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Low LDL-C level and intracranial haemorrhage risk after ischaemic stroke: a prospective cohort study
BACKGROUND AND PURPOSE: The Treat Stroke to Target trial has confirmed the benefit of targeting low-density lipoprotein cholesterol (LDL-C) of <1.8 mmol/L in patients who had an ischaemic stroke (IS). However, haemorrhagic risk brought by this target level (<1.8 mmol/L) or even lower level (&l...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10176994/ https://www.ncbi.nlm.nih.gov/pubmed/36162902 http://dx.doi.org/10.1136/svn-2022-001612 |
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author | Xu, Jie Chen, Zimo Wang, Meng Mo, Jinglin Jing, Jing Yalkun, Gulbahram Dai, Liye Meng, Xia Li, Hao Li, Zixiao Wang, Yongjun |
author_facet | Xu, Jie Chen, Zimo Wang, Meng Mo, Jinglin Jing, Jing Yalkun, Gulbahram Dai, Liye Meng, Xia Li, Hao Li, Zixiao Wang, Yongjun |
author_sort | Xu, Jie |
collection | PubMed |
description | BACKGROUND AND PURPOSE: The Treat Stroke to Target trial has confirmed the benefit of targeting low-density lipoprotein cholesterol (LDL-C) of <1.8 mmol/L in patients who had an ischaemic stroke (IS). However, haemorrhagic risk brought by this target level (<1.8 mmol/L) or even lower level (<1.4 mmol/L) of LDL-C should also be concerned. In this study, we aimed to demonstrate whether low LDL-C could increase the intracranial haemorrhage risk following IS. METHODS: Patients who had an IS from China Stroke Center Alliance programme with complete baseline information were prospectively enrolled. 793 572 patients who had an IS were categorised into 6 groups according to LDL-C level (<1.40 mmol/L, 1.40–1.79 mmol/L, 1.80–2.59 mmol/L, 2.60–2.99 mmol/L, 3.00–4.89 mmol/L, ≥4.90 mmol/L). The study outcome was defined as intracranial haemorrhage identified during hospitalisation. Logistic regression model was used to examine the association between different LDL-C levels and risk of intracranial haemorrhage. RESULTS: Compared with patients of LDL-C=1.80–2.59 mmol/L, both subgroups of LDL-C<1.40 mmol/L and LDL-C=1.40–1.79 mmol/L showed significantly higher risk of intracranial haemorrhage (OR=1.26, 95% CI=1.18 to 1.35; OR=1.22, 95% CI=1.14 to 1.30, respectively). Interaction effect was found to exist between the subgroups of intravenous thrombolytic therapy (p=0.04), rather than the subgroups of age, sex and body mass index. Moreover, the sensitivity analyses indicated that even patients who had an IS with minor stroke still suffered from the increased intracranial haemorrhage risk related to low LDL-C level. CONCLUSIONS: Among patients who had an IS, the low LDL-C level (<1.4 mmol/L or <1.8 mmol/L) at baseline is associated with increased risk of intracranial haemorrhage during acute stage. While actively lowering LDL-C level for patients who had an IS, clinicians should also concern about the haemorrhagic risk associated with low LDL-C level. |
format | Online Article Text |
id | pubmed-10176994 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-101769942023-05-13 Low LDL-C level and intracranial haemorrhage risk after ischaemic stroke: a prospective cohort study Xu, Jie Chen, Zimo Wang, Meng Mo, Jinglin Jing, Jing Yalkun, Gulbahram Dai, Liye Meng, Xia Li, Hao Li, Zixiao Wang, Yongjun Stroke Vasc Neurol Original Research BACKGROUND AND PURPOSE: The Treat Stroke to Target trial has confirmed the benefit of targeting low-density lipoprotein cholesterol (LDL-C) of <1.8 mmol/L in patients who had an ischaemic stroke (IS). However, haemorrhagic risk brought by this target level (<1.8 mmol/L) or even lower level (<1.4 mmol/L) of LDL-C should also be concerned. In this study, we aimed to demonstrate whether low LDL-C could increase the intracranial haemorrhage risk following IS. METHODS: Patients who had an IS from China Stroke Center Alliance programme with complete baseline information were prospectively enrolled. 793 572 patients who had an IS were categorised into 6 groups according to LDL-C level (<1.40 mmol/L, 1.40–1.79 mmol/L, 1.80–2.59 mmol/L, 2.60–2.99 mmol/L, 3.00–4.89 mmol/L, ≥4.90 mmol/L). The study outcome was defined as intracranial haemorrhage identified during hospitalisation. Logistic regression model was used to examine the association between different LDL-C levels and risk of intracranial haemorrhage. RESULTS: Compared with patients of LDL-C=1.80–2.59 mmol/L, both subgroups of LDL-C<1.40 mmol/L and LDL-C=1.40–1.79 mmol/L showed significantly higher risk of intracranial haemorrhage (OR=1.26, 95% CI=1.18 to 1.35; OR=1.22, 95% CI=1.14 to 1.30, respectively). Interaction effect was found to exist between the subgroups of intravenous thrombolytic therapy (p=0.04), rather than the subgroups of age, sex and body mass index. Moreover, the sensitivity analyses indicated that even patients who had an IS with minor stroke still suffered from the increased intracranial haemorrhage risk related to low LDL-C level. CONCLUSIONS: Among patients who had an IS, the low LDL-C level (<1.4 mmol/L or <1.8 mmol/L) at baseline is associated with increased risk of intracranial haemorrhage during acute stage. While actively lowering LDL-C level for patients who had an IS, clinicians should also concern about the haemorrhagic risk associated with low LDL-C level. BMJ Publishing Group 2022-09-26 /pmc/articles/PMC10176994/ /pubmed/36162902 http://dx.doi.org/10.1136/svn-2022-001612 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/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, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Original Research Xu, Jie Chen, Zimo Wang, Meng Mo, Jinglin Jing, Jing Yalkun, Gulbahram Dai, Liye Meng, Xia Li, Hao Li, Zixiao Wang, Yongjun Low LDL-C level and intracranial haemorrhage risk after ischaemic stroke: a prospective cohort study |
title | Low LDL-C level and intracranial haemorrhage risk after ischaemic stroke: a prospective cohort study |
title_full | Low LDL-C level and intracranial haemorrhage risk after ischaemic stroke: a prospective cohort study |
title_fullStr | Low LDL-C level and intracranial haemorrhage risk after ischaemic stroke: a prospective cohort study |
title_full_unstemmed | Low LDL-C level and intracranial haemorrhage risk after ischaemic stroke: a prospective cohort study |
title_short | Low LDL-C level and intracranial haemorrhage risk after ischaemic stroke: a prospective cohort study |
title_sort | low ldl-c level and intracranial haemorrhage risk after ischaemic stroke: a prospective cohort study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10176994/ https://www.ncbi.nlm.nih.gov/pubmed/36162902 http://dx.doi.org/10.1136/svn-2022-001612 |
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