Yanxi Long, Hui Liu, Rumeng Ban, Zifeng Xu, Tao Xu
{"title":"脑脊液代谢物与产后抑郁症之间的因果关系:一项双向孟德尔随机研究","authors":"Yanxi Long, Hui Liu, Rumeng Ban, Zifeng Xu, Tao Xu","doi":"10.2147/IJWH.S540467","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Postpartum depression (PPD) significantly affects maternal health and infant development, yet its underlying neurochemical mechanisms remain poorly understood. While observational studies have linked cerebrospinal fluid (CSF) metabolites with mood disorders, causal relationships are difficult to establish due to confounding environmental factors.</p><p><strong>Methods: </strong>We applied bidirectional two-sample Mendelian randomization (MR) to explore causal associations between 338 CSF metabolites and PPD. Genetic instruments were obtained from a metabolome-wide GWAS (n=291), and PPD summary statistics were derived from the FinnGen study (7604 PPD cases; 59,601 controls). Forward MR assessed how CSF metabolites affect PPD risk, while reverse MR evaluated the impact of PPD on metabolite levels. The primary analysis used inverse-variance weighting (IVW), supported by MR-Egger, weighted median/mode, and sensitivity tests including Cochran's Q and MR-PRESSO.</p><p><strong>Results: </strong>Forward MR identified 10 CSF metabolites with causal effects on PPD. Protective metabolites included guanosine, argininosuccinate, maleate, N6-methyllysine, and homocarnosine. In contrast, increased levels of N-acetyl-isoputreanine, glucose, benzoate, gluconate, and arachidonate were associated with higher PPD risk. Reverse MR showed that PPD may causally lower CSF maleate levels, suggesting mitochondrial involvement in disease progression. All findings were robust to sensitivity analyses, with no evidence of pleiotropy.</p><p><strong>Conclusion: </strong>This study is the first to use bidirectional MR to investigate the causal role of CSF metabolites in PPD. Our results highlight potential metabolic drivers and feedback mechanisms in PPD, especially the reciprocal link with maleate. These findings offer new insights into PPD's neurobiology and suggest novel targets for early detection and may inform novel therapeutic strategies in maternal mental health.</p>","PeriodicalId":14356,"journal":{"name":"International Journal of Women's Health","volume":"17 ","pages":"2919-2928"},"PeriodicalIF":2.6000,"publicationDate":"2025-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12421254/pdf/","citationCount":"0","resultStr":"{\"title\":\"Causal Links Between Cerebrospinal Fluid Metabolites and Postpartum Depression: A Bidirectional Mendelian Randomization Study.\",\"authors\":\"Yanxi Long, Hui Liu, Rumeng Ban, Zifeng Xu, Tao Xu\",\"doi\":\"10.2147/IJWH.S540467\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Postpartum depression (PPD) significantly affects maternal health and infant development, yet its underlying neurochemical mechanisms remain poorly understood. While observational studies have linked cerebrospinal fluid (CSF) metabolites with mood disorders, causal relationships are difficult to establish due to confounding environmental factors.</p><p><strong>Methods: </strong>We applied bidirectional two-sample Mendelian randomization (MR) to explore causal associations between 338 CSF metabolites and PPD. Genetic instruments were obtained from a metabolome-wide GWAS (n=291), and PPD summary statistics were derived from the FinnGen study (7604 PPD cases; 59,601 controls). Forward MR assessed how CSF metabolites affect PPD risk, while reverse MR evaluated the impact of PPD on metabolite levels. The primary analysis used inverse-variance weighting (IVW), supported by MR-Egger, weighted median/mode, and sensitivity tests including Cochran's Q and MR-PRESSO.</p><p><strong>Results: </strong>Forward MR identified 10 CSF metabolites with causal effects on PPD. Protective metabolites included guanosine, argininosuccinate, maleate, N6-methyllysine, and homocarnosine. In contrast, increased levels of N-acetyl-isoputreanine, glucose, benzoate, gluconate, and arachidonate were associated with higher PPD risk. Reverse MR showed that PPD may causally lower CSF maleate levels, suggesting mitochondrial involvement in disease progression. All findings were robust to sensitivity analyses, with no evidence of pleiotropy.</p><p><strong>Conclusion: </strong>This study is the first to use bidirectional MR to investigate the causal role of CSF metabolites in PPD. Our results highlight potential metabolic drivers and feedback mechanisms in PPD, especially the reciprocal link with maleate. These findings offer new insights into PPD's neurobiology and suggest novel targets for early detection and may inform novel therapeutic strategies in maternal mental health.</p>\",\"PeriodicalId\":14356,\"journal\":{\"name\":\"International Journal of Women's Health\",\"volume\":\"17 \",\"pages\":\"2919-2928\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2025-09-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12421254/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Women's Health\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.2147/IJWH.S540467\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"OBSTETRICS & GYNECOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Women's Health","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2147/IJWH.S540467","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"OBSTETRICS & GYNECOLOGY","Score":null,"Total":0}
Causal Links Between Cerebrospinal Fluid Metabolites and Postpartum Depression: A Bidirectional Mendelian Randomization Study.
Background: Postpartum depression (PPD) significantly affects maternal health and infant development, yet its underlying neurochemical mechanisms remain poorly understood. While observational studies have linked cerebrospinal fluid (CSF) metabolites with mood disorders, causal relationships are difficult to establish due to confounding environmental factors.
Methods: We applied bidirectional two-sample Mendelian randomization (MR) to explore causal associations between 338 CSF metabolites and PPD. Genetic instruments were obtained from a metabolome-wide GWAS (n=291), and PPD summary statistics were derived from the FinnGen study (7604 PPD cases; 59,601 controls). Forward MR assessed how CSF metabolites affect PPD risk, while reverse MR evaluated the impact of PPD on metabolite levels. The primary analysis used inverse-variance weighting (IVW), supported by MR-Egger, weighted median/mode, and sensitivity tests including Cochran's Q and MR-PRESSO.
Results: Forward MR identified 10 CSF metabolites with causal effects on PPD. Protective metabolites included guanosine, argininosuccinate, maleate, N6-methyllysine, and homocarnosine. In contrast, increased levels of N-acetyl-isoputreanine, glucose, benzoate, gluconate, and arachidonate were associated with higher PPD risk. Reverse MR showed that PPD may causally lower CSF maleate levels, suggesting mitochondrial involvement in disease progression. All findings were robust to sensitivity analyses, with no evidence of pleiotropy.
Conclusion: This study is the first to use bidirectional MR to investigate the causal role of CSF metabolites in PPD. Our results highlight potential metabolic drivers and feedback mechanisms in PPD, especially the reciprocal link with maleate. These findings offer new insights into PPD's neurobiology and suggest novel targets for early detection and may inform novel therapeutic strategies in maternal mental health.
期刊介绍:
International Journal of Women''s Health is an international, peer-reviewed, open access, online journal. Publishing original research, reports, editorials, reviews and commentaries on all aspects of women''s healthcare including gynecology, obstetrics, and breast cancer. Subject areas include: Chronic conditions including cancers of various organs specific and not specific to women Migraine, headaches, arthritis, osteoporosis Endocrine and autoimmune syndromes - asthma, multiple sclerosis, lupus, diabetes Sexual and reproductive health including fertility patterns and emerging technologies to address infertility Infectious disease with chronic sequelae including HIV/AIDS, HPV, PID, and other STDs Psychological and psychosocial conditions - depression across the life span, substance abuse, domestic violence Health maintenance among aging females - factors affecting the quality of life including physical, social and mental issues Avenues for health promotion and disease prevention across the life span Male vs female incidence comparisons for conditions that affect both genders.