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幽门螺杆菌、牙周病原体及其与大型全国性调查中全因和阿尔茨海默病痴呆症发病的交互关联。

Helicobacter pylori, periodontal pathogens, and their interactive association with incident all-cause and Alzheimer's disease dementia in a large national survey.

机构信息

Laboratory of Epidemiology and Population Sciences, National Institutes on Aging, NIA/NIH/IRP, Baltimore, MD, USA.

Fort Belvoir Community Hospital, Fort Belvoir, VA, USA.

出版信息

Mol Psychiatry. 2021 Oct;26(10):6038-6053. doi: 10.1038/s41380-020-0736-2. Epub 2020 May 4.

DOI:10.1038/s41380-020-0736-2
PMID:32366948
Abstract

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.

摘要

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。

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