Plasma Human Cartilage Glycoprotein‐39 and Cognitive Impairment After Acute Ischemic Stroke
Our study aimed at evaluating the association between plasma human cartilage glycoprotein-39 (YKL-40) and cognitive impairment at 3 months among patients with acute ischemic stroke. Plasma YKL-40 levels were measured in 604 participants from the China Antihypertensive Trial in Acute Ischemic Stroke....
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Published in | Journal of the American Heart Association Vol. 14; no. 2; p. e036790 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
John Wiley and Sons Inc
21.01.2025
Wiley |
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Abstract | Our study aimed at evaluating the association between plasma human cartilage glycoprotein-39 (YKL-40) and cognitive impairment at 3 months among patients with acute ischemic stroke.
Plasma YKL-40 levels were measured in 604 participants from the China Antihypertensive Trial in Acute Ischemic Stroke. Cognitive impairment outcomes were assessed at 3 months poststroke using the Mini-Mental State Examination and the Montreal Cognitive Assessment. According to the Mini-Mental State Examination score, patients in the highest quartile of YKL-40 had a 2.01-fold (95% CI, 1.23-3.29;
for trend=0.009) risk of poststroke cognitive impairment compared with those in the lowest quartile. Each 1 SD difference of logarithm-transformed YKL-40 was associated with a 28% (95% CI, 7-53) increased risk for the outcome. The multiple-adjusted spline regression model confirmed dose-response relationships between YKL-40 and poststroke cognitive impairment (
for linearity=0.01). Adding YKL-40 to a model containing conventional risk factors significantly improved the discriminatory power (area under the receiver operating characteristic curve improved by 0.02,
=0.03). When cognitive impairment was defined using the Montreal Cognitive Assessment score, similar findings were observed.
Elevated YKL-40 levels were associated with an increased risk of cognitive impairment at 3 months among patients with acute ischemic stroke.
URL: clinicaltrials.gov; Unique Identifier: NCT01840072. |
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AbstractList | Our study aimed at evaluating the association between plasma human cartilage glycoprotein-39 (YKL-40) and cognitive impairment at 3 months among patients with acute ischemic stroke.
Plasma YKL-40 levels were measured in 604 participants from the China Antihypertensive Trial in Acute Ischemic Stroke. Cognitive impairment outcomes were assessed at 3 months poststroke using the Mini-Mental State Examination and the Montreal Cognitive Assessment. According to the Mini-Mental State Examination score, patients in the highest quartile of YKL-40 had a 2.01-fold (95% CI, 1.23-3.29;
for trend=0.009) risk of poststroke cognitive impairment compared with those in the lowest quartile. Each 1 SD difference of logarithm-transformed YKL-40 was associated with a 28% (95% CI, 7-53) increased risk for the outcome. The multiple-adjusted spline regression model confirmed dose-response relationships between YKL-40 and poststroke cognitive impairment (
for linearity=0.01). Adding YKL-40 to a model containing conventional risk factors significantly improved the discriminatory power (area under the receiver operating characteristic curve improved by 0.02,
=0.03). When cognitive impairment was defined using the Montreal Cognitive Assessment score, similar findings were observed.
Elevated YKL-40 levels were associated with an increased risk of cognitive impairment at 3 months among patients with acute ischemic stroke.
