Section of Gastroenterology, Boston Medical Center, Boston University School of Medicine, Boston, Massachusetts.
Fatty Liver Program, Karsh Division of Gastroenterology and Hepatology, Cedars Sinai Medical Center, Los Angeles, California.
Gastroenterology. 2022 Sep;163(3):764-774.e1. doi: 10.1053/j.gastro.2022.06.023. Epub 2022 Jul 14.
Nonalcoholic fatty liver disease (NAFLD) is well recognized as a leading etiology for chronic liver disease, affecting >25% of the US and global populations. Up to 1 in 4 individuals with NAFLD have nonalcoholic steatohepatitis, which is associated with significant morbidity and mortality due to complications of liver cirrhosis, hepatic decompensation, and hepatocellular carcinoma. Although NAFLD is observed predominantly in persons with obesity and/or type 2 diabetes mellitus, an estimated 7%-20% of individuals with NAFLD have lean body habitus. Limited guidance is available to clinicians on appropriate clinical evaluation in lean individuals with NAFLD, such as for inherited/genetic disorders, lipodystrophy, drug-induced NAFLD, and inflammatory disorders. Emerging data now provide more robust evidence to define the epidemiology, natural history, prognosis, and mortality of lean individuals with NAFLD. Multiple studies have found that NAFLD among lean individuals is associated with increased cardiovascular, liver, and all-cause mortality relative to those without NAFLD. This American Gastroenterological Association Clinical Practice Update provides Best Practice Advice to assist clinicians in evidence-based approaches to the diagnosis, staging, and management of NAFLD in lean individuals.
This expert review was commissioned and approved by the American Gastroenterological Association (AGA) Institute Clinical Practice Updates Committee and the AGA Governing Board to provide timely guidance on a topic of high clinical importance to the AGA membership and underwent internal peer review by the Clinical Practice Updates Committee and external peer review through standard procedures of Gastroenterology. Best Practice Advice Statements BEST PRACTICE ADVICE 1: Lean NAFLD should be diagnosed in individuals with NAFLD and body mass index <25 kg/m (non-Asian race) or body mass index <23 kg/m (Asian race). BEST PRACTICE ADVICE 2: Lean individuals with NAFLD should be evaluated routinely for comorbid conditions, such as type 2 diabetes mellitus, dyslipidemia, and hypertension. BEST PRACTICE ADVICE 3: Lean individuals with NAFLD should be risk stratified for hepatic fibrosis to identify those with advanced fibrosis or cirrhosis. BEST PRACTICE ADVICE 4: Lean individuals in the general population should not undergo routine screening for NAFLD; however, screening should be considered for individuals older than 40 years with type 2 diabetes mellitus. BEST PRACTICE ADVICE 5: NAFLD should be considered in lean individuals with metabolic diseases (such as type 2 diabetes mellitus, dyslipidemia, and hypertension), elevated liver biochemical tests, or incidentally noted hepatic steatosis. BEST PRACTICE ADVICE 6: Clinicians should query patients routinely regarding alcohol consumption patterns in all patients with lean NAFLD. BEST PRACTICE ADVICE 7: In patients with lean NAFLD, other causes of liver disease should be ruled out, including other causes of fatty liver, such as HIV, lipodystrophy, lysosomal acid lipase deficiency, familial hypobetalipoproteinemia, and medication-induced hepatic steatosis (methotrexate, amiodarone, tamoxifen, and steroids). BEST PRACTICE ADVICE 8: Current evidence is inadequate to support routine testing for genetic variants in patients with lean NAFLD. BEST PRACTICE ADVICE 9: Liver biopsy, as the reference standard, should be considered if there is uncertainty regarding contributing causes of liver injury and/or the stage of liver fibrosis. BEST PRACTICE ADVICE 10: Serum indices (NAFLD fibrosis score and Fibrosis-4 score) and imaging techniques (transient elastography and magnetic resonance elastography) may be used as alternatives to liver biopsy for fibrosis staging and patient follow-up. These tests can be performed at the time of diagnosis and repeated at intervals of 6 months to 2 years, depending on fibrosis stage and the patient's response to intervention. BEST PRACTICE ADVICE 11: If noninvasive tests (eg, Fibrosis-4 and NAFLD fibrosis score) are indeterminate, a second noninvasive test (eg, transient elastography or magnetic resonance elastography) should be performed to confirm the stage and prognosis of NAFLD. BEST PRACTICE ADVICE 12: In lean patients with NAFLD, lifestyle intervention, including exercise, diet modification, and avoidance of fructose- and sugar-sweetened drinks, to target a modest weight loss of 3%-5% is suggested. BEST PRACTICE ADVICE 13: Administration of vitamin E may be considered in lean persons with biopsy-confirmed nonalcoholic steatohepatitis, but without type 2 diabetes mellitus or cirrhosis. Oral pioglitazone 30 mg daily may be considered in lean persons with biopsy-confirmed nonalcoholic steatohepatitis without cirrhosis. BEST PRACTICE ADVICE 14: The therapeutic role of glucagon-like peptide-1 agonists and sodium-glucose cotransporter-2 inhibitors in the management of lean NAFLD is not fully defined and requires further investigation. BEST PRACTICE ADVICE 15: Hepatocellular carcinoma surveillance with abdominal ultrasound with or without serum α-fetoprotein twice per year is suggested in patients with lean NAFLD and clinical markers compatible with liver cirrhosis.
