Coagulation factor XII contributes to renin activation, heart failure progression, and mortality

Inna P. Gladysheva, Ryan D. Sullivan, Sofiyan Saleem, Francis J. Castellino, Victoria A. Ploplis, Guy L. Reed
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Abstract

Symptomatic heart failure (sHF) with cardiac dysfunction, edema, and mortality are driven by overactivation of the renin-angiotensin-aldosterone system (RAAS). Renin is widely recognized as a key initiator of RAAS function, yet the mechanisms that activate renin remain a mystery. We discovered that activated coagulation factor XII generates active renin in the circulation and is directly linked to pathological activation of the systemic RAAS, development of sHF, and increased mortality. These findings suggest a new paradigm for therapeutically modulating the RAAS in sHF and other pathological conditions.
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凝血因子 XII 是肾素激活、心力衰竭进展和死亡率的诱因
肾素-血管紧张素-醛固酮系统(RAAS)的过度激活导致了伴有心功能不全、水肿和死亡的症状性心力衰竭(sHF)。肾素被公认为是 RAAS 功能的关键启动因子,但激活肾素的机制仍是一个谜。我们发现,活化的凝血因子 XII 会在血液循环中产生活性肾素,并与全身 RAAS 的病理激活、sHF 的发展和死亡率的增加直接相关。这些发现为在 sHF 和其他病理情况下调节 RAAS 提供了一种新的治疗模式。
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