Novel clinical biomarker for hepatic steatosis

The worldwide rise of obesity and metabolic syndrome has led to an increasing prevalence of nonalcoholic fatty liver disease. A subset of the one-quarter of affected patients globally have nonalcoholic fatty liver disease nonalcoholic steatohepatitis, which is an inflammatory disease that often advances to cirrhosis and end-stage liver failure. The enormous number of affected patients is accompanied with substantial morbidity, mortality and healthcare costs, presenting an emerging clinical challenge.
Life Sciences
Diagnostics
Reference
b82088
IP right year
2024
IP status
PCT filed, EP and US pending
Patentee
University of Regensburg
Contact
Charlotte Federhen

Challenge and innovation

Fatty liver disease constitutes a significant challenge in modern healthcare. Early stage intervention improves prognosis, but there is a lack of cost-effective and noninvasive diagnostic tests for detecting and staging hepatic steatosis. Presently, diagnosis depends on resource-intensive imaging by abdominal ultrasound or MRI, which sometimes must be followed up by liver biopsy.

Shedding of CD46 from hepatocytes into circulation reflects a stress response of hepatocytes to fat loading, which appears to be connected with activation of innate-like lymphocyte responses; therefore, soluble CD46 is unlike other established clinical liver markers by measuring a different type of hepatocyte property indicating cell injury, synthetic function, detoxifying activity, fibrosis or systemic inflammation. Soluble CD46 is a promising clinical marker of patients with steatosis at risk of developing early liver inflammation, a prevalent subset that could benefit from earlier clinical detection and intervention.

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