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Inflammation and Coronary Microvascular Dysfunction in Autoimmune Rheumatic Diseases
Elisabetta Zanatta1, Claudia Colombo2, Gianpiero D'Amico2
1Department of Medicine, Padova University Hospital, 35128 Padua, Italy.
Coronary microvascular dysfunction (CMD) is common in autoimmune rheumatic diseases (ARDs). Inflammation drives CMD in SLE and RA, responding to immunosuppressants, while SSc-CMD involves endothelial dysfunction, benefiting from calcium-channel blockers.
Area of Science:
- Rheumatology
- Cardiology
- Immunology
Background:
- Autoimmune rheumatic diseases (ARDs) encompass conditions like SLE, SSc, RA, IIMs, and vasculitis.
- Coronary microvascular dysfunction (CMD) is prevalent in ARDs, contributing to cardiovascular risks.
- Inflammation is a key factor in ARD pathogenesis, impacting both atherosclerosis and CMD.
Purpose of the Study:
- To review the current evidence on CMD occurrence in ARDs.
- To elucidate the role of inflammation in CMD pathogenesis across different ARDs.
- To explore potential therapeutic strategies for CMD in ARDs.
Main Methods:
- Systematic review of existing literature.
- Analysis of studies focusing on CMD in SLE, SSc, RA, IIMs, and systemic vasculitis.
- Evaluation of the impact of inflammation and therapeutic interventions on CMD.
Main Results:
- Inflammation significantly contributes to CMD in SLE and RA, with immunosuppressants/biologics showing efficacy.
- In SSc, CMD is primarily linked to endothelial dysfunction and microvascular ischemia, with calcium-channel blockers offering benefits.
- Limited data exists on CMD in IIMs and systemic vasculitis, necessitating further research.
Conclusions:
- CMD is a significant concern in ARDs, with varying pathogenic mechanisms.
- Targeting inflammation is crucial for managing CMD in SLE and RA.
- Further investigation is required to understand and manage CMD in IIMs and systemic vasculitis.
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