| Literature DB >> 32037737 |
Yuya Takahashi1, Sho Shindo2, Takashi Kanbayashi1,3, Masahiro Takeshima1, Aya Imanishi1, Kazuo Mishima1,3.
Abstract
We examined whether symptoms of dementia are improved by olfactory nerve stimulation in Alzheimer type dementia patients. First, a stick-type olfactory identification ability test was performed in patients with Alzheimer type dementia, to select patients without olfactory dysfunctions. Then, these patients were randomly assigned into the intervention (n = 19) and the control groups (n = 17). To evaluate the effects of olfactory nerve stimulation, we exposed the intervention group to a disinfecting ethanol with added aroma extracts from ceder and the control group to the ethanol without the added aroma extracts. Each group underwent the intervention for 8 weeks, cognitive and behavioral functions were evaluated before and after treatments using the Neuropsychiatric Inventory (NPI), the Japanese version of Zarit Caregiver Burden interview (J-ZBI), and the Alzheimer's Disease Assessment Scale-cognitive subscale (ADAS-cog). A significant improvement was observed in the NPI score and J-ZBI in the intervention group compared to the control group at 4 and 8 weeks. On the other hand, there was no significant difference in the score of ADAS-cog. Exposure to cedar fragrance improved behavioral and psychological symptoms of dementia (BPSD) in Alzheimer type dementia and may reduce the burden of nursing care. In addition to its effectiveness, the procedure is simple and minimally invasive and would be a valuable non-pharmaceutical treatment.Entities:
Keywords: alzheimer type dementia; aroma extracts from ceder; cognitive disorders; cognitive neuoscience; dementia; olfactory nerve
Mesh:
Substances:
Year: 2020 PMID: 32037737 PMCID: PMC7292212 DOI: 10.1002/npr2.12096
Source DB: PubMed Journal: Neuropsychopharmacol Rep ISSN: 2574-173X
Figure 1A, Room Fragrance Type. B, Spray Type
Background of Intervention and control groups. There was no significant difference between the 2 groups in back ground
| Intervention group (N = 19) | Control group (N = 17) | |
|---|---|---|
| Female, n(%) | 12 (63.2) | 10 (58.8) |
| Age, mean(SD), yr | 76.2 (9.8) | 75.8 (7.8) |
| Duration of illness, mean(SD), yr | 2.2 (1.5) | 2.1 (0.9) |
| Education, mean(SD), yr | 9.7 (1.6) | 9.6 (2.4) |
| FAST, mean(SD) | 2.6 (1.1) | 3.0 (0.9) |
| People on dementia medications, n(%) | 15 (78.9) | 14 (82.4) |
| OSIT‐J score, mean(SD) | 10 (1.1) | 11 (1.2) |
Abbreviations: FAST, Functional Assessment Staging; OSIT‐J, the Odor Stick Identification Test for Japan; SD, standard deviation.
Figure 2A, In the intervention group, the NPI score improved significantly after 4 and 8 wks. B, In the intervention group, the Japanese version of the Zarit Caregiver Burden interview (J‐ZBI) significantly decreased after 4 and 8 wks. C, There was no significant difference in ADAS ‐ cog between the intervention and the control groups
Figure 3A, This figure shows the following 3 out of 10 items of NPI, in which significant differences were observed: agitation, anxiety, and irritability. B, This figure shows the following 6 out of 22 items of J‐ZBI, in which significantly differences were observed: (Q2) Not having enough time for yourself, (Q4) Embarrassed of patient behavior, (Q5) Feel angry around patient, (Q9) Feel strained around patient, (Q16) Feel unable to take care of the patient much and (Q19) Feel uncertain of what to do