UNI-MB - logo
UMNIK - logo
 
E-viri
Celotno besedilo
Recenzirano
  • Association of BCAT2 and BC...
    Vargas-Morales, Juan M.; Guizar-Heredia, Rocio; Méndez-García, Ana L.; Palacios-Gonzalez, Berenice; Schcolnik-Cabrera, Alejandro; Granados, Omar; López-Barradas, Adriana M.; Vázquez-Manjarrez, Natalia; Medina-Vera, Isabel; Aguilar-López, Miriam; Tovar-Palacio, Claudia; Ordaz-Nava, Guillermo; Rocha-Viggiano, Ana K.; Medina-Cerda, Eduardo; Torres, Nimbe; Ordovas, José M.; Tovar, Armando R.; Guevara-Cruz, Martha; Noriega, Lilia G.

    Nutrition, metabolism, and cardiovascular diseases, 10/2021, Letnik: 31, Številka: 11
    Journal Article

    Circulating amino acids are modified by sex, body mass index (BMI) and insulin resistance (IR). However, whether the presence of genetic variants in branched-chain amino acid (BCAA) catabolic enzymes modifies circulating amino acids is still unknown. Thus, we determined the frequency of two genetic variants, one in the branched-chain aminotransferase 2 (BCAT2) gene (rs11548193), and one in the branched-chain ketoacid dehydrogenase (BCKDH) gene (rs45500792), and elucidated their impact on circulating amino acid levels together with clinical, anthropometric and biochemical parameters. We performed a cross-sectional comparative study in which we recruited 1612 young adults (749 women and 863 men) aged 19.7 ± 2.1 years and with a BMI of 24.9 ± 4.7 kg/m2. Participants underwent clinical evaluation and provided blood samples for DNA extraction and biochemical analysis. The single nucleotide polymorphisms (SNPs) were determined by allelic discrimination using real-time polymerase chain reaction (PCR). The frequencies of the less common alleles were 15.2 % for BCAT2 and 9.83 % for BCKDH. The subjects with either the BCAT2 or BCKDH SNPs displayed no differences in the evaluated parameters compared with subjects homozygotes for the most common allele at each SNP. However, subjects with both SNPs had higher body weight, BMI, blood pressure, glucose, and circulating levels of aspartate, isoleucine, methionine, and proline than the subjects homozygotes for the most common allele (P < 0.05, One-way ANOVA). Our findings suggest that the joint presence of both the BCAT2 rs11548193 and BCKDH rs45500792 SNPs induces metabolic alterations that are not observed in subjects without either SNP. •The less common alleles frequencies were 15.2% for the BCAT2 rs11548193 and 9.83% for the BCKDH rs45500792 polymorphisms.•BCAT2 polymorphism carriers presented lower isoleucine concentration than subjects homozygotes for the most common allele.•BCKDH SNPs carriers displayed no differences in the evaluated parameters compared with non-carrier homozygotes subjects.•Both SNPs carriers had higher BMI, blood pressure, glucose, Asp, Ile, Met, and Pro than non-carrier homozygotes subjects.