Mure Kanae, Yoshimura Noriko, Hashimoto Marowa, Muraki Shigeyuki, Oka Hiroyuki, Tanaka Sakae, Kawaguchi Hiroshi, Nakamura Kozo, Akune Toru, Takeshita Tatsuya
Department of Public Health, Wakayama Medical University School of Medicine, Wakayama, Japan.
Department of Joint Disease Research, 22nd Century Medical and Research Center, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Obesity (Silver Spring). 2015 Jul;23(7):1517-24. doi: 10.1002/oby.21130. Epub 2015 Jun 7.
To determine whether 8-iso-prostaglandin F2α (8-iso-PGF2α) is a reliable biomarker of the accumulation of metabolic risks [e.g., overweight, hypertension, impaired glucose tolerance (IGT), and dyslipidemia].
This was a cross-sectional study of the baseline characteristics of a Japanese general population cohort study: Research on Osteoarthritis/Osteoporosis Against Disability (ROAD). Of 1,690 participants, 1,527 fulfilled all questionnaires and examinations. Free and conjugated urinary 8-iso-PGF2α levels and metabolic syndrome (MetS) components including blood pressure, HbA1c, total cholesterol, high-density lipoprotein cholesterol (HDL-C), and non-HDL-C were analyzed. The data were analyzed by ANCOVA, multiple regression analysis, and multinomial logistic analysis.
8-iso-PGF2α was significantly associated with HbA1c and significantly inversely associated with total cholesterol and non-HDL-C. Notably, IGT with an HbA1c cut-off of 5.5% was significantly associated with 8-iso-PGF2α level in participants aged ≤50 years. Multinomial logistic regression analysis revealed 8-iso-PGF2α level was significantly associated with a greater number of MetS risks present; this association was stronger in younger participants. In participants aged ≥71 years, 8-iso-PGF2α was significantly associated with a greater number of MetS risks with higher IGT cut-offs.
Urinary 8-iso-PGF2α can be a reliable marker of IGT and the accumulation of MetS risks, especially in younger people.
确定8-异前列腺素F2α(8-iso-PGF2α)是否为代谢风险[如超重、高血压、糖耐量受损(IGT)和血脂异常]累积的可靠生物标志物。
这是一项针对日本普通人群队列研究基线特征的横断面研究:骨关节炎/骨质疏松症抗残疾研究(ROAD)。在1690名参与者中,1527名完成了所有问卷和检查。分析了游离和结合型尿8-iso-PGF2α水平以及包括血压、糖化血红蛋白(HbA1c)、总胆固醇、高密度脂蛋白胆固醇(HDL-C)和非HDL-C在内的代谢综合征(MetS)组分。数据通过协方差分析、多元回归分析和多项逻辑分析进行分析。
8-iso-PGF2α与HbA1c显著相关,与总胆固醇和非HDL-C显著负相关。值得注意的是,在年龄≤50岁的参与者中,HbA1c临界值为5.5%的IGT与8-iso-PGF2α水平显著相关。多项逻辑回归分析显示,8-iso-PGF2α水平与存在的更多MetS风险显著相关;这种关联在年轻参与者中更强。在年龄≥71岁的参与者中,8-iso-PGF2α与更高IGT临界值下的更多MetS风险显著相关。
尿8-iso-PGF2α可能是IGT以及MetS风险累积的可靠标志物,尤其是在年轻人中。