Abstract

It is established that chronic spirochetal infection can cause slowly progressive dementia, brain atrophy and amyloid deposition in late neurosyphilis. Recently it has been suggested that various types of spirochetes, in an analogous way to Treponema pallidum, could cause dementia and may be involved in the pathogenesis of Alzheimer's disease (AD). Here, we review all data available in the literature on the detection of spirochetes in AD and critically analyze the association and causal relationship between spirochetes and AD following established criteria of Koch and Hill. The results show a statistically significant association between spirochetes and AD (P = 1.5 × 10-17, OR = 20, 95% CI = 8-60, N = 247). When neutral techniques recognizing all types of spirochetes were used, or the highly prevalent periodontal pathogen Treponemas were analyzed, spirochetes were observed in the brain in more than 90% of AD cases. Borrelia burgdorferi was detected in the brain in 25.3% of AD cases analyzed and was 13 times more frequent in AD compared to controls. Periodontal pathogen Treponemas (T. pectinovorum, T. amylovorum, T. lecithinolyticum, T. maltophilum, T. medium, T. socranskii) and Borrelia burgdorferi were detected using species specific PCR and antibodies. Importantly, co-infection with several spirochetes occurs in AD. The pathological and biological hallmarks of AD were reproduced in vitro by exposure of mammalian cells to spirochetes. The analysis of reviewed data following Koch's and Hill's postulates shows a probable causal relationship between neurospirochetosis and AD. Persisting inflammation and amyloid deposition initiated and sustained by chronic spirochetal infection form together with the various hypotheses suggested to play a role in the pathogenesis of AD a comprehensive entity. As suggested by Hill, once the probability of a causal relationship is established prompt action is needed. Support and attention should be given to this field of AD research. Spirochetal infection occurs years or decades before the manifestation of dementia. As adequate antibiotic and anti-inflammatory therapies are available, as in syphilis, one might prevent and eradicate dementia.

Highlights

  • The recognition that pathogens can produce slowly progressive chronic diseases has resulted in a new concept of infectious diseases

  • The significantly higher frequency of B. burgdorferi in the brain of Alzheimer’s disease (AD) patients, the high risk factor and the results of the multifaceted analysis in three AD patients with concurrent Lyme neuroborreliosis, where B. burgdorferi was cultivated from the brain and species specific antigens and DNA were present in the cerebral cortex show that B. burgdorferi is involved in the pathogenesis of a subset of AD cases [85]

  • The association between periodontal pathogen spirochetes and AD was statistically significant as well (Table 1, Figure 2). They were detected in the brain in 93.7% of AD. These results show a strong, statistically significant association between spirochetes and AD and show that these microorganisms represent a strong risk for AD

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Summary

Introduction

The recognition that pathogens can produce slowly progressive chronic diseases has resulted in a new concept of infectious diseases. Using species-specific PCR, B. burgdorferi DNA was detected in the brains in 5 of 16 AD patients and in one of 18 controls [96] In these 6 positive cases (5 AD and 1 control) B. burgdorferi co-infected with oral Treponema spirochetes. The significantly higher frequency of B. burgdorferi in the brain of AD patients, the high risk factor and the results of the multifaceted analysis in three AD patients with concurrent Lyme neuroborreliosis, where B. burgdorferi was cultivated from the brain and species specific antigens and DNA were present in the cerebral cortex show that B. burgdorferi is involved in the pathogenesis of a subset of AD cases [85]. The analysis of historic and recent data available in the literature following Koch’s and Hill’s criteria is in favor of a causal relationship between neurospirochetosis and AD

Conclusions
Chiu B
17. Martin RJ
34. Koch R
59. Perusini G
66. Volland W
70. Miklossy J
81. Miklossy J
84. Miklossy J: Chronic inflammation and amyloidogenesis in Alzheimer’s disease
86. Miklossy J
93. Mattman LH
Findings
99. MacDonald AB
Full Text
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