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The role of adiposity, adipokines and polymorphisms of leptin and adiponectin in myelodysplastic syndromes

Published online by Cambridge University Press:  19 October 2023

Ana Patrícia Nogueira Aguiar*
Affiliation:
Cancer Cytogenomic Laboratory, Federal University of Ceará, Fortaleza, CE 60430-275, Brazil Center for Research and Drug Development (NPDM), Federal University of Ceará, Fortaleza, CE, Brazil
Priscila da Silva Mendonça
Affiliation:
Cancer Cytogenomic Laboratory, Federal University of Ceará, Fortaleza, CE 60430-275, Brazil Center for Research and Drug Development (NPDM), Federal University of Ceará, Fortaleza, CE, Brazil University Hospital Walter Cantidio, Brazilian Company of Hospital Services (EBSERH), Fortaleza, CE, Brazil
Roberto Cesar Pereira Lima Junior
Affiliation:
Center for Research and Drug Development (NPDM), Federal University of Ceará, Fortaleza, CE, Brazil Department of Physiology and Pharmacology, Federal University of Ceará, Fortaleza, CE, Brazil
Anacelia Gomes de Matos Mota
Affiliation:
Cancer Cytogenomic Laboratory, Federal University of Ceará, Fortaleza, CE 60430-275, Brazil Center for Research and Drug Development (NPDM), Federal University of Ceará, Fortaleza, CE, Brazil
Deysi Viviana Tenazoa Wong
Affiliation:
Center for Research and Drug Development (NPDM), Federal University of Ceará, Fortaleza, CE, Brazil Department of Pathology and Forensic Medicine, Federal University of Ceará, Fortaleza, CE, Brazil
Roberta Tatiane Germano de Oliveira
Affiliation:
Cancer Cytogenomic Laboratory, Federal University of Ceará, Fortaleza, CE 60430-275, Brazil Center for Research and Drug Development (NPDM), Federal University of Ceará, Fortaleza, CE, Brazil
Howard Lopes Ribeiro-Júnior
Affiliation:
Cancer Cytogenomic Laboratory, Federal University of Ceará, Fortaleza, CE 60430-275, Brazil Center for Research and Drug Development (NPDM), Federal University of Ceará, Fortaleza, CE, Brazil
Ronald Feitosa Pinheiro
Affiliation:
Cancer Cytogenomic Laboratory, Federal University of Ceará, Fortaleza, CE 60430-275, Brazil Center for Research and Drug Development (NPDM), Federal University of Ceará, Fortaleza, CE, Brazil Post-Graduate Program of Pathology, Federal University of Ceará, Fortaleza, CE, Brazil Department of Clinical Medicine, Federal University of Ceará, Fortaleza, CE, Brazil Post-graduate Program in Medical Science, Federal University of Ceará, Fortaleza, CE, Brazil
Silvia Maria Meira Magalhães
Affiliation:
Cancer Cytogenomic Laboratory, Federal University of Ceará, Fortaleza, CE 60430-275, Brazil Center for Research and Drug Development (NPDM), Federal University of Ceará, Fortaleza, CE, Brazil Department of Clinical Medicine, Federal University of Ceará, Fortaleza, CE, Brazil Post-graduate Program in Medical Science, Federal University of Ceará, Fortaleza, CE, Brazil
*
*Corresponding author: Dr A. P. N. Aguiar, email patricianogueiraaguiar@yahoo.com.br

Abstract

The aim of the present study was to investigate the relationship between leptin and adiponectin gene polymorphisms, circulating levels of leptin and adiponectin, adiposity and clinical markers in patients with myelodysplastic syndrome (MDS). This cross-sectional study was conducted with 102 adults and elderly MDS patients and 102 age- and sex-matched controls. Clinical characteristics, co-morbidities, anthropometric data, laboratory evaluation and genetic analysis (polymorphisms −2548G > A/rs7799039 of the LEP gene and +276G > T/rs1501299 of the ADIPOQ gene) were investigated. Serum leptin was higher and adiponectin lower in MDS when compared with controls. There was a significant positive correlation between serum leptin levels and BMI (r = 0·264, P = 0·025), waist circumference (r = 0·235, P = 0·047), body fat percentage (BF %) (r = 0·373, P = 0·001) and the fat mass index (FMI) (r = 0·371, P < 0·001). A lower mean adiponectin was found among patients with high BF %, higher visceral adiposity index and metabolic syndrome. A significant association was found between the AA genotype (mutant) of the LEP polymorphism rs7799039 and male sex and blast excess (≥ 5 %). In addition, a significant association was observed between the TT genotype (mutant) of the ADIPOQ rs1501299 polymorphism and Fe overload. These results demonstrate the importance of a comprehensive and systematic evaluation in patients with MDS in order to identify and control negative factors not related to the disease at an early stage.

Type
Research Article
Copyright
© The Author(s), 2023. Published by Cambridge University Press on behalf of The Nutrition Society

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