Skip to content

Advertisement

  • Commentary
  • Open Access

Herbal therapy: a new pathway for the treatment of Alzheimer's disease

Alzheimer's Research & Therapy20102:30

https://doi.org/10.1186/alzrt54

©  BioMed Central Ltd 2010

  • Published:

Abstract

It has been a clinical challenge to treat Alzheimer's disease (AD). In the present commentary we discuss whether herbal therapy could be a novel treatment method for AD on the basis of results from clinical trials, and discuss the implications for potential therapy for AD pathophysiology. There is evidence to suggest that single herbs or herbal formulations may offer certain complementary cognitive benefits to the approved drugs. The current evidence supporting their use alone, however, is inconclusive or inadequate owing to many methodological limitations. Herbal mixtures may have advantages with multiple target regulation compared with the single-target antagonist in the view of traditional Chinese medicine. Several clinical trials using herbal mixtures are being conducted in China and will hopefully show promising results for treating AD in the near future.

Keywords

  • Mild Cognitive Impairment
  • Memantine
  • Clinical Dementia Rate
  • Aniracetam
  • Ginkgo Biloba Extract

Introduction

The ultimate aim of Alzheimer's disease (AD) therapy is to stop or slow down the disease progression. Cholinesterase inhibitors have a modest clinical effect on the symptoms, however, and memantine - the currently available N-methyl-D-aspartate receptor antagonist - does not prevent the deterioration of dementia [1, 2]. Finding an effective method to treat AD still poses a significant clinical challenge.

Herbal medicine has long been used in China as therapy for dementia. The Complete Work of Jingyue published in 1624 contains the earliest known description in the world of a herbal therapeutic strategy for dementia. In the past 10 years, however, herbal drugs have seldom been approved for use alone in treating dementia. Overall, systematic review has identified a few single herbs and herbal formulations as possible effective medicine for AD (Table 1). According to the current evidence, some of these therapies show promising results in terms of their cognitive benefits. In the present commentary we discuss whether herbal therapy could be a novel pathway to treat AD, on the basis of the results from clinical trials, and the implications for potential therapy of AD pathophysiology.
Table 1

Different herbs and formulations effective in the treatment of Alzheimer's disease

Product

Composition

Design

Outcome measure

Source

Huperzine A

An extract from Lycopodium

A 12-week randomized, double-blind, placebo-controlled trial

ADAS-cog, MMSE, CIBIC-plus, ADL of patients with mild to moderate AD

Zhang and colleagues [7]

Gingko Biloba

EGb 761

A 24-week randomized, placebo- controlled, double-blind study

MMSE and CGI in patients with mild to moderate AD

Mazza and colleagues [4]

Panax ginseng

Ginsenosides

A 12-week open-label, randomized double-blind, placebo-controlled study

ADAS and MMSE scores of AD patients

Lee and colleagues [17]

Salvia officinalis

Leaf extract containing monoterpene, flavonoids, polyphenol

A 4-month, parallel-group, placebo- controlled trial

ADAS-cog and CDR in patients with mild to moderate AD

Akhondzadeh and colleagues [11]

Ba Wei Di Hunag Wan

Powder of Rehmannia with another seven plants mixed with honey

An 8-week randomized, double-blind, placebo-controlled trial

MMSE and Barthel Index scores in patients with mild to severe dementia

Iwasaki and colleagues [15]

Yi-Gan San formula

A mixture of seven different rootstock and branches, lyophilized dry extract

A 4-week randomized, observer-blind, controlled trial

NPI and ADL in patients with mild to severe dementia

Iwasaki and colleagues [16]

AD, Alzheimer disease; ADAS-cog, Alzheimer disease assessment scale-cognitive subscale; ADL, activities of daily living; CDR, Clinical Dementia Rating; CGI, Clinical Global Impression; CIBIC-plus, Clinician's Interview-Based Impression of Change plus Caregiver Input; MMSE, mini-mental state examination; NPI, neuropsychiatric Inventory.

