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- Open Access
Arterial stiffness as a model to dissect chronic inflammation in FMF
© Kukuy et al. 2015
- Published: 28 September 2015
- Chronic Inflammation
- Arterial Stiffness
- Pulse Wave Velocity
- Familial Mediterranean Fever
Familial Mediterranean fever (FMF) is an autoinflammatory disorder, characterized by short attacks of sterile serositis, successfully suppressed by continuous colchicine treatment. Subclinical chronic inflammation however, is a frequent finding in FMF, manifested with elevated levels of inflammatory markers
(CRP, SAA). While chronic inflammation is considered an important cardiovascular (CV) risk factor in most inflammatory disorders, findings on the impact of chronic inflammation in FMF are conflicting. Chronic inflammation is an important cause of arterial stiffness, an early sign and independent risk factor of cardiovascular atherosclerosis. Pulse wave velocity (PWV) measurement is a useful marker of arterial stiffness.
To study arterial stiffness in FMF and evaluate its predisposing factors.
Eighty consecutive FMF patients without known CV risk factors, were enrolled to the study, during their scheduled visit to the clinic. Demographic, genetic, clinical, and laboratory data were obtained from their file and examination. Arterial stiffness was determined through pulse wave velocity (PWV), measured by Sphygmocor system algorithm (AtCor Medical, Sydney, Australia). The recorded PWV values were standardized per age and blood pressure and coded as PWV_Z, relating to the reference general population.
Compared with the adjusted general population, FMF patients displayed normal PWV values, even with a significantly reduced dispersion around the mean (5% vs 10%, p=0.02). In a trial to identify pro- or counteracting driving factors no statistically significant variables were found, yet the dose of the colchicine demonstrated the strongest trend for normalizing PWV.
Arterial stiffness is not increased in FMF. Our data support a role for colchicine prophylaxis in this finding.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.