weighted variance method. Results: The genetic risk score was associated with self-reported ANM (P = 2.2 × 10–77) and predicted 4.8% of the variance in ANM. The ANM genetic risk score was not associated with POAG (Odds Ratio (OR) = 1.002; 95% Confidence Interval (CI): 0.998, 1.007; P = 0.28). No single genetic variant in the panel achieved nominal association with POAG (P ≥0.20). Compared to the middle 80 percent, there was also no association with the lowest 10th percentile or highest 90th percentile of genetic risk score with POAG (OR = 0.75; 95% CI: 0.47, 1.21; P = 0.23 and OR = 1.10; 95% CI: 0.72, 1.69; P = 0.65, respectively). Conclusions: A genetic risk score predicting 4.8% of ANM variation was not related to POAG; thus, genetic determinants of ANM are unlikely to explain the previously reported association between the two phenotypes.
- Subjects :
- 0301 basic medicine
Percentile
Aging
genetic structures
MESH: Menopause
Neurodegenerative
MESH: Risk Assessment
Medical and Health Sciences
MESH: Genotype
0302 clinical medicine
Risk Factors
MESH: Risk Factors
Reproductive history
MESH: Genetic Variation
Genetic risk
[STAT.AP]Statistics [stat]/Applications [stat.AP]
Natural menopause
MESH: Middle Aged
Age Factors
Obstetrics and Gynecology
Middle Aged
Genetic risk score
3. Good health
Open-Angle
ComputingMethodologies_DOCUMENTANDTEXTPROCESSING
Female
Menopause
Primary open-angle glaucoma
[STAT.ME]Statistics [stat]/Methodology [stat.ME]
Glaucoma, Open-Angle
medicine.medical_specialty
Genotype
Age at natural menopause
Risk Assessment
03 medical and health sciences
medicine
Genetics
MESH: United States
Humans
Obstetrics & Reproductive Medicine
Eye Disease and Disorders of Vision
Gynecology
MESH: Age Factors
MESH: Humans
business.industry
Human Genome
Genetic variants
Neurosciences
Genetic Variation
Glaucoma
Odds ratio
Original Articles
Confidence interval
United States
eye diseases
030104 developmental biology
Good Health and Well Being
[SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics
030221 ophthalmology & optometry
MESH: Glaucoma, Open-Angle
[SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie
[INFO.INFO-BI]Computer Science [cs]/Bioinformatics [q-bio.QM]
business
MESH: Female
Demography
Subjects
Details
- Language :
- English
- ISSN :
- 10723714
- Database :
- OpenAIRE
- Journal :
- Menopause, Menopause, Lippincott, Williams & Wilkins, 2017, 24 (2), pp.150-156. ⟨10.1097/GME.0000000000000741⟩, Menopause (New York, N.Y.), vol 24, iss 2, Menopause (New York, N.y.)
- Accession number :
- edsair.doi.dedup.....88080e30449fd5ce3a8f23c07d0c8316
- Full Text :
- https://doi.org/10.1097/GME.0000000000000741⟩