Astaxanthin
Astaxanthin is a red carotenoid from algae and marine animals; controlled studies show mainly higher HDL cholesterol, less muscle damage after exertion and, in diabetes, better blood glucose levels.
We evaluated 139 human studies on Astaxanthin, including 54 randomised controlled trials and 32 meta-analyses or systematic reviews; the controlled studies include 2,957 participants in total. As of 5 October 2026.
1. What Is Astaxanthin? Occurrence, Origin and Forms
Astaxanthin is a red carotenoid of the xanthophyll group. It gives marine animals such as crabs, shrimp and salmon, as well as flamingo feathers, their pink to red colour. It is sold as a dietary supplement in capsules, and in aquaculture it is used to pigment farmed fish.
Astaxanthin is formed in microalgae, above all in Haematococcus pluvialis, and in yeasts such as Xanthophyllomyces dendrorhous. Through the food chain it accumulates in krill, shrimp, crabs and salmon; in humans it is studied as a dietary supplement.
For study material, astaxanthin is mostly obtained from cultivated Haematococcus pluvialis algae, and also from yeast fermentation and chemical synthesis. What is tested are oil-based capsules with esterified or free astaxanthin, algal extracts, and occasionally preparations applied to the skin.
Forms and Preparations Studied
- Algal extract from Haematococcus pluvialis
- Astaxanthin from yeast fermentation
- Synthetically produced astaxanthin
- Esterified astaxanthin in an oil carrier
- Free astaxanthin
- Preparation for application to the skin
Not covered on this page:
- Krill oil and fish oil as a whole: they contain astaxanthin but are mixtures of omega-3 fatty acids and further substances.
- Other carotenoids such as beta-carotene, lutein, zeaxanthin and lycopene.
- Canthaxanthin, a different carotenoid that is likewise used for pigmentation.
- Astaxanthin as a feed additive in aquaculture when humans are not the subjects studied.
2. What Does Astaxanthin Do? Results by Area
| Area | Result in controlled studies | Strength of evidence | Studies | Participants |
|---|---|---|---|---|
| Oxidative stress and inflammation | mostly improved | high | 10 meta-analyses · 27 controlled · 22 other | 1,198 |
| Cardiometabolic markers | mostly improved | high | 9 meta-analyses · 14 controlled · 13 other | 810 |
| Exercise and physical performance | mostly improved | high | 3 meta-analyses · 12 controlled · 6 other | 268 |
| Skin | mostly improved | high | 2 meta-analyses · 2 controlled · 6 other | 88 |
| Cognition | mostly no difference | moderate | 2 meta-analyses · 2 controlled · 7 other | 121 |
| Eyes | mostly improved | low | 0 meta-analyses · 1 controlled · 6 other | 64 |
| Tolerability and safety | mostly no difference | unclear | 0 meta-analyses · 2 controlled · 15 other | 45 |
| Other investigations | mixed | high | 7 meta-analyses · 14 controlled · 19 other | 614 |
How to read the table: counted are human studies whose results concern the area. “High” means at least one meta-analysis and two controlled studies showing improvement, or at least three controlled studies of which three quarters show improvement, with at least 300 participants in total. “Moderate” means at least two controlled studies showing improvement, as a majority, or one meta-analysis alongside controlled studies. “Low” means one controlled study showing improvement. Where an area has no controlled study, the strength of evidence is at most “low” (result “reviews only” or “observational data only”). Everything else is “unclear”. A study counts as showing improvement when at least half of its outcomes in this area improved. Reviews of combination products do not count as meta-analyses; results that only describe side effects or shares of users do not count as an effect. The same study is counted only once.
3. What the Studies Show in Detail
Astaxanthin, Oxidative Stress and Inflammation: Human Studies
Compared with placebo, malondialdehyde, a marker of lipid peroxidation, fell more strongly in two randomized studies: in heart failure and after exhaustive cycling 3875. In the heart failure study, total antioxidant capacity and superoxide dismutase also rose more strongly than under placebo 38. In women with PCOS, catalase and total antioxidant capacity rose more strongly than under placebo, while malondialdehyde and superoxide dismutase did not 76. In type 2 diabetes under metformin, superoxide dismutase and catalase rose more strongly than under placebo, while malondialdehyde did not differ 55. Another randomized study found no difference from placebo for malondialdehyde 73, and a meta-analysis classifies the antioxidant effect overall as unclear 27. Inflammatory markers fell more strongly than under placebo in two randomized studies: TNF-α in heart failure 36, interleukin-6 and TNF-α in pneumonia 37. C-reactive protein fell in a meta-analysis only with a higher dose or longer intake 29. With dark chocolate in lycosome form, malondialdehyde and oxidized LDL fell more markedly than with astaxanthin alone 65. It remains open in which patient groups and at which doses the effect occurs reliably; this requires larger studies with uniform measures.
