嗜酸性粒细胞食管炎与 MASLD 之间的关联分析:2016-2020 年全国住院患者样本的回顾性、观察性、队列分析。

Isha Kohli, Aalam Sohal, Jay Patel, Marina Roytman
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引用次数: 0

摘要

背景和目的:嗜酸性粒细胞食管炎(EoE)是一种由免疫介导的慢性炎症。嗜酸性粒细胞食管炎的相关病理与代谢功能障碍相关性脂肪肝(MASLD)相似。本研究评估了代谢功能障碍相关性脂肪肝与肠易激综合征之间是否存在关联:我们使用 2020 年全国住院患者样本 (NIS) 数据来识别成年患者。我们使用 ICD-10 编码来识别 MASLD 和 EoE 患者。在调整了患者人口统计学特征、医院特征、Charlson合并症指数、肥胖、阻塞性睡眠呼吸暂停(OSA)、糖尿病、高血压(HTN)、高脂血症(HLD)、炎症性肠病(IBD)、乳糜泻(CD)、胃食管反流病(GERD)、吸烟、饮酒和肠易激综合征(IBS)等混杂因素后,通过多变量分析评估了MASLD与EoE之间的关系。研究结果在 2,600 万名患者中,4,820 人被诊断出患有肠易激综合征。大多数患者年龄在 18 至 44 岁之间(47.82%),男性(54.05%),有私人保险(50.1%),收入最高的四分位数(29.25%)。与无咽喉炎组相比,有咽喉炎组的 MASLD 发生率更高(6.1% 对 2.9%,p 结论:我们的研究报告了一项新发现,即 MASLD 与咽喉炎相关。今后需要开展前瞻性研究,以证实和了解这种关系的临床意义以及一种疾病如何影响另一种疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis of the Association between Eosinophilic Esophagitis and MASLD: Retrospective, Observational, Cohort Analysis of the National Inpatient Sample 2016-2020.

Background and aims: Eosinophilic esophagitis (EoE) is a chronic immune-mediated inflammatory condition. Associated pathologies for EoE are similar to those with metabolic-dysfunction-associated steatotic liver disease (MASLD). This study assesses whether an association exists between MASLD and EoE.

Methods: We used National Inpatient Sample (NIS) 2020 data to identify adult patients. ICD-10 codes were used to identify patients with MASLD and EoE. The relationship between MASLD and EoE was assessed by multivariate analysis after adjusting for confounding factors, such as patient demographics, hospital characteristics, Charlson comorbidity index, obesity, obstructive sleep apnea (OSA), diabetes, hypertension (HTN), hyperlipidemia (HLD), inflammatory bowel disease (IBD), celiac disease (CD), gastroesophageal reflux disease (GERD), smoking, alcohol use, and irritable bowel syndrome (IBS).

Results: Out of 26 million patients, 4,820 had a diagnosis of EoE. The majority of the patients were between 18 and 44 years of age (47.82%), male (54.05%), had private insurance (50.1%), and were in the highest income quartile (29.25%). A higher incidence of MASLD was noted in the EoE group than those without (6.1% vs.2.9%, p<0.001). After adjusting for confounding factors, MASLD had 2.38 times higher odds of having EoE (95% CI-1.82-3.11, p<0.001). Other factors noted to be associated with higher odds of EoE included younger age, Caucasian race, IBS, GERD, IBD, and CD.

Conclusions: Our study reports a novel finding that MASLD and EoE are associated. Future prospective studies are needed to confirm and understand the clinical significance of this relationship and how one disease affects the other.

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