Zhang Xinrong, Kam Leslie Yeeman, Barnett Scott D, Henry Linda, Cheung Ramsey, Nguyen Mindie H
Division of Gastroenterology and Hepatology, School of Medicine, Stanford University Medical Center, Palo Alto, California, USA.
Veterans Affairs Palo Alto Health Care System, Palo Alto, California, USA.
Dig Dis. 2025;43(1):36-45. doi: 10.1159/000541945. Epub 2024 Oct 14.
We compared clinical characteristics and outcomes in real-world metabolic dysfunction-associated steatotic liver disease (MASLD) patients with or without liver biopsy using a nationwide cohort in United States (USA) to fill in gaps in selection of biopsy patients.
We conducted a retrospective cohort study of adult MASLD patients using Marketscan® Databases (1/2007-12/2021). Patients were categorized into those with or without liver biopsy during follow-up.
We analyzed 540,326 MASLD patients: 23,732 with and 516,594 without biopsy. Only 4% of MASLD patients received liver biopsy and biopsy rate decreased in the last 5 years (9.4%-3.6%). After 1:5 propensity score matching on baseline characteristics including age, sex, and comorbidities, a total of 23,731 patients with biopsy and 118,396 matched patients without biopsy were analyzed. The incidence per 1,000 person-years for hepatocellular carcinoma (HCC) was 0.22 versus 2.18, cirrhosis 29.75 versus 90.44, and hepatic decompensation 15.84 versus 28.25 compared patients with and without biopsy. In multivariable analysis, patients with biopsy had more than 9 times higher risk of developing HCC, 3 times higher risk of cirrhosis, and 78% higher risk of hepatic decompensation. In subgroup analysis, the association remained consistent when stratified by age (<50 and ≥50), sex, and diabetes mellitus. Predictors of having biopsy included age, metabolic diseases, and living in North central or Northeast of USA.
These data can inform clinical patient management that biopsy patients likely represent a selected group at higher risk for disease progression, especially in clinical trials for MASLD therapies.
We compared clinical characteristics and outcomes in real-world metabolic dysfunction-associated steatotic liver disease (MASLD) patients with or without liver biopsy using a nationwide cohort in United States (USA) to fill in gaps in selection of biopsy patients.
We conducted a retrospective cohort study of adult MASLD patients using Marketscan® Databases (1/2007-12/2021). Patients were categorized into those with or without liver biopsy during follow-up.
We analyzed 540,326 MASLD patients: 23,732 with and 516,594 without biopsy. Only 4% of MASLD patients received liver biopsy and biopsy rate decreased in the last 5 years (9.4%-3.6%). After 1:5 propensity score matching on baseline characteristics including age, sex, and comorbidities, a total of 23,731 patients with biopsy and 118,396 matched patients without biopsy were analyzed. The incidence per 1,000 person-years for hepatocellular carcinoma (HCC) was 0.22 versus 2.18, cirrhosis 29.75 versus 90.44, and hepatic decompensation 15.84 versus 28.25 compared patients with and without biopsy. In multivariable analysis, patients with biopsy had more than 9 times higher risk of developing HCC, 3 times higher risk of cirrhosis, and 78% higher risk of hepatic decompensation. In subgroup analysis, the association remained consistent when stratified by age (<50 and ≥50), sex, and diabetes mellitus. Predictors of having biopsy included age, metabolic diseases, and living in North central or Northeast of USA.
These data can inform clinical patient management that biopsy patients likely represent a selected group at higher risk for disease progression, especially in clinical trials for MASLD therapies.
我们利用美国的一个全国性队列,比较了有或没有进行肝活检的真实世界中代谢功能障碍相关脂肪性肝病(MASLD)患者的临床特征和结局,以填补活检患者选择方面的空白。
我们使用Marketscan®数据库(2007年1月 - 2021年12月)对成年MASLD患者进行了一项回顾性队列研究。患者被分为随访期间进行或未进行肝活检的两类。
我们分析了540,326例MASLD患者:23,732例进行了活检,516,594例未进行活检。只有4%的MASLD患者接受了肝活检,且活检率在过去5年中有所下降(从9.4%降至3.6%)。在对包括年龄、性别和合并症在内的基线特征进行1:5倾向得分匹配后,共分析了23,731例进行活检的患者和118,396例匹配的未进行活检的患者。与未进行活检的患者相比,进行活检的患者每1000人年肝细胞癌(HCC)的发病率为0.22 vs 2.18,肝硬化发病率为29.75 vs 90.44,肝失代偿发病率为15.84 vs 28.25。在多变量分析中,进行活检的患者发生HCC的风险高出9倍多,发生肝硬化的风险高出3倍,发生肝失代偿的风险高出78%。在亚组分析中,按年龄(<50岁和≥50岁)、性别和糖尿病分层时,这种关联仍然一致。进行活检的预测因素包括年龄、代谢性疾病以及居住在美国中北部或东北部。
这些数据可为临床患者管理提供参考,即活检患者可能代表疾病进展风险较高的特定群体,尤其是在MASLD治疗的临床试验中。
我们利用美国的一个全国性队列,比较了有或没有进行肝活检的真实世界中代谢功能障碍相关脂肪性肝病(MASLD)患者的临床特征和结局,以填补活检患者选择方面的空白。
我们使用Marketscan®数据库(2007年1月 - 2021年12月)对成年MASLD患者进行了一项回顾性队列研究。患者被分为随访期间进行或未进行肝活检的两类。
我们分析了540,326例MASLD患者:23,732例进行了活检,516,594例未进行活检。只有4%的MASLD患者接受了肝活检,且活检率在过去5年中有所下降(从9.4%降至3.6%)。在对包括年龄、性别和合并症在内的基线特征进行1:5倾向得分匹配后,共分析了23,731例进行活检的患者和118,396例匹配的未进行活检的患者。与未进行活检的患者相比,进行活检的患者每1000人年肝细胞癌(HCC)的发病率为0.22 vs 2.18,肝硬化发病率为29.75 vs 90.44,肝失代偿发病率为15.84 vs 28.25。在多变量分析中,进行活检的患者发生HCC的风险高出9倍多,发生肝硬化的风险高出3倍,发生肝失代偿的风险高出78%。在亚组分析中,按年龄(<50岁和≥50岁)、性别和糖尿病分层时,这种关联仍然一致。进行活检的预测因素包括年龄、代谢性疾病以及居住在美国中北部或东北部。
这些数据可为临床患者管理提供参考,即活检患者可能代表疾病进展风险较高的特定群体,尤其是在MASLD治疗的临床试验中。