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Serum concentration of taurochenodeoxycholic acid predicts clinically significant portal hypertension

医学 门脉高压 门静脉压 胃肠病学 内科学 队列 逐步回归 逻辑回归 代理终结点 肝硬化
作者
Kateřina Žížalová,Barbora Nováková,Marek Vecka,J Petrtýl,Věra Lánská,Květa Pelinková,V. Šmíd,Radan Brůha,Libor Vı́tek,Martin Leníček
出处
期刊:Liver International [Wiley]
卷期号:43 (4): 888-895 被引量:10
标识
DOI:10.1111/liv.15481
摘要

Abstract Background & Aims Severity of portal hypertension is usually quantified by measuring the hepatic venous pressure gradient (HVPG). However, due to its invasiveness, alternative markers are being sought. Bile acids (BA), being synthesized, metabolized, and transported by the liver, seem to have the potential to serve as endogenous markers. The aim of the present study was to determine whether serum BA reflect the severity of portal hypertension. Methods We correlated serum concentrations of individual BA with portal pressure (as HVPG) in an exploratory cohort of 21 cirrhotic patients with portal hypertension. The predictive potential of selected candidates was then confirmed in an independent validation cohort ( n = 214). Additionally, nine previously published noninvasive markers were added to the stepwise logistic regression model to identify the most relevant ones, which were eventually used to create a prognostic index of portal hypertension. Results Serum levels of taurochenodeoxycholic acid (TCDCA) significantly correlated with HVPG and showed a high potential to predict clinically significant portal hypertension (HVPG ≥ 10 mm Hg: AUROC = 0.97 ± 0.06). This was confirmed in the validation cohort (AUROC = 0.96 ± 0.01). The predictive index (constructed based on AST/ALT, spleen diameter, and TCDCA concentration) was able to distinguish clinically significant portal hypertension with 95% sensitivity and 76% specificity. Conclusions TCDCA seems to be a promising noninvasive marker of clinically significant portal hypertension. Its predictive potential may be further enhanced when it is combined with both the AST/ALT ratio and spleen diameter.
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