| Study | Design · participants | Preparation · dose · duration · comparison | Result |
|---|---|---|---|
| 1 Zhong et al. 2025 | meta-analysis · 1,626 participants | Antioxidant supplementation, including astaxanthin; vs. Control (placebo/no supplementation) | Peripheral blood malondialdehyde: improved (SMD = -7.58; p = 0.001) |
| 3 Ma et al. 2022 | meta-analysis · 380 participants | Astaxanthin supplementation (source not reported); at least 1 week; vs. Placebo | Blood malondialdehyde: improved (SMD: -0.95; 95% CI, -1.67 to -0.23; P = .01); Malondialdehyde in T2DM patients: improved (SMD: -0.64; 95% CI, -1.26 to -0.01; P < .05); Superoxide dismutase activity: improved |
| 8 You et al. 2026 | meta-analysis · 188 participants | Astaxanthin supplementation, source not reported; 4-28 mg per day; 4 days to 12 weeks; vs. Control group of included RCTs | Advanced oxidation protein products (AOPP): improved (SMD = - 1.06; 95% CI - 1.49 to - 0.62; I2 = 48%); MDA/TBARS, SOD, SH, CK, IL-6: no difference |
| 9 Malcangi et al. 2026 | systematic review · 15 participants | Astaxanthin (ASX) supplementation; vs. not reported (review) | Pro-inflammatory cytokines (IL-6, TNF-α, TGF-β1): improved (consistently reduced); Antioxidant capacity (SOD, TAC): improved (increasing) |
| 10 Liu et al. 2026 | meta-analysis | Oral astaxanthin supplementation; vs. Placebo or control | Malondialdehyde: no difference; Interleukin-6: no difference |
| 11 Paparozzi et al. 2026 | systematic review | Astaxanthin as one of several carotenoids in a nutraceutical review; vs. different nutraceuticals compared with each other | PON1 activity: improved (2) |
| 12 Dehpahni et al. 2026 | meta-analysis | Astaxanthin (origin, esterification and carrier not reported); vs. Placebo in the clinical trials | Oxidative stress markers in animal models: improved (reductions in oxidative stress markers) |
| 13 Wang et al. 2026 | systematic review | Astaxanthin from Haematococcus pluvialis, dietary supplement | Nrf2 antioxidant pathway: improved; NF-κB inflammatory signaling pathway: improved |
Further studies in this area: 14 21 22 27 29 35 36 37 38 42 45 46 48 49 51 53 54 55 56 57 61 63 66 68 72 73 75 76 77 78 79 82 90 95 102 103 104 105 107 108 109 110 112 115 116 118 119 121 126 127 128
Astaxanthin and Cardiometabolic Markers: Human Studies
In prediabetes and type 2 diabetes, astaxanthin lowered fasting blood glucose, HbA1c, triglycerides, total and LDL cholesterol and raised HDL cholesterol compared with control in a meta-analysis 2. In type 2 diabetes, two randomized studies with the same design found lower blood glucose, HbA1c and blood lipid levels than under placebo 5152. In women with PCOS, fasting blood glucose, insulin resistance and LDL cholesterol decreased in a placebo-controlled study, while HDL cholesterol increased 48. In coronary heart disease, however, blood glucose levels did not differ from placebo 54. For blood lipids, the meta-analyses are inconsistent: HDL cholesterol increased in three of them 21529. LDL cholesterol decreased in two reviews 25, while three others found no effect on LDL and total cholesterol 61529. Body weight and body mass index did not change in two meta-analyses 219. Combinations with red yeast rice, berberine, policosanol, folic acid and coenzyme Q10 lowered LDL cholesterol, also in addition to a statin; this does not allow any statement about astaxanthin alone 3032. It remains open whether the better laboratory values translate into fewer cardiovascular events; studies with such endpoints are still pending.
