Cargando…

The role of age at menarche and age at menopause in Alzheimer’s disease: evidence from a bidirectional mendelian randomization study

The association between endogenous estrogen exposure and Alzheimer’s disease (AD) remains inconclusive in previous observational studies, and few Mendelian randomization (MR) studies have focused on their causality thus far. We performed a bidirectional MR study to clarify the causality and causal d...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Mingli, Lin, Jiali, Liang, Shuang, Chen, Zefeng, Bai, Yulan, Long, Xinyang, Huang, Shengzhu, Mo, Zengnan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8386554/
https://www.ncbi.nlm.nih.gov/pubmed/34347623
http://dx.doi.org/10.18632/aging.203384
_version_ 1783742283673239552
author Li, Mingli
Lin, Jiali
Liang, Shuang
Chen, Zefeng
Bai, Yulan
Long, Xinyang
Huang, Shengzhu
Mo, Zengnan
author_facet Li, Mingli
Lin, Jiali
Liang, Shuang
Chen, Zefeng
Bai, Yulan
Long, Xinyang
Huang, Shengzhu
Mo, Zengnan
author_sort Li, Mingli
collection PubMed
description The association between endogenous estrogen exposure and Alzheimer’s disease (AD) remains inconclusive in previous observational studies, and few Mendelian randomization (MR) studies have focused on their causality thus far. We performed a bidirectional MR study to clarify the causality and causal direction of age at menarche and age at menopause, which are indicators of endogenous estrogen exposure, on AD risk. We obtained all genetic datasets for the MR analyses using publicly available summary statistics based on individuals of European ancestry from the IEU GWAS database. The MR analyses indicated no significant causal relationship between the genetically determined age at menarche (outlier-adjusted inverse variance weighted odds ratio [IVWOR] = 0.926; 95% confidence interval [CI], 0.803-1.066) or age at menopause (outlier-adjusted IVWOR = 0.981; 95% CI, 0.941-1.022) and AD risk. Similarly, AD did not show any causal association with age at menarche or age at menopause. The sensitivity analyses yielded similar results. In contrast, an inverse association was detected between age at menarche and body mass index (BMI, outlier-adjusted IVW β = -0.043; 95% CI, -0.077 to -0.009). Our bidirectional MR study provides no evidence for a causal relationship between the genetically determined age at menarche or age at menopause and AD susceptibility, or vice versa. However, earlier menarche might be associated with higher adult BMI.
format Online
Article
Text
id pubmed-8386554
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Impact Journals
record_format MEDLINE/PubMed
spelling pubmed-83865542021-08-27 The role of age at menarche and age at menopause in Alzheimer’s disease: evidence from a bidirectional mendelian randomization study Li, Mingli Lin, Jiali Liang, Shuang Chen, Zefeng Bai, Yulan Long, Xinyang Huang, Shengzhu Mo, Zengnan Aging (Albany NY) Research Paper The association between endogenous estrogen exposure and Alzheimer’s disease (AD) remains inconclusive in previous observational studies, and few Mendelian randomization (MR) studies have focused on their causality thus far. We performed a bidirectional MR study to clarify the causality and causal direction of age at menarche and age at menopause, which are indicators of endogenous estrogen exposure, on AD risk. We obtained all genetic datasets for the MR analyses using publicly available summary statistics based on individuals of European ancestry from the IEU GWAS database. The MR analyses indicated no significant causal relationship between the genetically determined age at menarche (outlier-adjusted inverse variance weighted odds ratio [IVWOR] = 0.926; 95% confidence interval [CI], 0.803-1.066) or age at menopause (outlier-adjusted IVWOR = 0.981; 95% CI, 0.941-1.022) and AD risk. Similarly, AD did not show any causal association with age at menarche or