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Body composition after allogeneic haematopoietic cell transplantation/total body irradiation in children and young people: a restricted systematic review

PURPOSE: To collate evidence of changes in body composition following treatment of leukaemia in children, teenagers and young adults (CTYA, 0–24 years) with allogeneic haematopoietic stem cell transplant and total body irradiation (HSCT+TBI). METHODS: Papers were identified by searching Medline and...

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Autores principales: Lorenc, Ava, Hamilton-Shield, Julian, Perry, Rachel, Stevens, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7473918/
https://www.ncbi.nlm.nih.gov/pubmed/32388841
http://dx.doi.org/10.1007/s11764-020-00871-1
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author Lorenc, Ava
Hamilton-Shield, Julian
Perry, Rachel
Stevens, Michael
author_facet Lorenc, Ava
Hamilton-Shield, Julian
Perry, Rachel
Stevens, Michael
author_sort Lorenc, Ava
collection PubMed
description PURPOSE: To collate evidence of changes in body composition following treatment of leukaemia in children, teenagers and young adults (CTYA, 0–24 years) with allogeneic haematopoietic stem cell transplant and total body irradiation (HSCT+TBI). METHODS: Papers were identified by searching Medline and Google Scholar, reference lists/citations and contacting key authors, with no date or language restrictions. Inclusion criteria were as follows: leukaemia, HSCT+TBI, aged ≤ 24 years at HSCT and changes in body composition (total fat, central adiposity, adipose tissue function, muscle mass, muscle function). Quality was assessed using a brief Newcastle–Ottawa scale. RESULTS: Of 900 papers, 20 were included: seven controlled, five uncontrolled studies and eight case reports. Study quality appeared good. There was little evidence of differences in total fat/weight for HSCT + TBI groups (compared to healthy controls/population norms/short stature controls). There was some evidence of significantly higher central adiposity and differences in adipose tissue function (compared to leukaemic/non-leukaemic controls). Muscle mass was significantly lower (compared to healthy/obese controls). Muscle function results were inconclusive but suggested impairment. Case reports confirmed a lipodystrophic phenotype. CONCLUSIONS: Early remodelling of adipose tissue and loss of skeletal muscle are evident following HSCT + TBI for CTYA leukaemia, with extreme phenotype of overt lipodystrophy. There is some evidence for reduced muscle effectiveness. IMPLICATIONS FOR CANCER SURVIVORS: Body composition changes in patients after HSCT + TBI are apparent by early adult life and link with the risk of excess cardiometabolic morbidity seen in adult survivors. Interventions to improve muscle and/or adipose function, perhaps utilizing nutritional manipulation and/or targeted activity, should be investigated. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11764-020-00871-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-74739182020-09-16 Body composition after allogeneic haematopoietic cell transplantation/total body irradiation in children and young people: a restricted systematic review Lorenc, Ava Hamilton-Shield, Julian Perry, Rachel Stevens, Michael J Cancer Surviv Review PURPOSE: To collate evidence of changes in body composition following treatment of leukaemia in children, teenagers and young adults (CTYA, 0–24 years) with allogeneic haematopoietic stem cell transplant and total body irradiation (HSCT+TBI). METHODS: Papers were identified by searching Medline and Google Scholar, reference lists/citations and contacting key authors, with no date or language restrictions. Inclusion criteria were as follows: leukaemia, HSCT+TBI, aged ≤ 24 years at HSCT and changes in body composition (total fat, central adiposity, adipose tissue function, muscle mass, muscle function). Quality was assessed using a brief Newcastle–Ottawa scale. RESULTS: Of 900 papers, 20 were included: seven controlled, five uncontrolled studies and eight case reports. Study quality appeared good. There was little evidence of differences in total fat/weight for HSCT + TBI groups (compared to healthy controls/population norms/short stature controls). There was some evidence of significantly higher central adiposity and differences in adipose tissue function (compared to leukaemic/non-leukaemic controls). Muscle mass was significantly lower (compared to healthy/obese controls). Muscle function results were inconclusive but suggested impairment. Case reports confirmed a lipodystrophic phenotype. CONCLUSIONS: Early remodelling of adipose tissue and loss of skeletal muscle are evident following HSCT + TBI for CTYA leukaemia, with extreme phenotype of overt lipodystrophy. There is some evidence for reduced muscle effectiveness. IMPLICATIONS FOR CANCER SURVIVORS: Body composition changes in patients after HSCT + TBI are apparent by early adult life and link with the risk of excess cardiometabolic morbidity seen in adult survivors. Interventions to improve muscle and/or adipose function, perhaps utilizing nutritional manipulation and/or targeted activity, should be investigated. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11764-020-00871-1) contains supplementary material, which is available to authorized users. Springer US 2020-07-18 2020 /pmc/articles/PMC7473918/ /pubmed/32388841 http://dx.doi.org/10.1007/s11764-020-00871-1 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Review
Lorenc, Ava
Hamilton-Shield, Julian
Perry, Rachel
Stevens, Michael
Body composition after allogeneic haematopoietic cell transplantation/total body irradiation in children and young people: a restricted systematic review
title Body composition after allogeneic haematopoietic cell transplantation/total body irradiation in children and young people: a restricted systematic review
title_full Body composition after allogeneic haematopoietic cell transplantation/total body irradiation in children and young people: a restricted systematic review
title_fullStr Body composition after allogeneic haematopoietic cell transplantation/total body irradiation in children and young people: a restricted systematic review
title_full_unstemmed Body composition after allogeneic haematopoietic cell transplantation/total body irradiation in children and young people: a restricted systematic review
title_short Body composition after allogeneic haematopoietic cell transplantation/total body irradiation in children and young people: a restricted systematic review
title_sort body composition after allogeneic haematopoietic cell transplantation/total body irradiation in children and young people: a restricted systematic review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7473918/
https://www.ncbi.nlm.nih.gov/pubmed/32388841
http://dx.doi.org/10.1007/s11764-020-00871-1
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