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 inJournal of the American Heart Association Vol. 14; no. 2; p. e036790
Main Authors Wang, Ziyi, Zhang, Kaixin, Zhong, Chongke, Zhu, Zhengbao, Zheng, Xiaowei, Yang, Pinni, Che, Bizhong, Lu, Yaling, Zhang, Yonghong, Xu, Tian
Format Journal Article
LanguageEnglish
Published England John Wiley and Sons Inc 21.01.2025
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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.
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
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  surname: Xu
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Keywords YKL‐40
cognitive impairment
prognosis
biomarkers
ischemic stroke
Language English
License This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
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This manuscript was sent to Michelle H. Leppert, MD, MBA, Associate Editor, for review by expert referees, editorial decision, and final disposition.
For Sources of Funding and Disclosures, see page 8.
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  doi: 10.1016/j.biopsych.2010.08.025
– ident: e_1_3_2_30_2
  doi: 10.1161/STROKEAHA.114.006309
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  doi: 10.1161/JAHA.117.007776
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  doi: 10.1001/jama.2013.282543
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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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StartPage e036790
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
URI https://www.ncbi.nlm.nih.gov/pubmed/39819010
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https://pubmed.ncbi.nlm.nih.gov/PMC12054432
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Volume 14
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