Investigative Ophthalmology & Visual Science Cover Image for Volume 58, Issue 8
June 2017
Volume 58, Issue 8
Open Access
ARVO Annual Meeting Abstract  |   June 2017
Infection of A Keystone Bacterium in Periodontal Microbiota And Risk for Age-related Macular Degeneration
Author Affiliations & Notes
  • Chung-Jung Chiu
    Human Nutrition Res Ctr, Tufts University, Boston, Massachusetts, United States
  • Min-Lee Chang
    Human Nutrition Res Ctr, Tufts University, Boston, Massachusetts, United States
  • Allen Taylor
    Human Nutrition Res Ctr, Tufts University, Boston, Massachusetts, United States
  • Footnotes
    Commercial Relationships   Chung-Jung Chiu, None; Min-Lee Chang, None; Allen Taylor, None
  • Footnotes
    Support  RO1EY021826 (C-J.C.), RO1EY013250, RO1EY026979, and RO1EY021212 (A.T.) from the National Institutes of Health, the United States Department of Agriculture under agreements, 1950-5100-060-01A, and Kamada.
Investigative Ophthalmology & Visual Science June 2017, Vol.58, 1516. doi:
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    • Get Citation

      Chung-Jung Chiu, Min-Lee Chang, Allen Taylor; Infection of A Keystone Bacterium in Periodontal Microbiota And Risk for Age-related Macular Degeneration. Invest. Ophthalmol. Vis. Sci. 2017;58(8):1516.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : Using data from the Third National Health and Nutrition Examination Survey (NHANES III), our recent study indicated that dysbiotic oral microbiota, even without inducing clinically significant periodontitis, may have a significant impact on the risk for human disease and mortality, and that Porphyromonas gingivalis (P gingivalis) plays a keystone (catalyst) in the dysbiotic oral microbiota. While little is known about the relationship of human microbiota to age-related macular degeneration (AMD), it is interesting that AMD shares risk factors and etiological mechanisms with P gingivalis-related diseases including diabetes, cardiovascular disease, and Alzheimer's disease. We conducted a candidate microbe association study (CMAS) to test our hypothesis that infection with P gingivalis is associated with the occurrence of AMD.

Methods : We related serum P gingivalis immunoglobulin G (IgG) to the odds of early AMD (n=201 cases) among subjects aged 60 years or older in a case-control study in the NHANES III. Early AMD cases were defined as the presence of either drusen (≥63 µm in diameter, equivalent to Grade 3 drusen in the Wisconsin Age-related Maculopathy Grading System) or any drusen type with areas of depigmentation or hypopigmentation of the RPE without any visibility of choroidal vessels or with increased retinal pigment in the macular area.

Results : The multivariate-adjusted odds ratios (ORs) indicated that compared with the lowest IgG category (≤57 enzyme-linked immunosorbent assay units (EU)), the second higher category (58–119 EU) was associated with an over 30% increased odds (OR =1.33, 95% confidence interval (CI): 1.18 to 1.51) and the highest category (>119 EU) was associated with an over 60% increased odds (OR=1.61, 95% CI: 1.19 to 2.18; p for tend<0.001) of risk for early AMD.

Conclusions : This study is the first to show a significant association between a specific microbe in periodontal microbiota and AMD. The detailed mechanism warrants further study. Our findings imply that oral microbiota play a role in retinal eye health.

This is an abstract that was submitted for the 2017 ARVO Annual Meeting, held in Baltimore, MD, May 7-11, 2017.

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