Plasma miR-17-5p, miR-20a and miR-22 are down-regulated in women with endometriosis

Hum Reprod. 2013 Feb;28(2):322-30. doi: 10.1093/humrep/des413. Epub 2012 Nov 30.

Abstract

Study question: Can plasma microRNAs be used as a non-invasive diagnostic test for the detection of endometriosis?

Summary answer: Plasma miR-17-5p, miR-20a and miR-22 are down-regulated in women with endometriosis compared with those without endometriosis in mainland China.

What is known already: There is currently a pressing need to develop a non-invasive diagnostic test for endometriosis. Altered circulating microRNA profiles have already been linked to various disease states.

Study design, size, and duration: This was a prospective laboratory study in a tertiary-referral university hospital in Beijing, PR China, between January 2012 and May 2012. Twenty-three women with histologically proven endometriosis and 23 endometriosis-free controls were enrolled in this study.

Participants/materials, setting, and methods: Laparoscopic inspection of the abdominopelvic cavity was performed for each patient, and peripheral blood samples were collected before laparoscopy. Microarray-based microRNA expression profiling was used to identify differentially expressed microRNAs in plasma samples between women with and without endometriosis, and quantification of selected microRNAs was performed using quantitative RT-PCR.

Main results and the role of chance: Twenty-seven microRNAs were differentially expressed between women with and without endometriosis, of which six microRNAs (miR-15b-5p, miR-17-5p, miR-20a, miR-21, miR-22 and miR-26a) were selected for validation. MiR-17-5p, miR-20a and miR-22 were significantly down-regulated in women with endometriosis compared with controls (P = 0.011, 0.0020 and 0.0002, respectively), yielding an area under the receiver operator characteristics curve of 0.74 [95% confidence interval (CI): 0.58-0.90], 0.79 (95% CI: 0.65-0.93) and 0.85 (95% CI: 0.71-0.98) in discriminating endometriosis from controls, respectively.

Limitations and reasons for caution: Our sample size was small and all cases were rAFS stage III-IV, which may limit generalization of plasma microRNAs for early diagnosis of endometriosis. Moreover, only six microRNAs were selected for validation.

Wider implications of the findings: Plasma microRNAs provide a promising opportunity for detection of endometriosis.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult
  • Cluster Analysis
  • Down-Regulation
  • Endometriosis / blood
  • Endometriosis / diagnosis
  • Endometriosis / genetics*
  • Female
  • Gene Expression Profiling
  • Humans
  • MicroRNAs / blood*
  • Oligonucleotide Array Sequence Analysis
  • Prospective Studies
  • Real-Time Polymerase Chain Reaction

Substances

  • MIRN17 microRNA, human
  • MIRN20a microRNA, human
  • MIRN22 microRNA, human
  • MicroRNAs