Effect of the herbal extract combination Panax quinquefolium and Ginkgo biloba on attention-deficit hyperactivity disorder: a pilot study

M R Lyon, J C Cline, J Totosy de Zepetnek, J J Shan, P Pang, C Benishin, M R Lyon, J C Cline, J Totosy de Zepetnek, J J Shan, P Pang, C Benishin

Abstract

Objective: A combination herbal product containing American ginseng extract, Panax quinquefolium, (200 mg) and Ginkgo biloba extract (50 mg) (AD-FX; CV Technologies, Edmonton, Alta.) was tested for its ability to improve the symptoms of attention-deficit hyperactivity disorder (ADHD).

Design: Open study.

Patients: 36 children ranging in age from 3 to 17 years who fit the diagnostic criteria for ADHD.

Interventions: AD-FX capsules were taken twice a day on an empty stomach for 4 weeks. Patients were instructed not to change any other medications during the study.

Outcome measures: At the beginning of the study, after 2 weeks, and then at the end of the 4-week trial, parents completed the Conners' Parent Rating Scale--revised, long version, a questionnaire that assesses a broad range of problem behaviours (and was used as an indication of ADHD symptom severity).

Results: After 2 weeks of treatment, the proportion of the subjects exhibiting improvement (i.e., decrease in T-score of at least 5 points) ranged from 31% for the anxious-shy attribute to 67% for the psychosomatic attribute. After 4 weeks of treatment, the proportion of subjects exhibiting improvement ranged from 44% for the social problems attribute to 74% for the Conners' ADHD index and the DSM-IV hyperactive-impulsive attribute. Five (14%) of 36 subjects reported adverse events, only 2 of which were considered related to the study medication.

Conclusions: These preliminary results suggest AD-FX treatment may improve symptoms of ADHD and should encourage further research on the use of ginseng and Ginkgo biloba extracts to treat ADHD symptoms.

References

    1. Pharmacopsychiatry. 1997 Sep;30 Suppl 2:117-24
    1. J Pharm Pharmacol. 1992 Jan;44(1):24-7
    1. Int J Clin Pharmacol Res. 1984;4(2):89-93
    1. J Int Med Res. 1985;13(6):342-8
    1. J Ethnopharmacol. 1986 Apr-May;16(1):15-22
    1. J Abnorm Child Psychol. 1988 Oct;16(5):511-25
    1. Biochem Pharmacol. 1992 Dec 15;44(12):2395-401
    1. Neurochem Int. 1992 Jul;21(1):1-5
    1. J Formos Med Assoc. 1993 Feb;92(2):133-8
    1. Planta Med. 1993 Aug;59(4):302-7
    1. Am J Psychiatry. 1993 Dec;150(12):1792-8
    1. J Pharm Pharmacol. 1994 Apr;46(4):316-8
    1. Brain Res. 1994 Jun 27;649(1-2):7-11
    1. Life Sci. 1995;56(4):213-22
    1. Am J Orthopsychiatry. 1994 Oct;64(4):545-53
    1. Psychopharmacol Bull. 1995;31(1):147-58
    1. Life Sci. 1996;58(16):1315-21
    1. J Am Acad Child Adolesc Psychiatry. 1996 Mar;35(3):319-24
    1. J Assoc Physicians India. 1995 Nov;43(11):760-3
    1. Pharmacopsychiatry. 1996 Jul;29(4):150-5
    1. Psychol Bull. 1997 Jan;121(1):65-94
    1. Nature. 1997 Apr 24;386(6627):827-30
    1. JAMA. 1997 Oct 22-29;278(16):1327-32
    1. Chem Pharm Bull (Tokyo). 1989 Feb;37(2):481-4
    1. Planta Med. 1989 Oct;55(5):429-33
    1. Aust N Z J Psychiatry. 1991 Jun;25(2):277-83
    1. Psychiatr Clin North Am. 1992 Mar;15(1):1-27
    1. Am J Chin Med (Gard City N Y). 1977 Spring;5(1):1-23

Source: PubMed

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