4.6 Article

Repetitive Transcranial Magnetic Stimulation for Alzheimer's Disease Based on Apolipoprotein E Genotyping: Protocol for a Randomized Controlled Study

Journal

FRONTIERS IN AGING NEUROSCIENCE
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fnagi.2021.758765

Keywords

repetitive transcranial magnetic stimulation (rTMS); Alzheimer's disease (AD); APOE genotype; APOE4 carriers; randomized controlled Trail (RCT); preresults

Funding

  1. National Natural Science Foundation of China [82001447]
  2. China Postdoctoral Science Foundation [2020M682833]
  3. First Affiliated Hospital of Shantou University Medical College Supporting Funding
  4. Dengfeng Project for the Construction of High-Level Hospitals in Guangdong Province [202003-29]
  5. Li Ka Shing Foundation Cross-Disciplinary Research Grant [2020LKSFG11C]
  6. Beijing Tsinghua Changgung Hospital Fund [12015C1045]

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Currently, there is a lack of effective treatment strategies for Alzheimer's disease (AD) and repetitive transcranial magnetic stimulation (rTMS) can improve cognitive function in AD patients, but the effectiveness may vary depending on individual differences related to different apolipoprotein E (APOE) genotypes. Published clinical studies are highly heterogeneous, highlighting the need for well-developed randomized controlled trials (RCT) and precise treatment strategies.
To date, there is a shortage of effective treatment strategies for Alzheimer's disease (AD), and although repetitive transcranial magnetic stimulation (rTMS) can improve AD cognitive function, there are obvious individual differences, which may be related to different apolipoprotein E (APOE) genotypes. As the risk and pathogenesis of AD varies greatly among different genotypes precise treatment strategies should be implemented depending upon genotype, which has not been proved by clinical studies. Apart from that, the published clinical studies are highly heterogeneous, and therefore, systematic and well-developed randomized controlled Trails (RCT) and demonstration of precise administration protocols are required. To verify this hypothesis, this project designed a RCT study, and randomly divided apoE4 carrier AD and non-carrier AD into high-frequency rTMS (HF-rTMS) or low-frequency rTMS (LF-rTMS) treatment groups. Specifically, 80 patients with AD, namely 48 APOE4 carriers and 32 non-APOE4 carriers will be included in the study. After that, based on different stimulation frequencies of rTMS, they will be divided into the HF-rTMS group and the LF-rTMS group, when patients with AD will be randomly assigned to different treatment groups. After AD patients are involved in the study, their memory, cognition, anxiety, depression and activities of daily living will be tested before and during 2 weeks of rTMS. Furthermore, peripheral blood will be collected before and after treatment to detect changes in pathological indexes via MSD platform (Meso Scale Discovery), while 32-channel EEG data will be also collected to detect and analyze changes in gamma oscillation. In addition, these patients will be followed up for 6 months and their neuropsychological scale was also evaluated every month. At present, our study has included 18 AD patients (10 APOE4 carriers; 8 non-carriers). Our study is still in progress. The grouping has not been unblinded. But the preliminary data demonstrated that non-carriers had better MoCA score improvement than APOE4 carriers. The results indicated that the two populations of AD patients should be treated differently. Thus, this project will provide direction for precision rTMS in AD and also promotes a shift in relevant treatment philosophy.

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