| Study | Design · participants | Preparation · dose · duration · comparison | Result |
|---|---|---|---|
| 2 Molani-Gol et al. 2026 | meta-analysis · 403 participants | Astaxanthin supplementation (origin/esterification not reported); vs. Control group | Fasting blood sugar: improved (WMD: -16.126 mg/dl (95%CI: -28.968 to -3.285), P = .014); Glycated hemoglobin: improved (WMD: -0.338 (95%CI: -0.598 to -0.079), P = .011); Triglyceride: improved (WMD: -20.872 mg/dl, (95%CI: -38.205 to 3.540), P = .018) |
| 5 Leung et al. 2022 | systematic review · 321 participants | Astaxanthin (source, esterification, dose not reported); vs. Control groups of included RCTs | Total cholesterol: improved (marginal effects); Systolic blood pressure: improved (marginal effects); LDL cholesterol: improved (significant attenuating effect) |
| 6 Ursoniu et al. 2015 | meta-analysis · 280 participants | Oral astaxanthin supplementation; vs. Control group (117 participants) | Total cholesterol: no difference (WMD: -1.52 mg/dl, 95% CI: -8.69 to -5.66, p = 0.679); LDL-C: no difference (WMD: +1.25 mg/dl, 95% CI: -6.70 to +9.21, p = 0.758); HDL-C: no difference (WMD: +1.75 mg/dl, 95% CI: -0.92 to +4.42, p = 0.199) |
| 9 Malcangi et al. 2026 | systematic review · 15 participants | Astaxanthin (ASX) supplementation; vs. not reported (review) | Endothelial function and disease severity: improved (improved) |
| 13 Wang et al. 2026 | systematic review | Astaxanthin from Haematococcus pluvialis, dietary supplement | insulin sensitivity: improved |
| 15 Fornari et al. 2025 | meta-analysis | Astaxanthin supplement, source not stated; 6-24 mg/d, analyzed 6-20 mg/d; vs. Control groups of included RCTs | HDL cholesterol: improved (0.4200; 95% CI: 0.1081 to 0.7319); Triglycerides: improved (-0.3058; 95% CI: -0.5138 to -0.0978); LDL cholesterol: no difference (-0.0725; 95% CI: -0.3070 to 0.1620) |
| 19 Laurindo et al. 2025 | meta-analysis | Astaxanthin dietary supplement; dose-response assessed, not specified; vs. Control groups | Body mass index: no difference (-0.2162; 95% CI: -0.4697 to 0.0374); Body weight: no difference (0.0230; 95% CI: -0.4534 to 0.4994) |
| 20 Wan et al. 2024 | meta-analysis | Antioxidant functional lipid supplements, including astaxanthin; vs. Placebo | LDL cholesterol: improved (-0.11 [-0.21, -0.01] mmol/L); HDL cholesterol: improved (0.13 [0.05, 0.21] mmol/L); Total cholesterol: improved (-0.22 [-0.32, -0.12] mmol/L) |
Further studies in this area: 21 25 29 30 35 36 38 42 43 44 47 48 49 51 54 62 67 85 89 95 102 108 109 110 118 123 127 128
Astaxanthin, Exercise and Physical Performance: Human Studies
The most consistent finding is on recovery: in a meta-analysis of randomized studies, creatine kinase, a marker of muscle damage, was lower after exertion than under placebo 10. Randomized studies showed the same in young soccer players and after exhaustive cycling 6675. For performance, the meta-analyses are inconsistent: one found better physical performance when taken together with training 4. A larger meta-analysis, by contrast, found no improvement in maximum oxygen uptake, time trial performance or maximum performance 10. In small randomized studies with cyclists, astaxanthin shortened the time trial time and lengthened the time to exhaustion 7475. In older nursing home residents, the walking distance in the six-minute walk test was greater than under placebo 82. Fat burning during cycling was higher than under placebo in two randomized studies 7174, but not in another 73. An algal extract with astaxanthin and lutein did not reduce muscle damage after strength training 83; a crossover study with strength athletes also found no difference from placebo 85. It remains open whether the better recovery values translate into noticeably faster regeneration.
| Study | Design · participants | Preparation · dose · duration · comparison | Result |
|---|---|---|---|
| 4 Liu et al. 2024 | meta-analysis · 346 participants | Dietary astaxanthin supplement, source not reported; Subgroup analysis: dose ≥ 20 mg; 8–12 weeks; subgroup analysis > 12 weeks; vs. Control groups of included RCTs | Fat oxidation: improved (SMD: 2.56; 95% CI: 1.24-3.89); Physical performance: improved (SMD: .62; 95% CI: .17-1.06); Aerobic exercise performance: improved (SMD: .45; 95% CI: .13-.76) |
| 9 Malcangi et al. 2026 | systematic review · 15 participants | Astaxanthin (ASX) supplementation; vs. not reported (review) | Body composition, lipid profile, insulin sensitivity, immune recovery: improved (improved) |
| 10 Liu et al. 2026 | meta-analysis | Oral astaxanthin supplementation; vs. Placebo or control | Creatine kinase: improved (SMD = -0.45, 95% CI: -0.83 to -0.07); Lactate dehydrogenase: improved (SMD = -0.93, 95% CI: -1.39 to -0.48); VO2max: no difference |
| 62 Liu et al. 2021 | randomised controlled · 42 participants | Astaxanthin formulation (source not stated); 3 months; vs. Placebo during endurance training | Specific muscle endurance (contractions): improved (Pre 353 ± 26 vs. Post 472 ± 41 contractions); Submaximal GXT duration: no difference (PL 40.8 ± 9.1% and AX 41.1 ± 6.3%) |
