Key result
Astaxanthin improves total antioxidant capacity by 0.12 mmol/L vs. placebo in heart failure.
Why the study?
Does astaxanthin supplementation improve oxidative stress markers and clinical symptoms in patients with heart failure?
RCT (n=80)
Double-blind
randomly assigned
Does astaxanthin supplementation improve oxidative stress markers and clinical symptoms in patients with heart failure?
Answers are grounded in this paper and cite their sources.
Astaxanthin supplementation for 8 weeks significantly improves oxidative stress biomarkers, uric acid levels, and symptoms of dyspnea and fatigue in patients with heart failure.
BACKGROUND AND AIMS: Chronic heart failure (HF) is often linked to increased oxidative stress and metabolic issues like high uric acid, which can worsen outcomes. Astaxanthin (ASX), a strong antioxidant, may help reduce these harmful effects. This study aimed to investigate the effects of ASX supplementation on oxidative stress markers as the primary outcome and clinical symptoms in patients with HF. METHODS: In this randomized, double-blind, placebo-controlled clinical trial, 80 patients with HF were enrolled and randomly assigned to receive either ASX (20 mg/day) or a placebo (20 mg/day of maltodextrin) for 8 weeks. Biomarkers including total antioxidant capacity (TAC), malondialdehyde (MDA), superoxide dismutase (SOD), serum UA, and clinical symptoms (dyspnea, fatigue, appetite) were assessed pre-and post-intervention. RESULTS: After eight weeks, compared to the placebo group, participants receiving ASX supplementation showed a significant increase in TAC (0.12 vs. -0.04 mmol/L, P = 0.002) and SOD levels (156.92 vs. 36.14 U/mL, P < 0.001). In contrast, the ASX group demonstrated significantly greater reductions in MDA (-2.19 vs. -0.68 nmol/L, P < 0.001) and serum UA levels (-1.82 vs. -0.63 mg/dl, P = 0.003) compared to placebo. Furthermore, among ASX treated patients, improvements in dyspnea and fatigue were statistically significant (P < 0.001), while the increase in appetite was only marginally significant (P = 0.071). CONCLUSION: These findings suggest that ASX supplementation may be effective in improving oxidative stress biomarkers and clinical status in patients with HF. TRIAL REGISTRATION: Iranian Registry of Clinical Trials IRCT20200429047235N3. Registered on 26 March 2024, prior to the enrollment of the first participant. http://irct.behdasht.gov.ir/trial/75913 .
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Mohammadi et al. (2025) conducted an RCT in heart failure (n=80). Astaxanthin vs. Placebo (20 mg/day of maltodextrin) was evaluated on Oxidative stress markers (total antioxidant capacity change in mmol/L) (p=0.002). Astaxanthin supplementation for 8 weeks significantly increased total antioxidant capacity (0.12 vs. -0.04 mmol/L, P=0.002) and reduced malondialdehyde and uric acid in heart failure patients.
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