Radu Daniel, Parlițeanu Oana-Andreea, Nica Andra-Elena, Voineag Cristiana, Alexe Octavian-Sabin, Cristea Alexandra Maria, Georgescu Livia, Nemeș Roxana Maria, Tiron Andreea Taisia, Nemeș Alexandra Floriana
Department of Emergency, Ilfov County Emergency Clinical Hospital, 022104 Bucharest, Romania.
Department of Diabetes, 'Marius Nasta' Institute of Pneumology, 050159 Bucharest, Romania.
J Pers Med. 2025 Aug 1;15(8):336. doi: 10.3390/jpm15080336.
Insulin resistance (IR), a core component in the development of type 2 diabetes mellitus (T2DM), is increasingly recognized for its role in cardiovascular and pulmonary complications. This review explores the relationship between IR, right ventricular dysfunction (RVD), and decreased lung volume in patients with T2DM. Emerging evidence suggests that IR contributes to early structural and functional alterations in the right ventricle, independent of overt cardiovascular disease. The mechanisms involved include oxidative stress, inflammation, dyslipidemia, and obesity-factors commonly found in metabolic syndrome and T2DM. These pathophysiological changes compromise right ventricular contractility, leading to reduced pulmonary perfusion and respiratory capacity. RVD has been associated with chronic lung disease, pulmonary hypertension, and obstructive sleep apnea, all of which are prevalent in the diabetic population. As RVD progresses, it can result in impaired gas exchange, interstitial pulmonary edema, and exercise intolerance-highlighting the importance of early recognition and management. Therapeutic strategies should aim to improve insulin sensitivity and cardiac function through lifestyle interventions, pharmacological agents such as SGLT2 inhibitors and GLP-1/GIP analogs, and routine cardiac monitoring. These approaches may help slow the progression of RVD and its respiratory consequences. Considering the global burden of diabetes and obesity, and the growing incidence of related complications, further research is warranted to clarify the mechanisms linking IR, RVD, and respiratory dysfunction. Understanding this triad will be crucial for developing targeted interventions that improve outcomes and quality of life in affected patients.
胰岛素抵抗(IR)是2型糖尿病(T2DM)发生发展的核心组成部分,其在心血管和肺部并发症中的作用日益受到认可。本综述探讨了T2DM患者中IR、右心室功能障碍(RVD)和肺容积减少之间的关系。新出现的证据表明,IR促成右心室早期结构和功能改变,独立于明显的心血管疾病。涉及的机制包括氧化应激、炎症、血脂异常和肥胖——这些是代谢综合征和T2DM中常见的因素。这些病理生理变化损害右心室收缩力,导致肺灌注和呼吸能力降低。RVD与慢性肺病、肺动脉高压和阻塞性睡眠呼吸暂停有关,所有这些在糖尿病患者中都很常见。随着RVD进展,可导致气体交换受损、间质性肺水肿和运动不耐受——突出了早期识别和管理的重要性。治疗策略应旨在通过生活方式干预、诸如钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂和胰高血糖素样肽-1/葡萄糖依赖性促胰岛素多肽(GLP-1/GIP)类似物等药物制剂以及常规心脏监测来改善胰岛素敏感性和心脏功能。这些方法可能有助于减缓RVD及其呼吸后果的进展。考虑到糖尿病和肥胖的全球负担以及相关并发症发病率的不断上升,有必要进一步研究以阐明连接IR、RVD和呼吸功能障碍的机制。了解这三者关系对于制定改善受影响患者结局和生活质量的针对性干预措施至关重要。