β-cell Mass in Nondiabetic Autoantibody-Positive Subjects: An Analysis Based on the Network for Pancreatic Organ Donors Database

التفاصيل البيبلوغرافية
العنوان: β-cell Mass in Nondiabetic Autoantibody-Positive Subjects: An Analysis Based on the Network for Pancreatic Organ Donors Database
المؤلفون: Etienne Larger, Roberto Mallone, Marc Diedisheim, Christian Boitard
المصدر: The Journal of clinical endocrinology and metabolism. 101(4)
سنة النشر: 2016
مصطلحات موضوعية: 0301 basic medicine, Adult, Male, medicine.medical_specialty, Adolescent, Databases, Factual, Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, 030209 endocrinology & metabolism, Context (language use), Biochemistry, 03 medical and health sciences, Young Adult, 0302 clinical medicine, Endocrinology, Diabetes mellitus, Internal medicine, Insulin-Secreting Cells, medicine, Pancreatic mass, Humans, Organ donation, Child, Autoantibodies, Type 1 diabetes, business.industry, Biochemistry (medical), Autoantibody, Case-control study, Middle Aged, medicine.disease, Tissue Donors, 030104 developmental biology, medicine.anatomical_structure, Diabetes Mellitus, Type 1, Case-Control Studies, Child, Preschool, Female, Pancreas, business
الوصف: Context: Little information is available about β-cell mass in antibody-positive (Ab+) nondiabetic subjects. Objective: We have investigated whether the publicly available virtual slides of the Network for Pancreatic Organ Donors with Diabetes (nPOD) project can be used to assess β-cell mass and distribution in nondiabetic antibody-negative (Ab−) and antibody-positive (Ab+) subjects and in patients with recent-onset type 1 diabetes (T1D). Subjects and Methods: We developed a semi-automated quantification method and applied it to 415 insulin-stained slides from 69 Ab− subjects, 101 slides from 18 Ab+ subjects, and 46 slides from eight recent-onset ( Results: In Ab− subjects, the β-cell and endocrine mass were 0.66 ± 0.42 and 1.0 ± 0.65 g, respectively. Nonexocrine tissue represented 29% of pancreatic area, a proportion that increased with age. Proportional β-cell area relative to total pancreatic area was higher in the tail compared with head (0.83 vs 0.71%; P < .001). In Ab+ subjects, β-cell mass and β-cell area were similar to those of Ab− individuals, whereas these parameters were dramatically decreased in recent-onset T1D patients. Conclusion: The virtual slides of the nPOD project can be used for quantification projects. In Ab+ nondiabetic subjects, the β-cell mass was not decreased. However, as this cohort is largely composed of donors from the general population, with a single autoantibody, future studies with a larger number of donors with multiple autoantibodies and predisposing human leucocyte antigen genes are required to better define the dynamics of β-cell destruction in the preclinical phases of T1D.
تدمد: 1945-7197
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76ad0a3ef5bb445cac7a94c031998110Test
https://pubmed.ncbi.nlm.nih.gov/26829442Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....76ad0a3ef5bb445cac7a94c031998110
قاعدة البيانات: OpenAIRE