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Sex variation in colorectal cancer mortality: trends and implications for screening
BACKGROUND: Colorectal cancer (CRC) screening using faecal tests reduces disease-specific mortality. To investigate mortality and its association with sex, rates in women and men, and in different age ranges, were examined, before and after screening began in Scotland. METHODS: From 1990–99, no stru...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10066495/ https://www.ncbi.nlm.nih.gov/pubmed/36847663 http://dx.doi.org/10.1093/eurpub/ckad029 |
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author | Clark, Gavin R C Fraser, Callum G Strachan, Judith A Steele, Robert J C |
author_facet | Clark, Gavin R C Fraser, Callum G Strachan, Judith A Steele, Robert J C |
author_sort | Clark, Gavin R C |
collection | PubMed |
description | BACKGROUND: Colorectal cancer (CRC) screening using faecal tests reduces disease-specific mortality. To investigate mortality and its association with sex, rates in women and men, and in different age ranges, were examined, before and after screening began in Scotland. METHODS: From 1990–99, no structured screening existed. Three pilots ran from 2000 to 2007 and subsequent full roll-out completed in 2009. Crude mortality rates for 1990–2020 were calculated relative to Scottish population estimates, and age–sex standardized rates calculated for all, pre-screening (<50 years), screening (5–74 years) and post-screening (>74 years) age ranges. RESULTS: CRC mortality declined from 1990 to 2020, but not linearly, and differed between sexes. In women, 1990–99 showed a steady decline [average annual percentage change (AAPC): −2.1%, 95% confidence interval (CI): −2.8% to −1.4%], but a less marked decline after 2000 (AAPC: −0.7%, 95% CI: −0.9% to −0.4%). In men, no clear decline was seen from 1990 to 1999 (AAPC: −0.4%, 95% CI: −1.1% to 0.4%), but mortality declined from 2000 to 2020 (AAPC: −1.7%, 95% CI: −1.9% to −1.5%). This pattern was exaggerated in the screening age ranges. For 2000–20, the overall reduction in mortality was less in women and in the screening age range. In the post-screening age range, reductions were smaller, but an increase was seen in the pre-screening age range, greater in women. CONCLUSIONS: CRC mortality fell during 1990–2020, but the decline differed markedly between sexes, indicating a larger beneficial effect of screening on CRC mortality in men compared to women: use of different thresholds for the sexes might lead to equality. |
format | Online Article Text |
id | pubmed-10066495 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-100664952023-04-02 Sex variation in colorectal cancer mortality: trends and implications for screening Clark, Gavin R C Fraser, Callum G Strachan, Judith A Steele, Robert J C Eur J Public Health Cancer Screening BACKGROUND: Colorectal cancer (CRC) screening using faecal tests reduces disease-specific mortality. To investigate mortality and its association with sex, rates in women and men, and in different age ranges, were examined, before and after screening began in Scotland. METHODS: From 1990–99, no structured screening existed. Three pilots ran from 2000 to 2007 and subsequent full roll-out completed in 2009. Crude mortality rates for 1990–2020 were calculated relative to Scottish population estimates, and age–sex standardized rates calculated for all, pre-screening (<50 years), screening (5–74 years) and post-screening (>74 years) age ranges. RESULTS: CRC mortality declined from 1990 to 2020, but not linearly, and differed between sexes. In women, 1990–99 showed a steady decline [average annual percentage change (AAPC): −2.1%, 95% confidence interval (CI): −2.8% to −1.4%], but a less marked decline after 2000 (AAPC: −0.7%, 95% CI: −0.9% to −0.4%). In men, no clear decline was seen from 1990 to 1999 (AAPC: −0.4%, 95% CI: −1.1% to 0.4%), but mortality declined from 2000 to 2020 (AAPC: −1.7%, 95% CI: −1.9% to −1.5%). This pattern was exaggerated in the screening age ranges. For 2000–20, the overall reduction in mortality was less in women and in the screening age range. In the post-screening age range, reductions were smaller, but an increase was seen in the pre-screening age range, greater in women. CONCLUSIONS: CRC mortality fell during 1990–2020, but the decline differed markedly between sexes, indicating a larger beneficial effect of screening on CRC mortality in men compared to women: use of different thresholds for the sexes might lead to equality. Oxford University Press 2023-02-27 /pmc/articles/PMC10066495/ /pubmed/36847663 http://dx.doi.org/10.1093/eurpub/ckad029 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the European Public Health Association. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Cancer Screening Clark, Gavin R C Fraser, Callum G Strachan, Judith A Steele, Robert J C Sex variation in colorectal cancer mortality: trends and implications for screening |
title | Sex variation in colorectal cancer mortality: trends and implications for screening |
title_full | Sex variation in colorectal cancer mortality: trends and implications for screening |
title_fullStr | Sex variation in colorectal cancer mortality: trends and implications for screening |
title_full_unstemmed | Sex variation in colorectal cancer mortality: trends and implications for screening |
title_short | Sex variation in colorectal cancer mortality: trends and implications for screening |
title_sort | sex variation in colorectal cancer mortality: trends and implications for screening |
topic | Cancer Screening |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10066495/ https://www.ncbi.nlm.nih.gov/pubmed/36847663 http://dx.doi.org/10.1093/eurpub/ckad029 |
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