19
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Predictors of candesartan's effect on vascular reactivity in patients with coronary artery disease

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Summary

          Introduction and Aims

          Endothelial dysfunction and arterial stiffness have a prognostic value on adverse long‐term outcomes in coronary artery disease ( CAD) patients. We evaluated the efficacy on vascular reactivity of candesartan and analyzed predictors to control the candesartan's effect on vascular reactivity in CAD patients.

          Method

          Patients were prospectively enrolled and prescribed candesartan for 6 months. The effect on vascular reactivity was evaluated by the change in flow‐mediated dilation ( FMD) and pulse wave velocity ( PWV).

          Results

          A total of 124 patients completed the study. The better responder in FMD change (≥1.3%) showed significantly lower baseline FMD than the poor responder ( P < .001). In receiver operating characteristic analysis, baseline FMD 7.5% showed optimal predictive value (sensitivity 79%, specificity 79%) for predicting better responder. The baseline endothelial dysfunction ( FMD <7.5%) was the only significant predictor of the better responder to candesartan. The better responder in PWV change (≤−100 cm/s) showed greater blood pressure lowering and significantly higher baseline PWV than the poor responder (both P < .05). The poor responder in both FMD and PWV showed a higher prevalence of previous myocardial infarction (38.7% vs 17.2%, P = .013).

          Conclusion

          The candesartan's effect on vascular reactivity is more pronounced in patients with more severe endothelial dysfunction and arterial stiffness. Poor responders on both FMD and PWV showed higher prevalence of previous myocardial infarction.

          Related collections

          Most cited references22

          • Record: found
          • Abstract: found
          • Article: not found

          Validity, reproducibility, and clinical significance of noninvasive brachial-ankle pulse wave velocity measurement.

          The present study was conducted to evaluate the validity and reproducibility of noninvasive brachial-ankle pulse wave velocity (baPWV) measurements and to examine the alteration of baPWV in patients with coronary artery disease (CAD). Simultaneous recordings of baPWV by a simple, noninvasive method and aortic pulse wave velosity (PWV) using a catheter tip with pressure manometer were performed in 41 patients with CAD, vasospastic angina, or cardiomyopathy. In 32 subjects (15 controls and 17 patients with CAD), baPWV was recorded independently by two observers in a random manner. In 55 subjects (14 controls and 41 patients with CAD), baPWV was recorded twice by a single observer on different days. baPWV were compared among 172 patients with CAD (aged 62 +/- 8 years); 655 age-matched patients without CAD but with hypertension, diabetes mellitus, or dyslipidemia; and 595 age-matched healthy subjects without these risk factors. baPWV correlated well with aortic PWV (r=0.87, p<0.01). Pearson's correlation coefficients of interobserver and intraobserver reproducibility were r=0.98 and r=0.87, respectively. The corresponding coefficients of variation were 8.4% and 10.0%. baPWV were significantly higher in CAD patients than in non-CAD patients with risk factors, for both genders (p<0.01). In addition, baPWV were higher in non-CAD patients with risk factors than in healthy subjects without risk factors. Thus, the validity and reproducibility of baPWV measurements are considerably high, and this method seems to be an acceptable marker reflecting vascular damages. baPWV measured by this simple, noninvasive method is suitable for screening vascular damages in a large population.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Endothelial dysfunction, oxidative stress, and risk of cardiovascular events in patients with coronary artery disease.

            Endothelial function is impaired in coronary artery disease and may contribute to its clinical manifestations. Increased oxidative stress has been linked to impaired endothelial function in atherosclerosis and may play a role in the pathogenesis of cardiovascular events. This study was designed to determine whether endothelial dysfunction and vascular oxidative stress have prognostic impact on cardiovascular event rates in patients with coronary artery disease. Endothelium-dependent and -independent vasodilation was determined in 281 patients with documented coronary artery disease by measuring forearm blood flow responses to acetylcholine and sodium nitroprusside using venous occlusion plethysmography. The effect of the coadministration of vitamin C (24 mg/min) was assessed in a subgroup of 179 patients. Cardiovascular events, including death from cardiovascular causes, myocardial infarction, ischemic stroke, coronary angioplasty, and coronary or peripheral bypass operation, were studied during a mean follow-up period of 4.5 years. Patients experiencing cardiovascular events (n=91) had lower vasodilator responses to acetylcholine (P<0.001) and sodium nitroprusside (P<0.05), but greater benefit from vitamin C (P<0.01). The Cox proportional regression analysis for conventional risk factors demonstrated that blunted acetylcholine-induced vasodilation (P=0.001), the effect of vitamin C (P=0.001), and age (P=0.016) remained independent predictors of cardiovascular events. Endothelial dysfunction and increased vascular oxidative stress predict the risk of cardiovascular events in patients with coronary artery disease. These data support the concept that oxidative stress may contribute not only to endothelial dysfunction but also to coronary artery disease activity.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Long-term follow-up of patients with mild coronary artery disease and endothelial dysfunction.

