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Prevalence and risk factors for hyperhomocysteinemia: a population-based cross-sectional study from Hunan, China

OBJECTIVES: Hyperhomocysteinemia is an independent risk factor for cardiovascular diseases. We aimed to investigate the prevalence and risk factors for hyperhomocysteinemia, especially modifiable lifestyle factors, such as smoking behaviour and dietary factors. DESIGN: Population-based cross-section...

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Autores principales: Yang, Yide, Zeng, Yuan, Yuan, Shuqian, Xie, Ming, Dong, Yanhui, Li, Jian, He, Quanyuan, Ye, Xiangli, Lv, Yuan, Hocher, Carl-Friedrich, Kraemer, Bernhard K, Hong, Xiuqin, Hocher, Berthold
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8650492/
https://www.ncbi.nlm.nih.gov/pubmed/34872994
http://dx.doi.org/10.1136/bmjopen-2020-048575
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author Yang, Yide
Zeng, Yuan
Yuan, Shuqian
Xie, Ming
Dong, Yanhui
Li, Jian
He, Quanyuan
Ye, Xiangli
Lv, Yuan
Hocher, Carl-Friedrich
Kraemer, Bernhard K
Hong, Xiuqin
Hocher, Berthold
author_facet Yang, Yide
Zeng, Yuan
Yuan, Shuqian
Xie, Ming
Dong, Yanhui
Li, Jian
He, Quanyuan
Ye, Xiangli
Lv, Yuan
Hocher, Carl-Friedrich
Kraemer, Bernhard K
Hong, Xiuqin
Hocher, Berthold
author_sort Yang, Yide
collection PubMed
description OBJECTIVES: Hyperhomocysteinemia is an independent risk factor for cardiovascular diseases. We aimed to investigate the prevalence and risk factors for hyperhomocysteinemia, especially modifiable lifestyle factors, such as smoking behaviour and dietary factors. DESIGN: Population-based cross-sectional study. SETTING: Hunan Province, China PARTICIPANTS: A total of 4012 participants completed the study, between July 2013 and March 2014. The median age is 55 (interquartile range: 45–63) years, with 1644 males (41%) and 2368 females (59%). MAIN OUTCOME MEASURES: Homocysteine level were measured by the microplate enzyme immunoassay method. Hyperthomocysteinemia was defined as ≥15 µmol/L. Questionnaire was used to investigate potential risk factors of hyperhomocysteinemia. Crude odd ratio (OR) or adjusted OR with 95% CI were determined by using univariable or multivariable logistic regression models. RESULTS: The prevalence of hyperhomocysteinemia is 35.4% (45.4% vs 28.5% for men, women, respectively). One-year increase in age is significantly associated with 2% higher risk of hyperhomocysteinemia (OR=1.02, 95% CI: 1.01 to 1.03). One unit increase of BMI is associated with 5% higher risk of hyperhomocysteinemia (OR=1.05, 95% CI: 1.03 to 1.07). Compared with the non-smoker, smoking participants have a 24% higher risk of hyperhomocysteinemia (OR=1.24, 95% CI: 1.006 to 1.53), while the risk for those quitting smoking are not significantly different (OR=1.14, 95% CI: 0.85 to 1.54). compared with those consuming fruit and vegetable at least once every day, those consuming less than once every day had a significantly higher risk of hyperhomocysteinemia (OR=1.29, 95% CI:1.11 to 1.50). In addition, we found there were significant sex interaction with education level or alcohol drinking on the risk of hyperhomocysteinemia (p(interaction) <0.05). CONCLUSIONS: Higher BMI and older age are potential risk factors for hyperhomocysteinemia. Current smoking but not quitting smoking is associated with higher risk of hyperhomocysteinemia. Fruit and vegetable consumption may have protective effect against hyperhomocysteinemia. Alcohol consumption or education level might interact to influence the risk of hyperhomocysteinemia.
