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Published on: September 4, 2017
Harboring Cnm-expressing Streptococcus mutans in the oral cavity relates to both deep and lobar cerebral microbleeds
Shuhei Ikeda1,2,3, Satoshi Saito1,4,5, Satoshi Hosoki1
1Department of Neurology, National Cerebral and Cardiovascular Center, Suita, Japan.
Background:
Cerebral microbleeds (CMBs) influence long-term prognoses of stroke patients. Streptococcus mutans expressing the collagen-binding protein Cnm induces cerebrovascular inflammation, impairing blood brain barrier integrity and causing cerebral bleeding. Here, we examine the association of Cnm-positive S. mutans with CMBs.
Methods:
Acute stroke patients were selected from a single-center registry database. Oral carriage of Cnm-positive or Cnm-negative S. mutans was determined using polymerase chain reaction assays. The associations of Cnm-positive S. mutans with CMB number and specifically the presence of >10 CMBs were examined using quasi-Poisson and logistic regression models, respectively.
Results:
This study included 3154 stroke patients, of which 428 patients (median [interquartile range] age, 73.0 [63.0-81.0] years; 269 men [62.9%]) underwent oral bacterial examinations. In total, 326 patients harbored S. mutans. After excluding four patients without imaging data, we compared patients with Cnm-positive (n = 72) and Cnm-negative (n = 250) S. mutans. Harboring Cnm-positive S. mutans was independently associated with the presence of >10 CMBs (adjusted odds ratio 2.20 [1.18-4.10]) and higher numbers of deep and lobar CMBs (adjusted risk ratio 1.61 [1.14-2.27] for deep; 5.14 [2.78-9.51] for lobar), but not infratentorial CMBs, after adjusting for age, sex, hypertension, stroke type, National Institutes of Health Stroke Scale score, and cerebral amyloid angiopathy.
Conclusions:
Harboring Cnm-positive S. mutans was independently associated with a higher number of CMBs in deep and lobar locations. Reducing Cnm-positive S. mutans in the oral cavity may serve as a novel therapeutic approach for stroke.
Insights
Presence of Cnm-positive Streptococcus mutans in the mouth is linked to more cerebral microbleeds (CMBs) in stroke patients. Targeting this oral bacterium may offer a new stroke treatment strategy.
Area of Science:
- Neurology
- Infectious Diseases
- Cardiovascular Research
Background:
- Cerebral microbleeds (CMBs) significantly impact stroke patient prognoses.
- Streptococcus mutans, via its collagen-binding protein Cnm, can cause cerebrovascular inflammation and impair blood-brain barrier integrity, leading to cerebral bleeding.
- This study investigates the direct association between Cnm-positive S. mutans and the occurrence of CMBs.
Purpose of the Study:
- To determine the association between oral carriage of Cnm-positive Streptococcus mutans and the presence and number of cerebral microbleeds in acute stroke patients.
- To explore potential therapeutic targets for reducing CMBs in stroke survivors.
Main Methods:
- A cohort of acute stroke patients was analyzed from a single-center registry.
- Oral bacterial samples were tested for Cnm-positive and Cnm-negative S. mutans using polymerase chain reaction (PCR).
- Quasi-Poisson and logistic regression models were employed to assess the association between Cnm-positive S. mutans and CMB counts, including the presence of >10 CMBs, while controlling for confounding factors.
Main Results:
- The study included 428 patients for oral bacterial examination, with 326 found to harbor S. mutans.
- Patients with Cnm-positive S. mutans (n=72) showed a significant independent association with a higher number of CMBs, particularly in deep and lobar locations.
- Specifically, Cnm-positive S. mutans was linked to the presence of >10 CMBs (adjusted odds ratio 2.20) and increased counts of deep (adjusted risk ratio 1.61) and lobar CMBs (adjusted risk ratio 5.14).
Conclusions:
- Harboring Cnm-positive Streptococcus mutans is independently associated with an increased number of cerebral microbleeds in deep and lobar brain regions.
- Reducing the burden of Cnm-positive S. mutans in the oral cavity presents a potential novel therapeutic strategy for managing and preventing CMBs in stroke patients.
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