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Pulse wave velocity, augmentation index, and carotid intima-media thickness are each associated with different inflammatory protein signatures in young healthy adults: The lifestyle, biomarkers and atherosclerosis study
Örebro University, School of Medical Sciences. Department of Laboratory Medicine, Faculty of Medicine and Health, Örebro University Hospital, Örebro, Sweden; Department of Medical Biosciences/Clinical Chemistry, Umeå University, Umeå, Sweden.ORCID iD: 0000-0001-8458-6448
Örebro University, School of Medical Sciences. Örebro University Hospital. (Clinical Epidemiology and Biostatistics)ORCID iD: 0000-0002-3552-9153
Department of Laboratory Medicine, Faculty of Medicine and Health, Örebro University Hospital, Örebro, Sweden; School of Medicine, Faculty of Medicine and Health, Örebro University, Örebro, Sweden..
Department of Medical Biosciences/Clinical Chemistry, Umeå University, Umeå, Sweden.
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2020 (English)In: Atherosclerosis, ISSN 0021-9150, E-ISSN 1879-1484, Vol. 313, p. 150-155Article in journal (Refereed) Published
Abstract [en]

BACKGROUND AND AIMS: We aimed to identify plasma protein biomarkers related to inflammation that correlated with physiological measurements of vascular function and structure in healthy individuals.

METHODS: We used the OLINK proteomics panel, which measures 92 inflammatory proteins, in 834 young, healthy non-smokers (ages 18-26). Principal component analysis (PCA) was employed to identify patterns of proteins. The following measurements were used: pulse-wave velocity (PWV), carotid intima-media thickness (cIMT) and augmentation index (AIX). Established cardiovascular risk factors were included in multivariable models.

RESULTS: PCA showed four principal components (PC 1, PC 2, PC 3, PC 4). PC 3, comprising proteins related to hemostasis, was significantly and inversely correlated with PWV. Among the proteins with the highest factor loadings on PC 3, uPA was negatively correlated with PWV in multivariable regression models. AIX was significantly correlated with PC 2, comprising inflammatory cytokines. Among the proteins with the highest factor loadings on PC 2, interleukin-6 was significantly correlated with AIX in the multivariable model. cIMT was significantly correlated with PC 4, comprising proteins related to chemotaxis. Among the proteins with the highest factor loadings on PC 4, fractalkine was significantly correlated with cIMT in the multivariable model.

CONCLUSIONS: In young, healthy individuals, OLINK inflammatory proteins correlated with measures of vascular status. Each of the three measures PWV, AIX, and cIMT, which target different parts of the vasculature, correlated with its own specific protein signature, indicating that different subsets of inflammatory mediators affect different parts of the vasculature and are detectable already in young healthy adults.

Place, publisher, year, edition, pages
Elsevier, 2020. Vol. 313, p. 150-155
Keywords [en]
Correlation, Premature atherosclerosis, Principal component analysis, Proteomics, Vascular function
National Category
Clinical Laboratory Medicine
Identifiers
URN: urn:nbn:se:oru:diva-86802DOI: 10.1016/j.atherosclerosis.2020.09.027ISI: 000705333700008PubMedID: 33059161Scopus ID: 2-s2.0-8509250991OAI: oai:DiVA.org:oru-86802DiVA, id: diva2:1479363
Note

Funding agencies:

AFA Insurance, Sweden 130275

Region Örebro County's Research Committee, Örebro, Sweden OLL780061

Nyckelfonden, Örebro, Sweden OLL-787681

Umeå University, Umeå, Sweden RV-865861

Available from: 2020-10-26 Created: 2020-10-26 Last updated: 2021-10-28Bibliographically approved
In thesis
1. Biomarkers of vascular function and structure in young healthy adults
Open this publication in new window or tab >>Biomarkers of vascular function and structure in young healthy adults
2021 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Atherosclerosis is a disease affecting the blood vessels in the body. Its pathophysiologic mechanisms involve infiltration of the vessel walls by fatty matter and immune cells. This process is slow, starting in childhood but typically not manifesting as symptomatic disease until late adulthood (after 60 years of age). The identification of younger individuals with a high risk for early intervention has a higher potential of preventing morbidity and mortality.

In this thesis, part of the Lifestyle, Biomarkers and Atherosclerosis study (LBA), the earliest stages of vascular dysfunction have been examined in a population of young, healthy, non-smoking subjects. Vascularfunction and structure measurements predict a future risk of cardiovascular disease (CVD). The measurements were analyzed in relation to clinical chemistry analyses of various biomarkers in serum and plasma that have been associated with inflammation or cardiovascular risk. A secondary aim was to examine estrogen containing contraceptive use and its relation to the CVD biomarkers.

In Paper I and Paper II of the thesis, the association between inflammatory biomarkers, body fat percentage and vascular function and structure measurements was examined in multivariable linear regression models. A higher body fat percentage predicted an increased serum concentration of C-reactive protein (CRP) and orosomucoid. In Paper II, a higher body fat percentage and a higher CRP were associated with a more unfavorable vascular function and structure.

In Paper III and Paper IV, we employed two multiplex proteomics panels to analyze inflammatory proteins and proteins previously implicated in CVD. In multivariable linear regression models, proteins implicated in hemostasis, inflammatory signaling and chemoattraction correlated with different vascular function and structure measurements. InPaper IV, insulin-like growth factor-binding protein 1 (IGFBP1) and IGFBP2 were independently predictive of an increased vascular stiffness.

In conclusion, even in young, healthy individuals, altered concentrations of serum biomarkers can be detected in subjects with increased body fat and unfavorable vascular function and structure.

Place, publisher, year, edition, pages
Örebro: Örebro University, 2021. p. 94
Series
Örebro Studies in Medicine, ISSN 1652-4063 ; 226
Keywords
atherosclerosis, vascular function, vascular structure, body composition, age, inflammation, clinical chemistry, biomarker
National Category
General Practice
Identifiers
urn:nbn:se:oru:diva-87112 (URN)978-91-7529-363-9 (ISBN)
Public defence
2021-01-29, Örebro universitet, Campus USÖ, hörsal C1, Södra Grev Rosengatan 32, Örebro, 09:00 (Swedish)
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Available from: 2020-11-03 Created: 2020-11-03 Last updated: 2021-01-18Bibliographically approved

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Pettersson-Pablo, PaulCao, YangHurtig-Wennlöf, Anita

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