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One row per finding: what was tested, which way the result went, and how the study was built. The answer by area, and where the studies disagree, are on the main page.
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Showing 2 of 382 rows. One row per study per exposure: a study that tested two different things appears twice, once for each.
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| Exposure | Question | Direction | Outcome measured | Design | People | Effect size, as the source reported it | Source |
|---|---|---|---|---|---|---|---|
| Ginkgo biloba Diet and supplements | Treatment |
Mixed
whyIn dementia there may be small-to-moderate benefits at six months (low-certainty evidence, I2 88-96%); in MCI ginkgo probably has little or no effect (moderate certainty); in subjective cognitive complaints the effect is very uncertain. Adverse events were similar to placebo. |
Global clinical status, cognition and activities of daily living at 6 months in dementia and in MCI; adverse events | meta-analysis | 10,613 | Dementia Thirteen studies (3288 participants) compared ginkgo with placebo for dementia. At six months, low-certainty evidence suggests that people taking ginkgo may have better global clinical status on a six-point Likert scale (lower is better; MD -0.06, 95% CI -1.00 to -0.20; I² = 88%; 5 studies, 1359 participants), better cognition measured by decreases on a short cognitive performance test (Syndrom-Kurztest; MD -1.86, 95% CI -3.48 to -0.24; I² = 96%; 9 studies, 2801 participants) ... Mild cognitive impairment ... moderate-certainty evidence suggests that ginkgo probably has little to no effect on global clinical status measured on the Clinical Dementia Rating Scale (MD -0.03, 95% CI -0.06 to 0.01; 3 studies, 631 participants; I² = 0%) |
The Cochrane database of systematic reviews
2026 ✓ Peer-reviewed PMID 41641880 |
| Omega-3 / fish and fish oil Diet and supplements | Prevention |
Mixed
whyThe biochemical primary outcome was met (DHA raised the CSF DHA-to-arachidonic-acid ratio versus placebo), but there was no difference in cognition or brain volume over 24 months. The authors recommend against further supplementation trials of this kind. |
CSF DHA/AA ratio at 6 months (primary, target engagement); cognition and brain volumes at 24 months | phase 2 trial | 365 | DHA supplementation increased CSF DHA/AA ratio at 6 months vs placebo (0.17 [95% CI 0.15-0.18] vs -0.02 [95% CI -0.04 to -0.0004]; difference 0.19 [95% CI 0.16-0.21]; p < 0.0001), independent of APOE ε4 status (interaction p = 0.71). Dropout was 38%, mainly due to COVID-19. No treatment differences were observed in brain volumes or cognitive performance over 24 months |
EBioMedicine
2026 ✓ Peer-reviewed PMID 42315445 |