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Subjective cancer-related cognitive impairments and salience network connectivity in breast cancer survivors
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Metacognition and cognitive monitoring: A new area of cognitive–developmental inquiry
Flavell, J. H. (1979) · American Psychologist · doi:10.1037/0003-066x.34.10.906 · Cited by 11,282 · cited 1×
“Metacognition is a term that refers to self-monitoring of cognitive processes, or “thinking about thinking” [46, 47], that is relevant to subjective CRCI.”
BackgroundThe role of prefrontal cortex in cognitive control and executive function
Friedman, N. P., & Robbins, T. W. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-021-01132-0 · Cited by 1,737 · cited 1×
“1 3 prefrontal parietal cortices and the brain networks located within these regions [39, 40].”
BackgroundThe role of PFC networks in cognitive control and executive function
Menon, V., & D’Esposito, M. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-021-01152-w · Cited by 654
Common Dysfunction of Large-Scale Neurocognitive Networks Across Psychiatric Disorders
Sha, Z., Wager, T. D., Mechelli, A., & He, Y. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2018.11.011 · Cited by 367
Vaccaro, A. G., & Fleming, S. M. (2018) · Brain and Neuroscience Advances · doi:10.1177/2398212818810591 · Cited by 218
Research works printed but not linked: 48
- Lange M, Joly F, Vardy J, Ahles T, Dubois M, Tron L, Winocur G, De Ruiter MB, Castel H. Cancer-related cognitive impairment: an update on state of the art, detection, and management strategies in cancer survivors. Ann Oncol. 2019;30(12):1925–40. · DOI · Paper page
- Selamat MH, Loh SY, Mackenzie L, Vardy J. Chemobrain experienced by breast cancer survivors: a meta-ethnography study investigating research and care implications. PLoS One. 2014;9(9):e108002. · DOI
- Porro B, Durand MJ, Petit A, Bertin M, Roquelaure Y. Return to work of breast cancer survivors: toward an integrative and transactional conceptual model. J Cancer Surviv. 2021;16(3):590–603. · DOI
- Mayo SJ, Lustberg M, Dhillon HM, Nakamura ZM, Allen DH, Von ah D, Janelsins MC, Chan A, Olson K, Tan CJ, Toh YL, Oh J, Grech L, Cheung YT, Subbiah IM, Petranovic D, D’Olimpio J, Gobbo M, Koeppen S, Loprinzi CL, Pang L, Shinde S, Ntukidem O, Peters KB. Cancer-related cognitive impairment in patients with non-central nervous system malignancies: an overview for oncology providers from the MASCC Neurological Complications Study Group. Support Care Cancer. 2021;29(6):2821–40. · DOI
- Bray VJ, Dhillon HM, Vardy JL. Systematic review of self-reported cognitive function in cancer patients following chemotherapy treatment. J Cancer Surviv. 2018;12(4):537–59. · DOI
- Hutchinson AD, Hosking JR, Kichenadasse G, Mattiske JK, Wilson C. Objective and subjective cognitive impairment following chemotherapy for cancer: a systematic review. Cancer Treat Rev. 2012;38(7):926–34. · DOI
- Wefel JS, Kesler SR, Noll KR, Schagen SB. Clinical characteristics, pathophysiology, and management of noncentral nervous system cancer-related cognitive impairment in adults. CA Cancer J Clin. 2015;65(2):123–38. · DOI
- Kaiser J, Bledowski C, Dietrich J. Neural correlates of chemotherapy-related cognitive impairment. Cortex. 2014;54:33–50. · DOI
- Simo M, Rifa-Ros X, Rodriguez-Fornells A, Bruna J. Chemobrain: a systematic review of structural and functional neuroimaging studies. Neurosci Biobehav Rev. 2013;37(8):1311–21. · DOI
- Kesler S, Janelsins M, Koovakkattu D, Palesh O, Mustian K, Morrow G, Dhabhar FS. Reduced hippocampal volume and verbal memory performance associated with interleukin-6 and tumor necrosis factor-alpha levels in chemotherapy-treated breast cancer survivors. Brain Behav Immun. 2013;30(Suppl):S109–16. · DOI
- Kesler SR. Prevalence of cerebral small-vessel disease in long-term breast cancer survivors exposed to both adjuvant radiotherapy and chemotherapy. Breast Diseases: A Year Book Quarterly. 2015;26(4):353.
