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Metabolomic-based noninvasive serum test to diagnose nonalcoholic steatohepatitis: Results from discovery and validation cohorts
R. Mayo, J. Crespo, I. Martínez-Arranz, JM. Banales, M. Arias, I. Mincholé, R. Aller de la Fuente, R. Jimenez-Agüero, C. Alonso, DA. de Luis, L. Vitek, J. Stritesky, J. Caballería, M. Romero-Gómez, A. Martín-Duce, JM. Mugüerza Huguet, JI....
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články
NLK
Directory of Open Access Journals
od 2017
PubMed Central
od 2017
Europe PubMed Central
od 2017
ProQuest Central
od 2017-02-01 do 2022-12-31
Health & Medicine (ProQuest)
od 2017-02-01 do 2022-12-31
Wiley Free Content
od 2017 do 2022
Wiley-Blackwell Open Access Titles
od 2017 do 2022
ROAD: Directory of Open Access Scholarly Resources
od 2017
PubMed
30027139
DOI
10.1002/hep4.1188
Knihovny.cz E-zdroje
- Publikační typ
- časopisecké články MeSH
Nonalcoholic fatty liver disease (NAFLD) is the most common type of chronic liver disease worldwide and includes a broad spectrum of histologic phenotypes, ranging from simple hepatic steatosis or nonalcoholic fatty liver (NAFL) to nonalcoholic steatohepatitis (NASH). While liver biopsy is the reference gold standard for NAFLD diagnosis and staging, it has limitations due to its sampling variability, invasive nature, and high cost. Thus, there is a need for noninvasive biomarkers that are robust, reliable, and cost effective. In this study, we measured 540 lipids and amino acids in serum samples from biopsy-proven subjects with normal liver (NL), NAFL, and NASH. Using logistic regression analysis, we identified two panels of triglycerides that could first discriminate between NAFLD and NL and second between NASH and NAFL. These noninvasive tests were compared to blinded histology as a reference standard. We performed these tests in an original cohort of 467 patients with NAFLD (90 NL, 246 NAFL, and 131 NASH) that was subsequently validated in a separate cohort of 192 patients (7 NL, 109 NAFL, 76 NASH). The diagnostic performances of the validated tests showed an area under the receiver operating characteristic curve, sensitivity, and specificity of 0.88 ± 0.05, 0.94, and 0.57, respectively, for the discrimination between NAFLD and NL and 0.79 ± 0.04, 0.70, and 0.81, respectively, for the discrimination between NASH and NAFL. When the analysis was performed excluding patients with glucose levels >136 mg/dL, the area under the receiver operating characteristic curve for the discrimination between NASH and NAFL increased to 0.81 ± 0.04 with sensitivity and specificity of 0.73 and 0.80, respectively. Conclusion: The assessed noninvasive lipidomic serum tests distinguish between NAFLD and NL and between NASH and NAFL with high accuracy. (Hepatology Communications 2018;2:807-820).
CIC bioGUNE CIBERehd Bizkaia Technology Park Derio Bizkaia Spain
Department of Digestive Disease Clinic University Hospital University of Valladolid Valladolid Spain
Department of Pathology University Hospital Príncipe de Asturias Alcalá University Madrid Spain
Division of Digestive and Liver Diseases Cedars Sinai Medical Center Los Angeles CA United States
Faculty General Hospital and the 1st Faculty of Medicine Charles University Prague Czech Republic
Liver Unit Hospital Clinic CIBERehd IDIBAPS Barcelona Spain
OWL Metabolomics Bizkaia Technology Park Derio Spain
Surgery Department University Hospital Príncipe de Asturias Alcalá University Madrid Spain
Citace poskytuje Crossref.org
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