Benefits
Cognition: Class Evidence for Ginkgo, Not for This Product
Cognitive trials of ginkgo have used other preparations, mainly EGb 761, and their results are mixed. Ginkgoselect Phytosome itself has not been tested for memory, attention or any other cognitive outcome in people. Higher blood levels of terpene lactones do not by themselves show a cognitive effect, and no study has measured how much of the extract reaches brain tissue.
Cerebral Blood Flow: Proposed Mechanism, Not Measured
Ginkgo is widely described as increasing cerebral microcirculation, but no study has measured cerebral blood flow, perfusion or microcirculation in anyone taking Ginkgoselect Phytosome. Treat this as a proposed mechanism, not a demonstrated effect.
Peripheral Circulation: Not Measured for This Product
No study of Ginkgoselect Phytosome has measured walking distance, skin temperature, limb blood flow or any other circulatory outcome in people. Peripheral circulation is a proposed use for ginkgo, not a demonstrated effect of this product, and this is not a treatment for any circulatory condition.
Older Adults: Six Months of Use Was Tolerated, Benefit Untested
In the one randomized trial in older adults, 240 mg a day of a Ginkgoselect extract for six months caused no adverse clinical effects, no rise in liver injury markers and no genomic damage signal against placebo. That trial measured safety only. Mild cognitive impairment is a medical diagnosis and no trial of this product has enrolled that population.
Antioxidant Activity: Rodent and Laboratory Data Only
The only antioxidant data on ginkgo phytosome come from rats. In rat brain regions it prevented the fall in superoxide dismutase, catalase, glutathione peroxidase and glutathione reductase caused by sodium nitrite. No antioxidant marker has been measured in people taking this product, and such a marker would be a laboratory reading rather than a health outcome.
Enhanced Bioavailability vs Standard Ginkgo
This is the one claim with direct human data. In a single-dose study the phospholipid complex produced roughly double the peak plasma level of ginkgo terpene lactones compared with the same uncomplexed extract, with a later peak. Better absorption is not itself a health benefit, and no trial has shown that it produces one.
Mechanism of action
Ginkgo Flavonoids and Terpene Lactones
Active compounds: flavonoids (quercetin glycosides, kaempferol) — antioxidants; terpene lactones (ginkgolides A, B, C, J, bilobalide) — unique to ginkgo, antagonize platelet activating factor (PAF). Neuroprotective effects have been reported in cell and rodent models, not in people taking this product.
Cerebral Blood Flow Enhancement
Ginkgo is proposed to increase cerebral microcirculation. Neither cerebral blood flow nor brain perfusion has been measured with Ginkgoselect Phytosome, so this is a mechanism hypothesis rather than a finding.
Platelet-Activating Factor (PAF) Antagonism
Ginkgolides antagonize PAF, which produces a modest antiplatelet effect. This is the basis of the bleeding risk described below. No vascular benefit of this product has been measured in people.
Antioxidant Protection
In rats, ginkgo phytosome kept brain levels of superoxide dismutase, catalase, glutathione peroxidase and glutathione reductase from falling under chemically induced hypoxia. This has not been measured in people taking this product.
Phytosome® Bioavailability
Enhanced absorption of ginkgo bioactives via Phytosome complex.
Clinical trials
Randomized, double-blind, placebo-controlled trial part-funded by Indena. 120 mg of Ginkgoselect Plus twice daily or placebo for 6 months; 47 people completed it (27 treatment, 20 placebo).
Elderly residents of three Italian nursing homes.
No adverse clinical effects and no rise in liver injury markers over 6 months. Micronucleus frequency (mean ratio 1.01, 95% CI 0.86 to 1.18) and DNA breaks on the comet assay (mean ratio 0.91, 95% CI 0.58 to 1.43) did not differ from placebo. Cognition was not an endpoint, so this trial shows the product was tolerated, not that it works.
Single-dose plasma measurement study run with Indena scientists (Morazzoni, Bombardelli) using LC-MS. Both forms supplied 9.6 mg of total terpene lactones. Not a placebo-controlled trial and no health outcome was recorded.
Adult volunteers; the paper does not report how many took part or describe their health status.
Peak plasma concentration of ginkgolides A and B plus bilobalide was roughly twice as high after the phospholipid complex as after the free extract (181.8 versus 85.0 in the paper's stated units), and the peak arrived later, at 180 to 240 minutes versus 120 minutes. Elimination half-life was similar for both. Absorption only: no cognitive, circulatory or other health outcome was measured.