解锁哈普托格洛宾多态和非传染性人类疾病之间的联系:见解和影响
Joris R Delanghe1, Charlotte Delrue2, Reinhart Speeckaert3
1Department of Diagnostic Sciences, Ghent University, Ghent, Belgium.
Critical reviews in clinical laboratory sciences
|November 28, 2023
概括
哈普特球蛋白 (Hp) 基因变异影响健康. Hp 2-2表型与更高的疾病风险有关,而 Hp 1-1表型可能由于抗氧化和抗炎性质而提供保护.
科学领域:
- 生物化学 生物化学
- 遗传学 遗传学 是一个
- 免疫学 免疫学 免疫学
背景情况:
- 黑血球蛋白 (Hp) 是一种血红蛋白结合蛋白,对于清除自由血红蛋白,防止铁损失和抑制血红素诱导的氧化至关重要.
- 血在调节血管生成,氧化稳定,免疫反应和前列腺素合成方面发挥作用.
- 惠普基因的遗传变异导致不同的表型 (Hp 1-1,Hp 2-1,Hp 2-2),影响蛋白质功能和生物结果.
研究的目的:
- 审查当前对Haptoglobin (Hp) 基因多态性的理解.
- 探索HP表型与各种疾病之间的关联.
- 突出Hp多形态对健康和疾病的功能影响.
主要方法:
- 对调查哈普特蛋白 (Hp) 基因多态性的研究的文献综述.
- 对HP表型与诸如心血管疾病,炎症性肠病,癌症,移植和血红蛋白病等疾病之间的关联研究的分析.
- 检查Hp等位基因的功能作用,包括抗氧化,抗炎和免疫调节性质.
主要成果:
- Hp 2-2表型通常与疾病风险增加和预后较差有关.
- 具有Hp 2-2表型的个体通常在巨细胞上显示CD163表达的减少,这可能与血清抗氧化能力的降低有关.
- Hp 1-1表型可能具有保护作用,Hp1等位基具有显著的抗氧化,抗炎和免疫调节能力.
结论:
- 哈普特蛋白 (Hp) 基因多态性显著影响各种疾病的敏感性和结果.
- Hp 2-2表型与不良健康结果有关,可能是由于抗氧化剂防御机制受损.
- 这种Hp1等位基因表现出有益的特性,但其保护作用取决于环境,因遗传,环境和疾病特异性因素而有所不同.
更多相关视频
07:26High-resolution Melting PCR for Complement Receptor 1 Length Polymorphism Genotyping: An Innovative Tool for Alzheimer's Disease Gene Susceptibility Assessment
Published on: July 18, 2017
11.9K
08:07Personalized Peptide Arrays for Detection of HLA Alloantibodies in Organ Transplantation
Published on: September 6, 2017
10.1K
相关概念视频
Multiple Allele Traits
34.3K
The Concept of Multiple Allelism
34.3K
Single Nucleotide Polymorphisms-SNPs
15.1K
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,...
15.1K
Genome-wide Association Studies-GWAS
13.5K
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...
13.5K
Genetic Lingo
102.9K
Overview
102.9K
Gene Families
8.8K
Gene families consist of groups of genes proposed to have originated from a common ancestor. Typically these arise through events in which a gene or genes are mistakenly duplicated during cell division. Unlike their parent genes (which are subject to selection pressure to maintain function), these gene copies do not need to preserve their sequences and may evolve at a relatively faster rate.
Occasionally these regions can be adapted to take on new roles within the organism, becoming novel genes...
Occasionally these regions can be adapted to take on new roles within the organism, becoming novel genes...
8.8K
Blood Types
17.7K
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...
17.7K
