在北印度人口中人类白细胞抗原基因多态的流行
Brijesh Yadav1, Narayan Prasad1, Ravi Shanker Kushwaha1
1Department of Nephrology and Kidney Transplantation, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Indian journal of nephrology
|September 2, 2025
概括
这项研究分析了北印度的人类白细胞抗原 (HLA) 的基因频率. HLA-A*01,HLA-B*35,HLA-C*07,HLA-DRB1*07和HLA-DQA1*03是最常见的等位基因,对移植匹配至关重要.
科学领域:
- 免疫遗传学
- 种群遗传学
背景情况:
- 人类白细胞抗原 (HLA) 对免疫反应和自我/非自我识别至关重要.
- 了解HLA多样性有助于器官移植匹配.
- 这项研究侧重于北印度人群中的HLA等位基因流行.
研究的目的:
- 追溯分析HLA-A, -B, -C, -DRB1和 -DQA1等位基因的频率.
- 为潜在的移植应用提供北印度HLA多样性的数据.
主要方法:
- 对2259名移植患者的HLA抗原等位基因数据的回顾性分析.
- 对HLA-A, -B, -DRB1 (n=2259), -C (n=759) 和 -DQA1 (n=751) 的频率确定
主要成果:
- 最常见的HLA-A基因组:HLA-A*01 (25. 41%)
- 最常见的HLA-B等位基因:HLA-B*35 (20.54%).
- 最常见的HLA-C等位基因:HLA-C*07 (28.06%).
- 最常见的HLA-DRB1等位基因:HLA-DRB1*07 (21.60%).
- 最常见的HLA-DQA1等位基因:HLA-DQA1*03 (35. 42%)
结论:
- 确定了北印度人口中最常见的HLA基因.
- 这些发现对优化器官捐赠者与受体匹配具有重要意义.
- 提供了对这一特定人口群体的重要免疫遗传数据.
相关概念视频
Multiple Allele Traits
34.8K
The Concept of Multiple Allelism
34.8K
Genome-wide Association Studies-GWAS
14.1K
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...
14.1K
Single Nucleotide Polymorphisms-SNPs
15.8K
A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
15.8K
Blood Types
18.2K
Human blood is classified into different types based on the presence of antigens on the red blood cell's surface and antibodies in the plasma. Proper identification of blood type is essential for successful blood transfusion. The International Society of Blood Transfusion has identified 38 human blood types based on the surface antigens on the red blood cells. The most common types are ABO, Rh, and MNS blood types.
ABO blood group
ABO antigens are glycoproteins encoded by genes present on...
ABO blood group
ABO antigens are glycoproteins encoded by genes present on...
18.2K
Comparing Copy Number Variations and SNPs
17.9K
Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
17.9K
What is Population Genetics?
59.5K
A population is composed of members of the same species that simultaneously live and interact in the same area. When individuals in a population breed, they pass down their genes to their offspring. Many of these genes are polymorphic, meaning that they occur in multiple variants. Such variations of a gene are referred to as alleles. The collective set of all the alleles within a population is known as the gene pool.
59.5K


