Elevated plasma YKL-40, lipids and lipoproteins, and ischemic vascular disease in the general population

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Elevated plasma YKL-40, lipids and lipoproteins, and ischemic vascular disease in the general population. / Kjaergaard, Alisa D; Johansen, Julia S; Bojesen, Stig E; Nordestgaard, Børge G.

In: Stroke, Vol. 46, No. 2, 02.2015, p. 329-35.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Kjaergaard, AD, Johansen, JS, Bojesen, SE & Nordestgaard, BG 2015, 'Elevated plasma YKL-40, lipids and lipoproteins, and ischemic vascular disease in the general population', Stroke, vol. 46, no. 2, pp. 329-35. https://doi.org/10.1161/STROKEAHA.114.007657

APA

Kjaergaard, A. D., Johansen, J. S., Bojesen, S. E., & Nordestgaard, B. G. (2015). Elevated plasma YKL-40, lipids and lipoproteins, and ischemic vascular disease in the general population. Stroke, 46(2), 329-35. https://doi.org/10.1161/STROKEAHA.114.007657

Vancouver

Kjaergaard AD, Johansen JS, Bojesen SE, Nordestgaard BG. Elevated plasma YKL-40, lipids and lipoproteins, and ischemic vascular disease in the general population. Stroke. 2015 Feb;46(2):329-35. https://doi.org/10.1161/STROKEAHA.114.007657

Author

Kjaergaard, Alisa D ; Johansen, Julia S ; Bojesen, Stig E ; Nordestgaard, Børge G. / Elevated plasma YKL-40, lipids and lipoproteins, and ischemic vascular disease in the general population. In: Stroke. 2015 ; Vol. 46, No. 2. pp. 329-35.

Bibtex

@article{a28fd15cbf7b40dba3322c232def475a,
title = "Elevated plasma YKL-40, lipids and lipoproteins, and ischemic vascular disease in the general population",
abstract = "BACKGROUND AND PURPOSE: We tested the hypothesis that observationally and genetically elevated YKL-40 is associated with elevated lipids and lipoproteins and with increased risk of ischemic vascular disease.METHODS: We conducted cohort and Mendelian randomization studies in 96 110 individuals from the Danish general population, with measured plasma levels of YKL-40 (n=21 647), plasma lipids and lipoproteins (n=94 461), and CHI3L1 rs4950928 genotype (n=94 579).RESULTS: From 1977 to 2013, 3256 individuals developed ischemic stroke, 5629 ischemic cerebrovascular disease, 4183 myocardial infarction, and 10 271 developed ischemic heart disease. The 91% to 100% versus 0% to 33% YKL-40 percentile category was associated with a 34% increase in triglycerides, but only with minor changes in other lipids and lipoproteins. For these categories, the multifactorially adjusted hazard ratio was 1.99 (95% confidence interval, 1.49-2.67) for ischemic stroke, 1.85 (1.44-2.37) for ischemic cerebrovascular disease, 1.28 (0.95-1.73) for myocardial infarction, and 1.23 (1.01-1.51) for ischemic heart disease. When compared with rs4950928 CC homozygosity, the presence of G-allele was associated with a doubling (GC) or tripling (GG) in YKL-40 levels, but not with triglyceride levels or with risk of ischemic vascular disease. A doubling in YKL-40 was associated with a multifactorially adjusted observational hazard ratio for ischemic stroke of 1.18 (1.11-1.27), and a genetic odds ratio of 1.04 (0.95-1.15). Corresponding risk estimates were 1.15 (1.09-1.22) observationally and 1.06 (0.99-1.14) genetically for ischemic cerebrovascular disease, 1.08 (1.00-1.15) observationally and 1.04 (0.96-1.13) genetically for myocardial infarction, and 1.07 (1.02-1.12) observationally and 1.01 (0.96-1.07) genetically for ischemic heart disease.CONCLUSIONS: Elevated YKL-40 was associated with a 34% increase in triglyceride levels and with a 2-fold increased risk of ischemic stroke, whereas genetically elevated YKL-40 were not.",
keywords = "Adipokines, Aged, Biomarkers, Cerebrovascular Disorders, Cohort Studies, Female, Humans, Lectins, Lipids, Lipoproteins, Male, Middle Aged, Myocardial Infarction, Myocardial Ischemia, Population Surveillance, Prospective Studies, Risk Factors, Stroke, Triglycerides, Vascular Diseases",
author = "Kjaergaard, {Alisa D} and Johansen, {Julia S} and Bojesen, {Stig E} and Nordestgaard, {B{\o}rge G}",
note = "{\textcopyright} 2015 American Heart Association, Inc.",
year = "2015",
month = feb,
doi = "10.1161/STROKEAHA.114.007657",
language = "English",
volume = "46",
pages = "329--35",
journal = "Stroke",
issn = "0039-2499",
publisher = "Lippincott Williams & Wilkins",
number = "2",

}

RIS

TY - JOUR

T1 - Elevated plasma YKL-40, lipids and lipoproteins, and ischemic vascular disease in the general population

AU - Kjaergaard, Alisa D

AU - Johansen, Julia S

AU - Bojesen, Stig E

AU - Nordestgaard, Børge G

N1 - © 2015 American Heart Association, Inc.

