Multi‐photon microscopy for the evaluation of interstitial fibrosis in extended criteria donor kidneys: A proof‐of‐concept study
Introduction To evaluate the initial use of label‐free second harmonic generation (SHG) imaging with two‐photon excitation (2PE) auto‐fluorescence in multiphoton microscopy (MPM) for the quantification of collagen/fibrosis on preimplantation biopsies of extended criteria donors (ECD). Materials and...
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Published in | Clinical transplantation Vol. 36; no. 8; pp. e14717 - n/a |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Denmark
01.08.2022
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Subjects | |
Online Access | Get full text |
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Summary: | Introduction
To evaluate the initial use of label‐free second harmonic generation (SHG) imaging with two‐photon excitation (2PE) auto‐fluorescence in multiphoton microscopy (MPM) for the quantification of collagen/fibrosis on preimplantation biopsies of extended criteria donors (ECD).
Materials and methods
Twenty preimplantation core biopsies were extracted from 10 donor kidney samples, of which originated from seven donors. Kidney Donor Profile Index (KDPI) and Remuzzi scores of biopsies were calculated. Collagen parameters measured included quantification by the Collagen Area Ratio in Total Tissue (CART) and qualitative measurements by Collagen Reticulation Index (CRI).
Results
Biopsies classified with > 85% KDPI scores had significantly higher CART (p = .011) and lower CRI values (p = .025) than biopsies with ≤ 85% KDPI scores. Increase in CRI values correlated significantly with rise in recipient creatinine levels 1‐year post‐transplant (p = .027; 95% CI: 4.635‐66.797).
Conclusion
MPM is an evolving technology that enables the quantification of the amount (CART) and quality (CRI) of collagen deposition in unstained preimplantation biopsies of donor kidneys stratified by KDPI scores. This initial evaluation found significant differences in both parameters between donor kidneys with more or less than 85% KDPI. |
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Bibliography: | Journal: Clin Transplant ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0902-0063 1399-0012 |
DOI: | 10.1111/ctr.14717 |