| 63 Baralic et al. 2015 | randomised controlled · 40 participants | Astaxanthin (Asx); 4 mg Asx; 90 days; vs. Placebo | resting salivary IgA: improved; plasma muscle enzymes: unclear (reduced significantly) |
| 66 Djordjevic et al. 2012 | randomised controlled · 32 participants | Astaxanthin (Asx) supplementation; 90 days; vs. placebo, double-blind randomized | post-exercise CK and AST: improved (P<0.05) |
| 70 Fleischmann et al. 2019 | randomised controlled · 22 participants | Astaxanthin (ATX), source not stated; 12 mg/day per os; 30 days; vs. placebo (PLA), randomized double blind | rise in blood lactate after VO2max test: improved (9.4 ± 3.1 and 13.0 ± 3.1 mmole*l-1 in the ATX and PLA groups, respectively P < 0.02); change in oxygen uptake during recovery: improved (-2.02 ± 0.64 and 0.83 ± 0.79% of VO2 Max in the ATX and PLA group, respectively, p = 0.001); anaerobic threshold and VO2 Max: no difference |
| 71 Barker et al. 2026 | randomised controlled · 20 participants | Astaxanthin (AX), source/esterification not stated; 12 mg per day; 2 weeks supplementation, 2-week washout; vs. placebo, double-blind, crossover | Respiratory exchange ratio (RER) during submaximal cycling: improved (p = 0.04); Heart rate, blood lactate, rate of perceived exertion: no difference (p > 0.05) |
Further studies in this area: 73 74 75 82 83 84 85 94 95 110 117 121 124
Astaxanthin and Skin: Human Studies
In a small randomized study, skin tolerated more UV light until redness and lost less moisture when irradiated under astaxanthin than under placebo 69. In a placebo-controlled study with women in Japan, wrinkles and skin moisture worsened over the autumn months only under placebo, not under astaxanthin 79. Suspicion: A systematic review sees advantages for skin structure, wrinkles, moisture and UV protection; many of the included studies were small and company-funded 26. A combination with collagen hydrolysate improved elasticity and water loss of facial skin compared with placebo, but does not allow any statement about astaxanthin alone 80. It remains open whether the protective effect is confirmed in larger studies and outside Japan.
| Study | Design · participants | Preparation · dose · duration · comparison | Result |
|---|---|---|---|
| 16 Yang et al. 2025 | meta-analysis | Oral dietary supplements, including astaxanthin; typically ≤ 24 weeks; vs. Placebo | Skin photoaging / MED / skin elasticity: unclear (insufficient evidence to support the recommendation of other dietary supplements, such as astaxanthin) |
| 18 Natarelli et al. 2025 | systematic review | Dietary supplements incl. astaxanthin, carotenoids, polyphenols; vs. various supplements or controls | Photoprotection: improved |
| 21 Frumuzachi et al. 2024 | systematic review | Chocolate enriched/fortified with bioactive components, including co-crystalized astaxanthin; Chocolate intake 5 to 101 g per day; 2 weeks to 1 year; vs. Control groups of the included RCTs | Skin parameters: unclear |
| 26 Ng et al. 2021 | systematic review | Astaxanthin supplementation (source not stated); 3 to 6 mg/d; vs. Placebo in six randomized, double-blind trials; manufacturer-funded | Skin texture, appearance (wrinkles), moisture content: improved; UV-induced skin damage: improved |
| 69 Ito et al. 2018 | randomised controlled · 23 participants | capsule with 4 mg algal astaxanthin; 4 mg astaxanthin daily; 9 weeks of supplementation (10-week study); vs. placebo capsule, double-blind randomized | Minimal erythema dose (MED): improved; Loss of skin moisture in irradiated area: improved; Subjective skin improvement (rough skin, texture) in non-irradiated areas: improved |
| 79 Tominaga et al. 2017 | controlled · 65 participants | Oral astaxanthin, source not stated; 6 mg or 12 mg daily; 16 weeks; vs. Placebo | wrinkle parameters: improved; skin moisture content: improved |
| 101 Tominaga et al. 2012 | study | Astaxanthin from Haematococcus pluvialis, oral and topical; 6 mg/day oral; 2 ml (78.9 μM) topical daily; 8 weeks (women); 6 weeks (men); vs. Placebo (men); no control (women) | crow's feet wrinkle: improved; age spot size: improved; elasticity: improved |
| 114 Januszewski et al. 2023 | review | Astaxanthin as a nutritional supplement | Photoprotective effect: improved; Inflammatory skin diseases (atopic dermatitis, psoriasis): improved |
Further studies in this area: 116 118
Astaxanthin and Cognition: Human Studies
In healthy older adults with forgetfulness, individual cognitive tests improved with Haematococcus algae extract, without a confirmed difference from placebo 34. A meta-analysis found no effect on reaction time and only a borderline effect on cognitive accuracy 4. Clearer advantages over placebo were shown by combinations: with tocotrienols for memory 59, with Bacopa, lycopene and vitamin B12 in the Trail-Making Test and for verbal fluency 40. In athletically active young women, after mental fatigue, reaction time and speed in two tasks improved only with astaxanthin, not with placebo 81. Hypothesis: A review of older people sees indications of better cognition that are not statistically confirmed 23. For astaxanthin alone, larger studies with memory tests as the primary aim are needed.
