It is suggested that genetically predicted increased WP exerts beneficial effects against HF, partially mediated by obesity and sedentary habits, and targeting weight management and anti-sedentary interventions may mitigate HF risk in individuals with sarcopenia-related characteristics.
Abstract
Background
In this two-sample, two-step Mendelian randomization (MR) study, we aimed to elucidate the causal associations between sarcopenia-related characteristics and heart failure (HF) risk, and to identify the factors mediating these associations, with a particular focus on the mediating roles of obesity and sedentary habits.
Methods
Genetic instruments for appendicular lean mass (ALM), hand grip strength (HGS), walking pace (WP) and potential mediators were extracted from genome-wide association studies (GWASs). Inverse-variance weighting (IVW) was used as the primary analytical method, supplemented by MR-Egger regression, weighted median, and weighted mode analyses. Sensitivity analyses including Cochran's Q test and MR-Egger intercept method were performed to assess heterogeneity and pleiotropy. Bidirectional MR was conducted to exclude reverse causation.
Results
IVW revealed that a faster genetically predicted walking pace (WP) was associated with lower HF risk (odds ratio [OR] 0.44, 95% confidence interval [CI] 0.33-0.60, P = 5.806 × 10-7). The mediation analysis indicated that body mass index accounted for 32% of this effect, while time spent watching television accounted for 14%. Elevated appendicular lean mass showed a slight but significant positive association with HF risk (OR 1.06, 95% CI 1.03-1.09, P = 5.437 × 10-4). However, multivariable MR adjusting for BMI completely attenuated this association (P = 0.693), suggesting ALM reflects overall body composition rather than isolated muscle mass. No significant associations were found between HGS and HF. Bidirectional MR showed no robust reverse effects.
Conclusions
These findings suggest that genetically predicted increased WP exerts beneficial effects against HF, partially mediated by obesity and sedentary habits. Targeting weight management and anti-sedentary interventions may mitigate HF risk in individuals with sarcopenia-related characteristics.
This study identifies three genetic pathways linking biological aging to vascular disease, offering new molecular targets for its prevention and treatment.
Hao Yan, Shan Wei, Hui Hui et al.· Clinical and applied thrombo...· 0 citations
This bidirectional MR study identified several potential genetically predicted associations of domain-specific PA and SB traits with PsA and RA, and the findings for television viewing and RA may suggest a potential bidirectional association.
Tianyu Sun, Fei-Yao Zhang, Chang Liu et al.· Genes· 0 citations
Background Sarcopenia is observationally linked to venous thromboembolism, but the causal architecture and underlying biological pathways remain largely unclear. This study investigated the causal effects of sarcopenia-related traits on lower extremity deep vein thrombosis (DVT) and quantified potential mediating mecha...
Qi-Xiang Sun, Yi-Ming Hu, Zhen-Yong Yang et al.· Clinical and applied thrombo...· 0 citations
Genetic evidence supporting potential causal links between chronic pain and key phenotypic components of sarcopenia is provided, including hand grip strength, usual walking pace and appendicular lean mass.
Wei-Jie Wang, Qian-Kun Zhang, Zhen-Hua Wu· Journal of International Med...· 0 citations
AIMS/BACKGROUND
Coronary artery disease (CAD) has been epidemiologically linked to idiopathic pulmonary fibrosis (IPF); however, the genetic basis of this association remains unclear. Therefore, this study aims to investigate the potential causal relationships between IPF and CAD using a bidirectional two-sample Mendel...
Li-Rui Yang, Xin Zhao, Tingting Feng et al.· British journal of hospital...· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.