Single herbs or extracts from herbs

Ginkgo biloba

Ginkgo biloba extract is among the most widely used complementary therapies. A Cochrane review included 36 trials of gingko biloba, but most trials were small and of duration <3 months [3]. Nine trials were of 6 months duration and of adequate size, and were conducted to a reasonable standard. Of the four most recent trials to report results, three studies found no difference between Ginkgo biloba, at different doses, and placebo [3], and one study found very large treatment effects in favor of Ginkgo biloba, but the trial sample size was very small [4]. Another recent trial reported negative results in reducing cognitive decline in older adults with normal cognition or with mild cognitive impairment [5]. The current overall evidence that Ginkgo has a predictable and clinically significant benefit for people with dementia or cognitive impairment therefore seems inconsistent and unreliable.

Serrate clubmoss

Huperzine A extracted from the serrate clubmoss herb is a potent, reversible and selective inhibitor of acetyl-cholinesterase. Considering the available evidence from six trials, Huperzine A seems to have some beneficial effects on improvement of general cognitive function, global clinical status, behavioral disturbance and functional performance, with no obvious serious adverse events for patients with AD [6]. Only one study was of adequate quality and size, but the period during this study that found very large treatment effects was only 12 weeks [7]. Overall the current evidence supporting clinical use of Huperzine A is presently inconclusive or inadequate.

Ginseng

Panaxi ginseng's main active ingredient is panaxsaponin, which can enhance psychomotor and cognitive performance, and can benefit AD by improving brain cholinergic function, reducing the level of Aβ and repairing damaged neuronal networks [8]. The high-dose ginseng group showed statistically significant improvement on the Alzheimer Disease Assessment Scale (ADAS) and Clinical Dementia Rating (but not on the Mini-Mental State Examination) at the end of the study, when compared with the control group. This study was poorly designed, with an insufficient description of randomization and without blinding. Furthermore, the sample size was small (n = 15 for each group), and there was also a confounding effect due to concurrently administered western medications [9]. The evidence for ginseng as a treatment of AD is thus scarce and inconclusive. Further rigorous trials seem warranted [10].

Salvia officinalis

Salvia officinalis has been used in herbal medicine for many centuries. After 4 months of treatment, salvia officinalis extract produced a significantly better outcome on cognitive functions than placebo - as seen on the ADAS cognitive subscale and the Clinical Dementia Rating Sum of Boxes scale in patients with mild to moderate AD aged between 65 and 80 years [11]. There were no significant differences between salvia officinalis and placebo in terms of the observed side effects. In addition, salvia officinalis may reduce agitation in patients. More high-quality large-scale randomized controlled trials are needed, however, for further determination of the herb's efficacy [11].

Herbal formulations or mixtures of herbal ingredients

Herbal formulations or mixtures of herbal ingredients may have advantages with multiple target regulation compared with the single target antagonist in the view of traditional Chinese medicine, although there have been few clinical trials examining the efficacy and safety of herbal formulations in AD patients.

Shenwu capsule, a mixture of six herbs that is thought to reduce amyloid cytotoxicity, increased the memory score from baseline (n = 83) - but without significant difference from aniracetam (n = 83) - in a 12-week phase II trial for patients with mild cognitive impairment [12]. A phase III trial is now underway. Stilbene glycoside, an extract of Shenwu capsule, has been evaluated in a phase I trial for AD. Further results for both of these formulations will be available in the next few years.

GEPT, a combination of five active components extracted from Chinese herbs, may be valuable for the treatment of AD - reducing the level of Aβ via the inhibition of γ-secretase (presenilin-1) and the promotion of insulin-degrading enzyme and neprilysin, which has been reported in the brain of APPV717I transgenic mice [13]. A 24-week preliminary study of GEPT showed a significant improvement on cognitive function in patients with amnestic mild cognitive impairment, an early stage of AD (n = 101), consistently across different cognitive scales; for example, an improvement in the ADAS cognitive subscale from baseline of -4.19 points (95% confidence interval = -5.74 to -2.63), which declined at 24 weeks of follow-up after the GEPT withdrawal. This level of efficacy was comparable with that of -4.23 points found in the subjects taking Donepezil (n = 100) (Figure 1) [14]. GEPT is planned to apply for a shape II trial.
Figure 1
Figure 1

Cognitive function in patients with amnestic mild cognitive impairment. Mean change of the Alzheimer Disease Assessment Scale cognitive subscale (ADAS-cog) score from baseline after treatment in patients with amnestic mild cognitive impairment (aMCI). ITT-LOCF, Intent to Treat population Using the Last Observation Carried Forward Method.

