Key result
Novel strain index correlates moderately with shear wave elastography and accurately stages liver fibrosis.
Why the study?
Strain elastography is limited by its relative nature and inability to capture temporal changes, necessitating a novel quantitative strain index for liver fibrosis assessment.
Does a novel quantitative strain index (Q-SI) integrating spatiotemporal analysis of strain elastography improve the noninvasive evaluation of liver fibrosis compared to shear wave-based techniques in patients with chronic liver disease?
Observational (n=201)
Blinded to clinical, biochemical, and histological information at the time of acquisition
No
Does a novel quantitative strain index (Q-SI) integrating spatiotemporal analysis of strain elastography improve the noninvasive evaluation of liver fibrosis compared to shear wave-based techniques in patients with chronic liver disease?
Effect estimate: r = -0.51
p-value: p=<0.001
A novel quantitative strain index (Q-SI) provides diagnostic performance comparable to established shear wave-based techniques for assessing liver fibrosis, while remaining robust against the confounding effects of mild liver inflammation.
May offer inflammation-resistant alternative for fibrosis staging; leaves open adoption pending prospective validation.
Strain elastography is often limited by its relative nature and failure to capture temporal changes. This study aimed to establish a novel quantitative strain index (Q-SI) integrating spatiotemporal analysis and evaluate its utility for assessing liver fibrosis. This prospective study included patients with chronic liver disease (CLD) or chronic heart failure (CHF) between June 2020 and March 2022. The Q-SI was established by applying Q-Analysis to spatiotemporal strain map data, averaging values over 5–10 cardiac cycles. Correlations with two-dimensional shear wave elastography (2D-SWE) and vibration-controlled transient elastography (VCTE) were assessed. Diagnostic performance in histological fibrosis staging was compared using areas under the curve (AUC). A total of 201 participants (194 CLD, 7 CHF) were evaluated. In the CLD cohort, Q-SI showed a significant negative correlation with 2D-SWE ( r = − 0.51, P <0.001) and VCTE ( r = − 0.53, P <0.001). Q-SI also decreased significantly with advancing histological fibrosis stage. Diagnostic accuracy (AUC: ≥ F2, 0.74; ≥ F3, 0.73; F4, 0.84) was comparable to that of 2D-SWE (0.73, 0.76, and 0.76) and that of VCTE (0.77, 0.83, and 0.88). Unlike 2D-SWE and VCTE, Q-SI was not affected by high alanine aminotransferase levels. In the CHF cohort, the Q-SI correlated strongly with right atrial reservoir strain ( r = 0.90, P < 0.01), an indicator of right atrial pressure, but not with left ventricular ejection fraction. Q-SI provides a strain-based assessment of liver fibrosis comparable to that of shear wave-based techniques, with potential resilience to inflammation and independence from left ventricular function.
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Kobayashi et al. (2026) conducted an observational in Chronic liver disease (CLD) and chronic heart failure (CHF) (n=201). Quantitative strain index (Q-SI) via spatiotemporal analysis of strain elastography vs. Two-dimensional shear wave elastography (2D-SWE) and vibration-controlled transient elastography (VCTE) was evaluated on Correlation between Q-SI and 2D-SWE in the CLD cohort (r = -0.51, p=<0.001). The novel quantitative strain index (Q-SI) showed a significant negative correlation with 2D-SWE (r = -0.51) and VCTE (r = -0.53) in patients with chronic liver disease, providing comparable diagnostic accuracy for histological fibrosis staging.
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