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The influence of serum selenium in differential epigenetic and transcriptional regulation of CPT1B gene in women with obesity.
Watanabe, Lígia Moriguchi; Pereira, Vanessa Aparecida Batista; Noronha, Natalia Yumi; de Souza Pinhel, Marcela Augusta; Wolf, Leticia Santana; de Oliveira, Cristiana Cortes; Plaça, Jessica Rodrigues; Noma, Isabella Harumi Yonehara; da Silva Rodrigues, Guilherme; de Souza, Vanessa Cristina Oliveira; Júnior, Fernando Barbosa; Nonino, Carla Barbosa.
Affiliation
  • Watanabe LM; Department of Health Sciences, Division of Nutrition and Metabolism, Ribeirão Preto Medical School, University of São Paulo, FMRP/USP, Brazil. Electronic address: ligia.moriguchi@gmail.com.
  • Pereira VAB; Department of Health Sciences, Division of Nutrition and Metabolism, Ribeirão Preto Medical School, University of São Paulo, FMRP/USP, Brazil.
  • Noronha NY; Department of Internal Medicine, Ribeirão Preto Medical School, University of São Paulo, FMRP/USP, Brazil.
  • de Souza Pinhel MA; Department of Internal Medicine, Ribeirão Preto Medical School, University of São Paulo, FMRP/USP, Brazil; Departament of Molecular Biology - São Jose do Rio Preto Medical School, Sao Jose do Rio Preto, São Paulo, Brazil.
  • Wolf LS; Department of Internal Medicine, Ribeirão Preto Medical School, University of São Paulo, FMRP/USP, Brazil.
  • de Oliveira CC; Department of Internal Medicine, Ribeirão Preto Medical School, University of São Paulo, FMRP/USP, Brazil.
  • Plaça JR; National Institute of Science and Technology in Stem Cell and Cell Therapy (INCT/CNPq) and Center for Cell-Based Therapy, CEPID/FAPESP, Ribeirão Preto, São Paulo, Brazil.
  • Noma IHY; Department of Clinical and Toxicological Analyses, School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, São Paulo, Brazil.
  • da Silva Rodrigues G; Department of Internal Medicine, Ribeirão Preto Medical School, University of São Paulo, FMRP/USP, Brazil.
  • de Souza VCO; Department of Clinical and Toxicological Analyses and Bromatology, Faculty of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, FCFRP/USP, Brazil.
  • Júnior FB; Department of Clinical and Toxicological Analyses and Bromatology, Faculty of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, FCFRP/USP, Brazil.
  • Nonino CB; Department of Health Sciences, Division of Nutrition and Metabolism, Ribeirão Preto Medical School, University of São Paulo, FMRP/USP, Brazil; Department of Internal Medicine, Ribeirão Preto Medical School, University of São Paulo, FMRP/USP, Brazil.
J Trace Elem Med Biol ; 83: 127376, 2024 May.
Article in En | MEDLINE | ID: mdl-38183920
ABSTRACT

INTRODUCTION:

The increasing prevalence of obesity has become a major health problem worldwide. The causes of obesity are multifactorial and could be influenced by dietary patterns and genetic factors. Obesity has been associated with a decrease in micronutrient intake and consequently decreased blood concentrations. Selenium is an essential micronutrient for human health, and its metabolism could be affected by obesity, especially severe obesity. This study aimed to identify differential methylation genes associated with serum selenium concentration in women with and without obesity.

METHODOLOGY:

Thirty-four patients were enrolled in the study and divided into two groups Obese (Ob) n = 20 and Non-Obese (NOb) n = 14, according to the Body Mass Index (BMI). Anthropometry, body composition, serum selenium, selenium intake, and biochemical parameters were evaluated. DNA extraction and bisulfite conversion were performed to hybridize the samples on the 450k Methylation Chip Infinium Beadchip (Illumina). Bioinformatics analysis was performed using the R program and the Champ package. The differentially methylated regions (DMRs) were identified using the Bumphunter method. In addition, logarithmic conversion was performed for the analysis of serum selenium and methylation.

RESULTS:

In the Ob group, the body weight, BMI, fat mass, and free fat mass were higher than in the NOb group, as expected. Interestingly, the serum selenium was lower in the Ob than in the NOb group without differences in selenium intake. One DMR corresponding to the CPT1B gene, involved in lipid oxidation, was related to selenium levels. This region was hypermethylated in the Ob group, indicating that the intersection between selenium deficiency and hypermethylation could influence the expression of the CPT1B gene. The transcriptional analysis confirmed the lower expression of the CPT1B gene in the Ob group.

CONCLUSION:

Studies connecting epigenetics to environmental factors could offer insights into the mechanisms involving the expression of genes related to obesity and its comorbidities. Here we demonstrated that the mineral selenium might play an essential role in lipid oxidation via epigenetic and transcriptional regulation of the CPT1B gene in obesity.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Selenium / Carnitine O-Palmitoyltransferase / Epigenesis, Genetic / Obesity Type of study: Prognostic_studies / Risk_factors_studies Limits: Female / Humans Language: En Journal: J Trace Elem Med Biol / J. trace elem. med. biol / Journal of trace elements in medicine and biology Journal subject: METABOLISMO / SAUDE AMBIENTAL Year: 2024 Document type: Article Country of publication: Alemania

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Selenium / Carnitine O-Palmitoyltransferase / Epigenesis, Genetic / Obesity Type of study: Prognostic_studies / Risk_factors_studies Limits: Female / Humans Language: En Journal: J Trace Elem Med Biol / J. trace elem. med. biol / Journal of trace elements in medicine and biology Journal subject: METABOLISMO / SAUDE AMBIENTAL Year: 2024 Document type: Article Country of publication: Alemania