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Preventing and managing cardiovascular events in patients with inflammatory bowel diseases treated with
Pablo A Olivera1, Axel Dignass2, Marla C Dubinsky3
1IBD Unit, Gastroenterology Section, Department of Internal Medicine, Centro de Educación Médica e Investigación Clínica (CEMIC), Buenos Aires, Argentina; Zane Cohen Centre for Digestive Diseases, Lunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, Ontario, Canada.
Insights
Small molecule drugs (SMDs) like JAK inhibitors and S1P receptor modulators are used for inflammatory bowel disease (IBD). While generally safe, cardiovascular risk assessment is crucial before starting these IBD treatments.
Area of Science:
- Gastroenterology
- Cardiology
- Pharmacology
Background:
- Small molecule drugs (SMDs), including Janus kinase (JAK) inhibitors and sphingosine 1 phosphate (S1P) receptor modulators, are approved for inflammatory bowel disease (IBD) treatment.
- Clinical use of these SMDs may be constrained by potential cardiovascular concerns.
- Guidance is needed for risk assessment, monitoring, and management to mitigate cardiovascular risks associated with SMDs in IBD patients.
Purpose of the Study:
- To provide expert consensus guidance on managing cardiovascular risks in IBD patients treated with SMDs.
- To facilitate informed shared decision-making regarding the use of JAK inhibitors and S1P receptor modulators.
Main Methods:
- A systematic literature search was performed to gather relevant evidence.
- Proposed consensus statements were developed and reviewed.
- An international virtual consensus meeting involving IBD physicians and cardiovascular specialists was conducted.
- Anonymous voting determined agreement on consensus statements, with 75% consensus required.
Main Results:
- Consensus was achieved on eighteen statements regarding cardiovascular risk management for IBD patients on SMDs.
- Evidence suggests JAK inhibitors do not increase overall cardiovascular event risk in IBD, but risk may rise in patients with pre-existing cardiovascular risk factors.
- S1P receptor modulators may be linked to bradycardia, atrioventricular blocks, and hypertension.
Conclusions:
- Cardiovascular risk stratification is recommended prior to initiating JAK inhibitors or S1P receptor modulators for IBD.
- While overall cardiovascular risk appears low, specific patient profiles and drug types necessitate careful consideration and monitoring.
- Implementing these guidelines can help minimize cardiovascular risks and support optimal patient care in IBD management.
Abstract:
Janus kinase (JAK) inhibitors and sphingosine 1 phosphate (S1P) receptor modulators are small molecule drugs (SMDs) approved for IBD treatment. Their use in clinical practice might be limited due to cardiovascular concerns. We aimed to provide guidance on risk assessment, monitoring, and management strategies, aiming to minimize potential cardiovascular risks of SMDs and to facilitate an adequate shared decision-making. A systematic literature search was conducted, and proposed statements were prepared. A virtual consensus meeting was held, in which eleven IBD physicians and two cardiovascular specialists from ten countries attended. Proposed statements were voted upon in an anonymous manner. Agreement was defined as at least 75 % of participants voting as 'agree' with each statement. Consensus was reached for eighteen statements. Available evidence does not show a higher risk of cardiovascular events with JAK inhibitors in the overall IBD population, although it might be increased in patients with an unfavorable cardiovascular profile. S1P receptor modulators may be associated with a risk of bradycardia, atrioventricular blocks, and hypertension. Cardiovascular risk stratification should be done before initiation of SMDs. Although the risk of cardiovascular events in patients with IBD on SMDs appears to be low overall, caution should still be taken in certain scenarios.
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