PY - 2015/2

Y1 - 2015/2

N2 - BACKGROUND AND PURPOSE: We tested the hypothesis that observationally and genetically elevated YKL-40 is associated with elevated lipids and lipoproteins and with increased risk of ischemic vascular disease.METHODS: We conducted cohort and Mendelian randomization studies in 96 110 individuals from the Danish general population, with measured plasma levels of YKL-40 (n=21 647), plasma lipids and lipoproteins (n=94 461), and CHI3L1 rs4950928 genotype (n=94 579).RESULTS: From 1977 to 2013, 3256 individuals developed ischemic stroke, 5629 ischemic cerebrovascular disease, 4183 myocardial infarction, and 10 271 developed ischemic heart disease. The 91% to 100% versus 0% to 33% YKL-40 percentile category was associated with a 34% increase in triglycerides, but only with minor changes in other lipids and lipoproteins. For these categories, the multifactorially adjusted hazard ratio was 1.99 (95% confidence interval, 1.49-2.67) for ischemic stroke, 1.85 (1.44-2.37) for ischemic cerebrovascular disease, 1.28 (0.95-1.73) for myocardial infarction, and 1.23 (1.01-1.51) for ischemic heart disease. When compared with rs4950928 CC homozygosity, the presence of G-allele was associated with a doubling (GC) or tripling (GG) in YKL-40 levels, but not with triglyceride levels or with risk of ischemic vascular disease. A doubling in YKL-40 was associated with a multifactorially adjusted observational hazard ratio for ischemic stroke of 1.18 (1.11-1.27), and a genetic odds ratio of 1.04 (0.95-1.15). Corresponding risk estimates were 1.15 (1.09-1.22) observationally and 1.06 (0.99-1.14) genetically for ischemic cerebrovascular disease, 1.08 (1.00-1.15) observationally and 1.04 (0.96-1.13) genetically for myocardial infarction, and 1.07 (1.02-1.12) observationally and 1.01 (0.96-1.07) genetically for ischemic heart disease.CONCLUSIONS: Elevated YKL-40 was associated with a 34% increase in triglyceride levels and with a 2-fold increased risk of ischemic stroke, whereas genetically elevated YKL-40 were not.

AB - BACKGROUND AND PURPOSE: We tested the hypothesis that observationally and genetically elevated YKL-40 is associated with elevated lipids and lipoproteins and with increased risk of ischemic vascular disease.METHODS: We conducted cohort and Mendelian randomization studies in 96 110 individuals from the Danish general population, with measured plasma levels of YKL-40 (n=21 647), plasma lipids and lipoproteins (n=94 461), and CHI3L1 rs4950928 genotype (n=94 579).RESULTS: From 1977 to 2013, 3256 individuals developed ischemic stroke, 5629 ischemic cerebrovascular disease, 4183 myocardial infarction, and 10 271 developed ischemic heart disease. The 91% to 100% versus 0% to 33% YKL-40 percentile category was associated with a 34% increase in triglycerides, but only with minor changes in other lipids and lipoproteins. For these categories, the multifactorially adjusted hazard ratio was 1.99 (95% confidence interval, 1.49-2.67) for ischemic stroke, 1.85 (1.44-2.37) for ischemic cerebrovascular disease, 1.28 (0.95-1.73) for myocardial infarction, and 1.23 (1.01-1.51) for ischemic heart disease. When compared with rs4950928 CC homozygosity, the presence of G-allele was associated with a doubling (GC) or tripling (GG) in YKL-40 levels, but not with triglyceride levels or with risk of ischemic vascular disease. A doubling in YKL-40 was associated with a multifactorially adjusted observational hazard ratio for ischemic stroke of 1.18 (1.11-1.27), and a genetic odds ratio of 1.04 (0.95-1.15). Corresponding risk estimates were 1.15 (1.09-1.22) observationally and 1.06 (0.99-1.14) genetically for ischemic cerebrovascular disease, 1.08 (1.00-1.15) observationally and 1.04 (0.96-1.13) genetically for myocardial infarction, and 1.07 (1.02-1.12) observationally and 1.01 (0.96-1.07) genetically for ischemic heart disease.CONCLUSIONS: Elevated YKL-40 was associated with a 34% increase in triglyceride levels and with a 2-fold increased risk of ischemic stroke, whereas genetically elevated YKL-40 were not.

KW - Adipokines

KW - Aged

KW - Biomarkers

KW - Cerebrovascular Disorders

KW - Cohort Studies

KW - Female

KW - Humans

KW - Lectins

KW - Lipids

KW - Lipoproteins

KW - Male

KW - Middle Aged

KW - Myocardial Infarction

KW - Myocardial Ischemia

KW - Population Surveillance

KW - Prospective Studies

KW - Risk Factors

KW - Stroke

KW - Triglycerides

KW - Vascular Diseases

U2 - 10.1161/STROKEAHA.114.007657

DO - 10.1161/STROKEAHA.114.007657

M3 - Journal article

C2 - 25624368

VL - 46

SP - 329

EP - 335

JO - Stroke

JF - Stroke

SN - 0039-2499

IS - 2

ER -

ID: 162148668