Department of Medicine, Center for Esophageal Diseases, Baylor University Medical Center, Dallas, Texas; Center for Esophageal Research, Baylor Scott & White Research Institute, Dallas, Texas.
Department of Medicine, University of Utah, Salt Lake City, Utah.
Clin Gastroenterol Hepatol. 2024 Jan;22(1):34-41.e2. doi: 10.1016/j.cgh.2023.06.013. Epub 2023 Jun 28.
BACKGROUND & AIMS: Achalasia has been assumed to be an autoimmune disease targeting esophageal myenteric neurons. Recently, we proposed an alternative hypothesis that achalasia sometimes might be allergy-driven, caused by a form of eosinophilic esophagitis (EoE) in which activated eosinophils and/or mast cells infiltrating esophageal muscle release products that disrupt motility and damage myenteric neurons. To seek epidemiologic support for this hypothesis, we identified patients with achalasia in the Utah Population Database, and explored their frequency of having EoE and other allergic disorders.
We used International Classification of Diseases codes to identify patients with achalasia and allergic disorders including EoE, asthma, atopic dermatitis, contact dermatitis, allergic rhinitis, allergic conjunctivitis, hives/urticaria, and anaphylaxis. We calculated relative risk (RR) for each allergic disorder by comparing the number observed in patients with achalasia with the expected number in individuals matched for birthyear and sex, and we performed subanalyses for patients age ≤40 versus age >40 years.
Among 844 patients with achalasia identified (55% female; median age at diagnosis, 58 years), 402 (47.6%) had ≥1 allergic disorder. Fifty-five patients with achalasia (6.5%) had EoE (1.67 EoE cases expected), for a RR of 32.9 (95% confidence interval, 24.8-42.8; P < .001). In 208 patients with achalasia age ≤40 years, the RR for EoE was 69.6 (95% confidence interval, 46.6-100.0; P < .001). RR also was increased significantly for all other allergic disorders evaluated (all greater than 3-fold higher than population rates).
Achalasia is strongly associated with EoE and other allergic disorders. These data support the hypothesis that achalasia sometimes might have an allergic etiology.
贲门失弛缓症被认为是一种针对食管肌间神经元的自身免疫性疾病。最近,我们提出了一个替代假说,即贲门失弛缓症有时可能是由过敏引起的,由一种嗜酸性食管炎(EoE)引起,其中激活的嗜酸性粒细胞和/或浸润食管肌肉的肥大细胞释放的产物会破坏运动并损伤肌间神经元。为了寻求该假说的流行病学支持,我们在犹他州人群数据库中确定了贲门失弛缓症患者,并探讨了他们患 EoE 和其他过敏疾病的频率。
我们使用国际疾病分类代码来识别贲门失弛缓症患者和过敏疾病,包括 EoE、哮喘、特应性皮炎、接触性皮炎、过敏性鼻炎、过敏性结膜炎、荨麻疹/血管性水肿和过敏反应。我们通过比较观察到的贲门失弛缓症患者数量与按出生年份和性别匹配的个体的预期数量,计算了每种过敏疾病的相对风险(RR),并对≤40 岁和>40 岁的患者进行了亚分析。
在 844 名确诊的贲门失弛缓症患者中(55%为女性;中位诊断年龄为 58 岁),402 名(47.6%)至少有一种过敏疾病。55 名贲门失弛缓症患者(6.5%)患有 EoE(预期 1.67 例 EoE 病例),RR 为 32.9(95%置信区间,24.8-42.8;P<0.001)。在 208 名≤40 岁的贲门失弛缓症患者中,EoE 的 RR 为 69.6(95%置信区间,46.6-100.0;P<0.001)。评估的所有其他过敏疾病的 RR 也显著增加(均高于人群率的 3 倍以上)。
贲门失弛缓症与 EoE 和其他过敏疾病密切相关。这些数据支持贲门失弛缓症有时可能具有过敏病因的假说。