Evidence map›Paper›PMID 41957314›Full record

ArticleGeroScience2026

Restoration of gamma center frequency via personalized entrainment marks cognitive preservation in early Alzheimer's disease.

Yeseung Park, Hyeonwook Chae, Euisuk Yoon, Yejung Kim, Ji Won Han, Se Joon Woo, Seunghyup Yoo, Ki Woong Kim

Abstract read
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In one paragraph

Article in GeroScience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Yeseung Park *Department of Neuropsychiatry, College of Medicine, and Seoul National University Bundang Hospital, Seoul National University, 82, Gumi-Ro 173 Beon-Gil, Bundang-Gu, Seongnam-Si, Gyeonggi-Do, 13620, Republic of Korea.
Hyeonwook Chae *School of Electrical Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, 34141, Republic of Korea.
Euisuk YoonDepartment of Neuropsychiatry, College of Medicine, and Seoul National University Bundang Hospital, Seoul National University, 82, Gumi-Ro 173 Beon-Gil, Bundang-Gu, Seongnam-Si, Gyeonggi-Do, 13620, Republic of Korea.
Yejung KimDepartment of Neuropsychiatry, College of Medicine, and Seoul National University Bundang Hospital, Seoul National University, 82, Gumi-Ro 173 Beon-Gil, Bundang-Gu, Seongnam-Si, Gyeonggi-Do, 13620, Republic of Korea.
Ji Won HanDepartment of Neuropsychiatry, College of Medicine, and Seoul National University Bundang Hospital, Seoul National University, 82, Gumi-Ro 173 Beon-Gil, Bundang-Gu, Seongnam-Si, Gyeonggi-Do, 13620, Republic of Korea.
Se Joon WooDepartment of Ophthalmology, College of Medicine, Seoul National University, Seoul, 03080, Republic of Korea.
Seunghyup Yoo *School of Electrical Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, 34141, Republic of Korea.
Ki Woong Kim *Department of Neuropsychiatry, College of Medicine, and Seoul National University Bundang Hospital, Seoul National University, 82, Gumi-Ro 173 Beon-Gil, Bundang-Gu, Seongnam-Si, Gyeonggi-Do, 13620, Republic of Korea. kwkimmd@snu.ac.kr.ORCID http://orcid.org/0000-0002-1103-3858

Funding

Korea Health Industry Development Institute RS-2025-02223212National Research Foundation of Korea NRF-2017R1A5A1014708
6 · The paper itself

Abstract

Gamma entrainment shows promise for Alzheimer's disease (AD) treatment in preclinical models, but human trials have yielded heterogeneous results. We hypothesized that the clinical efficacy of gamma entrainment depends on individual neurophysiological receptivity, specifically the capacity for neural circuit plasticity. In this open-label pilot study, we screened 37 individuals and enrolled 16 participants with early AD (CDR 0.5-1.0, amyloid-positive) who completed 12 weeks of home-based flickering light stimulation at individually optimized gamma frequencies (32-40 Hz). Pre- and post-intervention assessments included 64-channel EEG recordings and MMSE. Participants demonstrated dichotomous neurophysiological responses: 43.8% showed center frequency (CF) increase (increased CF [ICF+]) while 56.3% showed no change/decrease (non-increased CF [ICF-]). CF restoration was significantly associated with cognitive preservation (r = 0.52, p = 0.039). Notably, future responders exhibited distinct baseline signatures of "neural reserve," characterized by higher temporal gamma power (Cohen's d = 0.70-0.92) and stronger frontotemporal connectivity (Cohen's d = 1.11-1.47). Almost 30% of screened candidates failed to show baseline entrainment, highlighting a distinct "non-responsive" biological subtype. CF restoration following personalized gamma entrainment identifies a neurophysiological subtype capable of meaningful plasticity. Rather than a universal remedy, gamma entrainment appears to act on specific neural substrates preserved in a subset of patients. These findings suggest that baseline electrophysiological profiling could unlock gamma entrainment's therapeutic potential by stratifying likely responders for precision neuromodulation.

Indexed as

Alzheimer’s diseaseCenter frequencyFunctional connectivityGamma entrainmentNeural reservePrecision neuromodulation

Identifiers

PMID41957314

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.