Detection comes too late
Conventional tests often identify kidney dysfunction only after significant, irreversible damage.
A new dimension of kidney function, from a single urine sample.
Chronic kidney disease affects more than 800 million people worldwide, yet today's standard tests often detect kidney dysfunction too late. Equilibrium Diagnostics has developed a fast, low-cost urine test that uncovers tubular dysfunction before conventional markers change.
Earlier detection. Better risk stratification. Fewer patients progressing to end-stage kidney disease.
CKD costs healthcare systems over €1 trillion annually, and affects more than one in ten adults globally. But the tools used to detect it (eGFR and albuminuria) measure only two dimensions of kidney function, and often not until damage is advanced.
Conventional tests often identify kidney dysfunction only after significant, irreversible damage.
Current diagnostics focus on filtration (eGFR) and barrier integrity (albuminuria). Tubular function, a critical new dimension, is overlooked, leaving clinicians without a full view of the kidney.
Many CKD patients progress to kidney failure because early tubular dysfunction goes unnoticed. Catching it earlier can delay or prevent end-stage disease, and the enormous human and financial cost that follows.
The urine Ammonium–pH Index (uAPI) is a new measure that quantifies renal tubular function: the kidney's ability to manage acid–base balance. A single urine sample, analysed on our AP Reader, produces the uAPI: a clear early-warning signal that conventional tests cannot capture.
The uAPI integrates seamlessly into existing clinical pathways. A single urine sample is all that is needed — no invasive procedures, no specialist equipment. Results deliver a new layer of clinical intelligence alongside standard kidney markers.
A routine, non-invasive urine sample collected at the clinic — no additional patient burden.
The AP Reader measures urinary ammonium and pH with gold-standard potentiometric precision.
The patented algorithm converts raw measurements into a single, clinically meaningful score.
Clinicians receive actionable risk stratification to guide referrals, treatment, and monitoring.
The AP Reader is an automated in-vitro diagnostic analyser designed to integrate seamlessly into research and clinical laboratory workflows. Robust, low-maintenance measurements with high accuracy in clinically relevant concentration ranges.
The AP Reader is the hardware entry point: an automated analyser that takes a standard urine sample and returns uAPI.
The uAPI isn't a hypothesis. It's the result of years of research at Aarhus University and validation across thousands of patient samples in international studies and clinical research collaborations.
In matched CKD Stage 3–4 patients with the same age, sex, BMI, eGFR, uACR, blood pressure and diabetes status, a low uAPI predicts a more than 7-fold higher risk of a serious kidney event.
Adding the uAPI to standard clinical variables (age, sex, BMI, eGFR, uACR, diabetes status, and systolic blood pressure) reclassifies >60% of patients into a more accurate risk category.
An independent 2025 health-economic study by the Nordic Institute of Health Economics modelled the impact of adding the uAPI to the KDIGO framework for CKD risk stratification and referral.
From adoption of the uAPI in CKD risk stratification and referral optimisation across the Danish CKD population of 242,729 patients.
Extrapolated from Danish data across EU member states, using KDIGO vs KDIGO + uAPI modelling. Dialysis and transplant costs excluded, so the true figure is likely higher.
Why it matters, and why early detection is so difficult.
Renal tubular acid handling is a highly relevant measure whenever acid-base regulation is under stress. Research into new indications is ongoing, with the goal of bringing precise acid-base diagnostics to more patients across multiple disease areas.
Cystic fibrosis is caused by mutations in the CFTR anion channel. CFTR channel defects impair epithelial bicarbonate secretion and is an important part of the pathogenesis in the disease. CFTR dysfunction also impairs renal bicarbonate excretion. Urine acid-base profiling can help reveal the extent of channel dysfunction and whether CFTR modulators are achieving meaningful functional benefit, providing an objective, low-cost response marker to complement expensive therapies.
Patients with short bowel anatomy lose bicarbonate through the gut, generating a persistent acid load that routine serum labs often underestimate or even miss. Renal net acid excretion offers a physiologically grounded measure of the true metabolic burden.
We offer comprehensive assessment of urine acid/base parameters and expert guidance regarding sample collection, storage, and interpretation on a case-by-case basis.
Equilibrium Diagnostics is a research-based venture spun out of Aarhus University, headquartered at the BioInnovation Institute in Copenhagen. We are developing a new diagnostic infrastructure for chronic kidney disease, grounded in more than ten years of foundational research in renal physiology, and built in close collaboration with the clinicians who will use it.
Whether you're a clinician, an investor, an IVD partner, or a researcher, we would love to hear from you.