Performance of continuous controlled attenuation parameter and liver stiffness measurement by the novel SmartExam in metabolic dysfunction‐associated steatotic liver disease

Author:

Song Sherlot J.12,Nogami Asako3,Liang Lilian Y.12ORCID,Yoneda Masato3,Leung Howard H.W.4,Nakajima Atsushi3,Lai Jimmy C.T.12ORCID,Wong Grace L.H.12ORCID,Shu Sally S.T.12,Wong Vincent W.S.12ORCID,Yip Terry C.F.12ORCID

Affiliation:

1. Medical Data Analytics Centre, Department of Medicine and Therapeutics The Chinese University of Hong Kong Hong Kong China

2. State Key Laboratory of Digestive Disease, Institute of Digestive Disease The Chinese University of Hong Kong Hong Kong China

3. Department of Gastroenterology and Hepatology Yokohama City University Graduate School of Medicine Yokohama Japan

4. Department of Anatomical and Cellular Pathology The Chinese University of Hong Kong Hong Kong China

Abstract

AbstractBackground & AimsFibroScan® Expert 630 and FibroScan® Mini+430 are novel vibration‐controlled transient elastography devices equipped with the same SmartExam software, which allows continuous measurement of controlled attenuation parameter (CAP) during the entire examination. This study aims to compare the CAP variabilities and the quantification for liver fibrosis and steatosis between the conventional FibroScan and the SmartExam‐equipped machines in patients with metabolic dysfunction‐associated steatotic liver disease (MASLD).MethodsThis retrospective study included 118 patients with biopsy‐proven MASLD who underwent liver biopsy at two tertiary centres between 2021 and 2023. Liver stiffness and steatosis measurements were performed using both FibroScan machines and M and XL probes for each individual. Liver histology was used as the reference standard for liver fibrosis and steatosis staging.ResultsStandard deviations of continuous CAP (cCAP) were significantly lower than those of CAP for all probes (p < .0001). CAP variability was significantly associated with body mass index (p < .01), probe selection (p < .001) as well as the random effect of centre. Only the effect of probe selection (p < .001) was significantly associated with cCAP variability. No significant difference was found in the performance of staging liver fibrosis and steatosis between two types of machines at the same cut‐offs.ConclusionsThe SmartExam‐based VCTE reduces the variability of CAP measurement and achieves a similar accuracy as the FibroScan 502 device for the estimation of both hepatic steatosis and fibrosis. Future studies should determine if cCAP is a better tool to monitor changes in steatosis than the original CAP.

Publisher

Wiley

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