التفاصيل البيبلوغرافية
| العنوان: |
Glycoprotein acetyls:a novel inflammatory biomarker of early cardiovascular risk in the young |
| المؤلفون: |
Chiesa, S. T. (Scott T.), Charakida, M. (Marietta), Georgiopoulos, G. (Georgios), Roberts, J. D. (Justin D.), Stafford, S. J. (Simon J.), Park, C. (Chloe), Mykkänen, J. (Juha), Kähönen, M. (Mika), Lehtimäki, T. (Terho), Ala‐Korpela, M. (Mika), Raitakari, O. (Olli), Pietiäinen, M. (Milla), Pussinen, P. (Pirkko), Muthurangu, V. (Vivek), Hughes, A. D. (Alun D.), Sattar, N. (Naveed), Timpson, N. J. (Nicholas J.), Deanfield, J. E. (John E.) |
| بيانات النشر: |
John Wiley & Sons |
| سنة النشر: |
2022 |
| المجموعة: |
Jultika - University of Oulu repository / Oulun yliopiston julkaisuarkisto |
| مصطلحات موضوعية: |
ALSPAC, CRP, GlycA, Young Finns Study, cardiovascular disease |
| الوصف: |
Background: Low‐grade inflammation in the young may contribute to the early development of cardiovascular disease. We assessed whether circulating levels of glycoprotein acetyls (GlycA) were better able to predict the development of adverse cardiovascular disease risk profiles compared with the more commonly used biomarker high‐sensitivity CRP (C‐reactive protein). Methods: A total of 3306 adolescents and young adults from the Avon Longitudinal Study of Parents and Children (mean age, 15.4±0.3; n=1750) and Cardiovascular Risk in Young Finns Study (mean age, 32.1±5.0; n=1556) were included. Baseline associations between inflammatory biomarkers, body composition, cardiovascular risk factors, and subclinical measures of vascular dysfunction were assessed cross‐sectionally in both cohorts. Prospective risk of developing hypertension and metabolic syndrome during 9‐to‐10‐year follow‐up were also assessed as surrogate markers for future cardiovascular risk. GlycA showed greater within‐subject correlation over 9‐to‐10‐year follow‐up in both cohorts compared with CRP, particularly in the younger adolescent group (r=0.36 versus 0.07). In multivariable analyses, GlycA was found to associate with multiple lifestyle‐related cardiovascular disease risk factors, cardiometabolic risk factor burden, and vascular dysfunction (eg, mean difference in flow‐mediated dilation=−1.2 [−1.8, −0.7]% per z‐score increase). In contrast, CRP levels appeared predominantly driven by body mass index and showed little relationship to any measured cardiovascular risk factors or phenotypes. In both cohorts, only GlycA predicted future risk of both hypertension (risk ratio [RR], ≈1.1 per z‐score increase for both cohorts) and metabolic syndrome (RR, ≈1.2–1.3 per z‐score increase for both cohorts) in 9‐to‐10‐year follow‐up. Conclusions: Low‐grade inflammation captured by the novel biomarker GlycA is associated with adverse cardiovascular risk profiles from as early as adolescence and predicts future risk of hypertension and metabolic ... |
| نوع الوثيقة: |
article in journal/newspaper |
| وصف الملف: |
application/pdf |
| اللغة: |
English |
| الإتاحة: |
http://urn.fi/urn:nbn:fi-fe2022081855778Test |
| حقوق: |
info:eu-repo/semantics/openAccess ; © 2022 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. ; https://creativecommons.org/licenses/by/4.0Test/ |
| رقم الانضمام: |
edsbas.BAD95B1B |
| قاعدة البيانات: |
BASE |
