Brain & Focus
Ginkgo and Memory: 277 Dementia Cases on Ginkgo, 246 on Placebo

Key takeaways
- GEM: 3,069 participants aged 75+, median follow-up 6.1 years, 120 mg twice daily versus identical placebo.
- Dementia: 277 cases on ginkgo, 246 on placebo. HR 1.12 (95% CI 0.94-1.33, P=0.21). Alzheimer's HR 1.16.
- Cognitive decline measured separately in the same cohort: no difference in memory, attention, visuospatial, language or executive function.
- Memory decline z-scores: 0.043 per year on ginkgo, 0.041 on placebo. Effectively identical.
- No effect modification by age, sex, race, education, APOE*E4 allele or baseline mild cognitive impairment.
- Cochrane: the evidence for predictable, clinically significant benefit is inconsistent and unreliable — but ginkgo appears safe.
Ginkgo is sold for memory. So somebody built the trial that would settle it, and then ran it for six years.
3,069 people, aged 75 and over. 120 mg twice daily or an identical placebo. Five academic medical centres. Assessment every six months. Median follow-up 6.1 years. Dropout and loss to follow-up: 6.3%.
The dementia result
| Ginkgo | Placebo | |
|---|---|---|
| Dementia cases | 277 | 246 |
| Rate per 100 person-years | 3.3 | 2.9 |
Hazard ratios, all three of them:
- All-cause dementia: 1.12 (95% CI 0.94–1.33, P=0.21)
- Alzheimer’s disease: 1.16 (0.97–1.39, P=0.11)
- Progression from mild cognitive impairment: 1.13 (0.85–1.50, P=0.39)
None is statistically significant, so this is not evidence that ginkgo causes dementia, and the page will not claim it.
But notice where all three landed: above 1. A preventive that worked would produce numbers below it. Three independent outcomes, three point estimates pointing the same wrong way.
The result that matters more to the person buying it
Almost nobody takes ginkgo to prevent a dementia diagnosis in fifteen years. They take it because they want their memory to be sharper.
So the same cohort was analysed again, this time for rate of cognitive decline across five domains.
| Domain | Ginkgo | Placebo |
|---|---|---|
| Memory | 0.043/yr | 0.041/yr |
| Attention | 0.043 | 0.048 |
| Visuospatial | 0.107 | 0.118 |
| Language | 0.045 | 0.041 |
| Executive function | 0.092 | 0.089 |
Nothing. Not a smaller effect than hoped — no separation at all, in any domain, over six years.
And the two summary scales agreed: 3MSE P=0.71, ADAS-Cog P=0.97.
They also looked for the subgroup
The usual rescue for a null trial is “it works for the right people.” GEM checked, and reported no significant effect modification by age, sex, race, education, APOE*E4 allele status, or baseline mild cognitive impairment — all P above 0.05.
The APOE*E4 one is the interesting entry. That allele is the best-known genetic risk factor for Alzheimer’s, and it is the first place you would look for a group that benefits.
There was not one.
So why does ginkgo have the reputation?
Cochrane answers this, and the answer is about the shape of the older literature rather than about the plant:
Many of the early trials used unsatisfactory methods, were small, and publication bias cannot be excluded. The evidence that Ginkgo biloba has predictable and clinically significant benefit for people with dementia or cognitive impairment is inconsistent and unreliable.
Small positive studies get published, quoted and repeated for years. The large null trial arrives later and travels a fraction as far.
What this is not
It is not a safety warning. Cochrane states that ginkgo appears to be safe in use with no excess side effects compared with placebo, and GEM reported similar adverse effect profiles in both groups.
That distinction is worth holding, because it is a different verdict from a supplement where the efficacy evidence is null and there is a safety signal. Here the cost of taking it is the money and the false reassurance.
And it is not a claim about every formulation. GEM tested 120 mg of extract twice daily. That is a standard studied dose taken for over six years, not a token one — but it is one preparation, and pretending the result covers every product ever sold would be overreaching.
No product box
There is nothing to link here.
