A new paradigm shift in diagnosis of Fibrillary GN(FGN) has occurred.
This rare form of organized deposit related GN might have a pathology staining
marker in the making.
Through the use of laser microdissection assisted liquid
chromatography tandem mass spectrometry , The Mayo pathologist recently discovered a novel proteomic
biomarker for FGN: DnaJ homolog subfamily B member 9 (DNAJB9), a member of the
molecular chaperone gene family. When looking at specific biopsy samples of FGN
vs non FGN cases, strong, homogeneous, smudgy DNAJB9 staining of glomerular
deposits was seen in all but 2 cases of FGN in one report published in KI-R.
This test had a 98% sensitivity and > 99%
specificity. Immunoelectron microscopy showed localization of DNAJB9 to FGN
fibrils but not to amyloid fibrils or immunotactoid glomerulopathy
microtubules. (http://www.kireports.org/article/S2468-0249(17)30341-8/pdf)
Another similar manuscript in JASN showed the same finding.
http://jasn.asnjournals.org/content/early/2017/11/02/ASN.2017050566.abstract(
below is the visual abstract)
Looks like we may have a diagnostic test and catch more cases of FGN
This comment has been removed by a blog administrator.
ReplyDelete