Ginkgo Biloba
In short
Summary of findings for quick reference
Ginkgo biloba is a living fossil, the sole survivor of an ancient lineage, but its tradition story is narrower than its age suggests. The old medicinal use is the seed (bai guo), recorded in Chinese materia medica from the Song dynasty around the 12th century and carried through the Yuan and Ming and into Japanese Kampo, for cough, asthmatic breathing and bladder complaints. That use is the seed, not the leaf. The cognitive and circulatory use that this entry is built around is something quite different: a standardised leaf extract developed in Germany from the 1960s. It is a modern rediscovery on a different part of the tree, so the antiquity of the seed does not belong to it.
What ginkgo does have is unusually strong modern regulatory standing for the leaf. The European Medicines Agency (EMA HMPCEuropean Medicines Agency, Committee on Herbal Medicinal Products (HMPC)) monograph on ginkgo leaf carries a well-established use indication for cognitive impairment and mild dementia, alongside a separate traditional use indication for minor circulatory disorders such as heaviness of the legs and cold hands and feet. The research behind it used EGb 761, one specific standardised dry leaf extract with declared flavone glycoside and terpene lactone content and a strict cap on ginkgolic acids. A generic ginkgo capsule without that declared standardisation is not the same thing as the studied extract.
The modern evidence is real but narrow. The signal is for symptomatic treatment of mild dementia with one specific extract at one specific dose, and the picture across trials is mixed. Ginkgo did not prevent dementia in a large six year study of healthy older adults, and the circulation evidence is weak. It also interacts with blood thinning, and the standard advice is to stop it at least two weeks before surgery. Ginkgo is best understood as a modern standardised leaf extract with a recognised but limited place, not as an ancient cognitive remedy and not as a way to prevent dementia.
Clinical evidence ↔ Historical significanceWe display two separate evidence categories: clinical evidence from modern trials and historical significance from documented healing tradition. Both are valuable, but they answer different questions.Read more
In every encyclopedia entry we evaluate two distinct categories of evidence. Clinical evidence as used in trials meets a narrower but scientifically essential bar. At the same time, the hundreds of thousands of plant species worldwide have only partially been captured and tested in modern studies.
Alongside the trial picture our researchers compile a comprehensive overview of where and since when a plant has been used across different traditions of natural medicine. When a plant has been used as a medicinal plant in many cultures across many generations, that historical significance deserves to be visible too.
Our position: a truly informative overview emerges only when both categories sit side by side. We communicate transparently what counts as what.
Overview
Ginkgo (Ginkgo biloba) is one of the oldest tree species on the planet, a single surviving lineage with no close living relatives. The fan shaped leaves are the part used in modern phytotherapy. Standardised leaf extracts have been studied in European clinical research since the 1970s, primarily around cognitive function in older adults and around peripheral circulation. Ginkgo trees grow well in Vienna and in many other European cities, where they are valued as ornamental street trees rather than as a foraged medicine.
The European Medicines Agency (EMA HMPCEuropean Medicines Agency, Committee on Herbal Medicinal Products (HMPC)) recognises a well established medicinal use for a specific dry extract of Ginkgo leaf (EGb 761) in the symptomatic treatment of mild dementia. That is a medicinal product indication assessed by a regulator. It is not a claim that any food supplement on the shelf will reproduce that effect. A separate traditional use indication covers symptoms of capillary fragility (heaviness in the legs, mild swelling). Outside those regulatory frames the picture is mixed, and the entry treats it that way.
History
Ginkgo biloba is a living fossil. The species has been part of the East Asian flora for about two hundred million years and survived in cultivation around Buddhist temples in China and Japan long before Western botanists encountered it in the 18th century. The seeds and leaves both have a place in traditional Chinese medicine, but it is the leaf, not the seed, that anchors modern European phytotherapy.
Modern Ginkgo phytotherapy is a 20th century German project. The standardised leaf extract EGb 761, developed at the Schwabe laboratories from the 1960s onwards, defined the dosage form used in most clinical trials and remains the reference extract in the EMA HMPCEuropean Medicines Agency, Committee on Herbal Medicinal Products (HMPC) well established use monograph. The documented medicinal record for the species begins in the Chinese materia medica, where the seed (bai guo) is recorded for cough and wheezing, and the tree itself reached Europe only in the 18th century, long after the medieval herbal writers. It entered the European market as a modern phytopharmaceutical, and the entry treats it that way.
