Prometheus Laboratories introduces the FIBROSpect NASH test, a new tool to help healthcare providers stratify NASH patients by risk, based on the severity of their liver fibrosis.
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[16-October-2017] |
SAN DIEGO, Oct. 16, 2017 /PRNewswire/ -- Prometheus Laboratories Inc. introduces the FIBROSpect® NASH test--a new tool to help healthcare providers stratify nonalcoholic steatohepatitis (NASH) patients by risk, based on the severity of their liver fibrosis. NASH is a potentially serious condition that is related to the more common and less severe nonalcoholic fatty liver disease (NAFLD). It is estimated that one third of the U.S. adult population may have NAFLD with approximately 25 percent of those progressing to NASH. As the incidence of these conditions grows, there is a critical need for noninvasive testing that measures the degree of fibrosis. Liver biopsy, an invasive procedure, is the current gold standard for diagnosing and staging liver fibrosis. Advanced stages of liver fibrosis have been proven to be the most significant independent risk factor for mortality in NASH patients. FIBROSpect NASH differentiates between mild and advanced liver fibrosis stages to help healthcare providers stratify the risk of their NASH patients and manage them accordingly. "The new FIBROSpect NASH serum test overcomes some of the limitations of current invasive and noninvasive liver assessment methods by pairing expert-developed proprietary algorithms with biomarkers that are clinically relevant to the development of liver fibrosis specifically in NASH patients," said Warren Cresswell, General Manager and Head of Diagnostics at Prometheus Laboratories Inc. "This is part of our new generation of diagnostic liver tests, based on scientific innovation and a strong investment, that anticipate and meet the changing needs of healthcare providers in the growing liver health category." "As more effective therapies become available to treat NASH patients, having noninvasive blood tests to assess the severity of the patient's fibrosis stage will allow us to better stratify their risk and select the most appropriate course of action accordingly," said Manal Abdelmalek, M.D., Associate Professor at the Duke University School of Medicine. The FIBROSpect NASH test was developed and clinically validated with well-characterized and biopsy-confirmed NASH patients. The clinical validation data is being presented at the 2017 American Association for the Study of Liver Diseases (AASLD) meeting, October 20-24, in Washington, D.C. About Prometheus About Nestlé Health Science PROMETHEUS, the Link Design, For the person in every patient, and FIBROSpect are registered trademarks of Société des Produits Nestlé S.A. Vevey, Switzerland. Contact for the media: Geri Vena-Shores, Head of Marketing
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