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spelling pubmed-86504922021-12-22 Prevalence and risk factors for hyperhomocysteinemia: a population-based cross-sectional study from Hunan, China Yang, Yide Zeng, Yuan Yuan, Shuqian Xie, Ming Dong, Yanhui Li, Jian He, Quanyuan Ye, Xiangli Lv, Yuan Hocher, Carl-Friedrich Kraemer, Bernhard K Hong, Xiuqin Hocher, Berthold BMJ Open Epidemiology OBJECTIVES: Hyperhomocysteinemia is an independent risk factor for cardiovascular diseases. We aimed to investigate the prevalence and risk factors for hyperhomocysteinemia, especially modifiable lifestyle factors, such as smoking behaviour and dietary factors. DESIGN: Population-based cross-sectional study. SETTING: Hunan Province, China PARTICIPANTS: A total of 4012 participants completed the study, between July 2013 and March 2014. The median age is 55 (interquartile range: 45–63) years, with 1644 males (41%) and 2368 females (59%). MAIN OUTCOME MEASURES: Homocysteine level were measured by the microplate enzyme immunoassay method. Hyperthomocysteinemia was defined as ≥15 µmol/L. Questionnaire was used to investigate potential risk factors of hyperhomocysteinemia. Crude odd ratio (OR) or adjusted OR with 95% CI were determined by using univariable or multivariable logistic regression models. RESULTS: The prevalence of hyperhomocysteinemia is 35.4% (45.4% vs 28.5% for men, women, respectively). One-year increase in age is significantly associated with 2% higher risk of hyperhomocysteinemia (OR=1.02, 95% CI: 1.01 to 1.03). One unit increase of BMI is associated with 5% higher risk of hyperhomocysteinemia (OR=1.05, 95% CI: 1.03 to 1.07). Compared with the non-smoker, smoking participants have a 24% higher risk of hyperhomocysteinemia (OR=1.24, 95% CI: 1.006 to 1.53), while the risk for those quitting smoking are not significantly different (OR=1.14, 95% CI: 0.85 to 1.54). compared with those consuming fruit and vegetable at least once every day, those consuming less than once every day had a significantly higher risk of hyperhomocysteinemia (OR=1.29, 95% CI:1.11 to 1.50). In addition, we found there were significant sex interaction with education level or alcohol drinking on the risk of hyperhomocysteinemia (p(interaction) <0.05). CONCLUSIONS: Higher BMI and older age are potential risk factors for hyperhomocysteinemia. Current smoking but not quitting smoking is associated with higher risk of hyperhomocysteinemia. Fruit and vegetable consumption may have protective effect against hyperhomocysteinemia. Alcohol consumption or education level might interact to influence the risk of hyperhomocysteinemia. BMJ Publishing Group 2021-12-06 /pmc/articles/PMC8650492/ /pubmed/34872994 http://dx.doi.org/10.1136/bmjopen-2020-048575 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Epidemiology
Yang, Yide
Zeng, Yuan
Yuan, Shuqian
Xie, Ming
Dong, Yanhui
Li, Jian
He, Quanyuan
Ye, Xiangli
Lv, Yuan
Hocher, Carl-Friedrich
Kraemer, Bernhard K
Hong, Xiuqin
Hocher, Berthold
Prevalence and risk factors for hyperhomocysteinemia: a population-based cross-sectional study from Hunan, China
title Prevalence and risk factors for hyperhomocysteinemia: a population-based cross-sectional study from Hunan, China
title_full Prevalence and risk factors for hyperhomocysteinemia: a population-based cross-sectional study from Hunan, China
title_fullStr Prevalence and risk factors for hyperhomocysteinemia: a population-based cross-sectional study from Hunan, China
title_full_unstemmed Prevalence and risk factors for hyperhomocysteinemia: a population-based cross-sectional study from Hunan, China
title_short Prevalence and risk factors for hyperhomocysteinemia: a population-based cross-sectional study from Hunan, China
title_sort prevalence and risk factors for hyperhomocysteinemia: a population-based cross-sectional study from hunan, china
topic Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8650492/
https://www.ncbi.nlm.nih.gov/pubmed/34872994
http://dx.doi.org/10.1136/bmjopen-2020-048575
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