Student or educator? Sign up with your school email and get 6 months of Pro free.
Cited by 27

The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.

Brain-derived neurotrophic factor as a biomarker in cancer-related cognitive impairment among adolescent and young adult cancer patients

Ng, Ding Quan, Cheng, Ivy, Wang, Claire, Tan, Chia Jie, Toh, Yi Long, Koh, Yong Qin, Ke, Yu, Foo, Koon Mian, Chan, Raymond J., Ho, Han Kiat, Chew, Lita, bin Harunal Rashid, Mohamad Farid, Chan, Alexandre·2023·Scientific Reports

Abstract

Brain-derived neurotrophic factor (BDNF) improves cognitive function by stimulating neurogenesis and neuroplasticity. We hypothesize that higher plasma BDNF levels are protective against cognitive toxicity among adolescent and young adult cancer patients (15–39 years old). In a prospective, longitudinal study, we recruited 74 newly diagnosed cancer and 118 age-matched non-cancer controls who completed the Cambridge Neuropsychological Test Automated Battery (CANTAB), Functional Assessment of Cancer Therapy-Cognitive Function questionnaire (FACT-Cog) and blood draws. Plasma BDNF was quantified using an enzyme-linked immunosorbent assay. Genomic DNA from buffy coat was genotyped for BDNF Val66Met. Most cancer participants were diagnosed with breast (24%) and head/neck (22%) cancers. After adjusting for sociodemographic variables (age, gender, race, marital status, education years), cancer participants had lower BDNF levels (ng/mL) at baseline (median: 10.7 vs 21.6, p < 0.001) and 6-months post-baseline (median: 8.2 vs 15.3, p = 0.001) compared to non-cancer controls. Through linear mixed modelling adjusted for sociodemographic variables, baseline cognition, fatigue, psychological distress, and time, we observed that among cancer participants, lower baseline BDNF levels were associated with worse attention (p = 0.029), memory (p = 0.018) and self-perceived cognitive abilities (p = 0.020) during cancer treatment. Met/Met was associated with enhanced executive function compared to Val/Val (p = 0.012). Plasma BDNF may serve as a predictive biomarker of cancer-related cognitive impairment.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1038/s41598-023-43581-1

