Key result
High levels of the lipid peroxidation marker Isoprostane (3rd tertile) were significantly associated with an increased risk of high carotid artery intima-media thickness (OR 14.21) after controlling for conventional risk factors.
Why the study?
Are oxidative damage markers associated with increased carotid artery intima-media thickness in men independent of conventional risk factors?
Case-Control (n=102)
No
Are oxidative damage markers associated with increased carotid artery intima-media thickness in men independent of conventional risk factors?
Oxidative damage markers, particularly Isoprostane, are strongly associated with increased carotid intima-media thickness in men independent of conventional cardiovascular risk factors.
Answers are grounded in this paper and cite their sources.
High isoprostane may flag elevated subclinical atherosclerosis risk independent of conventional factors; leaves open causality and prospective validation.
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.
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Yoon et al. (2015) conducted a case-control in Subclinical atherosclerosis (High Carotid Artery Intima-Media Thickness) (n=102). High levels of oxidative damage markers (Isoprostane, MDA, 8-OHdG) vs. Lowest tertile of oxidative damage markers was evaluated on High carotid artery intima-media thickness (CIMT ≥ 0.9 mm) (OR 14.21, 95% CI 3.34-60.56, p=<0.001). High levels of the lipid peroxidation marker Isoprostane (3rd tertile) were significantly associated with an increased risk of high carotid artery intima-media thickness (OR 14.21) after controlling for conventional risk factors.
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