Negative Association between Acrylamide Exposure and Metabolic Syndrome Markers in Adult Population

被引:10
作者
Hung, Chun-Chi [1 ,2 ]
Cheng, Yung-Wen [2 ,3 ]
Chen, Wei-Liang [2 ,3 ,4 ,5 ]
Fang, Wen-Hui [2 ,3 ]
机构
[1] Triserv Gen Hosp, Dept Orthopaed Surg, Taipei 114, Taiwan
[2] Natl Def Med Ctr, Sch Med, Taipei 114, Taiwan
[3] Triserv Gen Hosp, Dept Family & Community Med, Div Family Med, Taipei 114, Taiwan
[4] Triserv Gen Hosp, Dept Family & Community Med, Div Geriatr Med, Taipei 114, Taiwan
[5] Natl Def Med Ctr, Dept Biochem, Taipei 114, Taiwan
关键词
acrylamide; glycidamide; metabolic syndrome; NHANES; HEMOGLOBIN ADDUCTS; CANCER; CIRCUMFERENCE; INFLAMMATION; CHOLESTEROL; EXPRESSION; ADIPOKINES; BIOMARKERS; SMOKING; HEALTH;
D O I
10.3390/ijerph182211949
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Metabolic syndrome encompasses multiple conditions that increase the risk of cardiovascular disease, and exposure to environmental chemicals can cause metabolic syndrome. This cross-sectional study analyzed data from the US National Health and Nutrition Examination Survey (2003-2006) on 4318 adult participants to assess the association between acrylamide (AA) exposure and metabolic syndrome. Concentrations of hemoglobin-adducted AA (HbAA) and hemoglobin-adducted glycidamide (HbGA) were evaluated. Metabolic syndrome markers related to HbAA and HbGA and the effect of exposure to AA and GA on the prevalence of metabolic syndrome were studied by ANOVA and multivariate logistic regression analyses, respectively. HbAA concentration inversely correlated with the number of metabolic syndrome markers (p < 0.05). An increased HbAA concentration was noted with reduced high triglyceride and low high-density lipoprotein cholesterol levels in the adjusted model (p < 0.05). High fasting plasma glucose level significantly correlated with HbGA concentration in the adjusted model. In conclusion, AA exposure alters metabolic syndrome markers in adults. Additional clinical and animal studies will clarify the role of AA exposure at different stages in the progression of metabolic syndrome-related diseases.
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页数:10
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