Cosentino Francesco, Verma Subodh, Ambery Philip, Treppendahl Marianne Bach, van Eickels Martin, Anker Stefan D, Cecchini Michele, Fioretto Paola, Groop Per-Henrik, Hess David, Khunti Kamlesh, Lam Carolyn S P, Richard-Lordereau Isabelle, Lund Lars H, McGreavy Paul, Newsome Philip N, Sattar Naveed, Solomon Scott, Weidinger Franz, Zannad Faiez, Zeiher Andreas
Cardiology Unit, Department of Medicine Solna, Karolinska Institutet and Karolinska University Hospital, Solna, 171 76 Stockholm, Sweden.
Division of Cardiac Surgery, St Michael's Hospital, Unity Health Toronto, Toronto, ON, Canada.
Eur Heart J. 2023 Oct 14;44(39):4141-4156. doi: 10.1093/eurheartj/ehad445.
Metabolic comorbidities are common in patients with cardiorenal disease; they can cause atherosclerotic cardiovascular disease (ASCVD), speed progression, and adversely affect prognosis. Common comorbidities are Type 2 diabetes mellitus (T2DM), obesity/overweight, chronic kidney disease (CKD), and chronic liver disease. The cardiovascular system, kidneys, and liver are linked to many of the same risk factors (e.g. dyslipidaemia, hypertension, tobacco use, diabetes, and central/truncal obesity), and shared metabolic and functional abnormalities lead to damage throughout these organs via overlapping pathophysiological pathways. The COVID-19 pandemic has further complicated the management of cardiometabolic diseases. Obesity, T2DM, CKD, and liver disease are associated with increased risk of poor outcomes of COVID-19 infection, and conversely, COVID-19 can lead to worsening of pre-existing ASCVD. The high rates of these comorbidities highlight the need to improve recognition and treatment of ASCVD in patients with obesity, insulin resistance or T2DM, chronic liver diseases, and CKD and equally, to improve recognition and treatment of these diseases in patients with ASCVD. Strategies to prevent and manage cardiometabolic diseases include lifestyle modification, pharmacotherapy, and surgery. There is a need for more programmes at the societal level to encourage a healthy diet and physical activity. Many pharmacotherapies offer mechanism-based approaches that can target multiple pathophysiological pathways across diseases. These include sodium-glucose cotransporter-2 inhibitors, glucagon-like peptide-1 receptor agonists, selective mineralocorticoid receptor antagonists, and combined glucose-dependent insulinotropic peptide/glucagon-like peptide-1 receptor agonist. Non-surgical and surgical weight loss strategies can improve cardiometabolic disorders in individuals living with obesity. New biomarkers under investigation may help in the early identification of individuals at risk and reveal new treatment targets.
代谢合并症在心脏和肾脏疾病患者中很常见;它们可导致动脉粥样硬化性心血管疾病(ASCVD),加速疾病进展,并对预后产生不利影响。常见的合并症包括2型糖尿病(T2DM)、肥胖/超重、慢性肾脏病(CKD)和慢性肝病。心血管系统、肾脏和肝脏与许多相同的危险因素相关(如血脂异常、高血压、吸烟、糖尿病和中心性/躯干性肥胖),共同的代谢和功能异常通过重叠的病理生理途径导致这些器官受损。新冠疫情使心脏代谢疾病的管理更加复杂。肥胖、T2DM、CKD和肝病与新冠感染不良结局风险增加相关,反之,新冠可导致已有的ASCVD恶化。这些合并症的高发病率凸显了提高肥胖、胰岛素抵抗或T2DM、慢性肝病和CKD患者对ASCVD的识别和治疗的必要性,同样,也需要提高ASCVD患者对这些疾病的识别和治疗。预防和管理心脏代谢疾病的策略包括生活方式改变、药物治疗和手术。社会层面需要更多项目来鼓励健康饮食和体育活动。许多药物治疗提供基于机制的方法,可针对多种疾病的病理生理途径。这些药物包括钠-葡萄糖协同转运蛋白2抑制剂、胰高血糖素样肽1受体激动剂、选择性盐皮质激素受体拮抗剂以及葡萄糖依赖性促胰岛素多肽/胰高血糖素样肽1受体激动剂联合用药。非手术和手术减肥策略可改善肥胖个体的心脏代谢紊乱。正在研究的新生物标志物可能有助于早期识别高危个体并揭示新的治疗靶点。