A Comprehensive Analysis of Nuclear-Encoded Mitochondrial Genes in Schizophrenia

• Published in: Biological psychiatry (1969) Vol. 83; no. 9; pp. 780 - 789
• Main Authors: Gonçalves, Vanessa F., Cappi, Carolina, Hagen, Christian M., Sequeira, Adolfo, Vawter, Marquis P., Derkach, Andriy, Zai, Clement C., Hedley, Paula L., Bybjerg-Grauholm, Jonas, Pouget, Jennie G., Cuperfain, Ari B., Sullivan, Patrick F., Christiansen, Michael, Kennedy, James L., Sun, Lei
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.05.2018
• Subjects: Adolescent; Adult; Aged; Female; Gene-gene interaction; Genes, Mitochondrial; Genetic Predisposition to Disease; Genome-Wide Association Study; GWAS-HD; Humans; MAGMA; Male; Medicin och hälsovetenskap; Middle Aged; Mitochondria; Oxidative phosphorylation; Schizophrenia; Schizophrenia - genetics; Stratified FDR; Young Adult; Mitochondria; Oxidative phosphorylation; Schizophrenia; Stratified FDR; Gene-gene interaction; MAGMA; GWAS-HD
• ISSN: 0006-3223; 1873-2402; 1873-2402
• DOI: 10.1016/j.biopsych.2018.02.1175

The genetic risk factors of schizophrenia (SCZ), a severe psychiatric disorder, are not yet fully understood. Multiple lines of evidence suggest that mitochondrial dysfunction may play a role in SCZ, but comprehensive association studies are lacking. We hypothesized that variants in nuclear-encoded mitochondrial genes influence susceptibility to SCZ. We conducted gene-based and gene-set analyses using summary association results from the Psychiatric Genomics Consortium Schizophrenia Phase 2 (PGC-SCZ2) genome-wide association study comprising 35,476 cases and 46,839 control subjects. We applied the MAGMA method to three sets of nuclear-encoded mitochondrial genes: oxidative phosphorylation genes, other nuclear-encoded mitochondrial genes, and genes involved in nucleus-mitochondria crosstalk. Furthermore, we conducted a replication study using the iPSYCH SCZ sample of 2290 cases and 21,621 control subjects. In the PGC-SCZ2 sample, 1186 mitochondrial genes were analyzed, among which 159 had p values < .05 and 19 remained significant after multiple testing correction. A meta-analysis of 818 genes combining the PGC-SCZ2 and iPSYCH samples resulted in 104 nominally significant and nine significant genes, suggesting a polygenic model for the nuclear-encoded mitochondrial genes. Gene-set analysis, however, did not show significant results. In an in silico protein-protein interaction network analysis, 14 mitochondrial genes interacted directly with 158 SCZ risk genes identified in PGC-SCZ2 (permutation p = .02), and aldosterone signaling in epithelial cells and mitochondrial dysfunction pathways appeared to be overrepresented in this network of mitochondrial and SCZ risk genes. This study provides evidence that specific aspects of mitochondrial function may play a role in SCZ, but we did not observe its broad involvement even using a large sample.