The effect of birth weight on body composition: Evidence from a birth cohort and a Mendelian randomization study

PLoS One. 2019 Sep 10;14(9):e0222141. doi: 10.1371/journal.pone.0222141. eCollection 2019.

Abstract

Background: Lower birth weight is associated with diabetes although the underlying mechanisms are unclear. Muscle mass could be a modifiable link and hence a target of intervention. We assessed the associations of birth weight with muscle and fat mass observationally in a population with little socio-economic patterning of birth weight and using Mendelian randomization (MR) for validation.

Methods: In the population-representative "Children of 1997" birth cohort (n = 8,327), we used multivariable linear regression to assess the adjusted associations of birth weight (kg) with muscle mass (kg) and body fat (%) at ~17.5 years. Genetically predicted birth weight (effect size) was applied to summary genetic associations with fat-free mass and fat mass (kg) from the UK Biobank (n = ~331,000) to obtain unconfounded estimates using inverse-variance weighting.

Results: Observationally, birth weight was positively associated with muscle mass (3.29 kg per kg birth weight, 95% confidence interval (CI) 2.83 to 3.75) and body fat (1.09% per kg birth weight, 95% CI 0.54 to 1.65). Stronger associations with muscle mass were observed in boys than in girls (p for interaction 0.004). Using MR, birth weight was positively associated with fat-free mass (0.77 kg per birth weight z-score, 95% CI 0.22 to 1.33) and fat mass (0.58, 95% CI 0.01 to 1.15). No difference by sex was evident.

Conclusion: Higher birth weight increasing muscle mass may be relevant to lower birth weight increasing the risk of diabetes and suggests post-natal muscle mass as a potential target of intervention.

Publication types

  • Observational Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Birth Weight / genetics*
  • Body Composition / genetics*
  • China
  • Female
  • Humans
  • Infant, Newborn
  • Male
  • Mendelian Randomization Analysis
  • Polymorphism, Single Nucleotide

Grants and funding

This work is a substudy of the “Children of 1997” birth cohort which was initially supported by the Health Care and Promotion Fund, Health and Welfare Bureau, Government of the Hong Kong SAR [HCPF grant 216106] and reestablished in 2005 with support from the Health and Health Services Research Fund, Government of the Hong Kong SAR [HHSRF grant 03040771]; the Research Fund for the Control of Infectious Diseases in Hong Kong, the Government of Hong Kong SAR [RFCID grant 04050172]; the University Research Committee Strategic Research Theme (SRT) of Public Health, the University of Hong Kong. The Biobank clinical follow-up was partly supported by the WYNG Foundation. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.