Can oral infection be a risk factor for Alzheimer's disease?

被引:127
作者
Olsen, Ingar [1 ]
Singhrao, Sim K. [2 ]
机构
[1] Univ Oslo, Fac Dent, Dept Oral Biol, NO-0316 Oslo, Norway
[2] Univ Cent Lancashire, Coll Clin & Biomed Sci, Oral & Dent Sci Res Grp, Preston PR1 2HE, Lancs, England
关键词
Alzheimer's disease; pathogenesis; microorganisms; oral bacteria; direct cause; HERPES-SIMPLEX-VIRUS; AMYLOID-BETA-PROTEIN; GENOME-WIDE ASSOCIATION; APOLIPOPROTEIN-E; TOOTH LOSS; PORPHYROMONAS-GINGIVALIS; COMPLEMENT ACTIVATION; CHLAMYDIA-PNEUMONIAE; COGNITIVE FUNCTION; TNF-ALPHA;
D O I
10.3402/jom.v7.29143
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Alzheimer's disease (AD) is a scourge of longevity that will drain enormous resources from public health budgets in the future. Currently, there is no diagnostic biomarker and/or treatment for this most common form of dementia in humans. AD can be of early familial-onset or sporadic with a late-onset. Apart from the two main hallmarks, amyloid-beta and neurofibrillary tangles, inflammation is a characteristic feature of AD neuropathology. Inflammation may be caused by a local central nervous system insult and/or by peripheral infections. Numerous microorganisms are suspected in AD brains ranging from bacteria (mainly oral and non-oral Treponema species), viruses (herpes simplex type I), and yeasts (Candida species). A causal relationship between periodontal pathogens and non-oral Treponema species of bacteria has been proposed via the amyloid-beta and inflammatory links. Periodontitis constitutes a peripheral oral infection that can provide the brain with intact bacteria and virulence factors and inflammatory mediators due to daily, transient bacteremias. If and when genetic risk factors meet environmental risk factors in the brain, disease is expressed, in which neurocognition may be impacted, leading to the development of dementia. To achieve the goal of finding a diagnostic biomarker and possible prophylactic treatment for AD, there is an initial need to solve the etiological puzzle contributing to its pathogenesis. This review therefore addresses oral infection as the plausible etiology of late-onset AD (LOAD).
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页数:16
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