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Adverse events during longterm low-dose glucocorticoid treatment of polymyalgia rheumatica: a retrospective study
Maurizio Mazzantini1, Claudia Torre, Mario Miccoli
1Rheumatology Unit, Department of Internal Medicine, University of Pisa, Pisa, Italy. mmazzant@int.med.unipi.it
Objective:
To assess the occurrence of adverse events in a cohort of patients with polymyalgia rheumatica (PMR), treated with low-dose glucocorticoids (GC).
Methods:
This was a retrospective study by review of medical records.
Results:
We identified 222 patients who had a mean duration of followup of 60 ± 22 months and a mean duration of GC therapy of 46 ± 22 months. We found that 95 patients (43%) had at least 1 adverse event after a mean duration of GC therapy of 31 ± 22 months and a mean cumulative dose of 3.4 ± 2.4 g. In particular, 55 developed osteoporosis, 31 had fragility fractures; 27 developed arterial hypertension; 11 diabetes mellitus; 9 acute myocardial infarction; 3 stroke; and 2 peripheral arterial disease. Univariate analysis showed that the duration of GC treatment was significantly associated with osteoporosis (p < 0.0001), fragility fractures (p < 0.0001), arterial hypertension (p < 0.005), and acute myocardial infarction (p < 0.05). Cumulative GC dose was significantly associated with osteoporosis (p < 0.0001), fragility fractures (p < 0.0001), and arterial hypertension (p < 0.01). The adverse events occurred more frequently after 2 years of treatment. Multivariate analysis showed that GC duration was significantly associated with osteoporosis (adjusted OR 1.02, 95% CI 1.02-1.05) and arterial hypertension (adjusted OR 1.03, 95% CI 1.01-1.06); GC cumulative dose was significantly associated with fragility fractures (adjusted OR 1.4, 95% CI 1.03-1.8).
Conclusion:
Longterm, low-dose GC treatment of PMR is associated with serious adverse events such as osteoporosis, fractures, and arterial hypertension; these adverse events occur mostly after 2 years of treatment.
Insights
Low-dose glucocorticoids (GC) for polymyalgia rheumatica (PMR) can lead to serious adverse events like osteoporosis and fractures, particularly after two years of treatment. Careful monitoring is essential for patients on long-term GC therapy.
Area of Science:
- Rheumatology
- Endocrinology
- Pharmacology
Background:
- Polymyalgia rheumatica (PMR) is often treated with low-dose glucocorticoids (GC).
- Long-term GC use is associated with potential adverse events.
- Assessing these risks in PMR patients is crucial for patient safety.
Purpose of the Study:
- To evaluate the incidence and types of adverse events in patients with PMR receiving low-dose GC therapy.
- To identify risk factors associated with these adverse events.
Main Methods:
- Retrospective study involving the review of medical records of 222 PMR patients.
- Analysis of patient data including duration of follow-up, GC therapy duration, and cumulative GC dose.
- Statistical analysis (univariate and multivariate) to determine associations between GC treatment and adverse events.
Main Results:
- 43% of patients experienced at least one adverse event.
- Common adverse events included osteoporosis (55 patients), fragility fractures (31), and arterial hypertension (27).
- Longer GC treatment duration and higher cumulative doses were significantly associated with increased risk of osteoporosis, fractures, and hypertension, especially after two years.
Conclusions:
- Long-term, low-dose GC treatment for PMR is linked to significant adverse events, including osteoporosis, fractures, and hypertension.
- These adverse events predominantly manifest after two years of treatment.
- Clinical vigilance and monitoring are recommended for PMR patients on extended GC therapy.
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