| Title: | Blood metabolites, neurocognition and psychiatric disorders: a Mendelian randomization analysis to investigate causal pathways |
| Journal: | Translational Psychiatry |
| Published: | 16 Sep 2024 |
| Pubmed: | https://pubmed.ncbi.nlm.nih.gov/39285197/ |
| DOI: | https://doi.org/10.1038/s41398-024-03095-4 |
Publication 13482
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Abstract
BackgroundNeurocognitive dysfunction is observationally associated with the risk of psychiatric disorders. Blood metabolites, which are readily accessible, may become highly promising biomarkers for brain disorders. However, the causal role of blood metabolites in neurocognitive function, and the biological pathways underlying their association with psychiatric disorders remain unclear.MethodsTo explore their putative causalities, we conducted bidirectional two-sample Mendelian randomization (MR) using genetic variants associated with 317 human blood metabolites (nmax = 215,551), g-Factor (an integrated index of multiple neurocognitive tests with nmax = 332,050), and 10 different psychiatric disorders (n = 9,725 to 807,553) from the large-scale genome-wide association studies of European ancestry. Mediation analysis was used to assess the potential causal pathway among the candidate metabolite, neurocognitive trait and corresponding psychiatric disorder.ResultsMR evidence indicated that genetically predicted acetylornithine was positively associated with g-Factor (0.035 standard deviation units increase in g-Factor per one standard deviation increase in acetylornithine level; 95% confidence interval, 0.021 to 0.049; P = 1.15 × 10−6). Genetically predicted butyrylcarnitine was negatively associated with g-Factor (0.028 standard deviation units decrease in g-Factor per one standard deviation increase in genetically proxied butyrylcarnitine; 95% confidence interval, −0.041 to −0.015; P = 1.31 × 10−5). There was no evidence of associations between genetically proxied g-Factor and metabolites. Furthermore, the mediation analysis via two-step MR revealed that the causal pathway from acetylornithine to bipolar disorder was partly mediated by g-Factor, with a mediated proportion of 37.1%. Besides, g-Factor mediated the causal pathway from butyrylcarnitine to schizophrenia, with a mediated proportion of 37.5%. Other neurocognitive traits from different sources provided consistent findings.ConclusionOur results provide genetic evidence that acetylornithine protects against bipolar disorder through neurocognitive abilities, while butyrylcarnitine has an adverse effect on schizophrenia through neurocognition. These findings may provide insight into interventions at the metabolic level for risk of neurocognitive and related disorders.</p>
11 Keywords
- Biomarkers
- Bipolar Disorder
- Cognitive Dysfunction
- Genome-Wide Association Study
- Humans
- Mediation Analysis
- Mendelian Randomization Analysis
- Mental Disorders
- Neuropsychological Tests
- Polymorphism, Single Nucleotide
- Schizophrenia
13 Authors
- Jing Guo
- Ping Yang
- Jia-Hao Wang
- Shi-Hao Tang
- Ji-Zhou Han
- Shi Yao
- Ke Yu
- Cong-Cong Liu
- Shan-Shan Dong
- Kun Zhang
- Yuan-Yuan Duan
- Tie-Lin Yang
- Yan Guo
1 Application
| Application ID | Title |
|---|---|
| 46387 | Integration of regulatory elements and multi-trait genomic and phenomic data to improve the accuracy of risk prediction of human complex diseases/traits |
Enabling scientific discoveries that improve human health