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Development and Validation of Web-Based Tool to Predict Lamina Propria Fibrosis in Eosinophilic Esophagitis.
Hiremath, Girish; Sun, Lili; Correa, Hernan; Acra, Sari; Collins, Margaret H; Bonis, Peter; Arva, Nicoleta C; Capocelli, Kelley E; Falk, Gary W; King, Eileen; Gonsalves, Nirmala; Gupta, Sandeep K; Hirano, Ikuo; Mukkada, Vincent A; Martin, Lisa J; Putnam, Philip E; Spergel, Jonathan M; Wechsler, Joshua B; Yang, Guang-Yu; Aceves, Seema S; Furuta, Glenn T; Rothenberg, Marc E; Koyama, Tatsuki; Dellon, Evan S.
Afiliación
  • Hiremath G; Division of Pediatric Gastroenterology, Hepatology and Nutrition, Monroe Carell Jr. Children's Hospital at Vanderbilt, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Sun L; Department of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Correa H; Division of Pediatric Pathology, Monroe Carell Jr. Children's Hospital at Vanderbilt, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Acra S; Division of Pediatric Gastroenterology, Hepatology and Nutrition, Monroe Carell Jr. Children's Hospital at Vanderbilt, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Collins MH; Department of Pathology and Laboratory Medicine, Cincinnati Children's Hospital, Cincinnati, Ohio, USA.
  • Bonis P; Wolters Kluwer Health, Waltham, Massachusetts, USA.
  • Arva NC; Department of Pathology and Laboratory Medicine, Ann & Robert H. Laurie Children's Hospital at Chicago, Illinois, USA.
  • Capocelli KE; Department of Pathology, Children's Hospital Colorado, Aurora, Colorado, USA.
  • Falk GW; Department of Medicine, Perelman Center for Advanced Medicine, Philadelphia, Pennsylvania, USA.
  • King E; Division of Biostatistics and Epidemiology, Department of Pediatrics, Cincinnati Children's Hospital, Cincinnati, Ohio, USA.
  • Gonsalves N; Division of Gastroenterology and Hepatology, Northwestern Medicine, Chicago, Illinois, USA.
  • Gupta SK; Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Indiana University School of Medicine, Indianapolis, Indiana, USA.
  • Hirano I; Division of Gastroenterology and Hepatology, Northwestern Medicine, Chicago, Illinois, USA.
  • Mukkada VA; Department of Pediatrics, Cincinnati Children's Hospital, Cincinnati, Ohio, USA.
  • Martin LJ; Department of Pediatrics, Cincinnati Children's Hospital, Cincinnati, Ohio, USA.
  • Putnam PE; Department of Pediatrics, Cincinnati Children's Hospital, Cincinnati, Ohio, USA.
  • Spergel JM; Division of Allergy-Immunology, Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania, Pennsylvania, USA.
  • Wechsler JB; Division of Pediatric Gastroenterology, Hepatology and Nutrition, Monroe Carell Jr. Children's Hospital at Vanderbilt, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Yang GY; Division of Anatomical Pathology, Northwestern Feinberg School of Medicine, Chicago, Illinois, USA.
  • Aceves SS; Division of Rheumatology, Allergy and Immunology, Rady Children's Hospital, San Diego, San Diego, California, USA.
  • Furuta GT; Division of Pediatric Gastroenterology, Hepatology and Nutrition, Monroe Carell Jr. Children's Hospital at Vanderbilt, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Rothenberg ME; Division of Allergy and Immunology, Cincinnati Children's Hospital, Cincinnati, Ohio, USA.
  • Koyama T; Department of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Dellon ES; Division of Gastroenterology and Hepatology, University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, North Carolina, USA.
Am J Gastroenterol ; 117(2): 272-279, 2022 02 01.
Article en En | MEDLINE | ID: mdl-34932022
ABSTRACT

INTRODUCTION:

Approximately half of esophageal biopsies from patients with eosinophilic esophagitis (EoE) contain inadequate lamina propria, making it impossible to determine the lamina propria fibrosis (LPF). This study aimed to develop and validate a web-based tool to predict LPF in esophageal biopsies with inadequate lamina propria.

METHODS:

Prospectively collected demographic and clinical data and scores for 7 relevant EoE histology scoring system epithelial features from patients with EoE participating in the Consortium of Eosinophilic Gastrointestinal Disease Researchers observational study were used to build the models. Using the least absolute shrinkage and selection operator method, variables strongly associated with LPF were identified. Logistic regression was used to develop models to predict grade and stage of LPF. The grade model was validated using an independent data set.

RESULTS:

Of 284 patients in the discovery data set, median age (quartiles) was 16 (8-31) years, 68.7% were male patients, and 93.4% were White. Age of the patient, basal zone hyperplasia, dyskeratotic epithelial cells, and surface epithelial alteration were associated with presence of LPF. The area under the receiver operating characteristic curve for the grade model was 0.84 (95% confidence interval 0.80-0.89) and for stage model was 0.79 (95% confidence interval 0.74-0.84). Our grade model had 82% accuracy in predicting the presence of LPF in an external validation data set.

DISCUSSION:

We developed parsimonious models (grade and stage) to predict presence of LPF in esophageal biopsies with inadequate lamina propria and validated our grade model. Our predictive models can be easily used in the clinical setting to include LPF in clinical decisions and determine its effect on treatment outcomes.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Internet / Esófago / Esofagitis Eosinofílica / Membrana Mucosa Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Am J Gastroenterol Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Internet / Esófago / Esofagitis Eosinofílica / Membrana Mucosa Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Am J Gastroenterol Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos