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Identifying potential causal effects of age at menopause: a Mendelian randomization phenome-wide association study
Age at natural menopause (ANM) is associated with a range of health-related traits, including bone health, female reproductive cancers, and cardiometabolic health. Our objective was to conduct a Mendelian randomization phenome-wide association study (MR-pheWAS) of ANM. We conducted a hypothesis-free...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9529691/ https://www.ncbi.nlm.nih.gov/pubmed/36057072 http://dx.doi.org/10.1007/s10654-022-00903-3 |
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author | Magnus, Maria C. Borges, Maria Carolina Fraser, Abigail Lawlor, Deborah A. |
author_facet | Magnus, Maria C. Borges, Maria Carolina Fraser, Abigail Lawlor, Deborah A. |
author_sort | Magnus, Maria C. |
collection | PubMed |
description | Age at natural menopause (ANM) is associated with a range of health-related traits, including bone health, female reproductive cancers, and cardiometabolic health. Our objective was to conduct a Mendelian randomization phenome-wide association study (MR-pheWAS) of ANM. We conducted a hypothesis-free analysis of the genetic risk score (GRS) for ANM with 18,961 health-related traits among 181,279 women in UK Biobank. We also stratified the GRS according to the involvement of SNPs in DNA damage response. We sought to replicate our findings in independent cohorts. We conducted a negative control MR-pheWAS among men. Among women, we identified potential effects of ANM on 221 traits (1.17% of all traits) at a false discovery rate (P value ≤ 5.83 × 10(–4)), and 91 (0.48%) potential effects when using Bonferroni threshold (P value ≤ 2.64 × 10(–6)). Our findings included 55 traits directly related to ANM (e.g. hormone replacement therapy, gynaecological conditions and menstrual conditions), and liver function, kidney function, lung function, blood-cell composition, breast cancer and bone and cardiometabolic health. Replication analyses confirmed that younger ANM was associated with HbA1c (adjusted mean difference 0.003 mmol/mol; 95% CI 0.001, 0.006 per year decrease in ANM), breast cancer (adjusted OR 0.96; 95% CI 0.95, 0.98), and bone-mineral density (adjusted mean difference − 0.05; 95% CI − 0.07, − 0.03 for lumbar spine). In men, 30 traits were associated with the GRS at a false discovery rate (P value ≤ 5.49 × 10(–6)), and 11 potential effects when using Bonferroni threshold (P value ≤ 2.75 × 10(–6)). In conclusion, our results suggest that younger ANM has potential causal effects on a range of health-related traits. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10654-022-00903-3. |
format | Online Article Text |
id | pubmed-9529691 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-95296912022-10-05 Identifying potential causal effects of age at menopause: a Mendelian randomization phenome-wide association study Magnus, Maria C. Borges, Maria Carolina Fraser, Abigail Lawlor, Deborah A. Eur J Epidemiol Reproductive Epidemiology Age at natural menopause (ANM) is associated with a range of health-related traits, including bone health, female reproductive cancers, and cardiometabolic health. Our objective was to conduct a Mendelian randomization phenome-wide association study (MR-pheWAS) of ANM. We conducted a hypothesis-free analysis of the genetic risk score (GRS) for ANM with 18,961 health-related traits among 181,279 women in UK Biobank. We also stratified the GRS according to the involvement of SNPs in DNA damage response. We sought to replicate our findings in independent cohorts. We conducted a negative control MR-pheWAS among men. Among women, we identified potential effects of ANM on 221 traits (1.17% of all traits) at a false discovery rate (P value ≤ 5.83 × 10(–4)), and 91 (0.48%) potential effects when using Bonferroni threshold (P value ≤ 2.64 × 10(–6)). Our findings included 55 traits directly related to ANM (e.g. hormone replacement therapy, gynaecological conditions and menstrual conditions), and liver function, kidney function, lung function, blood-cell composition, breast cancer and bone and cardiometabolic health. Replication analyses confirmed that younger ANM was associated with HbA1c (adjusted mean difference 0.003 mmol/mol; 95% CI 0.001, 0.006 per year decrease in ANM), breast cancer (adjusted OR 0.96; 95% CI 0.95, 0.98), and bone-mineral density (adjusted mean difference − 0.05; 95% CI − 0.07, − 0.03 for lumbar spine). In men, 30 traits were associated with the GRS at a false discovery rate (P value ≤ 5.49 × 10(–6)), and 11 potential effects when using Bonferroni threshold (P value ≤ 2.75 × 10(–6)). In conclusion, our results suggest that younger ANM has potential causal effects on a range of health-related traits. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10654-022-00903-3. Springer Netherlands 2022-09-03 2022 /pmc/articles/PMC9529691/ /pubmed/36057072 http://dx.doi.org/10.1007/s10654-022-00903-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Reproductive Epidemiology Magnus, Maria C. Borges, Maria Carolina Fraser, Abigail Lawlor, Deborah A. Identifying potential causal effects of age at menopause: a Mendelian randomization phenome-wide association study |
title | Identifying potential causal effects of age at menopause: a Mendelian randomization phenome-wide association study |
title_full | Identifying potential causal effects of age at menopause: a Mendelian randomization phenome-wide association study |
title_fullStr | Identifying potential causal effects of age at menopause: a Mendelian randomization phenome-wide association study |
title_full_unstemmed | Identifying potential causal effects of age at menopause: a Mendelian randomization phenome-wide association study |
title_short | Identifying potential causal effects of age at menopause: a Mendelian randomization phenome-wide association study |
title_sort | identifying potential causal effects of age at menopause: a mendelian randomization phenome-wide association study |
topic | Reproductive Epidemiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9529691/ https://www.ncbi.nlm.nih.gov/pubmed/36057072 http://dx.doi.org/10.1007/s10654-022-00903-3 |
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