HTSNPedia:高血压相关基因的分子视角和风险估计数据库
Jeyanthi Sankar1, Agnal Arumugam2, A Antony Prakash2
1Pharmacogenomics and CADD Lab, Department of Bioinformatics, Alagappa University, Karaikudi, Tamil Nadu, 630 003, India.
Biochemical genetics
|August 25, 2025
概括
这种全球性健康问题涉及复杂的遗传和表观遗传因素. 一个新的数据库,HTSNPedia,整合了与高血压相关的SNP,途径和风险因素的数据,以帮助药物发现.
科学领域:
- 遗传学和表观遗传学
- 心血管疾病研究
- 生物信息学
背景情况:
- 全球超过10亿成年人患有高血压,
- 关键的信号通路如RAAS,KKS和内甲蛋白系统都与高血压的发展有关.
- 了解这些复杂的相互作用对于有效的高血压管理至关重要.
研究的目的:
- 开发一个全面的高血压研究知识库.
- 整合有关SNP,生物途径,风险因素和药物基因组学的信息.
- 促进新型药物治疗高血压的识别.
主要方法:
- 使用HTML和Java开发了HTSNPedia数据库.
- 与高血压相关的单核酸多态 (SNP) 的综合数据.
- 包括有关生物途径,风险评估,分子机制和药物基因组学的信息.
主要成果:
- 创建了一个公开的数据库,HTSNPedia.
- 该数据库有助于整合各种与高血压相关的信息.
- 预计将提高识别新药物标的效率.
结论:
- HTSNPedia增强了与高血压相关的数据的整合.
- 对于高血压的分子基础有更深入的了解,
- 该数据库支持研究新型高血压疗法和个性化医疗.
相关概念视频
Hypertension II: Pathophysiology
77
Hypertension is a chronic condition in which the blood's force against artery walls is excessively high, posing risks such as heart disease. The condition's underlying mechanisms involve complex interactions among the cardiovascular, kidney, and autonomic nervous systems.Renin-Angiotensin-Aldosterone System (RAAS): This system significantly influences blood pressure regulation. When blood pressure decreases, the kidneys secrete renin. This enzyme transforms angiotensinogen, a plasma protein,...
77
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
Hypertension I: Introduction
74
Hypertension is a widespread, long-term medical condition where blood pressure in the arteries remains elevated. It is characterized by systolic blood pressure readings of 130 mm Hg or above or diastolic blood pressure (DBP) readings of 80 mm Hg or higher. Unmanaged hypertension poses significant health risks, making the distinction between primary (or essential) hypertension and secondary hypertension crucial, as their management and implications vary.Primary HypertensionPrimary hypertension,...
74
Blood Pressure
2.5K
Blood pressure (BP) is the pressure or force of blood exerted on the artery's walls as it circulates through the body. It is essential for maintaining blood flow throughout the body.
The average BP in an adult is typically around 120/80 mmHg (millimeters of mercury). In this measurement, the numerator (120) indicates the systolic pressure, which is the pressure in the arteries during the contraction of the heart's ventricles as blood is expelled. The denominator (80) represents the...
The average BP in an adult is typically around 120/80 mmHg (millimeters of mercury). In this measurement, the numerator (120) indicates the systolic pressure, which is the pressure in the arteries during the contraction of the heart's ventricles as blood is expelled. The denominator (80) represents the...
2.5K
Hypertension and Regulation of Blood Pressure
3.1K
Hypertension, the most common cardiovascular disease, is diagnosed through repeated measurements of elevated blood pressure. Its risks, including damage to the kidney, heart, and brain, are directly proportional to blood pressure levels. Starting from 115/75 mm Hg, the risk of cardiovascular disease doubles with each increment of 20/10 mm Hg. The diagnosis relies on blood pressure measurements, not on patient symptoms, as hypertension is often asymptomatic until end-organ damage is imminent or...
3.1K
Single Nucleotide Polymorphisms-SNPs
15.9K
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,...
15.9K