非酒精性脂肪性肝病(NAFLD)是一种公认的慢性肝病主要病因,影响全球超过 25%的人群。多达 1/4 的 NAFLD 患者患有非酒精性脂肪性肝炎,由于肝硬化、肝功能失代偿和肝细胞癌等并发症,其发病率和死亡率较高。尽管 NAFLD 主要发生在肥胖和/或 2 型糖尿病患者中,但估计有 7%-20%的 NAFLD 患者体型偏瘦。对于 NAFLD 瘦体型患者,例如遗传性/遗传疾病、脂肪营养不良、药物性 NAFLD 和炎症性疾病,临床医生在适当的临床评估方面可获得的指导有限。目前的新兴数据为定义瘦体型 NAFLD 患者的流行病学、自然史、预后和死亡率提供了更有力的证据。多项研究发现,与无 NAFLD 者相比,瘦体型 NAFLD 患者的心血管疾病、肝脏和全因死亡率增加。美国胃肠病学会临床实践更新提供最佳实践建议,以帮助临床医生对瘦体型患者的 NAFLD 进行基于证据的诊断、分期和管理。
本专家综述由美国胃肠病学会(AGA)研究所临床实践更新委员会和 AGA 管理委员会委托和批准,为 AGA 会员高度关注的具有重要临床意义的主题提供及时的指导,并通过临床实践更新委员会进行内部同行评审,并通过胃肠病学的标准程序进行外部同行评审。
最佳实践建议 1:非亚裔人群中,BMI<25kg/m²(非亚裔种族)或 BMI<23kg/m²(亚裔种族)的 NAFLD 患者应诊断为瘦型 NAFLD。
最佳实践建议 2:应常规评估瘦型 NAFLD 患者的合并症,如 2 型糖尿病、血脂异常和高血压。
最佳实践建议 3:应评估瘦型 NAFLD 患者的肝纤维化风险,以识别有进展性纤维化或肝硬化的患者。
最佳实践建议 4:一般人群中的瘦体型者不进行常规 NAFLD 筛查;然而,对于年龄大于 40 岁且患有 2 型糖尿病的患者,应考虑进行筛查。
最佳实践建议 5:在患有代谢性疾病(如 2 型糖尿病、血脂异常和高血压)、肝生化指标升高或偶然发现的肝脂肪变性的瘦体型患者中,应考虑 NAFLD。
最佳实践建议 6:在所有瘦型 NAFLD 患者中,临床医生应常规询问患者的饮酒模式。
最佳实践建议 7:在瘦型 NAFLD 患者中,应排除其他原因引起的肝病,包括其他类型的脂肪肝,如 HIV、脂肪营养不良、溶酶体酸性脂肪酶缺乏症、家族性低β脂蛋白血症和药物性肝脂肪变性(甲氨蝶呤、胺碘酮、他莫昔芬和类固醇)。
最佳实践建议 8:目前证据不足以支持对瘦型 NAFLD 患者进行常规基因变异检测。
最佳实践建议 9:如果对导致肝损伤的原因和/或肝纤维化分期存在不确定性,应考虑肝活检作为参考标准。
最佳实践建议 10:血清指数(NAFLD 纤维化评分和纤维化-4 评分)和影像学技术(瞬时弹性成像和磁共振弹性成像)可替代肝活检用于纤维化分期和患者随访。这些测试可以在诊断时进行,并根据纤维化分期和患者的反应,每隔 6 个月至 2 年重复进行。
最佳实践建议 11:如果非侵入性测试(如纤维化-4 和 NAFLD 纤维化评分)不确定,应进行第二种非侵入性测试(如瞬时弹性成像或磁共振弹性成像)以确认 NAFLD 的分期和预后。
最佳实践建议 12:在瘦型 NAFLD 患者中,建议通过锻炼、饮食调整和避免果糖和含糖饮料等生活方式干预,将目标体重减轻 3%-5%,以达到适度减肥。
最佳实践建议 13:对于活检证实的非酒精性脂肪性肝炎但无 2 型糖尿病或肝硬化的瘦型患者,可以考虑给予维生素 E。对于活检证实的非酒精性脂肪性肝炎且无肝硬化的瘦型患者,可以考虑口服吡格列酮 30mg 每日一次。
最佳实践建议 14:在瘦型 NAFLD 中的作用尚未完全确定,需要进一步研究胰高血糖素样肽-1 激动剂和钠-葡萄糖共转运蛋白-2 抑制剂在管理中的作用。
最佳实践建议 15:在瘦型 NAFLD 患者中,伴有临床提示肝硬化的标志物的患者应每年进行两次腹部超声检查(伴或不伴血清α-胎蛋白)以进行肝细胞癌监测。