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Prediction Models for Celiac Disease Development in Children From High-Risk Families: Data From the PreventCD Cohort.
Meijer, Caroline R; Auricchio, Renata; Putter, Hein; Castillejo, Gemma; Crespo, Paula; Gyimesi, Judit; Hartman, Corina; Kolacek, Sanja; Koletzko, Sibylle; Korponay-Szabo, Ilma; Ojinaga, Eva Martinez; Polanco, Isabel; Ribes-Koninckx, Carmen; Shamir, Raanan; Szajewska, Hania; Troncone, Riccardo; Villanacci, Vincenzo; Werkstetter, Katharina; Mearin, M Luisa.
Afiliación
  • Meijer CR; Department of Pediatrics, Leiden University Medical Center, Leiden, the Netherlands. Electronic address: c.r.meijer-boekel@lumc.nl.
  • Auricchio R; Translational Medical Sciences and European Laboratory for the Investigation of Food-Induced Disease, University of Naples Federico II, Naples, Italy.
  • Putter H; Department of Medical Statistics, Leiden University Medical Center, Leiden, the Netherlands.
  • Castillejo G; Pediatric Gastroenterology Unit, Hospital Universitario Sant Joan de Reus, Reus, Spain.
  • Crespo P; ADViSE, Department of Health Sciences, European University Miguel de Cervantes, Hospital Recoletas Campo Grande, Valladolid, Spain.
  • Gyimesi J; Coeliac Disease Centre, Heim Pál National Paediatric Institute, Budapest, Hungary.
  • Hartman C; Institute for Gastroenterology, Nutrition and Liver Disease, Schneider Children's Medical Center, Sackler Faculty of Medicine Tel Aviv University, Tel Aviv, Israel.
  • Kolacek S; Referral Center Pediatric Gastroenterology and Nutrition, Zagreb University, Medical School, Zagreb, Croatia.
  • Koletzko S; Dr. von Hauner Children's Hospital, Department of Pediatrics, University Hospital, LMU Munich, Munich, Germany; Department of Pediatrics, Gastroenterology and Nutrition, School of Medicine Collegium Medicum University of Warmia and Mazury, Olsztyn, Poland.
  • Korponay-Szabo I; Coeliac Disease Centre, Heim Pál National Paediatric Institute, Budapest, Hungary.
  • Ojinaga EM; Pediatric Gastroenterology and Nutrition, La Paz University Hospital, Madrid, Spain.
  • Polanco I; Pediatric Gastroenterology and Nutrition, La Paz University Hospital, Madrid, Spain.
  • Ribes-Koninckx C; Pediatric Gastroenterology Unit, La Fe Hospital, Valencia, Spain.
  • Shamir R; Institute for Gastroenterology, Nutrition and Liver Disease, Schneider Children's Medical Center, Sackler Faculty of Medicine Tel Aviv University, Tel Aviv, Israel.
  • Szajewska H; Pediatrics, Warsaw, Medical University of Warsaw, Warsaw, Poland.
  • Troncone R; Translational Medical Sciences and European Laboratory for the Investigation of Food-Induced Disease, University of Naples Federico II, Naples, Italy.
  • Villanacci V; Institute of Pathology, ASST-Spedali Civili Brescia, Brescia, Italy.
  • Werkstetter K; Dr. von Hauner Children's Hospital, Department of Pediatrics, University Hospital, LMU Munich, Munich, Germany.
  • Mearin ML; Department of Pediatrics, Leiden University Medical Center, Leiden, the Netherlands.
Gastroenterology ; 163(2): 426-436, 2022 08.
Article en En | MEDLINE | ID: mdl-35487291
BACKGROUND & AIMS: Screening for celiac disease (CD) is recommended in children with affected first-degree relatives (FDR). However, the frequency of screening and at what age remain unknown. The aims of this study were to detect variables influencing the risk of CD development and develop and validate clinical prediction models to provide individualized screening advice. METHODS: We analyzed prospective data from the 10 years of follow-up of the PreventCD-birth cohort involving 944 genetically predisposed children with CD-FDR. Variables significantly influencing the CD risk were combined to determine a risk score. Landmark analyses were performed at different ages. Prediction models were created using multivariable Cox proportional hazards regression analyses, backward elimination, and Harrell's c-index for discrimination. Validation was done using data from the independent NeoCel cohort. RESULTS: In March 2019, the median follow-up was 8.3 years (22 days-12.0 years); 135/944 children developed CD (mean age, 4.3 years [range, 1.1-11.4]). CD developed significantly more often in girls (P = .005) and in Human Leukocyte Antigen (HLA)-DQ2 homozygous individuals (8-year cumulative incidence rate of 35.4% vs maximum of the other HLA-risk groups 18.2% [P < .001]). The effect of homozygosity DR3-DQ2/DR7-DQ2 on CD development was only present in girls (interaction P = .04). The prediction models showed good fit in the validation cohort (Cox regression 0.81 [0.54]). To calculate a personalized risk of CD development and provide screening advice, we designed the Prediction application https://hputter.shinyapps.io/preventcd/. CONCLUSION: Children with CD-FDR develop CD early in life, and their risk depends on gender, age and HLA-DQ, which are all factors that are important for sound screening advice. These children should be screened early in life, including HLA-DQ2/8-typing, and if genetically predisposed to CD, they should get further personalized screening advice using our Prediction application. TRIAL REGISTRATION NUMBER: ISRCTN74582487 (https://www.isrctn.com/search?q=ISRCTN74582487).
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad Celíaca Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Child / Child, preschool / Female / Humans Idioma: En Revista: Gastroenterology Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad Celíaca Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Child / Child, preschool / Female / Humans Idioma: En Revista: Gastroenterology Año: 2022 Tipo del documento: Article