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Abdominal Skeletal Muscle Index as a Potential Novel Biomarker in Adult Fontan Patients

BACKGROUND: Fontan palliation results in a chronic multisystem disorder with diminished exercise capacity and increased risk of muscle wasting. The aims of this study were to assess the feasibility of skeletal muscle mass measurements in Fontan patients undergoing magnetic resonance imaging liver su...

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Autores principales: Possner, Mathias, Alsaied, Tarek, Siddiqui, Saira, Morales, David, Trout, Andrew T., Veldtman, Gruschen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7067685/
https://www.ncbi.nlm.nih.gov/pubmed/32190826
http://dx.doi.org/10.1016/j.cjco.2019.12.004
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author Possner, Mathias
Alsaied, Tarek
Siddiqui, Saira
Morales, David
Trout, Andrew T.
Veldtman, Gruschen
author_facet Possner, Mathias
Alsaied, Tarek
Siddiqui, Saira
Morales, David
Trout, Andrew T.
Veldtman, Gruschen
author_sort Possner, Mathias
collection PubMed
description BACKGROUND: Fontan palliation results in a chronic multisystem disorder with diminished exercise capacity and increased risk of muscle wasting. The aims of this study were to assess the feasibility of skeletal muscle mass measurements in Fontan patients undergoing magnetic resonance imaging liver surveillance to compare muscle mass with a historic control and to assess its correlation with cardiorespiratory fitness. METHODS: Skeletal muscle area (SMA) and skeletal muscle index (SMI) were measured at T12 and L3. A young, healthy historic cohort was used as a comparison group. RESULTS: Forty patients with a Fontan circulation (mean age, 25.5 ± 7.9 years; 50% were men) were included. Measurements of SMA and SMI were feasible and highly reproducible. Mean SMA and SMI were significantly lower in women compared with men at both T12 (SMA: 25.1 ± 4.9 cm(2) vs 33.5 ± 8.4 cm(2), P < 0.001; SMI: 9.7 ± 2.1 cm(2)/m(2) vs 11.3 ± 2.7 cm(2)/m(2), P = 0.045) and L3 (SMA: 121 ± 12 cm(2) vs 162 ± 24 cm(2), P < 0.001; SMI: 46.9 ± 7.0 cm(2)/m(2) vs 54.5 ± 7.4 cm(2)/m(2), P = 0.002). Mean SMI at L3 was significantly lower in the male Fontan population compared with the healthy historic cohort (54.5 ± 7.4 cm(2)/m(2) vs 60.9 ± 7.8 cm(2)/m(2), P < 0.001), but was similar for women (46.9 ± 7.0 cm(2)/m(2) vs 47.5 ± 6.6 cm(2)/m(2), P = 0.692). SMI at L3, but not at T12, was positively correlated with peak oxygen consumption, oxygen pulse, and workload. Four patients (10%) met criteria for muscle wasting in the sarcopenic range based on L3 measurements. CONCLUSIONS: Abdominal skeletal muscle mass can be reproducibly determined on surveillance liver magnetic resonance imaging scans. Muscle wasting appears to occur commonly in Fontan patients. Further research is needed to better define the value of SMI as a biomarker in the Fontan population.
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spelling pubmed-70676852020-03-18 Abdominal Skeletal Muscle Index as a Potential Novel Biomarker in Adult Fontan Patients Possner, Mathias Alsaied, Tarek Siddiqui, Saira Morales, David Trout, Andrew T. Veldtman, Gruschen CJC Open Original Article BACKGROUND: Fontan palliation results in a chronic multisystem disorder with diminished exercise capacity and increased risk of muscle wasting. The aims of this study were to assess the feasibility of skeletal muscle mass measurements in Fontan patients undergoing magnetic resonance imaging liver surveillance to compare muscle mass with a historic control and to assess its correlation with cardiorespiratory fitness. METHODS: Skeletal muscle area (SMA) and skeletal muscle index (SMI) were measured at T12 and L3. A young, healthy historic cohort was used as a comparison group. RESULTS: Forty patients with a Fontan circulation (mean age, 25.5 ± 7.9 years; 50% were men) were included. Measurements of SMA and SMI were feasible and highly reproducible. Mean SMA and SMI were significantly lower in women compared with men at both T12 (SMA: 25.1 ± 4.9 cm(2) vs 33.5 ± 8.4 cm(2), P < 0.001; SMI: 9.7 ± 2.1 cm(2)/m(2) vs 11.3 ± 2.7 cm(2)/m(2), P = 0.045) and L3 (SMA: 121 ± 12 cm(2) vs 162 ± 24 cm(2), P < 0.001; SMI: 46.9 ± 7.0 cm(2)/m(2) vs 54.5 ± 7.4 cm(2)/m(2), P = 0.002). Mean SMI at L3 was significantly lower in the male Fontan population compared with the healthy historic cohort (54.5 ± 7.4 cm(2)/m(2) vs 60.9 ± 7.8 cm(2)/m(2), P < 0.001), but was similar for women (46.9 ± 7.0 cm(2)/m(2) vs 47.5 ± 6.6 cm(2)/m(2), P = 0.692). SMI at L3, but not at T12, was positively correlated with peak oxygen consumption, oxygen pulse, and workload. Four patients (10%) met criteria for muscle wasting in the sarcopenic range based on L3 measurements. CONCLUSIONS: Abdominal skeletal muscle mass can be reproducibly determined on surveillance liver magnetic resonance imaging scans. Muscle wasting appears to occur commonly in Fontan patients. Further research is needed to better define the value of SMI as a biomarker in the Fontan population. Elsevier 2020-01-20 /pmc/articles/PMC7067685/ /pubmed/32190826 http://dx.doi.org/10.1016/j.cjco.2019.12.004 Text en © 2020 Canadian Cardiovascular Society. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Possner, Mathias
Alsaied, Tarek
Siddiqui, Saira
Morales, David
Trout, Andrew T.
Veldtman, Gruschen
Abdominal Skeletal Muscle Index as a Potential Novel Biomarker in Adult Fontan Patients
title Abdominal Skeletal Muscle Index as a Potential Novel Biomarker in Adult Fontan Patients
title_full Abdominal Skeletal Muscle Index as a Potential Novel Biomarker in Adult Fontan Patients
title_fullStr Abdominal Skeletal Muscle Index as a Potential Novel Biomarker in Adult Fontan Patients
title_full_unstemmed Abdominal Skeletal Muscle Index as a Potential Novel Biomarker in Adult Fontan Patients
title_short Abdominal Skeletal Muscle Index as a Potential Novel Biomarker in Adult Fontan Patients
title_sort abdominal skeletal muscle index as a potential novel biomarker in adult fontan patients
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7067685/
https://www.ncbi.nlm.nih.gov/pubmed/32190826
http://dx.doi.org/10.1016/j.cjco.2019.12.004
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