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©2014 Baishideng Publishing Group Inc.
World J Cardiol. Aug 26, 2014; 6(8): 824-835
Published online Aug 26, 2014. doi: 10.4330/wjc.v6.i8.824
Published online Aug 26, 2014. doi: 10.4330/wjc.v6.i8.824
Ref. | Number of patients | Cohort | Asymptomatic Patients? | Length of follow-up (mo) | Outcome | Result | Independent value of FMD? |
Rossi et al[45] | 2264 | Post-menopausal women | Yes | 45 ± 13 | CV death, MI, revascularisation, TIA, stroke | FMD was a predictor of MACE independently of traditional cardiac risk factors. | Yes |
Patti et al[56] | 136 | Patients with single-vessel coronary artery disease undergoing PCI | No | 6 | In-stent restenosis | Patients with impaired FMD were more likely to suffer in-stent restenosis. | Yes |
Gokce et al[59] | 187 | Patients undergoing vascular surgery | No | 1 | CV death, MI, unstable angina, ventricular fibrillation, stroke, raised troponin | FMD was an independent predictor of MACE in the immediate post-operative period. | Yes |
Brevetti et al[58] | 139 | Patients with peripheral arterial disease | No | 23 ± 10 | CV death, MI, revascularisation, TIA, critical limb ischaemia | FMD was an independent predictor of events over the follow-up period. | Yes |
Chan et al[53] | 152 | Patients with coronary artery disease | No | 34 ± 10 | CV death, MI, revascularisation, claudication | FMD was a strong independent predictor of risk even accounting for carotid plaque burden. | Yes |
Shimbo et al[47] | 842 | Asymptomatic multi-ethnic cohort | Yes | 36 | Vascular death, MI, stroke | FMD was able to predict adverse events but not independently. | No |
Suzuki et al[43] | 819 | Asymptomatic multi-ethnic cohort including patients with metabolic syndrome | Yes | 81 ± 21 | Vascular death, MI, stroke | Patients with the combination of metabolic syndrome and endothelial dysfunction had a significantly worse outcome. | No |
Yeboah et al[44] | 2792 | Mixed cohort of patients > 65 yr | No | 60 | CVD death, MI, stroke, congestive heart failure, claudication, revascularisation | FMD was an independent predictor of risk but added little to traditional risk stratification. | Yes |
Muiesan et al[57] | 172 | Hypertensive patients | No | 95 ± 37 | CV death, MI, revascularisation, arrhythmia, TIA, critical limb ischaemia, retinal artery occlusion | FMD below median was independently associated with adverse outcome. | Yes |
Shechter et al[46] | 618 | Healthy subjects (mixed) | Yes | 55.2 ± 21.6 | CV death, MI, stroke, congestive revascularisation | FMD predicted adverse outcome independently. | Yes |
Katz et al[77] | 259 | Heart failure patients (LVEF < 40% and NYHA class 2-3) | No | 28 | Death or cardiac transplantation | FMD is associated with increased adverse outcome in ischaemic and non-ischaemic heart failure. | Yes |
Ref. | Drug | Cohort | Design | Results |
Mancini et al[94] | Quinapril | 105 normotensive patients with coronary artery disease | Randomised double-blind, placebo controlled | Quinapril improved endothelial function compared to placebo as measured by coronary artery diameter response to acetylcholine |
Higashi et al[96] | Various ACE inhibitors, beta-blockers, calcium channel blockers and diuretics | 296 hypertensive patients | Multi-centre cohort study | ACE inhibitors significantly improved endothelial dependent vasodilatation compared to other drug classes as measured by forearm blood flow |
Wassmann et al[97] | Candesartan, felodipine | 47 patients with high cholesterol | Randomised double-blind, placebo controlled | Candesartan improved forearm blood flow compared to felodipine or placebo |
Ghiadoni et al[98] | Nifedipine, amlodipine Perindopril, telmisartan, atenolol, nebivolol | 168 patients with hypertension | Randomized, single-blind, parallel-group | Only perindopril improved FMD (although perindopril, telmisartan, nifedipine and amlodipine reduced oxidative stress and increased plasma antioxidant capacity) |
Tzemos et al[99] | Valsartan, amlodipine | 25 hypertensive patients | Randomised double-blind, crossover | Valsartan improved forearm blood flow |
Takagi et al[100] | Telmisartan | Mixed; 398 patients | Meta-analysis of 7 studies | Statistically significant increase in FMD by 48.7% |
Farquaharson et al[101] | Spironolactone | 10 patients with NYHA class I-II heart failure | Randomised, double-blind placebo-controlled crossover study | Spironolactone improved forearm blood flow compared to placebo |
MacDonald et al[103] | Spironolactone | 43 patients with NYHA class I-II heart failure | Randomised, double-blind crossover study | Spironolactone improved forearm blood flow compared to placebo |
Abiose et al[104] | Spironolactone | 20 patients with NYHA class III-IV congestive heart failure | Cohort study | Spironolactone improved FMD at 4 wk with a sustained improvement at 8 wk |
Tzemos et al[107] | Nebivolol, atenolol | 12 hypertensive patients | Randomised, double-blind crossover study | Only nebivolol was able to improve endothelial dependent vasodilation |
Pasini et al[108] | Nebivolol, atenolol | 40 hypertensive patients with 40 controls | Randomised double-blind parallel group | FMD improved only in the group treated with nebivolol |
Matsuda et al[109] | Carvedilol | 29 patients with coronary artery disease | Randomised, placebo controlled | Carvedilol significantly improved FMD after 4 mo treatment |
Agewall et al[116] | Atorvastatin | 20 healthy smokers, 20 healthy non-smokers | Open label placebo controlled randomised cross-over | Smokers had a lower baseline FMD. Atorvastatin improved FMD in smokers but had no effect in non-smokers |
Ostad et al[117] | Atorvastatin, ezetimibe | 58 patients with coronary artery disease | Double-blind, randomised, parallel group | High-dose atorvastatin improved FMD significantly more than low dose atorvastatin + ezetimibe independently of improvement in LDL cholesterol |
Gounari et al[118] | Rosuvastatin, ezetimibe | Patients with heart failure | Double-blind, placebo controlled, cross-over trial | Rosuvastatin caused a significant improvement of FMD compared to ezetimibe and independent of LDL cholesterol and baseline brachial artery diameter |
Pitocco et al[121] | Metformin | 42 type 1 diabetics without overt cardiovascular disease | Randomised double-blind, placebo controlled | Significant improvement in FMD by 1.32% compared to placebo |
Lamendola et al[122] | Ranolazine | 30 type 2 (non-insulin dependent) diabetics without overt cardiovascular disease | Randomised double-blind, placebo controlled | Significant improvement in FMD compared to placebo after 2 wk of ranolazine therapy |
Kao et al[123] | Allopurinol | 67 patients with CKD stage 3 and LV hypertrophy | Randomized, double-blind, parallel-group | Significant improvement in FMD compared to placebo after 9 mo of allopurinol therapy |
- Citation: Mordi I, Tzemos N. Is reversal of endothelial dysfunction still an attractive target in modern cardiology? World J Cardiol 2014; 6(8): 824-835
- URL: https://www.wjgnet.com/1949-8462/full/v6/i8/824.htm
- DOI: https://dx.doi.org/10.4330/wjc.v6.i8.824