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Association of inflammatory markers with cerebral small vessel disease in community-based population

BACKGROUND: This study investigated the relationships of neutrophil count (NC), neutrophil-to-lymphocyte ratio (NLR) and systemic immune-inflammation index (SII) with cerebral small vessel disease (CSVD). METHODS: A total of 3052 community-dwelling residents from the Poly-vasculaR Evaluation for Cog...

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Autores principales: Jiang, Lingling, Cai, Xueli, Yao, Dongxiao, Jing, Jing, Mei, Lerong, Yang, Yingying, Li, Shan, Jin, Aoming, Meng, Xia, Li, Hao, Wei, Tiemin, Wang, Yongjun, Pan, Yuesong, Wang, Yilong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072153/
https://www.ncbi.nlm.nih.gov/pubmed/35513834
http://dx.doi.org/10.1186/s12974-022-02468-0
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author Jiang, Lingling
Cai, Xueli
Yao, Dongxiao
Jing, Jing
Mei, Lerong
Yang, Yingying
Li, Shan
Jin, Aoming
Meng, Xia
Li, Hao
Wei, Tiemin
Wang, Yongjun
Pan, Yuesong
Wang, Yilong
author_facet Jiang, Lingling
Cai, Xueli
Yao, Dongxiao
Jing, Jing
Mei, Lerong
Yang, Yingying
Li, Shan
Jin, Aoming
Meng, Xia
Li, Hao
Wei, Tiemin
Wang, Yongjun
Pan, Yuesong
Wang, Yilong
author_sort Jiang, Lingling
collection PubMed
description BACKGROUND: This study investigated the relationships of neutrophil count (NC), neutrophil-to-lymphocyte ratio (NLR) and systemic immune-inflammation index (SII) with cerebral small vessel disease (CSVD). METHODS: A total of 3052 community-dwelling residents from the Poly-vasculaR Evaluation for Cognitive Impairment and vaScular Events (PRECISE) study were involved in this cross-sectional study. CSVD burden and imaging markers, including white matter hyperintensity (WMH), lacunes, cerebral microbleeds (CMBs) and enlarged perivascular spaces in basal ganglia (BG-EPVS), were assessed according to total CSVD burden score. The associations of NC, NLR and SII with CSVD and imaging markers were evaluated using logistic regression models. Furthermore, two-sample Mendelian randomization (MR) analysis was performed to investigate the genetically predicted effect of NC on CSVD. The prognostic performances of NC, NLR and SII for the presence of CSVD were assessed. RESULTS: At baseline, the mean age was 61.2 ± 6.7 years, and 53.5% of the participants were female. Higher NC was suggestively associated with increased total CSVD burden and modified total CSVD burden (Q4 vs. Q1: common odds ratio (cOR) 1.33, 95% CI 1.05–1.70; cOR 1.28, 95% CI 1.02–1.60) and marginally correlated with the presence of CSVD (OR 1.29, 95% CI 1.00–1.66). Furthermore, elevated NC was linked to a higher risk of lacune (OR 2.13, 95% CI 1.25–3.62) and moderate-to-severe BG-EPVS (OR 1.67, 95% CI 1.14–2.44). A greater NLR was related to moderate-to-severe BG-EPVS (OR 1.68, 95% CI 1.16–2.45). Individuals with a higher SII had an increased risk of modified WMH burden (OR 1.35, 95% CI 1.08–1.69) and moderate-to-severe BG-EPVS (OR 1.70, 95% CI 1.20–2.41). MR analysis showed that genetically predicted higher NC was associated with an increased risk of lacunar stroke (OR 1.20, 95% CI 1.04–1.39) and small vessel stroke (OR 1.21, 95% CI 1.06–1.38). The addition of NC to the basic model with traditional risk factors improved the predictive ability for the presence of CSVD, as validated by the net reclassification index and integrated discrimination index (all p < 0.05). CONCLUSIONS: This community-based population study found a suggestive association between NC and CSVD, especially for BG-EPVS and lacune, and provided evidence supporting the prognostic significance of NC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12974-022-02468-0.
