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Age of natural menopause onset in BRCA1/2 carriers – systematic review and meta-analysis
INTRODUCTION: Germinal pathogenic variants in BRCA1 and BRCA2 genes are associated with high risk of cancers, including breast, ovary, fallopian tubes and primary peritoneal. Non-oncological implications of germline pathogenic variants in BRCA1 and BRCA2 genes, complicating reproductive health are l...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7812531/ https://www.ncbi.nlm.nih.gov/pubmed/33488327 http://dx.doi.org/10.5114/pm.2020.101946 |
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author | Kępczyński, Łukasz Połatyńska, Katarzyna Nykel, Anna Sałamunia, Jordan Kałużewski, Tadeusz Kużawczyk, Andrzej Gach, Agnieszka |
author_facet | Kępczyński, Łukasz Połatyńska, Katarzyna Nykel, Anna Sałamunia, Jordan Kałużewski, Tadeusz Kużawczyk, Andrzej Gach, Agnieszka |
author_sort | Kępczyński, Łukasz |
collection | PubMed |
description | INTRODUCTION: Germinal pathogenic variants in BRCA1 and BRCA2 genes are associated with high risk of cancers, including breast, ovary, fallopian tubes and primary peritoneal. Non-oncological implications of germline pathogenic variants in BRCA1 and BRCA2 genes, complicating reproductive health are less described. The influence of BRCA1 and BRCA2 on age of natural menopause remains inconclusive and controversial. MATERIAL AND METHODS: PubMed database was searched for potentially relevant abstracts. Studies which were not case-control, cohort or cross-sectional studies were subsequently excluded. Reference lists from systematic reviews or meta-analyses, dealing with the topic of menopause and BRCA1 and BRCA2 germinal pathogenic variants, were also checked to identify eligible studies. We also included our original, unpublished data from families, affected by BRCA1 or BRCA2 pathogenic variant, consisted of at least two postmenopausal female siblings with differing variant status. RESULTS AND CONCLUSIONS: Initial database search retrieved 193 abstracts. We identified 4 eligible studies for meta-analysis. Two studies not reporting dispersion measures and not reporting age of natural menopause in control group were left in summary for illustrational purposes, yet were excluded from meta-analysis. 4 studies and our original, unpublished data, combining data from 1535 germinal BRCA1 and BRCA2 pathogenic variant carriers and 3191 control individuals, did not support the hypothesis of association between germinal pathogenic variants of “breast cancer genes” and premature menopause. |
format | Online Article Text |
id | pubmed-7812531 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-78125312021-01-22 Age of natural menopause onset in BRCA1/2 carriers – systematic review and meta-analysis Kępczyński, Łukasz Połatyńska, Katarzyna Nykel, Anna Sałamunia, Jordan Kałużewski, Tadeusz Kużawczyk, Andrzej Gach, Agnieszka Prz Menopauzalny Special Issue Paper INTRODUCTION: Germinal pathogenic variants in BRCA1 and BRCA2 genes are associated with high risk of cancers, including breast, ovary, fallopian tubes and primary peritoneal. Non-oncological implications of germline pathogenic variants in BRCA1 and BRCA2 genes, complicating reproductive health are less described. The influence of BRCA1 and BRCA2 on age of natural menopause remains inconclusive and controversial. MATERIAL AND METHODS: PubMed database was searched for potentially relevant abstracts. Studies which were not case-control, cohort or cross-sectional studies were subsequently excluded. Reference lists from systematic reviews or meta-analyses, dealing with the topic of menopause and BRCA1 and BRCA2 germinal pathogenic variants, were also checked to identify eligible studies. We also included our original, unpublished data from families, affected by BRCA1 or BRCA2 pathogenic variant, consisted of at least two postmenopausal female siblings with differing variant status. RESULTS AND CONCLUSIONS: Initial database search retrieved 193 abstracts. We identified 4 eligible studies for meta-analysis. Two studies not reporting dispersion measures and not reporting age of natural menopause in control group were left in summary for illustrational purposes, yet were excluded from meta-analysis. 4 studies and our original, unpublished data, combining data from 1535 germinal BRCA1 and BRCA2 pathogenic variant carriers and 3191 control individuals, did not support the hypothesis of association between germinal pathogenic variants of “breast cancer genes” and premature menopause. Termedia Publishing House 2021-01-07 2020-12 /pmc/articles/PMC7812531/ /pubmed/33488327 http://dx.doi.org/10.5114/pm.2020.101946 Text en Copyright © 2020 Termedia http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0). License (http://creativecommons.org/licenses/by-nc-sa/4.0/) |
spellingShingle | Special Issue Paper Kępczyński, Łukasz Połatyńska, Katarzyna Nykel, Anna Sałamunia, Jordan Kałużewski, Tadeusz Kużawczyk, Andrzej Gach, Agnieszka Age of natural menopause onset in BRCA1/2 carriers – systematic review and meta-analysis |
title | Age of natural menopause onset in BRCA1/2 carriers – systematic review and meta-analysis |
title_full | Age of natural menopause onset in BRCA1/2 carriers – systematic review and meta-analysis |
title_fullStr | Age of natural menopause onset in BRCA1/2 carriers – systematic review and meta-analysis |
title_full_unstemmed | Age of natural menopause onset in BRCA1/2 carriers – systematic review and meta-analysis |
title_short | Age of natural menopause onset in BRCA1/2 carriers – systematic review and meta-analysis |
title_sort | age of natural menopause onset in brca1/2 carriers – systematic review and meta-analysis |
topic | Special Issue Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7812531/ https://www.ncbi.nlm.nih.gov/pubmed/33488327 http://dx.doi.org/10.5114/pm.2020.101946 |
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