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在一个儿科家庭肠外营养队列中,根据非侵入性工具评估的肝纤维化患病率。

The prevalence of liver fibrosis according to non-invasive tools in a pediatric home parenteral nutrition cohort.

作者信息

Nagelkerke Sjoerd C J, Draijer Laura G, Benninga Marc A, Koot Bart G P, Tabbers Merit M

机构信息

Amsterdam UMC, University of Amsterdam, Amsterdam Reproduction and Development Research Institute, Amsterdam, the Netherlands; Amsterdam UMC, University of Amsterdam, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam, the Netherlands; Amsterdam UMC, University of Amsterdam, Emma Children's Hospital, Department of Pediatric Gastroenterology, Hepatology and Nutrition, Amsterdam, the Netherlands.

Amsterdam UMC, University of Amsterdam, Amsterdam Reproduction and Development Research Institute, Amsterdam, the Netherlands; Amsterdam UMC, University of Amsterdam, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam, the Netherlands; Amsterdam UMC, University of Amsterdam, Emma Children's Hospital, Department of Pediatric Gastroenterology, Hepatology and Nutrition, Amsterdam, the Netherlands.

出版信息

Clin Nutr. 2021 Feb;40(2):460-466. doi: 10.1016/j.clnu.2020.05.039. Epub 2020 Jun 11.

Abstract

BACKGROUND & AIMS: Liver biopsy is no viable tool to routinely screen for liver fibrosis in children suffering from chronic intestinal failure (IF). We aim to assess the prevalence of liver fibrosis in a cohort of children with chronic IF by non-invasive tests: transient elastography (TE), aspartate-aminotransferase-to-platelet-ratio-index (APRI) and enhanced liver fibrosis (ELF) score.

METHODS

Cross sectional study where patients with chronic IF, receiving parenteral nutrition (PN) for at least 3 months, were enrolled. TE, APRI and ELF score were measured. Using Spearman's rank correlation coefficient and Kruskal-Wallis H test, the correlation between TE, APRI, ELF score and known risk factors for development of intestinal failure-associated liver disease (IFALD) were calculated.

RESULTS

32 patients were included (50% female), median age was 8 years and 4 months, median PN duration was 45 months. Six patients (21%) had TE ≥6.5 kPa, indicating significant fibrosis. Twelve patients (38%) had APRI ≥.5, indicating fibrosis. ELF score indicated moderate fibrosis in 17 patients (63%) and significant fibrosis in 10 patients (37%). TE and APRI correlated significantly with known risk factors for IFALD, but ELF showed poor correlation with known risk factors for IFALD.

CONCLUSION

In a cohort of pediatric patients suffering from chronic IF, TE measurement, APRI and ELF test show a varying, but substantial proportion of subjects with fibrosis. The diagnostic value of these tests and their role in the management of pediatric IF must be determined in larger cohorts with liver biopsy as reference standard.

TRIAL REGISTRATION

Academic Medical Center medical ethics committee number: METC 2017_185.

摘要

背景与目的

肝活检并非常规筛查慢性肠衰竭(IF)患儿肝纤维化的可行工具。我们旨在通过非侵入性检测评估慢性IF患儿队列中肝纤维化的患病率:瞬时弹性成像(TE)、天冬氨酸转氨酶与血小板比值指数(APRI)以及增强肝纤维化(ELF)评分。

方法

进行横断面研究,纳入接受肠外营养(PN)至少3个月的慢性IF患者。测量TE、APRI和ELF评分。使用Spearman等级相关系数和Kruskal-Wallis H检验,计算TE、APRI、ELF评分与已知的肠衰竭相关肝病(IFALD)发生风险因素之间的相关性。

结果

纳入32例患者(50%为女性),中位年龄为8岁4个月,中位PN持续时间为45个月。6例患者(21%)TE≥6.5 kPa,表明存在显著纤维化。12例患者(38%)APRI≥0.5,表明存在纤维化。ELF评分显示17例患者(63%)为中度纤维化,10例患者(37%)为显著纤维化。TE和APRI与已知的IFALD风险因素显著相关,但ELF与已知的IFALD风险因素相关性较差。

结论

在慢性IF的儿科患者队列中,TE测量、APRI和ELF检测显示不同比例但相当一部分受试者存在纤维化。这些检测的诊断价值及其在儿科IF管理中的作用必须在以肝活检为参考标准的更大队列中确定。

试验注册

学术医疗中心医学伦理委员会编号:METC 2017_185 。

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