The application of Chicago classification 4.0 in esophageal motility disorders of scleroderma: a case-control study in China.

IF 7 2区 医学 Q1 IMMUNOLOGY
Frontiers in Immunology Pub Date : 2026-10-05 eCollection Date: 2026-01-01 DOI:10.3389/fimmu.2026.1962332
Yinghui Yang, Siwei Xie, Minyi Xu, Zhiming Lin, Yanli Zhang
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引用次数: 0

Abstract

Background: Systemic sclerosis (SSc) is a rare autoimmune connective tissue disease characterized by multi-organ fibrosis and vasculopathy that frequently involves the esophagus. This study assessed esophageal motility disorders in patients with SSc using High-resolution manometry (HRM) and classified these disorders according to the Chicago Classification version 4.0, aims to investigate the associations between esophageal dysfunction and clinical phenotypes in Chinese SSc patients, while exploring potential modifications to enhance the applicability of the Chicago v4.0 protocol in SSc patients.

Methods: We retrospectively identified SSc patients fulfilling 2013 ACR criteria who underwent HRM classified by Chicago v4.0 at our center (2021-2023). Demographics, organ involvement, pulmonary-function tests, echocardiography and reflux symptom scores (RDQ/GERDQ) were extracted from the hospital information system; age and sex matched non-SSc HRM subjects served as controls. Associations between Chicago categories and clinical variables were examined by multinomial logistic regression.

Results: In our study, esophageal motility disorders were present in 76.7% of patients with systemic sclerosis, predominantly characterized by ineffective esophageal motility (IEM) (35%) and absent contractility (AC) (36.67%). The occurrence rate of AC rose with age. Symptoms of gastroesophageal reflux were more common in the AC group [Odds Ratio: 3.23 (1.02-10.22) vs 1.43(0.52-3.95), P<0.05, E value=2.99]. Diffusion capacity for carbon monoxide (DLCO) was significantly reduced in both IEM and AC (-2.03 vs -2.70, P value<0.05), with a more pronounced decrease in AC. Total lung capacity (TLC) and forced expiratory volume in one second (FEV1) exhibited stronger associations with AC (-1.04 and -0.8 respectively, p value<0.05). Upright HRM revealed more marked decreases in EGJ pressure and distal contractile integral (DCI) relative to the supine position in SSc patients, indicating that esophageal abnormalities may be more readily apparent during upright examination.

Conclusions: Esophageal motility disorders in SSc were common and significantly associated with older age, gastroesophageal reflux symptoms, and reduced lung function. Future studies are needed to clarify whether early esophageal motility disorders are associated with disease progression and prognosis in patients.

芝加哥4.0分型在硬皮病食管运动障碍中的应用:中国病例对照研究
背景:系统性硬化症(SSc)是一种罕见的自身免疫性结缔组织疾病,以多器官纤维化和血管病变为特征,常累及食道。本研究采用高分辨率测压法(HRM)评估SSc患者的食管运动障碍,并根据Chicago Classification version 4.0对这些疾病进行分类,旨在探讨中国SSc患者食管功能障碍与临床表型之间的关系,同时探索可能的修改,以增强Chicago v4.0方案在SSc患者中的适用性。方法:我们回顾性地确定了符合2013年ACR标准的SSc患者,这些患者在我们中心(2021-2023)接受了芝加哥v4.0分级的HRM。从医院信息系统中提取人口统计学、脏器受累、肺功能检查、超声心动图和反流症状评分(RDQ/GERDQ);年龄和性别匹配的非ssc人力资源管理受试者作为对照。采用多项逻辑回归检验芝加哥分类与临床变量之间的关系。结果:在我们的研究中,76.7%的系统性硬化症患者存在食道运动障碍,主要表现为食道运动无效(IEM)(35%)和食道收缩力缺失(AC)(36.67%)。AC的发生率随年龄的增长而上升。胃食管反流症状在AC组中更为常见[优势比:3.23 (1.02-10.22)vs 1.43(0.52-3.95), p结论:SSc患者食管运动障碍较为常见,且与年龄、胃食管反流症状和肺功能降低显著相关。需要进一步的研究来阐明早期食管运动障碍是否与患者的疾病进展和预后相关。
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来源期刊
CiteScore
9.80
自引率
11.00%
发文量
7153
审稿时长
14 weeks
期刊介绍: Frontiers in Immunology is a leading journal in its field, publishing rigorously peer-reviewed research across basic, translational and clinical immunology. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Immunology is the official Journal of the International Union of Immunological Societies (IUIS). Encompassing the entire field of Immunology, this journal welcomes papers that investigate basic mechanisms of immune system development and function, with a particular emphasis given to the description of the clinical and immunological phenotype of human immune disorders, and on the definition of their molecular basis.
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