Exome-Based Rare-Variant Analyses in CKD

Abstract

Significance Statement Studies have identified common CKD-associated gene variants, but the contribution of rare variants has not been systematically examined. The authors use exome sequencing and rare-variant collapsing analyses to compare rare genetic variants in 3150 cases (representing broad clinical CKD subtypes) with 9563 controls. For five known CKD-associated genes, they detected a significant enrichment of rare variants in PKD1 , PKD2 , COL4A5 , and found suggestive evidence for rare COL4A3 and COL4A4 variants. They also found evidence for four other genes not previously implicated in CKD. By demonstrating that rare-variant collapsing analyses can validate known genes and identify candidate genes and modifiers for nephropathy, these findings provide a rationale for larger-scale investigation of the rare variants’ contribution to disease risk across major clinical CKD categories. Background Studies have identified many common genetic associations that influence renal function and all-cause CKD, but these explain only a small fraction of variance in these traits. The contribution of rare variants has not been systematically examined. Methods We performed exome sequencing of 3150 individuals, who collectively encompassed diverse CKD subtypes, and 9563 controls. To detect causal genes and evaluate the contribution of rare variants we used collapsing analysis, in which we compared the proportion of cases and controls carrying rare variants per gene. Results The analyses captured five established monogenic causes of CKD: variants in PKD1 , PKD2 , and COL4A5 achieved study-wide significance, and we observed suggestive case enrichment for COL4A4 and COL4A3 . Beyond known disease-associated genes, collapsing analyses incorporating regional variant intolerance identified suggestive dominant signals in CPT2 and several other candidate genes. Biallelic mutations in CPT2 cause carnitine palmitoyltransferase II deficiency, sometimes associated with rhabdomyolysis and acute renal injury. Genetic modifier analysis among cases with APOL1 risk genotypes identified a suggestive signal in AHDC1 , implicated in Xia–Gibbs syndrome, which involves intellectual disability and other features. On the basis of the observed distribution of rare variants, we estimate that a two- to three-fold larger cohort would provide 80% power to implicate new genes for all-cause CKD. Conclusions This study demonstrates that rare-variant collapsing analyses can validate known genes and identify candidate genes and modifiers for kidney disease. In so doing, these findings provide a motivation for larger-scale investigation of rare-variant risk contributions across major clinical CKD categories.