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Dose-Response Association Between Systemic and Dermatologic Glucocorticoid Use and Type 2 Diabetes Mellitus: A
David Vadsholt1,2, Annika V Kvist1,2, Chano Sandiramoorthy2
1Steno Diabetes Center North Denmark, Aalborg University Hospital, Aalborg, Denmark.
Diabetes, Obesity & Metabolism
|June 16, 2026
Summary
Systemic and dermatologic glucocorticoid use increases Type 2 diabetes risk in a dose-dependent manner. Even low doses (<2.5 mg/day) showed increased odds, highlighting the need for careful prescribing and monitoring of cumulative exposure.
Area of Science:
- Endocrinology
- Pharmacology
- Public Health
Background:
- Glucocorticoids are widely used for their anti-inflammatory properties.
- Potential metabolic side effects, including an increased risk of Type 2 diabetes mellitus (T2DM), warrant investigation.
- Understanding the dose-response relationship is crucial for safe clinical practice.
Purpose of the Study:
- To examine the association between systemic and topical glucocorticoid use and the odds of developing Type 2 diabetes mellitus.
- To investigate the dose-response relationship for different routes of glucocorticoid administration.
Main Methods:
- A nationwide Danish case-control study was conducted using registry data from 2013-2021.
- Incident T2DM cases (n=149,113) aged ≥40 years were matched with controls (n=447,339).
- Glucocorticoid exposure was defined by prescription history, and dose-response was assessed using conditional logistic regression with prednisolone-equivalent doses.
Main Results:
- Higher glucocorticoid exposure and cumulative doses were observed in T2DM cases compared to controls.
- Oral systemic and dermatologic glucocorticoids showed a clear dose-dependent increase in T2DM odds, starting at doses <2.5 mg/day.
- Nasal, rectal, ophthalmic, or otic formulations did not show progressively significant associations with T2DM.
Conclusions:
- Systemic and dermatologic glucocorticoid use is associated with a dose-dependent increase in T2DM risk.
- Even low-dose glucocorticoids (<2.5 mg/day) were linked to elevated T2DM odds.
- Metabolically, other topical routes appear safe; cumulative exposure should guide prescribing and monitoring.
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