Furthermore, the herbal preparations Ba Wei Di Huang Wan and Yi-Gan San are individually reported to significantly improve cognition or behavior and function on the Mini-Mental State Examination, the Neuropsychiatric Inventory and the Barthel Index in the patients with AD [15, 16].

Conclusion

Single herbs or formulations may be able to complement approved drugs for AD. No serious adverse events have been reported. The current evidence to support their use alone, however, is inconclusive or inadequate. This uncertainty is mainly caused by methodological limitations such as poor study design, relatively small sample sizes without a power calculation, inappropriate outcome measures and primary and secondary end-point selection, and invalid statistical analysis. In addition, the herbs' potential value for prevention and treatment of AD only results from symptomatic changes and short treatment periods (< 6 months). Several studies currently underway or in early-stage development in China to evaluate herb mixtures will hopefully show promising results in the near future.

Abbreviations

AD: 

Alzheimer disease

ADAS: 

Alzheimer Disease Assessment Scale.

Declarations

Acknowledgements

The present work was supported by the 111 Project (No. B08006), the Beijing Cooperative Study Project of the Capital Foundation of Medical Developments (No. 2005-SF-1-007), New Century Excellent Talents in University (No. NCET-07-0117) and the Innovative Research Team of Alzheimer's Disease and Other Neurodegenerative Diseases of the Ministry of Education of China (No. IRT-08-010).

Authors’ Affiliations

(1)
BUCM Neurology Centre, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, 100700, China
(2)
Department of Preclinical Medicine, Hubei University of Chinese Medicine, Wuhan, 430065, China
(3)
Clinical Neuroscience Research Group, The University of Manchester, Hope Hospital, Stott Lane, Salford, Manchester, M6 8HD, UK
(4)
Institute of Clinical Medicine, China Academy of Chinese Medical Sciences, Beijing, 100700, China

