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Association between age at first birth and postpartum depression: A two-sample mendelian randomization analysis

BACKGROUND: Previous observational research has documented an association between age at first childbirth (AFB) and postpartum depression (PPD). However, the causal relationship remains unclear. This study aimed to assess the causal effects of AFB on PPD using a two-sample Mendelian randomization (M...

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Autores principales: Ou, Zhaoxing, Gao, Ziqing, Wang, Qi, Lin, Yuhong, Ye, Dalin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10543215/
https://www.ncbi.nlm.nih.gov/pubmed/37790979
http://dx.doi.org/10.1016/j.heliyon.2023.e20500
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author Ou, Zhaoxing
Gao, Ziqing
Wang, Qi
Lin, Yuhong
Ye, Dalin
author_facet Ou, Zhaoxing
Gao, Ziqing
Wang, Qi
Lin, Yuhong
Ye, Dalin
author_sort Ou, Zhaoxing
collection PubMed
description BACKGROUND: Previous observational research has documented an association between age at first childbirth (AFB) and postpartum depression (PPD). However, the causal relationship remains unclear. This study aimed to assess the causal effects of AFB on PPD using a two-sample Mendelian randomization (MR) analysis. METHODS: Three sets of instrumental variables were obtained from the United Kingdom Biobank (UK Biobank), Neale Lab consortium and a meta-analysis of genome-wide association studies (GWAS). Single-nucleotide polymorphisms (SNPs) associated with the PPD phenotype were obtained from the Finngen consortium, which included 13,657 cases and 236,178 controls. Inverse variance weighted (IVW), weighted median, weighted mode, and MR-Egger methods to evaluate causal effects. Heterogeneity was assessed using Cochran's Q test and funnel plots. Horizontal pleiotropy and sensitivity were assessed using the MR-Egger intercept test and “leave-one-out” analysis, respectively. Further meta-analysis was performed to validate the robustness of this relationship. Additionally, the potential mediating effects of risk factors associated with PPD were analyzed. RESULTS: Strong causal effects between AFB and PPD was found in both IVW and weighted median methods, which was further supported by meta-analysis (IVW, odds ratio [OR] 0.59 [95% confidence interval (CI) 0.36–0.96, p = 0.03]; weighted median, OR 0.59 [95% CI 0.37–0.95, p = 0.03]). The power of the MR supports the robustness of the findings. Heterogeneity or horizontal pleiotropy was not observed. Major depressive disorders, family income levels, and marital stress were identified as potential mediating factors in the causal relationships. CONCLUSION: Results of MR analysis supported the causal effect of increased AFB in reducing the risk for PPD.
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spelling pubmed-105432152023-10-03 Association between age at first birth and postpartum depression: A two-sample mendelian randomization analysis Ou, Zhaoxing Gao, Ziqing Wang, Qi Lin, Yuhong Ye, Dalin Heliyon Research Article BACKGROUND: Previous observational research has documented an association between age at first childbirth (AFB) and postpartum depression (PPD). However, the causal relationship remains unclear. This study aimed to assess the causal effects of AFB on PPD using a two-sample Mendelian randomization (MR) analysis. METHODS: Three sets of instrumental variables were obtained from the United Kingdom Biobank (UK Biobank), Neale Lab consortium and a meta-analysis of genome-wide association studies (GWAS). Single-nucleotide polymorphisms (SNPs) associated with the PPD phenotype were obtained from the Finngen consortium, which included 13,657 cases and 236,178 controls. Inverse variance weighted (IVW), weighted median, weighted mode, and MR-Egger methods to evaluate causal effects. Heterogeneity was assessed using Cochran's Q test and funnel plots. Horizontal pleiotropy and sensitivity were assessed using the MR-Egger intercept test and “leave-one-out” analysis, respectively. Further meta-analysis was performed to validate the robustness of this relationship. Additionally, the potential mediating effects of risk factors associated with PPD were analyzed. RESULTS: Strong causal effects between AFB and PPD was found in both IVW and weighted median methods, which was further supported by meta-analysis (IVW, odds ratio [OR] 0.59 [95% confidence interval (CI) 0.36–0.96, p = 0.03]; weighted median, OR 0.59 [95% CI 0.37–0.95, p = 0.03]). The power of the MR supports the robustness of the findings. Heterogeneity or horizontal pleiotropy was not observed. Major depressive disorders, family income levels, and marital stress were identified as potential mediating factors in the causal relationships. CONCLUSION: Results of MR analysis supported the causal effect of increased AFB in reducing the risk for PPD. Elsevier 2023-09-27 /pmc/articles/PMC10543215/ /pubmed/37790979 http://dx.doi.org/10.1016/j.heliyon.2023.e20500 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Ou, Zhaoxing
Gao, Ziqing
Wang, Qi
Lin, Yuhong
Ye, Dalin
Association between age at first birth and postpartum depression: A two-sample mendelian randomization analysis
title Association between age at first birth and postpartum depression: A two-sample mendelian randomization analysis
title_full Association between age at first birth and postpartum depression: A two-sample mendelian randomization analysis
title_fullStr Association between age at first birth and postpartum depression: A two-sample mendelian randomization analysis
title_full_unstemmed Association between age at first birth and postpartum depression: A two-sample mendelian randomization analysis
title_short Association between age at first birth and postpartum depression: A two-sample mendelian randomization analysis
title_sort association between age at first birth and postpartum depression: a two-sample mendelian randomization analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10543215/
https://www.ncbi.nlm.nih.gov/pubmed/37790979
http://dx.doi.org/10.1016/j.heliyon.2023.e20500
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