Combination of ACTN3 R577X and ACE I/D polymorphisms as a tool for prediction of obesity risk in children.
Patrícia Britto CostaLaura C AranaldePoliana E CorreiaGuilherme R F CardozoEvelise Sampaio da SilvaMonica Schiavon da CostaSandra Costa ValleRenata Torres Abib BertaccoSimone PienizRonaldo Carvalho AraujoAugusto SchneiderInes SchadockCarlos Castilho BarrosPublished in: International journal of obesity (2005) (2020)
The genetic influence in obesity prevalence is well described, but the role of genetic markers related to athletic strength/ endurance performance remains controversial. We investigated associations between obesity and the genetic polymorphisms alpha-actinin-3 (ACTN3) R577X and angiotensin-converting enzyme (ACE) I/D in schoolchildren aged 4-13 years from Southern Brazil. We collected sociodemographic data from parents through a questionnaire and conducted an anthropometric assessment. DNA was extracted from buccal cells and genotyping was performed by PCR. We found that 1.9% of the individuals were classified as low weight-for-age, 57.6% as normal weight and 40.5% as overweight/ obesity. Regarding allelic distribution, we found that 52.5% of individuals were DD, 30.8% ID, and 16.7% II for ACE; and 38.8% of individuals were RR, 40.2% RX and 21.0% XX for ACTN3. When both polymorphisms were combined, we observed a clear association between the composed genetic profile of these alleles and severe obesity in schoolchildren. Our data suggest that the combined analysis of ACTN3 R577X and ACE I/D polymorphisms may serve as a predictor for the risk of severe obesity in children. These data can contribute to a better understanding of the relationship between these polymorphisms and the body weight development of school-age children.
Keyphrases
- weight loss
- weight gain
- angiotensin converting enzyme
- insulin resistance
- metabolic syndrome
- type diabetes
- high fat diet induced
- angiotensin ii
- body weight
- body mass index
- young adults
- genome wide
- electronic health record
- skeletal muscle
- early onset
- big data
- dna methylation
- copy number
- adipose tissue
- high throughput
- cell proliferation
- machine learning
- cell death
- mass spectrometry
- endoplasmic reticulum stress
- cell free
- atomic force microscopy
- single cell
- cell cycle arrest