We place product links where the evidence points at a specific purchase — a form and a dose that produced a result in a trial. This article’s evidence is a 6.1-year trial in 3,069 people that found no effect on dementia and no effect on cognitive decline in any domain measured.
A buy button under that would tell you our buttons mean nothing.
Frequently asked questions
Does ginkgo biloba improve memory?
Not in the trial designed to answer it. The Ginkgo Evaluation of Memory study followed 3,069 community-dwelling participants aged 72 to 96 for a median of 6.1 years on 120 mg of extract twice daily or identical placebo, and measured cognitive change across five domains. Annual rates of decline did not differ between groups in any of them. For memory the annual z-score decline was 0.043 on ginkgo (95% CI 0.034 to 0.051) and 0.041 on placebo (95% CI 0.032 to 0.050). Attention, visuospatial abilities, language and executive function were the same story. The authors' conclusion is that ginkgo at 120 mg twice daily did not result in less cognitive decline in older adults with normal cognition or with mild cognitive impairment.
Does it prevent dementia?
No, and the direction of the result is worth knowing. Of 523 participants who developed dementia, 277 were in the ginkgo group and 246 on placebo. The rate was 3.3 per 100 person-years on ginkgo against 2.9 on placebo, giving a hazard ratio of 1.12 with a 95% confidence interval of 0.94 to 1.33 and P=0.21. For Alzheimer's disease the hazard ratio was 1.16 (0.97 to 1.39, P=0.11), and for progression to dementia among those with mild cognitive impairment, 1.13 (0.85 to 1.50, P=0.39). None of these is statistically significant, so this is not evidence that ginkgo causes dementia. What it does mean is that every point estimate landed above 1, which is the opposite of what a preventive would produce.
Was the trial big enough to detect a real effect?
That was the point of running it. The trial's own framing notes that adequately powered clinical trials testing ginkgo's effect on dementia incidence were lacking, which is why GEM was built: 3,069 participants, five academic medical centres, a median of 6.1 years of follow-up, assessment every six months, and dropout plus loss to follow-up of only 6.3%. This is not a small study that failed to find something. It is a large, long, well-retained study that looked hard and found nothing.
Then why does ginkgo have such a strong reputation?
Because the earlier literature was weaker than it looked, and Cochrane says so directly. Its review of ginkgo for cognitive impairment and dementia concluded that many of the early trials used unsatisfactory methods, were small, and publication bias cannot be excluded, and that the evidence ginkgo has predictable and clinically significant benefit for people with dementia or cognitive impairment is inconsistent and unreliable. Small positive studies get published and repeated; large null ones arrive later and travel less far.
Does it work better for some people than others?
GEM tested that explicitly and found no such group. There was no significant effect modification of treatment on the rate of cognitive decline by age, sex, race, education, APOE*E4 allele status or baseline mild cognitive impairment, all with P above 0.05. The APOE*E4 result is the notable one, since that allele is the best-known genetic risk factor for Alzheimer's disease and would be the obvious place to look for a subgroup that benefits. There was not one.
Is ginkgo dangerous?
That is not what this evidence says, and the distinction matters. Cochrane's review states that ginkgo biloba appears to be safe in use with no excess side effects compared with placebo, and GEM itself reported that adverse effect profiles were similar in both groups. So this is a page about something that does not work rather than something that harms. The cost of taking it is the money and the false reassurance, not a safety risk. That is a different verdict from supplements where the trial evidence is null and the safety signal is not.
What about a different dose or a different extract?
GEM used 120 mg of extract twice daily, which is a standard studied dose rather than a token one, for over six years. This page cannot tell you what a different dose or preparation would do, because that is not what was tested, and it would be dishonest to imply the null result generalises to every formulation ever sold. What can be said is that the largest, longest and best-retained trial of ginkgo for this purpose used a conventional dose and duration, and found nothing on either dementia incidence or cognitive decline.
Why is there no product recommendation here?
Because the conclusion does not support one. We place product links on articles where the evidence points at a specific purchase, such as a form and dose a trial actually used to produce a result. This article concludes that a 6.1-year trial in 3,069 people found no effect on dementia and no effect on cognitive decline in any domain. Putting a buy button under that would tell you our buttons mean nothing.
