S100A1 as a potential biomarker for the diagnosis of patients with acute aortic dissection
- PMID: 33823637
- PMCID: PMC8033472
- DOI: 10.1177/03000605211004512
S100A1 as a potential biomarker for the diagnosis of patients with acute aortic dissection
Abstract
Objective: Acute aortic dissection (AAD) is a common life-threatening cardiovascular disease. This retrospective study was conducted to analyze the plasma concentration of S100A1 and its diagnostic value for AAD through receiver operating characteristic (ROC) curve and logistic regression analyses.
Methods: Seventy-eight patients with AAD and 77 healthy controls were included, and the relevant clinical data for each group were collected. According to the Stanford classification, the AAD patients were divided into types A and B. The plasma levels of S100A1, D-dimer, hypersensitive C-reactive protein, and cardiac troponin T were detected by enzyme-linked immunosorbent assays.
Results: The S100A1 concentrations in the healthy control, Stanford A, and Stanford B groups were 0.7 ± 0.6, 4.9 ± 2.6, and 3.5 ± 2.2 ng/mL, respectively. The concentration of S100A1 was increased in patients with AAD complicated with aortic regurgitation, pericardial effusion, or in-hospital death. ROC curve analysis showed that the area under the curve was 0.89. Logistic regression analysis revealed that the S100A1 level was an important risk factor for the development of AAD.
Conclusion: Plasma S100A1 is significantly elevated in patients with AAD, and its concentration has potential clinical value for diagnosing AAD.
Keywords: Aortic disease; S100 protein; biological marker; calcium-binding protein; cardiovascular disease; diagnosis.
Conflict of interest statement
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References
-
- Gawinecka J, Schönrath F, Von Eckardstein A. Acute aortic dissection: pathogenesis, risk factors and diagnosis. Swiss Med Wkly 2017; 147: w14489. - PubMed
-
- Hagan PG, Nienaber CA, Isselbacher EM, et al.. The International Registry of Acute Aortic Dissection (IRAD): new insights into an old disease. JAMA 2000; 283: 897–903. - PubMed
-
- Clough RE, Nienaber CA. Management of acute aortic syndrome. Nat Rev Cardiol 2015; 12: 103–114. - PubMed
-
- Carroll BJ, Schermerhorn ML, Manning WJ. Imaging for acute aortic syndromes. Heart 2020; 106: 182–189. - PubMed
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