Panel of five microRNAs as potential biomarkers for the diagnosis and assessment of male infertility. Abu-Halima, M., Hammadeh, M., Backes, C., Fischer, U., Leidinger, P., Lubbad, A. M., Keller, A., & Meese, E. Fertility and sterility, 102:989–997.e1, October, 2014.
doi  abstract   bibtex   
To validate a set of five microRNAs (miRNAs) as specific biomarkers for the assessment of male infertility. Quantitative real-time polymerase chain reaction (qRT-PCR) validation study. University research and clinical institutes. Two hundred twenty-six men presenting at an infertility clinic. None. Validation analysis of a set of miRNAs in human purified spermatozoa and testicular biopsies. Five miRNAs (hsa-miR-34b*, hsa-miR-34b, hsa-miR-34c-5p, hsa-miR-429, and hsa-miR-122) were confirmed with the use of qRT-PCR analysis in validation sets in patients with different forms of spermatogenic impairments (subfertile and nonobstructive azoospermia [NOA]) and control subjects. We found that hsa-miR-429 was significantly increased and the four other miRNAs were decreased in both tested groups compared with normal control subjects. Computing the area under the receiver operating characteristic curve (AUC) value for each of the five miRNAs, we showed that they separated the tested groups with high accuracy (range 0.777-0.988), except for hsa-miR-429 (AUC 0.475), in patient samples with NOA. Furthermore, with the use of support vector machine classification combining these five miRNAs, we found that they discriminated individuals with, respectively, subfertility and NOA from control subjects with an accuracy of 98.65% and 99.91%, a specificity of 98.44% and 99.69%, and a sensitivity of 98.83% and 100%. Our finding suggests that these five miRNAs have potential as novel noninvasive biomarkers to diagnose patients with subfertility. Except for hsa-miR-429, the combination of these miRNAs with other conventional tests would improve the diagnostic accuracy for detecting patients with different forms of NOA.
@Article{Abu-Halima2014,
  author          = {Abu-Halima, Masood and Hammadeh, Mohamad and Backes, Christina and Fischer, Ulrike and Leidinger, Petra and Lubbad, Abdel Monem and Keller, Andreas and Meese, Eckart},
  title           = {Panel of five microRNAs as potential biomarkers for the diagnosis and assessment of male infertility.},
  journal         = {Fertility and sterility},
  year            = {2014},
  volume          = {102},
  pages           = {989--997.e1},
  month           = oct,
  issn            = {1556-5653},
  abstract        = {To validate a set of five microRNAs (miRNAs) as specific biomarkers for the assessment of male infertility. Quantitative real-time polymerase chain reaction (qRT-PCR) validation study. University research and clinical institutes. Two hundred twenty-six men presenting at an infertility clinic. None. Validation analysis of a set of miRNAs in human purified spermatozoa and testicular biopsies. Five miRNAs (hsa-miR-34b*, hsa-miR-34b, hsa-miR-34c-5p, hsa-miR-429, and hsa-miR-122) were confirmed with the use of qRT-PCR analysis in validation sets in patients with different forms of spermatogenic impairments (subfertile and nonobstructive azoospermia [NOA]) and control subjects. We found that hsa-miR-429 was significantly increased and the four other miRNAs were decreased in both tested groups compared with normal control subjects. Computing the area under the receiver operating characteristic curve (AUC) value for each of the five miRNAs, we showed that they separated the tested groups with high accuracy (range 0.777-0.988), except for hsa-miR-429 (AUC 0.475), in patient samples with NOA. Furthermore, with the use of support vector machine classification combining these five miRNAs, we found that they discriminated individuals with, respectively, subfertility and NOA from control subjects with an accuracy of 98.65% and 99.91%, a specificity of 98.44% and 99.69%, and a sensitivity of 98.83% and 100%. Our finding suggests that these five miRNAs have potential as novel noninvasive biomarkers to diagnose patients with subfertility. Except for hsa-miR-429, the combination of these miRNAs with other conventional tests would improve the diagnostic accuracy for detecting patients with different forms of NOA.},
  chemicals       = {Genetic Markers, MicroRNAs},
  citation-subset = {IM},
  completed       = {2014-11-28},
  country         = {United States},
  doi             = {10.1016/j.fertnstert.2014.07.001},
  issn-linking    = {0015-0282},
  issue           = {4},
  keywords        = {Case-Control Studies; Genetic Markers; Genetic Predisposition to Disease; Genetic Testing, methods; Humans; Infertility, Male, diagnosis, genetics, physiopathology; Male; MicroRNAs, genetics; Phenotype; Predictive Value of Tests; Real-Time Polymerase Chain Reaction; Reproducibility of Results; Spermatogenesis, genetics; Spermatozoa, chemistry; Testis, chemistry; male infertility; microRNA; nonobstructive azoospermia; seminal plasma; spermatozoa},
  nlm-id          = {0372772},
  owner           = {NLM},
  pii             = {S0015-0282(14)00596-2},
  pmid            = {25108464},
  pubmodel        = {Print-Electronic},
  pubstatus       = {ppublish},
  revised         = {2014-10-02},
}
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