在ACE基因I/D多态的插入等位基因. 抗胰岛素的一个候选基因?
A Panahloo1, C Andrès, V Mohamed-Ali
1Department of Medicine, University College London Medical School, Whittington Hospital, England.
Circulation
|December 15, 1995
概括
血管氨酸转化酶 (ACE) 删除基因型 (DD) 与冠心病 (CHD) 风险增加有关. 这项研究没有发现与胰岛素抵抗有任何关联,但在具有DD基因型的NIDDM受试者中显示胰岛素敏感性增加.
科学领域:
- 遗传学 是一个遗传学.
- 心血管疾病 心血管疾病
- 代谢综合征是代谢综合征的一种.
背景情况:
- 血管激素转化酶 (ACE) 插入/删除 (ID) 多态与冠心病 (CHD) 有关,但潜在的机制尚不清楚.
- 这项研究调查了ACE基因缺失等位基因与胰岛素抵抗之间的潜在关联.
研究的目的:
- 测试该假设,即ACE基因的删除等位基因与胰岛素抵抗有关.
- 探索ACE基因型与胰岛素抵抗综合征的组成部分之间的关系.
主要方法:
- 进行了ACE插入/删除 (ID) 多态的基因定型.
- 在103名非胰岛素依赖型糖尿病患者 (NIDDM) 和533名非糖尿病白人受试者中测量了胰岛素敏感性,胰岛素水平和des 31,32的亲胰岛素.
- 分析包括ANOVA和HOMA%计算.
主要成果:
- 与ID和II基因型相比,具有DD基因型的NIDDM受试者表现出明显较低的特定胰岛素水平.
- 不接受胰岛素治疗的DD基因型受试者表现出胰岛素敏感性增加和更低的亲胰岛素水平.
- 在糖尿病或非糖尿病组中,在ACE基因型之间没有观察到心脏病发病率,血压,血清脂质或PAI-1活性的显著差异.
结论:
- 与ACE DD基因型相关的心血管风险增加并非由胰岛素抵抗或纤维素分解异常介导.
- 在携带ACE DD基因型的NIDDM受试者中观察到胰岛素敏感性增加.
相关概念视频
Multiple Allele Traits
The Concept of Multiple Allelism
Cell Specific Gene Expression
Multicellular organisms contain a variety of structurally and functionally distinct cell types, but the DNA in all the cells originated from the same parent cells. The differences in the cells can be attributed to the differential gene expression. Liver cells, whose functions include detoxification of blood, production of bile to metabolize fats, and synthesis of proteins essential for metabolism, must express a specific set of genes to perform their functions. Gene expression also varies with...
Epistasis Analysis
Although Mendel chose seven unrelated traits in peas to study gene segregation, most traits involve multiple gene interactions that create a spectrum of phenotypes. When the interaction of various genes or alleles at different locations influences a phenotype, this is called epistasis. Epistasis often involves one gene masking or interfering with the expression of another (antagonistic epistasis). Epistasis often occurs when different genes are part of the same biochemical pathway. The...
Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase
Genetic polymorphisms in drug targets have emerged as critical determinants of interindividual variability in drug response and toxicity. Pharmacogenomic investigations increasingly focus on identifying these variations to personalize and optimize therapeutic interventions. A drug target may be a receptor, enzyme, or signaling protein involved in pharmacologic responses or disease-related pathways. While early pharmacogenetic studies focused primarily on drug metabolism, current research...
Insulin: The Receptor and Signaling Pathways
Insulin action is mediated through a receptor tyrosine kinase, akin to the IGF-1 receptor. The number of receptors per cell varies significantly, from 40 on erythrocytes to 300,000 on adipocytes and hepatocytes. The insulin receptor consists of linked α/β subunit dimers, forming a heterotetramer glycoprotein with two extracellular α subunits and two β subunits spanning the membrane. The α subunits inhibit the inherent tyrosine kinase activity of the β subunits, but this inhibition is released...
Type II Diabetes I: Introduction
Type 2 diabetes mellitus (T2DM) is a chronic metabolic disorder characterized by insulin resistance, in which target tissues such as the liver, muscle, and adipose tissue respond poorly to insulin. It is also associated with inadequate compensatory insulin secretion, where pancreatic β-cells fail to produce sufficient insulin. Together, these abnormalities lead to persistent hyperglycemia.EtiologyT2DM develops through a complex interaction of genetic predisposition and environmental or...


