A urinary Common Rejection Module (uCRM) score for non-invasive kidney transplant monitoring.
Tara K SigdelJoshua Y C YangOriol BestardAndrew SchroederSzu-Chuan HsiehJuliane M LibertoIzabella DammAnna Catharina Maria GeraedtsMinnie M SarwalPublished in: PloS one (2019)
A Common Rejection Module (CRM) consisting of 11 genes expressed in allograft biopsies was previously reported to serve as a biomarker for acute rejection (AR), correlate with the extent of graft injury, and predict future allograft damage. We investigated the use of this gene panel on the urine cell pellet of kidney transplant patients. Urinary cell sediments collected from patients with biopsy-confirmed acute rejection, borderline AR (bAR), BK virus nephropathy (BKVN), and stable kidney grafts with normal protocol biopsies (STA) were analyzed for expression of these 11 genes using quantitative polymerase chain reaction (qPCR). We assessed these 11 CRM genes for their abundance, autocorrelation, and individual expression levels. Expression of 10/11 genes were elevated in AR when compared to STA. Psmb9 and Cxcl10could classify AR versus STA as accurately as the 11-gene model (sensitivity = 93.6%, specificity = 97.6%). A uCRM score, based on the geometric mean of the expression levels, could distinguish AR from STA with high accuracy (AUC = 0.9886) and correlated specifically with histologic measures of tubulitis and interstitial inflammation rather than tubular atrophy, glomerulosclerosis, intimal proliferation, tubular vacuolization or acute glomerulitis. This urine gene expression-based score may enable the non-invasive and quantitative monitoring of AR.
Keyphrases
- poor prognosis
- genome wide
- genome wide identification
- liver failure
- gene expression
- oxidative stress
- end stage renal disease
- respiratory failure
- single cell
- high resolution
- genome wide analysis
- drug induced
- bioinformatics analysis
- binding protein
- randomized controlled trial
- heavy metals
- newly diagnosed
- cell therapy
- ejection fraction
- aortic dissection
- chronic kidney disease
- signaling pathway
- ultrasound guided
- prognostic factors
- mesenchymal stem cells
- transcription factor
- wastewater treatment
- intensive care unit
- peritoneal dialysis
- risk assessment
- fine needle aspiration
- high glucose