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MicroRNA in vitro diagnostics using immunoassay analyzers.
Kappel, Andreas; Backes, Christina; Huang, Yiwei; Zafari, Sachli; Leidinger, Petra; Meder, Benjamin; Schwarz, Herbert; Gumbrecht, Walter; Meese, Eckart; Staehler, Cord F; Keller, Andreas.
Afiliación
  • Kappel A; Corporate Technology, Siemens AG, Erlangen, Germany;
  • Backes C; Clinical Bioinformatics, Medical Faculty, Saarland University, and.
  • Huang Y; Corporate Technology, Siemens AG, Erlangen, Germany;
  • Zafari S; Clinical Bioinformatics, Medical Faculty, Saarland University, and.
  • Leidinger P; Department of Human Genetics, Saarland University, Saarbrücken, Germany;
  • Meder B; Internal Medicine III, University Hospital Heidelberg, Heidelberg, Germany;
  • Schwarz H; Siemens Healthcare Diagnostics Products GmbH, Marburg, Germany.
  • Gumbrecht W; Corporate Technology, Siemens AG, Erlangen, Germany;
  • Meese E; Department of Human Genetics, Saarland University, Saarbrücken, Germany;
  • Staehler CF; Strategy, Siemens Healthcare, Erlangen, Germany;
  • Keller A; Clinical Bioinformatics, Medical Faculty, Saarland University, and andreas.keller@ccb.uni-saarland.de.
Clin Chem ; 61(4): 600-7, 2015 Apr.
Article en En | MEDLINE | ID: mdl-25617425
BACKGROUND: The implementation of new biomarkers into clinical practice is one of the most important areas in medical research. Besides their clinical impact, novel in vitro diagnostic markers promise to have a substantial effect on healthcare costs. Although numerous publications report the discovery of biomarkers, only a fraction of those markers are routinely used. One key challenge is a measurement system that is compatible with clinical workflows. METHODS: We designed a new immunoassay for microRNA (miRNA) quantification. The assay combines streptavidin-linked microparticles, a biotinylated catcher oligonucleotide complementary to a single miRNA species, and finally, a monoclonal antibody to DNA/RNA heterohybrids labeled with acridinium ester. Importantly, our assay runs on standard immunoassay analyzers. After a technical validation of the assay, we evaluated the clinical performance on 4 Alzheimer disease miRNAs. RESULTS: Our assay has an analytical specificity of 99.4% and is at the same time sensitive (concentrations in the range of 1 pmol/L miRNA can be reliably profiled). Because the novel approach did not require amplification steps, we obtained high reproducibility for up to 40 biological replicates. Importantly, our assay prototype exhibited a time to result of <3 h. With human blood samples, the assay was able to measure 4 miRNAs that can detect Alzheimer disease with a diagnostic accuracy of 82% and showed a Pearson correlation >0.994 with the gold standard qRT-PCR. CONCLUSIONS: Our miRNA immunoassay allowed the measurement of miRNA signatures with sufficient analytical sensitivity and high specificity on commonly available laboratory equipment.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Inmunoensayo / Biomarcadores / MicroARNs / Enfermedad de Alzheimer / Anticuerpos Monoclonales Tipo de estudio: Diagnostic_studies / Evaluation_studies Límite: Humans Idioma: En Revista: Clin Chem Asunto de la revista: QUIMICA CLINICA Año: 2015 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Inmunoensayo / Biomarcadores / MicroARNs / Enfermedad de Alzheimer / Anticuerpos Monoclonales Tipo de estudio: Diagnostic_studies / Evaluation_studies Límite: Humans Idioma: En Revista: Clin Chem Asunto de la revista: QUIMICA CLINICA Año: 2015 Tipo del documento: Article