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Exocrine Pancreas Dysfunction in Type 1 Diabetes.
Foster, Timothy P; Bruggeman, Brittany; Campbell-Thompson, Martha; Atkinson, Mark A; Haller, Michael J; Schatz, Desmond A.
Afiliação
  • Foster TP; From the (1)Department of Pediatrics, College of Medicine, University of Florida, Gainesville, Florida, and.
  • Bruggeman B; From the (1)Department of Pediatrics, College of Medicine, University of Florida, Gainesville, Florida, and.
  • Campbell-Thompson M; Department of Pathology, Immunology, and Laboratory Medicine, Diabetes Institute, University of Florida, Gainesville, Florida.
  • Atkinson MA; From the (1)Department of Pediatrics, College of Medicine, University of Florida, Gainesville, Florida, and; Department of Pathology, Immunology, and Laboratory Medicine, Diabetes Institute, University of Florida, Gainesville, Florida.
  • Haller MJ; From the (1)Department of Pediatrics, College of Medicine, University of Florida, Gainesville, Florida, and.
  • Schatz DA; From the (1)Department of Pediatrics, College of Medicine, University of Florida, Gainesville, Florida, and. Electronic address: schatda@peds.ufl.edu.
Endocr Pract ; 26(12): 1505-1513, 2020 Dec.
Article em En | MEDLINE | ID: mdl-33471743
OBJECTIVE: Type 1 diabetes (T1D) is characterized by autoimmune ß-cell destruction, but exocrine pancreas abnormalities may also play a role in the disease pathophysiology. Herein, we review the current evidence of exocrine damage in T1D and discuss its underlying pathophysiology, clinical evaluation, and treatment. METHOD: Extensive literature search was performed for "type 1 diabetes" and "exocrine dysfunction" on PubMed and Google Scholar databases. RESULTS: T1D pancreata are significantly smaller than controls, both in weight and volume. T cells, dendritic cells, neutrophils, and products of complement activation are seen in T1D exocrine tissues. Exocrine pancreas fibrosis, arteriosclerosis, fatty infiltration, and acinar atrophy are also observed on histology. Pancreatic exocrine insufficiency (PEI) can be assessed through direct exocrine testing, fecal elastase concentration, and measurement of serum exocrine enzymes. The prevalence of PEI in T1D varies by modality and study but is consistently greater than controls. The clinical relevance of PEI in T1D is debatable, as many patients with laboratory evidence of PEI are asymptomatic. However, in PEI-symptomatic patients reported benefits of pancreatic enzyme replacement therapy (PERT) include relief of gastrointestinal symptoms, improved quality of life, better glycemic control, and optimal nutrition. CONCLUSION: Exocrine pancreas abnormalities often occur in T1D. Whether exocrine dysfunction occurs simultaneously with ß-cell destruction, as a result of ß-cell loss, or as a combination of both remains to be definitively answered. In T1D with gastrointestinal complaints, PEI should be evaluated, usually via fecal elastase measurements. PERT is recommended for T1D patients with symptoms and laboratory evidence of PEI. ABBREVIATIONS: AAb+ = autoantibody positive; AAb- = autoantibody negative; FEC = fecal elastase concentration; PEI = pancreatic exocrine insufficiency; PERT = pancreatic enzyme replacement therapy; PP = pancreatic polypep-tide; T1D = type 1 diabetes.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Insuficiência Pancreática Exócrina / Pâncreas Exócrino / Diabetes Mellitus Tipo 1 Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Endocr Pract Assunto da revista: ENDOCRINOLOGIA Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Insuficiência Pancreática Exócrina / Pâncreas Exócrino / Diabetes Mellitus Tipo 1 Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Endocr Pract Assunto da revista: ENDOCRINOLOGIA Ano de publicação: 2020 Tipo de documento: Article