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Factors associated with cognitive impairment during the first year of treatment for nonmetastatic breast cancer

BACKGROUND: Women with breast cancer are more likely to develop cognitive impairment (CI), insomnia, fatigue, and mood disturbance than individuals with other cancers. The main objectives of this study were to establish the prevalence of CI and examine the relationships between CI, insomnia, fatigue...

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Autores principales: Rodriguez, Nicole, Fawcett, Jonathan M., Rash, Joshua A., Lester, Renee, Powell, Erin, MacMillan, Connor D., Garland, Sheila N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7926005/
https://www.ncbi.nlm.nih.gov/pubmed/33455070
http://dx.doi.org/10.1002/cam4.3715
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author Rodriguez, Nicole
Fawcett, Jonathan M.
Rash, Joshua A.
Lester, Renee
Powell, Erin
MacMillan, Connor D.
Garland, Sheila N.
author_facet Rodriguez, Nicole
Fawcett, Jonathan M.
Rash, Joshua A.
Lester, Renee
Powell, Erin
MacMillan, Connor D.
Garland, Sheila N.
author_sort Rodriguez, Nicole
collection PubMed
description BACKGROUND: Women with breast cancer are more likely to develop cognitive impairment (CI), insomnia, fatigue, and mood disturbance than individuals with other cancers. The main objectives of this study were to establish the prevalence of CI and examine the relationships between CI, insomnia, fatigue, and mood over the first year of breast cancer treatment. METHODS: Participants were recruited after diagnosis and completed validated measures of insomnia, objective and perceived CI, fatigue, and mood disturbance at four time points during the first year of treatment. A random intercepts cross‐lagged panel model assessed relationships among symptoms over time. RESULTS: The sample included 98 women. Prevalence of objective CI ranged from 3.1% to 8.2% throughout the year, whereas 36.7% demonstrated a clinically meaningful decline in perceived CI from baseline to 4 months, which remained relatively stable. Greater perceived CI was associated with more fatigue (β = −0.78, z = 17.48, p < .01) and symptoms of insomnia (β = −0.58, z = 5.24, p < .01). Short‐term fluctuations in perceived CI (p < .05), but not fatigue or insomnia, predicted future perceived CI. Fatigue (p < .001) was a significant predictor of future reported symptoms of fatigue and insomnia. CONCLUSION: Subjective CI is more prevalent than objective impairments. Fatigue, insomnia, and perceived CI remain stable and are associated during the first year of treatment. Changes in insomnia and fatigue may have little effect on future perceived cognition. Women with breast cancer likely require targeted intervention for these side effects.
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spelling pubmed-79260052021-03-12 Factors associated with cognitive impairment during the first year of treatment for nonmetastatic breast cancer Rodriguez, Nicole Fawcett, Jonathan M. Rash, Joshua A. Lester, Renee Powell, Erin MacMillan, Connor D. Garland, Sheila N. Cancer Med Clinical Cancer Research BACKGROUND: Women with breast cancer are more likely to develop cognitive impairment (CI), insomnia, fatigue, and mood disturbance than individuals with other cancers. The main objectives of this study were to establish the prevalence of CI and examine the relationships between CI, insomnia, fatigue, and mood over the first year of breast cancer treatment. METHODS: Participants were recruited after diagnosis and completed validated measures of insomnia, objective and perceived CI, fatigue, and mood disturbance at four time points during the first year of treatment. A random intercepts cross‐lagged panel model assessed relationships among symptoms over time. RESULTS: The sample included 98 women. Prevalence of objective CI ranged from 3.1% to 8.2% throughout the year, whereas 36.7% demonstrated a clinically meaningful decline in perceived CI from baseline to 4 months, which remained relatively stable. Greater perceived CI was associated with more fatigue (β = −0.78, z = 17.48, p < .01) and symptoms of insomnia (β = −0.58, z = 5.24, p < .01). Short‐term fluctuations in perceived CI (p < .05), but not fatigue or insomnia, predicted future perceived CI. Fatigue (p < .001) was a significant predictor of future reported symptoms of fatigue and insomnia. CONCLUSION: Subjective CI is more prevalent than objective impairments. Fatigue, insomnia, and perceived CI remain stable and are associated during the first year of treatment. Changes in insomnia and fatigue may have little effect on future perceived cognition. Women with breast cancer likely require targeted intervention for these side effects. John Wiley and Sons Inc. 2021-01-16 /pmc/articles/PMC7926005/ /pubmed/33455070 http://dx.doi.org/10.1002/cam4.3715 Text en © 2021 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Rodriguez, Nicole
Fawcett, Jonathan M.
Rash, Joshua A.
Lester, Renee
Powell, Erin
MacMillan, Connor D.
Garland, Sheila N.
Factors associated with cognitive impairment during the first year of treatment for nonmetastatic breast cancer
title Factors associated with cognitive impairment during the first year of treatment for nonmetastatic breast cancer
title_full Factors associated with cognitive impairment during the first year of treatment for nonmetastatic breast cancer
title_fullStr Factors associated with cognitive impairment during the first year of treatment for nonmetastatic breast cancer
title_full_unstemmed Factors associated with cognitive impairment during the first year of treatment for nonmetastatic breast cancer
title_short Factors associated with cognitive impairment during the first year of treatment for nonmetastatic breast cancer
title_sort factors associated with cognitive impairment during the first year of treatment for nonmetastatic breast cancer
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7926005/
https://www.ncbi.nlm.nih.gov/pubmed/33455070
http://dx.doi.org/10.1002/cam4.3715
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