# Genome-Wide Genetic Analysis of Dropout in a Controlled Exercise Intervention in Sedentary Adults With Overweight or Obesity and Cardiometabolic Disease

## TL;DR

The study finds genetic variants linked to quitting exercise programs in sedentary adults with health issues.

## Contribution

Identifies a genetic variant cluster associated with exercise dropout in a controlled intervention.

## Key findings

- A genetic variant rs722069 is strongly linked to exercise intervention dropout.
- The variant affects gene expression and acylcarnitine levels in skeletal muscle.
- These findings suggest a genetic basis for difficulty in maintaining exercise programs.

## Abstract

Despite the benefits of exercise, many individuals are unable or unwilling to adopt an exercise intervention.

The purpose of this analysis was to identify putative genetic variants associated with dropout from exercise training interventions among individuals in the STRRIDE trials.

We used a genome-wide association study approach to identify genetic variants in 603 participants initiating a supervised exercise intervention. Exercise intervention dropout occurred when a subject withdrew from further participation in the study or was otherwise lost to follow-up.

Exercise intervention dropout was associated with a cluster of single-nucleotide polymorphisms with the top candidate being rs722069 (T/C, risk allele = C) (unadjusted p = 2.2 × 10−7, odds ratio = 2.23) contained within a linkage disequilibrium block on chromosome 16. In Genotype-Tissue Expression, rs722069 is an expression quantitative trait locus of the EARS2, COG7, and DCTN5 genes in skeletal muscle tissue. In subsets of the STRRIDE genetic cohort with available muscle gene expression (n = 37) and metabolic data (n = 82), at baseline the C allele was associated with lesser muscle expression of EARS2 (p < .002) and COG7 (p = .074) as well as lesser muscle concentrations of C2- and C3-acylcarnitines (p = .026).

Our observations imply that exercise intervention dropout is genetically moderated through alterations in gene expression and metabolic pathways in skeletal muscle. Individual genetic traits may allow the development of a biomarker-based approach for identifying individuals who may benefit from more intensive counseling and other interventions to optimize exercise intervention adoption.

STRRIDE I = NCT00200993; STRRIDE AT/RT = NCT00275145; STRRIDE-PD = NCT00962962.

Exercise intervention dropout appears to be genetically moderated through alterations in gene expression and metabolic pathways in skeletal muscle among sedentary adults with overweight or obesity and cardiometabolic disease.