Editorial: MASLD In Primary Care—Risk-Stratification as the First Step to Treatment

IF 6.8 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Alimentary Pharmacology & Therapeutics Pub Date : 2026-10-09 Epub Date: 2026-07-15 DOI:10.1111/apt.70841
Niharika Samala
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The conditionally FDA-approved pharmacotherapy, currently indicated only for individuals with “non-cirrhotic at-risk MASH”, has compelled us to switch from passive identification to active risk-stratification to find individuals at risk for MASLD with advanced fibrosis. 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引用次数: 0

Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) is associated with significant hepatic and extrahepatic clinical outcomes, including mortality [1, 2]. Notably, a subgroup with MASLD has a pronounced increase in risk of liver-related events, earning the name “at-risk metabolic dysfunction-associated steatohepatitis (MASH)” [3-5], and understandably deemed to be most likely to benefit from clinical interventions. However, the silence of MASLD until progression to liver failure challenges the timely identification of at-risk MASH. The conditionally FDA-approved pharmacotherapy, currently indicated only for individuals with “non-cirrhotic at-risk MASH”, has compelled us to switch from passive identification to active risk-stratification to find individuals at risk for MASLD with advanced fibrosis. In individuals with cardiometabolic risk factors, AASLD recommends FIB-4-guided risk-stratification, with referral to gastroenterology for individuals at high risk, or second-tier testing with the Enhanced Liver Fibrosis (ELF) test or transient elastography for intermediate risk and continued cardiometabolic optimization for those at low risk for advanced fibrosis.

In the current issue, Adams et al. examine the prevalence of probable at-risk MASH (using Fibrosis NASH Index (FNI)) and FIB-4 index-defined risk for advanced fibrosis among individuals with metabolic risk factors in primary care practices in Victoria, Australia, using two large linked data repositories—Primary Care Audit, Teaching and Research Open Network (PATRON) (de-identified electronic medical records) and Victorian Admitted Episodes Dataset (VAED) [6]. Of the third with metabolic dysfunction, the authors identified that one in five (4.3%) were at high-risk of advanced fibrosis and one in six (18%) were at intermediate-risk and would need additional risk-stratification. Nearly a quarter (24.3%) of those with metabolic dysfunction, and half with type-2 diabetes had at-risk MASH. We see comparable estimates of at-risk MASH (13.6%) and cirrhosis (5.6%) in individuals with type-2 diabetes in the U.S. [7], and advanced fibrosis (3.3%) from pooled studies [8]. Importantly, the authors found a strikingly high burden of probable at-risk MASH (25% vs. 15.5%) and high-risk for advanced fibrosis (5.4% vs. 4.4%) among individuals living in index of relative socioeconomic disadvantage (IRSD)-determined areas with the worst socio-economic disadvantage, compared to those living in areas with the least socio-economic disadvantage [6]. This finding is consistent with emerging evidence linking food insecurity, limited access to healthy foods, and neighbourhood-level deprivation with MASLD outcomes [9, 10].

Taken together, MASLD is a major public health burden that disproportionately affects individuals facing socio-economic disadvantage. Adams et al.'s paper reinforces that primary care is the key initial setting for identifying individuals at risk for MASLD with significant liver disease. In the absence of a structured risk-stratification pathway, a large proportion of patients are likely to remain undiagnosed and therefore untreated. The study observations should prompt consideration of socio-economic vulnerability as a guide for resource allocation at the healthcare system level, as well as in the design and implementation of risk-stratification frameworks for MASLD by medical societies. The current study underscores the need for collaboration between gastroenterology and primary care and endocrinology to facilitate risk-stratification of patients with cardiometabolic risk factors, thereby improving identification of MASLD with significant liver disease and ensuring timely treatment.

Niharika Samala: writing – original draft, conceptualization, supervision, writing – review and editing.

The author has nothing to report.

This article is linked to Adams et al. papers. To view this article, visit https://doi.org/10.1111/apt.70750.

The author has nothing to report.

社论:MASLD在初级保健-风险分层作为治疗的第一步
代谢功能障碍相关脂肪变性肝病(MASLD)与显著的肝脏和肝外临床结果相关,包括死亡率[1,2]。值得注意的是,MASLD亚组发生肝脏相关事件的风险明显增加,因此被称为“高危代谢功能障碍相关脂肪性肝炎(MASH)”[3-5],可以理解的是,该亚组最有可能从临床干预中获益。然而,在进展为肝功能衰竭之前,MASLD的沉默对及时识别有风险的MASH提出了挑战。fda有条件批准的药物治疗目前仅适用于“非肝硬化高危MASH”个体,这迫使我们从被动识别转向主动风险分层,以发现晚期纤维化的MASLD风险个体。对于有心脏代谢危险因素的个体,AASLD推荐fib -4引导的风险分层,对于高危个体转介到胃肠病学,或者对于中等风险的患者采用增强肝纤维化(ELF)试验或瞬态弹性成像进行二级检测,对于晚期纤维化低风险的患者则继续进行心脏代谢优化。在本期杂志中,Adams等人研究了澳大利亚维多利亚州初级保健实践中具有代谢危险因素的个体中可能存在风险的MASH(使用纤维化NASH指数(FNI))和FIB-4指数定义的晚期纤维化风险,使用两个大型关联数据库-初级保健审计,教学和研究开放网络(PATRON)(去识别电子医疗记录)和维多利亚州入院集数据集(VAED)[6]。在三分之一的代谢功能障碍患者中,作者发现五分之一(4.3%)处于晚期纤维化高风险,六分之一(18%)处于中等风险,需要额外的风险分层。近四分之一(24.3%)的代谢功能障碍患者和一半的2型糖尿病患者有危险的MASH。我们在美国的2型糖尿病患者中发现了相当的风险MASH(13.6%)和肝硬化(5.6%),在合并研究中发现了晚期纤维化(3.3%)。重要的是,作者发现生活在相对社会经济劣势指数(IRSD)确定的最严重社会经济劣势地区的个体与生活在社会经济劣势最小地区的个体相比,可能存在风险的MASH负担(25%对15.5%)和晚期纤维化高风险(5.4%对4.4%)惊人地高。这一发现与新出现的证据一致,这些证据将粮食不安全、获得健康食品的机会有限和社区层面的贫困与MASLD结果联系起来[9,10]。综上所述,MASLD是一项重大的公共卫生负担,对处于社会经济不利地位的个人产生了不成比例的影响。Adams等人的论文强调,初级保健是识别具有显著肝脏疾病的MASLD风险个体的关键初始设置。在缺乏结构化风险分层途径的情况下,很大一部分患者可能仍未得到诊断,因此得不到治疗。该研究的观察结果应促使人们考虑社会经济脆弱性,作为医疗保健系统层面资源分配的指导,以及医疗协会为MASLD设计和实施风险分层框架的指导。目前的研究强调了胃肠病学、初级保健和内分泌学之间合作的必要性,以促进具有心脏代谢危险因素的患者的风险分层,从而提高对伴有重大肝脏疾病的MASLD的识别并确保及时治疗。Niharika Samala:写作-原稿,构思,监督,写作-审查和编辑。作者没有什么可报道的。本文链接到Adams等人的论文。要查看这篇文章,请访问https://doi.org/10.1111/apt.70750.The,作者没有什么可报告的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
15.60
自引率
7.90%
发文量
527
审稿时长
3-6 weeks
期刊介绍: Alimentary Pharmacology & Therapeutics is a global pharmacology journal focused on the impact of drugs on the human gastrointestinal and hepato-biliary systems. It covers a diverse range of topics, often with immediate clinical relevance to its readership.
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