| Study | Design · participants | Preparation · dose · duration · comparison | Result |
|---|---|---|---|
| 4 Liu et al. 2024 | meta-analysis · 346 participants | Dietary astaxanthin supplement, source not reported; Subgroup analysis: dose ≥ 20 mg; 8–12 weeks; subgroup analysis > 12 weeks; vs. Control groups of included RCTs | Cognitive accuracy: unclear (SMD: .12; 95% CI: -.02-.26); Reaction time: no difference (SMD: -.08; 95% CI: -.26 to .10) |
| 23 Utomo et al. 2024 | systematic review | astaxanthin supplementation (source not stated) | subjective and objective cognitive amelioration: improved; statistical support for cognitive improvement: unclear (not being supported statistically) |
| 24 Martini et al. 2022 | systematic review | Carotenoids, including astaxanthin, lutein, lycopene | Emerging research topics: unclear (cognitive function and carotenoid-gut microbiota interactions) |
| 28 Nouchi et al. 2020 | systematic review | Oral carotenoid intake (lutein, astaxanthin); 10 mg lutein per day (astaxanthin dose not reported); twelve months (lutein); vs. Randomized controlled trials | Verbal episodic memory: improved (significant improvement); Cognitive functions overall: unclear (difficult to conclude) |
| 34 Katagiri et al. 2012 | randomised controlled · 96 participants | Capsule with astaxanthin-rich Haematococcus pluvialis extract; 6 mg or 12 mg astaxanthin per day; 12 weeks; vs. Placebo capsule | CogHealth battery scores: no difference; Groton Maze Learning Test scores: no difference |
| 81 Barker et al. 2025 | controlled · 25 participants | Astaxanthin or placebo; 12 mg/day; 4 weeks; vs. Placebo | Task-switching reaction time: unclear (~200 ms); Incongruent flanker reaction time: unclear (~50 ms); Task-switching speed: unclear (+20%) |
| 106 N et al. 2026 | review | Astaxanthin, fucoxanthin and canthaxanthin (marine xanthophylls) | Neuroprotective evidence base: improved (the most robust and extensive evidence base) |
| 111 Cunha et al. 2024 | review | Astaxanthin from Haematococcus pluvialis | symptoms of brain disorders: improved |
Further studies in this area: 113 116 118
Astaxanthin and Eyes: Human Studies
In schoolchildren with eye strain from screens, astaxanthin in a randomized study reduced complaints and visual fatigue more than placebo; visual acuity and accommodation did not change 45. A mixture with anthocyanin and lutein improved pupil response and focusing complaints in adults with screen fatigue compared with placebo 58. In dry eye, an antioxidant mixture with anthocyanosides, vitamins and herbal extracts improved the overall impression compared with placebo, but sicca complaints did not differ 60. Without a comparison group, in people of middle and older age with dry eye, complaints and tear film stability improved under algae extract from Haematococcus pluvialis 91. It remains open whether the findings of the mixtures are due to astaxanthin or to the combination partners.
