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1.
Trials ; 25(1): 518, 2024 Aug 01.
Article in English | MEDLINE | ID: mdl-39090754

ABSTRACT

BACKGROUND: Heart failure is a chronic and progressive disease where the heart muscle is unable to pump enough blood and oxygen to meet the body's needs. Oxidative stress and inflammation are key elements in the development and progression of heart failure. Astaxanthin, a carotenoid, has strong anti-inflammatory and antioxidant effects that may protect the cardiovascular system. A study will evaluate the effect of astaxanthin supplementation on inflammatory status, oxidative stress, lipid profile, uric acid levels, endothelial function, quality of life, and disease symptoms in people with heart failure. METHODS: The current study is a double-blind controlled randomized clinical trial for 8 weeks, in which people with heart failure were randomly assigned to two groups: intervention (one capsule containing 20 mg of astaxanthin per day, n = 40) and placebo (one capsule containing 20 mg of maltodextrin per day, n = 40) will be divided. At the beginning and end of the intervention, uric acid, lipid profile, oxidative stress indices, inflammatory markers, blood pressure, nitric oxide, and anthropometric factors will be measured, and questionnaires measuring quality of life, fatigue intensity, shortness of breath, and appetite will be completed. SPSS version 22 software will be used for statistical analysis. DISCUSSION: There is a growing global interest in natural and functional food products. This RCT contributes to the expanding body of research on the potential benefits of astaxanthin in heart failure patients, including its antioxidant, lipid-lowering, and anti-inflammatory effects. TRIAL REGISTRATION: Iranian Registry of Clinical Trials IRCT20200429047235N3. Registered on 26 March 2024.


Subject(s)
Biomarkers , Blood Pressure , Dietary Supplements , Heart Failure , Oxidative Stress , Quality of Life , Uric Acid , Xanthophylls , Humans , Xanthophylls/therapeutic use , Oxidative Stress/drug effects , Heart Failure/drug therapy , Heart Failure/physiopathology , Heart Failure/blood , Uric Acid/blood , Double-Blind Method , Biomarkers/blood , Blood Pressure/drug effects , Randomized Controlled Trials as Topic , Middle Aged , Male , Lipids/blood , Female , Antioxidants , Aged , Treatment Outcome , Inflammation Mediators/blood , Adult , Inflammation/blood , Anti-Inflammatory Agents/therapeutic use , Iran
2.
Phytother Res ; 33(1): 3-12, 2019 Jan.
Article in English | MEDLINE | ID: mdl-30281177

ABSTRACT

Despite a history of purslane usage as a herbal treatment for dyslipidemia and hyperglycemia management, existing evidence from clinical trials is controversial. The aim for the current study was to evaluate the efficacy of purslane supplementation on lipid parameters and glycemic status in adult populations. A systematic review was conducted in PubMed, Scopus, ISI Web of Science, and Google Scholar up to January 15, 2018, searching for randomized controlled trials that assessed the impact of purslane on fasting blood glucose (FBG), triglycerides, total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), and high-density lipoprotein cholesterol (HDL-C). Based on the detected heterogeneity between studies, a random- or fixed-effect model was applied in the meta-analysis. The findings from six randomized controlled trials, comprising 352 participants, indicated that purslane can reduce FBG (-4.54 mg/dl, 95% CI [-7.54, -1.53]; I2  = 0.53%) and triglycerides (-19.16 mg/dl, 95% CI [-38.17, -0.15]; I2  = 0%) levels. Changes in TC, LDL-C, and HDL-C concentrations did not reach a statistically significant level. Subgroup analysis showed a favorable effects of purslane on FBG, triglycerides, TC, and LDL-C in a subset of studies in which purslane was administered >1.5 g/day. Categorization based on gender showed that purslane was more effective in improving FBG, TC and LDL-C in females compared with males. This systematic review and meta-analysis suggested that the purslane might be effective on the improvement of blood lipid and glucose levels. Further robust studies with sufficient durations and dosages of supplementation are needed to confirm these results.


Subject(s)
Cholesterol, HDL/blood , Dyslipidemias/drug therapy , Glucose/metabolism , Lipids/blood , Portulaca/chemistry , Cholesterol, LDL/blood , Female , Humans , Male , Middle Aged , Randomized Controlled Trials as Topic
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