评论"一个常见的遗传变异与成人和儿童肥胖有关"
Ruth J F Loos1, Inês Barroso, Stephen O'rahilly
1Medical Research Council Epidemiology Unit, Cambridge, UK. ruth.loos@mrc-epid.cam.ac.uk
概括
在INSIG2基因附近的rs7566605遗传变异之前与更高的体重指数 (BMI) 有关. 我们的研究没有发现这种变体与大型队列中的BMI之间存在关联,这表明遗传发现可能存在差异.
科学领域:
- 遗传学 是一个遗传学.
- 代谢健康 代谢健康
- 人口研究 人口研究
背景情况:
- rs7566605单核酸多态 (SNP) 位于胰岛素诱导基因2 (INSIG2) 基因的上游.
- 以前的研究表明rs7566605与增加的体重指数 (BMI) 之间存在一致的关联.
研究的目的:
- 调查rs7566605遗传变异与身体质量指数 (BMI) 之间的关联.
- 验证或反驳赫伯特等人的发现. 关于rs7566605-BMI在独立队列中的协会.
主要方法:
- 来自两个大型,种族同质的基于人口的队列的遗传数据的分析.
- 对 rs7566605 变种的基因型定型.
- 统计分析以确定遗传变异与测量BMI之间的关联.
主要成果:
- 在任何一个队列中都没有发现rs7566605变体和BMI之间存在统计学上显著的关联证据.
- 观察到与之前报告的关联相反的趋势,尽管在统计学上并不显著.
结论:
- 赫伯特等人报告的rs7566605变种与BMI之间的关联. 在这些大,均质的群体中没有复制.
- 需要进一步的研究,以澄清rs7566605变异在人体质量调节中的作用和潜在的人口特异性影响.
相关概念视频
Human Genetics
Human genetics provides a profound framework for understanding the interplay between genetic predispositions and human psychology. At the heart of this discipline lies the study of how genes influence physical traits, behaviors, and susceptibility to diseases. Each person carries a unique genetic code that subtly or significantly shapes their psychological and behavioral landscape.
The complex relationship between genetics and psychology is observable through common biological components such...
The complex relationship between genetics and psychology is observable through common biological components such...
Obesity
The Body Mass Index (BMI) is a numerical value derived from a person's weight and height, used to categorize individuals into weight ranges. It is calculated using the formula: weight in kilograms divided by height in meters squared. Obesity is a health condition characterized by excessive accumulation of adipose tissue that poses health risks, often diagnosed with a BMI ≥ 30. This excess fat storage occurs when surplus dietary calories are converted into triglycerides and stored in adipocytes...
Genome-wide Association Studies-GWAS
Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
GWAS does not require the identification of the target gene involved in...
Polygenic Traits
When more than one gene is responsible for a given phenotype, the trait is considered polygenic. Human height is a polygenic trait. Studies have uncovered hundreds of loci that influence height, and there are believed to be many more. Due to the high number of genes involved, as well as environmental and nutritional factors, height varies significantly within a given population. The distribution of height forms a bell-shaped curve, with relatively few individuals in the population at the...
Polygenic Traits
When more than one gene is responsible for a given phenotype, the trait is considered polygenic. Human height is a polygenic trait. Studies have uncovered hundreds of loci that influence height, and there are believed to be many more. Due to the high number of genes involved, as well as environmental and nutritional factors, height varies significantly within a given population. The distribution of height forms a bell-shaped curve, with relatively few individuals in the population at the...
Principles of Pharmacogenetics: Types of Genetic Variants
The human genome is over 99.9% identical between individuals, yet genetic differences exist at millions of bases. The human genome contains approximately 3 million variant positions per individual, many of which are heterozygous, contributing to genetic diversity and individual traits. Genetic variations include single-nucleotide polymorphisms (SNPs), insertions, deletions, and copy number variations (CNVs).SNPs, the most common variation, involve single-base changes in DNA. These can be...

