Mendelian randomization study of telomere length and bone mineral density

Aging (Albany NY). 2020 Dec 15;13(2):2015-2030. doi: 10.18632/aging.202197. Epub 2020 Dec 15.

Abstract

Purpose: Some epidemiological studies and animal studies have reported a relationship between leukocyte telomere length (LTL) and bone mineral density (BMD). However, the causality underlying the purported relationship has not been determined. Here we performed a two-sample MR analysis to test the causal link between telomere length and BMD.

Results: Our research suggested no causal link of LTL and BMD using IVW method. The weighted median, MR-Egger regression and MR.RAPS method yielded a similar pattern of effects. MR-Egger intercept test demonstrated our results were not influenced by pleiotropy. Heterogeneities among the genetic variants on heel estimated BMD and TB-BMD vanished after excluding rs6028466. "Leave-one-out" sensitivity analysis confirmed the stability of our results.

Conclusion: Our MR analysis did not support causal effect of telomere length on BMD.

Methods: We utilized 5 independent SNPs robustly associated with LTL as instrument variables. The outcome results were obtained from GWAS summary data of BMD. The two-sample MR analysis was conducted using IVW, weighted median, MR-Egger regression and MR.RAPS method. MR-Egger intercept test, Cochran's Q test and I2 statistics and "leave-one-out" sensitivity analysis were performed to evaluate the horizontal pleiotropy, heterogeneities and stability of these genetic variants on BMD.

Keywords: bone mineral density; osteoporosis; telomere length; two-sample Mendelian randomization.

MeSH terms

  • Bone Density / genetics*
  • Causality
  • Humans
  • Leukocytes / metabolism*
  • Mendelian Randomization Analysis
  • Osteoporosis / epidemiology*
  • Osteoporosis / genetics
  • Polymorphism, Single Nucleotide
  • Telomere / metabolism*
  • Telomere Homeostasis