Abstract:Objective To assess the changes in body composition and nutritional risks faced by children with different stages of acute leukemia (AL). Methods Bioelectrical impedance analysis combined with anthropometric measurements was used to detect body composition. This prospective study was conducted from August 2023 to July 2024 at Shandong Provincial Hospital, examining the body composition and physical balance of children with various stages of AL and healthy children. Results The non-fat components of children with AL and healthy children both showed a linear increase with age. In the younger age group, there were no significant differences in body composition between children with AL and healthy children. However, in the older age group, the body composition of children undergoing chemotherapy for AL was significantly lower than that of healthy children (P<0.05), and muscle mass recovered first after the completion of AL chemotherapy. The proportion of children with increased trunk fat in AL children who completed chemotherapy was significantly lower than that in healthy children (P<0.05), while the incidence rate of severe left-right imbalance in body composition was significantly higher (P<0.05). Muscle distribution in children with AL primarily showed insufficient limb and overall muscle mass, whereas healthy children mainly exhibited insufficient upper limb muscle mass. Conclusions The body composition of children with AL varies at different treatment stages, indicating that nutritional status is affected by both the disease itself and the treatment. Early screening can provide a basis for reasonable nutritional intervention.
SHI Li-Xia,ZHAO Ming-Zhong,WANG Fei-Fei et al. Clinical analysis of nutritional components in children with acute leukemia[J]. CJCP, 2025, 27(3): 300-307.
Triarico S, Rinninella E, Cintoni M, et al. Impact of malnutrition on survival and infections among pediatric patients with cancer: a retrospective study[J]. Eur Rev Med Pharmacol Sci, 2019, 23(3): 1165-1175. PMID: 30779086. DOI: 10.26355/eurrev_201901_17009.
Gallo N, Horvath K, Czuppon K, et al. Different nutritional screening tools and recommended screening algorithm for pediatric oncology patients[J]. Clin Nutr, 2021, 40(6): 3836-3841. PMID: 34130030. DOI: 10.1016/j.clnu.2021.05.013.
Leiva Badosa E, Badia Tahull M, Virgili Casas N, et al. Hospital malnutrition screening at admission: malnutrition increases mortality and length of stay[J]. Nutr Hosp, 2017, 34(4): 907-913. PMID: 29095016. DOI: 10.20960/nh.657.
Allard JP, Keller H, Jeejeebhoy KN, et al. Decline in nutritional status is associated with prolonged length of stay in hospitalized patients admitted for 7 days or more: a prospective cohort study[J]. Clin Nutr, 2016, 35(1): 144-152. PMID: 25660316. DOI: 10.1016/j.clnu.2015.01.009.
Zhang H, Wang Y, Jiang ZM, et al. Impact of nutrition support on clinical outcome and cost-effectiveness analysis in patients at nutritional risk: a prospective cohort study with propensity score matching[J]. Nutrition, 2017, 37: 53-59. PMID: 28359363. DOI: 10.1016/j.nut.2016.12.004.
Cardenas D, Bermúdez C, Pérez A, et al. Nutritional risk is associated with an increase of in-hospital mortality and a reduction of being discharged home: results of the 2009-2015 nutritionDay survey[J]. Clin Nutr ESPEN, 2020, 38: 138-145. PMID: 32690148. DOI: 10.1016/j.clnesp.2020.05.014.
Zhang X, Tang T, Pang L, et al. Malnutrition and overall survival in older adults with cancer: a systematic review and meta-analysis[J]. J Geriatr Oncol, 2019, 10(6): 874-883. PMID: 30917937. DOI: 10.1016/j.jgo.2019.03.002.
Mejía-Aranguré JM, Fajardo-Gutiérrez A, Reyes-Ruíz NI, et al. Malnutrition in childhood lymphoblastic leukemia: a predictor of early mortality during the induction-to-remission phase of the treatment[J]. Arch Med Res, 1999, 30(2): 150-153. PMID: 10372451. DOI: 10.1016/s0188-0128(98)00026-8.
Rogers PC, Barr RD. The relevance of nutrition to pediatric oncology: a cancer control perspective[J]. Pediatr Blood Cancer, 2020,67Suppl 3:e28213. PMID: 32096351. DOI: 10.1002/pbc.28213.
Iniesta RR, Paciarotti I, Brougham MF, et al. Effects of pediatric cancer and its treatment on nutritional status: a systematic review[J]. Nutr Rev, 2015, 73(5): 276-295. PMID: 26011902. DOI: 10.1093/nutrit/nuu062.
Cederholm T, Bosaeus I, Barazzoni R, et al. Diagnostic criteria for malnutrition: an ESPEN consensus statement[J]. Clin Nutr, 2015, 34(3): 335-340. PMID: 25799486. DOI: 10.1016/j.clnu.2015.03.001.
