Evidence map›Paper›PMID 30382534›Full record

SynthesisMolecular neurobiology2019

Replication and Meta-analysis of the Association between BDNF Val66Met Polymorphism and Cognitive Impairment in Patients Receiving Chemotherapy.

Chia Jie Tan, Sheree Wan Ting Lim, Yi Long Toh, Terence Ng, Angie Yeo, Maung Shwe, Koon Mian Foo, Pat Chu, Amit Jain, Si-Lin Koo and 14 more

Open access · hybridAbstract readMeta-AnalysisMulticenter Study
In one paragraph

Synthesis in Molecular neurobiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 14% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
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  7. Potential role ofFrontiers in aging neuroscience · 2024
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  19. Role of Exosomes in Cancer-Related Cognitive Impairment.International journal of molecular sciences · 2020
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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

24 authors at 4 institutions in 1 country.

Chia Jie TanDepartment of Pharmacy, Faculty of Science, National University of Singapore, Block S4, 18 Science Drive 4, Singapore, 117543, Singapore.
Sheree Wan Ting LimDepartment of Pharmacy, Faculty of Science, National University of Singapore, Block S4, 18 Science Drive 4, Singapore, 117543, Singapore.
Yi Long TohDepartment of Pharmacy, Faculty of Science, National University of Singapore, Block S4, 18 Science Drive 4, Singapore, 117543, Singapore.
Terence NgDepartment of Pharmacy, Faculty of Science, National University of Singapore, Block S4, 18 Science Drive 4, Singapore, 117543, Singapore.
Angie YeoDepartment of Pharmacy, Faculty of Science, National University of Singapore, Block S4, 18 Science Drive 4, Singapore, 117543, Singapore.
Maung ShweDepartment of Pharmacy, Faculty of Science, National University of Singapore, Block S4, 18 Science Drive 4, Singapore, 117543, Singapore.
Koon Mian FooDepartment of Pharmacy, K.K. Women's and Children's Hospital, Singapore, Singapore.
Pat ChuSingapore Cord Blood Bank, Singapore, Singapore.
Amit JainDivision of Medical Oncology, National Cancer Centre, Singapore, Singapore.
Si-Lin KooDivision of Medical Oncology, National Cancer Centre, Singapore, Singapore.
Rebecca A DentDivision of Medical Oncology, National Cancer Centre, Singapore, Singapore.
Raymond Chee Hui NgDivision of Medical Oncology, National Cancer Centre, Singapore, Singapore.
Yoon Sim YapDivision of Medical Oncology, National Cancer Centre, Singapore, Singapore.
Elaine H LimDivision of Medical Oncology, National Cancer Centre, Singapore, Singapore.
Kiley Wei-Jen LohDivision of Medical Oncology, National Cancer Centre, Singapore, Singapore.
Wen Yee ChayDivision of Medical Oncology, National Cancer Centre, Singapore, Singapore.
Guek Eng LeeDivision of Medical Oncology, National Cancer Centre, Singapore, Singapore.
Tira Jing Ying TanDivision of Medical Oncology, National Cancer Centre, Singapore, Singapore.
Sok Yuen BehDivision of Medical Oncology, National Cancer Centre, Singapore, Singapore.
Mabel WongDivision of Medical Oncology, National Cancer Centre, Singapore, Singapore.
Jack Junjie ChanDivision of Medical Oncology, National Cancer Centre, Singapore, Singapore.
Chiea Chuen KhorHuman Genetics, Genome Institute of Singapore, Singapore, Singapore.
Han Kiat HoDepartment of Pharmacy, Faculty of Science, National University of Singapore, Block S4, 18 Science Drive 4, Singapore, 117543, Singapore.
Alexandre ChanDepartment of Pharmacy, Faculty of Science, National University of Singapore, Block S4, 18 Science Drive 4, Singapore, 117543, Singapore. phaac@nus.edu.sg.
National Cancer Centre Singapore · SGNational University of Singapore · SGGenome Institute of Singapore · SGKK Women's and Children's Hospital · SG

Funding

National Cancer Centre of Singapore NRFCB12131National Medical Research Council NMRC/CIRG/1386/2014, NMRC/CIRG/1471/2017National University of Singapore R-148-000-233-114
6 · The paper itself

Abstract

Cancer-related cognitive impairment (CRCI) adversely affects cancer patients. We had previously demonstrated that the BDNF Val66Met genetic polymorphism is associated with lower odds of subjective CRCI in the multitasking and verbal ability domains among breast cancer patients receiving chemotherapy. To further assess our previous findings, we evaluated the association of BDNF Val66Met polymorphism with subjective and objective CRCI in a temporally separate cohort of patients and pooled findings from both the original (n = 145) and current (n = 193) cohorts in a meta-analysis. Subjective CRCI was assessed using FACT-Cog. Objective CRCI was evaluated using computerized neuropsychological tests. Genotyping was carried out using Sanger sequencing. The association of BDNF Val66Met genotypes and CRCI was examined with logistic regression. A fixed-effect meta-analysis was conducted using the inverse variance method. In the meta-analysis (n = 338), significantly lower odds of CRCI were associated with Met allele carriers based on the global FACT-Cog score (OR = 0.52, 95% CI 0.29-0.94). Furthermore, Met allele carriers were at lower odds of developing impairment in the domains of memory (OR = 0.34, 95% CI: 0.17-0.70), multitasking (OR = 0.33, 95% CI: 0.18-0.59), and verbal ability (OR = 0.46, 95% CI: 0.24-0.88). Consistent with the previous study, lower odds of subjective CRCI among patients with the BDNF Met allele was observed after adjusting for potential confounders in the multitasking (OR = 0.30, 95% CI: 0.14-0.67) domain. In conclusion, carriers of the BDNF Met allele were protected against global subjective CRCI, particularly in the domains of memory, multitasking, and verbal ability. Our findings further contribute to the understanding of CRCI pathophysiology.

Indexed as

Genetic Predisposition to DiseaseAllelesAntineoplastic AgentsAnxietyBrain-Derived Neurotrophic FactorCognitive DysfunctionFatigueFemaleGene FrequencyHumansMiddle AgedOdds RatioPolymorphism, Single NucleotidePrevalenceReproducibility of ResultsAntineoplastic AgentsBrain-Derived Neurotrophic FactorBDNFBreast cancerCancer-related cognitive impairmentChemotherapyGenetic polymorphism

Identifiers

PMID30382534
PMCPMC6647505
OpenAlexW2898669956

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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.