Donor insulin use predicts beta-cell function after islet transplantation

Diabetes Obes Metab. 2020 Oct;22(10):1874-1879. doi: 10.1111/dom.14088. Epub 2020 Jun 14.

Abstract

Insulin is routinely used to manage hyperglycaemia in organ donors and during the peri-transplant period in islet transplant recipients. However, it is unknown whether donor insulin use (DIU) predicts beta-cell dysfunction after islet transplantation. We reviewed data from the UK Transplant Registry and the UK Islet Transplant Consortium; all first-time transplants during 2008-2016 were included. Linear regression models determined associations between DIU, median and coefficient of variation (CV) peri-transplant glucose levels and 3-month islet graft function. In 91 islet cell transplant recipients, DIU was associated with lower islet function assessed by BETA-2 scores (β [SE] -3.5 [1.5], P = .02), higher 3-month post-transplant HbA1c levels (5.4 [2.6] mmol/mol, P = .04) and lower fasting C-peptide levels (-107.9 [46.1] pmol/l, P = .02). Glucose at 10 512 time points was recorded during the first 5 days peri-transplant: the median (IQR) daily glucose level was 7.9 (7.0-8.9) mmol/L and glucose CV was 28% (21%-35%). Neither median glucose levels nor glucose CV predicted outcomes post-transplantation. Data on DIU predicts beta-cell dysfunction 3 months after islet transplantation and could help improve donor selection and transplant outcomes.

Keywords: insulin; islet; organ donor; pancreas; transplant.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blood Glucose
  • C-Peptide
  • Diabetes Mellitus, Type 1*
  • Glucose
  • Humans
  • Insulin
  • Insulin-Secreting Cells*
  • Islets of Langerhans Transplantation*
  • Tissue Donors

Substances

  • Blood Glucose
  • C-Peptide
  • Insulin
  • Glucose