Merchant RA, Seetharaman S, Au L, et al. Relationship of fat mass index and fat free mass index with body mass index and association with function, cognition and sarcopenia in pre-frail older adults[J]. Front Endocrinol (Lausanne), 2021, 12: 765415. PMID: 35002957. PMCID: PMC8741276. DOI: 10.3389/fendo.2021.765415.
Smith S, Madden AM. Body composition and functional assessment of nutritional status in adults: a narrative review of imaging, impedance, strength and functional techniques[J]. J Hum Nutr Diet, 2016, 29(6): 714-732. PMID: 27137882. DOI: 10.1111/jhn.12372.
Feng Y, Pan LY, Shen LY, et al. Changes in body composition in children with acute graft-versus-host disease within the first 100 days after hematopoietic stem cell transplantation[J]. Eur J Clin Nutr, 2018, 72(8): 1167-1175. PMID: 29269889. DOI: 10.1038/s41430-017-0057-y.
Seo YG, Kim JH, Kim Y, et al. Validation of body composition using bioelectrical impedance analysis in children according to the degree of obesity[J]. Scand J Med Sci Sports, 2018, 28(10): 2207-2215. PMID: 29938849. DOI: 10.1111/sms.13248.
Kyle UG, Earthman CP, Pichard C, et al. Body composition during growth in children: limitations and perspectives of bioelectrical impedance analysis[J]. Eur J Clin Nutr, 2015, 69(12): 1298-1305. PMID: 26039314. DOI: 10.1038/ejcn.2015.86.
Skipper A, Coltman A, Tomesko J, et al. Adult malnutrition (undernutrition) screening: an evidence analysis center systematic review[J]. J Acad Nutr Diet, 2020, 120(4): 669-708. PMID: 31866356. DOI: 10.1016/j.jand.2019.09.010.
Khoury JD, Solary E, Abla O, et al. The 5th edition of the World Health Organization classification of haematolymphoid tumours: myeloid and histiocytic/dendritic neoplasms[J]. Leukemia, 2022, 36(7):1703?1719. PMID:35732831. DOI: 10.1038/s41375-022-01613-1.
Sala A, Pencharz P, Barr RD. Children, cancer, and nutrition--a dynamic triangle in review[J]. Cancer, 2004, 100(4): 677-687. PMID: 14770421. DOI: 10.1002/cncr.11833.
Kazemi-Bajestani SM, Mazurak VC, Baracos V. Computed tomography-defined muscle and fat wasting are associated with cancer clinical outcomes[J]. Semin Cell Dev Biol, 2016, 54: 2-10. PMID: 26343952. DOI: 10.1016/j.semcdb.2015.09.001.
Martin L, Birdsell L, Macdonald N, et al. Cancer cachexia in the age of obesity: skeletal muscle depletion is a powerful prognostic factor, independent of body mass index[J]. J Clin Oncol, 2013, 31(12): 1539-1547. PMID: 23530101. DOI: 10.1200/JCO.2012.45.2722.
Chen JL, Colgan TD, Walton KL, et al. The TGF-β signalling network in muscle development, adaptation and disease[J]. Adv Exp Med Biol, 2016, 900: 97-131. PMID: 27003398. DOI: 10.1007/978-3-319-27511-6_5.
Bernardoni F, Bernhardt N, Pooseh S, et al. Metabolic state and value-based decision-making in acute and recovered female patients with anorexia nervosa[J]. J Psychiatry Neurosci, 2020, 45(4): 253-261. PMID: 32129584. PMCID: PMC7828930. DOI: 10.1503/jpn.190031.
Delhanty PJ, Huisman M, Julien M, et al. The acylated (AG) to unacylated (UAG) ghrelin ratio in esterase inhibitor-treated blood is higher than previously described[J]. Clin Endocrinol (Oxf), 2015, 82(1): 142-146. PMID: 24810977. DOI: 10.1111/cen.12489.
Davis TR, Pierce MR, Novak SX, et al. Ghrelin octanoylation by ghrelin O-acyltransferase: protein acylation impacting metabolic and neuroendocrine signalling[J]. Open Biol, 2021, 11(7): 210080. PMID: 34315274. PMCID: PMC8316800. DOI: 10.1098/rsob.210080.
Bizzarri C, Rigamonti AE, Luce A, et al. Children with Prader-Willi syndrome exhibit more evident meal-induced responses in plasma ghrelin and peptide YY levels than obese and lean children[J]. Eur J Endocrinol, 2010, 162(3): 499-505. PMID: 20019130. DOI: 10.1530/EJE-09-1033.
Moschovi M, Trimis G, Vounatsou M, et al. Serial plasma concentrations of PYY and ghrelin during chemotherapy in children with acute lymphoblastic leukemia[J]. J Pediatr Hematol Oncol, 2008, 30(10): 733-737. PMID: 19011469. DOI: 10.1097/MPH.0b013e318179a1d8.