Title of article :
Diagnostic Urinary Proteome Profile for Immunoglobulin A Nephropathy
Author/Authors :
Samavat, Shiva Shahid Beheshti University of Medical Sciences - Department of Nephrology , Kalantari, Shiva Shahid Beheshti University of Medical Sciences - Chronic Kidney Diseases Research Center , Nafar, Mohsen Shahid Beheshti University of Medical Sciences - Chronic Kidney Diseases Research Center , Rutishauser, Dorothea Karolinska Institute - Department of Medical Biochemistry and Biophysics , Rezaei-Tavirani, Mostafa Shahid Beheshti University of Medical Sciences - Department of Basic Sciences , Parvin, Mahmud Shahid Beheshti University of Medical Sciences - Department of Pathology , , Roman A Zubarev Karolinska Institute - Department of Medical Biochemistry and Biophysics
Abstract :
Introduction. Immunoglobulin A (IgA) nephropathy, the most
common type of glomerulonephritis, is only diagnosed by invasive
kidney biopsy. Urine proteome panel might help in noninvasive
diagnosis and also better understanding of pathogenesis of IgA
nephropathy.
Materials and Methods. Second mid-stream urine samples of 13
patients with biopsy-proven IgA nephropathy and 8 healthy controls
were investigated by means of nanoscale liquid chromatography
tandem mass spectrometry. Multivariate analysis of quantified
label-free proteins was performed by the principal component
analysis and partial least squares models.
Results. A total number of 493 unique proteins were quantified
by nanoscale liquid chromatography tandem mass spectrometry,
of which 46 proteins were considered as putative biomarkers of
IgA nephropathy, after multivariate analysis and additional filter
criterion and comparing the patients and the controls. Some of the
significant differentially expressed proteins were CD44, glycoprotein
2, vasorin, epidermal growth factor, CLM9, protocadherin,
utreoglobin, dipeptidyl peptidase IV, NHL repeat-containing protein
3, and SLAM family member 5. These proteins were related to
various involved pathogenic pathways of inflammatory response
and complement system.
Conclusions. This proteome profile could be utilized in the diagnosis
of IgA nephropathy. In addition, providing a noninvasive diagnostic
tool, it may shed light on the pathogenesis of IgA nephropathy.
Keywords :
mass spectrometry , proteomics , urine , IgA glomerulonephritis
Journal title :
Astroparticle Physics