A real-world study on the characteristics of autoimmune gastritis: A single-center retrospective cohort in China

IF 2.4 4区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY Clinics and research in hepatology and gastroenterology Pub Date : 2025-04-01 Epub Date: 2025-02-15 DOI:10.1016/j.clinre.2025.102556
Yu Chen , Xiaowei Ji , Weiyi Zhao , Jie Lin , Siyuan Xie , Jinghong Xu , Jianshan Mao
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Abstract

Background and Aim

Autoimmune gastritis (AIG) was previously considered a rare disease in China, and its clinical characteristics were not fully understood. This study aimed to demonstrate the characteristics of AIG in China and evaluate gastric oxyntic mucosal atrophy using a modified AIG-atrophic staging.

Methods

This was a single-center retrospective observational real-world study. The diagnosis of AIG was based on pathological results combined with parietal cell antibody (PCA) and intrinsic factor antibody (IFA) results, and endoscopic findings.

Results

A total of 745 patients were enrolled, the median age at diagnosis was 58 years old, and 69.9 % were female. The symptoms of AIG patients were nonspecific, and about 2/5 of the cases were asymptomatic. The proportions of cases from modified AIG-atrophic stage 1 to 4 were 0.8 %, 14.1 %, 73.8 %, and 11.3 %, respectively. Approximately 1/5 had autoimmune thyroiditis (AITD). Near 1/2 had one or more comorbidities: iron-deficiency anemia (IDA), pernicious anemia (PA), neuropathy, gastric hyperplastic polyps (GHP), gastric intraepithelial neoplasia (GIN), type 1 gastric neuroendocrine tumors (g-NET), or gastric adenocarcinoma (GAC). There was a high risk of type 1 g-NET (7.0 %) and GAC (9.1 %) in AIG patients.

Conclusions

AIG is not rare in China, and its early diagnosis is challenging, accompanied by a high risk of GAC. The modified four-stage AIG-atrophic staging can effectively represent the extent of oxyntic mucosal atrophy and the progression in AIG.
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自身免疫性胃炎特征的真实世界研究:中国单中心回顾性队列研究
背景和目的:自身免疫性胃炎(AIG)在中国以前被认为是一种罕见的疾病,其临床特征尚不完全清楚。本研究旨在阐明中国AIG的特点,并采用改良的AIG-萎缩分期来评价胃氧合性粘膜萎缩。方法本研究为单中心回顾性观察性真实世界研究。AIG的诊断是基于病理结果,结合壁细胞抗体(PCA)和内因子抗体(IFA)结果,以及内镜检查结果。结果共纳入745例患者,诊断时中位年龄为58岁,其中69.9%为女性。AIG患者的症状无特异性,约2/5的病例无症状。改良型aig萎缩1 ~ 4期的比例分别为0.8%、14.1%、73.8%、11.3%。约1/5患有自身免疫性甲状腺炎(AITD)。近1/2的患者有一种或多种合并症:缺铁性贫血(IDA)、恶性贫血(PA)、神经病变、胃增生性息肉(GHP)、胃上皮内瘤变(GIN)、1型胃神经内分泌肿瘤(g-NET)或胃腺癌(GAC)。AIG患者发生1型g-NET(7.0%)和GAC(9.1%)的风险较高。结论aig在中国并不罕见,其早期诊断具有挑战性,并伴有GAC的高风险。改良后的4期AIG萎缩分期能有效反映氧合性粘膜萎缩的程度和AIG的进展情况。
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来源期刊
CiteScore
4.30
自引率
3.70%
发文量
198
审稿时长
42 days
期刊介绍: Clinics and Research in Hepatology and Gastroenterology publishes high-quality original research papers in the field of hepatology and gastroenterology. The editors put the accent on rapid communication of new research and clinical developments and so called "hot topic" issues. Following a clear Editorial line, besides original articles and case reports, each issue features editorials, commentaries and reviews. The journal encourages research and discussion between all those involved in the specialty on an international level. All articles are peer reviewed by international experts, the articles in press are online and indexed in the international databases (Current Contents, Pubmed, Scopus, Science Direct). Clinics and Research in Hepatology and Gastroenterology is a subscription journal (with optional open access), which allows you to publish your research without any cost to you (unless you proactively chose the open access option). Your article will be available to all researchers around the globe whose institution has a subscription to the journal.
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