Medicus Economics, Boston, Massachusetts, United States of America.
Formerly of Madrigal Pharmaceuticals, Conshohocken, Pennsylvania, United States of America.
PLoS One. 2024 Aug 27;19(8):e0309617. doi: 10.1371/journal.pone.0309617. eCollection 2024.
NASH is considered a contributor to atherosclerotic cardiovascular disease (ASCVD) risk; however, its contribution beyond traditional risk factors for CVD, particularly diabetes, is less clearly understood. This study aimed to quantify the cardiovascular-event risk associated with NASH, independent of diabetes status.
A cross-sectional analysis was conducted using the 2017-2020 NHANES pre-pandemic cycle. NASH was defined based on presence of steatosis without other causes of liver disease, and FibroScan+AST score from vibration-controlled transient elastography (VCTE). Significant fibrosis (stages F2-F4) was identified by liver stiffness measurement from VCTE. Predicted primary CV-event risk was estimated using both the Pooled Cohort Equations (PCE) and the Framingham Risk Score (FRS). NASH patients were matched with non-NASH controls on age, sex, race/ethnicity, and diabetes status. Weighted logistic regression was conducted, modeling elevated predicted CV risk (binary) as the dependent variable and indicators for NASH / fibrosis stages as independent variables.
A sample of 125 NASH patients was matched with 2585 controls. NASH with significant fibrosis was associated with elevated predicted 10-year CV risk, although this association was only statistically significant in PCE analyses (odds ratio and 95% CI 2.34 [1.25, 4.36]). Analyses restricting to ages <65 years showed similar results, with associations of greater magnitude.
Independent of diabetes, a significant association was observed between NASH with significant liver fibrosis and predicted primary CV-event risk in US adults, particularly for those <65. These findings suggest the importance of accounting for NASH and liver-fibrosis stage in predicting CV-event risk.
NASH 被认为是动脉粥样硬化性心血管疾病(ASCVD)风险的一个因素;然而,它对心血管疾病(CVD)的风险贡献超出了传统的 CVD 危险因素,特别是糖尿病,这一点还不太清楚。本研究旨在定量评估 NASH 与心血管事件风险的关系,而不考虑糖尿病的状态。
利用 2017-2020 年 NHANES 大流行前周期进行横断面分析。根据无其他肝脏疾病原因的脂肪变性和振动控制瞬态弹性成像(VCTE)的 FibroScan+AST 评分定义 NASH。通过 VCTE 的肝硬度测量确定显著纤维化(F2-F4 期)。使用基于人群的队列方程(PCE)和弗雷明汉风险评分(FRS)估计主要 CV 事件的预测风险。NASH 患者与非 NASH 对照组在年龄、性别、种族/民族和糖尿病状态上进行匹配。采用加权逻辑回归,将升高的预测 CV 风险(二分类)作为因变量,将 NASH/纤维化分期作为自变量进行建模。
125 名 NASH 患者的样本与 2585 名对照进行了匹配。伴有显著纤维化的 NASH 与升高的预测 10 年 CV 风险相关,尽管这种关联仅在 PCE 分析中具有统计学意义(比值比和 95%置信区间 2.34[1.25, 4.36])。将年龄<65 岁的分析限制在年龄<65 岁,也得到了类似的结果,关联的程度更大。
在美国成年人中,独立于糖尿病,NASH 伴显著肝纤维化与预测的主要 CV 事件风险之间存在显著关联,尤其是年龄<65 岁的成年人。这些发现表明,在预测 CV 事件风险时,考虑 NASH 和肝纤维化分期非常重要。