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High prevalence of eosinophilic esophagitis in patients with inherited connective tissue disorders.
Abonia, J Pablo; Wen, Ting; Stucke, Emily M; Grotjan, Tommie; Griffith, Molly S; Kemme, Katherine A; Collins, Margaret H; Putnam, Philip E; Franciosi, James P; von Tiehl, Karl F; Tinkle, Brad T; Marsolo, Keith A; Martin, Lisa J; Ware, Stephanie M; Rothenberg, Marc E.
Afiliação
  • Abonia JP; Division of Allergy and Immunology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio 45229, USA.
J Allergy Clin Immunol ; 132(2): 378-86, 2013 Aug.
Article em En | MEDLINE | ID: mdl-23608731
ABSTRACT

BACKGROUND:

Eosinophilic esophagitis (EoE) is an emerging chronic inflammatory disease mediated by immune hypersensitization to multiple foods and strongly associated with atopy and esophageal remodeling.

OBJECTIVE:

We provide clinical and molecular evidence indicating a high prevalence of EoE in patients with inherited connective tissue disorders (CTDs).

METHODS:

We examined the rate of EoE among patients with CTDs and subsequently analyzed esophageal mRNA transcript profiles in patients with EoE with or without CTD features.

RESULTS:

We report a cohort of 42 patients with EoE with a CTD-like syndrome, representing 0.8% of patients with CTDs and 1.3% of patients with EoE within our hospital-wide electronic medical record database and our EoE research registry, respectively. An 8-fold risk of EoE in patients with CTDs (relative risk, 8.1; 95% confidence limit, 5.1-12.9; χ(2)1 = 112.0; P < 10(-3)) was present compared with the general population. Esophageal transcript profiling identified a distinct subset of genes, including COL8A2, in patients with EoE and CTDs.

CONCLUSION:

There is a remarkable association of EoE with CTDs and evidence for a differential expression of genes involved in connective tissue repair in this cohort. Thus, we propose stratification of patients with EoE and CTDs into a subset referred to as EoE-CTD.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Ehlers-Danlos / Esofagite Eosinofílica / Síndrome de Marfan Tipo de estudo: Etiology_studies / Prevalence_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2013 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Ehlers-Danlos / Esofagite Eosinofílica / Síndrome de Marfan Tipo de estudo: Etiology_studies / Prevalence_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2013 Tipo de documento: Article