posted on 2016-02-21, 15:34authored byJ. Barr, J. Caballería, I. Martínez-Arranz, A. Domínguez-Díez, C. Alonso, J. Muntané, M. Pérez-Cormenzana, C. García-Monzón, R. Mayo, A. Martín-Duce, M. Romero-Gómez, O. Lo Iacono, J. Tordjman, R. J. Andrade, M. Pérez-Carreras, Y. Le Marchand-Brustel, A. Tran, C. Fernández-Escalante, E. Arévalo, M. García-Unzueta, K. Clement, J. Crespo, P. Gual, M. Gómez-Fleitas, M. L. Martínez-Chantar, A. Castro, S. C. Lu, M. Vázquez-Chantada, J. M. Mato
Our understanding of the mechanisms by which nonalcoholic
fatty liver disease (NAFLD) progresses from simple steatosis to steatohepatitis
(NASH) is still very limited. Despite the growing number of studies
linking the disease with altered serum metabolite levels, an obstacle
to the development of metabolome-based NAFLD predictors has been the
lack of large cohort data from biopsy-proven patients matched for
key metabolic features such as obesity. We studied 467 biopsied individuals
with normal liver histology (n = 90) or diagnosed
with NAFLD (steatosis, n = 246; NASH, n = 131), randomly divided into estimation (80% of all patients) and
validation (20% of all patients) groups. Qualitative determinations
of 540 serum metabolite variables were performed using ultraperformance
liquid chromatography coupled to mass spectrometry (UPLC–MS).
The metabolic profile was dependent on patient body-mass index (BMI), suggesting that the NAFLD pathogenesis mechanism may be quite different depending on an individual’s level of obesity. A BMI-stratified multivariate model based on the NAFLD serum metabolic profile was used to separate patients with and without NASH. The area under the receiver operating characteristic curve was 0.87 in the estimation and 0.85 in the validation group. The cutoff (0.54) corresponding to maximum average diagnostic accuracy (0.82) predicted NASH with a sensitivity of 0.71 and a specificity of 0.92 (negative/positive predictive values = 0.82/0.84). The present data, indicating that a BMI-dependent serum metabolic profile may be able to reliably distinguish NASH from steatosis patients, have significant implications for the development of NASH biomarkers and potential novel targets for therapeutic intervention.