河北医科大学学报 ›› 2021, Vol. 42 ›› Issue (1): 47-53.doi: 10.3969/j.issn.1007-3205.2021.01.011

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妊娠期糖尿病患者不同孕周血浆Visfatin表达检测

  

  1. 山西省儿童医院山西省妇幼保健院妇产科,山西 太原  030000
  • 出版日期:2021-01-25 发布日期:2021-02-05
  • 作者简介:胡丽燕(1971-),女,山西太原人,山西省儿童医院山西省妇幼保健院主任医师,医学硕士,从事妊娠期糖尿病血糖诊治研究。

Plasma Visfatin expression in patients with gestational diabetes at different gestational weeks

  1. Department of Obstetrics and Gynecology, Shanxi Provincial Maternal and Child Health Hospital, Children′s Hospital of Shanxi Province, Taiyuan 030000, China
  • Online:2021-01-25 Published:2021-02-05

摘要: 目的  检测妊娠期糖尿病(gestational diabetes mellitus, GDM)患者不同孕周血浆Visfatin水平变化,分析其临床意义。
方法  选择我院系统检查的孕妇作为研究对象,所有入选孕妇均在孕24~26周作口服葡萄糖耐量试验(oral glucose tolerance test,OGTT),将确诊为GDM的孕妇 40例为GDM组,血糖正常的孕妇40例为正常糖耐量(normal glucose tolerance,NGT)组。采用酶联免疫吸附测定法检测2组孕24~26周血浆Visfatin含量,根据Visfatin中位数将GDM组分为高Visfatin亚组和低Visfatin亚组各20例,检测各组糖、脂代谢指标,并计算胰岛素抵抗指数(homeostasis model assessment insulin resistance,HOMA-IR);随访检测各组孕31~33周、38~40周血浆Visfatin含量,并记录新生儿体重、身长,计算ponderal指数。
结果  GDM组高Visfatin亚组、低Visfatin亚组及NGT组血浆Visfatin水平随孕周增加而升高(P<0.05);GDM组高Visfatin亚组孕24~26周血浆Visfatin高于低Visfatin亚组,且低Visfatin亚组高于NGT组(P<0.05),高Visfatin亚组、低Visfatin亚组孕31~33周、38~40周血浆Visfatin与NGT组比较差异无统计学意义(P>0.05);GDM组高Visfatin亚组孕24~26周空腹血糖、糖化血红蛋白、空腹胰岛素、HOMA-IR及总胆固醇、三酰甘油、低密度脂蛋白胆固醇均高于低Visfatin亚组,且低Visfatin亚组高于NGT组(P<0.05),GDM组高Visfatin亚组孕24~26周血浆高密度脂蛋白胆固醇低于低Visfatin亚组,且低Visfatin亚组低于NGT组,差异均有统计学意义(P<0.05);Pearson相关性分析显示,GDM组孕24~26周血浆Visfatin与孕24~26周HOMA-IR(r=0.429,P=0.036)、31~33周HOMA-IR(r=0.568,P=0.025)、孕38~40周HOMA-IR(r=0.672, P=0.003)均呈明显正相关;GDM组高Visfatin亚组新生儿体重、ponderal指数均高于低Visfatin亚组,且低Visfatin亚组高于NGT组,两两比较差异均有统计学意义(P<0.05)。
结论  血浆Visfatin含量随孕周增加而升高,GDM患者孕24~26周血浆Visfatin含量高于NGT孕妇;孕24~26周Visfatin与GDM患者糖类和脂质代谢紊乱有关,并促进胎儿宫内发育。


关键词: 糖尿病, 妊娠, 胰岛素抵抗, 糖脂代谢

Abstract: Objective  To detect the changes of plasma Visfatin levels in gestational diabetes mellitus(GDM) patients at different gestational weeks, and to analyze its clinical significance. 
Methods  The pregnant women systematically examined in our hospital were selected as the research subjects. All pregnant women enrolled underwent oral glucose tolerance test(OGTT) from 24 to 26 weeks of gestation; 40 cases diagnosed with GDM were assigned to GDM group, and 40 cases with normal glucose tolerance(NGT) to NGT group. The plasma Visfatin levels in the two groups were determined by ELISA at 24-26 weeks of gestation, and the GDM group was subdivided into the high Visfatin subgroup(n=20) and low Visfatin subgroup(n=20) according to the median Visfatin. Glycolipid metabolism indexes were detected and Homeostasis model assessment insulin resistance(HOMA-IR) was calculated. The plasma Visfatin was measured at 31-33 weeks and 38-40 weeks of gestation, and the neonatal body mass and body length were recorded to calculate ponderal index. 
Results  The plasma Visfatin level in high Visfatin subgroup, low Visfatin subgroup of the GDM group and NGT group were increased with the increase of gestational age(P<0.05). The plasma Visfatin level in high Visfatin subgroup of GDM group was higher than that in the low Visfatin subgroup at 24-26 weeks of gestation, and the level in low Visfatin subgroup was higher than that in the NGT group(P<0.05). There was no statistically difference of Visfatin level at 31-33 weeks and 38-40 weeks of gestation among high Visfatin subgroup, low Visfatin subgroup and NGT group(P>0.05). The pregnant fasting glucose, glycosylated hemoglobin, fasting insulin, HOMA-IR as well as triglyceride, total cholesterol, low density lipoprotein cholesterol at 24-26 weeks of gestation in high Visfatin subgroup were higher than that of low Visfatin subgroup, and the above indicators were higher in low Visfatin subgroup than in NGT group(P<0.05); the plasma high-density lipoprotein cholesterol at 24-26 weeks of gestation was lower in high Visfatin subgroup than in low Visfatin subgroup, and the level was lower in low Visfatin subgroup than in NGT group(P<0.05). Pearson correlation analysis showed that plasma Visfatin in GDM group was positively correlated with HOMA-IR(r=0.429, P=0.036) at 24-26 weeks of gestation, HOMA-IR(r=0.568, P=0.025) at 31-33 weeks of gestation, and HOMA-IR(r=0.672, P=0.003) at 38-40 weeks of gestation. The neonatal body mass and ponderal index in high Visfatin subgroup of GDM group were higher than that of the low Visfatin subgroup, which were higher in the low Visfatin subgroup than in the NGT group(P<0.05). 
Conclusion  The plasma Visfatin is increased with the increase of gestational age. The plasma Visfatin at 24-26 weeks of gestation in patients with GDM is higher than that of NGT pregnant women. Visfatin at 24-26 weeks of gestation is related to the disorder of glucose and lipid metabolism and promotes fetal intrauterine development in patients with GDM.


Key words: diabetes, gestational, insulin resistance, glucose and lipid metabolism