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Stroke in systemic lupus erythematosus: a meta-analysis of population-based cohort studies

Previous studies of stroke in systemic lupus erythematosus (SLE) have had limited statistical power, combined stroke subtypes into composite outcomes, and lacked a reference population estimate. Therefore, we conducted a systematic review and meta-analysis of cohort studies to summarise the stroke s...

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Autores principales: Holmqvist, Marie, Simard, Julia F, Asplund, Kjell, Arkema, Elizabeth V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4692049/
https://www.ncbi.nlm.nih.gov/pubmed/26719816
http://dx.doi.org/10.1136/rmdopen-2015-000168
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author Holmqvist, Marie
Simard, Julia F
Asplund, Kjell
Arkema, Elizabeth V
author_facet Holmqvist, Marie
Simard, Julia F
Asplund, Kjell
Arkema, Elizabeth V
author_sort Holmqvist, Marie
collection PubMed
description Previous studies of stroke in systemic lupus erythematosus (SLE) have had limited statistical power, combined stroke subtypes into composite outcomes, and lacked a reference population estimate. Therefore, we conducted a systematic review and meta-analysis of cohort studies to summarise the stroke subtype-specific risk in patients with SLE compared to the general population. A systematic search of MEDLINE and EMBASE was performed for cohort studies examining the risk of stroke in SLE and including a general population comparator. Random effects models were used to pool the risk ratio (RR) for stroke. Subgroup analyses were carried out to investigate potential sources of heterogeneity. 10 studies were included which reported RRs for overall stroke (n=5), ischaemic stroke (n=6), intracerebral haemorrhage (n=3) and subarachnoid haemorrhage (n=3). The pooled RR for overall stroke was 2.53 (95% CI 1.96 to 3.26), ischaemic stroke 2.10 (95% CI 1.68 to 2.62), intracerebral haemorrhage 2.72 (95% CI 2.15 to 3.44) and subarachnoid haemorrhage 3.85 (95% CI 3.20 to 4.64). Significant heterogeneity among studies for ischaemic stroke was detected (p=0.002). Relative risk of stroke was highest among individuals younger than 50 years of age. Individuals with SLE have a twofold higher risk of ischaemic stroke, a threefold higher risk of intracerebral haemorrhage, and an almost fourfold higher risk of subarachnoid haemorrhage compared to the general population. Future studies should focus on whether comorbidity and disease flares are related to stroke, when individuals are at the highest risk, and how the targeting of specific groups of patients with SLE may reduce this risk.
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spelling pubmed-46920492015-12-30 Stroke in systemic lupus erythematosus: a meta-analysis of population-based cohort studies Holmqvist, Marie Simard, Julia F Asplund, Kjell Arkema, Elizabeth V RMD Open Lupus Previous studies of stroke in systemic lupus erythematosus (SLE) have had limited statistical power, combined stroke subtypes into composite outcomes, and lacked a reference population estimate. Therefore, we conducted a systematic review and meta-analysis of cohort studies to summarise the stroke subtype-specific risk in patients with SLE compared to the general population. A systematic search of MEDLINE and EMBASE was performed for cohort studies examining the risk of stroke in SLE and including a general population comparator. Random effects models were used to pool the risk ratio (RR) for stroke. Subgroup analyses were carried out to investigate potential sources of heterogeneity. 10 studies were included which reported RRs for overall stroke (n=5), ischaemic stroke (n=6), intracerebral haemorrhage (n=3) and subarachnoid haemorrhage (n=3). The pooled RR for overall stroke was 2.53 (95% CI 1.96 to 3.26), ischaemic stroke 2.10 (95% CI 1.68 to 2.62), intracerebral haemorrhage 2.72 (95% CI 2.15 to 3.44) and subarachnoid haemorrhage 3.85 (95% CI 3.20 to 4.64). Significant heterogeneity among studies for ischaemic stroke was detected (p=0.002). Relative risk of stroke was highest among individuals younger than 50 years of age. Individuals with SLE have a twofold higher risk of ischaemic stroke, a threefold higher risk of intracerebral haemorrhage, and an almost fourfold higher risk of subarachnoid haemorrhage compared to the general population. Future studies should focus on whether comorbidity and disease flares are related to stroke, when individuals are at the highest risk, and how the targeting of specific groups of patients with SLE may reduce this risk. BMJ Publishing Group 2015-12-16 /pmc/articles/PMC4692049/ /pubmed/26719816 http://dx.doi.org/10.1136/rmdopen-2015-000168 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ 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 Lupus
Holmqvist, Marie
Simard, Julia F
Asplund, Kjell
Arkema, Elizabeth V
Stroke in systemic lupus erythematosus: a meta-analysis of population-based cohort studies
title Stroke in systemic lupus erythematosus: a meta-analysis of population-based cohort studies
title_full Stroke in systemic lupus erythematosus: a meta-analysis of population-based cohort studies
title_fullStr Stroke in systemic lupus erythematosus: a meta-analysis of population-based cohort studies
title_full_unstemmed Stroke in systemic lupus erythematosus: a meta-analysis of population-based cohort studies
title_short Stroke in systemic lupus erythematosus: a meta-analysis of population-based cohort studies
title_sort stroke in systemic lupus erythematosus: a meta-analysis of population-based cohort studies
topic Lupus
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4692049/
https://www.ncbi.nlm.nih.gov/pubmed/26719816
http://dx.doi.org/10.1136/rmdopen-2015-000168
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