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Updated: Oct 29, 2026

Using Multi-fluorinated Bile Acids and In Vivo Magnetic Resonance Imaging to Measure Bile Acid Transport
Published on: November 27, 2016
Laboratory indicators combined with liver function scores for predicting suboptimal hepatobiliary phase imaging
Fuhe Qiu1, Fuling Huang1, Haihui Pan1
1Department of Medical Imaging, Guangxi Medical University Cancer Hospital, Nanning, China.
Background:
Suboptimal hepatobiliary-phase (HBP) enhancement may limit the diagnostic quality of gadoxetic acid-enhanced MRI. We investigated whether routinely available laboratory indicators and liver function scores could identify patients at increased risk of suboptimal HBP imaging.
Methods:
This retrospective study included 555 patients with focal liver lesions who underwent gadoxetic acid-enhanced MRI, including 460 with good and 95 with suboptimal HBP image quality. Associations between laboratory indicators, liver function scores, and HBP image quality were evaluated using correlation and logistic regression analyses. Model discrimination, calibration, internal validation, and potential clinical utility were assessed using ROC analysis, bootstrap resampling, calibration analysis, and decision-curve analysis.
Results:
The ALBI score (OR=2.391, 95% CI: 1.364-4.190), GGT (OR=1.003, 95% CI: 1.001-1.004), TBA (OR=1.010, 95% CI: 1.003-1.017), and Hb (OR=0.982, 95% CI: 0.971-0.993) were independently associated with suboptimal HBP imaging. The combined model yielded an AUC of 0.758 (95% CI: 0.701-0.816), with 63.16% sensitivity and 78.70% specificity. Bootstrap internal validation that repeated the entire model-development procedure yielded a mean AUC optimism of 0.044 and an optimism-corrected AUC of 0.714, indicating that moderate discrimination was retained after correction for model-development optimism. The apparent and optimism-corrected Brier scores were 0.116 and 0.128, respectively.
Conclusions:
A model combining the ALBI score, GGT, TBA, and Hb showed moderate discrimination for suboptimal HBP imaging. These routinely available indicators may assist pre-MRI risk stratification, but external validation is required before clinical implementation.
