Cited by 10Pancreatic function and diabetesDiabetes and associated disordersTransplantation: Methods and Outcomes

A Golden Hour and Golden Opportunity for β-Cell Preservation

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Evans-Molina, Carmella, Oram, Richard A.·2024·Diabetes

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Crossref · 10.2337/dbi24-0019

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18 of 18 references verified0 citation errors · 0 not checkable

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  • Natural history studies, intervention trials, and transplantation studies consistently show that higher C-peptide responses to a mixed meal are associated with improved glycaemic control, fewer hypoglycaemic episodes, and reduced long-term complications.

    “natural history studies, intervention trials, and transplantation studies consistently show that higher Cpeptide responses to a mixed meal are associated with improved glycaemic control, fewer hypoglycaemic episodes, and reduced longterm complications.[55][56][57]”

    From The future of type 1 diabetes therapy (2025) · cites this paper as [56]

    In the section discussing DCCT/EDIC and the intervention-trial evidence (page not provided), the paper links preserved C-peptide with improved glycaemic control and describes indirect evidence for fewer hypoglycaemic episodes and complications. It says hypoglycaemia was inconsistently measured across trials, so the claim overstates how consistently all three study types show all three outcomes. (LLM, conf=0.85)

    Experimental — accuracy not yet measured

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Authors
Evans-Molina, C., & Oram, R. A.
Affiliations
  • 1Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN
  • National Health Service (GB)
Corresponding author
Oram, Richard A.
Venue
Diabetes
Published
2024-05-20
Volume
73
Issue
6
Pages
834-836
ISSN
0012-1797 (ISSN-L)
OpenAlex
W4398143848
Cited by
10
References
18
Citations by year
2026: 1 · 2025: 9
Type
journal article
Language
en
Open access
Locations
  • Diabetes (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • IUScholarWorks (Indiana University) (submittedVersion)
  • Royal Devon and Exeter Research Repository (Royal Devon and Exeter) (submittedVersion)
Funders
  • Larry M and Leona B Helmsley Charitable Trust
  • Randox Ltd
  • U.S. Department of Veterans Affairs Merit Award (I01BX001733)
  • Ball Brothers Foundation
  • Sigma Beta Sorority
  • National Institute for Health and Care Research (NIHR) Exeter Biomedical Research Centre
  • National Institute of Diabetes and Digestive and Kidney Diseases (R01 DK121843-01, R01DK093954, R01DK127236, R01DK127308, U01DK127382-01, U01DK127786, UC4DK104166)
  • George and Frances Ball Foundation
  • Diabetes UK Harry Keen Fellowship (16/0005529)
  • JDRF (2-SRA-2002-1259-S-B, 2-SRA-2022-1258-M-B, 2-SRA-2022-1261-S-B, 3-SRA-2019-827-S-B, 3-SRA-2022-1241-S-B)
Topics
  • Health Sciences › Medicine › Surgery › Pancreatic function and diabetes
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Diabetes and associated disorders
  • Health Sciences › Medicine › Surgery › Transplantation: Methods and Outcomes
Keywords
beta-cell preservation, beta-cell function, pancreatic islets
MeSH terms
Animals, Diabetes Mellitus, Type 1, Humans, Preservation, Biological, United States Food and Drug Administration, Islets of Langerhans Transplantation, Drug Approval, Insulin-Secreting Cells, Antibodies, Monoclonal, Humanized

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