Serum miRNAs in women affected by hyperandrogenic polycystic ovary syndrome: the potential role of miR-155 as a biomarker for monitoring the estroprogestinic treatment.
Walter ArancioMarco Calogero AmatoMiriam MagliozzoGiuseppe PizzolantiRosalia VescoCarla GiordanoPublished in: Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology (2018)
MicroRNAs can be used as very efficient circulating biomarkers. The role of microRNAs in polycystic ovary syndrome (PCOS) and the effects of antiandrogen therapy on microRNA expression is still not fully understood. A panel of serum microRNAs were retrotranscribed via looped reverse primer transcription specific for each miRNA and quantified via probe specific RT-PCR in 16 Caucasian hyperandrogenic PCOS women selected according to the Rotterdam criteria and in a subset of seven patients after four months of sequential reverse antiandrogenic therapy. All women recruited underwent an oral glucose tolerance test (OGTT) and a baseline total cholesterol, high density lipoproteins cholesterol, triglycerides, AST and ALT dosage. In the follicular phase women were evaluated for total testosterone, Δ4-androstenedione, DHEAS, 17OHpg, FSH, LH, and 17-β-E2. The AUC2hglucose, ISI Matsuda, oral disposition index (DIo) and visceral adipose index (VAI) were also calculated. We suggest that miR-155 might have a role as biomarker in hyperandrogenic PCOS patients to monitor the effect of antiandrogen therapy.
Keyphrases
- polycystic ovary syndrome
- insulin resistance
- end stage renal disease
- high density
- ejection fraction
- cell proliferation
- long non coding rna
- newly diagnosed
- adipose tissue
- chronic kidney disease
- metabolic syndrome
- prognostic factors
- peritoneal dialysis
- poor prognosis
- transcription factor
- long noncoding rna
- replacement therapy
- patient reported outcomes
- mesenchymal stem cells
- binding protein
- living cells
- pregnancy outcomes
- single molecule