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Published on: August 4, 2018
An exploratory, open-label, randomized, multicenter trial of hachimijiogan for mild Alzheimer's disease
Mosaburo Kainuma1, Shinji Ouma2, Shinobu Kawakatsu3
1Department of Japanese Oriental Medicine, Toyama University Hospital, Toyama, Japan.
Insights
Hachimijiogan (HJG) may help slow cognitive decline in mild Alzheimer's disease (AD) when used with standard treatments. This study suggests HJG could be a beneficial add-on therapy for managing AD progression.
Area of Science:
- Neurology
- Pharmacology
- Geriatrics
Background:
- Alzheimer's disease (AD) is a leading cause of dementia, necessitating early intervention.
- Current treatments for mild AD, such as acetylcholinesterase inhibitors (AChEIs), have limited efficacy.
- Novel therapeutic strategies for mild AD are urgently needed.
Purpose of the Study:
- To evaluate the effectiveness of hachimijiogan (HJG), a traditional Japanese herbal medicine, as an adjunct therapy for mild AD.
- To assess HJG's impact on cognitive function and daily living activities in patients with mild AD.
Main Methods:
- An exploratory, open-label, randomized, multicenter trial involving patients with mild AD (MMSE > 21).
- Participants received either AChEI plus HJG extract (7.5 g/day) or AChEI alone.
- Primary outcome: change in Alzheimer's Disease Assessment Scale-cognitive component-Japanese version (ADAS-Jcog) at 6 months.
Main Results:
- The study analyzed data from 69 patients (34 HJG, 35 control).
- No significant difference in ADAS-Jcog change was observed between groups at 6 months (difference: 1.29, p=0.293).
- Subgroup analyses suggested potential benefits in women and older adults at 3 months, but results were not statistically significant.
Conclusions:
- Hachimijiogan (HJG) shows potential as an adjuvant therapy for acetylcholinesterase inhibitors in mild Alzheimer's disease.
- Further research is warranted to confirm HJG's role in delaying cognitive decline in AD patients.
Abstract:
Background: Alzheimer's disease (AD) is a progressive neurodegeneration and is the most prevalent form of dementia. Intervention at an early stage is imperative. Although three acetylcholinesterase inhibitors (AChEIs) are currently approved for the treatment of mild AD, they are not sufficiently effective. Novel treatments for mild AD are of utmost importance. Objective: To assess the effectiveness of hachimijiogan (HJG), a traditional Japanese herbal medicine (Kampo), in the treatment of mild AD. Methods: This exploratory, open-label, randomized, multicenter trial enrolled patients with mild AD whose score on the Mini Mental State Examination (MMSE) was over 21points. All participants had been taking the same dosage of AChEI for more than 3 months. The participants were randomly assigned to an HJG group taking HJG extract 7.5 g/day in addition to AChEI or to a control group treated only with AChEI. The primary outcome was the change from baseline to 6 months post treatment initiation on the Alzheimer's Disease Assessment Scale-cognitive component- Japanese version(ADAS-Jcog). The secondary outcomes were change from baseline of the Instrumental Activity of Daily Life (IADL), Apathy scale, and Neuropsychiatric Inventory (NPI) -Q score. Results: Among the 77 enrollees, the data of 69(34 HJG and 35 control)were available for analysis. The difference in the change of ADAS-Jcog from baseline to 6 months of the HJG and control groups was 1.29 (90% Confidence interval (CI), -0.74 to 3.32 p = 0.293). In the subgroup analysis, the differences in the change from baseline to 3 and 6 months for women were 3.70 (90% CI ,0.50 to 6.91, p = 0.059) and 2.90 (90% CI,0.09 to 5.71, p = 0.090), respectively. For patients over 65 years, the difference at 3 months was 2.35 (90%CI, 0.01 to 4.68 p = 0.099). No significant differences were found between the HJG and control groups in IADL score, Apathy scale, or NPI-Q score. Conclusion: Although not conclusive, our data indicate that HJG has an adjuvant effect for acetylcholinesterase inhibitors and that it delays the deterioration of the cognitive dysfunction of mild Altzheimer's disease patients. Clinical Trial Registration: http://clinicaltrials.gov Japan Registry of clinical trials, identifier jRCTs 071190018.
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