| Study | Design · participants | Preparation · dose · duration · comparison | Result |
|---|---|---|---|
| 17 Martinez-Perez et al. 2025 | systematic review | Nutritional supplementation with carotenoids, including astaxanthin; vs. Placebo or active controls | macular pigment optical density (MPOD): improved; visual fatigue: improved; axial elongation (one pediatric trial): improved |
| 24 Martini et al. 2022 | systematic review | Carotenoids, including astaxanthin, lutein, lycopene | Main study topics: unclear (eye and cardiovascular health) |
| 45 Hecht et al. 2025 | randomised controlled · 64 participants | Astaxanthin (AstaReal®) soft capsule; 4 mg daily; 84 days; vs. Placebo, double-blind randomized | CVS-Q score: improved (- 4.00 ± 4.05 arbitrary units (A.U.) from baseline, p < 0.0001); Visual fatigue Likert scale: improved (11.55 ± 5.78 A.U.); Stereopsis after acute visual load: improved (p < 0.05, p < 0.0001 vs. placebo) |
| 91 Tian et al. 2021 | study · 60 participants | Astaxanthin tablets (Weihong Haematococcus Pluvialis Astaxanthin); 6 mg orally twice daily; 30 ± 2 days; vs. no control group, before/after comparison | OSDI score: improved (P < 0.05); NIBUT: improved (P < 0.05); FBUT: improved (P < 0.05) |
| 93 Hsu et al. 2023 | study · 34 participants | Lutein/DHA complex with 30 mg astaxanthin from red algae extract; 30 mg astaxanthin (red algae extract) daily; 12 weeks; vs. no control group (single-arm) | Tear break-up time: improved (significantly increased); Intraocular pressure: improved (significantly decreased) |
| 100 D'Aloisio et al. 2022 | case-control study | Oral nutritional supplement with astaxanthin, bromelain, vitamin D3, folic acid, lutein, and antioxidants; at least 6 months; vs. Control group without supplement | choriocapillary vessel density: improved (p < 0.001); choroidal thickness: improved (p < 0.001) |
| 118 Donoso et al. 2021 | review | Astaxanthin (origin, esterification, dose not stated) | Treatment of eye diseases (glaucoma, cataracts, uveitis): unclear |
Astaxanthin, Tolerability and Safety: Human Studies
Under astaxanthin alone, in controlled studies neither side effects nor differences in safety values compared with placebo were noted 34454988. In pneumonia, astaxanthin as an addition to standard therapy was safe and well tolerated 37. Two systematic reviews report no serious adverse events or notable laboratory findings 2326. Mixed preparations with astaxanthin, for example with krill oil and hyaluronic acid or with red yeast rice and berberine, were also well tolerated 3133. Data on intake for more than a few months are still pending.
| Study | Design · participants | Preparation · dose · duration · comparison | Result |
|---|---|---|---|
| 23 Utomo et al. 2024 | systematic review | astaxanthin supplementation (source not stated) | unwanted issues on physical and laboratory examinations |
| 26 Ng et al. 2021 | systematic review | Astaxanthin supplementation (source not stated); 3 to 6 mg/d; vs. Placebo in six randomized, double-blind trials; manufacturer-funded | Serious adverse events (No serious adverse events were reported) |
| 34 Katagiri et al. 2012 | randomised controlled · 96 participants | Capsule with astaxanthin-rich Haematococcus pluvialis extract; 6 mg or 12 mg astaxanthin per day; 12 weeks; vs. Placebo capsule | Adverse effects (No adverse effect on the subjects was observed) |
| 37 Youssef et al. 2025 | randomised controlled · 80 participants | Astaxanthin (ASX) as adjunct to standard antibiotic therapy; 12 mg/day; 7 days; vs. Placebo in addition to standard antibiotic therapy | Safety and tolerability |
| 45 Hecht et al. 2025 | randomised controlled · 64 participants | Astaxanthin (AstaReal®) soft capsule; 4 mg daily; 84 days; vs. Placebo, double-blind randomized | Safety variables |
| 49 Urakaze et al. 2021 | randomised controlled · 53 participants | astaxanthin or placebo, source not stated; 12 mg astaxanthin once daily; 12 weeks; vs. placebo, randomized controlled | adverse effects (without adverse effects) |
| 64 Spiller et al. 2003 | randomised controlled · 35 participants | Algal extract (H. pluvialis) in safflower oil gelcaps; 6 mg astaxanthin/day (3 gelcaps of 2 mg); 8 weeks; vs. Placebo (safflower oil gelcaps) | Blood pressure and blood chemistry: no difference (No significant differences were detected); Serum calcium, total protein, eosinophils: unclear (P <.01) |
| 75 Tsao et al. 2025 | randomised controlled · 10 participants | oral astaxanthin, source not stated; 28 mg/day; 4 days; vs. placebo | profile of mood states: no difference |
Further studies in this area: 78 88 92 96 102 122 123 127 128
Astaxanthin: Further Outcomes in Studies
In women with PCOS before artificial fertilization, the proportion of mature eggs was higher than under placebo in two randomized studies 5676. In one of them, the proportion of high-quality embryos also increased 76. A meta-analysis confirms the higher maturation proportion; pregnancy rates did not differ either there or in the randomized study 2276. In men with impaired sperm quality, astaxanthin did not change any semen parameter in a randomized study 39. In rheumatoid arthritis, disease activity fell more than under placebo 46, in pneumonia, severity scores improved in addition to standard therapy 37. In knee or hip osteoarthritis, a mixed preparation of krill oil, astaxanthin and hyaluronic acid relieved joint pain more than placebo 31. These findings each come from individual small studies and need independent replication.
