Key result
In patients with end-stage left heart failure, severely impaired right ventricular function was associated with significantly increased oxidative DNA damage compared to those with normal right ventricular function.
Why the study?
Pathomechanisms underlying the transition from maladaptive right ventricular remodeling to right heart failure upon pressure overload remain incompletely understood.
Does mitochondrial oxidative stress promote the transition of maladaptive right ventricular remodeling to right heart failure upon pressure overload?
Case-Control (n=21)
No
Does mitochondrial oxidative stress promote the transition of maladaptive right ventricular remodeling to right heart failure upon pressure overload?
Mitochondrial oxidative stress is a key driver in the transition from maladaptive right ventricular remodeling to right heart failure.
Answers are grounded in this paper and cite their sources.
Association of oxidative damage with RV dysfunction is hypothesis-generating; leaves open mitochondrial stress as driver of maladaptive remodeling.
We sought to unravel pathomechanisms of the transition of maladaptive right ventricular (RV) remodeling to right heart failure (RHF) upon pressure overload. Exposure of C57BL/6J and C57BL/6N mice to pulmonary artery banding disclosed a tight relation of structural remodeling with afterload, but a dissociation from RV systolic function. Reduced release of mitochondrial reactive oxygen species in C57BL/6J mice prevented the development of RHF. In patients with left heart failure, increased oxidative damage in RV sections was associated with severely impaired RV function. In conclusion, reactive oxygen species are involved in the transition of maladaptive RV remodeling to RHF.
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Müller et al. (2022) conducted a case-control in Dilated cardiomyopathy (n=21). Severely impaired right ventricular function vs. Normal right ventricular function was evaluated on Oxidative DNA damage in right ventricular sections. In patients with end-stage left heart failure, severely impaired right ventricular function was associated with significantly increased oxidative DNA damage compared to those with normal right ventricular function.
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