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Volume 2, Issue 4, Pages 298-303 (August 2008)


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High levels of urinary F2-isoprostanes predict cardiovascular mortality in postmenopausal women

Mark Roest, PhDa, Hieronymus A.M. Voorbij, PhDa, Yvonne T. Van der Schouw, PhDb, Petra H.M. Peeters, PhDb, Tom Teerlink, PhDc, Peter G. Scheffer, PhDcCorresponding Author Informationemail address

Received 20 March 2008; accepted 8 June 2008. published online 16 June 2008.

Background

F2-isoprostanes are prostaglandin-like compounds formed via arachidonic acid oxidation during oxidative stress.

Objective

To study the relation between urinary concentrations of 8-iso-prostaglandin F2α (8-iso PGF2α) and mortality due to cardiovascular disease (CVD) in a nested case-cohort design.

Methods

Follow-up duration of this prospective study among postmenopausal women was 18 years. Cases included 141 women who died of coronary heart disease and 109 women who died of stroke, whereas controls were a random cohort sample of 142 women. The concentration of 8-iso PGF2α was determined with liquid chromatography/tandem mass spectrometry in urine samples collected at baseline.

Results

Smokers had 34.8% higher urinary 8-iso PGF2α concentrations than nonsmokers (P < 0.001). High levels of urinary 8-iso PGF2α were associated with increased incidence of fatal CVD. Women who were in the highest quartile of urinary 8-iso PGF2α levels had, independently of age, an odds ratio of 1.8 (95% confidence interval, 1.1–3.1, P < 0.05) for CVD mortality. Further adjustment by systolic blood pressure, history of CVD, diabetes, smoking, and body mass index did not attenuate this association.

Conclusion

Women with high levels of urinary 8-iso PGF2α had an 80% increased risk of dying of coronary heart disease or stroke, supporting involvement of oxidative stress in the pathophysiology of cardiovascular disease.

a Research Laboratory of the Department of Clinical Chemistry and Haematology, University Medical Center Utrecht, the Netherlands

b The Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, the Netherlands

c Department of Clinical Chemistry, VU University Medical Center, Amsterdam, The Netherlands

Corresponding Author InformationCorresponding author.

PII: S1933-2874(08)00265-1

doi:10.1016/j.jacl.2008.06.004


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