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Real-world effects of anti-dementia treatment on mortality in patients with Alzheimer´s dementia
To examine the real-world effects of the cholinesterase inhibitors (AChEI) on all-cause mortality. A nationwide, retrospective cohort study. Participants were diagnosed with incident AD in Denmark from January 1, 2000 to December 31, 2011 with follow-up until December 31, 2012. A total of 36,513 par...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666173/ https://www.ncbi.nlm.nih.gov/pubmed/36397447 http://dx.doi.org/10.1097/MD.0000000000031625 |
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author | Nielsen, René Ernst Grøntved, Simon Lolk, Annette Andersen, Kjeld Valentin, Jan B. |
author_facet | Nielsen, René Ernst Grøntved, Simon Lolk, Annette Andersen, Kjeld Valentin, Jan B. |
author_sort | Nielsen, René Ernst |
collection | PubMed |
description | To examine the real-world effects of the cholinesterase inhibitors (AChEI) on all-cause mortality. A nationwide, retrospective cohort study. Participants were diagnosed with incident AD in Denmark from January 1, 2000 to December 31, 2011 with follow-up until December 31, 2012. A total of 36,513 participants were included in the current study with 22,063 deaths during 132,426 person-years of follow-up. At baseline, patients not treated with AChEI (n = 28,755 [9961 males (35%)]) had a mean age ± standard deviation (SD) of 80.33 ± 7.98 years (78.97 ± 8.26 for males and 81.04 ± 7.98 for females), as compared to 79.95 ± 7.67 (78.87 ± 7.61 for males and 80.61 ± 7.63 for females) in the group exposed at baseline. Patients treated with AChEI had a beneficial hazard ratio (HR) of 0.69, 95% confidence interval (CI) (0.67–0.71) for all-cause mortality as compared to patients not treated, with donepezil (HR 0.80, 95% CI [0.77–0.82]) and galantamine (HR 0.93,95% CI [0.89–0.97]) having beneficial effects on mortality rate as compared to non-treatment, whereas rivastigmine (HR 0.99, 95% CI [0.95–1.03]) was associated with a mortality rate comparable to non-treatment with AChEI. Patients were primarily exposed to donepezil (65.8%) with rivastigmine (19.8%) and galantamine (14.4%) being used less often. These findings underscore the effect of AChEI on not only reducing speed of cognitive decline but also directly prolonging life, which could result in changes in treatment recommendation for when to stop treatment. |
format | Online Article Text |
id | pubmed-9666173 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-96661732022-11-16 Real-world effects of anti-dementia treatment on mortality in patients with Alzheimer´s dementia Nielsen, René Ernst Grøntved, Simon Lolk, Annette Andersen, Kjeld Valentin, Jan B. Medicine (Baltimore) 4200 To examine the real-world effects of the cholinesterase inhibitors (AChEI) on all-cause mortality. A nationwide, retrospective cohort study. Participants were diagnosed with incident AD in Denmark from January 1, 2000 to December 31, 2011 with follow-up until December 31, 2012. A total of 36,513 participants were included in the current study with 22,063 deaths during 132,426 person-years of follow-up. At baseline, patients not treated with AChEI (n = 28,755 [9961 males (35%)]) had a mean age ± standard deviation (SD) of 80.33 ± 7.98 years (78.97 ± 8.26 for males and 81.04 ± 7.98 for females), as compared to 79.95 ± 7.67 (78.87 ± 7.61 for males and 80.61 ± 7.63 for females) in the group exposed at baseline. Patients treated with AChEI had a beneficial hazard ratio (HR) of 0.69, 95% confidence interval (CI) (0.67–0.71) for all-cause mortality as compared to patients not treated, with donepezil (HR 0.80, 95% CI [0.77–0.82]) and galantamine (HR 0.93,95% CI [0.89–0.97]) having beneficial effects on mortality rate as compared to non-treatment, whereas rivastigmine (HR 0.99, 95% CI [0.95–1.03]) was associated with a mortality rate comparable to non-treatment with AChEI. Patients were primarily exposed to donepezil (65.8%) with rivastigmine (19.8%) and galantamine (14.4%) being used less often. These findings underscore the effect of AChEI on not only reducing speed of cognitive decline but also directly prolonging life, which could result in changes in treatment recommendation for when to stop treatment. Lippincott Williams & Wilkins 2022-11-11 /pmc/articles/PMC9666173/ /pubmed/36397447 http://dx.doi.org/10.1097/MD.0000000000031625 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC) (https://creativecommons.org/licenses/by-nc/4.0/) , where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. |
spellingShingle | 4200 Nielsen, René Ernst Grøntved, Simon Lolk, Annette Andersen, Kjeld Valentin, Jan B. Real-world effects of anti-dementia treatment on mortality in patients with Alzheimer´s dementia |
title | Real-world effects of anti-dementia treatment on mortality in patients with Alzheimer´s dementia |
title_full | Real-world effects of anti-dementia treatment on mortality in patients with Alzheimer´s dementia |
title_fullStr | Real-world effects of anti-dementia treatment on mortality in patients with Alzheimer´s dementia |
title_full_unstemmed | Real-world effects of anti-dementia treatment on mortality in patients with Alzheimer´s dementia |
title_short | Real-world effects of anti-dementia treatment on mortality in patients with Alzheimer´s dementia |
title_sort | real-world effects of anti-dementia treatment on mortality in patients with alzheimer´s dementia |
topic | 4200 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666173/ https://www.ncbi.nlm.nih.gov/pubmed/36397447 http://dx.doi.org/10.1097/MD.0000000000031625 |
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