{"title":"Causal Relationship Between Brain Functional Networks and Sleep Disorders: A Mendelian Randomization Study.","authors":"Wenting Lin, Xiaoqin Chen, Yuxing Wei, Lu Yang, Hui Li, Tianmin Zhu","doi":"10.1002/brb3.70870","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Dysfunction of brain resting-state functional networks has been widely reported in sleep disorders, but their causal relationships remain controversial.</p><p><strong>Objective: </strong>To investigate causal relationships between 191 resting-state functional magnetic resonance imaging (rsfMRI) phenotypes and eight sleep disorders using bidirectional two-sample Mendelian randomization (MR), with multivariable MR (MVMR) adjusting for addictive behaviors.</p><p><strong>Methods: </strong>Genome-wide association study (GWAS) data from UK Biobank and FinnGen were analyzed. Instrumental variables (IVs) were selected adhering to MR assumptions. Causal estimates were primarily derived via inverse-variance weighted (IVW), with sensitivity analyses using MR-Egger, weighted median, weighted mode, simple mode, and MR Pleiotropy Residual Sum and Outlier (MR-PRESSO).</p><p><strong>Results: </strong>We found increased functional connectivity within the salience and default mode networks in insular, cingulate, and frontal regions (OR = 0.94, 95% CI: 0.92-0.97, pFDR = 0.042) was causally associated with a 6% reduced risk of daytime napping. For obstructive sleep apnea (OSA), elevated functional connectivity within the default mode and central executive networks localized to precuneus/occipital regions (OR = 1.16, 95% CI: 1.08-1.25, pFDR = 0.042) and elevated functional connectivity within the default mode and central executive networks localized to parietal/temporal regions (OR = 1.18, 95% CI: 1.09-1.27, pFDR = 0.016) having a causal effect, associated with a 16% and 18% elevated risk of OSA respectively. MVMR analysis revealed that coffee intake did not confound associations between rsfMRI phenotypes and sleep disorders, while smoking, alcohol consumption, tea intake, and cannabis use may act as confounding factors affecting these links.</p><p><strong>Conclusion: </strong>This study provides robust evidence for causal associations between specific rsfMRI phenotype signatures and sleep disorders. It highlights brain functional networks as potential targets for non-invasive interventions, particularly within the context of addictive behaviors.</p>","PeriodicalId":9081,"journal":{"name":"Brain and Behavior","volume":"15 10","pages":"e70870"},"PeriodicalIF":2.7000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12504808/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brain and Behavior","FirstCategoryId":"102","ListUrlMain":"https://doi.org/10.1002/brb3.70870","RegionNum":3,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BEHAVIORAL SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Dysfunction of brain resting-state functional networks has been widely reported in sleep disorders, but their causal relationships remain controversial.
Objective: To investigate causal relationships between 191 resting-state functional magnetic resonance imaging (rsfMRI) phenotypes and eight sleep disorders using bidirectional two-sample Mendelian randomization (MR), with multivariable MR (MVMR) adjusting for addictive behaviors.
Methods: Genome-wide association study (GWAS) data from UK Biobank and FinnGen were analyzed. Instrumental variables (IVs) were selected adhering to MR assumptions. Causal estimates were primarily derived via inverse-variance weighted (IVW), with sensitivity analyses using MR-Egger, weighted median, weighted mode, simple mode, and MR Pleiotropy Residual Sum and Outlier (MR-PRESSO).
Results: We found increased functional connectivity within the salience and default mode networks in insular, cingulate, and frontal regions (OR = 0.94, 95% CI: 0.92-0.97, pFDR = 0.042) was causally associated with a 6% reduced risk of daytime napping. For obstructive sleep apnea (OSA), elevated functional connectivity within the default mode and central executive networks localized to precuneus/occipital regions (OR = 1.16, 95% CI: 1.08-1.25, pFDR = 0.042) and elevated functional connectivity within the default mode and central executive networks localized to parietal/temporal regions (OR = 1.18, 95% CI: 1.09-1.27, pFDR = 0.016) having a causal effect, associated with a 16% and 18% elevated risk of OSA respectively. MVMR analysis revealed that coffee intake did not confound associations between rsfMRI phenotypes and sleep disorders, while smoking, alcohol consumption, tea intake, and cannabis use may act as confounding factors affecting these links.
Conclusion: This study provides robust evidence for causal associations between specific rsfMRI phenotype signatures and sleep disorders. It highlights brain functional networks as potential targets for non-invasive interventions, particularly within the context of addictive behaviors.
期刊介绍:
Brain and Behavior is supported by other journals published by Wiley, including a number of society-owned journals. The journals listed below support Brain and Behavior and participate in the Manuscript Transfer Program by referring articles of suitable quality and offering authors the option to have their paper, with any peer review reports, automatically transferred to Brain and Behavior.
* [Acta Psychiatrica Scandinavica](https://publons.com/journal/1366/acta-psychiatrica-scandinavica)
* [Addiction Biology](https://publons.com/journal/1523/addiction-biology)
* [Aggressive Behavior](https://publons.com/journal/3611/aggressive-behavior)
* [Brain Pathology](https://publons.com/journal/1787/brain-pathology)
* [Child: Care, Health and Development](https://publons.com/journal/6111/child-care-health-and-development)
* [Criminal Behaviour and Mental Health](https://publons.com/journal/3839/criminal-behaviour-and-mental-health)
* [Depression and Anxiety](https://publons.com/journal/1528/depression-and-anxiety)
* Developmental Neurobiology
* [Developmental Science](https://publons.com/journal/1069/developmental-science)
* [European Journal of Neuroscience](https://publons.com/journal/1441/european-journal-of-neuroscience)
* [Genes, Brain and Behavior](https://publons.com/journal/1635/genes-brain-and-behavior)
* [GLIA](https://publons.com/journal/1287/glia)
* [Hippocampus](https://publons.com/journal/1056/hippocampus)
* [Human Brain Mapping](https://publons.com/journal/500/human-brain-mapping)
* [Journal for the Theory of Social Behaviour](https://publons.com/journal/7330/journal-for-the-theory-of-social-behaviour)
* [Journal of Comparative Neurology](https://publons.com/journal/1306/journal-of-comparative-neurology)
* [Journal of Neuroimaging](https://publons.com/journal/6379/journal-of-neuroimaging)
* [Journal of Neuroscience Research](https://publons.com/journal/2778/journal-of-neuroscience-research)
* [Journal of Organizational Behavior](https://publons.com/journal/1123/journal-of-organizational-behavior)
* [Journal of the Peripheral Nervous System](https://publons.com/journal/3929/journal-of-the-peripheral-nervous-system)
* [Muscle & Nerve](https://publons.com/journal/4448/muscle-and-nerve)
* [Neural Pathology and Applied Neurobiology](https://publons.com/journal/2401/neuropathology-and-applied-neurobiology)