Department of Cardiovascular and Metabolic Medicine, University of Liverpool, Liverpool, UK.
Metabolism & Nutrition Research Group, Liverpool University Hospitals NHS Foundation Trust, Liverpool, UK.
Liver Int. 2024 Nov;44(11):3031-3049. doi: 10.1111/liv.16086. Epub 2024 Sep 2.
The cumulative impact of metabolic syndrome (MetS) components on micro- and macrovascular disease in metabolic dysfunction-associated steatotic liver disease (MASLD) is unclear. We aimed to determine whether the number of the MetS components increases the risk of micro- and macrovascular disease in patients with MASLD.
We performed a retrospective cohort study of electronic medical records using the TriNetX network, a global federated database. The exposure arm was patients with hepatic steatosis (defined via International Classification of Diseases, 10th Revision coding, or modified hepatic steatosis index), and ≥1 MetS components (obesity/central adiposity, insulin resistance, hypertension, or dyslipidaemia), compared with a reference arm of adults without any MetS components or hepatic steatosis. Our propensity score matched (1:1) for confounders with 5 years of follow-up. Primary outcomes included microvascular (peripheral neuropathy, retinopathy, and nephropathy) and macrovascular (cardiovascular events, cerebrovascular accidents, and peripheral vascular disease) disease. Secondary analyses assessed the impact of additional MetS components on these outcomes, as well as the impact of sex.
MASLD, defined by hepatic steatosis and insulin resistance (n = 15 937), carried the highest risk of microvascular disease (HR 13.93 (95% CI 8.55-22.68)), whilst MASLD, defined by hepatic steatosis and hypertension (n = 53 028), carried the highest risk of macrovascular disease (7.23 (6.45-8.13)). MASLD with all MetS components carried greatest risk of both micro- (31.20 (28.88-33.70) (n = 462 789)) and macrovascular (8.04 (7.33-8.82) (n = 336 010)) disease.
We demonstrate a differential effect of MetS components on micro- and macrovascular disease risk in patients with MASLD, with a cumulative impact of multiple MetS on overall risk. The impact of MetS components was most pronounced in women. Aggressive metabolic risk factor management is critical for prevention of micro- and macrovascular complications.
代谢综合征(MetS)各组分对代谢相关脂肪性肝病(MASLD)中微血管和大血管疾病的累积影响尚不清楚。我们旨在确定 MASLD 患者中 MetS 组分的数量是否会增加微血管和大血管疾病的风险。
我们使用 TriNetX 网络(一个全球联合数据库)进行了电子病历的回顾性队列研究。暴露组为患有肝脂肪变性(通过国际疾病分类,第 10 版编码或改良肝脂肪变性指数定义)和≥1 个 MetS 组分(肥胖/中心性肥胖、胰岛素抵抗、高血压或血脂异常)的患者,与没有任何 MetS 组分或肝脂肪变性的成人参考组进行比较。我们通过 5 年的随访进行了混杂因素的倾向评分匹配(1:1)。主要结局包括微血管(周围神经病变、视网膜病变和肾病)和大血管(心血管事件、中风和外周血管疾病)疾病。次要分析评估了其他 MetS 组分对这些结局的影响,以及性别的影响。
由肝脂肪变性和胰岛素抵抗定义的 MASLD(n=15937)微血管疾病风险最高(HR 13.93(95%CI 8.55-22.68)),而由肝脂肪变性和高血压定义的 MASLD(n=53028)大血管疾病风险最高(7.23(6.45-8.13))。具有所有 MetS 组分的 MASLD 发生微血管疾病(31.20(28.88-33.70)(n=462789))和大血管疾病(8.04(7.33-8.82)(n=336010))的风险最高。
我们证明了 MetS 组分对 MASLD 患者微血管和大血管疾病风险的影响存在差异,多种 MetS 对总体风险具有累积影响。MetS 组分的影响在女性中最为明显。积极的代谢危险因素管理对于预防微血管和大血管并发症至关重要。