2009
DOI: 10.1016/j.amjcard.2009.04.047
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Usefulness of Elevations in Serum Choline and Free F2-Isoprostane to Predict 30-Day Cardiovascular Outcomes in Patients With Acute Coronary Syndrome

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Cited by 59 publications
(49 citation statements)
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“…Atherosclerosis and inflammation have been identified as the key mechanisms underlying AMD. Increased F2-IsoPs have also been shown to be associated with atherosclerosis, [15][16][17] atherosclerotic CVD, 21,45,46 and markers of inflammation including serum amyloid A and C-reactive protein (CRP) in previous studies. [18][19][20][21][22] In addition, F2-IsoPs have also been shown to be associated with several proatherogenic factors including smoking, diabetes, and hypertension.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Atherosclerosis and inflammation have been identified as the key mechanisms underlying AMD. Increased F2-IsoPs have also been shown to be associated with atherosclerosis, [15][16][17] atherosclerotic CVD, 21,45,46 and markers of inflammation including serum amyloid A and C-reactive protein (CRP) in previous studies. [18][19][20][21][22] In addition, F2-IsoPs have also been shown to be associated with several proatherogenic factors including smoking, diabetes, and hypertension.…”
Section: Discussionmentioning
confidence: 99%
“…In line with this hypothesis, in the current study, those with higher levels of F2-isoPs had lower levels of BMI. It could also be due to selective mortality of those with higher levels of F2-IsoPs and diabetes, hypertension, or CVD 21,45 given that elevated levels of F2-IsoPs have been shown to predict the extent and severity of coronary artery disease. 51 In addition, CVD in the current study was self-reported and FIGURE.…”
Section: Discussionmentioning
confidence: 99%
“…Choline in plasma (Adamczyk et al 2006) or serum (LeLeiko et al 2009) has been associated with early events related to tissue ischemia, whereas whole-blood choline predicts events related to coronary plaque instability (such as myocardial infarction) during follow-up (Danne et al 2007), particularly in patients with low to moderate risk (Mockel et al 2008). The reported associations between ischemic heart diseases and choline in plasma versus whole blood are complex and somewhat inconsistent (Body et al 2009) and have been explained by activation of phospholipases A2 and D in ischemic heart tissue and activated blood cells, leading to release of choline into plasma and secondary uptake into blood cells (Danne et al 2007).…”
Section: Cardiovascular Disease and Metabolic Syndromementioning
confidence: 99%
“…Notably, other work has revealed a positive association between blood choline levels and increased CVD risk [74][75][76]. In fact, whole-blood choline, plasma choline and serum choline have recently been characterized as emerging biomarkers to detect vulnerable plaques in patients with acute coronary syndrome (ACS) [77].…”
Section: Human Studiesmentioning
confidence: 99%