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    Research bench · no dosing

    Eye Health Supplements

    Lutein and zeaxanthin, the AREDS2 pair, next to astaxanthin and citicoline (CDP-choline)

    no dosing on this page human data on 4 of 4 the trials ran from four weeks (the astaxanthin blood-flow study) to a median of five years in AREDS2, with ten years of follow-up; in a year-long trial in healthy young adults, blood lutein and zeaxanthin were up by the first three-month visit (Hammond 2014) beginner

    01Overview

    the Eye Health Supplements bench sets lutein and zeaxanthin, the pair the AREDS2 trial tested, beside astaxanthin and citicoline. AREDS2 tested lutein with zeaxanthin in 4,203 people aged 50 to 85 who already had intermediate age-related macular degeneration, or advanced disease in one eye, so its results describe them, not healthy eyes. the bench gives no amounts and no timing.

    02 Read this first

    nothing on the Eye Health Supplements bench is an amount, a schedule or a treatment for any eye disease, and all four compounds are sold as supplements. the anchor trial, AREDS2, enrolled 4,203 people aged 50 to 85 who already had intermediate age-related macular degeneration, a third of them with advanced disease in one eye, and added lutein and zeaxanthin to a vitamin and zinc formula, so its results describe that group, not healthy eyes. the hard stops: beta-carotene, which the original AREDS formula contained, for anyone who smokes or used to, since AREDS2 found more lung cancers with it, mostly in former smokers; any new blur, distortion or loss in central vision, which calls for an eye exam, not a supplement; and citicoline in place of eye-pressure treatment, since the glaucoma trials here gave it alongside pressure-lowering treatment.

    03The bench: 4 compounds

    roles and evidence, not amounts. this page does not publish doses or schedules for research compounds.

    evidence ladder

    human data on 4 of 4

    • 2 human trials
    • 2 small human trials

    01Luteinhuman trials

    the guide

    the macula's main yellow pigment, with zeaxanthin: a Florida group identified the human macular pigment as lutein and zeaxanthin in 1985 (Bone 1985), and in donor retinas lutein outnumbered zeaxanthin toward the edge of the retina while zeaxanthin led at the center (Bone 1988).

    evidence: the anchor human trial is AREDS2. it enrolled 4,203 people aged 50 to 85 with large drusen in both eyes, or large drusen in one eye and advanced age-related macular degeneration in the other, asked them to take the AREDS vitamin and zinc formula or a variant of it, and randomized them to lutein with zeaxanthin, fish oils, both, or placebo for a median of five years (AREDS2 2013). adding lutein and zeaxanthin did not significantly reduce progression to advanced disease in the primary analysis. in exploratory comparisons the pair did better than the beta-carotene it replaced (AREDS2 report 3, 2014), and the ten-year follow-up kept that direction (AREDS2 report 28, 2022). a 2023 Cochrane review rated the evidence for lutein and zeaxanthin against placebo as low certainty, with similar or slightly lower risk of progression (Evans 2023). across 20 trials, supplements raised macular pigment density in patients and in healthy people (Ma 2016), and in 115 healthy young adults a year of the pair improved recovery from a bright flash and color contrast but not glare disability, in a trial where three of the five authors worked for DSM Nutritional Products (Hammond 2014).

    watch for: AREDS2 tested lutein and zeaxanthin in place of beta-carotene because beta-carotene had raised lung cancer risk in smokers and former smokers and because the pair is part of the retina (AREDS2 report 3, 2014); in the trial more lung cancers appeared with beta-carotene, mostly in former smokers (AREDS2 2013), and at ten years beta-carotene nearly doubled the odds while lutein and zeaxanthin showed no significant rise (AREDS2 report 28, 2022). more is not always better: a woman in her sixties who had taken a lutein supplement for eight years on top of a very high-lutein diet developed glistening crystals in both foveas, without vision loss, and they began to clear in one eye after she stopped (Choi 2016). a rise in macular pigment density is a measurement, not proof that eye disease was prevented.

    02Zeaxanthinhuman trials, mostly with lutein

    the guide

    the other macular carotenoid, concentrated at the center: in donor retinas, zeaxanthin outnumbered lutein about 2.4 to 1 in the central quarter millimeter, and the ratio reversed toward the edge (Bone 1988). part of the central pigment is meso-zeaxanthin, which the Florida group proposed the retina makes from lutein (Bone 1997).

    evidence: every large trial gave it with lutein, so its own effect has not been separated: AREDS2 tested lutein plus zeaxanthin as one arm (AREDS2 2013). the trials that gave zeaxanthin alone are small. in a year-long trial of 60 patients with early atrophic macular degeneration, 57 of them men, the control arm took lutein rather than a placebo, and macular pigment rose in all three arms with no difference between them (Richer 2011); high-contrast acuity improved by 1.5 lines in the zeaxanthin arm, while the lutein arm did better on low-contrast acuity, contrast sensitivity and glare recovery. in eight people with macular telangiectasia type 2 given zeaxanthin alone for two years, macular pigment rose around the fovea but no objective gain in vision was found (Choi 2017).

    watch for: zeaxanthin's safety record in AREDS2 is the pair's record, since the trial never gave it alone (AREDS2 2013; AREDS2 report 28, 2022). in the two-year trial of zeaxanthin alone in macular telangiectasia, one woman developed crystals in the macula, with no change in visual acuity, and they cleared several months after she stopped (Choi 2017). the year-long zeaxanthin trial ran at a veterans' health care facility, enrolled almost only men, and had no placebo arm (Richer 2011).

