Andrew D Schreiner, Jingwen Zhang, Chelsey A Petz, William P Moran, David G Koch, Justin Marsden, Chloe Bays, Patrick D Mauldin, Mulugeta Gebregziabher
{"title":"Statin prescriptions and progression of advanced fibrosis risk in primary care patients with MASLD.","authors":"Andrew D Schreiner, Jingwen Zhang, Chelsey A Petz, William P Moran, David G Koch, Justin Marsden, Chloe Bays, Patrick D Mauldin, Mulugeta Gebregziabher","doi":"10.1136/bmjgast-2024-001404","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>We aimed to determine the association of statins with progression to a high risk for advanced fibrosis in primary care patients with metabolic dysfunction-associated steatotic liver disease (MASLD).</p><p><strong>Design: </strong>This retrospective cohort study of electronic health record data included patients with MASLD and an initial low or indeterminate risk for advanced fibrosis, determined by Fibrosis-4 Index (FIB-4) score (<2.67). Patients were followed from the index FIB-4 until the primary outcome of a high-risk FIB-4 (≥2.67) or the end of the study period. Prescription for a statin during follow-up was the primary exposure. We developed Cox regression models for the time to a high-risk FIB-4 score with statin therapy as the primary covariate and adjusting for baseline fibrosis risk, demographic and comorbidity variables.</p><p><strong>Results: </strong>The cohort of 1238 patients with MASLD was followed for a mean of 3.3 years, with 47% of patients receiving a prescription for a statin, and 18% of patients progressing to a high-risk FIB-4. In the adjusted Cox model with statin prescription as the primary exposure, statins were associated with a lower risk (HR 0.60; 95% CI 0.45 to 0.80) of progressing to a FIB-4≥2.67. In the adjusted Cox models with statin prescription intensity as the exposure, moderate (HR 0.60; 95% CI 0.42 to 0.84) and high intensity (HR 0.61; 95% CI 0.42 to 0.88) statins were associated with a lower risk of progressing to a high-risk FIB-4.</p><p><strong>Conclusion: </strong>Statin prescriptions, and specifically moderate and high intensity statin prescriptions, demonstrate a protective association with fibrosis risk progression in primary care patients with MASLD.</p>","PeriodicalId":9235,"journal":{"name":"BMJ Open Gastroenterology","volume":"11 1","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2024-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11256061/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMJ Open Gastroenterology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1136/bmjgast-2024-001404","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GASTROENTEROLOGY & HEPATOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: We aimed to determine the association of statins with progression to a high risk for advanced fibrosis in primary care patients with metabolic dysfunction-associated steatotic liver disease (MASLD).
Design: This retrospective cohort study of electronic health record data included patients with MASLD and an initial low or indeterminate risk for advanced fibrosis, determined by Fibrosis-4 Index (FIB-4) score (<2.67). Patients were followed from the index FIB-4 until the primary outcome of a high-risk FIB-4 (≥2.67) or the end of the study period. Prescription for a statin during follow-up was the primary exposure. We developed Cox regression models for the time to a high-risk FIB-4 score with statin therapy as the primary covariate and adjusting for baseline fibrosis risk, demographic and comorbidity variables.
Results: The cohort of 1238 patients with MASLD was followed for a mean of 3.3 years, with 47% of patients receiving a prescription for a statin, and 18% of patients progressing to a high-risk FIB-4. In the adjusted Cox model with statin prescription as the primary exposure, statins were associated with a lower risk (HR 0.60; 95% CI 0.45 to 0.80) of progressing to a FIB-4≥2.67. In the adjusted Cox models with statin prescription intensity as the exposure, moderate (HR 0.60; 95% CI 0.42 to 0.84) and high intensity (HR 0.61; 95% CI 0.42 to 0.88) statins were associated with a lower risk of progressing to a high-risk FIB-4.
Conclusion: Statin prescriptions, and specifically moderate and high intensity statin prescriptions, demonstrate a protective association with fibrosis risk progression in primary care patients with MASLD.
目的我们旨在确定他汀类药物与代谢功能障碍相关性脂肪性肝病(MASLD)初级保健患者进展为晚期纤维化高风险的关系:这项对电子健康记录数据进行的回顾性队列研究纳入了根据纤维化-4指数(FIB-4)评分确定的晚期纤维化初始低风险或不确定风险的MASLD患者(结果:1238名MASLD患者的队列中包含了他汀类药物:对1238名MASLD患者进行了平均为期3.3年的随访,其中47%的患者接受了他汀类药物处方,18%的患者进展为FIB-4高风险。在以他汀类药物处方为主要暴露的调整Cox模型中,他汀类药物与较低的FIB-4进展风险(HR 0.60;95% CI 0.45至0.80)相关,FIB-4≥2.67。在以他汀类药物处方强度为暴露的调整Cox模型中,中度(HR 0.60;95% CI 0.42至0.84)和高强度(HR 0.61;95% CI 0.42至0.88)他汀类药物与进展为高风险FIB-4的较低风险相关:他汀类药物处方,特别是中等强度和高强度他汀类药物处方,与MASLD初级保健患者的纤维化风险进展有保护作用。
期刊介绍:
BMJ Open Gastroenterology is an online-only, peer-reviewed, open access gastroenterology journal, dedicated to publishing high-quality medical research from all disciplines and therapeutic areas of gastroenterology. It is the open access companion journal of Gut and is co-owned by the British Society of Gastroenterology. The journal publishes all research study types, from study protocols to phase I trials to meta-analyses, including small or specialist studies. Publishing procedures are built around continuous publication, publishing research online as soon as the article is ready.