URL: clinicaltrials.gov; Unique Identifier: NCT01840072. Background Our study aimed at evaluating the association between plasma human cartilage glycoprotein‐39 (YKL‐40) and cognitive impairment at 3 months among patients with acute ischemic stroke. Methods and Results Plasma YKL‐40 levels were measured in 604 participants from the China Antihypertensive Trial in Acute Ischemic Stroke. Cognitive impairment outcomes were assessed at 3 months poststroke using the Mini‐Mental State Examination and the Montreal Cognitive Assessment. According to the Mini‐Mental State Examination score, patients in the highest quartile of YKL‐40 had a 2.01‐fold (95% CI, 1.23–3.29; P for trend=0.009) risk of poststroke cognitive impairment compared with those in the lowest quartile. Each 1 SD difference of logarithm‐transformed YKL‐40 was associated with a 28% (95% CI, 7–53) increased risk for the outcome. The multiple‐adjusted spline regression model confirmed dose–response relationships between YKL‐40 and poststroke cognitive impairment (P for linearity=0.01). Adding YKL‐40 to a model containing conventional risk factors significantly improved the discriminatory power (area under the receiver operating characteristic curve improved by 0.02, P=0.03). When cognitive impairment was defined using the Montreal Cognitive Assessment score, similar findings were observed. Conclusions Elevated YKL‐40 levels were associated with an increased risk of cognitive impairment at 3 months among patients with acute ischemic stroke. Registration URL: clinicaltrials.gov; Unique Identifier: NCT01840072. Our study aimed at evaluating the association between plasma human cartilage glycoprotein-39 (YKL-40) and cognitive impairment at 3 months among patients with acute ischemic stroke.BACKGROUNDOur study aimed at evaluating the association between plasma human cartilage glycoprotein-39 (YKL-40) and cognitive impairment at 3 months among patients with acute ischemic stroke.Plasma YKL-40 levels were measured in 604 participants from the China Antihypertensive Trial in Acute Ischemic Stroke. Cognitive impairment outcomes were assessed at 3 months poststroke using the Mini-Mental State Examination and the Montreal Cognitive Assessment. According to the Mini-Mental State Examination score, patients in the highest quartile of YKL-40 had a 2.01-fold (95% CI, 1.23-3.29; P for trend=0.009) risk of poststroke cognitive impairment compared with those in the lowest quartile. Each 1 SD difference of logarithm-transformed YKL-40 was associated with a 28% (95% CI, 7-53) increased risk for the outcome. The multiple-adjusted spline regression model confirmed dose-response relationships between YKL-40 and poststroke cognitive impairment (P for linearity=0.01). Adding YKL-40 to a model containing conventional risk factors significantly improved the discriminatory power (area under the receiver operating characteristic curve improved by 0.02, P=0.03). When cognitive impairment was defined using the Montreal Cognitive Assessment score, similar findings were observed.METHODS AND RESULTSPlasma YKL-40 levels were measured in 604 participants from the China Antihypertensive Trial in Acute Ischemic Stroke. Cognitive impairment outcomes were assessed at 3 months poststroke using the Mini-Mental State Examination and the Montreal Cognitive Assessment. According to the Mini-Mental State Examination score, patients in the highest quartile of YKL-40 had a 2.01-fold (95% CI, 1.23-3.29; P for trend=0.009) risk of poststroke cognitive impairment compared with those in the lowest quartile. Each 1 SD difference of logarithm-transformed YKL-40 was associated with a 28% (95% CI, 7-53) increased risk for the outcome. The multiple-adjusted spline regression model confirmed dose-response relationships between YKL-40 and poststroke cognitive impairment (P for linearity=0.01). Adding YKL-40 to a model containing conventional risk factors significantly improved the discriminatory power (area under the receiver operating characteristic curve improved by 0.02, P=0.03). When cognitive impairment was defined using the Montreal Cognitive Assessment score, similar findings were observed.Elevated YKL-40 levels were associated with an increased risk of cognitive impairment at 3 months among patients with acute ischemic stroke.CONCLUSIONSElevated YKL-40 levels were associated with an increased risk of cognitive impairment at 3 months among patients with acute ischemic stroke.URL: clinicaltrials.gov; Unique Identifier: NCT01840072.REGISTRATIONURL: clinicaltrials.gov; Unique Identifier: NCT01840072. |
