Affiliations 

  • 1 Duke-NUS Singapore, National Neuroscience Institute, Singapore, Singapore
  • 2 Hasan Sadikin General Hospital, Bandung, Indonesia
  • 3 School of Medicine and Health Science, Atma Jaya Catholic University of Indonesia, Jakarta, Indonesia
  • 4 Changi General Hospital, Singapore, Singapore
  • 5 Singapore General Hospital, Singapore, Singapore
  • 6 Department of Medicine, National University of Singapore, Singapore, Singapore
  • 7 Department of Pharmacology, National University of Singapore, Singapore, Singapore
  • 8 St Luke's Medical Center, Quezon City, Philippines
  • 9 University of Santo Tomas, Metro Manila, Philippines
  • 10 Can Tho University of Medicine and Pharmacy, Can Tho, Vietnam
  • 11 Hospital Sultan Ismail, Johor, Malaysia
  • 12 Hospital Kuala Lumpur, Kuala Lumpur, Malaysia
  • 13 Subang Jaya Medical Centre, Selangor, Malaysia
  • 14 Ramathibodi Hospital, Bangkok, Thailand
  • 15 Faculty of Pharmacy, Mahidol University, Bangkok, Thailand
  • 16 Siriraj Hospital, Bangkok, Thailand
  • 17 Beijing Tiantan Hospital, Capital Medical University, Beijing, China
  • 18 Sahara Hospital, Lucknow, India
  • 19 Alexian Hospital, Krefeld, Germany
CNS Neurosci Ther, 2019 02;25(2):288-298.
PMID: 30648358 DOI: 10.1111/cns.13095

Abstract

BACKGROUND: The Ginkgo biloba special extract, EGb 761® has been widely used in the treatment of neuropsychiatric disorders, including Alzheimer's disease (AD).

METHODS: To guide clinical practice in the Asian region, the Asian Clinical Expert Group on Neurocognitive Disorders compiled evidence-based consensus recommendations regarding the use of EGb 761® in neurocognitive disorders with/without cerebrovascular disease.

RESULTS: Key randomized trials and robust meta-analyses have demonstrated significant improvement in cognitive function, neuropsychiatric symptoms, activities of daily living (ADL) and quality of life with EGb 761® versus placebo in patients with mild-to-moderate dementia. In those with mild cognitive impairment (MCI), EGb 761® has also demonstrated significant symptomatic improvement versus placebo. World Federation of Societies of Biological Psychiatry guidelines list EGb 761® with the same strength of evidence as acetylcholinesterase inhibitors and N-methyl-D-aspartate (NMDA) antagonists e.g. memantine (Grade 3 recommendation; Level B evidence). Only EGb 761® had Level B evidence in improving cognition, behaviour, and ADL in both AD and vascular dementia patients. Safety analyses show EGb 761® to have a positive risk-benefit profile. While concerns have been raised regarding a possible increased bleeding risk, several randomized trials and two meta-analyses have not supported this association.

CONCLUSIONS: The Expert Group foresee an important role for EGb 761® , used alone or as an add-on therapy, in the treatment of MCI and dementias, particularly when patients do not derive benefit from acetylcholinesterase inhibitors or NMDA antagonists. EGb 761® should be used in alignment with local clinical practice guidelines.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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