Photoacoustic imaging of kidney fibrosis for assessing pretransplant organ quality

Eno Hysi, Xiaolin He, Muhannad N. Fadhel, Tianzhou Zhang, Adriana Krizova, Michael Ordon, Monica Farcas, Kenneth T. Pace, Victoria Mintsopoulos, Warren L. Lee, Michael C. Kolios, Darren A. Yuen*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

32 Scopus citations

Abstract

Roughly 10% of the world's population has chronic kidney disease (CKD). In its advanced stages, CKD greatly increases the risk of hospitalization and death. Although kidney transplantation has revolutionized the care of advanced CKD, clinicians have limited ways of assessing donor kidney quality. Thus, optimal donor kidney-recipient matching cannot be performed, meaning that some patients receive damaged kidneys that function poorly. Fibrosis is a form of chronic damage often present in donor kidneys, and it is an important predictor of future renal function. Currently, no safe, easy-to-perform technique exists that accurately quantifies renal fibrosis. We describe a potentially novel photoacoustic (PA) imaging technique that directly images collagen, the principal component of fibrotic tissue. PA imaging noninvasively quantifies whole kidney fibrotic burden in mice, and cortical fibrosis in pig and human kidneys, with outstanding accuracy and speed. Remarkably, 3-dimensional PA imaging exhibited sufficiently high resolution to capture intrarenal variations in collagen content. We further show that PA imaging can be performed in a setting that mimics human kidney transplantation, suggesting the potential for rapid clinical translation. Taken together, our data suggest that PA collagen imaging is a major advance in fibrosis quantification that could have widespread preclinical and clinical impact.

Original languageEnglish (US)
Article numbere136995
JournalJCI Insight
Volume5
Issue number10
DOIs
StatePublished - May 2020

Funding

This work was supported by a Collaborative Health Research Project grant cofunded by Canadian Institutes of Health Research (CIHR) and the Natural Sciences and Engineering Research Council of Canada (NSERC; awarded to MCK and DAY), a Banting and Best Diabetes Centre Pilot and Feasibility grant (awarded to MCK and DAY), a Canadian Society of Transplantation and Canadian National Transplant Research Program Basic Research Catalyst grant (awarded to MCK and DAY), and funds from the St. Michael’s Hospital Foundation (awarded to DAY). EH is supported by a Vanier Canada Graduate Scholarship. WLL is a Canada Research Chair in Mechanisms of Endothelial Permeability, and work in his laboratory is funded by a Collaborative Health Research Project from CIHR and NSERC. DAY is supported by a CIHR New Investigator Award. The authors wish to thank research staff Lindita Rapi, Weiqiu Yuan, and Michelle Nash for assistance in ethics board approvals, data collection, and study coordination. Danielle Bince’s assistance with handling pig kidneys is also gratefully acknowledged.

ASJC Scopus subject areas

  • General Medicine

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