Mechanism
Standardised Ginkgo leaf extracts contain two main groups of bioactives. Flavone glycosides (around twenty four per cent in EGb 761, with kaempferol, quercetin and isorhamnetin derivatives as the main components) and terpene lactones (around six per cent in EGb 761, made up of ginkgolides A, B and C, plus bilobalide). The standardised label values (twenty four per cent flavone glycosides, six per cent terpene lactones) are the regulatory standard for EGb 761 and the closely related LI 1370 extract. The extract is also defined by a maximum content of ginkgolic acids (below 5 parts per million) because of allergenic concerns at higher levels.
Proposed mechanisms in the published literature include vasodilation and improved microcirculation, antioxidant activity at the level of mitochondrial membranes, and platelet activating factor antagonism (mainly attributed to ginkgolide B). The platelet activating factor pathway is the mechanism most often cited in discussions of the bleeding interactions covered in the safety section. The link between any specific bioactive and a specific clinical effect in people is plausible but not firmly established, and a meaningful share of the older mechanistic work is in vitro or in animal models rather than in controlled human trials.
The Cochrane review by Birks and Grimley Evans (2009) summarised more than thirty randomised controlled trials of Ginkgo extracts in people with cognitive impairment or dementia. The conclusion was mixed. Some trials, particularly those using EGb 761 at 240 mg per day over six months, showed measurable improvements on cognitive scales and on clinician rated impressions of change. Other trials showed no benefit over placebo. The Cochrane authors described the overall evidence as inconsistent and rated the methodological quality of many older trials as low to moderate.
The Ginkgo Evaluation of Memory (GEM) study reported by DeKosky et al. in 2008 was a large multi centre trial of EGb 761 at 240 mg per day for the prevention of all cause dementia in older adults. It enrolled more than three thousand participants over six years and did not find a preventive benefit. The combined reading across Birks 2009 and DeKosky 2008 is that there is a real signal for symptomatic treatment of mild dementia with one specific extract at one specific dose (which is why EMA HMPCEuropean Medicines Agency, Committee on Herbal Medicinal Products (HMPC) recognised the well established use indication) and no convincing evidence that Ginkgo prevents dementia in healthy adults. A separate small body of research covers peripheral arterial disease (intermittent claudication, walking distance); the signal there is weak and inconsistent.
Evidence
| Outcome | Class | Grade | Effect | Studies |
|---|---|---|---|---|
| Cognitive function in mild dementiaBirks and Grimley Evans 2009 Cochrane review of 30+ RCTs in cognitive impairment and dementia. Some trials with EGb 761 at 240 mg per day for six months showed measurable improvements; others showed no benefit. Overall evidence inconsistent; many older trials low to moderate methodological quality.Older adults with mild cognitive impairment or mild dementia | EmergingEmerging research. Early small trials suggest an effect but await replication. | CEvidence quality grade C. Mixed or limited evidence. Small trials, signals, or traditional use under an EMA HMPC traditional-use monograph. This is an evidence rating, not a product endorsement. | Mixed Effect | |
| Peripheral arterial disease, walking distanceSmall body of trials on standardised Ginkgo extract in intermittent claudication. Signals on pain free walking distance are weak and inconsistent across studies. Used as the anchor for the EMA HMPC traditional use indication on capillary fragility.Adults with intermittent claudication | EmergingEmerging research. Early small trials suggest an effect but await replication. | CEvidence quality grade C. Mixed or limited evidence. Small trials, signals, or traditional use under an EMA HMPC traditional-use monograph. This is an evidence rating, not a product endorsement. | Mixed Effect | |
| Dementia prevention in healthy older adultsDeKosky et al. 2008 GEM study followed more than three thousand older adults on EGb 761 240 mg per day for six years and did not find a preventive benefit for all cause dementia.Healthy older adults without baseline dementia | InsufficientInsufficient data. No reliable trials or traditional sources available. | DEvidence quality grade D. Preliminary signal. A single small trial, pilot result, or laboratory or animal model. Clinical relevance unclear. This is an evidence rating, not a product endorsement. | No Effect | |
