Genetic loci implicated in meta-analysis of body shape in Africans

Nutr Metab Cardiovasc Dis. 2022 Jun;32(6):1511-1518. doi: 10.1016/j.numecd.2022.03.010. Epub 2022 Mar 26.

Abstract

Background and aims: Obesity is one of the leading causes of non-communicable diseases (NCD). Thus, NCD risk varies in obese individuals based on the location of their fat depots; while subcutaneous adiposity is protective, visceral adiposity increases NCD risk. Although, previously anthropometric traits have been used to quantify body shape in low-income settings, there is no consensus on how it should be assessed. Hence, there is a growing interest to evaluate body shape derived from the principal component analysis (PCA) of anthropometric traits; however, this is yet to be explored in individuals of African ancestry whose body shape is different from those of Europeans. We set out to capture body shape in its multidimensional structure and examine the association between genetic variants and body shape in individuals of African ancestry.

Method and results: We performed a genome-wide association study (GWAS) for body shape derived from PCA analysis of anthropometric traits in the Ugandan General Population Cohort (GPC, n = 6407) and the South African Zulu Cohort (SZC, n = 2595), followed by a GWAS meta-analysis to assess the genetic variants associated with body shape. We identified variants in FGF12, GRM8, TLX1NB and TRAP1 to be associated with body shape. These genes were different from the genes been associated with BMI, height, weight, WC and waist-hip ration in continental Africans. Notably, we also observed that a standard deviation change in body shape was associated with an increase in blood pressure and blood lipids.

Conclusion: Variants associated with body shape, as a composite variable might be different for those of individual anthropometric traits. Larger studies are required to further explore these phenomena.

Keywords: Anthropometric traits; Body shape; Principal components; Uganda; Zulu.

Publication types

  • Meta-Analysis
  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Adiposity / genetics
  • Body Mass Index
  • Fibroblast Growth Factors
  • Genetic Loci
  • Genome-Wide Association Study* / methods
  • HSP90 Heat-Shock Proteins / genetics
  • Humans
  • Noncommunicable Diseases*
  • Obesity / diagnosis
  • Obesity / epidemiology
  • Obesity / genetics
  • Somatotypes
  • Waist-Hip Ratio

Substances

  • FGF12 protein, human
  • HSP90 Heat-Shock Proteins
  • TRAP1 protein, human
  • Fibroblast Growth Factors