Summary
| Direction in NAFLD / MASH (Metabolic-Associated Steatohepatitis) | ↑ Elevated — higher than in the comparison group |
|---|---|
| Category | Hepatic |
| Compared against | NASH vs without NASH/healthy controls |
| Source | Feldstein et al. 2009 — doi:10.1002/hep.23050 |
| Condition atlas | NAFLD / MASH (Metabolic-Associated Steatohepatitis) Biomarker Atlas |
Related Hepatic markers in NAFLD / MASH (Metabolic-Associated Steatohepatitis)
Full list: NAFLD / MASH (Metabolic-Associated Steatohepatitis) Biomarker Atlas.
Frequently asked questions
Is Cytokeratin-18 (CK-18) high or low in NAFLD / MASH (Metabolic-Associated Steatohepatitis)?
Elevated. Studies summarised in the OSMF atlas report higher Cytokeratin-18 (CK-18) in NAFLD / MASH (Metabolic-Associated Steatohepatitis) than in the reference group of the cited comparison (NASH vs without NASH/healthy controls). Source: Feldstein et al. 2009.
Which test measures Cytokeratin-18 (CK-18)?
The atlas record does not list a standardised clinical test code (LOINC) for Cytokeratin-18 (CK-18), which usually means it was measured with research assays or study-specific protocols rather than a routine clinical panel. Check the cited source for the exact method.
Is one abnormal Cytokeratin-18 (CK-18) result diagnostic of NAFLD / MASH (Metabolic-Associated Steatohepatitis)?
No. No single biomarker is diagnostic of NAFLD / MASH (Metabolic-Associated Steatohepatitis). Cytokeratin-18 (CK-18) findings come from group comparisons, overlap considerably between patients and controls, and vary with study design, timing and comparison group. A result should be interpreted by a clinician alongside symptoms, history and other tests.
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Last reviewed: 2026-07-03 · Page generated from nafld-mash-metabolic-associated-steatohepatitis.json · Browse: NAFLD / MASH (Metabolic-Associated Steatohepatitis) atlas · Biomarker Index · All marker pages
Disclaimer: This page is an educational synthesis of published, peer-reviewed research and is not medical advice. Biomarker findings vary across studies with case definitions, comparison groups, timing and assay methods. Direction of change reflects the predominant finding in the cited source and does not establish a diagnostic threshold. Discuss any test result with a qualified clinician.