Cognitive dysfunction in young subjects with periodontal disease.

TitleCognitive dysfunction in young subjects with periodontal disease.
Publication TypeJournal Article
Year of Publication2021
AuthorsHategan SI, Kamer SA, Craig RG, Sinescu C, de Leon MJ, Jianu DC, Marian C, Bora BI, Dan T-F, Birdac CD, Marcu A, Kamer AR, Negrutiu MLavinia
JournalNeurol Sci
Volume42
Issue11
Pagination4511-4519
Date Published2021 Nov
ISSN1590-3478
KeywordsAged, Alzheimer Disease, Cognitive Dysfunction, Cross-Sectional Studies, Female, Humans, Male, Mental Status and Dementia Tests, Neuropsychological Tests, Periodontal Diseases
Abstract

BACKGROUND: Periodontal disease is an inflammatory, dysbiotic condition. Studies have shown that in the elderly, periodontal disease was associated with cognitive dysfunction and Alzheimer's disease.

OBJECTIVE: To investigate whether young healthy subjects with periodontal disease have lower cognition compared to those without periodontal disease. The salivary cytokines (IL-1β, TNF-α) levels in relation to cognition were also tested.

METHODS: In a monocenter, cross-sectional study, forty subjects [mean age (SD) = 34 (5) and 48% female] from western Romania were classified into periodontal disease conditions using radiographic assessment: 10 subjects had aggressive periodontitis (AGG_P), 20 chronic mild-moderate periodontitis (CR_P), and 10 no periodontitis (NL_P). Neuropsychological assessment performed by standardized neurologists and psychologist included Rey Auditory Verbal Learning Test (RAVLT), Montreal Cognitive Assessment test (MOCA), Mini-Mental State Examination (MMSE), and Prague tests. Salivary cytokines levels were determined by ELISA.

RESULTS: RAVLT and MOCA delayed recall scores were lower in AGG_P group compared to NL_P and CR_P. The learning curve was also different with subjects with AGG_P showing reduced learning performance. Contrary to our hypothesis, salivary IL-1β associated with immediate but not delayed cognitive scores.

CONCLUSIONS: These results showed for the first time that subjects with AGG_P had cognitive dysfunction and IL-1β may play a role in this process.

DOI10.1007/s10072-021-05115-3
Alternate JournalNeurol Sci
PubMed ID33606127
PubMed Central IDPMC8519837
Grant ListP30 AG066512 / AG / NIA NIH HHS / United States
Related Institute: 
Brain Health Imaging Institute (BHII)

Weill Cornell Medicine
Department of Radiology
525 East 68th Street New York, NY 10065