人类乳头瘤病毒基因型特异性流行率和感染风险:美国10年人口研究
Cosette M Wheeler1,2, Rachael Adcock1, William C Hunt1
1Center for HPV Prevention, University of New Mexico Comprehensive Cancer Center, Albuquerque, NM 87131, United States.
Journal of the National Cancer Institute
|December 10, 2024
概括
四价人乳头瘤病毒 (HPV) 疫苗显著降低了HPV-16/18的流行率和高度状内皮病变. 然而,非疫苗HPV类型的增加可能会影响未来的减少,尽管疫苗接种的好处仍然很大.
科学领域:
- 流行病学 流行病学
- 疫苗学 疫苗学 疫苗学
- 公共卫生 公共卫生
背景情况:
- 人类乳头瘤病毒 (HPV) 疫苗对基因型特异分布的影响正在调查中.
- 这项研究在美国引入四价HPV疫苗十年后,对HPV基因型流行率进行了最大的基于人口的分析.
研究的目的:
- 在实施四价HPV疫苗 (针对HPV-6/11/16/18) 之后,评估HPV的基因型特异性流行率.
- 评估疫苗对HPV感染率和癌前宫病变的影响.
主要方法:
- 来自新墨西哥州15-30岁的宫细胞学样本使用广谱HPV基因型鉴定进行了分析.
- 在HPV类型特定患病率的加权相对差异是通过比较2007-2009年与2013-2016年的数据来计算的.
- 权重后勤回归估计了特定类型的HPV感染的相对风险.
主要成果:
- 在HPV-16,HPV-18,HPV-31和HPV-33的流行率中观察到显著的减少.
- 其他致癌型HPV的患病率 (不包括HPV-16/18) 增加了19.5%.
- 2007年至2018年,高度状内皮层病变或更严重的病变在2007年至2018年期间减少了49.4%.
结论:
- 四价HPV疫苗导致疫苗型HPV患病率和癌前病变的实质性减少.
- 非疫苗HPV基因型的增加可能会部分抵消未来HPV相关异常的减少.
- 尽管一些非疫苗类型的疫苗增加,但HPV疫苗接种的整体益处仍然很大.
相关概念视频
Cancer Prevention
6.1K
Several factors can increase the risk of cancer in an individual. About 50% of cancer cases can be prevented by adopting a healthy lifestyle, regular exercise, eating healthy, and following a modest cancer prevention diet. Epidemiological studies have consistently shown that populations with vegetable and fruit-rich diets have reduced the incidence of cancer. On the other hand, populations who have a diet rich in animal fat, red meat, junk food, or high calories are predisposed to cancer.
Some...
Some...
6.1K
Sexually Transmitted Infections
271
Sexually transmitted infections (STIs) are diseases transmitted primarily through unsafe sexual interactions. Bacteria, viruses, or parasites cause them and can result in severe health complications if untreated.ChlamydiaThe bacterium Chlamydia trachomatis is responsible for the disease Chlamydia, the most common STI in the United States. This peculiar pathogen requires human cells to reproduce, residing intracellularly. The initial infection often goes unnoticed because it typically does not...
271
Single Nucleotide Polymorphisms-SNPs
14.0K
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,...
14.0K


