Comparison of different normalization strategies for the analysis of glomerular microRNAs in IgA nephropathy

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作者
Clemens L. Bockmeyer
Karen Säuberlich
Juliane Wittig
Marc Eßer
Sebastian S. Roeder
Udo Vester
Peter F. Hoyer
Putri A. Agustian
Philip Zeuschner
Kerstin Amann
Christoph Daniel
Jan U. Becker
机构
[1] Friedrich Alexander University (FAU) Erlangen-Nuremberg,Department of Nephropathology
[2] Institute of Pathology,Department of Nephrology
[3] Hannover Medical School,undefined
[4] Institute of Pathology,undefined
[5] University Hospital of Cologne,undefined
[6] Children’s Hospital,undefined
[7] Pediatrics II,undefined
[8] University of Duisburg-Essen,undefined
[9] Hannover Medical School,undefined
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Small nucleolar RNAs (snoRNAs) have been used for normalization in glomerular microRNA (miRNA) quantification without confirmation of validity. Our aim was to identify glomerular reference miRNAs in IgA nephropathy. We compared miRNAs in human paraffin-embedded renal biopsies from patients with cellular-crescentic IgA-GN (n = 5; crescentic IgA-GN) and non-crescentic IgA-GN (n = 5; IgA-GN) to mild interstitial nephritis without glomerular abnormalities (controls, n = 5). Laser-microdissected glomeruli were used for expression profiling of 762 miRNAs by low-density TaqMan arrays (cards A and B). The comparison of different normalization methods (GeNormPlus, NormFinder, global mean and snoRNAs) in crescentic IgA-GN, IgA-GN and controls yielded similar results. However, levels of significance and the range of relative expression differed. In median, two normalization methods demonstrated similar results. GeNormPlus and NormFinder gave different top ranked reference miRNAs. Stability ranking for snoRNAs varied between cards A and B. In conclusion, we suggest the geometric mean of the most stable reference miRNAs found in GeNormPlus (miR-26b-5p), NormFinder (miR-28-5p) and snoRNAs (RNU44) as reference. It should be considered that significant differences could be missed using one particular normalization method. As a starting point for glomerular miRNA studies in IgA nephropathy we provide a library of miRNAs.
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