Association of increased levels of plasma tumor necrosis factor alpha with primary open-angle glaucoma
Altaf A Kondkar, Tahira Sultan, Faisal A Almobarak, Hatem Kalantan, Saleh A Al-Obeidan, Khaled K Abu-Amero Glaucoma Research Chair, Department of Ophthalmology, College of Medicine, King Saud University, Riyadh, Saudi Arabia Purpose: Retinal ganglion cell (RGC) death is a key feature of glaucoma....
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Dove Medical Press
2018
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oai:doaj.org-article:55d603a719f14e7e87546687ad7a3f1d2021-12-02T04:03:30ZAssociation of increased levels of plasma tumor necrosis factor alpha with primary open-angle glaucoma1177-5483https://doaj.org/article/55d603a719f14e7e87546687ad7a3f1d2018-04-01T00:00:00Zhttps://www.dovepress.com/association-of-increased-levels-of-plasma-tumor-necrosis-factor-alpha--peer-reviewed-article-OPTHhttps://doaj.org/toc/1177-5483Altaf A Kondkar, Tahira Sultan, Faisal A Almobarak, Hatem Kalantan, Saleh A Al-Obeidan, Khaled K Abu-Amero Glaucoma Research Chair, Department of Ophthalmology, College of Medicine, King Saud University, Riyadh, Saudi Arabia Purpose: Retinal ganglion cell (RGC) death is a key feature of glaucoma. Elevated levels of tumor necrosis factor alpha (TNF-α), a pro-inflammatory cytokine, can induce RGC apoptosis and play a critical role in glaucomatous neurodegeneration. Based on the possible role of inflammation and oxidative stress in the pathogenesis of primary open-angle glaucoma (POAG), we investigated the association between plasma levels of TNF-α and POAG or its clinical indices in comparison to non-glaucomatous controls. Patients and methods: In a case–control retrospective cohort of 51 POAG cases and 88 controls, plasma TNF-α levels were measured using an enzyme-linked immunosorbent assay (ELISA). The assay was performed in duplicates on an automated ELISA analyzer. Results: Mean TNF-α level was significantly elevated in POAG cases (1.88 ± 2.17 pg/mL) than the controls (0.93 ± 1.49 pg/mL; p = 0.003). The overall dose–response trend was significant (Χ2 = 6.12, df = 2; p = 0.047). No statistical difference was seen in age, gender and systemic disease distribution. A modest negative and significant correlation was seen between TNF-α level and number of antiglaucoma medications, an important clinical index of POAG severity. Moreover, logistic regression analysis showed that the risk of POAG was most significantly affected by TNF-α level and not by age and sex. Conclusion: High systemic level of an inflammatory cytokine, TNF-α, is associated with POAG; however, its possible use as a biomarker for early glaucoma diagnosis and/or disease severity needs further investigation. Keywords: apoptosis, biomarker, cytokines, ELISA, inflammation, neurodegeneration, oxidative stressKondkar AASultan TAlmobarak FAKalantan HAl-Obeidan SAAbu-Amero KKDove Medical Pressarticleglaucomainflammationoxidative stressPOAGTNF-αOphthalmologyRE1-994ENClinical Ophthalmology, Vol Volume 12, Pp 701-706 (2018) |
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glaucoma inflammation oxidative stress POAG TNF-α Ophthalmology RE1-994 |
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glaucoma inflammation oxidative stress POAG TNF-α Ophthalmology RE1-994 Kondkar AA Sultan T Almobarak FA Kalantan H Al-Obeidan SA Abu-Amero KK Association of increased levels of plasma tumor necrosis factor alpha with primary open-angle glaucoma |
description |
Altaf A Kondkar, Tahira Sultan, Faisal A Almobarak, Hatem Kalantan, Saleh A Al-Obeidan, Khaled K Abu-Amero Glaucoma Research Chair, Department of Ophthalmology, College of Medicine, King Saud University, Riyadh, Saudi Arabia Purpose: Retinal ganglion cell (RGC) death is a key feature of glaucoma. Elevated levels of tumor necrosis factor alpha (TNF-α), a pro-inflammatory cytokine, can induce RGC apoptosis and play a critical role in glaucomatous neurodegeneration. Based on the possible role of inflammation and oxidative stress in the pathogenesis of primary open-angle glaucoma (POAG), we investigated the association between plasma levels of TNF-α and POAG or its clinical indices in comparison to non-glaucomatous controls. Patients and methods: In a case–control retrospective cohort of 51 POAG cases and 88 controls, plasma TNF-α levels were measured using an enzyme-linked immunosorbent assay (ELISA). The assay was performed in duplicates on an automated ELISA analyzer. Results: Mean TNF-α level was significantly elevated in POAG cases (1.88 ± 2.17 pg/mL) than the controls (0.93 ± 1.49 pg/mL; p = 0.003). The overall dose–response trend was significant (Χ2 = 6.12, df = 2; p = 0.047). No statistical difference was seen in age, gender and systemic disease distribution. A modest negative and significant correlation was seen between TNF-α level and number of antiglaucoma medications, an important clinical index of POAG severity. Moreover, logistic regression analysis showed that the risk of POAG was most significantly affected by TNF-α level and not by age and sex. Conclusion: High systemic level of an inflammatory cytokine, TNF-α, is associated with POAG; however, its possible use as a biomarker for early glaucoma diagnosis and/or disease severity needs further investigation. Keywords: apoptosis, biomarker, cytokines, ELISA, inflammation, neurodegeneration, oxidative stress |
format |
article |
author |
Kondkar AA Sultan T Almobarak FA Kalantan H Al-Obeidan SA Abu-Amero KK |
author_facet |
Kondkar AA Sultan T Almobarak FA Kalantan H Al-Obeidan SA Abu-Amero KK |
author_sort |
Kondkar AA |
title |
Association of increased levels of plasma tumor necrosis factor alpha with primary open-angle glaucoma |
title_short |
Association of increased levels of plasma tumor necrosis factor alpha with primary open-angle glaucoma |
title_full |
Association of increased levels of plasma tumor necrosis factor alpha with primary open-angle glaucoma |
title_fullStr |
Association of increased levels of plasma tumor necrosis factor alpha with primary open-angle glaucoma |
title_full_unstemmed |
Association of increased levels of plasma tumor necrosis factor alpha with primary open-angle glaucoma |
title_sort |
association of increased levels of plasma tumor necrosis factor alpha with primary open-angle glaucoma |
publisher |
Dove Medical Press |
publishDate |
2018 |
url |
https://doaj.org/article/55d603a719f14e7e87546687ad7a3f1d |
work_keys_str_mv |
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_version_ |
1718401430816030720 |