炎症易感基因与中国儿童近视的关联
Xuhui Liu1, Xiaofeng Hu2, Yi Zhen3
1Department of General Ophthalmology, Chinese PLA General Hospital, Beijing, China.
International ophthalmology
|October 25, 2025
概括
炎症相关基因的遗传变异与中国儿童高近视有关. 特定的单核酸多态 (SNP) 可能作为早期指标来识别患有高近视风险的儿童.
科学领域:
- 眼科医生 眼科 眼科
- 遗传学 遗传学是一种遗传学.
- 分子生物学分子生物学
背景情况:
- 高近视是全球范围内一个重大的公共卫生问题.
- 遗传因素在折射误差的发展中起着至关重要的作用,包括高近视.
- 了解高近视的遗传基础对于早期发现和干预至关重要.
研究的目的:
- 研究与炎症相关的基因中的单核酸多态 (SNP) 与中国儿童高近视之间的关联.
- 为了确定潜在的遗传标记,以便早期识别高近视风险.
主要方法:
- 一组458名中国学生 (年龄在10-13岁) 患有高近视或视,对47个向SNP进行了基因定型.
- 在SNP基因定型中使用了MassARRAY平台.
- 进行了物流回归和哈普洛型分析,以评估SNP和高近视之间的关联.
主要成果:
- 与炎症相关的基因中的几个SNP,包括CCL2,TGFβ1,MMP1,IL1RN和IL1β,与高近视相关.
- 在CCL2和TGFβ1中,特定的单元类型分别被确定为风险和保护因素.
结论:
- 与炎症相关的基因的多态性与中国儿童高近视的发病有关.
- 这些遗传变异可能作为预测高近视发展的有价值的生物标志物.
相关概念视频
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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,...
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At the molecular level, visual signals trigger transformations in photopigment molecules, resulting in changes in the photoreceptor cell's membrane potential. The photon's energy level is denoted by its wavelength, with each specific wavelength of visible light associated with a distinct color. The spectral range of visible light, classified as electromagnetic radiation, spans from 380 to 720 nm. Electromagnetic radiation wavelengths exceeding 720 nm fall under the infrared category, whereas...


