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Histological validation of a type 1 diabetes clinical diagnostic model for classification of diabetes.
Carr, A L J; Perry, D J; Lynam, A L; Chamala, S; Flaxman, C S; Sharp, S A; Ferrat, L A; Jones, A G; Beery, M L; Jacobsen, L M; Wasserfall, C H; Campbell-Thompson, M L; Kusmartseva, I; Posgai, A; Schatz, D A; Atkinson, M A; Brusko, T M; Richardson, S J; Shields, B M; Oram, R A.
Afiliação
  • Carr ALJ; Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.
  • Perry DJ; Department of Pathology, Immunology and Laboratory Medicine, University of Florida Diabetes Institute, Gainesville, FL, USA.
  • Lynam AL; Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.
  • Chamala S; Department of Pathology, Immunology and Laboratory Medicine, University of Florida Diabetes Institute, Gainesville, FL, USA.
  • Flaxman CS; Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.
  • Sharp SA; Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.
  • Ferrat LA; Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.
  • Jones AG; Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.
  • Beery ML; Department of Pathology, Immunology and Laboratory Medicine, University of Florida Diabetes Institute, Gainesville, FL, USA.
  • Jacobsen LM; Department of Pediatrics, College of Medicine, University of Florida Diabetes Institute, Gainesville, FL, USA.
  • Wasserfall CH; Department of Pathology, Immunology and Laboratory Medicine, University of Florida Diabetes Institute, Gainesville, FL, USA.
  • Campbell-Thompson ML; Department of Pathology, Immunology and Laboratory Medicine, University of Florida Diabetes Institute, Gainesville, FL, USA.
  • Kusmartseva I; Department of Pathology, Immunology and Laboratory Medicine, University of Florida Diabetes Institute, Gainesville, FL, USA.
  • Posgai A; Department of Pathology, Immunology and Laboratory Medicine, University of Florida Diabetes Institute, Gainesville, FL, USA.
  • Schatz DA; Department of Pediatrics, College of Medicine, University of Florida Diabetes Institute, Gainesville, FL, USA.
  • Atkinson MA; Department of Pathology, Immunology and Laboratory Medicine, University of Florida Diabetes Institute, Gainesville, FL, USA.
  • Brusko TM; Department of Pediatrics, College of Medicine, University of Florida Diabetes Institute, Gainesville, FL, USA.
  • Richardson SJ; Department of Pathology, Immunology and Laboratory Medicine, University of Florida Diabetes Institute, Gainesville, FL, USA.
  • Shields BM; Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.
  • Oram RA; Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.
Diabet Med ; 37(12): 2160-2168, 2020 12.
Article em En | MEDLINE | ID: mdl-32634859
ABSTRACT

AIMS:

Misclassification of diabetes is common due to an overlap in the clinical features of type 1 and type 2 diabetes. Combined diagnostic models incorporating clinical and biomarker information have recently been developed that can aid classification, but they have not been validated using pancreatic pathology. We evaluated a clinical diagnostic model against histologically defined type 1 diabetes.

METHODS:

We classified cases from the Network for Pancreatic Organ donors with Diabetes (nPOD) biobank as type 1 (n = 111) or non-type 1 (n = 42) diabetes using histopathology. Type 1 diabetes was defined by lobular loss of insulin-containing islets along with multiple insulin-deficient islets. We assessed the discriminative performance of previously described type 1 diabetes diagnostic models, based on clinical features (age at diagnosis, BMI) and biomarker data [autoantibodies, type 1 diabetes genetic risk score (T1D-GRS)], and singular features for identifying type 1 diabetes by the area under the curve of the receiver operator characteristic (AUC-ROC).

RESULTS:

Diagnostic models validated well against histologically defined type 1 diabetes. The model combining clinical features, islet autoantibodies and T1D-GRS was strongly discriminative of type 1 diabetes, and performed better than clinical features alone (AUC-ROC 0.97 vs. 0.95; P = 0.03). Histological classification of type 1 diabetes was concordant with serum C-peptide [median < 17 pmol/l (limit of detection) vs. 1037 pmol/l in non-type 1 diabetes; P < 0.0001].

CONCLUSIONS:

Our study provides robust histological evidence that a clinical diagnostic model, combining clinical features and biomarkers, could improve diabetes classification. Our study also provides reassurance that a C-peptide-based definition of type 1 diabetes is an appropriate surrogate outcome that can be used in large clinical studies where histological definition is impossible. Parts of this study were presented in abstract form at the Network for Pancreatic Organ Donors Conference, Florida, USA, 19-22 February 2019 and Diabetes UK Professional Conference, Liverpool, UK, 6-8 March 2019.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ilhotas Pancreáticas / Diabetes Mellitus Tipo 1 / Diabetes Mellitus Tipo 2 Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Diabet Med Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ilhotas Pancreáticas / Diabetes Mellitus Tipo 1 / Diabetes Mellitus Tipo 2 Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Diabet Med Ano de publicação: 2020 Tipo de documento: Article