June 2021
Volume 62, Issue 8
Open Access
ARVO Annual Meeting Abstract  |   June 2021
From gut to glaucoma: translating the microbiome to the eye
Author Affiliations & Notes
  • Joëlle Vergroesen
    Ophthalmology, Erasmus MC, Rotterdam, Zuid-Holland, Netherlands
    Epidemiology, Erasmus MC, Rotterdam, Zuid-Holland, Netherlands
  • Robert Kraaij
    Internal Medicine, Erasmus MC, Rotterdam, Zuid-Holland, Netherlands
  • Cornelia van Duijn
    University of Oxford Nuffield Department of Population Health, Oxford, Oxfordshire, United Kingdom
  • Caroline C. W. Klaver
    Ophthalmology/Epidemiology, Erasmus MC, Rotterdam, Netherlands
    Institute of Molecular and Clinical Ophthalmology, Basel, Switzerland
  • Wishal D Ramdas
    Ophthalmology, Erasmus MC, Rotterdam, Zuid-Holland, Netherlands
  • Footnotes
    Commercial Relationships   Joëlle Vergroesen, None; Robert Kraaij, None; Cornelia van Duijn, None; Caroline Klaver, None; Wishal Ramdas, None
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science June 2021, Vol.62, 2240. doi:
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      Joëlle Vergroesen, Robert Kraaij, Cornelia van Duijn, Caroline C. W. Klaver, Wishal D Ramdas; From gut to glaucoma: translating the microbiome to the eye. Invest. Ophthalmol. Vis. Sci. 2021;62(8):2240.

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

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Abstract

Purpose : Several studies provided compelling evidence that the immune system is involved in the pathogenesis of open-angle glaucoma (OAG). Reactive oxygen species and cytokines produced by the gut microbiome may play a role in this process, traveling from the gut mucosa to the eye. Therefore it is of interest to find changes in the microbiome of patients with OAG.

Methods : Population-based cohort study. All participants underwent extensive ophthalmic examinations, including intra-ocular pressure (IOP), retinal nerve fiber layer (RNFL), and vertical cup-to-disc ratio (VCDR) measurements, and provided a stool sample. A 16S rRNA gene profile dataset was generated and PICRUSt tool was used to obtain predicted bacterial functions. Beta-diversity was calculated and compared using Bray-Curtis dissimilarity matrices. The relationship between alpha-diversity and OAG and OAG-associated parameters was assessed by logistic and linear regression analyses, respectively, adjusted for age, sex, body-mass index, and medication use. The same analyses were performed to assess these relationships at taxa level.

Results : When comparing OAG cases with controls, no differences in alpha- and beta diversity were observed. On taxa level, a higher abundance of the family Rikenellaceae, more specifically the genus Alistipes (OR [95% CI]=1.69 [1.17-2.54]), was associated with higher OAG risk (OR [95% CI]=1.60 [1.11-2.38]). The family Clostridiaceae1 was associated with a lower IOP (estimate=-0.121; p-value=0.001) and smaller VCDR (estimate=-0.024; p-value=0.002). At genus level, Clostridiumsensustricto1 showed the same effects (estimate=-0.120; p-value=0.002 and estimate=-0.023; p-value=0.003, respectively). Predicted functional metagenome analysis showed an association between the lysosome and OAG (OR [95% CI]=2.50 [1.18-4.68]) and RNFL (estimate=-5.273; p-value=0.007).

Conclusions : This study showed associations between the gut microbiome and OAG, as well as with OAG-associated parameters. Predicted functional metagenome analysis revealed the lysosome as potentially interesting for the development of glaucoma. Although replication studies are necessary, our findings display a new pathway in the pathogenesis of glaucoma.

This is a 2021 ARVO Annual Meeting abstract.

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