Meta-analysis: Histological severity of biopsy-proven metabolic dysfunction-associated steatotic liver disease in pediatric patients.

IF 2.6 3区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY
Matheus Souza, Samira Mohamad Khalil, Fabiana Dolovitsch de Oliveira
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Abstract

The burden of metabolic dysfunction-associated steatotic liver disease (MASLD) is increasing in children and adolescents. However, the severity of disease at diagnosis by liver biopsy remains uncertain and has not been systematically evaluated. We conducted a systematic review and meta-analysis to determine the prevalence of metabolic dysfunction-associated steatohepatitis (MASH), significant and advanced fibrosis in this population. PubMed and Embase databases were systematically searched (from inception to September 17, 2024) for studies reporting liver histology in pediatric patients (≤21 years) with biopsy-proven MASLD. Meta-analysis of proportions was performed using a generalized linear mixed model with Clopper-Pearson intervals to obtain pooled prevalence estimates. Of 4761 records identified, we included 35 studies with 5898 pediatric patients with biopsy-proven MASLD (33.4% girls; mean age 12.6 years). The pooled prevalences of MASH, significant fibrosis (defined as ≥F2) and advanced fibrosis (defined as ≥F3) based on histology were 59.95% (n = 18 studies, 95% confidence interval [CI]: 46.89-71.73, I² = 97%), 30.53% (n = 26 studies, 95% CI: 22.32-40.20, I² = 94%), and 11.77% (n = 28 studies, 95% CI: 8.10-16.80, I² = 89%), respectively. Subgroup analyses showed higher prevalence of advanced fibrosis in studies with <100 patients compared to larger studies. Meta-regressions did not show an influence of age, sex, and body mass index on the prevalences. Sensitivity analyses did not modify these results. Pediatric patients have considerable severity of MASLD at diagnosis by liver biopsy. Developing effective screening and risk stratification strategies for this group is urgently needed.

荟萃分析:小儿患者活检证实的代谢功能障碍相关脂肪变性肝病的组织学严重程度
在儿童和青少年中,代谢功能障碍相关脂肪变性肝病(MASLD)的负担正在增加。然而,通过肝活检诊断疾病的严重程度仍然不确定,也没有系统的评估。我们进行了一项系统回顾和荟萃分析,以确定该人群中代谢功能障碍相关脂肪性肝炎(MASH)、显著和晚期纤维化的患病率。系统检索PubMed和Embase数据库(从成立到2024年9月17日),以报告活检证实为MASLD的儿科患者(≤21岁)肝脏组织学的研究。比例的荟萃分析使用广义线性混合模型与Clopper-Pearson区间进行,以获得合并的患病率估计。在确定的4761份记录中,我们纳入了35项研究,涉及5898名活检证实的MASLD儿童患者(33.4%的女孩;平均年龄12.6岁)。基于组织学的MASH、显著纤维化(定义为≥F2)和晚期纤维化(定义为≥F3)的总患病率分别为59.95% (n = 18项研究,95%可信区间[CI]: 46.89-71.73, I²= 97%)、30.53% (n = 26项研究,95% CI: 22.32-40.20, I²= 94%)和11.77% (n = 28项研究,95% CI: 8.10-16.80, I²= 89%)。亚组分析显示,晚期纤维化的患病率较高
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来源期刊
CiteScore
5.30
自引率
13.80%
发文量
467
审稿时长
3-6 weeks
期刊介绍: ​The Journal of Pediatric Gastroenterology and Nutrition (JPGN) provides a forum for original papers and reviews dealing with pediatric gastroenterology and nutrition, including normal and abnormal functions of the alimentary tract and its associated organs, including the salivary glands, pancreas, gallbladder, and liver. Particular emphasis is on development and its relation to infant and childhood nutrition.
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