Evidence map›Paper›PMID 41555676›Full record

ArticleJournal of movement disorders2026

Longitudinal Implications of the BDNF rs6265 Polymorphism for Motor and Nonmotor Features of Parkinson's Disease in the Korean Population.

Sang-Won Yoo, Yun Joong Kim, Dong-Woo Ryu, Yoonsang Oh, Seunggyun Ha, Joong-Seok Kim

Abstract read
In one paragraph

Article in Journal of movement disorders, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Sang-Won YooDepartment of Neurology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Yun Joong KimDepartment of Neurology, Yonsei University College of Medicine, Seoul, Korea.
Dong-Woo RyuDepartment of Neurology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Yoonsang OhDepartment of Neurology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Seunggyun HaDivision of Nuclear Medicine, Department of Radiology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Joong-Seok KimDepartment of Neurology, College of Medicine, The Catholic University of Korea, Seoul, Korea.

Funding

Korea National Institute of Health 2024ER100202Ministry of Education RS-2021-NR065151Ministry of Science and ICTMinistry of Science, ICT and Future Planning 2017R1D1A1B06028086Ministry of Science, ICT and Future Planning RS-2017-NR027859National Research Foundation of Korea 2021R1I1A1A01050492National Research Foundation of Korea RS-2024-00452428
6 · The paper itself

Abstract

objectiveBrain-derived neurotrophic factor (BDNF) has been suggested to support the endurance and dopamine release of dopaminergic neurons. Its Val66Met polymorphism might modify Parkinson's disease (PD) evolution, although evidence in Asian populations remains limited. This study aimed to explore how the BDNF rs6265 genotype is associated with the clinical characteristics and longitudinal progression patterns of PD patients in a Korean population.

methodsA total of 247 patients were enrolled and followed for a mean duration of 50.9±23.9 months. Baseline and/or periodic assessments captured motor severity, nonmotor burden, cognition, orthostatic stress, cardiac denervation, and presynaptic dopamine transporter availability. The repeated measures were manipulated to infer any genotypic differences in the trajectories of each clinical domain.

resultsThe genotype frequencies were 31.2% (77/247) for Val/Val carriers and 68.8% (170/247) for Met-allele carriers. Baseline clinical characteristics and presynaptic dopamine transporter availability were comparable between genotypes. Initially, Val homozygotes showed more preserved myocardial innervation and poorer nonfrontal cognitive performance. Longitudinal analyses demonstrated genotype-specific increases in motor and cognitive severity. Compared with Met-allele carriers, the homozygous Val group exhibited accelerated motor progression and a more rapid decline in the frontal domain after 3 years of follow-up.

conclusionThe differences in myocardial denervation at diagnosis, cognitive profiles, and motor progression might suggest a potential modulatory role of BDNF polymorphisms in PD progression in the Korean population.

Indexed as

BDNF rs6265 polymorphismBrain-derived neurotrophic factorDisease progressionGenotypic differenceParkinson’s disease

Identifiers

PMID41555676
PMCPMC13175727

What Socratic holds

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LicenceCC BY-NC
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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.