Novel Saliva-based Renal Function Test Platform - Project Summary
Chronic Kidney Disease (CKD) affects millions of people worldwide, including 20 million adults and children in
the USA. Timely detection of kidney function deterioration can improve management of CKD, including in kidney
transplanted recipients. Without a blood draw, an acute kidney injury (AKI) event or a transplant rejection could
remain unrecognized for extended periods of time, leading to irreversible loss of kidney function and structure.
Novel patient-friendly methods of kidney function measurement with high levels of precision and reproducibility
are urgently needed to ensure more frequent and reliable monitoring in the home and for point-of-care screening.
Currently, invasive phlebotomy followed by laborious blood specimen processing and reporting are the only way
to measure the three major kidney filtration markers: serum creatinine, urea, and cystatin C. However, saliva has
been proven to mirror blood biomarker levels. Limited preliminary data suggest that salivary creatinine and urea
levels correlate with those in serum in CKD patients. Measurable levels of cystatin C have been assayed in
saliva without being affected by periodontal disease. Based on these findings, Intelligent Optical Systems (IOS),
in collaboration with the University of California (UC) Irvine and UC San Francisco, plans to develop (Phase I,
12 months) a novel means of detecting creatinine, cystatin C, and urea in saliva, using a highly sensitive and
selective enzyme-based lateral flow assay (ELF assay). In this novel, compact, single-step, enzymatic
multiplexed assay, highly fluorescent dyes yield reliable quantitative measurements on a portable analyzer. The
innovatively developed methods will be subsequently (Fast-Track) validated in 200 CKD patients from UCI
nephrology and transplant clinics (Phase II, 24 months). The proposed development builds on extensive IOS
expertise in complex assay development, using saliva matrix that has been successfully validated in clinics for
bone metabolism markers and rapid testing for drug of abuse. In Phase I we will demonstrate the feasibility of
recording reproducible and sensitive measurements of salivary creatinine, cystatin C, and urea, using spiked
and laboratory tested human saliva samples obtained from BioreclamationIVT. Assay specification, sensitivity
LOD, specificity, and stability will be reported by the end of Phase I in accordance with IOS-established protocols
for salivary assay development and optimization. Building on a successful Phase I demonstration of an ELF
assay, and validating the results against the predetermined milestone criteria, we will then conduct the clinical
validation in Phase II, testing saliva measurements against blood levels in 200 human subjects with CKD –
including 50 kidney transplant recipients – with a broad range of GFR of 10-60 mL/min/1.73 m2 BSA. Our
proposed Fast-Track design is efficient, feasible, and innovative, and has a high likelihood of sustained powerful
influence and immediate clinical applicability. The availability of non-invasive, point-of-care, multiplex measures
of kidney function would have a dramatic impact on the care and monitoring of patients with CKD, particularly in
remote locations.