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Higher Levels of Lipoprotein Associated Phospholipase A2 is associated with Increased Prevalence of Cognitive Impairment: the APAC Study
Lipoprotein-associated phospholipase A(2) (Lp-PLA(2)) is a unique circulating phospholipase with inflammatory and oxidative activities and the limited data regarding the relationship between Lp-PLA(2) and cognitive impairment are conflicted. We conducted a cross-sectional study including 1,374 Chine...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5017024/ https://www.ncbi.nlm.nih.gov/pubmed/27609335 http://dx.doi.org/10.1038/srep33073 |
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author | Jiang, Ruixuan Chen, Shengyun Shen, Yuan Wu, Jianwei Chen, Shuohua Wang, Anxin Wu, Shouling Zhao, Xingquan |
author_facet | Jiang, Ruixuan Chen, Shengyun Shen, Yuan Wu, Jianwei Chen, Shuohua Wang, Anxin Wu, Shouling Zhao, Xingquan |
author_sort | Jiang, Ruixuan |
collection | PubMed |
description | Lipoprotein-associated phospholipase A(2) (Lp-PLA(2)) is a unique circulating phospholipase with inflammatory and oxidative activities and the limited data regarding the relationship between Lp-PLA(2) and cognitive impairment are conflicted. We conducted a cross-sectional study including 1,374 Chinese adults recruited from 2010 to 2011, aiming to evaluate the relationship between Lp-PLA(2) levels and the prevalence of cognitive impairment in a Chinese community-based population. Participants underwent standardized evaluation. Serum Lp-PLA2 mass was measured by ELISA. Cognition status was evaluated via the Mini-Mental Status Exam (MMSE) and cognitive impairment was identified as MMSE <24. Multivariable logistic regression models were used to assess the associations of Lp-PLA(2) mass with cognitive impairment. Lp-PLA(2) mass was significantly associated with the prevalence of cognitive impairment after adjusting for other potential confounding factors (compared with the first quartile, adjusted ORs of the second, third, and fourth quartile were 2.058 (95% CI, 0.876–4.835), 2.834 (95% CI, 1.255–6.398), and 4.882 (95% CI, 2.212–10.777), p < 0.0001). In conclusion, elevated level of Lp-PLA(2) mass was independently associated with the prevalence of cognitive impairment in Chinese adults. |
format | Online Article Text |
id | pubmed-5017024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50170242016-09-12 Higher Levels of Lipoprotein Associated Phospholipase A2 is associated with Increased Prevalence of Cognitive Impairment: the APAC Study Jiang, Ruixuan Chen, Shengyun Shen, Yuan Wu, Jianwei Chen, Shuohua Wang, Anxin Wu, Shouling Zhao, Xingquan Sci Rep Article Lipoprotein-associated phospholipase A(2) (Lp-PLA(2)) is a unique circulating phospholipase with inflammatory and oxidative activities and the limited data regarding the relationship between Lp-PLA(2) and cognitive impairment are conflicted. We conducted a cross-sectional study including 1,374 Chinese adults recruited from 2010 to 2011, aiming to evaluate the relationship between Lp-PLA(2) levels and the prevalence of cognitive impairment in a Chinese community-based population. Participants underwent standardized evaluation. Serum Lp-PLA2 mass was measured by ELISA. Cognition status was evaluated via the Mini-Mental Status Exam (MMSE) and cognitive impairment was identified as MMSE <24. Multivariable logistic regression models were used to assess the associations of Lp-PLA(2) mass with cognitive impairment. Lp-PLA(2) mass was significantly associated with the prevalence of cognitive impairment after adjusting for other potential confounding factors (compared with the first quartile, adjusted ORs of the second, third, and fourth quartile were 2.058 (95% CI, 0.876–4.835), 2.834 (95% CI, 1.255–6.398), and 4.882 (95% CI, 2.212–10.777), p < 0.0001). In conclusion, elevated level of Lp-PLA(2) mass was independently associated with the prevalence of cognitive impairment in Chinese adults. Nature Publishing Group 2016-09-09 /pmc/articles/PMC5017024/ /pubmed/27609335 http://dx.doi.org/10.1038/srep33073 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Jiang, Ruixuan Chen, Shengyun Shen, Yuan Wu, Jianwei Chen, Shuohua Wang, Anxin Wu, Shouling Zhao, Xingquan Higher Levels of Lipoprotein Associated Phospholipase A2 is associated with Increased Prevalence of Cognitive Impairment: the APAC Study |
title | Higher Levels of Lipoprotein Associated Phospholipase A2 is associated with Increased Prevalence of Cognitive Impairment: the APAC Study |
title_full | Higher Levels of Lipoprotein Associated Phospholipase A2 is associated with Increased Prevalence of Cognitive Impairment: the APAC Study |
title_fullStr | Higher Levels of Lipoprotein Associated Phospholipase A2 is associated with Increased Prevalence of Cognitive Impairment: the APAC Study |
title_full_unstemmed | Higher Levels of Lipoprotein Associated Phospholipase A2 is associated with Increased Prevalence of Cognitive Impairment: the APAC Study |
title_short | Higher Levels of Lipoprotein Associated Phospholipase A2 is associated with Increased Prevalence of Cognitive Impairment: the APAC Study |
title_sort | higher levels of lipoprotein associated phospholipase a2 is associated with increased prevalence of cognitive impairment: the apac study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5017024/ https://www.ncbi.nlm.nih.gov/pubmed/27609335 http://dx.doi.org/10.1038/srep33073 |
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