Evidence map›Paper›PMID 38379321›Full record

ArticleCancer medicine2024

Associations of brain-derived neurotrophic factor rs6265 polymorphism and cognitive function in breast cancer survivors from a cross-sectional study.

Taichi Goto, Leorey N Saligan, Xiaobai Li, Lichen Xiang, Catherine Kwiat, Christopher Nguyen, Adele Crouch, Diane Von Ah

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
4.2field-weighted citation impact, top 6% of its field
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

8 citing papers in PubMed, 10 citations in OpenAlex.

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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 at 4 institutions in 1 country.

Taichi GotoSymptoms Biology Unit, Division of Intramural Research, National Institute of Nursing Research, National Institutes of Health, Bethesda, Maryland, USA.ORCID 0000-0001-7140-8175
Leorey N SaliganSymptoms Biology Unit, Division of Intramural Research, National Institute of Nursing Research, National Institutes of Health, Bethesda, Maryland, USA.ORCID 0000-0001-9481-7836
Xiaobai LiDepartment of Biostatistics, National Institutes of Health Clinical Center, Bethesda, Maryland, USA.
Lichen XiangSymptoms Biology Unit, Division of Intramural Research, National Institute of Nursing Research, National Institutes of Health, Bethesda, Maryland, USA.
Catherine KwiatSymptoms Biology Unit, Division of Intramural Research, National Institute of Nursing Research, National Institutes of Health, Bethesda, Maryland, USA.
Christopher NguyenSymptoms Biology Unit, Division of Intramural Research, National Institute of Nursing Research, National Institutes of Health, Bethesda, Maryland, USA.
Adele CrouchIndiana University School of Nursing, Indianapolis, Indiana, USA.
Diane Von AhThe Ohio State University College of Nursing, Columbus, Ohio, USA.ORCID 0000-0002-3189-1307
National Institutes of Health · USIndiana University – Purdue University Indianapolis · USNational Institutes of Health Clinical Center · USThe Ohio State University · US

Funding

Investigating Molecular-Genetic Correlates of FatigueZIANR000019 · NINR · NATIONAL INSTITUTE OF NURSING RESEARCH · PI SALIGAN, LEOREY · 2010 to 2025
$12.8M
NINR NIH HHS
6 · The paper itself

Abstract

backgroundBreast cancer survivors (BCS) often complain of cancer-related cognitive impairment (CRCI) during and even months after completing primary cancer treatments, particularly chemotherapy. The etiology of CRCI is unknown, but associations of CRCI with germline genetic polymorphisms have been reported, including Brain-Derived Neurotrophic Factor (BDNF) rs6265 polymorphism. The current study investigated the associations of specific BDNF rs6265 with CRCI.

methodsCancer-related cognitive impairment was assessed using subjective reports of cognitive symptoms (the version 1.0, 8-item short-forms of the Patient-Reported Outcomes Measurement Information System®) and computerized objective cognitive function scores (CANTAB®). BDNF rs6265 genotypes were determined from buccal swabs. The associations of specific BDNF rs6265 with CRCI were examined by either one-way analysis of variance or the Kruskal-Wallis test followed by post hoc tests and rank-based regression analysis.

resultsWe examined 356 female BCS. The mean (SD) age was 55.6 (9.8) years old, the median (IQR) years since cancer diagnosis were 4.0 (6.0), and 331 (92.7%) were self-described as White. BCS carrying the Met/Met genotype showed poorer results on 'visual episodic memory and new learning' and 'spatial working memory and executive function.' This relationship was observed regardless of prior chemotherapy.

conclusionOur findings suggest that carrying the BDNF rs6265 Met/Met genotype increases the risk for CRCI in BCS. These results are foundational in nature and provide important information to identify mechanisms underpinning CRCI.

Indexed as

Breast NeoplasmsCancer SurvivorsAgedBrain-Derived Neurotrophic FactorCognitionCross-Sectional StudiesFemaleGenotypeHumansMiddle AgedPolymorphism, Single NucleotideBDNF protein, humanBrain-Derived Neurotrophic FactorBDNFcancer-related cognitive impairmentVal66Metworking memory and executive function

Identifiers

PMID38379321
PMCPMC10839126
OpenAlexW4391545774

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LicenceCC BY
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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 OpenQuestion graph.