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Sample Preparation to Bioinformatics Analysis of DNA Methylation: Association Strategy for Obesity and Related Trait Studies
Published on: May 6, 2022
SAA1 gene variants and childhood obesity in China
Xiao Zhang1, Qi-Zhu Tang, Ai-Ying Wan
1Department of Pediatric, RenMin Hospital of Wuhan University, Jie Fang Road, Wuchang district, Wuhan 430060, China. xiaozhan_g@163.com.
Insights
Obesity in children is linked to SAA1 gene variations. Specific SAA1 polymorphisms, particularly rs4638289, were more frequent in obese children and correlated with higher SAA plasma levels.
Area of Science:
- Genetics
- Pediatrics
- Metabolic Health
Background:
- Obesity is a risk factor for insulin resistance and metabolic syndrome in children.
- Serum amyloid A (SAA) is an apolipoprotein crucial for glucose and lipid homeostasis.
Purpose of the Study:
- To investigate the association between SAA1 gene allelic variants and obesity in school-age children.
- To explore the role of SAA1 polymorphisms in pediatric obesity and metabolic parameters.
Main Methods:
- Study included 520 children aged 5-15 years, categorized as obese (BMI z score ≥1.65) or non-obese.
- Genotyping of four SAA1 gene SNPs (rs12218, rs4638289, rs7131332, rs11603089) using PCR-RFLP.
- Analysis of SAA levels, LDL-C, TG, and TC concentrations in relation to obesity and genotypes.
Main Results:
- Obese children exhibited higher circulating SAA, LDL-C, TG, and TC levels compared to non-obese children.
- Increased frequency of SAA1 polymorphisms rs12218 and rs4638289 was observed in obese children.
- The rs4638289 polymorphism was significantly associated with elevated SAA plasma levels.
Conclusions:
- SAA1 genetic polymorphisms are associated with obesity in Chinese children.
- The rs4638289 variant may contribute to increased SAA levels and obesity risk.
Background:
Obesity increases the risk for insulin resistance and metabolic syndrome in both adults and children. SAA is a member of apolipoprotein and plays an important role in maintaining glucose and lipid homeostasis. The purpose of this study was to assess SAA1 allelic variants with obesity in young school-age children.
Methods:
A total of 520 consecutive children ages 5-15 years were recruited. Children were divided based on BMI z score into Obese (OB; BMI z score ≥1.65; n = 253) and non-obese (NOB; n = 267). Four SNPs of the human SAA1 gene (rs12218, rs4638289, rs7131332 and rs11603089) were genotyped by use of polymerase chain reaction - restriction fragment length polymorphism (PCR-RFLP) method.
Results:
Compared to NOB, circulating SAA levels were increased in OB, as were LDL-C, TG and TC concentration. Obese children showed increased frequency of rs12218 and rs4638289 polymorphism compared to control children. There were no differences between OB and NOB for the other 2 polymorphisms. Only the rs4638289 polymorphism showed significant contributions to higher SAA plasma levels.
Conclusions:
SAA1 genetic polymorphism was associated with obesity in Chinese children.
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