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The effects of coenzyme Q10 supplementation on biomarkers of inflammation and oxidative stress in among coronary artery disease: a systematic review and meta-analysis of randomized controlled trials
被引:37
|作者:
Jorat, Mohammad Vahid
[1
]
Tabrizi, Reza
[2
]
Kolahdooz, Fariba
[3
]
Akbari, Maryam
[2
]
Salami, Maryamalsadat
[4
]
Heydari, Seyed Taghi
[5
]
Asemi, Zatollah
[6
]
机构:
[1] Shiraz Univ Med Sci, Dept Cardiol, Shiraz, Iran
[2] Shiraz Univ Med Sci, Inst Hlth, Ctr Hlth Policy Res, Student Res Comm, Shiraz, Iran
[3] Univ Alberta, Dept Med, Indigenous & Global Hlth Res Grp, Edmonton, AB, Canada
[4] Shiraz Univ Med Sci, Shiraz, Iran
[5] Shiraz Univ Med Sci, Inst Hlth, Ctr Hlth Policy Res, Shiraz, Iran
[6] Kashan Univ Med Sci, Res Ctr Biochem & Nutr Metab Dis, Kashan, Iran
关键词:
CoQ10;
Inflammation;
Oxidative stress;
Coronary artery disease;
Meta-analysis;
DOUBLE-BLIND;
HEART-FAILURE;
MYOCARDIAL-INFARCTION;
RISK;
MARKERS;
Q(10);
INTERLEUKIN-6;
PREVENTION;
RADICALS;
THERAPY;
D O I:
10.1007/s10787-019-00572-x
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
ObjectiveSystemic inflammation and oxidative stress significantly contribute in developing coronary artery disease (CAD). This systematic review and meta-analysis was aimed to determine the effects of coenzyme Q10 (CoQ10) supplementation on biomarkers of inflammation and oxidative stress among patients with CAD.MethodsThe electronic databases including MEDLINE, EMBASE, Scopus, Web of Science, and Cochrane Library databases were systematically searched until Oct 2018. The quality assessment and heterogeneity of the selected randomized clinical Trials (RCTs) were examined using the Cochrane Collaboration risk of bias tool, and Q and I-2 tests, respectively. Given the presence of heterogeneity, random-effects model or fixed-effect model were used to pool standardized mean differences (SMDs) as summary effect sizes.ResultsA total of 13 clinical RCTs of 912 potential citations were found to be eligible for the current meta-analysis. The pooled findings for biomarkers of inflammation and oxidative stress demonstrated that CoQ10 supplementation significantly increased superoxide dismutase (SOD) (SMD 2.63; 95% CI, 1.17, 4.09, P<0.001; I-2=94.5%) and catalase (CAT) levels (SMD 1.00; 95% CI, 0.57, 1.43, P<0.001; I-2=24.5%), and significantly reduced malondialdehyde (MDA) (SMD -4.29; 95% CI -6.72, -1.86, P=0.001; I-2=97.6%) and diene levels (SMD -2.40; 95% CI -3.11, -1.68, P<0.001; I-2=72.6%). We did not observe any significant effect of CoQ10 supplementation on C-reactive protein (CRP) (SMD -0.62; 95% CI -1.31, 0.08, P=0.08; I-2=87.9%), tumor necrosis factor alpha (TNF-) (SMD 0.22; 95% CI -1.07, 1.51, P=0.73; I-2=89.7%), interleukin-6 (IL-6) (SMD -1.63; 95% CI -3.43, 0.17, P=0.07; I-2=95.2%), and glutathione peroxidase (GPx) levels (SMD 0.14; 95% CI -0.77, 1.04, P=0.76; I-2=78.7%).ConclusionsOverall, this meta-analysis demonstrated CoQ10 supplementation increased SOD and CAT, and decreased MDA and diene levels, but did not affect CRP, TNF-, IL-6, and GPx levels among patients with CAD.
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页码:233 / 248
页数:16
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