Exploring the shared genetic basis of major depressive disorder and frailty.

Major depressive disorder (MDD) and frailty impose substantial health and economic burdens. MDD is recognized as a significant risk factor for frailty, but the genetic associations between these conditions remain unclear. This study investigates the genetic correlation, shared pleiotropic loci, causal relationships, and comorbid genes between MDD and frailty. The genetic correlation between MDD and frailty was assessed using linkage disequilibrium score regression (LDSC) based on data from genome-wide association studies (GWAS). A detailed analysis was performed to identify shared pleiotropic loci and causal relationships through cross-phenotype association tests and Mendelian randomization. Additionally, tissue enrichment analysis was conducted using stratified LDSC, gene-based associations with both conditions were assessed using Multimarker Analysis of Genomic Annotation (MAGMA), and pathway analysis of comorbid genes was performed using the g: GOSt tool. Our findings revealed a significant positive genetic correlation between MDD and frailty (r g = 0.65, P = 1.49E-219). We identified 57 shared risk SNPs between the two conditions, including 6 novel SNPs. Mendelian randomization analyses indicated robust causal effects of MDD on frailty and vice versa. Furthermore, we observed tissue-specific heritability enrichment in 9 brain tissues. By combining MAGMA and CPASSOC analyses, we identified 10 comorbid genes associated with both MDD and frailty, primarily involved in synapse formation, modulation, plasticity, and desaturase activity. This study provides strong evidence for a shared genetic basis between MDD and frailty. The identification of comorbid genes offers new insights into the mechanisms underlying the relationship between these conditions. • A remarkably positive genetic correlation between major depressive disorder and frailty. • A total of 57 shared risk SNPs were identified between major depressive disorder and frailty, including 6 newly identified shared SNPs. • Multiple mendelian randomization methods suggest robust bidirectional causal relationship between major depressive disorder and frailty. • Both major depressive disorder and frailty were was significantly heritability enrichments in 9 brain tissues, including anterior cingulate cortex, frontal cortex, hippocampus, hypothalamus, amygdala, nucleus accumbens, putamen, caudate, and cerebellum. • Ten comorbid genes were identified. These comorbid genes are mainly enriched in synapse formation, modulation, plasticity, and desaturase activity. [ABSTRACT FROM AUTHOR]