    03Astaxanthinsmall human trials, mostly company-run

    the guide

    a red carotenoid from microalgae and seafood (EFSA 2020), sold for the eyes but not part of the macular pigment, which is lutein, zeaxanthin and meso-zeaxanthin (Bone 1985; Bone 1997). its eye claims rest on blood flow and eye-strain measures, not on pigment.

    evidence: small trials, most of them short and most run by companies or given in mixes. in 20 healthy volunteers, blood flow velocity in the choroid under the macula rose after four weeks compared with each person's own starting value, with no change on placebo; the abstract reports changes within each arm, not a comparison between arms (Saito 2012). in 64 children aged 10 to 14 with heavy screen use, an astaxanthin capsule beat placebo on an eye-strain questionnaire over 84 days but not on focusing distance, visual acuity or a tear test; seven of the 12 authors list AstaReal, the brand tested, or Fuji Chemical Industries as their employer (Hecht 2025). the longest eye trial gave astaxanthin only inside a mix with lutein, zeaxanthin and other antioxidants: in 145 people with age-related macular degeneration, those given the mix had better visual acuity at two years than those given no supplement, in an open-label trial (Piermarocchi 2012).

    watch for: EU food-safety experts found astaxanthin from supplements, at the level they assessed, plus a normal diet within their acceptable daily intake for adults but over it for children aged 10 to 13 (EFSA 2020), and EFSA's 2025 opinions on astaxanthin in foods hold only if children and adolescents do not take astaxanthin supplements on the same day (EFSA 2025). apart from eye-strain trials, the only study we found that gave astaxanthin on its own to people with an eye disease and followed the disease itself had no comparison group: 60 middle-aged and older adults with mild to moderate dry eye improved on symptom and tear-film scores over a month (Tian 2022).

    04Citicoline (CDP-choline)small human trials, mostly glaucoma

    the guide

    CDP-choline, an intermediate the body uses to build phosphatidylcholine for cell membranes; swallowed, it releases cytidine and choline (Secades 2006, a review whose first author worked in the medical department of the drug company Grupo Ferrer). it is approved in some countries as a stroke drug (Davalos 2012), and eye researchers test it as a protector of the retinal ganglion cells, the neurons that connect the eye to the brain and die in glaucoma (Prinz 2023).

    evidence: small glaucoma trials, most from eye clinics in Rome and Milan, using injections, an oral solution and eye drops. a Rome group reported better retinal and visual-cortex electrical responses after citicoline injections into muscle in 40 patients (Parisi 1999) and after eye drops or an oral solution in later small trials (Parisi 2015; Parisi 2026). in a three-year placebo-controlled trial of citicoline eye drops in 80 patients, 40 in each arm, loss on the standard 24-2 visual field test did not differ significantly, while loss on the central 10-2 field and in nerve fiber thickness was slower on citicoline; the eye-drop maker co-funded the trial and the authors called it a pilot (Rossetti 2020). a 2023 systematic review of 10 studies and 424 patients found no difference from controls in eye pressure, visual field, nerve fiber layer or retinal electrical response (Prinz 2023).

    watch for: the forms differ: the trials used injections, an oral solution and eye drops, not only the capsules sold as supplements. a phase 3 trial of citicoline eye drops, sponsored by their maker Omikron Italia, plans 1,000 patients and listed no results when read on 25 October 2026 (NCT05710198). outside the eye, two large citicoline trials found no benefit: 2,298 people after stroke, with no difference in safety measures from placebo (Davalos 2012), and 1,213 people after brain injury (Zafonte 2012).

    04At a glance

    form
    capsules, softgels and powders, as sold
    human data
    one large randomized trial with ten years of follow-up for lutein and zeaxanthin together, plus small trials of macular pigment; no large trial of zeaxanthin alone; small, mostly company-run or mixed-product trials for astaxanthin, the longest a two-year macular degeneration trial of a mix and the only dry-eye study of astaxanthin alone uncontrolled; small glaucoma trials for citicoline, mostly from Italian centers, and a systematic review that found no clear benefit
    evidence
    2 human trials, 2 small human trials
    level
    beginner
    timeline
    the trials ran from four weeks (the astaxanthin blood-flow study) to a median of five years in AREDS2, with ten years of follow-up; in a year-long trial in healthy young adults, blood lutein and zeaxanthin were up by the first three-month visit (Hammond 2014)
    schedule
    not applicable, no schedule published. AREDS2 ran a median of five years, and the citicoline eye-drop trial three years.

