Ukraintseva Svetlana, Yashkin Arseniy P, Akushevich Igor, Arbeev Konstantin, Duan Hongzhe, Gorbunova Galina, Stallard Eric, Yashin Anatoliy
Biodemography of Aging Research Unit, Social Science Research Institute, Duke University, Durham, NC, USA.
Biodemography of Aging Research Unit, Social Science Research Institute, Duke University, Durham, NC, USA.
Exp Gerontol. 2024 Jun 1;190:112411. doi: 10.1016/j.exger.2024.112411. Epub 2024 Apr 2.
Diverse pathogens (viral, bacterial, fungal) have been associated with Alzheimer's disease (AD) and related traits in various studies. This suggests that compromised immunity, rather than specific microbes, may play a role in AD by increasing an individual's vulnerability to various infections, which could contribute to neurodegeneration. If true, then vaccines that have heterologous effects on immunity, extending beyond protection against the targeted disease, may hold a potential for AD prevention.
We evaluated the associations of common adult infections (herpes simplex, zoster (shingles), pneumonia, and recurrent mycoses), and vaccinations against shingles and pneumonia, with the risks of AD and other dementias in a pseudorandomized sample of the Health and Retirement Study (HRS).
Shingles, pneumonia and mycoses, diagnosed between ages 65 and 75, were all associated with significantly increased risk of AD later in life, by 16 %-42 %. Pneumococcal and shingles vaccines administered between ages 65-75 were both associated with a significantly lower risk of AD, by 15 %-21 %. These effects became less pronounced when AD was combined with other dementias.
Our findings suggest that both the pneumococcal polysaccharide vaccine and the live attenuated zoster vaccine can offer significant protection against AD. It remains to be determined if non-live shingles vaccine has a similar beneficial effect on AD. This study also found significant associations of various infections with the risk of AD, but not with the risks of other dementias. This indicates that vulnerability to infections may play a more significant role in AD than in other types of dementia, which warrants further investigation.
在各项研究中,多种病原体(病毒、细菌、真菌)都与阿尔茨海默病(AD)及相关特征有关。这表明免疫功能受损,而非特定微生物,可能通过增加个体对各种感染的易感性在AD中发挥作用,而这可能导致神经退行性变。如果这一观点正确,那么对免疫具有异源效应、超出针对目标疾病保护范围的疫苗可能具有预防AD的潜力。
我们在健康与退休研究(HRS)的伪随机样本中,评估了常见成人感染(单纯疱疹、带状疱疹、肺炎和复发性真菌病)以及针对带状疱疹和肺炎的疫苗接种与AD及其他痴呆症风险之间的关联。
65至75岁之间诊断出的带状疱疹、肺炎和真菌病,均与晚年AD风险显著增加相关,增幅为16% - 42%。65至75岁之间接种的肺炎球菌疫苗和带状疱疹疫苗均与AD风险显著降低相关,降幅为15% - 21%。当将AD与其他痴呆症合并时,这些效应变得不那么明显。
我们的研究结果表明,肺炎球菌多糖疫苗和减毒活带状疱疹疫苗都能为AD提供显著保护。非活性带状疱疹疫苗对AD是否具有类似的有益效果仍有待确定。本研究还发现各种感染与AD风险之间存在显著关联,但与其他痴呆症风险无关。这表明对感染的易感性在AD中可能比在其他类型的痴呆症中发挥更重要的作用,这值得进一步研究。