Li Hongwei, Yin Qian, Li Ning, Ouyang Zhenbo, Zhong Mei
Department of Obstetrics & Gynecology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Department of Obstetrics & Gynecology, Puyang Oilfield General Hospital, Puyang, China.
Obstet Gynecol Int. 2016;2016:3865454. doi: 10.1155/2016/3865454. Epub 2016 Oct 10.
To determine plasma markers of oxidative stress during the second and third trimester of pregnancy in patients with gestational diabetes mellitus (GDM). We conducted a prospective nested case-control study involving 400 pregnant women, 22 of whom developed GDM. As control group, 30 normal pregnant women were chosen randomly. Plasma samples were analyzed for 8-iso-prostaglandin F2 (8-iso-PGF2), advanced oxidative protein products (AOPPs), protein carbonyl (PCO), glutathione peroxidase-3 (GPX-3), and paraoxonase-1 (PON1) at 16-20 weeks, 24-28 weeks, and 32-36 weeks of gestation. Compared to control subjects, the plasma levels of PCO, AOPPs, and 8-iso-PGF2 were elevated at 16-20 weeks' and 32-36 weeks' gestation in GDM. There was no significant difference in PCO and 8-iso-PGF2 at 24-28 weeks in GDM. GPX-3 was statistically significantly increased at 16-20 weeks and 32-36 weeks in GDM. PON1 reduced in patients with GDM. No significant differences were found at 24-28 and 32-36 weeks between the GDM and control groups. In GDM, PCO, AOPPs, and 8-iso-PGF2 levels were higher and GPX-3 and PON1 levels were lower in the second than the third trimester. Oxidation status increased in GDM, especially protein oxidation, which may contribute to the pathogenesis of GDM.
确定妊娠期糖尿病(GDM)患者妊娠中期和晚期氧化应激的血浆标志物。我们进行了一项前瞻性巢式病例对照研究,纳入400名孕妇,其中22名患GDM。作为对照组,随机选取30名正常孕妇。在妊娠16 - 20周、24 - 28周和32 - 36周时,对血浆样本进行8 - 异前列腺素F2(8 - iso - PGF2)、晚期氧化蛋白产物(AOPPs)、蛋白羰基(PCO)、谷胱甘肽过氧化物酶 - 3(GPX - 3)和对氧磷酶 - 1(PON1)分析。与对照组相比,GDM患者在妊娠16 - 20周和32 - 36周时血浆PCO、AOPPs和8 - iso - PGF2水平升高。GDM患者在24 - 28周时PCO和8 - iso - PGF2无显著差异。GDM患者在16 - 20周和32 - 36周时GPX - 3在统计学上显著升高。GDM患者PON1降低。GDM组与对照组在24 - 28周和32 - 36周时未发现显著差异。在GDM中,妊娠中期的PCO、AOPPs和8 - iso - PGF2水平高于晚期,而GPX - 3和PON1水平低于晚期。GDM中氧化状态增加,尤其是蛋白质氧化,这可能有助于GDM的发病机制。