Cargando…

Influences of genetic variants on stroke recovery: a meta-analysis of the 31,895 cases

BACKGROUND: The influences of genetic variants on functional clinical outcomes following stroke are unclear. In order to reliably quantify these influences, we undertook a comprehensive meta-analysis of outcomes after acute intracerebral haemorrhage (ICH) or ischaemic stroke (AIS) in relation to dif...

Descripción completa

Detalles Bibliográficos
Autores principales: Math, Nikhil, Han, Thang S., Lubomirova, Irina, Hill, Robert, Bentley, Paul, Sharma, Pankaj
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6848040/
https://www.ncbi.nlm.nih.gov/pubmed/31359356
http://dx.doi.org/10.1007/s10072-019-04024-w
_version_ 1783469007222865920
author Math, Nikhil
Han, Thang S.
Lubomirova, Irina
Hill, Robert
Bentley, Paul
Sharma, Pankaj
author_facet Math, Nikhil
Han, Thang S.
Lubomirova, Irina
Hill, Robert
Bentley, Paul
Sharma, Pankaj
author_sort Math, Nikhil
collection PubMed
description BACKGROUND: The influences of genetic variants on functional clinical outcomes following stroke are unclear. In order to reliably quantify these influences, we undertook a comprehensive meta-analysis of outcomes after acute intracerebral haemorrhage (ICH) or ischaemic stroke (AIS) in relation to different genetic variants. METHODS: PubMed, PsycInfo, Embase and Medline electronic databases were searched up to January 2019. Outcomes, defined as favourable or poor, were assessed by validated scales (Barthel index, modified Rankin scale, Glasgow outcome scale and National Institutes of Health stroke scale). RESULTS: Ninety-two publications comprising 31,895 cases met our inclusion criteria. Poor outcome was observed in patients with ICH who possessed the APOE4 allele: OR =2.60 (95% CI = 1.25–5.41, p = 0.01) and in AIS patients with the GA or AA variant at the BDNF-196 locus: OR = 2.60 (95% CI = 1.25–5.41, p = 0.01) or a loss of function allele of CYP2C19: OR = 2.36 (95% CI = 1.56–3.55, p < 0.0001). Poor outcome was not associated with APOE4: OR = 1.02 (95% CI = 0.81–1.27, p = 0.90) or IL6-174 G/C: OR = 2.21 (95% CI = 0.55–8.86, p = 0.26) in patients with AIS. CONCLUSIONS: We demonstrate that recovery of AIS was unfavourably associated with variants of BDNF and CYP2C19 genes whilst recovery of ICH was unfavourably associated with APOE4 gene. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10072-019-04024-w) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6848040
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Springer International Publishing
record_format MEDLINE/PubMed
spelling pubmed-68480402019-11-22 Influences of genetic variants on stroke recovery: a meta-analysis of the 31,895 cases Math, Nikhil Han, Thang S. Lubomirova, Irina Hill, Robert Bentley, Paul Sharma, Pankaj Neurol Sci Review Article BACKGROUND: The influences of genetic variants on functional clinical outcomes following stroke are unclear. In order to reliably quantify these influences, we undertook a comprehensive meta-analysis of outcomes after acute intracerebral haemorrhage (ICH) or ischaemic stroke (AIS) in relation to different genetic variants. METHODS: PubMed, PsycInfo, Embase and Medline electronic databases were searched up to January 2019. Outcomes, defined as favourable or poor, were assessed by validated scales (Barthel index, modified Rankin scale, Glasgow outcome scale and National Institutes of Health stroke scale). RESULTS: Ninety-two publications comprising 31,895 cases met our inclusion criteria. Poor outcome was observed in patients with ICH who possessed the APOE4 allele: OR =2.60 (95% CI = 1.25–5.41, p = 0.01) and in AIS patients with the GA or AA variant at the BDNF-196 locus: OR = 2.60 (95% CI = 1.25–5.41, p = 0.01) or a loss of function allele of CYP2C19: OR = 2.36 (95% CI = 1.56–3.55, p < 0.0001). Poor outcome was not associated with APOE4: OR = 1.02 (95% CI = 0.81–1.27, p = 0.90) or IL6-174 G/C: OR = 2.21 (95% CI = 0.55–8.86, p = 0.26) in patients with AIS. CONCLUSIONS: We demonstrate that recovery of AIS was unfavourably associated with variants of BDNF and CYP2C19 genes whilst recovery of ICH was unfavourably associated with APOE4 gene. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10072-019-04024-w) contains supplementary material, which is available to authorized users. Springer International Publishing 2019-07-29 2019 /pmc/articles/PMC6848040/ /pubmed/31359356 http://dx.doi.org/10.1007/s10072-019-04024-w Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Review Article
Math, Nikhil
Han, Thang S.
Lubomirova, Irina
Hill, Robert
Bentley, Paul
Sharma, Pankaj
Influences of genetic variants on stroke recovery: a meta-analysis of the 31,895 cases
title Influences of genetic variants on stroke recovery: a meta-analysis of the 31,895 cases
title_full Influences of genetic variants on stroke recovery: a meta-analysis of the 31,895 cases
title_fullStr Influences of genetic variants on stroke recovery: a meta-analysis of the 31,895 cases
title_full_unstemmed Influences of genetic variants on stroke recovery: a meta-analysis of the 31,895 cases
title_short Influences of genetic variants on stroke recovery: a meta-analysis of the 31,895 cases
title_sort influences of genetic variants on stroke recovery: a meta-analysis of the 31,895 cases
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6848040/
https://www.ncbi.nlm.nih.gov/pubmed/31359356
http://dx.doi.org/10.1007/s10072-019-04024-w
work_keys_str_mv AT mathnikhil influencesofgeneticvariantsonstrokerecoveryametaanalysisofthe31895cases
AT hanthangs influencesofgeneticvariantsonstrokerecoveryametaanalysisofthe31895cases
AT lubomirovairina influencesofgeneticvariantsonstrokerecoveryametaanalysisofthe31895cases
AT hillrobert influencesofgeneticvariantsonstrokerecoveryametaanalysisofthe31895cases
AT bentleypaul influencesofgeneticvariantsonstrokerecoveryametaanalysisofthe31895cases
AT sharmapankaj influencesofgeneticvariantsonstrokerecoveryametaanalysisofthe31895cases