Clinical study on the association between pregnancy-induced hypertension and insulin resistance

被引:14
作者
Chen, Zhifang [1 ]
Liu, Weiling [1 ]
Sun, Xiaoqin [1 ]
Zhu, Lingling [1 ]
机构
[1] Nantong Univ, Nantong Matern & Child Hlth Care Hosp, Dept Obstet & Gynecol, 399 Century Ave, Nantong 226018, Jiangsu, Peoples R China
关键词
HOMA-IR; HOMA-ISI; HOMA-beta%; insulin resistance; pregnancy-induced hypertension; METABOLIC SYNDROME; RISK-FACTOR; PREECLAMPSIA; WOMEN; SUSCEPTIBILITY; SENSITIVITY; DISORDERS; TRIMESTER; EWES;
D O I
10.3892/etm.2017.4169
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The aim of the present study was to explore the association between pregnancy-induced hypertension (PIH) and insulin resistance (IR). A total of 50 cases of PIH and 50 healthy pregnant women with a similar gestational age were enrolled. The hyperinsulinemic-euglycemic clamp technique was used to evaluate the degree of IR and all 100 subjects were divided into an IR and a non-IR group accordingly. Subsequently, the correlation between the systolic or diastolic blood pressure was assessed; furthermore, a homeostasis model assessment of IR (HOMA-IR), a HOMA of the insulin sensitivity index (HOMA-ISI) and a HOMA of beta cell function (HOMA-beta%) were performed. Moreover, the effect of IR on PIH was assessed and the protein expression of insulin receptor substrate (IRS)-1, phosphorylated (p)-IRS-1, AKT and p-AKT were detected in the placental plasma by western blot analysis. The results showed that in the PIH group, the p-IRS-1/IRS-1 and p-AKT/AKT ratios were decreased compared with those in the control group. Blood flow parameters, including perfusion index, retinal resistive index and systolic maximum velocity/end-diastolic velocity ratio in the IR group were higher, while time averaged velocity was lower compared with that in the non-IR group. Furthermore, the HOMA-ISI and HOMA-beta% were decreased, while the HOMA-IR was increased in the PIH group compared to that in the control group; alongside the blockage of the insulin signaling pathway, these factors may therefore cause PIH. The present study may provide novel therapeutic approaches for PIH.
引用
收藏
页码:2065 / 2070
页数:6
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