医学
内科学
自身免疫性肝炎
回顾性队列研究
肝移植
原发性硬化性胆管炎
队列
肝病学
比例危险模型
肝炎
移植
疾病
作者
CD Slooter,Floris F. van den Brand,Ana Lleò,Francesca Colapietro,Marco Lenzi,Paolo Muratori,Nanda Kerkar,George Ν. Dalekos,Kalliopi Zachou,M. Isabel Lucena,Mercedes Robles‐Díaz,Daniel E. Di Zeo-Sánchez,Raúl J. Andrade,Aldo J. Montaño‐Loza,Ellina Lytvyak,Birgit I. Lissenberg‐Witte,Patrick Maisonneuve,Gerd Bouma,Guilherme Macedo,Rodrigo Liberal,Ynto S. de Boer
出处
期刊:Hepatology
[Wiley]
日期:2023-09-04
卷期号:79 (3): 538-550
被引量:12
标识
DOI:10.1097/hep.0000000000000589
摘要
Background and Aims: The International Autoimmune Hepatitis Group retrospective registry (IAIHG-RR) is a web-based platform with subjects enrolled with a clinical diagnosis of autoimmune hepatitis (AIH). As prognostic factor studies with enough power are scarce, this study aimed to ascertain data quality and identify prognostic factors in the IAIHG-RR cohort. Methods: This retrospective, observational, multicenter study included all patients with a clinical diagnosis of AIH from the IAIHG-RR. The quality assessment consisted of external validation of completeness and consistency for 29 predefined variables. Cox regression was used to identify risk factors for liver-related death and liver transplantation (LT). Results: This analysis included 2559 patients across 7 countries. In 1700 patients, follow-up was available, with a completeness of individual data of 90% (range: 30–100). During a median follow-up period of 10 (range: 0–49) years, there were 229 deaths, of which 116 were liver-related, and 143 patients underwent LT. Non-White ethnicity (HR 4.1 95% CI: 2.3–7.1), cirrhosis (HR 3.5 95% CI: 2.3–5.5), variant syndrome with primary sclerosing cholangitis (PSC) (HR 3.1 95% CI: 1.6–6.2), and lack of complete biochemical response within 6 months (HR 5.7 95% CI: 3.4–9.6) were independent prognostic factors. Conclusions: The IAIHG-RR represents the world’s largest AIH cohort with moderate-to-good data quality and a relevant number of liver-related events. The registry is a suitable platform for patient selection in future studies. Lack of complete biochemical response to treatment, non-White ethnicity, cirrhosis, and PSC-AIH were associated with liver-related death and LT.
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