- Correa DD, Ahles TA. Neurocognitive changes in cancer survivors. Cancer J. 2008;14(6):396–400. · DOI
- Wefel JS, Vardy J, Ahles T, Schagen SB. International Cognition and Cancer Task Force recommendations to harmonise studies of cognitive function in patients with cancer. Lancet Oncol. 2011;12(7):703–8. · DOI
- Janelsins MC, Kohli S, Mohile SG, Usuki K, Ahles TA, Morrow GR. An update on cancer- and chemotherapy-related cognitive dysfunction: current status. Semin Oncol. 2011;38(3):431–8. · DOI
- Vardy J. Cognitive function in breast cancer survivors. Cancer Treat Res. 2009;151:387–419. · DOI
- Wefel JS, Saleeba AK, Buzdar AU, Meyers CA. Acute and late onset cognitive dysfunction associated with chemotherapy in women with breast cancer. Cancer. 2010;116(14):3348–56. · DOI
- Jansen CE, Miaskowski C, Dodd M, Dowling G, Kramer J. A metaanalysis of studies of the effects of cancer chemotherapy on various domains of cognitive function. Cancer. 2005;104(10):2222–33. · DOI
- McDonald BC, Conroy SK, Smith DJ, West JD, Saykin AJ. Frontal gray matter reduction after breast cancer chemotherapy and association with executive symptoms: a replication and extension study. Brain Behav Immun. 2013;30(Suppl):S117–25. · DOI
- Kesler SR, Kent JS, O’Hara R. Prefrontal cortex and executive function impairments in primary breast cancer. Arch Neurol. 2011;68(11):1447–53. · DOI
- Askren MK, Jung M, Berman MG, Zhang M, Therrien B, Peltier S, Ossher L, Hayes DF, Reuter-Lorenz PA, Cimprich B. Neuromarkers of fatigue and cognitive complaints following chemotherapy for breast cancer: a prospective fMRI investigation. Breast Cancer Res Treat. 2014;147(2):445–55. · DOI
- Apple AC, Schroeder MP, Ryals AJ, Wagner LI, Cella D, Shih PA, Reilly J, Penedo FJ, Voss JL, Wang L. Hippocampal functional connectivity is related to self-reported cognitive concerns in breast cancer patients undergoing adjuvant therapy. NeuroImage Clin. 2018;20:110–8. · DOI
- S.R. Kesler, T. Tang, A.M. Henneghan, M. Wright, M.W. Gaber, O. Palesh, Cross-sectional characterization of local brain network connectivity pre and post breast cancer treatment and distinct association with subjective cognitive and psychological function, Frontiers in neurology 12(1969) (2021). · DOI
- Kesler SR, Wefel JS, Hosseini SM, Cheung M, Watson CL, Hoeft F. Default mode network connectivity distinguishes chemotherapy-treated breast cancer survivors from controls. Proc Natl Acad Sci USA. 2013;110(28):11600–5. · DOI
- Dumas JA, Makarewicz J, Schaubhut GJ, Devins R, Albert K, Dittus K, Newhouse PA. Chemotherapy altered brain functional connectivity in women with breast cancer: a pilot study. Brain Imaging Behav. 2013;7(4):524–32. · DOI
- Zeng Y, Cheng ASK, Song T, Sheng X, Zhang Y, Liu X, Chan CCH. Subjective cognitive impairment and brain structural networks in Chinese gynaecological cancer survivors compared with age-matched controls: a cross-sectional study. BMC Cancer. 2017;17(1):796. · DOI
- Chand GB, Wu J, Hajjar I, Qiu D. Interactions of the salience network and its subsystems with the default-mode and the central-executive networks in normal aging and mild cognitive impairment. Brain Connectivity. 2017;7(7):401–12. · DOI
- Seeley WW. The salience network: a neural system for perceiving and responding to homeostatic demands. J Neurosci. 2019;39(50):9878–82. · DOI · Paper page
- Chong JSX, Ng GJP, Lee SC, Zhou J. Salience network connectivity in the insula is associated with individual differences in interoceptive accuracy. Brain Struct Funct. 2017;222(4):1635–44. · DOI · Paper page
- Roth RM, Lance CE, Isquith PK, Fischer AS, Giancola PR. Confirmatory factor analysis of the behavior rating inventory of executive function-adult version in healthy adults and application to attention-deficit/hyperactivity disorder. Arch Clin Neuropsychol. 2013;28(5):425–34. · DOI · Paper page
- Troyer AK, Rich JB. Psychometric Properties of a New Metamemory Questionnaire for Older Adults. J Gerontol B Psychol Sci Soc Sci. 2002;57(1):P19–27. · DOI
- AAghakhani EK Chan Test Reviews: Bracken BA, Howell K 2004. Clinical Assessment of Depression Odessa, FL: Psychological Assessment Resources. J Psychoeduc Assess. 2007;25(4):416–22. · DOI
