Risk factors for severe cranial ischaemic events in patients with giant cell arteritis
Chagai Grossman1, Iris Barshack2, Nira Koren-Morag3
1Department of Internal Medicine F and Rheumatology Unit, The Chaim Sheba Medical Center, Tel-Hashomer, affiliated to Sackler Faculty of Medicine, Tel-Aviv University, Israel. chagaigr@gmail.com.
Insights
Giant cell arteritis (GCA) patients with severe cranial ischaemic events showed lower inflammation and higher beta-blocker use. Cardiovascular risk factors and antiplatelet therapy did not influence event occurrence in GCA.
Area of Science:
- Rheumatology
- Neurology
- Vascular Medicine
Background:
- Giant cell arteritis (GCA) is an inflammatory vasculitis.
- Cranial ischaemic events are a serious complication of GCA.
- Identifying risk factors for these events is crucial for patient management.
Purpose of the Study:
- To investigate associations between cardiovascular risk factors, medications, and clinical features with severe cranial ischaemic events in GCA patients.
- To identify predictors of severe cranial ischaemic complications in GCA.
Main Methods:
- Retrospective analysis of 83 GCA patients.
- Collected data included baseline clinical features, laboratory results, comorbidities, cardiovascular risk factors, and medications.
- Comparison between GCA patients with and without severe cranial ischaemic complications.
Main Results:
- 29% of GCA patients developed severe cranial ischaemic events.
- Patients with events had lower erythrocyte sedimentation rate (ESR) at diagnosis and higher prevalence of jaw claudication.
- Lower ESR and use of beta-blockers were identified as predictors of severe cranial ischaemic events.
Conclusions:
- GCA patients experiencing severe cranial ischaemic events exhibit reduced inflammatory markers and increased beta-blocker usage.
- Cardiovascular risk factors and antiplatelet therapy did not demonstrate a significant impact on the occurrence of severe cranial ischaemic events in this cohort.
- Lower ESR and beta-blocker use are associated with an increased risk of severe cranial ischaemic complications in GCA.
Objectives:
Cranial ischaemic events constitute a significant component in the clinical spectrum of giant cell arteritis (GCA). Our aim was to investigate whether cardiovascular risk factors, specific medications and baseline clinical features are associated with the development of severe cranial ischaemic events in GCA patients.
Methods:
Retrospective analysis of GCA patients. Information collected included baseline clinical and laboratory data, comorbidities, cardiovascular risk factors and medications. GCA Patients with and without severe cranial ischaemic complications were compared.
Results:
A total of 83 patients with GCA were included in the study. Among them, 24 (29%) patients developed severe cranial ischaemic events. Compared with patients without severe cranial ischaemic events, those with severe cranial ischaemic events had lower erythrocyte sedimentation rate (ESR) levels at diagnosis (81±17 vs. 93±21, p=0.018) and were more likely to have jaw claudication (37.5% vs. 17%, p=0.043). Rate of cardiovascular risk factors and rate of use of anti-platelets and statins were similar between the two groups. The use of β-blockers was higher among patients with severe ischaemic events (46% vs. 20%, p=0.019). Logistic regression analysis showed that lower ESR levels (OR=0.967, 95% CI, 0.94, 0.99) and β-blockers use (OR=4.35, 95% CI, 1.33, 14.2) predicted development of severe cranial ischaemic complications.
Conclusions:
The present study demonstrated that GCA patients with severe cranial ischaemic events had lower inflammatory responses and were more likely to have been treated with β-blockers. Cardiovascular risk factors and antiplatelet therapy had no effect on the occurrence of severe cranial ischaemic events.
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