Sources
Every claim above is drawn from these primary sources. Last checked July 2026.
- 1.DeKosky ST, Williamson JD, Fitzpatrick AL, Kronmal RA, Ives DG, Saxton JA, Lopez OL, Burke G, Carlson MC, Fried LP, Kuller LH, Robbins JA, Tracy RP, Woolard NF, Dunn L, Snitz BE, Nahin RL, Furberg CD. Ginkgo biloba for prevention of dementia: a randomized controlled trial. JAMA. 2008;300(19):2253-62. PMID 19017911. Randomised, double-blind, placebo-controlled trial in 5 US academic medical centres between 2000 and 2008, median follow-up 6.1 years. 3,069 community volunteers aged 75 or older with normal cognition (n=2,587) or mild cognitive impairment (n=482), assessed every 6 months for incident dementia. Twice-daily 120 mg extract of G. biloba (n=1,545) or placebo (n=1,524). 523 individuals developed dementia (246 receiving placebo, 277 receiving G. biloba), with 92% of cases classified as possible or probable Alzheimer's disease, or AD with evidence of vascular disease of the brain. Dropout and loss to follow-up 6.3%; adverse effect profiles similar in both groups. Overall dementia rate 3.3 per 100 person-years on G. biloba versus 2.9 on placebo. Hazard ratio for all-cause dementia 1.12 (95% CI 0.94-1.33, P=.21); for AD 1.16 (95% CI 0.97-1.39, P=.11); for progression to dementia in participants with MCI 1.13 (95% CI 0.85-1.50, P=.39). Authors' conclusion: G. biloba at 120 mg twice a day was not effective in reducing either the overall incidence rate of dementia or AD incidence in elderly individuals with normal cognition or those with MCI. Checked 14 August 2026
- 2.Snitz BE, O'Meara ES, Carlson MC, Arnold AM, Ives DG, Rapp SR, Saxton J, Lopez OL, Dunn LO, Sink KM, DeKosky ST; Ginkgo Evaluation of Memory (GEM) Study Investigators. Ginkgo biloba for preventing cognitive decline in older adults: a randomized trial. JAMA. 2009;302(24):2663-70. PMID 20040554. Same GEM cohort: 3,069 community-dwelling participants aged 72 to 96, 6 US academic medical centres, median follow-up 6.1 years, 120 mg twice daily (n=1,545) versus identical-appearing placebo (n=1,524). Annual rates of decline in z scores did not differ between groups in any domain: memory (0.043; 95% CI 0.034-0.051 vs 0.041; 95% CI 0.032-0.050), attention (0.043; 0.037-0.050 vs 0.048; 0.041-0.054), visuospatial abilities (0.107; 0.097-0.117 vs 0.118; 0.108-0.128), language (0.045; 0.037-0.054 vs 0.041; 0.033-0.048) and executive functions (0.092; 0.086-0.099 vs 0.089; 0.082-0.096). For the 3MSE and ADAS-Cog, rates of change varied by baseline cognitive status but there were no differences between treatment groups (3MSE P=.71; ADAS-Cog P=.97). No significant effect modification by age, sex, race, education, APOE*E4 allele or baseline mild cognitive impairment (all P>.05). Conclusion: compared with placebo, G. biloba 120 mg twice daily did not result in less cognitive decline. Checked 14 August 2026
- 3.Birks J, Grimley Evans J. Ginkgo biloba for cognitive impairment and dementia. Cochrane Database Syst Rev. 2009;(1):CD003120. PMID 19160216. Authors' conclusions verbatim: 'Ginkgo biloba appears to be safe in use with no excess side effects compared with placebo. Many of the early trials used unsatisfactory methods, were small, and publication bias cannot be excluded. The evidence that Ginkgo biloba has predictable and clinically significant benefit for people with dementia or cognitive impairment is inconsistent and unreliable.' Cited here both for the safety statement and for the explanation of why the earlier literature looked more favourable than it was. Checked 14 August 2026