Laboratory of Epidemiology and Population Sciences, National Institutes on Aging, NIA/NIH/IRP, Baltimore, MD, USA.
Fort Belvoir Community Hospital, Fort Belvoir, VA, USA.
Mol Psychiatry. 2021 Oct;26(10):6038-6053. doi: 10.1038/s41380-020-0736-2. Epub 2020 May 4.
Co-infection between Helicobacter pylori (Hp) and groups of periodontal pathogens may alter the onset of Alzheimer's disease (AD) and all-cause dementia. We examined the interactive associations among Hp sero-positivity, periodontal disease (Pd), and infections with incident AD and all-cause dementia, among older adults (≥65 years at baseline). Up to 1431 participants from phase 1 of the National Health and Nutrition Survey III (1988-1991) had complete data till January 1st, 2014 on Hp sero-positivity with a mean follow-up of 10-11 years for AD and all-cause dementia incidence. Exposures consisted of 19 periodontal pathogens, constructed factors and clusters, and two Pd markers- probing depth and clinical attachment loss (CAL). Cox proportional hazards models were performed. Around 55% of the selected sample was Hp. We found that Prevotella intermedia, Campylobacter Rectus, Factor 2 (Pi/Prevotella nigrescens/Prevotella melaninogenica), and the Orange-Red cluster interacted synergistically with Hp sero-positivity, particularly with respect to AD incidence. The presence of higher levels of Actinomyces Naeslundii (An) enhanced the effect of being Hp on both AD and all-cause dementia incidence. In contrast, Fusobacterim nucleatum (Fn), and Factor 1 (which included Fn), exhibited an antagonistic interaction with Hp in relation to all-cause dementia. Both probing depth and CAL had direct associations with all-cause dementia among Hp individuals, despite nonsignificant interaction. Selected periodontal pathogen titers, factors, and clusters interacted mostly synergistically, with Hp sero-positivity, to alter the risk of AD and all-cause dementia. Ultimately, a randomized controlled trial is needed, examining effects of co-eradication of Hp and select periodontal pathogens on neurodegenerative disease.
幽门螺杆菌(Hp)与牙周病病原体群的合并感染可能改变阿尔茨海默病(AD)和全因痴呆的发病。我们研究了 Hp 血清阳性、牙周病(Pd)与 AD 和全因痴呆发病之间的相互关联,研究对象为年龄在 65 岁及以上的老年人(基线时)。截至 2014 年 1 月 1 日,来自美国国家健康和营养调查 III 期(1988-1991 年)第 1 阶段的 1431 名参与者完成了 Hp 血清阳性的完整数据,其 AD 和全因痴呆的平均随访时间为 10-11 年。暴露因素包括 19 种牙周病原体、构建因子和聚类,以及 Pd 标志物——探诊深度和临床附着丧失(CAL)。采用 Cox 比例风险模型进行分析。所选样本中约有 55%的人感染了 Hp。我们发现中间普雷沃菌、直肠弯曲菌、因子 2(Pi/普雷沃菌属/黑色素普雷沃菌)和橙色-红色聚类与 Hp 血清阳性呈协同作用,特别是与 AD 发病相关。较高水平的放线菌(An)的存在增强了 Hp 对 AD 和全因痴呆发病的影响。相比之下,核梭杆菌(Fn)和因子 1(包含 Fn)与 Hp 之间存在拮抗作用,与全因痴呆发病相关。尽管交互作用不显著,但探诊深度和 CAL 与 Hp 个体的全因痴呆发病均存在直接关联。选定的牙周病原体滴度、因子和聚类主要与 Hp 血清阳性呈协同作用,改变 AD 和全因痴呆的发病风险。最终,需要开展一项随机对照试验,研究 Hp 和选定的牙周病原体共同根除对神经退行性疾病的影响。