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Increased aortic tortuosity indicates a more severe aortic phenotype in adults with Marfan syndrome.
- Source :
-
International journal of cardiology [Int J Cardiol] 2015 Sep 01; Vol. 194, pp. 7-12. Date of Electronic Publication: 2015 May 15. - Publication Year :
- 2015
-
Abstract
- Background: Patients with Marfan syndrome (MFS) have a highly variable occurrence of aortic complications. Aortic tortuosity is often present in MFS and may help to identify patients at risk for aortic complications.<br />Methods: 3D-visualization of the total aorta by MR imaging was performed in 211 adult MFS patients (28% with prior aortic root replacement) and 20 controls. A method to assess aortic tortuosity (aortic tortuosity index: ATI) was developed and reproducibility was tested. The relation between ATI and age, and body size and aortic dimensions at baseline was investigated. Relations between ATI at baseline and the occurrence of a clinical endpoint (aortic dissection, and/or aortic surgery) and aortic dilatation rate during 3 years of follow-up were investigated.<br />Results: ATI intra- and interobserver agreements were excellent (ICC: 0.968 and 0.955, respectively). Mean ATI was higher in 28 age-matched MFS patients than in the controls (1.92 ± 0.2 vs. 1.82 ± 0.1, p=0.048). In the total MFS cohort, mean ATI was 1.87 ± 0.20, and correlated with age (r=0.281, p<0.001), aortic root diameter (r=0.223, p=0.006), and aortic volume expansion rate (r=0.177, p=0.026). After 49.3 ± 8.8 months follow-up, 33 patients met the combined clinical endpoint (7 dissections) with a significantly higher ATI at baseline than patients without endpoint (1.98 ± 0.2 vs. 1.86 ± 0.2, p=0.002). Patients with an ATI>1.95 had a 12.8 times higher probability of meeting the combined endpoint (log rank-test, p<0.001) and a 12.1 times higher probability of developing an aortic dissection (log rank-test, p=0.003) compared to patients with an ATI<1.95.<br />Conclusions: Increased ATI is associated with a more severe aortic phenotype in MFS patients.<br /> (Copyright © 2015 Elsevier Ireland Ltd. All rights reserved.)
- Subjects :
- Adult
Aortic Dissection pathology
Angiotensin II Type 1 Receptor Blockers administration & dosage
Angiotensin II Type 1 Receptor Blockers adverse effects
Aorta drug effects
Aorta pathology
Aortic Diseases drug therapy
Dilatation, Pathologic drug therapy
Dilatation, Pathologic pathology
Female
Fibrillins
Follow-Up Studies
Humans
Losartan administration & dosage
Losartan adverse effects
Magnetic Resonance Imaging
Male
Marfan Syndrome drug therapy
Marfan Syndrome genetics
Microfilament Proteins metabolism
Middle Aged
Mutation
Phenotype
Reproducibility of Results
Aortic Diseases pathology
Marfan Syndrome pathology
Subjects
Details
- Language :
- English
- ISSN :
- 1874-1754
- Volume :
- 194
- Database :
- MEDLINE
- Journal :
- International journal of cardiology
- Publication Type :
- Academic Journal
- Accession number :
- 26005802
- Full Text :
- https://doi.org/10.1016/j.ijcard.2015.05.072