Optimizing surveillance of low-risk metabolic dysfunction associated steatotic liver disease using transient elastography

Author:

Gopalakrishna Harish1,Nair Gayatri B.2,Salman Roghani Roham13,Ravendhran Natarajan45,Rotman Yaron1

Affiliation:

1. Liver & Energy Metabolism Section, Liver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland

2. Department of Pulmonary and Sleep Medicine, Medstar Georgetown University Hospital, Washington DC

3. Department of Internal Medicine, Eisenhower Health, Rancho Mirage, California

4. Digestive Disease Associates

5. Department of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland, USA

Abstract

Background Most people with metabolic dysfunction-associated steatotic liver disease (MASLD) lack significant fibrosis and are considered low-risk. Surveillance strategy for low-risk MASLD remains uncertain. Aim Identify which low-risk subjects can avoid follow-up vibration-controlled transient elastography (VCTE) within 1 year. Methods Retrospective analysis of two independent low-risk MASLD cohorts (baseline liver stiffness [LS] < 8kPa) with routine 6–12 months follow-up VCTE. The primary outcome was LS ≥ 8kPa on follow-up, requiring referral and further work-up according to current guidance. Predictors of the primary outcome on univariate and multivariate logistic regression were incorporated into a decision algorithm, and validated in an independent cohort. Results Of 206 subjects in the derivation cohort, 96 were low-risk. After a median of 10 months, 24 (25%) low-risk subjects had LS ≥ 8kPa. Baseline LS (P < 0.01) and ALT change from baseline (P = 0.02) (multivariate AUROC = 0.84 [0.74–0.94]) predicted the primary outcome, and were incorporated to a two-step decision algorithm. Low-risk subjects with baseline LS < 5.5 kPa can avoid repeating VCTE in a year, while those with LS > 6.8 kPa require one. For intermediate baseline LS (5.5–6.8kPa), repeat VCTE is only indicated when ALT increase > 6 U/L. The algorithm had 92% negative predictive value, 78% specificity, and 78% accuracy in the derivation cohort. In the validation cohort (n = 64), it had 91% NPV, 72% specificity, and 71% accuracy. Conclusion In low-risk MASLD, a simple algorithm combining baseline LS and ALT change can be used to safely avoid a repeat VCTE in a year.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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