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Association between Lipoprotein (a) Levels and Metabolic Syndrome in a Middle-aged and Elderly Chinese Cohort.

Authors :
WU, Xue Yan
LIN, Lin
Yan, Qi Hong
DU, Rui
HU, Chun Yan
MA, Li Na
PENG, Kui
LI, Mian
XU, Yu
XU, Min
CHEN, Yu Hong
LU, Jie Li
BI, Yu Fang
WANG, Wei Qing
NING, Guang
Source :
Biomedical & Environmental Sciences; Jul2019, Vol. 32 Issue 7, p477-485, 9p
Publication Year :
2019

Abstract

The association between lipoprotein (a) [Lp(a)] levels and metabolic syndrome (MetS) remains uncertain, especially in the Asian population. The purpose of this study was to demonstrate the association between Lp(a) levels and MetS in a middle-aged and elderly Chinese cohort. A cross-sectional study of 10,336 Chinese adults aged 40 years or older was conducted in Jiading District, Shanghai, China. Logistic regression analysis was used to evaluate the association between serum Lp(a) levels and MetS. In the overall population, 37.5% of participants had MetS. Compared with individuals in the lowest quartile of serum Lp(a) levels, those in the highest quartile had a lower prevalence of MetS (30.9% vs. 46.9%, P for trend < 0.0001). Multivariate logistic regression analyses showed that compared with participants in the bottom quartile of serum Lp(a) levels, those in the top quartile had decreased odds ratio (OR) for prevalent MetS [multivariate-adjusted OR 0.45 (95% confidence interval 0.39-0.51); P < 0.0001]. Additionally, Lp(a) level was conversely associated with the risk of central obesity, high fasting glucose, high triglycerides, and low HDL cholesterol, but not with hypertension. Stratified analyses suggested that increasing levels of Lp(a) was associated with decreased risk of MetS in all the subgroups. Serum Lp(a) level was inversely associated with the risk of prevalent MetS in a middle-aged and elderly Chinese cohort. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
08953988
Volume :
32
Issue :
7
Database :
Supplemental Index
Journal :
Biomedical & Environmental Sciences
Publication Type :
Academic Journal
Accession number :
141902481
Full Text :
https://doi.org/10.3967/bes2019.065