OP- 4 EPIDEMIOLOGY OF PRIMARY BILIARY CHOLANGITIS IN LATIN AMERICA: PRELIMINARY RESULTS FROM ALLATIN COHORT

IF 4.4 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY Annals of hepatology Pub Date : 2024-12-01 Epub Date: 2024-12-06 DOI:10.1016/j.aohep.2024.101602
Guilherme Grossi Lopes Cançado , Rafael Theodoro , Ezequiel Ridruejo , Lorena Castro Solari , Cristiane Alves Villela-Nogueira , Pablo Andres Coste Murillo , Harlim Rodríguez , Carlos Benítez Gajardo , Álvaro Urzúa , Eira Cerda Reyes , Paulo Lisboa Bittencourt , Alejandro Sosa , Emilia Vera , Luciana Costa Faria , Maria Lucia Ferraz , Mario Guimarães Pessoa , Debora Raquel Benedita Terrabuio , Eduardo Luiz Rachid Cançado , Claudia Alves Couto
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引用次数: 0

Abstract

Conflict of interest

No

Introduction and Objectives

Primary biliary cholangitis (PBC) may present differently depending on various factors such as ethnicity and genetic background. Latin America has a highly admixed population with a unique genetic diversity compared to other regions of the world. However, there is limited information available on the presentation and epidemiology of PBC in this region. This study aims to address the epidemiology of PBC in Latin America.

Patients / Materials and Methods

Ongoing retrospective, international, multicentric cohort study sponsored by ALEH that enrolls PBC patients from different countries in Latin America.

Results and Discussion

Data were accrued on 231 patients [Brazil (52%), Argentina (27.4%), Chile (10.8%), Costa Rica (4.5%), Cuba (3.6%), and Mexico (0.9%)], 92.1% female (mean age at diagnosis 50.5 years), 25.6% with cirrhosis at baseline. Overlap with autoimmune hepatitis was reported in 16.0% of cases. Most patients were symptomatic (67.9%) at diagnosis, with fatigue (41.9%) and pruritus (40.5%) being the main symptoms. Anti-mitochondrial antibodies (AMA) were positive in 70.8% and antinuclear antibodies (ANA) in 60.6%. Hashimoto thyroiditis (23.7%) and Sjogren syndrome (9.1%) were the most common extrahepatic autoimmune diseases associated with PBC. Mean baseline alkaline phosphatase, alanine aminotransferase, aspartate aminotransferase, and bilirubin levels were 445.9 (± 407), 89.8 (± 137.2), 37.6 (± 8.9) U/L, and 1.6 (± 3.1) mg/dL, respectively. Almost all patients (99.1%) were treated with ursodeoxycholic acid (UDCA). 67.4% achieved adequate response to UDCA according to the Toronto criteria and 32% normalized alkaline phosphatase at 12 months. Only 19.9% received second-line therapy, all with fibrates (89.1% bezafibrate, 8.7% ciprofibrate, 4.3% fenofibrate). Of the patients, 9% died, with 33% of deaths being liver-related, while 6% underwent liver transplantation. Hepatocellular carcinoma was diagnosed in 1.7% of patients.

Conclusions

In this unprecedented study, the epidemiology of PBC in Latin America appears similar to that in other parts of the world. However, lower rates of AMA positivity were observed, and most patients were still diagnosed with symptomatic disease. Second-line therapy options were limited to the availability of fibrates only.
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拉丁美洲原发性胆管炎的流行病学:allatin队列的初步结果
利益冲突介绍和目的原发性胆管炎(PBC)可能因种族和遗传背景等因素而表现不同。与世界其他地区相比,拉丁美洲人口高度混合,具有独特的遗传多样性。然而,关于该地区PBC的表现和流行病学的信息有限。本研究旨在探讨拉丁美洲PBC的流行病学。患者/材料和方法一项由ALEH赞助的回顾性、国际性、多中心队列研究,纳入了来自拉丁美洲不同国家的PBC患者。231例患者[巴西(52%)、阿根廷(27.4%)、智利(10.8%)、哥斯达黎加(4.5%)、古巴(3.6%)和墨西哥(0.9%)]的数据累积,92.1%为女性(诊断时平均年龄50.5岁),25.6%基线时为肝硬化。16.0%的病例报告与自身免疫性肝炎重叠。大多数患者在诊断时有症状(67.9%),以疲劳(41.9%)和瘙痒(40.5%)为主要症状。抗线粒体抗体(AMA)阳性率为70.8%,抗核抗体(ANA)阳性率为60.6%。桥本甲状腺炎(23.7%)和干燥综合征(9.1%)是与PBC相关的最常见的肝外自身免疫性疾病。平均基线碱性磷酸酶、丙氨酸转氨酶、天冬氨酸转氨酶和胆红素水平分别为445.9(±407)、89.8(±137.2)、37.6(±8.9)U/L和1.6(±3.1)mg/dL。几乎所有患者(99.1%)接受熊去氧胆酸(UDCA)治疗。67.4%的患者根据多伦多标准对UDCA有足够的反应,32%的患者在12个月时碱性磷酸酶正常化。只有19.9%接受了二线治疗,全部使用贝特类药物(贝扎贝特89.1%,环丙贝特8.7%,非诺贝特4.3%)。9%的患者死亡,其中33%的死亡与肝脏有关,而6%的患者接受了肝移植。1.7%的患者被诊断为肝细胞癌。结论在这项前所未有的研究中,拉丁美洲的PBC流行病学与世界其他地区相似。然而,AMA阳性率较低,大多数患者仍被诊断为有症状的疾病。二线治疗选择仅限于贝特类药物的可用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Annals of hepatology
Annals of hepatology 医学-胃肠肝病学
CiteScore
7.90
自引率
2.60%
发文量
183
审稿时长
4-8 weeks
期刊介绍: Annals of Hepatology publishes original research on the biology and diseases of the liver in both humans and experimental models. Contributions may be submitted as regular articles. The journal also publishes concise reviews of both basic and clinical topics.
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