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Jitka Starekova

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Review Open access Jul 2026

High-Throughput Quantitative Chemical Shift-Encoded MRI of the Liver.

BACKGROUND Access to MRI is limited by lengthy exam times and inefficient utilization. Focused protocols can reduce exam times, but workflow variability and inefficient room turnaround contribute to conservative scheduling with long exam slots. PURPOSE To develop and evaluate a high-throughput clinical MRI suite architecture and workflow, using an AI-prescribed free-breathing chemical shift-encoded (CSE) MRI exam to quantify liver proton density fat fraction (PDFF) in under 5 min of total MRI room time. STUDY TYPE Prospective. SUBJECTS 24 healthy volunteers in two cohorts: 12 research staff (7 women/5 men; age 26.8 ± 5.8 years) and 12 community volunteers (6 women/6 men; age 41.3 ± 13.5 years). FIELD STRENGTH/SEQUENCE 1.5 T; free-breathing 2D multi-echo gradient echo CSE-MRI. ASSESSMENT Each participant underwent three nonconsecutive CSE-MRI exams in a continuously queued workflow to characterize timing and PDFF repeatability. Workflow intervals were recorded from timestamped video review and image metadata. Staff cohort exams included two CSE-MRI acquisitions to assess within-exam repeatability, while community cohort exams included one to simulate clinical practice. Three radiologists (8/13/14 years of experience) independently evaluated AI-automated prescriptions for complete liver coverage and rated CSE-MRI image quality (five-point Likert scale). STATISTICAL TESTS Student's t-tests; Gwet's AC2; repeatability coefficients (RCs) with bootstrap 95% confidence intervals; Bland-Altman analysis. p < 0.05 was significant. RESULTS Diagnostic image quality was achieved in all 72 exams (median PDFF Likert score 5/5, inter-rater AC2 ≥ 0.86). Total MRI room times averaged 4:09 ± 0:14 min (staff) and 3:35 ± 0:34 min (community). Turnaround times averaged under 2 min, enabling throughput of 16.1 exams per hour in the community cohort. Automated prescription achieved complete liver coverage in all exams. PDFF RCs were 0.78% (staff within-exam), 0.99% (staff between-exam), and 1.21% (community between-exam) absolute PDFF. DATA CONCLUSION The proposed high-throughput MRI workflow achieved over 16 exams per hour with highly repeatable liver fat quantification, demonstrating a framework for improving MRI utilization and access. EVIDENCE LEVEL 1. STAGE OF TECHNICAL EFFICACY 2.

Garrett C Fullerton, Jiayi Tang, Jitka Starekova et al. · 1 citation
Aug 2026

Normative values for quantitative MRI biomarkers of the liver in collegiate athletes.

PURPOSE Quantitative MRI biomarkers are increasingly used to assess liver health; however, athlete-specific normative values are lacking. This study aimed to establish liver-specific normative values for proton density fat fraction (PDFF), R2*-based liver iron concentration (LIC), and T1 and T2 relaxation times in collegiate athletes. METHODS In this retrospective single-center study, collegiate athletes undergoing return-to-play cardiac MRI (1.5 T/3.0 T) following Coronavirus Disease 2019 recovery were identified. Whole-liver PDFF and R2* were obtained from chemical shift-encoded MRI, T1 and T2 relaxation times were derived from cardiac mapping with partial liver coverage. LIC was calculated from R2*. PDFF and LIC were considered field-strength-independent, whereas R2*, T1, and T2 were analyzed by field strength. Biomarkers are reported as median (interquartile range). RESULTS A total of 211 athletes (64.0% males; median age 19.9 years) were included. PDFF and LIC were 2.2% (1.7, 2.8) and 0.67 mg/g (0.58, 0.74) in males and 1.8% (1.5, 2.3) and 0.57 mg/g (0.50, 0.67) in females. At 1.5 T, R2*, T1 and T2 were 34.0 s-1 (31.9, 36.4), 571 ms (552, 593), and 45.4 ms (43.3, 47.0) in males and 32.0 s-1 (29.5, 34.6), 588 ms (577, 600), and 49.4 ms (46.4, 52.2) in females. At 3.0 T, values were 44.1 s-1 (41.8, 48.8), 755 ms (727, 783), and 40.9 ms (38.3, 43.4) in males and 41.6 s-1 (37.7, 44.0), 806 ms (791, 822), and 42.8 ms (38.9, 44.3) in females. CONCLUSIONS We established sex- and field strength-specific normative values for quantitative liver MRI biomarkers in collegiate athletes, providing a foundation for baseline clinical interpretation and longitudinal monitoring of liver health.

Alexandra A Anagnostopoulos, J. Heidenreich, Amirhossein Roshanshad et al. · 0 citations