| Bleeding events with anticoagulants or antiplateletsPublished case reports of post operative bleeding, intracranial bleeding, and increased bleeding tendency when Ginkgo extract is combined with warfarin, aspirin, clopidogrel, or chronic NSAIDs. Standard recommendation is to stop two weeks before any surgery.Adults on warfarin, aspirin, clopidogrel, or chronic NSAIDs | TraditionalTraditional use. Long-standing folk practice or EMA HMPC traditional-use monograph. | FEvidence quality grade F. Evidence of harm at typical dose. Use not recommended. This is an evidence rating, not a product endorsement. | Net Detriment |
Usage
Forms and preparation
In modern phytotherapy the relevant form is a standardised dry leaf extract in capsules or tablets. EGb 761 and the closely related LI 1370 are the two extracts that account for most of the clinical research. When you buy a Ginkgo product, look on the label for the standardisation: twenty four per cent flavone glycosides and six per cent terpene lactones is the reference. Products that do not declare this standardisation are not comparable to the research extracts and should not be assumed to reproduce the same effects. Fresh Ginkgo leaves and home made teas are not the same product as the standardised extract. Fresh leaf preparations contain ginkgolic acids at much higher levels than the regulated extract maximum (5 ppm), with a real allergenic risk on contact and an irritant risk when ingested. The fan leaves you see on a Vienna street tree are not a foraging target. Take Ginkgo only as a standardised commercial extract from a reputable manufacturer.
Dosage
The dose used in the EMA HMPC well established use indication and in the bulk of the cognitive trials is 240 mg per day of a standardised dry leaf extract (EGb 761 or LI 1370), taken as one dose or split into two doses with food. Lower doses (120 mg per day) appear in some older trials and remain on the market, mostly for the traditional use indication. Effects in the well established use indication are assessed over months, not days. Most trials in this space ran six months or longer. Start at the manufacturer recommended dose and do not stack Ginkgo on top of other blood thinning supplements (for example fish oil at high doses, garlic at high doses, vitamin E at high doses). If you are on a prescription anticoagulant, an antiplatelet, or chronic non steroidal anti inflammatory drugs, do not start Ginkgo without talking to your prescribing doctor first. The bleeding interaction is the gating safety question, not the dose itself.
Safety
Look-alikes
FAQs
Is a generic Ginkgo supplement the same as EGb 761?
Not necessarily. EGb 761 is a specific standardised dry leaf extract with declared content of flavone glycosides (around twenty four per cent) and terpene lactones (around six per cent), and a regulatory cap on ginkgolic acids (below 5 parts per million). LI 1370 is the closely related extract used in some other trials. Generic Ginkgo capsules without a declared standardisation are not comparable to the research extracts. Look on the label and pick a standardised product if you want a research aligned dose.
Can I take Ginkgo together with low dose aspirin?
Not without talking to your doctor first. Both Ginkgo and aspirin act on platelet function, and case reports of bleeding events (including intracranial bleeding) have been published for this combination. If you are on a daily low dose of aspirin for cardiovascular prevention you are by definition in the population where the combined antiplatelet effect matters. Talk to your prescribing doctor before adding Ginkgo, and do not start it on your own.
I have surgery scheduled. When should I stop Ginkgo?
Stop Ginkgo at least two weeks before the procedure, and tell your anaesthetist and surgeon that you have taken it. The two week washout is the standard recommendation in anaesthesia and surgical guidelines on herbal supplements. The same rule applies to dental extractions and other invasive procedures. If your surgery is sooner than two weeks away, stop immediately and inform the team.
Can I make tea from fresh Ginkgo leaves in autumn?
We do not recommend it. Fresh Ginkgo leaves contain ginkgolic acids at much higher concentrations than the regulatory maximum allowed for the standardised extract (below 5 parts per million). Ginkgolic acids are allergenic on skin contact and irritant on ingestion. The clinical research behind the EMA HMPC indications used the standardised extract, not home made tea. The yellow autumn leaves on Vienna street trees are not a foraging target. Take Ginkgo only as a standardised commercial extract from a reputable manufacturer.
Legal notice: The depiction of historical significance and traditional use is context within our encyclopedia and not a health claim for any product, not a treatment promise, and not a substitute for medical advice. What may be stated on product labels, product pages, or in advertising is governed by the applicable legal requirements.