References

  1. Reisberg B, Doody R, Stöffler A, Schmitt F, Ferris S, Möbius HJ, Memantine Study Group: Memantine in moderate-to-severe Alzheimer's disease. N Engl J Med. 2003, 348: 1333-1341. 10.1056/NEJMoa013128.View ArticlePubMedGoogle Scholar
  2. Porsteinsson AP, Grossberg GT, Mintzer J, Olin JT, Memantine MEM-MD-12 Study Group: Memantine treatment in patients with mild to moderate Alzheimer's disease already receiving a cholinesterase inhibitor: a randomized, double-blind, placebo-controlled trial. Curr Alzheimer Res. 2008, 5: 83-89. 10.2174/156720508783884576.View ArticlePubMedGoogle Scholar
  3. Birks J, Grimley Evans J: Ginkgo biloba for cognitive impairment and dementia. Cochrane Database Syst Rev. 2009, 1: CD003120-PubMedGoogle Scholar
  4. Mazza M, Capuano A, Bria P, Mazza S: Ginkgo biloba and donepezil: a comparison in the treatment of Alzheimer's dementia in a randomized placebo-controlled double-blind study. Eur J Neurol. 2006, 13: 981-985. 10.1111/j.1468-1331.2006.01409.x.View ArticlePubMedGoogle Scholar
  5. Snitz BE, O'Meara ES, Carlson MC, Arnold AM, Ives DG, Rapp SR, Saxton J, Lopez OL, Dunn LO, Sink KM, DeKosky ST, Ginkgo Evaluation of Memory Study I: Ginkgo biloba for preventing cognitive decline in older adults: a randomized trial. JAMA. 2009, 302: 2663-2670. 10.1001/jama.2009.1913.PubMed CentralView ArticlePubMedGoogle Scholar
  6. Li J, Wu HM, Zhou RL, Liu GJ, Dong BR: Huperzine A for Alzheimer's disease. Cochrane Database Syst Rev. 2008, 2: CD005592-PubMedGoogle Scholar
  7. Zhang Z, Wang X, Chen Q, Shu L, Wang J, Shan G: Clinical efficacy and safety of huperzine Alpha in treatment of mild to moderate Alzheimer disease, a placebo-controlled, double-blind, randomized trial [in Chinese]. Zhonghua Yi Xue Za Zhi. 2002, 82: 941-944.PubMedGoogle Scholar
  8. Chen F, Eckman EA, Eckman CB: Reductions in levels of the Alzheimer's amyloid beta peptide after oral administration of ginsenosides. Faseb J. 2006, 20: 1269-1271. 10.1096/fj.05-5530fje.View ArticlePubMedGoogle Scholar
  9. Fu LM, Li JT: A systematic review of single Chinese herbs for Alzheimer's disease treatment. Evid Based Complement Alternat Med. 2009,Google Scholar
  10. Lee MS, Yang EJ, Kim JI, Ernst E: Ginseng for cognitive function in Alzheimer's disease: a systematic review. J Alzheimers Dis. 2009, 18: 339-344.PubMedGoogle Scholar
  11. Akhondzadeh S, Noroozian M, Mohammadi M, Ohadinia S, Jamshidi AH, Khani M: Salvia officinalis extract in the treatment of patients with mild to moderate Alzheimer's disease: a double blind, randomized and placebocontrolled trial. J Clin Pharm Ther. 2003, 28: 53-59. 10.1046/j.1365-2710.2003.00463.x.View ArticlePubMedGoogle Scholar
  12. Zhong J, Tian JZ, Zhu AH, Yang CZ: Clinical study on a randomized, doubleblind control of Shenwu gelatin capsule in treatment of mild cognitive impairment [in Chinese]. Zhongguo Zhong Yao Za Zhi. 2007, 32: 1800-1803.PubMedGoogle Scholar
  13. Tian J, Shi J, Zhang L, Yin J, Hu Q, Xu Y, Sheng S, Wang P, Ren Y, Wang R, Wang Y: GEPT extract reduces a beta deposition by regulating the balance between production and degradation of amyloid-beta in APPV717I transgenic mice. Curr Alzheimer Res. 2009, 6: 118-131. 10.2174/156720509787602942.View ArticlePubMedGoogle Scholar
  14. Miao YC: Part 5: a randomized, double-blind and parallel control study of GEPT extract in the treatment of amnestic mild cognitive impairment. PhD thesis. 2008, Beijing University of Chinese Medicine, 95-117.Google Scholar
  15. Iwasaki K, Kobayashi S, Chimura Y, Taguchi M, Inoue K, Cho S, Akiba T, Arai H, Cyong JC, Sasaki H: A randomized, double-blind, placebo-controlled clinical trial of the Chinese herbal medicine 'Ba wei di huang wan' in the treatment of dementia. J Am Geriatr Soc. 2004, 52: 1518-1521. 10.1111/j.1532-5415.2004.52415.x.View ArticlePubMedGoogle Scholar
  16. Iwasaki K, Satoh-Nakagawa T, Maruyama M, Monma Y, Nemoto M, Tomita N, Tanji H, Fujiwara H, Seki T, Fujii M, Arai H, Sasaki H: A randomized, observerblind, controlled trial of the traditional Chinese medicine yi-gan san for improvement of behavioral and psychological symptoms and activities of daily living in dementia patients. J Clin Psychiatry. 2005, 66: 248-252. 10.4088/JCP.v66n0214.View ArticlePubMedGoogle Scholar
  17. Lee ST, Chu K, Sim JY, Heo JH, Kim M: Panax ginseng enhances cognitive performance in Alzheimer disease. Alzheimer Dis Assoc Disord. 2008, 22: 222-226. 10.1097/WAD.0b013e31816c92e6.View ArticlePubMedGoogle Scholar

Copyright

© BioMed Central Ltd 2010

Comments

Advertisement

Alzheimer's Research & Therapy

ISSN: 1758-9193