    05Why these together

    lutein and zeaxanthin sit together because they are the macular pigment and because AREDS2 gave them as a pair (Bone 1985; AREDS2 2013). astaxanthin and citicoline are here as eye supplements built on other claims: astaxanthin as a red carotenoid credited with blood-flow and eye-strain effects, citicoline as a membrane-building nutrient tested on the optic nerve in glaucoma. side by side, only the carotenoid pair has a large eye trial, and that trial was in people who already had macular degeneration.

    06Overlap

    the carotenoids overlap and citicoline does not. lutein and zeaxanthin are the same kind of pigment laid down in different parts of the macula (Bone 1988), and every large trial gave them together, so their effects cannot be told apart. astaxanthin is a carotenoid too, but the macular pigment is lutein, zeaxanthin and meso-zeaxanthin (Bone 1985; Bone 1997), and its eye trials mostly come as mixes: with lutein, zeaxanthin and other antioxidants in 145 people with macular degeneration (Piermarocchi 2012), with lutein and zeaxanthin in healthy screen workers in a trial whose first four authors work for Senju Pharmaceutical (Yoshida 2023), and with lutein and anthocyanins in a second screen-work trial (Kizawa 2021). citicoline is tested for a different job, protecting the retinal ganglion cells that die in glaucoma (Prinz 2023), and we found no trial pairing it with any of the three carotenoids (PubMed search, 25 October 2026).

    07 Conflicts

    beta-carotene with smoking: the original AREDS formula held beta-carotene, AREDS2 found more lung cancers with it, mostly in former smokers (AREDS2 2013), and at ten years beta-carotene nearly doubled the odds of lung cancer (AREDS2 report 28, 2022). zinc in AREDS-type formulas: zinc was linked to more genitourinary problems in men in AREDS (Evans 2023). lutein at very high long-term intake: one case of foveal crystals that began to clear after the supplement stopped (Choi 2016). zeaxanthin alone: in a two-year trial, one patient's macular crystals cleared after she stopped (Choi 2017). astaxanthin in children and adolescents: EFSA found combined intake from diet and supplements over its acceptable daily intake for children aged 10 to 13 and made its 2025 food opinions conditional on no same-day supplements for children and adolescents (EFSA 2020; EFSA 2025). citicoline in place of glaucoma treatment: the citicoline eye-drop trials in glaucoma gave the drops alongside pressure-lowering treatment (Rossetti 2020; Parisi 2015).

    08 What the evidence actually is

    lutein and zeaxanthin: one 4,203-person randomized trial, AREDS2, in which adding the pair to the AREDS formula did not significantly slow progression to advanced macular degeneration, while exploratory and ten-year analyses favored the pair over beta-carotene; Cochrane rates the evidence against placebo as low certainty; small trials show macular pigment rising, in healthy people too. zeaxanthin alone: small trials only, among them a year-long 60-person trial without a true placebo and a two-year trial in eight people with a rare macular disease, one of whom developed crystals that cleared after she stopped. astaxanthin: small trials, most of them short and most run by companies or given in mixes; the two-year macular degeneration trial gave it inside a mix, and the one dry-eye study of astaxanthin alone had no comparison group. citicoline: small glaucoma trials mostly from Italian centers, a three-year eye-drop trial significant on the central field test and nerve fiber thinning but not on the standard field test, a systematic review finding no clear benefit, and a phase 3 eye-drop trial with no results posted. all four together: never tested.

    09 What people report

    what trials measured, not reports: higher macular pigment density with lutein and zeaxanthin in patients and healthy people (Ma 2016); no significant extra slowing of advanced macular degeneration when the pair was added to the AREDS formula, though it did better than beta-carotene in exploratory comparisons (AREDS2 2013; AREDS2 report 3, 2014); lower eye-strain questionnaire scores with astaxanthin in a company-run children's trial (Hecht 2025); and electrical-response changes with citicoline in small glaucoma trials that a systematic review did not confirm (Prinz 2023).

    Who It's For

    people searching for eye health supplements who want to see what AREDS2 actually tested, and in whom, before reading about astaxanthin or citicoline

    What to Track

    eye strain after screen work on a fixed scale, glare and night-vision changes, any new blur or distortion in central vision, and the date of the last dilated eye exam

    Read the compound guides

    10Frequently Asked Questions

    the Eye Health Supplements bench sets lutein and zeaxanthin, the pair the AREDS2 trial tested, beside astaxanthin and citicoline. AREDS2 tested lutein with zeaxanthin in 4,203 people aged 50 to 85 who already had intermediate age-related macular degeneration, or advanced disease in one eye, so its results describe them, not healthy eyes. the bench gives no amounts and no timing. the Eye Health Supplements bench covers 4 compounds: Lutein, Zeaxanthin, Astaxanthin, Citicoline (CDP-choline).

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