Cites

5 of 5 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 5 references

Research works printed but not linked: 33

  1. Huang, E. J. & Reichardt, L. F. Neurotrophins: Roles in neuronal development and function. Annu. Rev. Neurosci. 24, 677–736. https://doi.org/10.1146/annurev.neuro.24.1.677 (2001). · DOI · Paper page
  2. Teixeira, A. L., Barbosa, I. G., Diniz, B. S. & Kummer, A. Circulating levels of brain-derived neurotrophic factor: Correlation with mood, cognition and motor function. Biomark. Med. 4(6), 871–887. https://doi.org/10.2217/bmm.10.111 (2010). · DOI
  3. Cheeran, B. et al. A common polymorphism in the brain-derived neurotrophic factor gene (BDNF) modulates human cortical plasticity and the response to rTMS. J. Physiol. 586(23), 5717–5725. https://doi.org/10.1113/jphysiol.2008.159905 (2008). · DOI
  4. Fritsch, B. et al. Direct current stimulation promotes BDNF-dependent synaptic plasticity: Potential implications for motor learning. Neuron 66(2), 198–204. https://doi.org/10.1016/j.neuron.2010.03.035 (2010). · DOI · Paper page
  5. Gunstad, J. et al. Serum brain-derived neurotrophic factor is associated with cognitive function in healthy older adults. J. Geriatr. Psychiatry Neurol. 21(3), 166–170. https://doi.org/10.1177/0891988708316860 (2008). · DOI
  6. Shimada, H. et al. A large, cross-sectional observational study of serum BDNF, cognitive function, and mild cognitive impairment in the elderly. Front. Aging Neurosci. 6, 69. https://doi.org/10.3389/fnagi.2014.00069 (2014). · DOI
  7. Ng, D. Q. et al. Evidence of brain-derived neurotrophic factor in ameliorating cancer-related cognitive impairment: A systematic review of human studies. Crit. Rev. Oncol. Hematol. 176, 103748. https://doi.org/10.1016/j.critrevonc.2022.103748 (2022). · DOI
  8. Yap, N. Y. et al. Associations of plasma brain-derived neurotrophic factor (BDNF) and Val66Met polymorphism (rs6265) with long-term cancer-related cognitive impairment in survivors of breast cancer. Breast Cancer Res. Treat. 183(3), 683–696. https://doi.org/10.1007/s10549-020-05807-y (2020). · DOI
  9. Zimmer, P. et al. Post-chemotherapy cognitive impairment in patients with B-cell non-Hodgkin lymphoma: A first comprehensive approach to determine cognitive impairments after treatment with rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone or rituximab and bendamustine. Leuk Lymphoma. 56(2), 347–352. https://doi.org/10.3109/10428194.2014.915546 (2015). · DOI
  10. Bury-Kamińska, M. et al. Chemotherapy-related differences in cognitive functioning and their biological predictors in patients with multiple myeloma. Brain Sci. 11(9), 1166. https://doi.org/10.3390/brainsci11091166 (2021). · DOI
  11. Guo, J. C. et al. Functional rs6265 polymorphism in the brain-derived neurotrophic factor gene confers protection against neurocognitive dysfunction in posttraumatic stress disorder among Chinese patients with hepatocellular carcinoma. J. Cell Biochem. 120(6), 10434–10443. https://doi.org/10.1002/jcb.28328 (2019). · DOI
  12. Jehn, C. F. et al. Neurocognitive function, brain-derived neurotrophic factor (BDNF) and IL-6 levels in cancer patients with depression. J. Neuroimmunol. 287, 88–92. https://doi.org/10.1016/j.jneuroim.2015.08.012 (2015). · DOI
  13. Egan, M. F. et al. The BDNF val66met polymorphism affects activity-dependent secretion of BDNF and human memory and hippocampal function. Cell 112(2), 257–269. https://doi.org/10.1016/S0092-8674(03)00035-7 (2003). · DOI · Paper page
  14. Tan, C. J. et al. Replication and meta-analysis of the association between BDNF Val66Met polymorphism and cognitive impairment in patients receiving chemotherapy. Mol. Neurobiol. 56(7), 4741–4750. https://doi.org/10.1007/s12035-018-1410-4 (2019). · DOI
  15. Ng, T. et al. Brain-derived neurotrophic factor genetic polymorphism (rs6265) is protective against chemotherapy-associated cognitive impairment in patients with early-stage breast cancer. Neuro Oncol. 18(2), 244–251. https://doi.org/10.1093/neuonc/nov162 (2016). · DOI
  16. Chan, A. et al. Cognitive impairment in adolescent and young adult cancer patients: Pre-treatment findings of a longitudinal study. Cancer Med. https://doi.org/10.1002/cam4.5295 (2022). · DOI
  17. Usmani, M. T. et al. BDNF augmentation using riluzole reverses doxorubicin-induced decline in cognitive function and neurogenesis. Neurotherapeutics https://doi.org/10.1007/s13311-022-01339-z (2023). · DOI
  18. Li, F. et al. The clinical significance of serum adipocytokines level in patients with lung cancer. J. Thorac. Dis. 11(8), 3547–3555. https://doi.org/10.21037/jtd.2019.07.66 (2019). · DOI
