| Literature DB >> 35899271 |
Yijun Zhan1, Qinhui Fu1, Jian Pei1, Mingxia Fan2, Qiurong Yu2, Miao Guo2, Houguang Zhou3, Tao Wang4, Liaoyao Wang1, Yaoxin Chen1.
Abstract
Background: Functional brain imaging changes have been proven as potential pathophysiological targets in early-stage AD. Current longitudinal neuroimaging studies of AD treated by acupuncture, which is one of the growingly acknowledged non-pharmacological interventions, have neither adopted comprehensive acupuncture protocols, nor explored the changes after a complete treatment duration. Thus, the mechanisms of acupuncture effects remain not fully investigated. Objective: This study aimed to investigate the changes in spontaneous brain activity and functional connectivity and provide evidence for central mechanism of a 12-week acupuncture program on mild-to-moderate AD.Entities:
Keywords: Alzheimer's disease; Donepezil; acupuncture; fractional amplitude of low-frequency fluctuation (fALFF); functional connectivity (FC); functional magnetic resonance imaging (fMRI)
Year: 2022 PMID: 35899271 PMCID: PMC9309357 DOI: 10.3389/fneur.2022.912923
Source DB: PubMed Journal: Front Neurol ISSN: 1664-2295 Impact factor: 4.086
Baseline characteristics of participants.
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| 61.82 ± 6.118 | 60.52 ± 7.420 | 60.97 ± 7.274 |
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| 9 (45.0%) | 8 (40.0%) | 10 (50.0%) |
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| 15 (12) | 14 (14) | / |
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| illiteracy | 2 (10.0%) | 2 (10.0%) | 2 (10.0%) |
| Primary school | 5 (25.0%) | 3 (15.0%) | 4 (20.0%) |
| Middle school | 4 (20.0%) | 7 (35.0%) | 5 (25.0%) |
| High school | 5 (25.0%) | 3 (15.0%) | 4 (20.0%) |
| College | 4 (20.0%) | 5 (25.0%) | 5 (25.0%) |
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| Hypertension | 9 (45.0%) | 10 (50.0%) | 9 (45.0%) |
| Heart disease | 4 (20.0%) | 5 (25.0%) | 4 (20.0%) |
| Diabetes | 5 (25.0%) | 5 (25.0%) | 4 (20.0%) |
| Hyperlipidemia | 8 (40.0%) | 7 (35.0%) | 7 (35.0%) |
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| 3 (15.0%) | 2 (10.0%) | 3 (15.0%) |
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| 5 (25.0%) | 4 (20.0%) | 4 (20.0%) |
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| 17 (5) | 18 (6) | 27 (4) |
Regions showing significant fALFF value differences between healthy subject and AD.
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| Inferior temporal gyrus | R | 37 | 48 | −70 | −4 | −7.03 | 68 |
| Inferior frontal gyrus | R | / | 45 | 5 | 26 | −6.63 | 16 |
| Superior temporal gyrus | R | 22 | 66 | −43 | 11 | −5.94 | 22 |
| Postcentral gyrus | R | 3 | 45 | −22 | 53 | −5.95 | 155 |
| Middle frontal gyrus | R | 6 | 30 | −1 | 50 | −5.54 | 30 |
| Middle occipital gyrus | R | 19 | 39 | −79 | 8 | −5.01 | 18 |
| Superior temporal gyrus | L | / | −57 | 8 | 2 | −4.83 | 14 |
| Precuneus | L | / | −9 | −73 | 35 | −4.76 | 14 |
R, right; L, left; MNI, Montreal Neurological Institute. p < 0.05, FDR–corrected.
Figure 1Regions showing significant fALFF value differences between healthy subjects and AD. The results were FDR-corrected with p < 0.05.
Regions showing significant fALFF value changes between the treatment group and control group.
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| Precuneus | R | / | 6 | −58 | 65 | 8.94 | 15 |
| Inferior temporal gyrus | L | / | −51 | −46 | −25 | 8.08 | 27 |
| Lingual gyrus | L | / | −18 | −82 | −22 | 7.89 | 9 |
| Thalamus | L | / | −12 | −10 | 11 | 7.30 | 6 |
R, right; L, left; MNI, Montreal Neurological Institute. p < 0.001, uncorrected.
Figure 2Regions showing significant fALFF value changes between the treatment group and control group. The results were uncorrected with p < 0.001.
Change in ADAS–cog values within and between groups (mean ± SD).
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| Week 0 | 19.32 ± 1.89 | 19.98 ± 1.59 |
| Week 12 | 16.52 ± 1.47 | 18.08 ± 1.49 |
| ΔWeek 12–Week 0 | 2.80 ± 1.51 | 1.90 ± 1.36 |
p < 0.05 within group;
p < 0.05 between groups.
Regions showing significant correlation in the change in fALFF in the treatment group to the change in ADAS–cog.
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| Inferior temporal gyrus | L | / | −24 | −45 | 0 | 7.57 | 7 |
| Middle temporal gyrus | R | / | 42 | −78 | 21 | −5.06 | 6 |
R, right; L, left; MNI, Montreal Neurological Institute. p < 0.05, FWE–corrected.
Figure 3Regions showing significant correlation in the change in fALFF in the treatment group to the change in ADAS-cog. (A) Multiple regression correlation results of significant correlation between fALFF value changes and ADAS-cog value changes in the treatment group (p < 0.001, FWE-corrected). (B) Pearson correlation results of the change in fALFF value of the left inferior temporal gyrus and the change in ADAS-cog value. (C) Pearson correlation results of the change in fALFF value of the right middle temporal gyrus and the change in ADAS-cog value.
Figure 4Seed point of the right precuneus for functional connection analysis.
Regions showing significant FC changes between the treatment group and control group.
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| Middle temporal gyrus | R | / | 51 | −42 | −3 | 10.84 | 5 |
| Middle temporal gyrus | L | 21 | −57 | −48 | 3 | 7.86 | 5 |
| Middle frontal gyrus | L | / | −12 | 42 | 24 | 6.15 | 7 |
R, right; L, left; MNI; Montreal Neurological Institute. p < 0.001, uncorrected.
Figure 5Regions showing significant FC changes between the treatment group and control group. The results were uncorrected with 5 < 0.001.
Regions showing significant correlation in the change in FC in the treatment group to the change in ADAS–cog.
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| Superior occipital gyrus | R | / | 21 | −102 | 6 | −4.42 | 12 |
| Superior temporal gyrus | R | 41 | 48 | −33 | 9 | −6.07 | 18 |
| Precuneus | L | / | −12 | −57 | 51 | −8.00 | 34 |
R, right; L, left; MNI, Montreal Neurological Institute. p < 0.001, FDR–corrected.
Figure 6Regions showing significant correlation in the change in FC in the treatment group to the change in ADAS-cog. (A) Multiple regression correlation results of significant correlation between FC changes and ADAS-cog value changes in the treatment group (p < 0.001, FDR-corrected). (B) Pearson correlation results of the change in FC to the right superior occipital gyrus and the change in ADAS-cog value. (C) Pearson correlation results of the change in FC to the right superior temporal gyrus and the change in ADAS-cog value. (D) Pearson correlation results of the change in FC to the right superior temporal gyrus and the change in ADAS-cog value.