Longitudinal Assessment of 11C-5-Hydroxytryptophan Uptake in Pancreas After Debut of Type 1 Diabetes

Author:

Espes Daniel12ORCID,Carlsson Per-Ola12ORCID,Selvaraju Ram Kumar3,Rosestedt Maria3,Cheung Pierre3,Ahlström Håkan45,Korsgren Olle6ORCID,Eriksson Olof3ORCID

Affiliation:

1. Department of Medical Cell Biology, Uppsala University, Uppsala, Sweden

2. Department of Medical Sciences, Uppsala University, Uppsala, Sweden

3. Science for Life Laboratory, Department of Medicinal Chemistry, Uppsala University, Uppsala, Sweden

4. Department of Surgical Sciences, Uppsala University, Uppsala, Sweden

5. Antaros Medical AB, Mölndal, Sweden

6. Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden

Abstract

The longitudinal alterations of the pancreatic β-cell and islet mass in the progression of type 1 diabetes (T1D) are still poorly understood. The objective of this study was to repeatedly assess the endocrine volume and the morphology of the pancreas for up to 24 months after T1D diagnosis (n = 16), by 11C-5-hydroxytryptophan (11C-5-HTP) positron emission tomography (PET) and MRI. Study participants were examined four times by PET/MRI: at recruitment and then after 6, 12, and 24 months. Clinical examinations and assessment of β-cell function by a mixed-meal tolerance test and fasting blood samples were performed in connection with the imaging examination. Pancreas volume has a tendency to decrease from 50.2 ± 10.3 mL at T1D debut to 42.2 ± 14.6 mL after 24 months (P < 0.098). Pancreas uptake of 11C-5-HTP (e.g., the volume of the endocrine pancreas) did not decrease from T1D diagnosis (0.23 ± 0.10 % of injected dose) to 24-month follow-up, 0.21 ± 0.14% of injected dose, and exhibited low interindividual changes. Pancreas perfusion was unchanged from diagnosis to 24-month follow-up. The pancreas uptake of 11C-5-HTP correlated with the long-term metabolic control as estimated by HbA1c (P < 0.05). Our findings argue against a major destruction of β-cell or islet mass in the 2-year period after diagnosis of T1D.

Funder

JDRF

European Foundation for the Study of Diabetes

Swedish Research Council

Science for Life Laboratory

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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