It is urgent that we restart by coming to a consensus on the terminology of this disease. In cases of heart failure, there seems to be no other currently used terminology for that condition, which might be the first important step towards the current achievements in treating heart failure. This may be the key to the possible differences in the academic content and achievements in the fields of heart failure and bladder failure. The term “bladder failure” still remains surrounded by ambiguity with a lack of accepted terminology [2]. In our opinion, the terminology for any disease should be simple and easily recognizable by the patients as well as physicians. Although “bladder failure” may give the impression of an all-or-nothing event, giving the condition a name may be the first step toward an expansion in the development of bladder failure research.

The heart and bladder are harder-working organs than any others in the body, continuously pumping blood or urine out. The failure of these organs may have similar underlying mechanistic causes and pathogenesis. In this issue of International Neurourology Journal, Marquez et al. [3] introduces a close relationship between the heart and mitochondrial function in the regulation of cellular energetics and metabolism, and describes the beneficial effect of targeting mitochondrial biogenesis in failing hearts. Furthermore, although there are currently no pharmacologic agents that directly affect mitochondrial biogenesis in heart failure, this article shows current advances in the development of heart failure therapies, including mitochondrial biogenesis, mitochondrial oxidative stress, and mitochondrial pore transition proteins. A similar relationship between the bladder and mitochondrial function was described previously in a study of bladder failure [4,5]. However, researchers in the field of bladder failure seem to have much work to do in the future.