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Safety of JAK inhibitors: focus on cardiovascular and thromboembolic events
Fabiola Atzeni1, Călin D Popa2, Valeria Nucera1
1Rheumatology Unit, Department of Experimental and Internal Medicine, University of Messina, Messina, Italy.
Insights
Janus kinase inhibitors (JAKis) for rheumatoid arthritis (RA) and psoriatic arthritis (PsA) may impact cardiovascular risk and thromboembolic events. Further research is needed to clarify their role in RA patients
Area of Science:
- Rheumatology and Immunology
- Cardiovascular Medicine
- Pharmacology
Background:
- Four Janus kinase inhibitors (JAKis) are approved for rheumatoid arthritis (RA) and psoriatic arthritis (PsA) treatment.
- While most disease-modifying antirheumatic drugs (DMARDs) may be cardioprotective, the cardiovascular (CV) risk modulation by JAKis is not fully understood.
- RA patients have an inherent increased risk of cardiovascular comorbidities and venous thromboembolism (VTE) due to chronic inflammation.
Purpose of the Study:
- To review the impact of JAKis on cardiovascular risk, atherosclerosis, and major adverse cardiovascular events (MACE).
- To examine the effect of JAKis on thromboembolic risk in patients with RA and PsA.
Main Methods:
- Review of existing literature and clinical data on JAKis, cardiovascular risk, and thromboembolic events.
- Analysis of the relationship between JAK inhibition, inflammation, atherosclerosis, and VTE.
Main Results:
- The precise effect of JAKis on cardiovascular risk and atherosclerosis remains under investigation.
- The role of JAKis in modulating the risk of venous thromboembolism (VTE), including deep vein thrombosis (DVT) and pulmonary embolism (PE), is a significant concern in RA patients.
Conclusions:
- Understanding the cardiovascular and thromboembolic effects of JAKis is crucial for managing RA and PsA patients.
- Further studies are essential to determine whether JAKis control or induce cardiovascular complications and VTE in the context of chronic inflammation.
Introduction:
To date, four Janus kinase inhibitors (JAKis) are licensed for the treatment of rheumatoid arthritis (RA) and/or psoriatic arthritis (PsA) in North America and/or Europe: tofacitinib, baricitinib, upadacitinib, and filgotinib. Most DMARDs have cardioprotective potential, yet for some of them, including JAKi, the modulatory effect on cardiovascular risk remains undetermined. Since their commercialization, the risk of venous thromboembolism (VTE) including deep vein thrombosis (DVT) and pulmonary embolism (PE) is taking on a relevant role in RA patients.
Areas Covered:
In this article, we will review the effect of JAKi on CV risk and atherosclerosis process as major contributor to MACE. Furthermore, we will present the effect of JAKi on thromboembolic risk.
Expert Opinion:
Although the effect of JAKi on CV and thrombosis is one of the most relevant topic regarding RA patients, it is necessary to underline that these patients have an increased risk of these comorbidities due to the inflammation process, and further study are needed in order to understand the real role of JAKi in controlling or inducing these complications.
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