- Glover GH, Lai S. Self-navigated spiral fMRI: interleaved versus single-shot. Magn Reson Med. 1998;39(3):361–8. · DOI
- Ashburner J. SPM: a history. Neuroimage. 2012;62(2):791–800. · DOI
- Whitfield-Gabrieli S, Nieto-Castanon A. Conn: a functional connectivity toolbox for correlated and anticorrelated brain networks. Brain Connectivity. 2012;2(3):125–41. · DOI · Paper page
- Behzadi Y, Restom K, Liau J, Liu TT. A component based noise correction method (CompCor) for BOLD and perfusion based fMRI. Neuroimage. 2007;37(1):90–101. · DOI · Paper page
- Tzourio-Mazoyer N, Landeau B, Papathanassiou D, Crivello F, Etard O, Delcroix N, Mazoyer B, Joliot M. Automated anatomical labeling of activations in SPM using a macroscopic anatomical parcellation of the MNI MRI single-subject brain. Neuroimage. 2002;15(1):273–89. · DOI · Paper page
- Van der Gucht K, Ahmadoun S, Melis M, de Cloe E, Sleurs C, Radwan A, Blommaert J, Takano K, Vandenbulcke M, Wildiers H, Neven P, Kuppens P, Raes F, Smeets A, Sunaert S, Deprez S. Effects of a mindfulness-based intervention on cancer-related cognitive impairment: results of a randomized controlled functional magnetic resonance imaging pilot study. Cancer. 2020;126(18):4246–55. · DOI
- R.M. Roth, P.K. Isquith, G. Gioia, Behavioral rating inventory of executive function - adult version, Psychological Assessment Resources, Lutz, FL, 2005. · DOI · Paper page
- Bernstein LJ, Edelstein K, Sharma A, Alain C. Chemo-brain: an activation likelihood estimation meta-analysis of functional magnetic resonance imaging studies. Neurosci Biobehav Rev. 2021;130:314–25. · DOI · Paper page
- Gratton C, Sun H, Petersen SE. Control networks and hubs. Psychophysiol. 2018;55(3):e13032. · DOI
- Hou J, Song B, Chen ACN, Sun C, Zhou J, Zhu H, Beauchaine TP. Review on neural correlates of emotion regulation and music: implications for emotion dysregulation. Front Psychol. 2017;8:501.
- Conley CC, Bishop BT, Andersen BL. Emotions and emotion regulation in breast cancer survivorship. Healthcare (Basel). 2016;4(3):56. · DOI
- Arndt J, Das E, Schagen SB, Reid-Arndt SA, Cameron LD, Ahles TA. Broadening the cancer and cognition landscape: the role of self-regulatory challenges. Psychooncol. 2014;23(1):1–8. · DOI
- Perrier J, Joue G, Desgranges B, Allouache D, Levy C, Noal S, Dayan J, Eustache F, Joly F, Viard A, Giffard B. Self-referential processes and resting-state connectivity in breast cancer patients before and 1 year after chemotherapy. Eur J Neurosci. 2022;55(2):624–36. · DOI
- Kesler SR, Wayfull JS, Hosseini SM, Cheung M, Watson CL, Hoeft F. Default mode network connectivity distinguishes chemotherapy-treated breast cancer survivors from controls. Proc Natl Acad Sci USA. 2013;110(28):11600–5. · DOI
- Sharma N, Murari G, Vandermorris S, Verhoeff N, Herrmann N, Chen JJ, Mah L. Functional connectivity between the posterior default mode network and parahippocampal gyrus is disrupted in older adults with subjective cognitive decline and correlates with subjective memory ability. J Alzheimer’s Disease : JAD. 2021;82(1):435–45. · DOI
- Costa DSJ, Fardell JE. Why are objective and perceived cognitive function weakly correlated in patients with cancer? J Clin Oncol. 2019;37(14):1154–8. · DOI
- Janelsins MC, Kesler SR, Ahles TA, Morrow GR. Prevalence, mechanisms, and management of cancer-related cognitive impairment. Int Rev Psychiatry. 2014;26(1):102–13. · DOI · Paper page
Metadata
- Authors
- Henneghan, A. M., & Kesler, S. R.
- Venue
- Journal of Cancer Survivorship
- Published
- 2022-12-05
- Volume
- 17
- Issue
- 4
- Pages
- 967-973
- ISSN
- 1932-2259
- 1932-2267
- Cited by
- 15
- References
- 5
- Language
- en
- Licence
- Funders
- National Institute of Nursing Research (K01NR018970)
- National Cancer Institute (R01CA226080)
- NIH Office of the Director (DP2OD004445)
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- Henneghan, A. M., & Kesler, S. R. (2023). Subjective cancer-related cognitive impairments and salience network connectivity in breast cancer survivors. Journal of Cancer Survivorship. https://doi.org/10.1007/s11764-022-01307-8
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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.