Treatment outcomes with oral anti‐hyperglycaemic therapies in people with diabetes secondary to a pancreatic condition (type 3c diabetes): A population‐based cohort study
dc.contributor.author | Hopkins, R | |
dc.contributor.author | Young, KG | |
dc.contributor.author | Thomas, NJ | |
dc.contributor.author | Jones, AG | |
dc.contributor.author | Hattersley, AT | |
dc.contributor.author | Shields, BM | |
dc.contributor.author | Dennis, JM | |
dc.contributor.author | McGovern, AP | |
dc.date.accessioned | 2025-03-25T14:37:36Z | |
dc.date.issued | 2025-01-06 | |
dc.date.updated | 2025-03-25T13:47:18Z | |
dc.description.abstract | Aims: To assess outcomes of oral anti-hyperglycaemic therapies in people with diabetes secondary to a pancreatic condition (type 3c), where specific treatment guidance is limited. Materials and Methods: Using hospital-linked UK primary care records (Clinical Practice Research Datalink; 2004–2020), we identified 7084 people with a pancreatic condition (acute pancreatitis, chronic pancreatitis, pancreatic cancer and haemochromatosis) preceding diabetes diagnosis (type 3c cohort), initiating oral glucose-lowering therapy (metformin, sulphonylureas, SGLT2-inhibitors, DPP4-inhibitors or thiazolidinediones), and without concurrent insulin treatment. We stratified by pancreatic exocrine insufficiency [PEI] (n = 5917 without PEI, 1167 with PEI) and matched to 97 227 type 2 diabetes (T2D) controls. 12-month HbA1c response and weight change and 6-month treatment discontinuation were compared in type 3c versus T2D. Results: People with type 3c diabetes had substantial mean HbA1c reduction with oral therapies in those without PEI (12.2 [95%CI 12.0–12.4] mmol/mol) and with PEI (9.4 [8.9–10.0] mmol/mol). Compared to T2D controls, people with type 3c without PEI had similar mean HbA1c reduction (0.7 [0.4–1.0] mmol/mol difference) and odds of discontinuation (Odds ratio [OR] 1.08 [0.98–1.19]). In contrast, people with type 3c and PEI had lower mean HbA1c response (3.5 [2.9–4.1] mmol/mol lesser reduction) and greater discontinuation (OR 2.03 [1.73–2.36]) versus T2D controls. Weight change in type 3c was similar to T2D. Results were largely consistent across underlying pancreatic conditions and drug classes. Conclusions: Oral anti-hyperglycaemic therapies are effective in people with type 3c diabetes and could provide an important component of glycaemic management. PEI could identify people with type 3c requiring closer monitoring of treatment response. | en_GB |
dc.description.sponsorship | Medical Research Council (MRC) | en_GB |
dc.description.sponsorship | Research England | en_GB |
dc.description.sponsorship | National Institute for Health and Care Research (NIHR) | en_GB |
dc.description.sponsorship | Wellcome Trust | en_GB |
dc.format.extent | 1544-1553 | |
dc.format.medium | Print-Electronic | |
dc.identifier.citation | Vol. 27(3), pp. 1544-1553 | en_GB |
dc.identifier.doi | https://doi.org/10.1111/dom.16163 | |
dc.identifier.grantnumber | MR/N00633X/1 | en_GB |
dc.identifier.grantnumber | 227 070/Z/23/Z | en_GB |
dc.identifier.uri | http://hdl.handle.net/10871/140670 | |
dc.language.iso | en | en_GB |
dc.publisher | Wiley | en_GB |
dc.relation.url | https://www.ncbi.nlm.nih.gov/pubmed/39762966 | en_GB |
dc.rights | © 2025 The Author(s). Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. | en_GB |
dc.subject | antidiabetic drug | en_GB |
dc.subject | effectiveness | en_GB |
dc.subject | glycaemic control | en_GB |
dc.subject | observational study | en_GB |
dc.subject | primary care | en_GB |
dc.subject | real-world evidence | en_GB |
dc.title | Treatment outcomes with oral anti‐hyperglycaemic therapies in people with diabetes secondary to a pancreatic condition (type 3c diabetes): A population‐based cohort study | en_GB |
dc.type | Article | en_GB |
dc.date.available | 2025-03-25T14:37:36Z | |
dc.identifier.issn | 1462-8902 | |
exeter.place-of-publication | England | |
dc.description | This is the final version. Available on open access from Wiley via the DOI in this record | en_GB |
dc.description | Data availability statement: No additional data are available from the authors although CPRD data are available by application to CPRD Independent Scientific Advisory Committee. | en_GB |
dc.identifier.eissn | 1463-1326 | |
dc.identifier.journal | Diabetes, Obesity and Metabolism: A Journal of Pharmacology and Therapeutics | en_GB |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0 | en_GB |
dcterms.dateAccepted | 2024-12-18 | |
dcterms.dateSubmitted | 2024-11-04 | |
rioxxterms.version | VoR | en_GB |
rioxxterms.licenseref.startdate | 2025-01-06 | |
rioxxterms.type | Journal Article/Review | en_GB |
refterms.dateFCD | 2025-03-25T14:33:14Z | |
refterms.versionFCD | VoR | |
refterms.dateFOA | 2025-03-25T14:37:41Z | |
refterms.panel | A | en_GB |
refterms.dateFirstOnline | 2025-01-06 | |
exeter.rights-retention-statement | Yes |
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Except where otherwise noted, this item's licence is described as © 2025 The Author(s). Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.