Causal associations of Insomnia and postpartum depression: a two-sample mendelian randomization study

Background Postpartum depression (PPD), a prevalent social-mental condition, impacts the mother and the newborn and several facets of their lives. It has been suggested that insomnia is related to both the occurrence and progression of PPD. However, because o f lingering confounding and bias, it is...

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Veröffentlicht in:Archives of gynecology and obstetrics 2024-09, Vol.310 (3), p.1409-1416
Hauptverfasser: Shen, Xiao, Qiao, Dongyan, Wang, Yixiao, Obore, Nathan, Tao, Yuchen, Yu, Hong
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container_issue 3
container_start_page 1409
container_title Archives of gynecology and obstetrics
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creator Shen, Xiao
Qiao, Dongyan
Wang, Yixiao
Obore, Nathan
Tao, Yuchen
Yu, Hong
description Background Postpartum depression (PPD), a prevalent social-mental condition, impacts the mother and the newborn and several facets of their lives. It has been suggested that insomnia is related to both the occurrence and progression of PPD. However, because o f lingering confounding and bias, it is impossible to determine the cause of this connection using observational analysis. In this study, we evaluate the causal importance of insomnia on postpartum depression using Mendelian randomization (MR). Methods Utilizing summary data from genome-wide association studies (GWAS), a two-sample MR study was conducted. A GWAS dataset of IEU study of the United Kingdom Biobank phenotypes comprising 462,341 people of European heritage yielded 38 single-nucleotide polymorphisms (SNPs) for insomnia. The PPD data were provided by the FinnGen project and comprised 7604 cases and 59,601 controls. Inverse variance weighting (IVW) was utilized for the primary MR analysis, with weighted median and MR-Egger as sensitivity analyses. Results As a result, we found that genetically predicted insomnia was positively associated with postpartum depression. The odds ratios (OR) of PPD were 1.849 (95% (confidence interval) CI 1.011–3.381; p  = 0.046). Conclusion For the first time, the causative role of sleeplessness for postpartum depression has been extensively evaluated in the current two-sample MR investigation. Our findings show that insomnia and PPD are related causally.
doi_str_mv 10.1007/s00404-023-07302-3
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It has been suggested that insomnia is related to both the occurrence and progression of PPD. However, because o f lingering confounding and bias, it is impossible to determine the cause of this connection using observational analysis. In this study, we evaluate the causal importance of insomnia on postpartum depression using Mendelian randomization (MR). Methods Utilizing summary data from genome-wide association studies (GWAS), a two-sample MR study was conducted. A GWAS dataset of IEU study of the United Kingdom Biobank phenotypes comprising 462,341 people of European heritage yielded 38 single-nucleotide polymorphisms (SNPs) for insomnia. The PPD data were provided by the FinnGen project and comprised 7604 cases and 59,601 controls. Inverse variance weighting (IVW) was utilized for the primary MR analysis, with weighted median and MR-Egger as sensitivity analyses. Results As a result, we found that genetically predicted insomnia was positively associated with postpartum depression. The odds ratios (OR) of PPD were 1.849 (95% (confidence interval) CI 1.011–3.381; p  = 0.046). Conclusion For the first time, the causative role of sleeplessness for postpartum depression has been extensively evaluated in the current two-sample MR investigation. Our findings show that insomnia and PPD are related causally.</description><identifier>ISSN: 1432-0711</identifier><identifier>ISSN: 0932-0067</identifier><identifier>EISSN: 1432-0711</identifier><identifier>DOI: 10.1007/s00404-023-07302-3</identifier><identifier>PMID: 38112721</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Depression, Postpartum - epidemiology ; Depression, Postpartum - genetics ; Endocrinology ; Female ; Genome-Wide Association Study ; Gynecology ; Human Genetics ; Humans ; Insomnia ; Maternal-Fetal Medicine ; Medicine ; Medicine &amp; Public Health ; Mendelian Randomization Analysis ; Obstetrics/Perinatology/Midwifery ; Polymorphism, Single Nucleotide ; Postpartum depression ; Sleep Initiation and Maintenance Disorders - epidemiology ; Sleep Initiation and Maintenance Disorders - genetics ; United Kingdom - epidemiology</subject><ispartof>Archives of gynecology and obstetrics, 2024-09, Vol.310 (3), p.1409-1416</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023. 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It has been suggested that insomnia is related to both the occurrence and progression of PPD. However, because o f lingering confounding and bias, it is impossible to determine the cause of this connection using observational analysis. In this study, we evaluate the causal importance of insomnia on postpartum depression using Mendelian randomization (MR). Methods Utilizing summary data from genome-wide association studies (GWAS), a two-sample MR study was conducted. A GWAS dataset of IEU study of the United Kingdom Biobank phenotypes comprising 462,341 people of European heritage yielded 38 single-nucleotide polymorphisms (SNPs) for insomnia. The PPD data were provided by the FinnGen project and comprised 7604 cases and 59,601 controls. Inverse variance weighting (IVW) was utilized for the primary MR analysis, with weighted median and MR-Egger as sensitivity analyses. Results As a result, we found that genetically predicted insomnia was positively associated with postpartum depression. The odds ratios (OR) of PPD were 1.849 (95% (confidence interval) CI 1.011–3.381; p  = 0.046). Conclusion For the first time, the causative role of sleeplessness for postpartum depression has been extensively evaluated in the current two-sample MR investigation. 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It has been suggested that insomnia is related to both the occurrence and progression of PPD. However, because o f lingering confounding and bias, it is impossible to determine the cause of this connection using observational analysis. In this study, we evaluate the causal importance of insomnia on postpartum depression using Mendelian randomization (MR). Methods Utilizing summary data from genome-wide association studies (GWAS), a two-sample MR study was conducted. A GWAS dataset of IEU study of the United Kingdom Biobank phenotypes comprising 462,341 people of European heritage yielded 38 single-nucleotide polymorphisms (SNPs) for insomnia. The PPD data were provided by the FinnGen project and comprised 7604 cases and 59,601 controls. Inverse variance weighting (IVW) was utilized for the primary MR analysis, with weighted median and MR-Egger as sensitivity analyses. Results As a result, we found that genetically predicted insomnia was positively associated with postpartum depression. The odds ratios (OR) of PPD were 1.849 (95% (confidence interval) CI 1.011–3.381; p  = 0.046). Conclusion For the first time, the causative role of sleeplessness for postpartum depression has been extensively evaluated in the current two-sample MR investigation. Our findings show that insomnia and PPD are related causally.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>38112721</pmid><doi>10.1007/s00404-023-07302-3</doi><tpages>8</tpages></addata></record>
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subjects Depression, Postpartum - epidemiology
Depression, Postpartum - genetics
Endocrinology
Female
Genome-Wide Association Study
Gynecology
Human Genetics
Humans
Insomnia
Maternal-Fetal Medicine
Medicine
Medicine & Public Health
Mendelian Randomization Analysis
Obstetrics/Perinatology/Midwifery
Polymorphism, Single Nucleotide
Postpartum depression
Sleep Initiation and Maintenance Disorders - epidemiology
Sleep Initiation and Maintenance Disorders - genetics
United Kingdom - epidemiology
title Causal associations of Insomnia and postpartum depression: a two-sample mendelian randomization study
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