Xie Min, Eyting Markus, Bommer Christian, Ahmed Haroon, Geldsetzer Pascal
Division of Primary Care and Population Health, Department of Medicine, Stanford University, Stanford, California, USA.
Heidelberg Institute of Global Health, Heidelberg University, Heidelberg, Germany.
medRxiv. 2024 Aug 23:2024.08.23.24312457. doi: 10.1101/2024.08.23.24312457.
The varicella zoster virus, a neurotropic herpesvirus, has been hypothesized to play a role in the pathophysiology of dementia, such as through neuroinflammatory processes or intracerebral vasculopathy. Using unique natural experiments, our group has previously found that live-attenuated herpes zoster (HZ) vaccination reduced the incidence of new diagnoses of dementia in both Wales and Australia. To inform further research and ultimately clinical care, it is crucial to understand at which stage of the disease course of dementia the HZ vaccine has its effect. Representing the two opposing ends of the dementia disease course as it can be ascertained from electronic health record data, the aims of this study were twofold: to determine the effect of HZ vaccination on i) new diagnoses of mild cognitive impairment (MCI) among individuals without any record of cognitive impairment, and ii) deaths due to dementia among individuals living with dementia. Our approach took advantage of the fact that at the time of the start date (September 1 2013) of the HZ vaccination program in Wales, individuals who had their eightieth birthday just after this date were eligible for HZ vaccination for one year whereas those who had their eightieth birthday just before were ineligible and remained ineligible for life. This eligibility rule created comparison groups just on either side of the September 2 1933 date-of-birth eligibility threshold who differed in their age by merely a week but had a large difference in their probability of receiving HZ vaccination. The key strength of our study is that these comparison groups should be similar in their health characteristics and behaviors except for a minute difference in age. We used regression discontinuity analysis to estimate the difference in our outcomes between individuals born just on either side of the date-of-birth eligibility threshold for HZ vaccination. Our dataset consisted of detailed country-wide electronic health record data from primary care in Wales, linked to hospital records and death certificates. We restricted our dataset to individuals born between September 1 1925 and September 1 1942. Among our study cohort of 282,557 without any record of cognitive impairment at baseline, HZ vaccination eligibility and receipt reduced the incidence of a new MCI diagnosis by 1.5 (95% CI: 0.5 - 2.9, p=0.006) and 3.1 (95% CI: 1.0 - 6.2, p=0.007) percentage points over nine years, respectively. Similarly, among our study cohort of 14,350 individuals who were living with dementia at baseline, being eligible for and receiving HZ vaccination reduced deaths due to dementia by 8.5 (95% CI: 0.6 - 18.5, p=0.036) and 29.5 (95% CI: 0.6 - 62.9, p=0.046) percentage points over nine years, respectively. Except for dementia, HZ vaccination did not have an effect on any of the ten most common causes of morbidity and mortality among adults aged 70 years and older in Wales in either of our two study cohorts. The protective effects of HZ vaccination for both MCI and deaths due to dementia were larger among women than men. Our findings suggest that the live-attenuated HZ vaccine has benefits for the dementia disease process at both ends of the disease course of dementia.
水痘带状疱疹病毒是一种嗜神经性疱疹病毒,据推测它在痴呆症的病理生理学中发挥作用,比如通过神经炎症过程或脑内血管病变。利用独特的自然实验,我们团队此前发现,减毒活带状疱疹(HZ)疫苗降低了威尔士和澳大利亚痴呆症新诊断病例的发生率。为了为进一步研究及最终的临床护理提供信息,了解HZ疫苗在痴呆症病程的哪个阶段发挥作用至关重要。鉴于从电子健康记录数据中可以确定痴呆症病程的两个相反端点,本研究的目的有两个:一是确定HZ疫苗对i)无任何认知障碍记录的个体中新诊断的轻度认知障碍(MCI)的影响,二是确定HZ疫苗对痴呆症患者中因痴呆症导致的死亡的影响。我们的方法利用了这样一个事实:在威尔士HZ疫苗接种计划开始日期(2013年9月1日)时,恰好在该日期之后过80岁生日的个体有资格接种HZ疫苗一年,而恰好在该日期之前过80岁生日的个体则没有资格且终生无资格。这一资格规则在1933年9月2日出生日期资格阈值的两侧创建了比较组,这两组年龄仅相差一周,但接种HZ疫苗的概率有很大差异。我们研究的关键优势在于,除了年龄上的微小差异外,这些比较组在健康特征和行为方面应该相似。我们使用回归断点分析来估计在HZ疫苗接种出生日期资格阈值两侧出生的个体在我们的研究结果上的差异。我们的数据集包括来自威尔士初级保健的详细全国电子健康记录数据,并与医院记录和死亡证明相链接。我们将数据集限制在1925年9月1日至1942年9月1日之间出生的个体。在我们282,557名基线时无任何认知障碍记录的研究队列中,HZ疫苗接种资格和接种在九年内分别将新MCI诊断的发生率降低了1.5(95%置信区间:0.5 - 2.9,p = 0.006)和3.1(95%置信区间:1.0 - 6.2,p = 0.007)个百分点。同样,在我们14,350名基线时患有痴呆症的研究队列中,有资格接种并接种HZ疫苗在九年内分别将因痴呆症导致的死亡降低了8.5(95%置信区间:0.6 - 18.5,p = 0.036)和29.5(95%置信区间:0.6 - 62.9,p = 0.046)个百分点。在我们的两个研究队列中,除了痴呆症外,HZ疫苗对威尔士70岁及以上成年人中十种最常见发病原因和死亡原因中的任何一种均无影响。HZ疫苗对MCI和因痴呆症导致的死亡的保护作用在女性中比男性更大。我们的研究结果表明,减毒活HZ疫苗在痴呆症病程的两端对痴呆症疾病进程均有益处。