Key result
Rare lipolysis gene variants are linked to unfavorable body fat distribution and cardiometabolic risk.
Why the study?
Difficulties in identifying causal variants and genes underlying genetic associations have limited the translational potential of genetic studies of body fat distribution, and the contribution of rare variant associations to fat distribution is understudied.
Observational (n=450,562)
p-value: p=<5×10-08
Should not yet change practice; hypothesis-generating for lipolysis pathways in cardiometabolic risk.
Difficulties in identifying causal variants and genes underlying genetic associations have limited the translational potential of genetic studies of body fat distribution, an important, partly-heritable risk factor for cardio-metabolic disease. Rare variant associations facilitate fine-mapping of causal alleles, but their contribution to fat distribution is understudied. We performed a genome-wide scan of rare nonsynonymous variants for body mass index-adjusted waist-to-hip-ratio (BMI-adjusted WHR; a widely-used measure of fat distribution) in 450,562 European ancestry individuals, followed by systematic Bayesian fine-mapping at six genome-wide (p<5×10 −08 ; main-analysis) and two subthreshold signals (significant at a Bonferroni-corrected p<1.3×10 −06 ). We found strong statistical evidence of causal association for nonsynonymous alleles in CALCRL (p.L87P, p conditional =5.9×10 −12 ; posterior-probability of association [PPA]=52%), PLIN1 (p.L90P, p conditional =5.5×10 −13 ; PPA>99%), PDE3B (p.R783X, p conditional =6.2×10 −15 ; PPA>99%), ACVR1C (p.I195T; p conditional =5.4×10 −12 ; PPA>99%), and FGF1 (p.G21E, p conditional =1.6×10 −07 ; PPA=98%). Alleles at the four likely-causal main-analysis genes affected fat distribution primarily via larger hip-rather than smaller waist-circumference and six of nine conditionally-independent WHR-lowering index-variants were associated with protection from cardiovascular or metabolic disease. All four genes are expressed in adipose tissue and have been linked with the regulation of intracellular lipolysis, which controls fat retention in mature cells. Targeted follow-up analyses of key intracellular-lipolysis genes revealed associations for a variant in the initiator of intracellular lipolysis PNPLA2 (p.N252K) with higher BMI-adjusted-WHR and higher cardio-metabolic risk. This study provides human genetic evidence of a link between intracellular lipolysis, fat-distribution and its cardio-metabolic complications in the general population.
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Lotta et al. (2018) conducted an observational in Body fat distribution (n=450,562). Rare nonsynonymous genetic variants in intracellular lipolysis genes vs. Non-carriers was evaluated on BMI-adjusted waist-to-hip ratio (p=<5×10-08). Rare nonsynonymous variants in intracellular lipolysis genes, including CALCRL, PLIN1, PDE3B, and ACVR1C, were significantly associated with BMI-adjusted waist-to-hip ratio and cardio-metabolic risk.
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