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spelling pubmed-90721532022-05-06 Association of inflammatory markers with cerebral small vessel disease in community-based population Jiang, Lingling Cai, Xueli Yao, Dongxiao Jing, Jing Mei, Lerong Yang, Yingying Li, Shan Jin, Aoming Meng, Xia Li, Hao Wei, Tiemin Wang, Yongjun Pan, Yuesong Wang, Yilong J Neuroinflammation Research BACKGROUND: This study investigated the relationships of neutrophil count (NC), neutrophil-to-lymphocyte ratio (NLR) and systemic immune-inflammation index (SII) with cerebral small vessel disease (CSVD). METHODS: A total of 3052 community-dwelling residents from the Poly-vasculaR Evaluation for Cognitive Impairment and vaScular Events (PRECISE) study were involved in this cross-sectional study. CSVD burden and imaging markers, including white matter hyperintensity (WMH), lacunes, cerebral microbleeds (CMBs) and enlarged perivascular spaces in basal ganglia (BG-EPVS), were assessed according to total CSVD burden score. The associations of NC, NLR and SII with CSVD and imaging markers were evaluated using logistic regression models. Furthermore, two-sample Mendelian randomization (MR) analysis was performed to investigate the genetically predicted effect of NC on CSVD. The prognostic performances of NC, NLR and SII for the presence of CSVD were assessed. RESULTS: At baseline, the mean age was 61.2 ± 6.7 years, and 53.5% of the participants were female. Higher NC was suggestively associated with increased total CSVD burden and modified total CSVD burden (Q4 vs. Q1: common odds ratio (cOR) 1.33, 95% CI 1.05–1.70; cOR 1.28, 95% CI 1.02–1.60) and marginally correlated with the presence of CSVD (OR 1.29, 95% CI 1.00–1.66). Furthermore, elevated NC was linked to a higher risk of lacune (OR 2.13, 95% CI 1.25–3.62) and moderate-to-severe BG-EPVS (OR 1.67, 95% CI 1.14–2.44). A greater NLR was related to moderate-to-severe BG-EPVS (OR 1.68, 95% CI 1.16–2.45). Individuals with a higher SII had an increased risk of modified WMH burden (OR 1.35, 95% CI 1.08–1.69) and moderate-to-severe BG-EPVS (OR 1.70, 95% CI 1.20–2.41). MR analysis showed that genetically predicted higher NC was associated with an increased risk of lacunar stroke (OR 1.20, 95% CI 1.04–1.39) and small vessel stroke (OR 1.21, 95% CI 1.06–1.38). The addition of NC to the basic model with traditional risk factors improved the predictive ability for the presence of CSVD, as validated by the net reclassification index and integrated discrimination index (all p < 0.05). CONCLUSIONS: This community-based population study found a suggestive association between NC and CSVD, especially for BG-EPVS and lacune, and provided evidence supporting the prognostic significance of NC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12974-022-02468-0. BioMed Central 2022-05-06 /pmc/articles/PMC9072153/ /pubmed/35513834 http://dx.doi.org/10.1186/s12974-022-02468-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Jiang, Lingling
Cai, Xueli
Yao, Dongxiao
Jing, Jing
Mei, Lerong
Yang, Yingying
Li, Shan
Jin, Aoming
Meng, Xia
Li, Hao
Wei, Tiemin
Wang, Yongjun
Pan, Yuesong
Wang, Yilong
Association of inflammatory markers with cerebral small vessel disease in community-based population
title Association of inflammatory markers with cerebral small vessel disease in community-based population
title_full Association of inflammatory markers with cerebral small vessel disease in community-based population
title_fullStr Association of inflammatory markers with cerebral small vessel disease in community-based population
title_full_unstemmed Association of inflammatory markers with cerebral small vessel disease in community-based population
title_short Association of inflammatory markers with cerebral small vessel disease in community-based population
title_sort association of inflammatory markers with cerebral small vessel disease in community-based population
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072153/
https://www.ncbi.nlm.nih.gov/pubmed/35513834
http://dx.doi.org/10.1186/s12974-022-02468-0
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