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Biomarkers for diagnosis and prognostic stratification of aortic dissection: challenges and perspectives
Fulvio Morello1, Pavel Piler, Miroslav Novak
1Emergency Department, A.O. Città della Salute e della Scienza, Molinette Hospital, Turin, Italy.
Insights
Circulating biomarkers show promise for diagnosing aortic dissection (AD), a serious vascular condition. These markers could aid in screening, risk identification, and prognosis, potentially improving patient outcomes.
Area of Science:
- Cardiovascular Medicine
- Biomarker Discovery
- Vascular Surgery
Background:
- Aortic dissection (AD) is a life-threatening vascular emergency.
- Current AD diagnosis relies heavily on clinical judgment and urgent imaging.
- There is a need for improved diagnostic and prognostic tools for AD.
Purpose of the Study:
- To review current data on circulating biomarkers for aortic dissection.
- To discuss the potential of these biomarkers in AD diagnosis and risk stratification.
- To explore future perspectives for biomarker-based AD management.
Main Methods:
- Literature review of studies identifying potential AD biomarkers.
- Analysis of biomarkers from extracellular matrix, vascular smooth muscle cells, coagulation, and inflammation.
- Discussion of biomarker utility in screening, diagnosis, and prognosis.
Main Results:
- Several potential biomarkers have been identified in patients with AD.
- These include markers related to extracellular matrix, smooth muscle cells, coagulation, and inflammation.
- Elevated circulating levels of these biomarkers are observed in AD patients.
Conclusions:
- Circulating biomarkers hold significant potential for AD diagnosis and prognostic stratification.
- Biomarkers could aid in screening, ruling out AD, and identifying high-risk patients.
- Further research is needed to validate and implement these biomarkers in clinical practice.
Abstract:
Aortic dissection (AD) is a severe vascular disease associated with major morbidity and mortality. The diagnosis of AD requires the performance of urgent aortic imaging exams such as computed tomography angiography, but the decision to perform these exams now essentially relies on clinical judgment. Several studies have identified a range of potential biomarkers stemming from the aortic extracellular matrix (matrix metalloproteinases, TGF-β, soluble elastin fragments), vascular smooth muscle cells (smooth muscle myosin heavy chain, creatine kinase, calponin), coagulation (D-dimer, platelets) and inflammation (C-reactive protein), whose circulating levels increase in patients affected by AD. Biomarkers of AD could be potentially used to screen patients with compatible symptoms, to identify patients at higher risk of AD, to rule out AD in patients with non-high clinical probability of AD and/or to obtain prognostic stratification of affected patients. This review will summarize available data and discuss present and future perspectives of circulating biomarkers for the diagnosis and prognostic stratification of AD.
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