Abstract
X-chromosomal genetic variants are understudied but can yield valuable insights into sexually dimorphic human traits and diseases. We performed a sex-stratified cross-ancestry X-chromosome-wide association meta-analysis of seven kidney-related traits (n = 908,697), identifying 23 loci genome-wide significantly associated with two of the traits: 7 for uric acid and 16 for estimated glomerular filtration rate (eGFR), including four novel eGFR loci containing the functionally plausible prioritized genes ACSL4, CLDN2, TSPAN6 and the female-specific DRP2. Further, we identified five novel sex-interactions, comprising male-specific effects at FAM9B and AR/EDA2R, and three sex-differential findings with larger genetic effect sizes in males at DCAF12L1 and MST4 and larger effect sizes in females at HPRT1. All prioritized genes in loci showing significant sex-interactions were located next to androgen response elements (ARE). Five ARE genes showed sex-differential expressions. This study contributes new insights into sex-dimorphisms of kidney traits along with new prioritized gene targets for further molecular research.
Original language | English |
---|---|
Article number | 586 |
Journal | Nature Communications |
Volume | 15 |
Issue number | 1 |
DOIs | |
Publication status | Published - 18 Jan 2024 |
Publication type | A1 Journal article-refereed |
Keywords
- Humans
- Male
- Female
- Androgens/genetics
- Genome-Wide Association Study
- Kidney
- Chromosomes, Human, X/genetics
- Response Elements
- Polymorphism, Single Nucleotide
- Genetic Predisposition to Disease
- Tetraspanins/genetics
Publication forum classification
- Publication forum level 3
ASJC Scopus subject areas
- Genetics(clinical)
- Nephrology
- General Medicine