Brain and behavior · 2026
Unveiling Shared Genetic Architectures and Causality: Intestinal Diseases and Neurological Diseases.
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Zhao Ning, Tan Shiheng, Fu Qingzhen, Li Yanbing, Tian Tian, Cheng Zesong, Zhang Ding, Gao Lijing, Bao Weiwei, Zhang Depei, Li Zinan, Liu Jinyin, Wang Liwan, Zhang Zhuobo, Wang Fan, Zhao Yashuang
Аннотация
BACKGROUND: The "gut-brain axis" provides a theoretical foundation for the connection between intestinal and neurological diseases, but whether this reflects a shared genetic etiology or causal relationships exist remains unclear.
METHODS: We used genome-wide association study summary data from FinnGen and UK Biobank to investigate the genetic correlations and causal relationships between three intestinal diseases and six neurological diseases.
RESULTS: We observed positive global genetic correlations between irritable bowel syndrome and epilepsy (rg = 0.429, p = 1.53 × 10-2), and stroke (rg = 0.368, p = 2.56×10-2). Upon dividing the whole genome into 1703 independent regions, local genetic correlations were identified in a region between ulcerative colitis and multiple sclerosis (Chr6: 31571218-32682664). We also identified 12 novel pleiotropic SNPs shared between intestinal and neurological diseases, as well as a functional gene shared between ulcerative colitis and multiple sclerosis. SNP heritability enrichment analysis indicated that ulcerative colitis and multiple sclerosis have enrichment in several immune cells. Two-sample Mendelian randomization indicated the causal effect of Crohn's disease on Parkinson's disease (FDR = 1.34 × 10-2, OR = 1.092). The methylome Mendelian randomization analysis also showed causal relationships between several intestinal and neurological diseases.
CONCLUSIONS: Through comprehensive and systematic statistical analysis, we identified the global and local genetic correlations and causal relationships between several intestinal and neurological diseases and discovered shared pleiotropic loci and genes between them. Furthermore, the consistent SNP heritability enrichment observed in immune cells also indicated the crucial role of the immune system in the "gut-brain axis."
METHODS: We used genome-wide association study summary data from FinnGen and UK Biobank to investigate the genetic correlations and causal relationships between three intestinal diseases and six neurological diseases.
RESULTS: We observed positive global genetic correlations between irritable bowel syndrome and epilepsy (rg = 0.429, p = 1.53 × 10-2), and stroke (rg = 0.368, p = 2.56×10-2). Upon dividing the whole genome into 1703 independent regions, local genetic correlations were identified in a region between ulcerative colitis and multiple sclerosis (Chr6: 31571218-32682664). We also identified 12 novel pleiotropic SNPs shared between intestinal and neurological diseases, as well as a functional gene shared between ulcerative colitis and multiple sclerosis. SNP heritability enrichment analysis indicated that ulcerative colitis and multiple sclerosis have enrichment in several immune cells. Two-sample Mendelian randomization indicated the causal effect of Crohn's disease on Parkinson's disease (FDR = 1.34 × 10-2, OR = 1.092). The methylome Mendelian randomization analysis also showed causal relationships between several intestinal and neurological diseases.
CONCLUSIONS: Through comprehensive and systematic statistical analysis, we identified the global and local genetic correlations and causal relationships between several intestinal and neurological diseases and discovered shared pleiotropic loci and genes between them. Furthermore, the consistent SNP heritability enrichment observed in immune cells also indicated the crucial role of the immune system in the "gut-brain axis."