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IGFBP-1 and IGFBP-2 are associated with a decreased pulse-wave velocity in young, healthy adults
BACKGROUND AND AIMS: In healthy, young adults we analyzed a panel of cardiovascular disease related proteins in plasma and compared them with the vascular health of the subjects. The aim was to identify proteins with a relationship to the early atherosclerotic process in healthy individuals. METHODS...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7949246/ https://www.ncbi.nlm.nih.gov/pubmed/33706704 http://dx.doi.org/10.1186/s12872-021-01914-w |
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author | Pettersson-Pablo, Paul Nilsson, Torbjörn K. Breimer, Lars H. Hurtig-Wennlöf, Anita |
author_facet | Pettersson-Pablo, Paul Nilsson, Torbjörn K. Breimer, Lars H. Hurtig-Wennlöf, Anita |
author_sort | Pettersson-Pablo, Paul |
collection | PubMed |
description | BACKGROUND AND AIMS: In healthy, young adults we analyzed a panel of cardiovascular disease related proteins in plasma and compared them with the vascular health of the subjects. The aim was to identify proteins with a relationship to the early atherosclerotic process in healthy individuals. METHODS: We employed the proximity extension assay from OLINK proteomics to analyze 92 cardiovascular disease (CVD) related proteins on 833 subjects (men and women, ages 18–26). The women were further divided into an estrogen-using group and non-users. Protein expression was analyzed using principal component analysis (PCA). The following vascular examinations were performed: Pulse-wave velocity (PWV), augmentation index (AIX), carotid-intima media thickness (cIMT). RESULTS: Three principal components were obtained using PCA to analyze the protein expression. None of the obtained principal components correlated significantly with AIX or cIMT. One of the components, explaining 6% of the total variance of the data, was significantly correlated with PWV. Upon examination of the proteins with the highest factor loadings on this component independently in a multivariable model, adjusting for established CVD risk biomarkers, insulin-like growth factor-binding protein 1 (IGFBP-1) and insulin-like growth factor-binding protein 2 (IGFBP-2) were found to independently, negatively correlate with PWV. Among the established risk factors included in the multivariable model, age was significantly and adversely correlated with all vascular measurements. CONCLUSIONS: In this population of healthy, young adults, groups of CVD related proteins correlate with PWV, but not AIX or cIMT. This group of proteins, of which IGFBP-1 and IGFBP-2 were independently, negatively correlated in a multivariable model with PWV, could have benificial effects on vascular stiffness. The robust association between age and PWV, AIX and cIMT provide insight into the impact of aging on the vasculature, which is detectable even in a population of young, healthy, non-smoking individuals of ages spanning only 8 years. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12872-021-01914-w. |
format | Online Article Text |
id | pubmed-7949246 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-79492462021-03-11 IGFBP-1 and IGFBP-2 are associated with a decreased pulse-wave velocity in young, healthy adults Pettersson-Pablo, Paul Nilsson, Torbjörn K. Breimer, Lars H. Hurtig-Wennlöf, Anita BMC Cardiovasc Disord Research Article BACKGROUND AND AIMS: In healthy, young adults we analyzed a panel of cardiovascular disease related proteins in plasma and compared them with the vascular health of the subjects. The aim was to identify proteins with a relationship to the early atherosclerotic process in healthy individuals. METHODS: We employed the proximity extension assay from OLINK proteomics to analyze 92 cardiovascular disease (CVD) related proteins on 833 subjects (men and women, ages 18–26). The women were further divided into an estrogen-using group and non-users. Protein expression was analyzed using principal component analysis (PCA). The following vascular examinations were performed: Pulse-wave velocity (PWV), augmentation index (AIX), carotid-intima media thickness (cIMT). RESULTS: Three principal components were obtained using PCA to analyze the protein expression. None of the obtained principal components correlated significantly with AIX or cIMT. One of the components, explaining 6% of the total variance of the data, was significantly correlated with PWV. Upon examination of the proteins with the highest factor loadings on this component independently in a multivariable model, adjusting for established CVD risk biomarkers, insulin-like growth factor-binding protein 1 (IGFBP-1) and insulin-like growth factor-binding protein 2 (IGFBP-2) were found to independently, negatively correlate with PWV. Among the established risk factors included in the multivariable model, age was significantly and adversely correlated with all vascular measurements. CONCLUSIONS: In this population of healthy, young adults, groups of CVD related proteins correlate with PWV, but not AIX or cIMT. This group of proteins, of which IGFBP-1 and IGFBP-2 were independently, negatively correlated in a multivariable model with PWV, could have benificial effects on vascular stiffness. The robust association between age and PWV, AIX and cIMT provide insight into the impact of aging on the vasculature, which is detectable even in a population of young, healthy, non-smoking individuals of ages spanning only 8 years. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12872-021-01914-w. BioMed Central 2021-03-11 /pmc/articles/PMC7949246/ /pubmed/33706704 http://dx.doi.org/10.1186/s12872-021-01914-w Text en © The Author(s) 2021 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/. The Creative Commons Public Domain Dedication waiver (http://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 Article Pettersson-Pablo, Paul Nilsson, Torbjörn K. Breimer, Lars H. Hurtig-Wennlöf, Anita IGFBP-1 and IGFBP-2 are associated with a decreased pulse-wave velocity in young, healthy adults |
title | IGFBP-1 and IGFBP-2 are associated with a decreased pulse-wave velocity in young, healthy adults |
title_full | IGFBP-1 and IGFBP-2 are associated with a decreased pulse-wave velocity in young, healthy adults |
title_fullStr | IGFBP-1 and IGFBP-2 are associated with a decreased pulse-wave velocity in young, healthy adults |
title_full_unstemmed | IGFBP-1 and IGFBP-2 are associated with a decreased pulse-wave velocity in young, healthy adults |
title_short | IGFBP-1 and IGFBP-2 are associated with a decreased pulse-wave velocity in young, healthy adults |
title_sort | igfbp-1 and igfbp-2 are associated with a decreased pulse-wave velocity in young, healthy adults |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7949246/ https://www.ncbi.nlm.nih.gov/pubmed/33706704 http://dx.doi.org/10.1186/s12872-021-01914-w |
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