A Sidney Barritt, Elliot B Tapper, Philip N Newsome, Derek Gazis, Heather Morris, Andrea R Mospan, Anthony Daniel Perez, Yestle Kim, Brent A Neuschwander-Tetri, Rohit Loomba, Arun Sanyal
{"title":"Cardiovascular risk assessment tools are insufficient for patients with metabolic dysfunction associated steatotic liver disease.","authors":"A Sidney Barritt, Elliot B Tapper, Philip N Newsome, Derek Gazis, Heather Morris, Andrea R Mospan, Anthony Daniel Perez, Yestle Kim, Brent A Neuschwander-Tetri, Rohit Loomba, Arun Sanyal","doi":"10.14309/ajg.0000000000003595","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Risk for cardiovascular (CV) events is estimated by the Framingham Risk Score (FRS), Pooled Cohort Equation (PCE) and the American Heart Association Predicting Risk of CVD EVENTs (PREVENT) equation. The applicability of these risk tools in patients with MASLD is uncertain. This study sought to determine the accuracy of the FRS, PCE, and PREVENT in a real-world cohort of patients with MASLD.</p><p><strong>Methods: </strong>This analysis included US adults ≥ age 30 with MASLD in the TARGET-NASH study. Five to ten-year CV risk was estimated using original and recalibrated versions of the FRS and PCE, and original PREVENT equation. Discrimination among prediction models was assessed using Harrell's concordance statistic and calibration was evaluated using a modified Hosmer Lemeshow test comparing observed and predicted CV events. Logistic regression was used to assess the contribution of liver disease to observed CV events.</p><p><strong>Results: </strong>Overall, 1,090 patients were included. There was an increase in observed CV events from MASL to cirrhosis. FRS demonstrated a weak ability to identify patients who went on to experience a CV event (C-statistic 0.58, 95% CI 0.52-0.63) as did the AHA PREVENT model (C-statistic 0.60, 95% CI 0.54-0.65). Both the FRS and PCE demonstrated a significant lack of calibration (p<0.01), with overestimation in the highest deciles and underestimation in the lowest deciles of predicted risk.</p><p><strong>Conclusions: </strong>Commonly used tools to identify CV risk performed poorly in a cohort of patients with MASLD. As CV related death is the greatest source of mortality among patients with MASLD, better risk assessment tools are required.</p>","PeriodicalId":7608,"journal":{"name":"American Journal of Gastroenterology","volume":" ","pages":""},"PeriodicalIF":8.0000,"publicationDate":"2025-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Gastroenterology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.14309/ajg.0000000000003595","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GASTROENTEROLOGY & HEPATOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction: Risk for cardiovascular (CV) events is estimated by the Framingham Risk Score (FRS), Pooled Cohort Equation (PCE) and the American Heart Association Predicting Risk of CVD EVENTs (PREVENT) equation. The applicability of these risk tools in patients with MASLD is uncertain. This study sought to determine the accuracy of the FRS, PCE, and PREVENT in a real-world cohort of patients with MASLD.
Methods: This analysis included US adults ≥ age 30 with MASLD in the TARGET-NASH study. Five to ten-year CV risk was estimated using original and recalibrated versions of the FRS and PCE, and original PREVENT equation. Discrimination among prediction models was assessed using Harrell's concordance statistic and calibration was evaluated using a modified Hosmer Lemeshow test comparing observed and predicted CV events. Logistic regression was used to assess the contribution of liver disease to observed CV events.
Results: Overall, 1,090 patients were included. There was an increase in observed CV events from MASL to cirrhosis. FRS demonstrated a weak ability to identify patients who went on to experience a CV event (C-statistic 0.58, 95% CI 0.52-0.63) as did the AHA PREVENT model (C-statistic 0.60, 95% CI 0.54-0.65). Both the FRS and PCE demonstrated a significant lack of calibration (p<0.01), with overestimation in the highest deciles and underestimation in the lowest deciles of predicted risk.
Conclusions: Commonly used tools to identify CV risk performed poorly in a cohort of patients with MASLD. As CV related death is the greatest source of mortality among patients with MASLD, better risk assessment tools are required.
心血管(CV)事件的风险是通过Framingham风险评分(FRS)、合并队列方程(PCE)和美国心脏协会预测CVD事件风险(prevention)方程来估计的。这些风险工具在MASLD患者中的适用性尚不确定。本研究旨在确定真实世界MASLD患者队列中FRS、PCE和PREVENT的准确性。方法:该分析纳入了TARGET-NASH研究中年龄≥30岁的美国MASLD患者。使用原始和重新校准版本的FRS和PCE,以及原始的PREVENT方程来估计5至10年的CV风险。使用Harrell’s一致性统计评估预测模型之间的区别,使用改进的Hosmer Lemeshow检验比较观察到的CV事件和预测的CV事件来评估校准。使用Logistic回归来评估肝脏疾病对观察到的CV事件的贡献。结果:共纳入1090例患者。从MASL到肝硬化,观察到的CV事件有所增加。FRS在识别继续经历CV事件的患者方面表现出较弱的能力(c -统计量0.58,95% CI 0.52-0.63), AHA PREVENT模型也是如此(c -统计量0.60,95% CI 0.54-0.65)。FRS和PCE都显示出明显缺乏校准(结论:在MASLD患者队列中,常用的心血管风险识别工具表现不佳)。由于心血管相关死亡是MASLD患者死亡的最大来源,因此需要更好的风险评估工具。
期刊介绍:
Published on behalf of the American College of Gastroenterology (ACG), The American Journal of Gastroenterology (AJG) stands as the foremost clinical journal in the fields of gastroenterology and hepatology. AJG offers practical and professional support to clinicians addressing the most prevalent gastroenterological disorders in patients.