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Comparative Study
. 2021 Apr 1;16(4):e0249491.
doi: 10.1371/journal.pone.0249491. eCollection 2021.

Comparison between magnetic resonance and ultrasound-derived indicators of hepatic steatosis in a pooled NAFLD cohort

Affiliations
Comparative Study

Comparison between magnetic resonance and ultrasound-derived indicators of hepatic steatosis in a pooled NAFLD cohort

Cayden Beyer et al. PLoS One. .

Abstract

Background & aims: MRI-based proton density fat fraction (PDFF) and the ultrasound-derived controlled attenuation parameter (CAP) are non-invasive techniques for quantifying liver fat, which can be used to assess steatosis in patients with non-alcoholic fatty liver disease (NAFLD). This study compared both of these techniques to histopathological graded steatosis for the assessment of fat levels in a large pooled NAFLD cohort.

Methods: This retrospective study pooled N = 581 participants from two suspected NAFLD cohorts (mean age (SD) 56 (12.7), 60% females). Steatosis was graded according to NASH-CRN criteria. Liver fat was measured non-invasively using PDFF (with Liver MultiScan's Iterative Decomposition of water and fat with Echo Asymmetry and Least-squares estimation method, LMS-IDEAL, Perspectum, Oxford) and CAP (FibroScan, Echosens, France), and their diagnostic performances were compared.

Results: LMS-IDEAL and CAP detected steatosis grade ≥ 1 with AUROCs of 1.00 (95% CI, 0.99-1.0) and 0.95 (95% CI, 0.91-0.99), respectively. LMS-IDEAL was superior to CAP for detecting steatosis grade ≥ 2 with AUROCs of 0.77 (95% CI, 0.73-0.82] and 0.60 (95% CI, 0.55-0.65), respectively. Similarly, LMS-IDEAL outperformed CAP for detecting steatosis grade ≥ 3 with AUROCs of 0.81 (95% CI, 0.76-0.87) and 0.63 (95% CI, 0.56-0.70), respectively.

Conclusion: LMS-IDEAL was able to diagnose individuals accurately across the spectrum of histological steatosis grades. CAP performed well in identifying individuals with lower levels of fat (steatosis grade ≥1); however, its diagnostic performance was inferior to LMS-IDEAL for higher levels of fat (steatosis grades ≥2 and ≥3).

Trial registration: ClinicalTrials.gov (NCT03551522); https://clinicaltrials.gov/ct2/show/NCT03551522. UMIN Clinical Trials Registry (UMIN000026145); https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000026145.

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Conflict of interest statement

RB is the CEO and founder of Perspectum. AD, CB, CH, AA are employees of Perspectum. DK is employed by Texas Digestive Disease Consultants (GI Alliance). KI and AN are employees of Yokohoma City University Hospital. This does not alter our adherence to PLOS ONE policies on sharing data and materials.

Figures

Fig 1
Fig 1. Example LMS-IDEAL PDFF maps.
Fig 2
Fig 2. Box plots showing the minimum, median, maximum and interquartile ranges (IQR) values for LMS-IDEAL, and CAP with corresponding steatosis scores.
(left) LMS-IDEAL values plotted against steatosis CRN scores, (right) CAP values plotted against steatosis CRN scores.
Fig 3
Fig 3. Scatter plot showing CAP values plotted against LMS-IDEAL PDFF values.
Fig 4
Fig 4. ROC curves illustrating diagnostic accuracies for LMS-IDEAL (black) and CAP (grey).
Values represent AUROC (95% CI). (A) LMS-IDEAL and CAP for diagnosing steatosis grades of ≥ 1. (B) LMS-IDEAL and CAP for diagnosing steatosis grades of ≥ 2. (C) LMS-IDEAL and CAP for diagnosing steatosis grades of ≥ 3.

References

    1. Sattar N, Forrest E, Preiss D. Non-alcoholic fatty liver disease. Br Med J. 2014; 349:g4596. - PMC - PubMed
    1. Araújo AR, Rosso N, Bedogni G, et al.. Global epidemiology of non-alcoholic fatty liver disease/non-alcoholic steatohepatitis: What we need in the future. Liver International 2018;S1:47–51. 10.1111/liv.13643 - DOI - PubMed
    1. Estes C, Razavi H, Loomba R, et al.. Modeling the epidemic of nonalcoholic fatty liver disease demonstrates an exponential increase in burden of disease. Journal of Hepatology 2018;67:123–133. 10.1002/hep.29466 - DOI - PMC - PubMed
    1. Perumpail BJ, Khan MA, Yoo ER, et al.. Clinical epidemiology and disease burden of nonalcoholic fatty liver disease. World Journal of Gastroenterology 2017;23:8263–8276. 10.3748/wjg.v23.i47.8263 - DOI - PMC - PubMed
    1. Benjamin A, Zubajlo R, Dhyani M, et al. Non-Invasive Diagnosis of Non-Alcoholic Fatty Liver Disease (NAFLD) using Ultrasound Image Echogenicity. Conference Proceedings IEEE Engineering in Medicine and Biology Society 2017;2920–2923. - PMC - PubMed

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