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Relationship between BRSK1 rs12611091 variant and age at natural menopause based on physical activity

OBJECTIVES: The rs12611091 variant in the BR serine/threonine kinase 1 gene is one of the variants previously associated with age at natural menopause. So far, this variant has not been replicated in Taiwanese women. The purpose of this study was to determine the association between rs12611091 and a...

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Autores principales: Su, Chun-Lang, Tsai, Yi-Ling, Nfor, Oswald Ndi, Liu, Wen-Hsiu, Ho, Chien Chang, Lung, Chia-Chi, Lin, Yi-Tien, Wang, Lee, Liaw, Yung-Po
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott-Raven Publishers 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7147414/
https://www.ncbi.nlm.nih.gov/pubmed/31895179
http://dx.doi.org/10.1097/GME.0000000000001481
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author Su, Chun-Lang
Tsai, Yi-Ling
Nfor, Oswald Ndi
Liu, Wen-Hsiu
Ho, Chien Chang
Lung, Chia-Chi
Lin, Yi-Tien
Wang, Lee
Liaw, Yung-Po
author_facet Su, Chun-Lang
Tsai, Yi-Ling
Nfor, Oswald Ndi
Liu, Wen-Hsiu
Ho, Chien Chang
Lung, Chia-Chi
Lin, Yi-Tien
Wang, Lee
Liaw, Yung-Po
author_sort Su, Chun-Lang
collection PubMed
description OBJECTIVES: The rs12611091 variant in the BR serine/threonine kinase 1 gene is one of the variants previously associated with age at natural menopause. So far, this variant has not been replicated in Taiwanese women. The purpose of this study was to determine the association between rs12611091 and age at natural menopause based on physical activity. METHODS: A total of 1,758 women were eligible for analysis whose information about menopause was collected from the Taiwan Biobank. Multiple linear regression analysis was used for analysis. RESULTS: The mean age (standard deviation) at natural menopause was 50.82 (3.59) years. Of the eligible participants, 56.94% were rs12611091 CC carriers, 36.69% were TC carriers, and 6.37% were TT carriers. Compared to CC carriers, TC and TT carriers were associated with early menopause (β = −0.42, P = 0.02 and −0.87, P = 0.01, respectively). There was a significant interaction between rs12611091 and physical activity (P for interaction = 0.02). Compared to rs12611091 CC carriers, TC and TT carriers who were physically inactive were significantly associated with earlier menopause (β = −0.88, P < 0.01 and −1.25, P = 0.02, respectively). CONCLUSION: We demonstrated that rs12611091 variant was associated with age at natural menopause especially among inactive women in Taiwan. That is, women with TC and TT genotypes who were physically inactive were significantly associated with earlier natural menopause compared to those with CC genotype.
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spelling pubmed-71474142020-04-24 Relationship between BRSK1 rs12611091 variant and age at natural menopause based on physical activity Su, Chun-Lang Tsai, Yi-Ling Nfor, Oswald Ndi Liu, Wen-Hsiu Ho, Chien Chang Lung, Chia-Chi Lin, Yi-Tien Wang, Lee Liaw, Yung-Po Menopause Original Studies OBJECTIVES: The rs12611091 variant in the BR serine/threonine kinase 1 gene is one of the variants previously associated with age at natural menopause. So far, this variant has not been replicated in Taiwanese women. The purpose of this study was to determine the association between rs12611091 and age at natural menopause based on physical activity. METHODS: A total of 1,758 women were eligible for analysis whose information about menopause was collected from the Taiwan Biobank. Multiple linear regression analysis was used for analysis. RESULTS: The mean age (standard deviation) at natural menopause was 50.82 (3.59) years. Of the eligible participants, 56.94% were rs12611091 CC carriers, 36.69% were TC carriers, and 6.37% were TT carriers. Compared to CC carriers, TC and TT carriers were associated with early menopause (β = −0.42, P = 0.02 and −0.87, P = 0.01, respectively). There was a significant interaction between rs12611091 and physical activity (P for interaction = 0.02). Compared to rs12611091 CC carriers, TC and TT carriers who were physically inactive were significantly associated with earlier menopause (β = −0.88, P < 0.01 and −1.25, P = 0.02, respectively). CONCLUSION: We demonstrated that rs12611091 variant was associated with age at natural menopause especially among inactive women in Taiwan. That is, women with TC and TT genotypes who were physically inactive were significantly associated with earlier natural menopause compared to those with CC genotype. Lippincott-Raven Publishers 2019-12-30 /pmc/articles/PMC7147414/ /pubmed/31895179 http://dx.doi.org/10.1097/GME.0000000000001481 Text en Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The North American Menopause Society. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Original Studies
Su, Chun-Lang
Tsai, Yi-Ling
Nfor, Oswald Ndi
Liu, Wen-Hsiu
Ho, Chien Chang
Lung, Chia-Chi
Lin, Yi-Tien
Wang, Lee
Liaw, Yung-Po
Relationship between BRSK1 rs12611091 variant and age at natural menopause based on physical activity
title Relationship between BRSK1 rs12611091 variant and age at natural menopause based on physical activity
title_full Relationship between BRSK1 rs12611091 variant and age at natural menopause based on physical activity
title_fullStr Relationship between BRSK1 rs12611091 variant and age at natural menopause based on physical activity
title_full_unstemmed Relationship between BRSK1 rs12611091 variant and age at natural menopause based on physical activity
title_short Relationship between BRSK1 rs12611091 variant and age at natural menopause based on physical activity
title_sort relationship between brsk1 rs12611091 variant and age at natural menopause based on physical activity
topic Original Studies
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7147414/
https://www.ncbi.nlm.nih.gov/pubmed/31895179
http://dx.doi.org/10.1097/GME.0000000000001481
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