Evidence map›Paper›PMID 40414756›Full record

ArticleThe journal of prevention of Alzheimer's disease2025

Serum BDNF and progression to MCI in cognitively normal older adults: A prospective cohort study.

Kyungtae Kim, Min Soo Byun, Dahyun Yi, Joon Hyung Jung, Bo Kyung Sohn, Gijung Jung, Hyejin Ahn, Jun-Young Lee, Yun-Sang Lee, Yu Kyeong Kim and 3 more

Abstract read
In one paragraph

Article in The journal of prevention of Alzheimer's disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 pooled it
–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

6 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Review
  6. Article
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

13 authors.

Kyungtae KimDepartment of Neuropsychiatry, Seoul National University Hospital, Seoul, Republic of Korea. Electronic address: youthdukt@naver.com.
Min Soo ByunDepartment of Neuropsychiatry, Seoul National University Hospital, Seoul, Republic of Korea; Department of Psychiatry, Seoul National University College of Medicine, Seoul, Republic of Korea.
Dahyun YiInstitute of Human Behavioral Medicine, Medical Research Center, Seoul National University, Seoul, Republic of Korea.
Joon Hyung JungDepartment of Psychiatry, Chungbuk National University Hospital, Cheongju, Republic of Korea. Electronic address: bban29@naver.com.
Bo Kyung SohnDepartment of Psychiatry, Inje University Sanggye Paik Hospital, Seoul, Republic of Korea. Electronic address: bksohn1221@daum.net.
Gijung JungInstitute of Human Behavioral Medicine, Medical Research Center, Seoul National University, Seoul, Republic of Korea. Electronic address: gijung1004@naver.com.
Hyejin AhnInterdisciplinary program of cognitive science, Seoul National University, Seoul, Republic of Korea.
Jun-Young LeeDepartment of Neuropsychiatry, SMG-SNU Boramae Medical Center, Republic of Korea. Electronic address: benji@snu.ac.kr.
Yun-Sang LeeDepartment of Nuclear Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea. Electronic address: wonza43@snu.ac.kr.
Yu Kyeong KimDepartment of Nuclear Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea. Electronic address: yk3181@snu.ac.kr.
Kwangsik NhoIndiana Alzheimer's Disease Research Center, Indiana University School of Medicine, Indianapolis, USA; Department of Radiology and Imaging Sciences, Indiana University School of Medicine, Indianapolis, USA. Electronic address: knho@iu.edu.
Dong Young LeeDepartment of Neuropsychiatry, Seoul National University Hospital, Seoul, Republic of Korea; Department of Psychiatry, Seoul National University College of Medicine, Seoul, Republic of Korea; Institute of Human Behavioral Medicine, Medical Research Center, Seoul National University, Seoul, Republic of Korea; Interdisciplinary program of cognitive science, Seoul National University, Seoul, Republic of Korea. Electronic address: selfpsy@snu.ac.kr.
KBASE Research Group

Funding

KBASE2: Korean Brain Aging Study, Longitudinal Endophenotypes and Systems BiologyU01AG072177 · NIA · INDIANA UNIVERSITY INDIANAPOLIS · PI LEE, DONG YOUNG, NHO, KWANGSIK TIMOTHY · 2021 to 2025
$11.2M
NIA NIH HHS U01 AG072177
6 · The paper itself

Abstract

backgroundBrain-derived neurotrophic factor (BDNF) is the most abundant neurotrophin in the mammalian brain. Preclinical studies suggest that BDNF influences the pathophysiology of Alzheimer's disease. In humans, higher blood BDNF levels have been associated with a lower risk of dementia. However, the relationship between serum BDNF levels and the progression to mild cognitive impairment (MCI) in cognitively normal (CN) individuals remains uncertain.

objectivesTo examine whether higher serum BDNF levels in CN older adults are associated with a reduced incidence of MCI over a 4-year follow-up period and to identify potential moderators of this relationship.

designLongitudinal analyses were conducted using follow-up data from the Korean Brain Aging Study for Early Diagnosis and Prediction of Alzheimer's Disease, an ongoing prospective cohort study. Data were collected from January 1, 2014, to May 31, 2021, and analyzed from May 1, 2023, to September 30, 2023.

settingCommunity and memory clinic setting.

participantsA total of 274 CN older adults aged 55-90 years were included at baseline. MEASUREMENT: Progression to MCI over the 4-year follow-up period.

resultsAmong the 274 participants, 26 developed MCI during follow-up. The high BDNF group had a significantly lower incidence of MCI compared to the low BDNF group (hazard ratio [HR], 0.27; 95 % confidence interval [CI], 0.11-0.69; P = 0.006). This association persisted even after adjusting for BDNF Val66Met polymorphism, amyloid PET positivity, vascular risk factors, cholesterol levels, triglycerides, homocysteine, BMI, smoking, alcohol, TBI history, CES-D, and MMSE scores (HR, 0.14; 95 % CI, 0.05-0.40; P < 0.001). Subgroup analyses further revealed that the association was significant only in women (HR, 0.12; 95 % CI, 0.03-0.48; P = 0.002), individuals aged <75 years (HR, 0.16; 95 % CI, 0.03-0.77; P = 0.022), those with less than a college degree (HR, 0.23; 95 % CI, 0.07-0.74; P = 0.013), and amyloid PET-negative (HR, 0.29; 95 % CI, 0.11-0.72; P = 0.014) individuals.

conclusionsThese findings suggest a protective role of BDNF against clinical progression to MCI in cognitively healthy older individuals. This effect appears to be more prominent in women, as well as in relatively younger, less educated, and amyloid PET-negative individuals.

Indexed as

Brain-Derived Neurotrophic FactorCognitive DysfunctionAgedAged, 80 and overBiomarkersCognitionDisease ProgressionFemaleHumansIncidenceLongitudinal StudiesMaleMiddle AgedProspective StudiesBDNF protein, humanBiomarkersBrain-Derived Neurotrophic FactorAlzheimer's diseaseBrain-derived neurotrophic factor (BDNF)Cognitively normalMild cognitive impairment (MCI)Neurotrophins

Identifiers

PMID40414756
PMCPMC12321615

What Socratic holds

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LicenceCC BY-NC-ND
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Registered trials

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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 Socratic graph.