Arja O Rydin, Yuri Milaneschi, Femke Lamers, Rick Quax, Noah van de Bunt, Angela Koloi, Bennard Doornbos, Brenda W J H Penninx
{"title":"抑郁症状、代谢综合征、炎症和心脏代谢疾病的轨迹:纵向贝叶斯网络方法。","authors":"Arja O Rydin, Yuri Milaneschi, Femke Lamers, Rick Quax, Noah van de Bunt, Angela Koloi, Bennard Doornbos, Brenda W J H Penninx","doi":"10.1016/j.bbi.2025.106120","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Both cardiometabolic diseases (CMD) and depression carry high burden of disease and have a striking bi-directional comorbidity. Understanding mechanisms of this comorbidity is key in improving health outcomes. Through Bayesian network analysis and quantitative centrality assessments we disentangled longitudinal associational pathways connecting depressive symptoms with immuno-metabolic dysregulations and CMD.</p><p><strong>Methods: </strong>Data are from the Netherlands Study of Depression and Anxiety (NESDA), an ongoing longitudinal cohort study. Subjects (N = 1059, 68 % female, mean age 42.4 ± 12.5) had a lifetime depression diagnosis at baseline, and data at baseline, 2-, 6- and 9-year follow-up. Variables included depressive symptoms, metabolic syndrome components, inflammation, diabetes and atherosclerotic disease. Individual changes over time, determined using generalised mixed models, were fed into a Bayesian network model, resulting in a directed acyclic graph (DAG). For centrality evaluation, indegree and outdegree of variables (nodes) were assessed.</p><p><strong>Results: </strong>The DAG showed a path starting with the depressive symptom low energy, leading to appetite/weight alterations and hypersomnia, ultimately leading to the nodes of diabetes and markers related to dyslipidaemia and inflammation. Waist circumference was the node with highest centrality. This result remained robust in sensitivity analyses.</p><p><strong>Discussion: </strong>The findings traced a pathway linking specific energy-related depressive symptoms (e.g. low energy, appetite/weight oscillations and hypersomnia) to inflammation, dyslipidaemia and diabetes. Depressive symptoms and biological markers connected in this identified pathway may provide a valuable target to reduce cardiometabolic risk related to depression.</p>","PeriodicalId":9199,"journal":{"name":"Brain, Behavior, and Immunity","volume":" ","pages":"106120"},"PeriodicalIF":7.6000,"publicationDate":"2025-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Trajectories of depressive symptoms, metabolic syndrome, inflammation, and cardiometabolic diseases: A longitudinal Bayesian network approach.\",\"authors\":\"Arja O Rydin, Yuri Milaneschi, Femke Lamers, Rick Quax, Noah van de Bunt, Angela Koloi, Bennard Doornbos, Brenda W J H Penninx\",\"doi\":\"10.1016/j.bbi.2025.106120\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Both cardiometabolic diseases (CMD) and depression carry high burden of disease and have a striking bi-directional comorbidity. Understanding mechanisms of this comorbidity is key in improving health outcomes. Through Bayesian network analysis and quantitative centrality assessments we disentangled longitudinal associational pathways connecting depressive symptoms with immuno-metabolic dysregulations and CMD.</p><p><strong>Methods: </strong>Data are from the Netherlands Study of Depression and Anxiety (NESDA), an ongoing longitudinal cohort study. Subjects (N = 1059, 68 % female, mean age 42.4 ± 12.5) had a lifetime depression diagnosis at baseline, and data at baseline, 2-, 6- and 9-year follow-up. Variables included depressive symptoms, metabolic syndrome components, inflammation, diabetes and atherosclerotic disease. Individual changes over time, determined using generalised mixed models, were fed into a Bayesian network model, resulting in a directed acyclic graph (DAG). For centrality evaluation, indegree and outdegree of variables (nodes) were assessed.</p><p><strong>Results: </strong>The DAG showed a path starting with the depressive symptom low energy, leading to appetite/weight alterations and hypersomnia, ultimately leading to the nodes of diabetes and markers related to dyslipidaemia and inflammation. Waist circumference was the node with highest centrality. This result remained robust in sensitivity analyses.</p><p><strong>Discussion: </strong>The findings traced a pathway linking specific energy-related depressive symptoms (e.g. low energy, appetite/weight oscillations and hypersomnia) to inflammation, dyslipidaemia and diabetes. Depressive symptoms and biological markers connected in this identified pathway may provide a valuable target to reduce cardiometabolic risk related to depression.</p>\",\"PeriodicalId\":9199,\"journal\":{\"name\":\"Brain, Behavior, and Immunity\",\"volume\":\" \",\"pages\":\"106120\"},\"PeriodicalIF\":7.6000,\"publicationDate\":\"2025-09-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Brain, Behavior, and Immunity\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/j.bbi.2025.106120\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brain, Behavior, and Immunity","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.bbi.2025.106120","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
Trajectories of depressive symptoms, metabolic syndrome, inflammation, and cardiometabolic diseases: A longitudinal Bayesian network approach.
Introduction: Both cardiometabolic diseases (CMD) and depression carry high burden of disease and have a striking bi-directional comorbidity. Understanding mechanisms of this comorbidity is key in improving health outcomes. Through Bayesian network analysis and quantitative centrality assessments we disentangled longitudinal associational pathways connecting depressive symptoms with immuno-metabolic dysregulations and CMD.
Methods: Data are from the Netherlands Study of Depression and Anxiety (NESDA), an ongoing longitudinal cohort study. Subjects (N = 1059, 68 % female, mean age 42.4 ± 12.5) had a lifetime depression diagnosis at baseline, and data at baseline, 2-, 6- and 9-year follow-up. Variables included depressive symptoms, metabolic syndrome components, inflammation, diabetes and atherosclerotic disease. Individual changes over time, determined using generalised mixed models, were fed into a Bayesian network model, resulting in a directed acyclic graph (DAG). For centrality evaluation, indegree and outdegree of variables (nodes) were assessed.
Results: The DAG showed a path starting with the depressive symptom low energy, leading to appetite/weight alterations and hypersomnia, ultimately leading to the nodes of diabetes and markers related to dyslipidaemia and inflammation. Waist circumference was the node with highest centrality. This result remained robust in sensitivity analyses.
Discussion: The findings traced a pathway linking specific energy-related depressive symptoms (e.g. low energy, appetite/weight oscillations and hypersomnia) to inflammation, dyslipidaemia and diabetes. Depressive symptoms and biological markers connected in this identified pathway may provide a valuable target to reduce cardiometabolic risk related to depression.
期刊介绍:
Established in 1987, Brain, Behavior, and Immunity proudly serves as the official journal of the Psychoneuroimmunology Research Society (PNIRS). This pioneering journal is dedicated to publishing peer-reviewed basic, experimental, and clinical studies that explore the intricate interactions among behavioral, neural, endocrine, and immune systems in both humans and animals.
As an international and interdisciplinary platform, Brain, Behavior, and Immunity focuses on original research spanning neuroscience, immunology, integrative physiology, behavioral biology, psychiatry, psychology, and clinical medicine. The journal is inclusive of research conducted at various levels, including molecular, cellular, social, and whole organism perspectives. With a commitment to efficiency, the journal facilitates online submission and review, ensuring timely publication of experimental results. Manuscripts typically undergo peer review and are returned to authors within 30 days of submission. It's worth noting that Brain, Behavior, and Immunity, published eight times a year, does not impose submission fees or page charges, fostering an open and accessible platform for scientific discourse.