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Pre-eclampsia and risk of dementia later in life: nationwide cohort study

OBJECTIVE: To explore associations between pre-eclampsia and later dementia, overall and by dementia subtype and timing of onset. DESIGN: Nationwide register based cohort study. SETTING: Denmark. POPULATION: All women with at least one live birth or stillbirth between 1978 and 2015. MAIN OUTCOME MEA...

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Detalles Bibliográficos
Autores principales: Basit, Saima, Wohlfahrt, Jan, Boyd, Heather A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group Ltd. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6191824/
https://www.ncbi.nlm.nih.gov/pubmed/30333106
http://dx.doi.org/10.1136/bmj.k4109
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author Basit, Saima
Wohlfahrt, Jan
Boyd, Heather A
author_facet Basit, Saima
Wohlfahrt, Jan
Boyd, Heather A
author_sort Basit, Saima
collection PubMed
description OBJECTIVE: To explore associations between pre-eclampsia and later dementia, overall and by dementia subtype and timing of onset. DESIGN: Nationwide register based cohort study. SETTING: Denmark. POPULATION: All women with at least one live birth or stillbirth between 1978 and 2015. MAIN OUTCOME MEASURE: Hazard ratios comparing dementia rates among women with and without a history of pre-eclampsia, estimated using Cox regression. RESULTS: The cohort consisted of 1 178 005 women with 20 352 695 person years of follow-up. Women with a history of pre-eclampsia had more than three times the risk of vascular dementia (hazard ratio 3.46, 95% confidence interval 1.97 to 6.10) later in life, compared with women with no history of pre-eclampsia. The association with vascular dementia seemed to be stronger for late onset disease (hazard ratio 6.53, 2.82 to 15.1) than for early onset disease (2.32, 1.06 to 5.06) (P=0.08). Adjustment for diabetes, hypertension, and cardiovascular disease attenuated the hazard ratios only moderately; sensitivity analyses suggested that body mass index was unlikely to explain the association with vascular dementia. In contrast, only modest associations were observed for Alzheimer’s disease (hazard ratio 1.45, 1.05 to 1.99) and other/unspecified dementia (1.40, 1.08 to 1.83). CONCLUSIONS: Pre-eclampsia was associated with an increased risk of dementia, particularly vascular dementia. Cardiovascular disease, hypertension, and diabetes were unlikely to mediate the associations substantially, suggesting that pre-eclampsia and vascular dementia may share underlying mechanisms or susceptibility pathways. Asking about a history of pre-eclampsia could help physicians to identify women who might benefit from screening for early signs of disease, allowing for early clinical intervention.
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spelling pubmed-61918242018-10-19 Pre-eclampsia and risk of dementia later in life: nationwide cohort study Basit, Saima Wohlfahrt, Jan Boyd, Heather A BMJ Research OBJECTIVE: To explore associations between pre-eclampsia and later dementia, overall and by dementia subtype and timing of onset. DESIGN: Nationwide register based cohort study. SETTING: Denmark. POPULATION: All women with at least one live birth or stillbirth between 1978 and 2015. MAIN OUTCOME MEASURE: Hazard ratios comparing dementia rates among women with and without a history of pre-eclampsia, estimated using Cox regression. RESULTS: The cohort consisted of 1 178 005 women with 20 352 695 person years of follow-up. Women with a history of pre-eclampsia had more than three times the risk of vascular dementia (hazard ratio 3.46, 95% confidence interval 1.97 to 6.10) later in life, compared with women with no history of pre-eclampsia. The association with vascular dementia seemed to be stronger for late onset disease (hazard ratio 6.53, 2.82 to 15.1) than for early onset disease (2.32, 1.06 to 5.06) (P=0.08). Adjustment for diabetes, hypertension, and cardiovascular disease attenuated the hazard ratios only moderately; sensitivity analyses suggested that body mass index was unlikely to explain the association with vascular dementia. In contrast, only modest associations were observed for Alzheimer’s disease (hazard ratio 1.45, 1.05 to 1.99) and other/unspecified dementia (1.40, 1.08 to 1.83). CONCLUSIONS: Pre-eclampsia was associated with an increased risk of dementia, particularly vascular dementia. Cardiovascular disease, hypertension, and diabetes were unlikely to mediate the associations substantially, suggesting that pre-eclampsia and vascular dementia may share underlying mechanisms or susceptibility pathways. Asking about a history of pre-eclampsia could help physicians to identify women who might benefit from screening for early signs of disease, allowing for early clinical intervention. BMJ Publishing Group Ltd. 2018-10-17 /pmc/articles/PMC6191824/ /pubmed/30333106 http://dx.doi.org/10.1136/bmj.k4109 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Research
Basit, Saima
Wohlfahrt, Jan
Boyd, Heather A
Pre-eclampsia and risk of dementia later in life: nationwide cohort study
title Pre-eclampsia and risk of dementia later in life: nationwide cohort study
title_full Pre-eclampsia and risk of dementia later in life: nationwide cohort study
title_fullStr Pre-eclampsia and risk of dementia later in life: nationwide cohort study
title_full_unstemmed Pre-eclampsia and risk of dementia later in life: nationwide cohort study
title_short Pre-eclampsia and risk of dementia later in life: nationwide cohort study
title_sort pre-eclampsia and risk of dementia later in life: nationwide cohort study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6191824/
https://www.ncbi.nlm.nih.gov/pubmed/30333106
http://dx.doi.org/10.1136/bmj.k4109
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