Arriola-Montenegro Jose, Beas Renato, Cerna-Viacava Renato, Chaponan-Lavalle Andres, Hernandez Randich Karla, Chambergo-Michilot Diego, Flores Sanga Herson, Mutirangura Pornthira
Department of Internal Medicine, University of Minnesota, Minneapolis, MN 55455, United States.
Department of Medicine, Indiana University School of Medicine, Indiana, IN 46202, United States.
World J Cardiol. 2023 Jul 26;15(7):328-341. doi: 10.4330/wjc.v15.i7.328.
Heart failure with reduced ejection fraction (HFrEF) and nonalcoholic fatty liver disease (NAFLD) are two common comorbidities that share similar pathophysiological mechanisms. There is a growing interest in the potential of targeted therapies to improve outcomes in patients with coexisting HFrEF and NAFLD. This manuscript reviews current and potential therapies for patients with coexisting HFrEF and NAFLD. Pharmacological therapies, including angiotensin-converting enzyme inhibitors/angiotensin receptor blockers, mineralocorticoids receptor antagonist, and sodium-glucose cotransporter-2 inhibitors, have been shown to reduce fibrosis and fat deposits in the liver. However, there are currently no data showing the beneficial effects of sacubitril/valsartan, ivabradine, hydralazine, isosorbide nitrates, digoxin, or beta blockers on NAFLD in patients with HFrEF. This study highlights the importance of considering HFrEF and NAFLD when developing treatment plans for patients with these comorbidities. Further research is needed in patients with coexisting HFrEF and NAFLD, with an emphasis on novel therapies and the importance of a multidisciplinary approach for managing these complex comorbidities.
射血分数降低的心力衰竭(HFrEF)和非酒精性脂肪性肝病(NAFLD)是两种具有相似病理生理机制的常见合并症。对于针对同时患有HFrEF和NAFLD的患者改善预后的靶向治疗潜力,人们的兴趣日益浓厚。本文综述了同时患有HFrEF和NAFLD患者的现有及潜在治疗方法。包括血管紧张素转换酶抑制剂/血管紧张素受体阻滞剂、盐皮质激素受体拮抗剂和钠-葡萄糖协同转运蛋白2抑制剂在内的药物治疗已被证明可减少肝脏纤维化和脂肪沉积。然而,目前尚无数据表明沙库巴曲/缬沙坦、伊伐布雷定、肼屈嗪、硝酸异山梨酯、地高辛或β受体阻滞剂对HFrEF患者的NAFLD有有益作用。本研究强调了在为这些合并症患者制定治疗方案时考虑HFrEF和NAFLD的重要性。对于同时患有HFrEF和NAFLD的患者,需要进一步研究,重点是新疗法以及多学科方法管理这些复杂合并症的重要性。