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Lack of cognitive impairment in long-term survivors of colorectal cancer

BACKGROUND: Our longitudinal study reported cognitive impairment in 43% of people following diagnosis of localised colorectal cancer (CRC) versus 15% in healthy controls (p < 0.001) and 50% versus 13% 1–2 years later (p < 0.001). Here we evaluate cognitive function and neuroimaging in a subgro...

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Autores principales: Vardy, Janette L., Pond, Gregory R., Cysique, Lucette A., Gates, Thomas M., Lagopoulos, Jim, Renton, Corrinne, Waite, Louise M., Tannock, Ian F., Dhillon, Haryana M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9135780/
https://www.ncbi.nlm.nih.gov/pubmed/35420329
http://dx.doi.org/10.1007/s00520-022-07008-3
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author Vardy, Janette L.
Pond, Gregory R.
Cysique, Lucette A.
Gates, Thomas M.
Lagopoulos, Jim
Renton, Corrinne
Waite, Louise M.
Tannock, Ian F.
Dhillon, Haryana M.
author_facet Vardy, Janette L.
Pond, Gregory R.
Cysique, Lucette A.
Gates, Thomas M.
Lagopoulos, Jim
Renton, Corrinne
Waite, Louise M.
Tannock, Ian F.
Dhillon, Haryana M.
author_sort Vardy, Janette L.
collection PubMed
description BACKGROUND: Our longitudinal study reported cognitive impairment in 43% of people following diagnosis of localised colorectal cancer (CRC) versus 15% in healthy controls (p < 0.001) and 50% versus 13% 1–2 years later (p < 0.001). Here we evaluate cognitive function and neuroimaging in a subgroup at long-term follow-up. PATIENTS AND METHODS: Cancer-free Australian participants in the study, and controls, completed cognitive and functional assessments. Neuroimaging was optional. Blood tests included inflammatory markers, clotting factors, sex hormones and apolipoprotein E genotype. The primary endpoint was demographically and practice effect-corrected cognitive scores comparing CRC survivors with controls over time examined using a linear mixed model, adjusted for baseline performance. Secondary endpoints included cognitive impairment rate using the Global Deficit Score [GDS > 0.5], Functional Deficit Score, blood results and neuroimaging. RESULTS: The study included 25 CRC survivors (60% men, median age 72) at mean 9 years after baseline (9 received adjuvant chemotherapy) and 25 controls (44% men, median age 68) at mean 6 years after baseline. There were no significant differences in cognitive scores or proportion with cognitive impairment (16 vs. 8%) between survivors and controls and no evidence of accelerated ageing in CRC survivors. Baseline cognitive performance predicted for subsequent cognitive function. There were no differences in functional tests or blood tests between groups. In 18 participants undergoing neuroimaging, 10 CRC survivors had higher myoinositol levels than 8 controls, and lower volume in the right amygdala and caudate and left hippocampal regions. CONCLUSIONS: There was no difference in cognitive capacity and function between CRC survivors and controls 6–12 years after diagnosis. Differences in neuroimaging require confirmation in a larger sample. HIGHLIGHTS: • No evidence of long term cognitive impairment in colorectal cancer survivors compared to controls 6–12 years after diagnosis • No evidence of accelerated cognitive ageing in colorectal cancer survivors • No evidence of long-term functional impairment in colorectal cancer survivors SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00520-022-07008-3.
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spelling pubmed-91357802022-05-28 Lack of cognitive impairment in long-term survivors of colorectal cancer Vardy, Janette L. Pond, Gregory R. Cysique, Lucette A. Gates, Thomas M. Lagopoulos, Jim Renton, Corrinne Waite, Louise M. Tannock, Ian F. Dhillon, Haryana M. Support Care Cancer Original Article BACKGROUND: Our longitudinal study reported cognitive impairment in 43% of people following diagnosis of localised colorectal cancer (CRC) versus 15% in healthy controls (p < 0.001) and 50% versus 13% 1–2 years later (p < 0.001). Here we evaluate cognitive function and neuroimaging in a subgroup at long-term follow-up. PATIENTS AND METHODS: Cancer-free Australian participants in the study, and controls, completed cognitive and functional assessments. Neuroimaging was optional. Blood tests included inflammatory markers, clotting factors, sex hormones and apolipoprotein E genotype. The primary endpoint was demographically and practice effect-corrected cognitive scores comparing CRC survivors with controls over time examined using a linear mixed model, adjusted for baseline performance. Secondary endpoints included cognitive impairment rate using the Global Deficit Score [GDS > 0.5], Functional Deficit Score, blood results and neuroimaging. RESULTS: The study included 25 CRC survivors (60% men, median age 72) at mean 9 years after baseline (9 received adjuvant chemotherapy) and 25 controls (44% men, median age 68) at mean 6 years after baseline. There were no significant differences in cognitive scores or proportion with cognitive impairment (16 vs. 8%) between survivors and controls and no evidence of accelerated ageing in CRC survivors. Baseline cognitive performance predicted for subsequent cognitive function. There were no differences in functional tests or blood tests between groups. In 18 participants undergoing neuroimaging, 10 CRC survivors had higher myoinositol levels than 8 controls, and lower volume in the right amygdala and caudate and left hippocampal regions. CONCLUSIONS: There was no difference in cognitive capacity and function between CRC survivors and controls 6–12 years after diagnosis. Differences in neuroimaging require confirmation in a larger sample. HIGHLIGHTS: • No evidence of long term cognitive impairment in colorectal cancer survivors compared to controls 6–12 years after diagnosis • No evidence of accelerated cognitive ageing in colorectal cancer survivors • No evidence of long-term functional impairment in colorectal cancer survivors SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00520-022-07008-3. Springer Berlin Heidelberg 2022-04-14 2022 /pmc/articles/PMC9135780/ /pubmed/35420329 http://dx.doi.org/10.1007/s00520-022-07008-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Vardy, Janette L.
Pond, Gregory R.
Cysique, Lucette A.
Gates, Thomas M.
Lagopoulos, Jim
Renton, Corrinne
Waite, Louise M.
Tannock, Ian F.
Dhillon, Haryana M.
Lack of cognitive impairment in long-term survivors of colorectal cancer
title Lack of cognitive impairment in long-term survivors of colorectal cancer
title_full Lack of cognitive impairment in long-term survivors of colorectal cancer
title_fullStr Lack of cognitive impairment in long-term survivors of colorectal cancer
title_full_unstemmed Lack of cognitive impairment in long-term survivors of colorectal cancer
title_short Lack of cognitive impairment in long-term survivors of colorectal cancer
title_sort lack of cognitive impairment in long-term survivors of colorectal cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9135780/
https://www.ncbi.nlm.nih.gov/pubmed/35420329
http://dx.doi.org/10.1007/s00520-022-07008-3
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