| Study | Design · participants | Preparation · dose · duration · comparison | Result |
|---|---|---|---|
| 1 Zhong et al. 2025 | meta-analysis · 1,626 participants | Antioxidant supplementation, including astaxanthin; vs. Control (placebo/no supplementation) | Pelvic pain (continuous): improved (SMD = -2.68; p < 0.00001); Pelvic pain (binary): improved (RR = 9.31; p < 0.0001); Dysmenorrhea (continuous): improved (SMD = -1.77; p = 0.01) |
| 4 Liu et al. 2024 | meta-analysis · 346 participants | Dietary astaxanthin supplement, source not reported; Subgroup analysis: dose ≥ 20 mg; 8–12 weeks; subgroup analysis > 12 weeks; vs. Control groups of included RCTs | Subjective fatigue: improved |
| 7 Arefpour et al. 2024 | meta-analysis · 196 participants | Astaxanthin supplement, source not reported; 6 to 12 mg/day; 4 to 48 weeks; vs. placebo group | alanine transaminase (ALT): worsened (WMD: 1.92 U/L, 95% CI: 0.16 to 3.68, P=0.03); aspartate transaminase (AST): no difference (WMD: 0.72 U/L, 95% CI: -0.85 to 2.29, P=0.36); gamma-glutamyl transferase (GGT): no difference (WMD: 0.48 U/L, 95% CI: -2.71 to 3.67, P=0.76) |
| 9 Malcangi et al. 2026 | systematic review · 15 participants | Astaxanthin (ASX) supplementation; vs. not reported (review) | Oocyte and embryo quality in PCOS/endometriosis: improved (improved) |
| 12 Dehpahni et al. 2026 | meta-analysis | Astaxanthin (origin, esterification and carrier not reported); vs. Placebo in the clinical trials | Semen parameters in humans: no difference (no statistically significant improvements in any semen parameters); Sperm count in animal models: improved (MD = 27.15); Sperm motility in animal models: improved (MD = 11.29%) |
| 13 Wang et al. 2026 | systematic review | Astaxanthin from Haematococcus pluvialis, dietary supplement | cellular apoptosis: improved |
| 14 Rodrigues et al. 2025 | meta-analysis | Astaxanthin supplementation (source not stated); variable, not specified in abstract; not reported in abstract; vs. Control groups of included RCTs | Oocyte quality and number of high-quality embryos: improved (moderate improvements); Fertilization rates and pregnancy outcomes: no difference (insignificant) |
| 21 Frumuzachi et al. 2024 | systematic review | Chocolate enriched/fortified with bioactive components, including co-crystalized astaxanthin; Chocolate intake 5 to 101 g per day; 2 weeks to 1 year; vs. Control groups of the included RCTs | Immune function: unclear |
Further studies in this area: 22 24 36 37 38 39 46 50 53 54 56 70 76 86 87 88 90 92 94 97 98 99 103 104 108 109 110 116 118 120 125 129
4. How Is Astaxanthin Dosed? Preparation, Dose and Duration in Studies
The studies used predominantly oral astaxanthin capsules, some with algal extract from Haematococcus pluvialis or extract from Paracoccus carotinifaciens, some without stated origin. Individual investigations tested combination preparations, for example with lutein, tocotrienols, krill oil, collagen or dark chocolate. Origin and esterification of the astaxanthin are not reported in many studies; the doses are shown in the table.
| Preparation or form | Dose | Duration | Study |
|---|---|---|---|
| FlexPro MD (krill oil, astaxanthin, hyaluronic acid) | once daily | 12 weeks | 31 |
| Armolipid Plus (red yeast rice, policosanol, berberine, folic acid, coenzyme Q10, astaxanthin) plus low-dose statin | — | 3 months | 32 |
| Armolipid Plus (nutraceutical mixture containing astaxanthin) | — | 3 months, then 12 months combination | 33 |
| Capsule with astaxanthin-rich Haematococcus pluvialis extract | 6 mg or 12 mg astaxanthin per day | 12 weeks | 34 |
| astaxanthin supplementation (source not stated) | 8 mg/day | 8 weeks | 35 |
| Astaxanthin 20 mg/day or placebo, double-blind | 20 mg/day | 8 weeks | 36 |
| Astaxanthin (ASX) as adjunct to standard antibiotic therapy | 12 mg/day | 7 days | 37 |
| astaxanthin capsules (source not stated) | 20 mg/day | 8 weeks | 38 |
| Oral astaxanthin, source not stated | 16 mg daily | 3 months | 39 |
| Antioxidant mix containing bacopa, lycopene, astaxanthin, and vitamin B12 | — | 8 weeks, once daily | 40 |
| Nutraceutical-combined pill containing astaxanthin 0.5 mg | Astaxanthin 0.5 mg daily | 12 months | 41 |
| oral astaxanthin (source not stated) | 10 mg/day | 12 weeks | 42 |
| astaxanthin capsule or placebo | 20 mg/d daily | 12 weeks | 43 |
| Astaxanthin capsule or placebo | 20 mg/day | 12 weeks | 44 |
| Astaxanthin (AstaReal®) soft capsule | 4 mg daily | 84 days | 45 |
5. Is Astaxanthin Safe? Side Effects in Studies
In placebo-controlled studies with astaxanthin alone, no side effects or differences in safety values were observed 344549. In a study on a combination preparation of krill oil, astaxanthin and hyaluronic acid, fewer participants reported adverse events than under placebo; gastrointestinal complaints were most common in both groups 31. Long-term data are still pending, because the studies were mostly small and lasted from a few weeks to months.