Author | Zhong, Chongke Zhang, Kaixin Zhu, Zhengbao Lu, Yaling Xu, Tian Che, Bizhong Yang, Pinni Zheng, Xiaowei Zhang, Yonghong Wang, Ziyi |
AuthorAffiliation | 1 Department of Neurology, Affiliated Hospital of Nantong University Medical School of Nantong University Nantong China 4 Department of Neurology Affiliated Hospital of Nantong University Nantong China 2 Department of Clinical Research Center Wuxi No. 2 People’s Hospital (Jiangnan University Medical Center) Wuxi China 3 Department of Epidemiology, School of Public Health and Jiangsu Key Laboratory of Preventive and Translational Medicine for Major Chronic Non‐communicable Diseases, MOE Key Laboratory of Geriatric Diseases and Immunology Suzhou Medical College of Soochow University Suzhou China |
AuthorAffiliation_xml | – name: 1 Department of Neurology, Affiliated Hospital of Nantong University Medical School of Nantong University Nantong China – name: 3 Department of Epidemiology, School of Public Health and Jiangsu Key Laboratory of Preventive and Translational Medicine for Major Chronic Non‐communicable Diseases, MOE Key Laboratory of Geriatric Diseases and Immunology Suzhou Medical College of Soochow University Suzhou China – name: 4 Department of Neurology Affiliated Hospital of Nantong University Nantong China – name: 2 Department of Clinical Research Center Wuxi No. 2 People’s Hospital (Jiangnan University Medical Center) Wuxi China |
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Cites_doi | 10.1080/00365510050184886 10.3978/j.issn.2305-5839.2014.08.05 10.1161/STROKEAHA.111.633586 10.7150/thno.75069 10.1161/01.str.20.7.864 10.1186/s12974-021-02234-8 10.1016/S1474-4422(24)00038-3 10.1002/sim.4780080504 10.1177/1747493016660094 10.3760/j.issn:0253-3758.2007.05.003 10.1111/ane.12709 10.1161/STROKEAHA.114.005380 10.1161/01.STR.31.7.1494 10.1161/STROKEAHA.121.036143 10.1186/s40478-016-0350-3 10.1002/sim.2929 10.1161/01.HYP.0000150859.47929.8e 10.1042/BCJ20160505 10.1158/1055-9965.EPI-05-0011 10.1016/S1474-4422(21)00252-0 10.1136/jnnp-2020-325796 10.3389/fpsyt.2021.725511 10.1186/1742-2094-7-34 10.1186/s12974-018-1269-3 10.1161/CIRCRESAHA.122.319951 10.1038/s41582-023-00822-1 10.3760/cma.j.issn.0254-9026.2021.03.001 10.1016/j.biopha.2018.02.050 10.1161/JAHA.122.026263 10.1161/01.str.24.1.35 10.1161/STROKEAHA.110.579888 10.1161/STROKEAHA.122.040798 10.3389/fimmu.2022.841290 10.1016/j.cca.2020.09.035 10.1002/acn3.266 10.1016/0022-3956(75)90026-6 10.1111/j.1532-5415.2005.53221.x 10.3233/JAD-2012-120787 10.1016/j.neuroscience.2024.06.028 10.1146/annurev-immunol-051116-052358 10.1016/j.biopsych.2010.08.025 10.1161/STROKEAHA.114.006309 10.1161/JAHA.117.007776 10.1001/jama.2013.282543 |
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Keywords | YKL‐40 cognitive impairment prognosis biomarkers ischemic stroke |
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Snippet | Our study aimed at evaluating the association between plasma human cartilage glycoprotein-39 (YKL-40) and cognitive impairment at 3 months among patients with... Background Our study aimed at evaluating the association between plasma human cartilage glycoprotein‐39 (YKL‐40) and cognitive impairment at 3 months among... |
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SubjectTerms | Aged biomarkers Biomarkers - blood China - epidemiology Chitinase-3-Like Protein 1 - blood Cognitive Dysfunction - blood Cognitive Dysfunction - diagnosis Cognitive Dysfunction - epidemiology Cognitive Dysfunction - etiology cognitive impairment Female Humans ischemic stroke Ischemic Stroke - blood Ischemic Stroke - complications Ischemic Stroke - diagnosis Ischemic Stroke - psychology Male Mental Status and Dementia Tests Middle Aged Original Research prognosis Risk Factors Time Factors YKL‐40 |
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Title | Plasma Human Cartilage Glycoprotein‐39 and Cognitive Impairment After Acute Ischemic Stroke |
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