age at menopause. The sensitivity analyses yielded similar results. In contrast, an inverse association was detected between age at menarche and body mass index (BMI, outlier-adjusted IVW β = -0.043; 95% CI, -0.077 to -0.009). Our bidirectional MR study provides no evidence for a causal relationship between the genetically determined age at menarche or age at menopause and AD susceptibility, or vice versa. However, earlier menarche might be associated with higher adult BMI. Impact Journals 2021-08-04 /pmc/articles/PMC8386554/ /pubmed/34347623 http://dx.doi.org/10.18632/aging.203384 Text en Copyright: © 2021 Li et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Li, Mingli
Lin, Jiali
Liang, Shuang
Chen, Zefeng
Bai, Yulan
Long, Xinyang
Huang, Shengzhu
Mo, Zengnan
The role of age at menarche and age at menopause in Alzheimer’s disease: evidence from a bidirectional mendelian randomization study
title The role of age at menarche and age at menopause in Alzheimer’s disease: evidence from a bidirectional mendelian randomization study
title_full The role of age at menarche and age at menopause in Alzheimer’s disease: evidence from a bidirectional mendelian randomization study
title_fullStr The role of age at menarche and age at menopause in Alzheimer’s disease: evidence from a bidirectional mendelian randomization study
title_full_unstemmed The role of age at menarche and age at menopause in Alzheimer’s disease: evidence from a bidirectional mendelian randomization study
title_short The role of age at menarche and age at menopause in Alzheimer’s disease: evidence from a bidirectional mendelian randomization study
title_sort role of age at menarche and age at menopause in alzheimer’s disease: evidence from a bidirectional mendelian randomization study
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8386554/
https://www.ncbi.nlm.nih.gov/pubmed/34347623
http://dx.doi.org/10.18632/aging.203384
work_keys_str_mv AT limingli theroleofageatmenarcheandageatmenopauseinalzheimersdiseaseevidencefromabidirectionalmendelianrandomizationstudy
AT linjiali theroleofageatmenarcheandageatmenopauseinalzheimersdiseaseevidencefromabidirectionalmendelianrandomizationstudy
AT liangshuang theroleofageatmenarcheandageatmenopauseinalzheimersdiseaseevidencefromabidirectionalmendelianrandomizationstudy
AT chenzefeng theroleofageatmenarcheandageatmenopauseinalzheimersdiseaseevidencefromabidirectionalmendelianrandomizationstudy
AT baiyulan theroleofageatmenarcheandageatmenopauseinalzheimersdiseaseevidencefromabidirectionalmendelianrandomizationstudy
AT longxinyang theroleofageatmenarcheandageatmenopauseinalzheimersdiseaseevidencefromabidirectionalmendelianrandomizationstudy
AT huangshengzhu theroleofageatmenarcheandageatmenopauseinalzheimersdiseaseevidencefromabidirectionalmendelianrandomizationstudy
AT mozengnan theroleofageatmenarcheandageatmenopauseinalzheimersdiseaseevidencefromabidirectionalmendelianrandomizationstudy
AT limingli roleofageatmenarcheandageatmenopauseinalzheimersdiseaseevidencefromabidirectionalmendelianrandomizationstudy
AT linjiali roleofageatmenarcheandageatmenopauseinalzheimersdiseaseevidencefromabidirectionalmendelianrandomizationstudy
AT liangshuang roleofageatmenarcheandageatmenopauseinalzheimersdiseaseevidencefromabidirectionalmendelianrandomizationstudy
AT chenzefeng roleofageatmenarcheandageatmenopauseinalzheimersdiseaseevidencefromabidirectionalmendelianrandomizationstudy
AT baiyulan roleofageatmenarcheandageatmenopauseinalzheimersdiseaseevidencefromabidirectionalmendelianrandomizationstudy
AT longxinyang roleofageatmenarcheandageatmenopauseinalzheimersdiseaseevidencefromabidirectionalmendelianrandomizationstudy
AT huangshengzhu roleofageatmenarcheandageatmenopauseinalzheimersdiseaseevidencefromabidirectionalmendelianrandomizationstudy
AT mozengnan roleofageatmenarcheandageatmenopauseinalzheimersdiseaseevidencefromabidirectionalmendelianrandomizationstudy