              Coronary endothelial dysfunction is characterized by vasoconstrictive response to the endothelium-dependent vasodilator acetylcholine. Although endothelial dysfunction is considered an early phase of coronary atherosclerosis, there is a paucity of information regarding the outcome of these patients. Thus, this study was designed to evaluate the outcome of patients with mild coronary artery disease on the basis of their endothelial function. Follow-up was obtained in 157 patients with mildly diseased coronary arteries who had undergone coronary vascular reactivity evaluation by graded administration of intracoronary acetylcholine, adenosine, and nitroglycerin and intracoronary ultrasound at the time of diagnostic study. Patients were divided on the basis of their response to acetylcholine into 3 groups: group 1 (n=83), patients with normal endothelial function; group 2 (n=32), patients with mild endothelial dysfunction; and group 3 (n=42), patients with severe endothelial dysfunction. Over an average 28-month follow-up (range, 11 to 52 months), none of the patients from group 1 or 2 had cardiac events. However, 6 (14%) with severe endothelial dysfunction had 10 cardiac events (P<0.05 versus groups 1 and 2). Cardiac events included myocardial infarction, percutaneous or surgical coronary revascularization, and/or cardiac death. Severe endothelial dysfunction in the absence of obstructive coronary artery disease is associated with increased cardiac events. This study supports the concept that coronary endothelial dysfunction may play a role in the progression of coronary atherosclerosis.
                Bookmark

                Author and article information

                Contributors
                shkimmd@snu.ac.kr
                usahyosoo@gmail.com , hyosoo@snu.ac.kr
                Journal
                Cardiovasc Ther
                Cardiovasc Ther
                10.1111/(ISSN)1755-5922
                CDR
                Cardiovascular Therapeutics
                John Wiley and Sons Inc. (Hoboken )
                1755-5914
                1755-5922
                14 September 2017
                October 2017
                : 35
                : 5 ( doiID: 10.1111/cdr.2017.35.issue-5 )
                : e12291
                Affiliations
                [ 1 ] Division of Cardiology Department of Internal Medicine/Cardiovascular Center Seoul National University Hospital Seoul Korea
                [ 2 ] Department of Cardiology Cardiovascular Center Seoul National University Bundang Hospital Seongnam Korea
                [ 3 ] Division of Cardiology Department of Internal Medicine Seoul National University Boramae Medical Center Seoul Korea
                Author notes
                [*] [* ] Correspondence

                H.‐S. Kim, M.D., Ph.D., Department of Internal Medicine and Cardiovascular Center, Seoul National University Hospital, Seoul, Korea.

                Emails: usahyosoo@ 123456gmail.com , hyosoo@ 123456snu.ac.kr

                and

                S.‐H. Kim, M.D., Ph.D., Division of Cardiology, Department of Internal Medicine, Seoul Boramae Medical Center, Seoul, Korea.

                Email: shkimmd@ 123456snu.ac.kr

                Author information
                http://orcid.org/0000-0003-0847-5329
                Article
                CDR12291
                10.1111/1755-5922.12291
                5639377
                28796934
                134649cf-6a37-4103-8763-77c09f8461d0
                © 2017 The Authors. Cardiovascular Therapeutics Published by John Wiley & Sons Ltd

                This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

                History
                : 01 September 2016
                : 23 June 2017
                : 06 August 2017
                Page count
                Figures: 3, Tables: 3, Pages: 10, Words: 6537
                Funding
                Funded by: Korea Health Technology R&D Project
                Funded by: Ministry of Health & Welfare, Republic of Korea
                Award ID: HI14C1277
                Categories
                Original Research Article
                Original Research Articles
                Custom metadata
                2.0
                cdr12291
                October 2017
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.2.1 mode:remove_FC converted:13.10.2017

                Cardiovascular Medicine
                angiotensin ii type 1 receptor blockers,arterial stiffness,endothelial dysfunction,flow‐mediated dilation,pulse wave velocity

                Comments

                Comment on this article