Research Laboratory of the Department of Clinical Chemistry and Haematology, University Medical Center Utrecht, the Netherlands.
J Clin Lipidol. 2008 Aug;2(4):298-303. doi: 10.1016/j.jacl.2008.06.004. Epub 2008 Jun 13.
F2-isoprostanes are prostaglandin-like compounds formed via arachidonic acid oxidation during oxidative stress.
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.
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.
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.
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.
F2-异前列腺素是在氧化应激时通过花生四烯酸氧化形成的类前列腺素化合物。
在巢式病例对照设计中研究尿液中 8-异前列腺素 F2α(8-iso PGF2α)浓度与心血管疾病(CVD)死亡率之间的关系。
这项针对绝经后妇女的前瞻性研究的随访时间为 18 年。病例包括 141 例死于冠心病和 109 例死于中风的妇女,而对照组是随机抽取的 142 例妇女。在基线时采集的尿液样本中,采用液相色谱/串联质谱法测定 8-iso PGF2α 的浓度。
吸烟者尿液 8-iso PGF2α 浓度比不吸烟者高 34.8%(P<0.001)。高水平的尿液 8-iso PGF2α 与致命 CVD 的发生率增加有关。尿液 8-iso PGF2α 水平最高四分位数的女性,不论年龄大小,患 CVD 死亡率的比值比为 1.8(95%置信区间,1.1-3.1,P<0.05)。进一步调整收缩压、CVD 病史、糖尿病、吸烟和体重指数并没有减弱这种关联。
尿液 8-iso PGF2α 水平较高的女性死于冠心病或中风的风险增加了 80%,这支持氧化应激参与了心血管疾病的病理生理学过程。