In a quiet laboratory partnership between a Melbourne university and an Australian diagnostics firm, an old medical problem is being approached from a new angle. Kidney injury often slips past clinicians in its earliest hours, when treatment could still change its course, because today's tests read the kidney's slow chemical echoes rather than the damage itself. A research team is now trying to listen to the structure of the organ directly, hoping that a simple blood test might one day catch failure before it hardens into a lifelong condition, and perhaps even let people watch over their own k
RMIT and Nexsen Develop Blood Tests to Detect Kidney Injury Hours Earlier and Enable At-Home Monitoring
Changes in kidney function trail the damage to the kidney's structure
Why does a few hours matter so much for kidney injury?
Because the current signals lag. Urine output and creatinine can take six and 24 hours respectively to show a problem, and in intensive care that's the window when intervention counts.
And the new approach is different how?
It targets biomarkers of structural damage using patented DNA aptamers, rather than waiting for function to decline. Professor Kumta says function changes trail the damage itself.
Worth being clear: this is a research contract, not a validated test. The claim that it will detect injury hours earlier is the team's aim, not a trial result.
So nothing has been tested in kidney patients yet?
The source doesn't report any kidney trial data. What it does report is a funded development project.
The GBS test is the proof of platform, though. Devices are manufactured and a trial is approved at Northern Health.
Approved to begin, not completed. And a platform working for a bacterium doesn't automatically carry over to kidney biomarkers.
What about the home monitoring idea?
The 850 million figure is the potential reach, and the comparison to diabetic glucose checks is a suggested model.
Also note the closeness here: Bansal is both an RMIT professor and Nexsen's Chief Innovation Officer, and RMIT holds equity. That's disclosed, but it's context for the optimistic quotes.
O Pulso
- Current tests can take six to 24 hours to reveal acute kidney injury, leaving intensive care teams working partly in the dark.
- Nearly one in three intensive care patients develops acute kidney injury, and the window for effective treatment is narrow.
- RMIT and Nexsen are building blood tests on patented DNA aptamers that look for signs of structural kidney damage rather than waiting for creatinine to rise.
- The same platform has already produced devices for Group B Streptococcus, with a clinical trial at Northern Health due to begin this year.
- The kidney tests remain at the research-contract stage, and the Group B Streptococcus trial will be the first real test of whether the platform works in patients.
In a quiet laboratory partnership between a Melbourne university and an Australian diagnostics firm, an old medical problem is being approached from a new angle. Kidney injury often slips past clinicians in its earliest hours, when treatment could still change its course, because today's tests read the kidney's slow chemical echoes rather than the damage itself. A research team is now trying to listen to the structure of the organ directly, hoping that a simple blood test might one day catch failure before it hardens into a lifelong condition, and perhaps even let people watch over their own kidneys from home.
A research team at RMIT University and the Australian diagnostics company Nexsen Limited has signed a AUD $1.125 million contract to develop blood tests for kidney disease. The aim is to catch damage faster than hospitals can today, and eventually to let people monitor their kidneys at home.
The urgency begins in intensive care, where nearly one in three patients develops acute kidney injury. The condition is hardest to see in its earliest stages, which is exactly when treatment matters most. Further along, around 13 percent of people live with chronic kidney disease, a leading cause of premature death.
Professor Shekhar Kumta, a clinician who manages kidney failure in trauma and complex surgical patients, explains the core problem. Current tests track how well the kidney filters creatinine, but that chemical builds up slowly, so changes can take hours or days to appear. The damage to the kidney's structure has already happened by then. A test that looks directly at that structural damage, he says, would be a real game-changer.
The team is building patented DNA aptamers to detect biomarkers linked to that damage. For chronic disease, similar tests could be used at home, much like the glucose monitoring many people with diabetes already do, and could reach more than 850 million patients worldwide.
The partnership rests on an existing relationship and a platform already developed for Group B Streptococcus, a bacterium that can seriously harm newborns. A clinical trial for that test is set to begin at Northern Health in Melbourne this year. For now, the kidney tests are still in the research stage, and that trial will be the nearest sign of how well the platform performs in real patients.
A research team at RMIT University and an Australian diagnostics company, Nexsen Limited, have signed a AUD $1.125 million research contract to build blood tests for kidney disease that work faster than what hospitals use now, and that could one day be used at home.
The need starts in intensive care. Nearly one-third of ICU patients develop acute kidney injury, and the condition is hard to catch in its earliest stages, which is exactly when treatment matters most. Further along the disease spectrum, an estimated 13% of people live with chronic kidney disease, which remains a leading cause of premature death.
The two tests the team is developing are aimed at those two problems. One would identify acute kidney injury hours sooner than current methods. The other would let people with chronic kidney disease monitor themselves at home, which the researchers describe as a first. Professor Vipul Bansal, who directs RMIT's Sir Ian Potter NanoBioSensing Facility, says the approach could be more timely, cheaper and simpler than the pathology-based kidney function tests now in use.
Bansal points to the delay built into today's methods. Diagnosis relies on reduced urine output and rising serum creatinine, which can take six and 24 hours respectively to show up. He says the rapid onset of the injury, paired with the lack of a reliable test, makes timely intervention a major challenge for clinicians. Acting earlier, he explained, can improve outcomes and stop acute injury from progressing into irreversible chronic disease.
Professor Shekhar Kumta explains why the lag exists. A clinician experienced in managing kidney failure in trauma and complex surgical patients, he also heads the Clinical Translational Research Partnership between RMIT and Northern Hospital. Standard tests measure kidney function, such as how well the organs filter creatinine, but creatinine builds up slowly, so a noticeable change can take hours or days. In his words, changes in function trail the damage to the kidney's complex structure. A test that looks directly at damage to different parts of the kidney, he said, would be a real game-changer.
That is what the team is trying to build. They are developing patented DNA aptamers designed to detect specific biomarkers tied to structural kidney damage. Kumta says such blood tests should be able to diagnose the root cause of an injury early, helping define the best management plan for each patient. For chronic disease, similar tests tailored to regular home use could serve more than 850 million patients worldwide, and could sit alongside the blood glucose monitoring many people with diabetes already do daily.
The project builds on an existing relationship. RMIT and Nexsen have signed a memorandum of understanding setting the terms of a long-term strategic partnership, and RMIT recently took an equity position in the company. Several joint appointments tie them together, including Bansal's roles as Nexsen's Chief Innovation Officer and Chair of its Advisory Board.
The platform technology has already been developed for another target: Group B Streptococcus, a bacterium carried by 1 in 5 pregnant women that can cause serious complications for babies. Investigational GBS devices have been manufactured, and a clinical trial at Northern Health in Melbourne has been approved to begin this year, ahead of schedule. Nexsen Executive Chairman Reece O'Connell says both projects aim to deliver rapid, affordable tests for hospitals, clinics and eventually homes, targeting unmet clinical needs in globally significant markets.
The kidney tests are at the research-contract stage. The GBS trial, due to begin at Northern Health, will be the nearest indication of how well the platform performs in patients.
Citações Notáveis
A new test that can directly investigate the damage to different parts of the kidneys will be a real game-changer.— Professor Shekhar Kumta, RMIT and Northern Hospital
Our first products are targeting key unmet clinical needs in globally significant markets such as GBS and kidney disease.— Reece O'Connell, Executive Chairman, Nexsen