  19. Brierley, G. V. et al. Serum concentrations of brain-derived neurotrophic factor (BDNF) are decreased in colorectal cancer patients. Cancer Biomark. 13(2), 67–73. https://doi.org/10.3233/CBM-130345 (2013). · DOI
  20. Erickson, K. I., Miller, D. L. & Roecklein, K. A. The aging hippocampus: Interactions between exercise, depression, and BDNF. Neuroscientist 18(1), 82–97. https://doi.org/10.1177/1073858410397054 (2012). · DOI
  21. Califf, R. M. Biomarker definitions and their applications. Exp. Biol. Med. 243(3), 213–221. https://doi.org/10.1177/1535370217750088 (2018). · DOI
  22. Altshuler, D. B. et al. BDNF, COMT, and DRD2 polymorphisms and ability to return to work in adult patients with low- And high-grade glioma. Neuro-Oncol. Pract. 6(5), 375–385. https://doi.org/10.1093/nop/npy059 (2019). · DOI
  23. Wefel, J. S., Vardy, J., Ahles, T. & Schagen, S. B. International Cognition and Cancer Task Force recommendations to harmonise studies of cognitive function in patients with cancer. Lancet Oncol. 12(7), 703–708. https://doi.org/10.1016/S1470-2045(10)70294-1 (2011). · DOI
  24. Maassen, G. H., Bossema, E. & Brand, N. Reliable change and practice effects: Outcomes of various indices compared. J. Clin. Exp. Neuropsychol. 31(3), 339–352. https://doi.org/10.1080/13803390802169059 (2009). · DOI
  25. Jacobson, N. S. & Truax, P. Clinical significance: A statistical approach to defining meaningful change in psychotherapy research. J. Consult. Clin. Psychol. 59(1), 12–19. https://doi.org/10.1037/0022-006X.59.1.12 (1991). · DOI · Paper page
  26. Cheung, Y. T., Lim, S. R., Shwe, M., Tan, Y. P. & Chan, A. Psychometric properties and measurement equivalence of the english and chinese versions of the functional assessment of cancer therapy-cognitive in Asian patients with breast cancer. Value Health 16(6), 1001–1013. https://doi.org/10.1016/j.jval.2013.06.017 (2013). · DOI
  27. Cheung, Y. T. et al. Minimal clinically important difference (MCID) for the functional assessment of cancer therapy: Cognitive function (FACT-Cog) in breast cancer patients. J. Clin. Epidemiol. 67(7), 811–820. https://doi.org/10.1016/j.jclinepi.2013.12.011 (2014). · DOI
  28. Chan, A. et al. Assessment of psychological distress among Asian adolescents and young adults (AYA) cancer patients using the distress thermometer: A prospective, longitudinal study. Support Care Cancer 26(9), 3257–3266. https://doi.org/10.1007/s00520-018-4189-y (2018). · DOI
  29. Chan, A. et al. Psychometric properties and measurement equivalence of the Multidimensional Fatigue Syndrome Inventory- Short Form (MFSI-SF) amongst breast cancer and lymphoma patients in Singapore. Health Qual. Life Outcomes 16(1), 1–14. https://doi.org/10.1186/s12955-018-0846-6 (2018). · DOI
  30. Chan, A. et al. Minimal clinically important difference of the multidimensional fatigue symptom inventory-short form (MFSI-SF) for fatigue worsening in Asian breast cancer patients. J. Pain Sympt. Manage. 55(3), 992-997.e2. https://doi.org/10.1016/j.jpainsymman.2017.10.014 (2018). · DOI
  31. Brown, L. D., Cai, T. T. & Das Gupta, A. Interval estimation for a binomial proportion. Stat. Sci. 16(2), 213286. https://doi.org/10.1214/ss/1009213286 (2001). · DOI
  32. Puthenpura, V. et al. Loss to follow-up of minorities, adolescents, and young adults on clinical trials: A report from the Children’s Oncology Group. Cancer 129(10), 1547–1556. https://doi.org/10.1002/cncr.34701 (2023). · DOI
  33. Tan, C. J. et al. Self-reported cognitive outcomes among adolescent and young adult patients with noncentral nervous system cancers. Psychooncology 29(8), 1355–1362. https://doi.org/10.1002/pon.5456 (2020). · DOI

Metadata

Authors
Ng, D. Q., Cheng, I., Wang, C., Tan, C. J., Toh, Y. L., Koh, Y. Q., Ke, Y., Foo, K. M., Chan, R. J., Ho, H. K., Chew, L., bin Harunal Rashid, M. F., & Chan, A.
Venue
Scientific Reports
Published
2023-09-28
Volume
13
Issue
1
ISSN
2045-2322
Cited by
27
References
5
Language
en
Funders
National Medical Research Council (NMRC/CIRG/1471/2017)

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: Brain-derived neurotrophic factor as a biomarker in cancer-related cognitive impairment among adolescent and young adult cancer patients. https://app.cochat.ai/papers/10.1038/s41598-023-43581-1
The paper
Ng, D. Q., Cheng, I., Wang, C., Tan, C. J., Toh, Y. L., Koh, Y. Q., Ke, Y., Foo, K. M., Chan, R. J., Ho, H. K., Chew, L., bin Harunal Rashid, M. F., & Chan, A. (2023). Brain-derived neurotrophic factor as a biomarker in cancer-related cognitive impairment among adolescent and young adult cancer patients. Scientific Reports. https://doi.org/10.1038/s41598-023-43581-1

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.