Transplantation Proceedings
Volume 36, Issue 10 , Pages 2991-2992, December 2004

Methenamine silver staining quantitative digital histochemistry in chronic allograft nephropathy

The Dokuz Eylul University School of Medicine, Izmir, Turkey

Abstract 

Renal function and final outcome of renal allografts have been correlated with irreversible damage. This study describes a quantitative histochemical method relying on periodic acid methenamine silver (PAMS) staining of all renal compartments. Among 60 renal allograft biopsies from 43 patients, 15 biopsies showing pure chronic allograft nephropathy were selected to determine PAMS-stained area percentage (SAP), using image analysis with quantitative histochemistry. Of the 15 cases, 9 (60%) were grade I and 6 (40%) were grade II chronic allograft nephropathy (CAN). The mean serum creatinine (sCr) value was 1.86 ± 0.47 for allograft biopsies. The mean (±SD) SAP for the implantation biopsies was 10.58 ± 1.87%, and for allograft biopsies 25.26 ± 9.67 (P << .000). The serum creatinine (sCr) values for grade I versus II CAN were 1.63 ± 0.24 versus 2.20 ± 0.54 mg/dL, respectively (P = .019), and SAP values were 18.97 ± 0.24 versus 34.7 ± 5.89 (P = .003). There was a strong positive correlation between sCr values and SAP (P = .005; r = 0.64). These findings show the PAMS approach to be a useful alternative method for reflecting damage in more than one compartment of the renal tissue. Also, the method can discriminated implantation and allograft biopsies as well as grade I and II CAN cases. The series is small for a multivariate analysis of the value of SAP measurements in PAMS-stained sections as a prognosticator, but the data support its use.

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0041-1345(04)01231-X

doi:10.1016/j.transproceed.2004.10.043

Transplantation Proceedings
Volume 36, Issue 10 , Pages 2991-2992, December 2004