| Study | Reported side effects |
|---|---|
| 7 Arefpour et al. 2024 | not reported |
| 14 Rodrigues et al. 2025 | Long-term safety and benefits stated as needing further study |
| 16 Yang et al. 2025 | All oral supplements safe during study period |
| 23 Utomo et al. 2024 | no unwanted issues on physical and laboratory examinations |
| 26 Ng et al. 2021 | No serious adverse events reported |
| 31 Hill et al. 2023 | Adverse events 4% vs. 16% placebo, mostly gastrointestinal |
| 32 Marazzi et al. 2017 | 6 patients (3 per group) dropped out due to myalgia |
| 33 Marazzi et al. 2015 | no important undesirable effects |
| 34 Katagiri et al. 2012 | No adverse effects observed |
| 37 Youssef et al. 2025 | ASX was safe and well-tolerated |
| 41 Marazzi et al. 2011 | No differences in safety parameters; well tolerated |
| 45 Hecht et al. 2025 | no significant differences in safety variables |
6. What Remains Open: Limits of the Evidence
- Origin and esterification of the astaxanthin are not reported in many studies; which form is most effective remains open.
- Many controlled studies are small and short, which limits the transferability of the results.
- Some of the findings come from combination preparations and do not allow any statement about astaxanthin alone.
- Most findings concern blood and measured values; for clinical endpoints such as pregnancy rate, the studies found no difference.
7. Bottom Line: What Is Established About Astaxanthin
Astaxanthin is a carotenoid from the xanthophyll group that is offered as a dietary supplement in capsules. The clearest evidence is for higher HDL cholesterol and less muscle damage after exertion, and in prediabetes and diabetes also for better blood glucose levels. For oxidative stress, the results are inconsistent; for skin, eyes and memory, the evidence comes from small studies and partly from combination preparations. Meta-analyses showed no effect on body weight, maximum oxygen uptake and reaction time. The findings apply to the preparations studied, mostly capsules, often with algal extract from Haematococcus pluvialis; combination preparations do not allow any statement about astaxanthin alone. Next, larger and longer studies with clearly described preparations are needed that also capture clinical endpoints.
Frequently Asked Questions
How well has Astaxanthin been studied in humans?
We evaluated 139 human studies on Astaxanthin, including 54 randomised controlled trials and 32 meta-analyses or systematic reviews; the controlled studies include 2,957 participants in total. As of 5 October 2026.
Does Astaxanthin help with oxidative stress and inflammation? What the studies show
Does Astaxanthin help with cardiometabolic markers? What the studies show
Does Astaxanthin help with exercise and physical performance? What the studies show
Does Astaxanthin help with skin? What the studies show
Does Astaxanthin help with cognition? What the studies show
Does Astaxanthin help with eyes? What the studies show
What is astaxanthin?
Astaxanthin is a red carotenoid from the xanthophyll group. It colors marine animals such as crabs, shrimp and salmon as well as the feathers of flamingos pink to red. As a dietary supplement it is offered in capsules, and in aquaculture it serves to pigment farmed fish.
What effects do studies in humans show?
Which forms of astaxanthin were studied?
The studies used predominantly oral capsules, some with algal extract from Haematococcus pluvialis or extract from Paracoccus carotinifaciens, some without stated origin. Individual investigations tested combination preparations, for example with lutein, tocotrienols, krill oil, collagen or dark chocolate. Origin and esterification of the astaxanthin are not reported in many studies.
How well tolerated is astaxanthin?
In placebo-controlled studies with astaxanthin alone, no side effects or differences in safety values were noted 344549. In a study on a combination preparation of krill oil, astaxanthin and hyaluronic acid, fewer participants reported adverse events than under placebo; the most common in both groups were gastrointestinal complaints 31. Long-term data beyond several months are still pending.
What should be considered with combination preparations?
Many preparations combine astaxanthin with other substances, for example lutein, tocotrienols, krill oil or collagen; their results do not allow any statement about astaxanthin alone. Thus the advantages over placebo for memory and eyes come predominantly from combinations, for example with tocotrienols, bacopa or lutein 405859. A distinction must also be made between measured values in the blood or skin and clinically detectable endpoints.
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Every statement on this page carries its evidence tier — proven, plausible or hypothesis — and leads to the original work. The decision in the individual case rests with the practitioner; we provide the connections.