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Positive syphilis serology contributes to intracranial stenosis in ischemic stroke patients
BACKGROUND AND PURPOSE: The risk of ischemic stroke is increased among people living with syphilis infection; however, whether syphilis is an independently risk for stenosis is unclear. We investigated the clinical, laboratory, and vascular stenosis features of ischemic stroke patients living with p...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7821556/ https://www.ncbi.nlm.nih.gov/pubmed/33089668 http://dx.doi.org/10.1002/brb3.1906 |
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author | Xiang, Lei Zhang, Tao Zhang, Biao Zhang, Chao Cui, Wanzhen Yue, Wei |
author_facet | Xiang, Lei Zhang, Tao Zhang, Biao Zhang, Chao Cui, Wanzhen Yue, Wei |
author_sort | Xiang, Lei |
collection | PubMed |
description | BACKGROUND AND PURPOSE: The risk of ischemic stroke is increased among people living with syphilis infection; however, whether syphilis is an independently risk for stenosis is unclear. We investigated the clinical, laboratory, and vascular stenosis features of ischemic stroke patients living with positive syphilis serology to evaluate the role of syphilis in cerebral artery stenosis. METHODS: The demographic, clinical characteristics, and the distribution of cerebral artery stenosis were compared between 668 syphilis‐positive and 785 syphilis‐negative ischemic stroke patients. Multivariate logistic regression analysis was performed to determine the degree and distribution of stenosis associated with positive syphilis serology and estimate the factors related to artery stenosis in the syphilis‐positive ischemic stroke patients. RESULTS: Syphilis‐positive ischemic stroke patients were distinct from the nonsyphilis population, with a younger age, fewer women, and a different risk factor profile. Positive syphilis serology was independently associated with moderate stenosis (OR, 2.31; 95% CI 2.02–2.69; p = .003) and severe stenosis (OR, 6.15; 95% CI, 2.85–8.94; p < .001), mainly intracranial stenosis (OR, 1.49; 95% CI, 1.15–1.92; p = .002) rather than extracranial stenosis. Among stroke patients with positive syphilis serology, the higher RPR titer (OR, 1.18, 95% CI, 1.07–1.89 for RPR titer 1:16; OR, 5.16, 95% CI 2.99–8.89 for RPR titer > 1:32) and previous unknown or untreated syphilis (OR, 3.63; 95% CI, 2.72–4.03; p < .001) were the factors related to stenosis. CONCLUSIONS: Syphilis infection, especially when less well controlled, may play an important role in intracranial stenosis of ischemic stroke patients. |
format | Online Article Text |
id | pubmed-7821556 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78215562021-01-29 Positive syphilis serology contributes to intracranial stenosis in ischemic stroke patients Xiang, Lei Zhang, Tao Zhang, Biao Zhang, Chao Cui, Wanzhen Yue, Wei Brain Behav Original Research BACKGROUND AND PURPOSE: The risk of ischemic stroke is increased among people living with syphilis infection; however, whether syphilis is an independently risk for stenosis is unclear. We investigated the clinical, laboratory, and vascular stenosis features of ischemic stroke patients living with positive syphilis serology to evaluate the role of syphilis in cerebral artery stenosis. METHODS: The demographic, clinical characteristics, and the distribution of cerebral artery stenosis were compared between 668 syphilis‐positive and 785 syphilis‐negative ischemic stroke patients. Multivariate logistic regression analysis was performed to determine the degree and distribution of stenosis associated with positive syphilis serology and estimate the factors related to artery stenosis in the syphilis‐positive ischemic stroke patients. RESULTS: Syphilis‐positive ischemic stroke patients were distinct from the nonsyphilis population, with a younger age, fewer women, and a different risk factor profile. Positive syphilis serology was independently associated with moderate stenosis (OR, 2.31; 95% CI 2.02–2.69; p = .003) and severe stenosis (OR, 6.15; 95% CI, 2.85–8.94; p < .001), mainly intracranial stenosis (OR, 1.49; 95% CI, 1.15–1.92; p = .002) rather than extracranial stenosis. Among stroke patients with positive syphilis serology, the higher RPR titer (OR, 1.18, 95% CI, 1.07–1.89 for RPR titer 1:16; OR, 5.16, 95% CI 2.99–8.89 for RPR titer > 1:32) and previous unknown or untreated syphilis (OR, 3.63; 95% CI, 2.72–4.03; p < .001) were the factors related to stenosis. CONCLUSIONS: Syphilis infection, especially when less well controlled, may play an important role in intracranial stenosis of ischemic stroke patients. John Wiley and Sons Inc. 2020-10-21 /pmc/articles/PMC7821556/ /pubmed/33089668 http://dx.doi.org/10.1002/brb3.1906 Text en © 2020 The Authors. Brain and Behavior published by Wiley Periodicals LLC This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Xiang, Lei Zhang, Tao Zhang, Biao Zhang, Chao Cui, Wanzhen Yue, Wei Positive syphilis serology contributes to intracranial stenosis in ischemic stroke patients |
title | Positive syphilis serology contributes to intracranial stenosis in ischemic stroke patients |
title_full | Positive syphilis serology contributes to intracranial stenosis in ischemic stroke patients |
title_fullStr | Positive syphilis serology contributes to intracranial stenosis in ischemic stroke patients |
title_full_unstemmed | Positive syphilis serology contributes to intracranial stenosis in ischemic stroke patients |
title_short | Positive syphilis serology contributes to intracranial stenosis in ischemic stroke patients |
title_sort | positive syphilis serology contributes to intracranial stenosis in ischemic stroke patients |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7821556/ https://www.ncbi.nlm.nih.gov/pubmed/33089668 http://dx.doi.org/10.1002/brb3.1906 |
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