没有证据表明ACE2或TMPRSS2在COVID风险方面推动了人口差异
Nathaniel M Pearson1, John Novembre2
1Root Deep Insight, Boston, MA, USA. nathaniel.pearson@gmail.com.
BMC medicine
|August 25, 2024
概括
早期研究表明,ACE2和TMPRSS2基因变异在某些人群中增加了COVID-19风险. 这项研究澄清了采样偏差,而不是遗传差异,创造了这种外观,其他基因是更重要的风险因素.
科学领域:
- 遗传学和基因组学 遗传学和基因组学
- 流行病学 流行病学
- 传染病研究传染病研究.
背景情况:
- 最初的研究表明,ACE2和TMPRSS2的特定人群遗传变异影响了COVID-19风险.
- 这些早期的解释依赖于预测工具和潜在的罕见变异,而不是临床结果.
相关概念视频
Single Nucleotide Polymorphisms-SNPs
14.9K
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,...
14.9K
Gene Flow
35.0K
Gene flow is the transfer of genes among populations, resulting from either the dispersal of gametes or from the migration of individuals.
35.0K
Retroviruses
12.2K
Retroviruses and retrotransposons both insert copies of their genetic elements into the genome of the host cell. Thus, the viral genes are passed on when the host genome is replicated or translated. A typical retroviral DNA sequence contains 3-4 genes that encode the different proteins required for its structural assembly and function as a molecular parasite. This DNA is transcribed into a single mRNA, which is very similar in structure to conventional mRNAs, i.e., it is capped at the 5’...
12.2K


