Division of Internal Medicine, Warren Alpert Medical School of Brown University, Rhode Island Hospital, Providence, Rhode Island.
Division of Infectious Diseases, Warren Alpert Medical School of Brown University, Rhode Island Hospital, Providence, Rhode Island.
Clin Gastroenterol Hepatol. 2023 Jul;21(7):1708-1722. doi: 10.1016/j.cgh.2023.01.001. Epub 2023 Jan 13.
Liver disease remains a leading cause of morbidity and mortality among people living with HIV (PLWH). Emerging data suggest that PLWH are at high risk for developing nonalcoholic fatty liver disease (NAFLD). The aim of this review is to examine the current literature and provide an accurate estimate of the prevalence of NAFLD, nonalcoholic steatohepatitis (NASH), and fibrosis, and identify potential risk factors for NAFLD in PLWH.
We searched PubMed and Embase databases to identify studies reporting the prevalence of NAFLD and/or fibrosis in PLWH monoinfection. We performed a random effects meta-analysis of proportions to estimate the pooled prevalence of NAFLD, NASH, and fibrosis among PLWH monoinfection. We also examined potential risk factors for NAFLD by comparing characteristics of PLWH monoinfection with and without NAFLD.
A total of 43 studies, reporting data for 8230 patients, met our eligibility criteria and were included in the meta-analysis. Based on imaging studies the overall pooled prevalence of NAFLD and moderate liver fibrosis (METAVIR ≥ F2) among PLWH monoinfection was 33.9% (95% confidence interval [CI], 29.67%-38.39%), and 12.00% (95% CI, 10.02%-14.12%), respectively. Based on biopsy studies, prevalence of NASH and significant liver fibrosis (stage ≥F2 on histology) was 48.77% (95% CI, 34.30%-63.34%) and 23.34% (95% CI, 14.98%-32.75%), respectively. Traditional metabolic syndrome and HIV-related factors were associated with NAFLD in PLWH.
Our study confirms that the burden of NAFLD, NASH, and fibrosis is high among PLWH monoinfection. Prospective longitudinal studies are needed to delineate NAFLD, NASH, and fibrosis risk factors, and identify early interventions and new therapies for NAFLD in this population.
肝脏疾病仍然是导致人类免疫缺陷病毒(HIV)感染者(PLWH)发病率和死亡率的主要原因。新出现的数据表明,PLWH 发生非酒精性脂肪性肝病(NAFLD)的风险很高。本综述的目的是检查当前的文献,并提供一个准确的估计,NAFLD、非酒精性脂肪性肝炎(NASH)和纤维化的患病率,并确定 PLWH 中 NAFLD 的潜在危险因素。
我们检索了 PubMed 和 Embase 数据库,以确定报告 PLWH 单感染中 NAFLD 和/或纤维化患病率的研究。我们对比例进行了随机效应荟萃分析,以估计 PLWH 单感染中 NAFLD、NASH 和纤维化的总体患病率。我们还通过比较 PLWH 单感染中有无 NAFLD 的特征,检查了 NAFLD 的潜在危险因素。
共有 43 项研究,报告了 8230 名患者的数据,符合我们的纳入标准,并纳入了荟萃分析。根据影像学研究,PLWH 单感染中 NAFLD 和中度肝纤维化(METAVIR≥F2)的总体合并患病率分别为 33.9%(95%置信区间[CI],29.67%-38.39%)和 12.00%(95% CI,10.02%-14.12%)。根据活检研究,NASH 和显著肝纤维化(组织学上≥F2 期)的患病率分别为 48.77%(95% CI,34.30%-63.34%)和 23.34%(95% CI,14.98%-32.75%)。传统的代谢综合征和 HIV 相关因素与 PLWH 中的 NAFLD 相关。
我们的研究证实,PLWH 单感染中 NAFLD、NASH 和纤维化的负担很高。需要前瞻性纵向研究来描绘 NAFLD、NASH 和纤维化的危险因素,并为该人群中的 NAFLD 确定早期干预和新疗法。