Association study of common functional genetic polymorphisms in SLC6A4 (5-HTT) and MAOA genes with obesity in portuguese children

Arch Physiol Biochem. 2022 Dec;128(6):1510-1515. doi: 10.1080/13813455.2020.1779312. Epub 2020 Jun 18.

Abstract

Objectives: To investigate the association of polymorphisms in SLC6A4 and MAOA genes with obesity indices in children.

Material and methods: A total of 637 Portuguese children (317 girls; 320 boys) aged 3-11 years-old were genotyped for the SLC6A4 polymorphisms, 5-HTTLPR and STin2, and for a MAOA VNTR. Polymorphisms were analysed by PCR-based methods.

Results: Although non-significant (p = .089), our study revealed the Stin2 10 minor allele with a marked higher frequency in girls with overweight/obesity (0.466) in comparison with controls (0.376). Combining the two SLC6A4 polymorphisms, haplotype S/12 revealed in girls significant or nominally significant protective effects against BMI (β = -0.615; p = .009), BMI Z-score (β = -0.251; p = .006), WC (β = -1.4; p = .02) and WHtR (β = -0.008; p = .04).

Conclusions: We found some evidences for the role of SLC6A4 gene in measures of childhood obesity, mainly in girls.

Keywords: MAOA; Obesity; SLC6A4; children; serotonin.

MeSH terms

  • Child
  • Child, Preschool
  • Female
  • Genotype
  • Humans
  • Male
  • Pediatric Obesity* / genetics
  • Polymorphism, Single Nucleotide*
  • Portugal
  • Serotonin Plasma Membrane Transport Proteins / genetics

Substances

  • SLC6A4 protein, human
  • Serotonin Plasma Membrane Transport Proteins