1. The possible link between coeliac and Kawasaki diseases in Brazil: a cross-sectional study
- Author
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Claudia B. Pratesi, Nicole Selleski, Alessandra dos Santos Domingues, Lenora Gandolfi, Cristina Medeiros Ribeiro de Magalhães, and Rosa Harumi Uenishi
- Subjects
Male ,medicine.medical_specialty ,Duodenum ,Cross-sectional study ,Biopsy ,prevalence ,Population ,Gastroenterology and Hepatology ,Mucocutaneous Lymph Node Syndrome ,Gastroenterology ,Coeliac disease ,Autoimmune Diseases ,Serology ,03 medical and health sciences ,0302 clinical medicine ,Reference Values ,HLA-DQ Antigens ,030225 pediatrics ,Internal medicine ,medicine ,Humans ,Child ,education ,Alleles ,Autoantibodies ,Autoimmune disease ,education.field_of_study ,Kawasaki disease ,business.industry ,Research ,General Medicine ,Hepatology ,medicine.disease ,Celiac Disease ,Cross-Sectional Studies ,Case-Control Studies ,Child, Preschool ,Female ,030211 gastroenterology & hepatology ,business ,Brazil ,Molecular Chaperones ,Systemic vasculitis - Abstract
BackgroundKawasaki disease (KD) is a self-limited acute systemic vasculitis of unknown aetiology that predominantly affects infants and young children eventually associated with immunological abnormalities. Coeliac disease (CD) is an inflammatory autoimmune disease characterised by a permanent gluten intolerance, which affects genetically susceptible individuals of any age group, and can cause intestinal and systemic symptoms. Association of CD with KD has been previously described in a single study that disclosed a surprisingly high prevalence of CD in children with a history of KD.ObjectiveTo confirm the existence of a higher prevalence of CD among individuals with a history of KD, which would turn the screening for CD in patients with history of KD highly advisable.SettingChildren with history of KD, diagnosed and followed at the Rheumatology Clinic of the Children’s Hospital of Brasilia (Brasilia, Brazil).ParticipantsThis study included 110 children with history of KD and a control group composed of 110 presumably healthy children.InterventionsParticipants underwent anti-transglutaminase and anti-endomysial antibodies tests and genetic typing for the presence of CD predisposing alleles (HLA-DQ2 and DQ8). Jejunal biopsy was performed when necessary, according the European Society of Paediatric Gastroenterology, Hepatology and Nutrition guidelines.ResultsDiagnosis of CD was confirmed in one (0.91%) patient with KD by positive serological tests, presence of predisposing alleles and CD typical lesions on duodenal biopsy. All serological tests were negative among the controls. The prevalence of CD predisposing alleles among patients with KD was 29.09%, similar to the prevalence found among controls, 33.64%.ConclusionThe detected CD prevalence (0.91%) does not confirm the existence of an association between KD and CD since this prevalence is similar to that found in the general population (≃1%).
- Published
- 2018
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