Cited by 57Acute Lymphoblastic Leukemia researchRegulation of Appetite and ObesityAdipokines, Inflammation, and Metabolic Diseases

Short‐term effects of prednisolone and dexamethasone on circulating concentrations of leptin and sex hormone‐binding globulin in children being treated for acute lymphoblastic leukaemia

Wallace, A. M., Tucker, P., Williams, D. M., Hughes, I. A., Ahmed, S. F.·2003·Clinical Endocrinology

Abstract

Summary: objective Disturbances in body weight regulation are often encountered during glucocorticoid treatment and are associated with increased insulin resistance and truncal fat accumulation. Children were investigated who were receiving glucocorticoid treatment for acute lymphoblastic leukaemia (ALL). They were randomized to receive either prednisolone or dexamethasone as part of induction of remission. This randomization process provided a suitable opportunity to compare the effects of these two administered steroid on surrogate markers of adipocyte activity (leptin) and hyperinsulinaemia/insulin resistance (SHBG). design and patients Prospective study over 16 weeks of children randomized to receive prednisolone (40 mg/m 2) or dexamethasone (6·5 mg/m 2) as part of the MRC‐ALL97/99 induction chemotherapy for ALL. Nineteen children (8 male, 11 female) with a median age 5·9 years (range 2·6–13 years) were recruited into the study. Main outcome measures were body mass index (BMI), serum leptin and sex hormone binding globulin (SHBG). results Glucocorticoid administration for 5 weeks resulted in significant (P < 0·05) increases in BMI, leptin (corrected for BMI) and the leptin : SHBG ratio and lowering of SHBG. Dose for dose, dexamethasone was significantly more potent than prednisolone in altering these parameters. conclusions Short‐term glucocorticoid treatment has significant effects on BMI, leptin and SHBG. The leptin : SHBG ratio increase indicates that this may be a novel and sensitive biochemical marker of metabolic change. Our results suggest that glucocorticoid treatment regimens should be kept as short as possible to avoid possible detrimental effects associated with increased adiposity and insulin resistance.

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Crossref · 10.1046/j.1365-2265.2003.01790.x

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Authors
Wallace, A. M., Tucker, P., Williams, D. M., Hughes, I. A., & Ahmed, S. F.
Affiliations
  • University of Cambridge (GB)
  • Royal Hospital for Children (GB)
Venue
Clinical Endocrinology
Publisher
Wiley
Published
2003-06
Volume
58
Issue
6
Pages
770-776
ISSN
  • 0300-0664 (ISSN-L)
  • 1365-2265
OpenAlex
W2006456070
Cited by
57
References
2
Citations by year
2026: 2 · 2025: 3 · 2023: 1 · 2022: 3 · 2021: 2 · 2020: 1 · 2019: 3 · 2018: 1 · 2017: 3 · 2016: 2 · 2015: 3 · 2014: 2 · 2013: 1 · 2012: 4
FWCI
3.72
Type
journal article
Language
en
Open access
closed
Locations
  • Clinical Endocrinology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Acute Lymphoblastic Leukemia research
  • Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
  • Health Sciences › Medicine › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
Keywords
prednisolone, dexamethasone, glucocorticoids, acute lymphoblastic leukemia, children, leptin, sex hormone-binding globulin, body mass index, insulin resistance, hyperinsulinemia, adiposity, induction chemotherapy, metabolic side effects
MeSH terms
Adolescent, Child, Child, Preschool, Dexamethasone, Female, Glucocorticoids, Humans, Male, Prednisolone, Prospective Studies, Sex Hormone-Binding Globulin, Time Factors, Body Mass Index, Leptin, Precursor Cell Lymphoblastic Leukemia-Lymphoma

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