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Published on: August 9, 2024
Coronary artery disease in heart transplantation: new concepts for an old disease
Mandy Langstraat1, Kyra J S Musters1, Olivier Manintveld2
1School of Medicine, Erasmus MC, Rotterdam, The Netherlands.
Insights
Cardiac allograft vasculopathy (CAV) is a major long-term risk after heart transplants. Recent evidence highlights varying pathology and emphasizes prevention through risk factor control and targeted immunosuppression over treatment.
Area of Science:
- Cardiology
- Transplantation Immunology
- Medical Research
Background:
- Cardiac allograft vasculopathy (CAV) is a primary long-term complication following heart transplantation.
- Understanding evolving risk factors, pathology, and therapeutic strategies for CAV is crucial for improving patient outcomes.
Purpose of the Study:
- To systematically review recent (6-year) literature on cardiac allograft vasculopathy (CAV).
- To reappraise novel evidence regarding risk factors, pathology, prevention, and treatment of CAV.
Main Methods:
- Conducted a systematic literature search on PubMed using a defined search string.
- Included 98 studies focusing on CAV risk factors, pathology, prevention, and treatment.
- Excluded studies focused solely on diagnosis, biomarkers, imaging, or other disease complications.
Main Results:
- Identified 48 articles on CAV risk factors, 13 on pathology, 24 on prevention, and 13 on treatment.
- Found evidence that CAV pathophysiology may differ based on time post-transplant and the balance of metabolic versus immune factors.
- Selective revascularization of focal lesions showed some clinical benefit.
Conclusions:
- CAV prevention, by managing risk factors and employing targeted immunosuppression, is the most evidence-based strategy.
- This approach is superior to treatment for reducing disease progression.
- Pathophysiological understanding of CAV continues to evolve, influenced by transplant duration and risk factor profiles.
Abstract:
Cardiac allograft vasculopathy (CAV) remains one of the main long-term complications after heart transplantation. We performed a systematic review focused on articles published in the previous 6 years to reappraise the novel evidences supporting risk factors, pathology, prevention, and treatment of CAV. We identified a search string for a literature search on PubMed. We excluded articles specifically focused on diagnosis/biomarkers/imaging only or complications of other diseases. We included 98 studies out of our search. Forty-eight articles describe risk factors for CAV, 13 pathology, 24 prevention, and 13 treatment for CAV. While confirming known concepts, we found supportive evidence that CAV pathophysiology may vary according to the time post-transplant and the prevalence of metabolic versus immune-mediated risk factors. Selective revascularization of focal lesions in patients with CAV may result in some clinical benefit, but CAV prevention, rather than treatment, by controlling risk factors and by using targeted immunosuppressive therapies is the most evidence-based approach to reduce disease progression.
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