Key result
In patients with polymyalgia rheumatica and giant cell arteritis, 40 weeks of glucocorticoid treatment was associated with a significant decrease in aortic pulse wave velocity (p<0.001), alongside decreased bone mineral content and increased fat mass.
Why the study?
Identifying comorbidities in PMR/GCA is crucial for patient outcomes, prompting evaluation of the impact of the inflammatory process and glucocorticoid treatment on aortic arterial stiffness and body composition.
Does glucocorticoid treatment and inflammation reduction improve arterial stiffness and alter body composition in patients with PMR/GCA?
Cohort (n=77)
No
Does glucocorticoid treatment and inflammation reduction improve arterial stiffness and alter body composition in patients with PMR/GCA?
Absolute Event Rate: 11.4% vs 11.8%
p-value: p=<0.001
In patients with PMR/GCA, treatment with glucocorticoids is associated with a decrease in arterial stiffness but leads to adverse changes in body composition, including decreased bone mineral content and increased fat mass.
Glucocorticoid effects on stiffness and body composition warrant monitoring in PMR/GCA; leaves open whether benefits outweigh long-term risks.
Identifying comorbidities in polymyalgia rheumatica/giant cell arteritis (PMR/GCA) is crucial for patients' outcomes. The present study aimed to evaluate the impact of the inflammatory process and glucocorticoid treatment on aortic arterial stiffness and body composition in PMR/GCA. 77 patients with newly diagnosed PMR/GCA were treated with oral glucocorticoids and followed for 40 weeks. Aortic pulse wave velocity (PWV) was measured at baseline and during the follow-up period and compared to the results of temporal artery biopsy (TAB) and 18F-FDG PET/CT. Body composition was assessed by total body DXA at baseline and the end of the study. Of 77 patients (49 (63.6%) female, mean of age: (71.8 ± 8.0)), 64 (83.1%) had pure PMR, 10 (13.0%) concomitant PMR and GCA, and 3 (3.9%) pure GCA. Compared to baseline values, aortic PWV was initially decreased at week 16 (p = 0.010) and remained lower than baseline at week 28 (p = 0.002) and week 40 (p < 0.001), with no association with results of TAB and 18F-FDG PET/CT. Aortic PWV was significantly associated with age, male gender, left systolic and diastolic blood pressure, right diastolic blood pressure, and CRP. Total bone mineral content (BMC) was decreased in both genders (p < 0.001), while fat mass (FM) was significantly increased (p < 0.001). However, lean body mass did not significantly change during the study. Changes in FM were correlated with cumulative prednisolone dose (rho: 0.26, p = 0.031). Glucocorticoid treatment of patients with PMR/GCA had several prognostic impacts. Arterial stiffness was decreased due either to the treatment or a reduction in the inflammatory load. Additionally, treatment led to changes in body composition, including a decrease in BMC and FM excess.
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Emamifar et al. (2021) conducted a cohort in Polymyalgia rheumatica and giant cell arteritis (n=77). Oral glucocorticoids vs. Baseline (pre-treatment) was evaluated on Aortic pulse wave velocity (PWV) at week 40 (p=<0.001). In patients with polymyalgia rheumatica and giant cell arteritis, 40 weeks of glucocorticoid treatment was associated with a significant decrease in aortic pulse wave velocity (p<0.001), alongside decreased bone mineral content and increased fat mass.
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