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Advanced glycation end products measured by skin autofluorescence and subclinical cardiovascular disease: the Rotterdam Study
BACKGROUND: Advanced glycation end products (AGEs) have been linked to cardiovascular disease (CVD), especially coronary heart disease (CHD), but their role in CVD pathogenesis remains unclear. Therefore, we investigated cross-sectional associations of skin AGEs with subclinical atherosclerosis, art...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10685533/ https://www.ncbi.nlm.nih.gov/pubmed/38017418 http://dx.doi.org/10.1186/s12933-023-02052-7 |
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author | Chen, Jinluan Arshi, Banafsheh Waqas, Komal Lu, Tianqi Bos, Daniel Ikram, M. Arfan Uitterlinden, André G. Kavousi, Maryam Zillikens, M. Carola |
author_facet | Chen, Jinluan Arshi, Banafsheh Waqas, Komal Lu, Tianqi Bos, Daniel Ikram, M. Arfan Uitterlinden, André G. Kavousi, Maryam Zillikens, M. Carola |
author_sort | Chen, Jinluan |
collection | PubMed |
description | BACKGROUND: Advanced glycation end products (AGEs) have been linked to cardiovascular disease (CVD), especially coronary heart disease (CHD), but their role in CVD pathogenesis remains unclear. Therefore, we investigated cross-sectional associations of skin AGEs with subclinical atherosclerosis, arterial stiffness, and hypertension after confirming their relation with CHD. METHODS: In the population-based Rotterdam Study, skin AGEs were measured as skin autofluorescence (SAF). Prevalent MI was obtained from digital medical records. Carotid plaques, carotid intima-media thickness (IMT), coronary artery calcification (CAC), pulse wave velocity (PWV), and hypertension were assessed. Associations of SAF with endophenotypes were investigated in logistic and linear regression models adjusting for common cardiovascular risk factors. Effect modification by sex, diabetes mellitus, and chronic kidney disease (CKD) was tested. RESULTS: 3001 participants were included (mean age 73 (SD 9) years, 57% women). One unit higher SAF was associated with the presence of carotid plaques (OR 1.2 (0.92, 1.57)), a higher max IMT (0.08 SD (0.01, 0.15)), higher CAC (OR 2.2 (1.39, 3.48)), and PWV (0.09 SD (0.01, 0.16)), but not with hypertension (OR 0.99 (0.81, 1.21)). The associations with endophenotypes were more pronounced in men and participants with diabetes or CKD with significant interactions. CONCLUSIONS: Previously documented associations between SAF and CVD, also found in our study, may be explained by the endophenotypes atherosclerosis and arterial stiffness, especially in men and individuals with diabetes or CKD, but not by hypertension. Longitudinal studies are needed to replicate these findings and to test if SAF is an independent risk factor or biomarker of CVD. Trial registration: The Rotterdam Study has been entered into the Netherlands National Trial Register (NTR; www.trialregister.nl) and the WHO International Clinical Trials Registry Platform (ICTRP; www.who.int/ictrp/network/primary/en/) under shared catalogue number NTR6831. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12933-023-02052-7. |
format | Online Article Text |
id | pubmed-10685533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-106855332023-11-30 Advanced glycation end products measured by skin autofluorescence and subclinical cardiovascular disease: the Rotterdam Study Chen, Jinluan Arshi, Banafsheh Waqas, Komal Lu, Tianqi Bos, Daniel Ikram, M. Arfan Uitterlinden, André G. Kavousi, Maryam Zillikens, M. Carola Cardiovasc Diabetol Research BACKGROUND: Advanced glycation end products (AGEs) have been linked to cardiovascular disease (CVD), especially coronary heart disease (CHD), but their role in CVD pathogenesis remains unclear. Therefore, we investigated cross-sectional associations of skin AGEs with subclinical atherosclerosis, arterial stiffness, and hypertension after confirming their relation with CHD. METHODS: In the population-based Rotterdam Study, skin AGEs were measured as skin autofluorescence (SAF). Prevalent MI was obtained from digital medical records. Carotid plaques, carotid intima-media thickness (IMT), coronary artery calcification (CAC), pulse wave velocity (PWV), and hypertension were assessed. Associations of SAF with endophenotypes were investigated in logistic and linear regression models adjusting for common cardiovascular risk factors. Effect modification by sex, diabetes mellitus, and chronic kidney disease (CKD) was tested. RESULTS: 3001 participants were included (mean age 73 (SD 9) years, 57% women). One unit higher SAF was associated with the presence of carotid plaques (OR 1.2 (0.92, 1.57)), a higher max IMT (0.08 SD (0.01, 0.15)), higher CAC (OR 2.2 (1.39, 3.48)), and PWV (0.09 SD (0.01, 0.16)), but not with hypertension (OR 0.99 (0.81, 1.21)). The associations with endophenotypes were more pronounced in men and participants with diabetes or CKD with significant interactions. CONCLUSIONS: Previously documented associations between SAF and CVD, also found in our study, may be explained by the endophenotypes atherosclerosis and arterial stiffness, especially in men and individuals with diabetes or CKD, but not by hypertension. Longitudinal studies are needed to replicate these findings and to test if SAF is an independent risk factor or biomarker of CVD. Trial registration: The Rotterdam Study has been entered into the Netherlands National Trial Register (NTR; www.trialregister.nl) and the WHO International Clinical Trials Registry Platform (ICTRP; www.who.int/ictrp/network/primary/en/) under shared catalogue number NTR6831. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12933-023-02052-7. BioMed Central 2023-11-28 /pmc/articles/PMC10685533/ /pubmed/38017418 http://dx.doi.org/10.1186/s12933-023-02052-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 Chen, Jinluan Arshi, Banafsheh Waqas, Komal Lu, Tianqi Bos, Daniel Ikram, M. Arfan Uitterlinden, André G. Kavousi, Maryam Zillikens, M. Carola Advanced glycation end products measured by skin autofluorescence and subclinical cardiovascular disease: the Rotterdam Study |
title | Advanced glycation end products measured by skin autofluorescence and subclinical cardiovascular disease: the Rotterdam Study |
title_full | Advanced glycation end products measured by skin autofluorescence and subclinical cardiovascular disease: the Rotterdam Study |
title_fullStr | Advanced glycation end products measured by skin autofluorescence and subclinical cardiovascular disease: the Rotterdam Study |
title_full_unstemmed | Advanced glycation end products measured by skin autofluorescence and subclinical cardiovascular disease: the Rotterdam Study |
title_short | Advanced glycation end products measured by skin autofluorescence and subclinical cardiovascular disease: the Rotterdam Study |
title_sort | advanced glycation end products measured by skin autofluorescence and subclinical cardiovascular disease: the rotterdam study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10685533/ https://www.ncbi.nlm.nih.gov/pubmed/38017418 http://dx.doi.org/10.1186/s12933-023-02052-7 |
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