Please use this identifier to cite or link to this item: https://doi.org/10.1186/s12885-017-3861-9
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dc.titleEvaluation of plasma brain-derived neurotrophic factor levels and self-perceived cognitive impairment post-chemotherapy: A longitudinal study
dc.contributor.authorNg T.
dc.contributor.authorLee Y.Y.
dc.contributor.authorChae J.-W.
dc.contributor.authorYeo A.H.L.
dc.contributor.authorShwe M.
dc.contributor.authorGan Y.X.
dc.contributor.authorNg R.C.H.
dc.contributor.authorChu P.P.Y.
dc.contributor.authorKhor C.C.
dc.contributor.authorHo H.K.
dc.contributor.authorChan A.
dc.date.accessioned2020-09-09T10:32:42Z
dc.date.available2020-09-09T10:32:42Z
dc.date.issued2017
dc.identifier.citationNg T., Lee Y.Y., Chae J.-W., Yeo A.H.L., Shwe M., Gan Y.X., Ng R.C.H., Chu P.P.Y., Khor C.C., Ho H.K., Chan A. (2017). Evaluation of plasma brain-derived neurotrophic factor levels and self-perceived cognitive impairment post-chemotherapy: A longitudinal study. BMC Cancer 17 (1) : 867. ScholarBank@NUS Repository. https://doi.org/10.1186/s12885-017-3861-9
dc.identifier.issn1471-2407
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/175411
dc.description.abstractBackground: Preliminary evidence suggests that changes in plasma brain-derived neurotrophic factor (BDNF) levels may contribute to the occurrence of chemotherapy-associated cognitive impairment (CACI), and a previous study suggested that carriers of the BDNF Met homozygous genotype are protected from CACI. Methods: This multicenter, prospective cohort study involved chemotherapy-receiving early-stage breast cancer (ESBC) patients. Self-perceived cognitive function was longitudinally assessed using the validated FACT-Cog (ver. 3) across three time points: Prior to chemotherapy (T1), during chemotherapy (T2), and at the end of chemotherapy (T3). Plasma BDNF levels were quantified using enzyme-linked immunosorbent assay. Genotyping was performed using Sanger Sequencing. Results: A total of 51 chemotherapy-receiving ESBC patients (mean age: 52.6 ± 9.5 years) were recruited, and 11 patients (21.6%) reported subjective cognitive impairment post-chemotherapy. Overall, there was a reduction in median plasma BDNF levels over time (T1: 5423.0 pg/ml; T2: 5313.6 pg/ml; T3: 4050.3 pg/ml; p < 0.01). After adjusting for confounding factors, longitudinal analysis revealed that BDNF levels were associated with self-reported concentration deficit (p = 0.032). Carriers of Val/Val (p = 0.011) and Val/Met (p = 0.003) BDNF genotypes demonstrated a significant reduction in plasma BDNF levels over time; however, plasma BDNF levels were similar across all time points among Met homozygous carriers (p = 0.107). Conclusion: There was a statistically significant change in BDNF levels post-chemotherapy in ESBC patients, and plasma BDNF levels were associated with self-perceived concentration deficit in patients receiving chemotherapy. © 2017 The Author(s).
dc.sourceUnpaywall 20200831
dc.subjectantineoplastic agent
dc.subjectbrain derived neurotrophic factor
dc.subjectscatter factor receptor
dc.subjectbrain derived neurotrophic factor
dc.subjectbrain-derived neurotrophic factor, human
dc.subjectadult
dc.subjectArticle
dc.subjectbreast cancer
dc.subjectcancer chemotherapy
dc.subjectcancer staging
dc.subjectclinical evaluation
dc.subjectcognition
dc.subjectcognitive defect
dc.subjectcohort analysis
dc.subjectconcentration loss
dc.subjectdisease association
dc.subjectenzyme linked immunosorbent assay
dc.subjectfunctional assessment
dc.subjectFunctional Assessment of Cancer Therapy Cognitive Function
dc.subjectgene frequency
dc.subjectgenetic polymorphism
dc.subjectgenotype
dc.subjectheterozygote
dc.subjecthomozygosity
dc.subjecthuman
dc.subjectlongitudinal study
dc.subjectmajor clinical study
dc.subjectmiddle aged
dc.subjectpilot study
dc.subjectprospective study
dc.subjectprotein blood level
dc.subjectquestionnaire
dc.subjectSanger sequencing
dc.subjectself report
dc.subjectaged
dc.subjectblood
dc.subjectbreast tumor
dc.subjectchemically induced
dc.subjectcognitive defect
dc.subjectfemale
dc.subjectgenetic association study
dc.subjectgenetic predisposition
dc.subjectgenetics
dc.subjectmale
dc.subjectpathology
dc.subjectsingle nucleotide polymorphism
dc.subjectAdult
dc.subjectAged
dc.subjectBrain-Derived Neurotrophic Factor
dc.subjectBreast Neoplasms
dc.subjectCognitive Dysfunction
dc.subjectFemale
dc.subjectGenetic Association Studies
dc.subjectGenetic Predisposition to Disease
dc.subjectGenotype
dc.subjectHumans
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectNeoplasm Staging
dc.subjectPolymorphism, Single Nucleotide
dc.typeArticle
dc.contributor.departmentPHARMACY
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.1186/s12885-017-3861-9
dc.description.sourcetitleBMC Cancer
dc.description.volume17
dc.description.issue1
dc.description.page867
dc.published.statePublished
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