Presença de polimorfismos genéticos no receptor de vitamina D e padrão da reserva corporal de micronutrientes e suas relações com os marcadores do controle glicêmico, perfis lipídico e inflamatório de indivíduos com diabetes mellitus tipo 2

• Ano de defesa: 2024
• Autor(a) principal: Santos, Ramara Kadija Fonseca
• Orientador(a): Silva, Ana Mara de Oliveira e
• Tipo de documento: Tese
• Tipo de acesso: Acesso aberto
• Idioma: por
• Programa de Pós-Graduação: Pós-Graduação em Ciências da Saúde
• Palavras-chave em Português: Diabetes tipo 2; Vitamina D; Glicemia; Inflamação; Micronutrientes; Receptor de vitamina D; Polimorfismo genético
• Palavras-chave em Inglês: Type 2 diabetes; Vitamin D; Glycemia; Inflammation; Micronutrients; Vitamin D receptor; Genetic polymorphism
• Link de acesso: https://ri.ufs.br/jspui/handle/riufs/23615

Genetic single nucleotide polymorphisms (SNPs) and haplotypes in the vitamin D receptor (VDR), and deficiencies in vitamin D, magnesium (Mg), zinc (Zn), calcium (Ca) and potassium (K) are factors that alone contribute to inadequate metabolic control in individuals with type 2 diabetes mellitus (DM2). Thus, the aim of this study is to associate the presence of SNPs in the VDR, haplotypes and patterns of micronutrient body reserves with markers of glycemic control, lipid levels and inflammatory profile in individuals with DM2. To this end, a meta-analysis evaluated the association between the presence of SNPs in the VDR and markers of glycemic control, lipid levels and inflammatory profile in individuals with DM2, following the MOOSE guidelines and registered with PROSPERO (nºCRD42021268152). A systematic search of the data was carried out in the PubMed, EMBASE and SCOPUS databases. Studies comparing the values of markers of glycemic control, lipid profile and inflammation between the identified genotypes were included. The quality of the studies was assessed using the Newcastle-Ottawa scale. Effect sizes were tested using a random-effects model and reported as standardized mean difference (SMD) and 95% confidence interval (95%CI). In parallel, an observational, cross-sectional study was carried out with 160 adults with DM2, both sexes, living in Sergipe. Sociodemographic information was collected, anthropometric and body composition assessments were carried out, and blood was drawn to identify SNPs and assess biochemical markers of glycemic and lipid control. The frequency of SNPs, linkage disequilibrium and the Hardy-Weinberg test were calculated and SNPs with a frequency greater than 1% were inserted into the haplotype model. The SNPs and haplotypes, and the micronutrient body reserve patterns established by principal component analysis and stratified into quartiles, were entered into the binary logistic regression model tests (dependent variables therapeutic target values for fasting glycemia, percent of glycated hemoglobin (%HbA1c) and Homeostasis Model Assessment - Insulin Resistance (HOMA-IR) adjusted for gender, age, time of diagnosis and BMI, significance p<0.05. The meta-analysis identified four SNPs: Fokl (rs2228570); BsmI (rs1544410); Taql (rs731236) and Apal (rs7975232). The Fokl and BsmI SNPs were associated with higher %HbA1c (SMD=0.409, p=0.002) and triacylglycerol (SMD=0.206, p=0.023), respectively. In the observational study, the Bsml SNP was associated with increased %HbA1c (OR=2.071, p=0.045), but the haplotypes did not contribute to inadequate glycemic control. Two patterns of body micronutrient reserve were established. The lowest quartile of Pattern 1 (Mg, Zn, Ca and K) and Pattern 2 (25(OH)D and Zn) were 4.319 (p=0.019) and 3.970 (p=0.038) times more likely to increase HOMA-IR and %HbA1c values, respectively. It is concluded that SNPs in the VDR and the pattern of micronutrient body reserves explained by the lower concentration of 25(OH)D, Zn, Mg, Ca and K contribute to poor metabolic control in individuals with DM2.