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Myosteatosis predicts survival after surgery for periampullary cancer: a novel method using MRI.

David P J van Dijk ,
Frans C H Bakers ,
Sebastian Sanduleanu ,
Rianne D W Vaes ,
Sander S Rensen ,
Cornelis H C Dejong ,
Regina G H Beets-Tan ,
Steven W M Olde Damink

Abstract

METHODS

Patients were selected from a prospective cohort of 236 surgical patients with periampullary cancer. The MRI-muscle signal intensity and CT-muscle radiation attenuation were assessed at the level of the third lumbar vertebra and related to survival.

CONCLUSIONS

Myosteatosis may be adequately assessed using either MRI-muscle signal intensity or CT-muscle radiation attenuation.

RESULTS

Forty-seven patients were included in the study. Inter-observer variability for MRI assessment was low (R2 = 0.94). MRI-muscle signal intensity was associated with short survival: median survival 9.8 (95%-CI: 1.5-18.1) vs. 18.2 (95%-CI: 10.7-25.8) months for high vs. low intensity, respectively (p = 0.038). Similar results were found for CT-muscle radiation attenuation (low vs. high radiation attenuation: 10.8 (95%-CI: 8.5-13.1) vs. 15.9 (95%-CI: 10.2-21.7) months, respectively; p = 0.046). MRI-signal intensity correlated negatively with CT-radiation attenuation (r=-0.614, p < 0.001).

BACKGROUND

Myosteatosis, characterized by inter- and intramyocellular fat deposition, is strongly related to poor overall survival after surgery for periampullary cancer. It is commonly assessed by calculating the muscle radiation attenuation on computed tomography (CT) scans. However, since magnetic resonance imaging (MRI) is replacing CT in routine diagnostic work-up, developing methods based on MRI is important. We developed a new method using MRI-muscle signal intensity to assess myosteatosis and compared it with CT-muscle radiation attenuation.

More about this publication

HPB : the official journal of the International Hepato Pancreato Biliary Association

Volume 20
Issue nr. 8
Pages 715-720
Publication date 01-08-2018

Full text links

Publisher website (DOI) 10.1016/j.hpb.2018.02.378
Europe PubMed Central 29519644
Pubmed 29519644

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