Role of Serum miRNAs in the Prediction of Ovarian Hyperstimulation Syndrome in Polycystic Ovarian Syndrome Patients

被引:26
作者
Zhao, Chun [1 ]
Liu, Xiaoguang [2 ]
Shi, Zhonghua [1 ]
Zhang, Jing [1 ]
Zhang, Junqiang [1 ]
Jia, Xuemei [2 ]
Ling, Xiufeng [1 ]
机构
[1] Nanjing Med Univ, Nanjing Matern & Child Hlth Care Hosp, Dept Reprod, State Key Lab Reprod Med, Nanjing 210004, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Affiliated Hosp 1, Dept Obstet & Gynecol, Nanjing 210004, Jiangsu, Peoples R China
关键词
PCOS; MicroRNA; OHSS; Predictor; Microarray; CIRCULATING MICRORNAS; CANCER; WOMEN; IVF; PREVENTION; BIOMARKERS; CONSENSUS; MARKERS; PLASMA; VEGF;
D O I
10.1159/000373934
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background: Polycystic ovarian syndrome (PCOS) causes a significantly increased risk of ovarian hyperstimulation syndrome (OHSS). Here, we focused on the altered expression of serum miRNAs and their predictive value for OHSS in PCOS patients. Methods: We used the TaqMan low density array followed by individual quantitative reverse transcription-polymerase chain reaction to identify and validate the expression of serum miRNAs in PCOS patients likely to develop severe OHSS. Results: The miR-16 and miR-223 expression levels were significantly reduced in the patients who were likely to develop severe OHSS than in the control subjects who were likely to develop mild or no OHSS. The sensitivity and specificity of the basal LH, basal LH/FSH, and body mass index (BMI) as OHSS predictors were also evaluated. miR-16 was the most efficient for OHSS prediction as it yielded the highest AUC. Logistic binary regression analyses revealed a positive association of miR-223 and BMI. Conclusion: Serum miRNAs are differentially expressed in PCOS patients likely to suffer from severe OHSS. We identified and validated two serum miRNAs that have potential for use as novel noninvasive biomarkers to accurately predict OHSS before controlled ovarian hyperstimulation (COH) for PCOS patients. Copyright (C) 2015 S. Karger AG, Basel
引用
收藏
页码:1086 / 1094
页数:9
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