4.5 Article

Flow Mediated Dilatation and Progression of Abdominal Aortic Aneurysms

Journal

Publisher

W B SAUNDERS CO LTD
DOI: 10.1016/j.ejvs.2017.03.001

Keywords

Abdominal aortic aneurysm; Biomarkers; Flow mediated dilatation; AAA Progression

Funding

  1. Medical Sciences Division, University of Oxford Medical Research Fund
  2. Jackie Walton Vascular Studies Unit, Oxford University Hospitals NHS Foundation Trust
  3. Oxford Regional Vascular Services Unit, Oxford University Hospitals NHS Foundation Trust
  4. Oxford Biomedical Research Centre Research Capacity Fund
  5. Academy of Medical Sciences UK
  6. Academy of Medical Sciences (AMS) [AMS-SGCL13-Lee] Funding Source: researchfish
  7. National Institute for Health Research [NF-SI-0514-10166] Funding Source: researchfish

Ask authors/readers for more resources

Objective/Background: Biomarker(s) for prediction of the future progression rate of abdominal aortic aneurysms (AAA) may be useful to stratify the management of individual patients. AAAs are associated with features of systemic inflammation and endothelial dysfunction. Flow mediated dilatation (FMD) of the brachial artery is a recognised non-invasive measurement for endothelial function. We hypothesised that FMD is a potential biomarker of AAA progression and reflects the temporal changes of endothelial function during AAA progression. Methods: In a prospectively recruited cohort of patients with AAAs (Oxford Abdominal Aortic Aneurysm Study), AAA size was recorded by antero-posterior diameter (APD) (outer to outer) on ultrasound. Annual AAA progression was calculated by (AAPD/APD at baseline)/(number of days lapsed/365 days). FMD was assessed at the same time as AAA size measurement. Analyses of data were performed in the overall cohort, and further in subgroups of AAA by size (small: 30-39 mm; moderate: 40-55 mm; large: > 55 mm). Results: FMD is inversely correlated with the diameter of AAAs in all patients (n = 162, Spearman's r=-.28, p < .001). FMD is inversely correlated with AAA diameter progression in the future 12 months (Spearman's r=-.35, p = .001), particularly in the moderate size group. Furthermore, FMD deteriorates during the course of AAA surveillance (from a median of 2.0% at baseline to 1.2% at follow-up; p = .004), while surgical repair of AAAs (n = 50 [open repair n = 22, endovascular repair n = 28)] leads to an improvement in FMD (from 1.1% pre-operatively to 3.8% post-operatively; p < .001), irrespective of the type of surgery. Conclusion: FMD is inversely correlated with future AAA progression in humans. FMD deteriorates during the natural history of AAA, and is improved by surgery. The utility of FMD as a potential biomarker in the context of AAA warrants further investigation. (C) 2017 The Authors. Published by Elsevier Ltd on behalf of European Society for Vascular Surgery.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available