Please use this identifier to cite or link to this item:
https://doi.org/10.1186/s12885-017-3861-9
DC Field | Value | |
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dc.title | Evaluation of plasma brain-derived neurotrophic factor levels and self-perceived cognitive impairment post-chemotherapy: A longitudinal study | |
dc.contributor.author | Ng T. | |
dc.contributor.author | Lee Y.Y. | |
dc.contributor.author | Chae J.-W. | |
dc.contributor.author | Yeo A.H.L. | |
dc.contributor.author | Shwe M. | |
dc.contributor.author | Gan Y.X. | |
dc.contributor.author | Ng R.C.H. | |
dc.contributor.author | Chu P.P.Y. | |
dc.contributor.author | Khor C.C. | |
dc.contributor.author | Ho H.K. | |
dc.contributor.author | Chan A. | |
dc.date.accessioned | 2020-09-09T10:32:42Z | |
dc.date.available | 2020-09-09T10:32:42Z | |
dc.date.issued | 2017 | |
dc.identifier.citation | Ng 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.issn | 1471-2407 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/175411 | |
dc.description.abstract | Background: 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.source | Unpaywall 20200831 | |
dc.subject | antineoplastic agent | |
dc.subject | brain derived neurotrophic factor | |
dc.subject | scatter factor receptor | |
dc.subject | brain derived neurotrophic factor | |
dc.subject | brain-derived neurotrophic factor, human | |
dc.subject | adult | |
dc.subject | Article | |
dc.subject | breast cancer | |
dc.subject | cancer chemotherapy | |
dc.subject | cancer staging | |
dc.subject | clinical evaluation | |
dc.subject | cognition | |
dc.subject | cognitive defect | |
dc.subject | cohort analysis | |
dc.subject | concentration loss | |
dc.subject | disease association | |
dc.subject | enzyme linked immunosorbent assay | |
dc.subject | functional assessment | |
dc.subject | Functional Assessment of Cancer Therapy Cognitive Function | |
dc.subject | gene frequency | |
dc.subject | genetic polymorphism | |
dc.subject | genotype | |
dc.subject | heterozygote | |
dc.subject | homozygosity | |
dc.subject | human | |
dc.subject | longitudinal study | |
dc.subject | major clinical study | |
dc.subject | middle aged | |
dc.subject | pilot study | |
dc.subject | prospective study | |
dc.subject | protein blood level | |
dc.subject | questionnaire | |
dc.subject | Sanger sequencing | |
dc.subject | self report | |
dc.subject | aged | |
dc.subject | blood | |
dc.subject | breast tumor | |
dc.subject | chemically induced | |
dc.subject | cognitive defect | |
dc.subject | female | |
dc.subject | genetic association study | |
dc.subject | genetic predisposition | |
dc.subject | genetics | |
dc.subject | male | |
dc.subject | pathology | |
dc.subject | single nucleotide polymorphism | |
dc.subject | Adult | |
dc.subject | Aged | |
dc.subject | Brain-Derived Neurotrophic Factor | |
dc.subject | Breast Neoplasms | |
dc.subject | Cognitive Dysfunction | |
dc.subject | Female | |
dc.subject | Genetic Association Studies | |
dc.subject | Genetic Predisposition to Disease | |
dc.subject | Genotype | |
dc.subject | Humans | |
dc.subject | Male | |
dc.subject | Middle Aged | |
dc.subject | Neoplasm Staging | |
dc.subject | Polymorphism, Single Nucleotide | |
dc.type | Article | |
dc.contributor.department | PHARMACY | |
dc.contributor.department | DUKE-NUS MEDICAL SCHOOL | |
dc.description.doi | 10.1186/s12885-017-3861-9 | |
dc.description.sourcetitle | BMC Cancer | |
dc.description.volume | 17 | |
dc.description.issue | 1 | |
dc.description.page | 867 | |
dc.published.state | Published | |
Appears in Collections: | Staff Publications Elements |
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