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The Association Between Chronological Age and Dyslipidemia: A Cross-Sectional Study in Chinese Aged Population

BACKGROUND AND AIMS: Dyslipidemia is obviously an important risk factor for cardiovascular diseases, which might further lead to disability and death in aged population. We thus performed the current study to evaluate the association between chronological age and dyslipidemia. SUBJECTS AND METHODS:...

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Autores principales: Li, Qingyao, Jiang, Ying, Song, Anqi, Li, Yun, Xu, Xinyi, Xu, Renying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10124621/
https://www.ncbi.nlm.nih.gov/pubmed/37101655
http://dx.doi.org/10.2147/CIA.S406237
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author Li, Qingyao
Jiang, Ying
Song, Anqi
Li, Yun
Xu, Xinyi
Xu, Renying
author_facet Li, Qingyao
Jiang, Ying
Song, Anqi
Li, Yun
Xu, Xinyi
Xu, Renying
author_sort Li, Qingyao
collection PubMed
description BACKGROUND AND AIMS: Dyslipidemia is obviously an important risk factor for cardiovascular diseases, which might further lead to disability and death in aged population. We thus performed the current study to evaluate the association between chronological age and dyslipidemia. SUBJECTS AND METHODS: A total number of 59,716 Chinese aged population (31,174 men and 28,542 women, average age 67.8y) were included in the current study. Age and sex were abstracted from medical records. Height, body weight, and blood pressure were measured by trained nurses. Serum concentration of total cholesterol (TC) and total triglycerides were performed by enzyme-linked immunosorbent method after at least 8-h fast. Dyslipidemia was defined if total cholesterol≥5.7 mmol/L, or total triglycerides≥1.7 mmol/L, or self-reported history of dyslipidemia. RESULTS: The prevalence of dyslipidemia was 50.4% in the current study population. Compared to the youngest age group (60–64y), the adjusted odds ratio was 0.88 (95% CI: 0.84, 0.92), 0.77 (95% CI: 0.73, 0.81), 0.66 (95% CI: 0.61, 0.70), 0.55 (95% CI: 0.50, 0.59) for the participants who were 65 to 69, 70–74, 75–79, and ≥80 years old (p trend <0.001). Excluding participants with low body weight and with overweight and obesity, with high blood pressure and history of hypertension, with high fasting blood glucose and history of diabetes, generated similar results with main analysis. CONCLUSION: Chronological age was closely associated with the risk of dyslipidemia in Chinese aged population.
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spelling pubmed-101246212023-04-25 The Association Between Chronological Age and Dyslipidemia: A Cross-Sectional Study in Chinese Aged Population Li, Qingyao Jiang, Ying Song, Anqi Li, Yun Xu, Xinyi Xu, Renying Clin Interv Aging Original Research BACKGROUND AND AIMS: Dyslipidemia is obviously an important risk factor for cardiovascular diseases, which might further lead to disability and death in aged population. We thus performed the current study to evaluate the association between chronological age and dyslipidemia. SUBJECTS AND METHODS: A total number of 59,716 Chinese aged population (31,174 men and 28,542 women, average age 67.8y) were included in the current study. Age and sex were abstracted from medical records. Height, body weight, and blood pressure were measured by trained nurses. Serum concentration of total cholesterol (TC) and total triglycerides were performed by enzyme-linked immunosorbent method after at least 8-h fast. Dyslipidemia was defined if total cholesterol≥5.7 mmol/L, or total triglycerides≥1.7 mmol/L, or self-reported history of dyslipidemia. RESULTS: The prevalence of dyslipidemia was 50.4% in the current study population. Compared to the youngest age group (60–64y), the adjusted odds ratio was 0.88 (95% CI: 0.84, 0.92), 0.77 (95% CI: 0.73, 0.81), 0.66 (95% CI: 0.61, 0.70), 0.55 (95% CI: 0.50, 0.59) for the participants who were 65 to 69, 70–74, 75–79, and ≥80 years old (p trend <0.001). Excluding participants with low body weight and with overweight and obesity, with high blood pressure and history of hypertension, with high fasting blood glucose and history of diabetes, generated similar results with main analysis. CONCLUSION: Chronological age was closely associated with the risk of dyslipidemia in Chinese aged population. Dove 2023-04-20 /pmc/articles/PMC10124621/ /pubmed/37101655 http://dx.doi.org/10.2147/CIA.S406237 Text en © 2023 Li et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Li, Qingyao
Jiang, Ying
Song, Anqi
Li, Yun
Xu, Xinyi
Xu, Renying
The Association Between Chronological Age and Dyslipidemia: A Cross-Sectional Study in Chinese Aged Population
title The Association Between Chronological Age and Dyslipidemia: A Cross-Sectional Study in Chinese Aged Population
title_full The Association Between Chronological Age and Dyslipidemia: A Cross-Sectional Study in Chinese Aged Population
title_fullStr The Association Between Chronological Age and Dyslipidemia: A Cross-Sectional Study in Chinese Aged Population
title_full_unstemmed The Association Between Chronological Age and Dyslipidemia: A Cross-Sectional Study in Chinese Aged Population
title_short The Association Between Chronological Age and Dyslipidemia: A Cross-Sectional Study in Chinese Aged Population
title_sort association between chronological age and dyslipidemia: a cross-sectional study in chinese aged population
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10124621/
https://www.ncbi.nlm.nih.gov/pubmed/37101655
http://dx.doi.org/10.2147/CIA.S406237
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