2010
DOI: 10.1007/s11695-010-0204-1
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A Biomarker Panel for Non-alcoholic Steatohepatitis (NASH) and NASH-Related Fibrosis

Abstract: This NAFLD Diagnostic Panel based on a clinical and laboratory data has good performance characteristics and is easy to use. This biomarker panel could become useful in the management of patients with NAFLD.

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Cited by 141 publications
(115 citation statements)
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“…In other reports, TIMP-1 levels have been included in non-invasive algorithms to classify the extent of fibrosis (36,37). In support of such a role, animal models have shown that TIMP-1 overexpression promotes liver fibrosis (12) and retards fibrosis resolution (13), and the administration of TIMP-1 blocking antibodies attenuates fibrosis (38).…”
Section: Discussionmentioning
confidence: 99%
“…In other reports, TIMP-1 levels have been included in non-invasive algorithms to classify the extent of fibrosis (36,37). In support of such a role, animal models have shown that TIMP-1 overexpression promotes liver fibrosis (12) and retards fibrosis resolution (13), and the administration of TIMP-1 blocking antibodies attenuates fibrosis (38).…”
Section: Discussionmentioning
confidence: 99%
“…As clearly demonstrated by Bedossa et al, liver biopsy sampling variability is especially prominent in the cases of discriminating stages of fibrosis [1]. In fact, the METAVIR scoring system which was used for staging fibrosis on a typical 15-mm liver biopsy core was correct approximately 65% of the times, reflecting an AUC of only 0.82 [1]. Because of this relatively low performance, using core liver biopsy as a "gold standard" for validating non-invasive biomarkers is difficult at best.…”
Section: Replymentioning
confidence: 91%
“…We are fully aware of these drawbacks, especially those related to the performance of a biomarker panel in comparison to tests containing only a single biomarker. It is important to note that some of the variables included in a panel of biomarker such as ours (presence of diabetes, gender, BMI, triglycerides, and AST) are routinely available in clinical practice [1]. Therefore, adding these parameters to a "biomarker panel" should not increase the associated costs.…”
Section: Replymentioning
confidence: 99%
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“…A kaszpáz 3 aktivációja során a citokeratin 18 (CK18) hasítása követ-kezik be, amely egy átmeneti fi lamentum a májsejtekben. Az ebből létrejövő CK18-M30 részlet (fragmentum) koncentrációja jól korrelál a NASH súlyosságával számos vizsgálat alapján [40,41,42], ugyanúgy, mint a CK18-M65 szintje (AUROC: 0,8) [32].…”
Section: A Steatosis Progressziójának Markereiunclassified