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Oxidative damage markers are significantly associated with the carotid artery intima-media thickness after controlling for conventional risk factors of atherosclerosis in men

Authors
 Jin-Ha Yoon  ;  Jang-Young Kim  ;  Jong-Ku Park  ;  Sang-Baek Ko 
Citation
 PLOS ONE, Vol.10(3) : e0119731, 2015 
Journal Title
PLOS ONE
Issue Date
2015
MeSH
Adult ; Aged ; Aged, 80 and over ; Atherosclerosis/diagnostic imaging ; Atherosclerosis/etiology* ; Atherosclerosis/metabolism ; Biomarkers/blood ; Carotid Arteries/diagnostic imaging ; Carotid Arteries/metabolism* ; Carotid Artery Diseases/diagnostic imaging ; Carotid Artery Diseases/etiology* ; Carotid Artery Diseases/metabolism ; Carotid Intima-Media Thickness ; Case-Control Studies ; Cohort Studies ; Deoxyguanosine/analogs & derivatives ; Deoxyguanosine/blood ; Humans ; Isoprostanes/blood ; Male ; Malondialdehyde/blood ; Middle Aged ; Oxidative Stress/physiology* ; Risk Factors
Abstract
BACKGROUND: This study aimed to assess the association between oxidative damage markers and carotid artery intima-media thickness (CIMT) after controlling for conventional risk factors of atherosclerosis in multiple logistic regression models.

METHODS AND FINDINGS: Fifty-one case male participants (CIMT ≥ 0.9 mm) were enrolled during their visits to Korean Genomic Rural Cohort Study of Wonju centers between May 1 and August 31, 2011, along with 51 control participants (CIMT < 0.9 mm) selected using frequency matching by age group. The levels of oxidative damage markers, 8-hydroxy-2'-deoxyquuanosine (8-OHdG), malondialdehyde (MDA), and 8-iso-prostaglandin F2α (Isoprostane), were measured. Conditional logistic regression models were used to evaluate relative relationships between the oxidative damage markers and the risk of high CIMT.

RESULTS: The markers of oxidative lipid (Isoprostane and MDA) and DNA (8-OHdG) damage were associated with CIMT after controlling for the conventional risk factors, including age, low density lipoprotein, body mass index, smoking history, alcohol consumption, and metabolic syndrome (ORs [95% CI] for Isoprostane: 3rd tertile, 8.47 [2.59-27.67]; for MDA: 3rd tertile, 8.47 [2.59-27.67]; for 8-OHdG: 3rd tertile, 5.58 [1.79-17.33]). When all the oxidative damage markers were incorporated in the same logistic regression model, only Isoprostane was significantly related to CIMT (OR [95% CI]: 4.22 [1.31-13.53] in 2nd tertile and 14.21 [3.34-60.56] in 3rd tertile).

CONCLUSIONS: In this nested case-control study, the oxidative damage markers of lipid and DNA were associated with CIMT even after controlling for the conventional risk factors of cardiovascular diseases.
Files in This Item:
T201505118.pdf Download
DOI
10.1371/journal.pone.0119731
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Preventive Medicine (예방의학교실) > 1. Journal Papers
Yonsei Authors
Yoon, Jin Ha(윤진하) ORCID logo https://orcid.org/0000-0003-4198-2955
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/157033
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