Causal relationship of interleukin-6 and its receptor on sarcopenia traits using mendelian randomization

Nutr J. 2024 May 15;23(1):51. doi: 10.1186/s12937-024-00958-w.

Abstract

Background: Previous research has extensively examined the role of interleukin 6 (IL-6) in sarcopenia. However, the presence of a causal relationship between IL-6, its receptor (IL-6R), and sarcopenia remains unclear.

Method: In this study, we utilized summary-level data from genome-wide association studies (GWAS) focused on appendicular lean mass (ALM), hand grip strength, and walking pace. Single nucleotide polymorphisms (SNPs) were employed as genetic instruments for IL-6 and IL-6R to estimate the causal effect of sarcopenia traits. We adopted the Mendelian randomization (MR) approach to investigate these associations using the inverse variance weighted (IVW) method as the primary analytical approach. Additionally, we performed sensitivity analyses to validate the reliability of the MR results.

Result: This study revealed a significant negative association between main IL-6R and eQTL IL-6R on the left grip strength were - 0.013 (SE = 0.004, p < 0.001) and -0.029 (SE = 0.007, p < 0.001), respectively. While for the right grip strength, the estimates were - 0.011 (SE = 0.001, p < 0.001) and - 0.021 (SE = 0.008, p = 0.005). However, no evidence of an association for IL-6R with ALM and walking pace. In addition, IL-6 did not affect sarcopenia traits.

Conclusion: Our study findings suggest a negative association between IL-6R and hand grip strength. Additionally, targeting IL-6R may hold potential value as a therapeutic approach for the treatment of hand grip-related issues.

Keywords: Genome-wide association studies; IL-6 receptor; Interleukin 6; Mendelian randomization; Sarcopenia.

MeSH terms

  • Genome-Wide Association Study* / methods
  • Hand Strength* / physiology
  • Humans
  • Interleukin-6* / blood
  • Interleukin-6* / genetics
  • Mendelian Randomization Analysis* / methods
  • Polymorphism, Single Nucleotide*
  • Receptors, Interleukin-6* / genetics
  • Sarcopenia* / genetics