Sultan Danish, Brundel Bianca J J M, Kurakula Kondababu
Department of Physiology, Amsterdam UMC, Vrije Universiteit, Amsterdam Cardiovascular Sciences, Heart Failure and Arrhythmias, Pulmonary Hypertension and Thrombosis, 1081 HZ Amsterdam, The Netherlands.
Cells. 2025 Jun 4;14(11):839. doi: 10.3390/cells14110839.
Pulmonary hypertension (PH) is a progressive lung disease characterized by abnormal pulmonary vascular pressure and right ventricular (RV) dysfunction. Atrial arrhythmias, including atrial fibrillation (AF) and atrial flutter, are common in patients with PH and significantly contribute to disease progression and mortality. A bidirectional pathophysiological link exists between PH and AF, encompassing shared mechanisms such as endothelial dysfunction, DNA damage, autophagy, inflammation, and oxidative stress, as well as mutual risk factors, including diabetes, obesity, heart disease, and aging. Despite these shared pathways, limited research has been conducted to fully understand the intertwined relationship between PH and AF, hindering the development of effective treatments. In this review, we provide a comprehensive overview of the epidemiology of PH, the molecular mechanisms underlying the development of AF in PH, and the overlap in their pathophysiology. We also identify novel druggable targets and propose mechanism-based therapeutic approaches to treat this specific patient group. By shedding light on the molecular connection between PH and AF, this review aims to fuel the design and validation of innovative treatments to address this challenging comorbidity.
肺动脉高压(PH)是一种进行性肺部疾病,其特征为肺血管压力异常和右心室(RV)功能障碍。房性心律失常,包括心房颤动(AF)和心房扑动,在PH患者中很常见,并显著促进疾病进展和增加死亡率。PH与AF之间存在双向病理生理联系,包括内皮功能障碍、DNA损伤、自噬、炎症和氧化应激等共同机制,以及糖尿病、肥胖、心脏病和衰老等共同危险因素。尽管存在这些共同途径,但为充分理解PH与AF之间相互交织的关系所开展的研究有限,这阻碍了有效治疗方法的开发。在本综述中,我们全面概述了PH的流行病学、PH中AF发生发展的分子机制及其病理生理学重叠情况。我们还确定了新的可成药靶点,并提出了基于机制的治疗方法来治疗这一特定患者群体。通过阐明PH与AF之间的分子联系,本综述旨在推动针对这一具有挑战性的合并症的创新治疗方法的设计与验证。