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Using Multi-fluorinated Bile Acids and In Vivo Magnetic Resonance Imaging to Measure Bile Acid Transport
Published on: November 27, 2016
Altered Serum Bile Acid Pattern as an Independent Factor for Covert and Overt Hepatic Encephalopathy in Patients With
Takao Miwa1, Hajime Ueda2, Teruo Miyazaki2
1Department of Gastroenterology/Internal Medicine, Graduate School of Medicine, Gifu University, Gifu, Japan.
Insights
High bile acid (BA) levels impact liver disease. Elevated conjugated primary BAs predict overt hepatic encephalopathy (HE) and mortality in cirrhosis patients, while non-conjugated BAs indicate covert HE.
Area of Science:
- Hepatology
- Gastroenterology
- Biochemistry
Background:
- Bile acid (BA) signaling is implicated in hepatic encephalopathy (HE) pathogenesis.
- Clinical impact of BA signaling in cirrhosis patients, especially for covert HE (CHE) and overt HE (OHE), remains understudied.
Purpose of the Study:
- To investigate the clinical significance of BA levels in cirrhosis patients.
- To assess the association between BA levels and the development of CHE, OHE, and mortality.
Main Methods:
- Retrospective study of 189 cirrhosis patients with CHE assessment.
- Quantification of BAs using liquid chromatography-tandem mass spectrometry.
- Statistical analysis including logistic, Fine-Gray competing risk, and Cox regression models.
Main Results:
- 28.0% of patients had CHE; 15.9% developed OHE and 33.3% died during follow-up.
- High conjugated primary BA levels independently predicted OHE development (aHR 3.44) and mortality (HR 2.06).
- High non-conjugated primary BA levels independently predicted CHE (OR 2.18).
Conclusions:
- Elevated serum conjugated primary BA levels are independent predictors of OHE and mortality in cirrhosis.
- Elevated non-conjugated primary BA levels are associated with CHE in cirrhosis patients.
Aim:
Bile acid (BA) signaling plays an important role in the pathogenesis of hepatic encephalopathy (HE), including covert (CHE) and overt HE (OHE). However, few studies have examined its clinical impact in patients with cirrhosis.
Methods:
This retrospective study included patients with cirrhosis who underwent CHE assessment using a computer-aided neuropsychiatric test. BAs were quantified using liquid chromatography-tandem mass spectrometry. Patients were divided into high and low groups according to their BA levels. Independent factors, namely CHE, OHE development, and mortality, were assessed using logistic, Fine-Gray competing risk, and Cox proportional hazards regression models.
Results:
Among the 189 patients, the median age was 71 years, 74.1% were male, and 28.0% were diagnosed with CHE. During a median follow-up period of 3.1 years, 15.9% (n = 30) developed OHE, and 33.3% (n = 63) died. Considering mortality as a competing risk, multivariable analysis identified a high conjugated primary BA level (subdistribution hazard ratio [HR] 3.44; 95% confidence interval [CI] 1.08-10.97) as an independent factor for OHE development. Additionally, a high non-conjugated primary BA level (odds ratio 2.18; 95% CI 1.06-4.46) was an independent factor of CHE. Furthermore, a high conjugated primary BA level (HR 2.06; 95% CI 1.11-3.83) was an independent predictor of mortality.
Conclusions:
Elevated serum conjugated primary BA levels are an independent factor for OHE development and mortality in patients with cirrhosis. Additionally, elevated non-conjugated primary BA levels were an independent factor for CHE in these patients.
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