• Mustafa Bulut, Nursen Keles, Zuhal Caliskan, Osman Kostek, Feyza Aksu, Kamil Ozdil, Mustafa Akcakoyun, Kenan Demircioglu, Yusuf Yilmaz, Mehmet Kanbay, and Mustafa Caliskan.
• Istanbul Kartal KosuyoluYuksek Ihtisas Training and Research Hospital, Department of Cardiology, Istanbul, Turkey.
• Atherosclerosis. 2016 Aug 1; 251: 389-395.

Background And AimsSystemic amyloid A protein (AA) amyloidosis may occur as a complication of many chronic inflammatory disorders. Patients receiving inadequate anti-inflammatory and immunosuppressive therapies have an increased risk of developing systemic AA amyloidosis. Inflammation plays a role in all stages and the thrombotic complications of atherosclerosis. In the absence of epicardial coronary stenosis, coronary flow reserve (CFR) reflects coronary microvascular dysfunction. In the present study, we hypothesized that amyloid advanced subclinical inflammation in chronic inflammatory diseases (CID) patients may further affect coronary microcirculation.MethodsThirty-two patients with biopsy-diagnosed renal AA, 73 patients with non-amyloid CID, and a group of healthy volunteers were included in the study. The measurements of coronary flow velocity were performed by a single investigator with expertise in transthoracic Doppler harmonic echocardiography (TTDE).ResultsThe AA amyloidosis subgroup had significantly lower CFR values than other non-amyloid CID patients and the control individuals (1.8 (1.5-2.1) vs. 2.1 (2.0-2.4) and 3.0 (2.8-3.2), p < 0.001). Multivariate logistic regression analysis indicated that the presence of AA amyloidosis and elevated hs - CRP independently predict impairment of the CFR (p < 0.05).ConclusionsThe presence of AA amyloidosis is related to decreased CFR values and the presence of AA amyloidosis and elevated hs - CRP independently predict impairment of the CFR. Therefore, patients with AA amyloidosis may have an increased risk of developing coronary artery diseases.Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.

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