Evidence map›Paper›PMID 42108220›Full record

ArticleMedical physics2026

Correlation of ultrasound attenuation with proton density fat fraction across multiple organs in healthy volunteers.

Adrien Rohfritsch, Jules Courgenay, Antoine Biénassis, Elorri Olhagaray, Manon Basso, Benjamin Leporq, Benoit Allignet, David Melodelima

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Article in Medical physics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Adrien RohfritschLaboratory of Therapeutic Applications of Ultrasound, INSERM, Centre Léon Bérard, Université Lyon 1, Lyon, France.
Jules CourgenayLaboratory of Therapeutic Applications of Ultrasound, INSERM, Centre Léon Bérard, Université Lyon 1, Lyon, France.
Antoine BiénassisLaboratory of Therapeutic Applications of Ultrasound, INSERM, Centre Léon Bérard, Université Lyon 1, Lyon, France.
Elorri OlhagarayLaboratory of Therapeutic Applications of Ultrasound, INSERM, Centre Léon Bérard, Université Lyon 1, Lyon, France.
Manon BassoLaboratory of Therapeutic Applications of Ultrasound, INSERM, Centre Léon Bérard, Université Lyon 1, Lyon, France.
Benjamin LeporqUniv Lyon, INSA-Lyon, Université Claude Bernard Lyon 1, Villeurbanne, France.
Benoit AllignetUniv Lyon, INSA-Lyon, Université Claude Bernard Lyon 1, Villeurbanne, France.
David MelodelimaLaboratory of Therapeutic Applications of Ultrasound, INSERM, Centre Léon Bérard, Université Lyon 1, Lyon, France.

Funding

SIRIC Lyrican INCa-DGOSINSERM- ITMO cancer 18003
6 · The paper itself

Abstract

backgroundLocal determination of the attenuation in biological tissues has been the focus of extensive research over the past decades. Its characterization is of major interest for both noninvasive thermal therapies and diagnostic applications. Numerous ultrasound (US)-based methods have been investigated in recent years to assess attenuation in vivo. PURPOSE: In this article, we aim to map US attenuation in four organs of human volunteers: liver, pancreas, kidney, and breast. We propose to compare the mean attenuation values obtained in each tissue with the corresponding proton density fat fraction (PDFF) derived from quantitative magnetic resonance imaging (qMRI). This comparison allows us to (i) present a direct calculation method of the local US attenuation and (ii) investigate the relationship between the average fat content of each organ and its global US attenuation.

methodsThe ultrasonic measurement method is in line with techniques originating from the spectral difference method. Here, the attenuation coefficient (AC) is estimated by insonifying tissues with a single plane wave and acquiring the backscattered echoes. This approach avoids the need for a reference medium to compensate for diffraction and focusing effects. The method is characterized and validated on a calibrated phantom and compared with two commonly used techniques on ex vivo liver tissues. Subsequently, attenuation maps and average values obtained from US imaging in healthy volunteers are compared with PDFF values measured by qMRI. Hepatic (

resultsMeasurements on the calibrated phantom showed relative errors between the measured mean values and the manufacturer values of 2% and 9%, respectively. Average AC of each organ was included in the confidence interval of the corresponding literature value. The Pearson correlation coefficient between

conclusionsThis work presents an alternative method for in vivo characterization of US attenuation based on the emission of a plane wave, and highlights the impact of fat density on inter-organ attenuation variations. Together, these results provide new insights into the relationship between tissue microstructure and US attenuation.

Indexed as

Adipose TissueHealthy VolunteersProtonsAdultBreastFemaleHumansImage Processing, Computer-AssistedKidneyLiverMagnetic Resonance ImagingPancreasPhantoms, ImagingUltrasonographyProtonsfat fractionquantitative MRIultrasonic attenuation

Identifiers

PMID42108220
PMCPMC13158173

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.