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Exposure to Porphyromonas gingivalis and Modifiable Risk Factors Modulate Risk for Early Diabetic Retinopathy
PURPOSE: We hypothesized that exposure to Porphyromonas gingivalis (Pg) increases the risk for early diabetic retinopathy (DR) and that the risk can be modulated. METHODS: We identified 116 early DR cases, and 116 non-DR controls were selected randomly by frequency matching for age, sex, race, and e...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Association for Research in Vision and Ophthalmology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7900844/ https://www.ncbi.nlm.nih.gov/pubmed/34003908 http://dx.doi.org/10.1167/tvst.10.2.23 |
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author | Chiu, Chung-Jung Chang, Min-Lee Kantarci, Alpdogan Van Dyke, Thomas E. Shi, Wenyuan |
author_facet | Chiu, Chung-Jung Chang, Min-Lee Kantarci, Alpdogan Van Dyke, Thomas E. Shi, Wenyuan |
author_sort | Chiu, Chung-Jung |
collection | PubMed |
description | PURPOSE: We hypothesized that exposure to Porphyromonas gingivalis (Pg) increases the risk for early diabetic retinopathy (DR) and that the risk can be modulated. METHODS: We identified 116 early DR cases, and 116 non-DR controls were selected randomly by frequency matching for age, sex, race, and education from the US Third National Health and Nutrition Examination Survey. DR was assessed using non-mydriatic fundus photographs and graded by trained graders using the Modified Airlie House Classification scheme and the Early Treatment for Diabetic Retinopathy Study severity scale. Serum Pg immunoglobulin G (IgG) antibody (Ab) was measured in enzyme-linked immunosorbent assay units. Logistic regression was used to relate serum Pg IgG Ab levels to the risk for early DR. RESULTS: Per tenfold increase in Pg IgG Ab levels, there was an over 60% increased risk for early DR (odds ratio = 1.64; 95% confidence interval, 1.36–1.97), and a linear trend was noted for the estimated probabilities of early DR at various Pg IgG Ab levels (P for trend = 0.0053). The analysis also suggested that moderate alcohol consumption (less than 12 drinks in the past 12 months; P for interaction = 0.0003) and maintaining a normal serum glycated hemoglobulin level (HbA1c ≤ 5.7%; P for interaction < 0.0001) helped reduce the Pg-related DR risk. CONCLUSIONS: The increased Pg-related DR risk could be alleviated by managing alcohol consumption and maintaining a normal blood glucose level. TRANSLATIONAL RELEVANCE: Findings from this study provide new directions for developing novel therapeutics and prevention strategies for DR. |
format | Online Article Text |
id | pubmed-7900844 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Association for Research in Vision and Ophthalmology |
record_format | MEDLINE/PubMed |
spelling | pubmed-79008442021-02-26 Exposure to Porphyromonas gingivalis and Modifiable Risk Factors Modulate Risk for Early Diabetic Retinopathy Chiu, Chung-Jung Chang, Min-Lee Kantarci, Alpdogan Van Dyke, Thomas E. Shi, Wenyuan Transl Vis Sci Technol Article PURPOSE: We hypothesized that exposure to Porphyromonas gingivalis (Pg) increases the risk for early diabetic retinopathy (DR) and that the risk can be modulated. METHODS: We identified 116 early DR cases, and 116 non-DR controls were selected randomly by frequency matching for age, sex, race, and education from the US Third National Health and Nutrition Examination Survey. DR was assessed using non-mydriatic fundus photographs and graded by trained graders using the Modified Airlie House Classification scheme and the Early Treatment for Diabetic Retinopathy Study severity scale. Serum Pg immunoglobulin G (IgG) antibody (Ab) was measured in enzyme-linked immunosorbent assay units. Logistic regression was used to relate serum Pg IgG Ab levels to the risk for early DR. RESULTS: Per tenfold increase in Pg IgG Ab levels, there was an over 60% increased risk for early DR (odds ratio = 1.64; 95% confidence interval, 1.36–1.97), and a linear trend was noted for the estimated probabilities of early DR at various Pg IgG Ab levels (P for trend = 0.0053). The analysis also suggested that moderate alcohol consumption (less than 12 drinks in the past 12 months; P for interaction = 0.0003) and maintaining a normal serum glycated hemoglobulin level (HbA1c ≤ 5.7%; P for interaction < 0.0001) helped reduce the Pg-related DR risk. CONCLUSIONS: The increased Pg-related DR risk could be alleviated by managing alcohol consumption and maintaining a normal blood glucose level. TRANSLATIONAL RELEVANCE: Findings from this study provide new directions for developing novel therapeutics and prevention strategies for DR. The Association for Research in Vision and Ophthalmology 2021-02-16 /pmc/articles/PMC7900844/ /pubmed/34003908 http://dx.doi.org/10.1167/tvst.10.2.23 Text en Copyright 2021 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. |
spellingShingle | Article Chiu, Chung-Jung Chang, Min-Lee Kantarci, Alpdogan Van Dyke, Thomas E. Shi, Wenyuan Exposure to Porphyromonas gingivalis and Modifiable Risk Factors Modulate Risk for Early Diabetic Retinopathy |
title | Exposure to Porphyromonas gingivalis and Modifiable Risk Factors Modulate Risk for Early Diabetic Retinopathy |
title_full | Exposure to Porphyromonas gingivalis and Modifiable Risk Factors Modulate Risk for Early Diabetic Retinopathy |
title_fullStr | Exposure to Porphyromonas gingivalis and Modifiable Risk Factors Modulate Risk for Early Diabetic Retinopathy |
title_full_unstemmed | Exposure to Porphyromonas gingivalis and Modifiable Risk Factors Modulate Risk for Early Diabetic Retinopathy |
title_short | Exposure to Porphyromonas gingivalis and Modifiable Risk Factors Modulate Risk for Early Diabetic Retinopathy |
title_sort | exposure to porphyromonas gingivalis and modifiable risk factors modulate risk for early diabetic retinopathy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7900844/ https://www.ncbi.nlm.nih.gov/pubmed/34003908 http://dx.doi.org/10.1167/tvst.10.2.23 |
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