Defining outcomes for β-cell replacement therapy in the treatment of diabetes: a consensus report on the Igls criteria from the IPITA/EPITA opinion leaders workshop

  • Michael R. Rickels
  • , Peter G. Stock
  • , Eelco J.P. de Koning
  • , Lorenzo Piemonti
  • , Johann Pratschke
  • , Rodolfo Alejandro
  • , Melena D. Bellin
  • , Thierry Berney
  • , Pratik Choudhary
  • , Paul R. Johnson
  • , Raja Kandaswamy
  • , Thomas W.H. Kay
  • , Bart Keymeulen
  • , Yogish C. Kudva
  • , Esther Latres
  • , Robert M. Langer
  • , Roger Lehmann
  • , Barbara Ludwig
  • , James F. Markmann
  • , Marjana Marinac
  • Jon S. Odorico, François Pattou, Peter A. Senior, James A.M. Shaw, Marie Christine Vantyghem, Steven White

Research output: Contribution to journalReview articlepeer-review

33 Scopus citations

Abstract

β-cell replacement therapy, available currently as pancreas or islet transplantation, has developed without a clear definition of graft functional and clinical outcomes. The International Pancreas & Islet Transplant Association (IPITA) and European Pancreas & Islet Transplantation Association (EPITA) held a workshop to develop consensus for an IPITA/EPITA Statement on the definition of function and failure of current and future forms of β-cell replacement therapy. There was consensus that β-cell replacement therapy could be considered as a treatment for β-cell failure, regardless of etiology and without requiring undetectable C-peptide, accompanied by glycemic instability with either problematic hypoglycemia or hyperglycemia. Glycemic control should be assessed at a minimum by glycated hemoglobin (HbA1c) and the occurrence of severe hypoglycemia. Optimal β-cell graft function is defined by near-normal glycemic control [HbA1c ≤ 6.5% (48 mmol/mol)] without severe hypoglycemia or requirement for insulin or other antihyperglycemic therapy, and with an increase over pretransplant measurement of C-peptide. Good β-cell graft function requires HbA1c < 7.0% (53 mmol/mol) without severe hypoglycemia and with a significant (>50%) reduction in insulin requirements and restoration of clinically significant C-peptide production. Marginal β-cell graft function is defined by failure to achieve HbA1c < 7.0% (53 mmol/mol), the occurrence of any severe hypoglycemia, or less than 50% reduction in insulin requirements when there is restoration of clinically significant C-peptide production documented by improvement in hypoglycemia awareness/severity, or glycemic variability/lability. A failed β-cell graft is defined by the absence of any evidence for clinically significant C-peptide production. Optimal and good functional outcomes are considered successful clinical outcomes.

Original languageEnglish (US)
Pages (from-to)343-352
Number of pages10
JournalTransplant International
Volume31
Issue number4
DOIs
StatePublished - Apr 2018

Keywords

  • Outcome
  • islet clinical
  • pancreas clinical

ASJC Scopus subject areas

  • Transplantation

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