Key result
Genetic predisposition for heart failure significantly increased the risk of chronic kidney disease (OR 1.12), whereas genetic predictors of chronic kidney disease were not associated with a higher risk of heart failure.
Why the study?
Although shared risk factors for heart failure and chronic kidney disease are recognized, the exact causal relationship between these conditions remains unclear.
Does genetic predisposition to heart failure causally increase the risk of chronic kidney disease and renal dysfunction in European populations?
Observational
Mendelian Randomization
Yes
Does genetic predisposition to heart failure causally increase the risk of chronic kidney disease and renal dysfunction in European populations?
Effect estimate: OR 1.12 (95% CI 1.03-1.21)
p-value: p=0.009
Genetic predisposition to heart failure is causally associated with an increased risk of chronic kidney disease, highlighting the importance of HF management in preventing CKD progression.
HF genetic risk may elevate CKD odds; leaves open bidirectional causality and need for interventional confirmation.
BACKGROUND: Heart Failure (HF) is a widespread condition that affects millions of people, and it is caused by issues with the heart and blood vessels. Even though we know hypertension, coronary artery disease, obesity, diabetes, and genetics can increase the risk of HF and Chronic Kidney Disease (CKD), the exact cause of these conditions remains a mystery. To bridge this gap, we adopted Mendelian Randomization (MR), which relies on genetic variants as proxies. METHODS: We used data from European populations for our Bidirectional Two-Sample MR Study, which included 930,014 controls and 47,309 cases of HF from the HERMES consortium, as well as 736,396 controls and 51,256 cases of CKD. We also employed several MR variations, including MR-Egger, Inverse Variance Weighted (IVW), and Weighted Median Estimator (WME), to guarantee the results were accurate and comprehensive.). RESULTS: In this study, the MR analysis found that individuals with a genetic predisposition for HF have an elevated risk of CKD. Our study revealed a significant association between the genetic prediction of HF and the risk of CKD, as evidenced by the IVW method [with an odds ratio (OR) of 1.12 (95% CI, 1.03-1.21), p = 0.009] and the WME [with an OR of 1.14 (95% CI, 1.03-1.26), p = 0.008]. This causal relationship remained robust even after conducting MR analysis while adjusting for the effects of diabetes and hypertension, yielding ORs of 1.13 (IVW:95% CI, 1.03-1.23), 1.12 (MR-Egger: 95% CI, 0.85-1.48), and 1.15 (WME:95% CI, 1.04-1.27) (p = 0.008). However, in the reverse analysis aiming to explore CKD and renal function as exposures and HF as the outcome, we did not observe a statistically significant causal link between CKD and HF. CONCLUSION: Our study demonstrates the significance of HF in CKD progression, thus having meaningful implications for treatment and the potential for discovering new therapies. To better understand the relationship between HF and CKD, we need to conduct research in a variety of populations.
No takes yet. Share an insight, caveat, or question.
Zhang et al. (2023) conducted an observational in Heart Failure and Chronic Kidney Disease. Genetic predisposition for Heart Failure vs. Control (no genetic predisposition) was evaluated on Risk of Chronic Kidney Disease (CKD) (OR 1.12, 95% CI 1.03-1.21, p=0.009). Genetic predisposition for heart failure significantly increased the risk of chronic kidney disease (OR 1.12), whereas genetic predictors of chronic kidney disease were not associated with a higher risk of heart failure.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: