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Decreased Circulating Levels of Dickkopf-1 in Patients with Exudative Age-related Macular Degeneration

Aberrant activation of the Wnt/β-catenin signaling pathway plays a pathogenic role in retinal inflammation and neovascularization. Here, we investigated whether circulating levels of Dickkopf-1 (DKK-1), a specific inhibitor of this pathway, are altered in patients with exudative age-related macular...

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Autores principales: Qiu, Fangfang, Liu, Zhen, Zhou, Yueping, He, Jia, Gong, Songjian, Bai, Xue, Zeng, Yingxia, Liu, Zuguo, Ma, Jian-xing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5430640/
https://www.ncbi.nlm.nih.gov/pubmed/28455497
http://dx.doi.org/10.1038/s41598-017-01119-2
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author Qiu, Fangfang
Liu, Zhen
Zhou, Yueping
He, Jia
Gong, Songjian
Bai, Xue
Zeng, Yingxia
Liu, Zuguo
Ma, Jian-xing
author_facet Qiu, Fangfang
Liu, Zhen
Zhou, Yueping
He, Jia
Gong, Songjian
Bai, Xue
Zeng, Yingxia
Liu, Zuguo
Ma, Jian-xing
author_sort Qiu, Fangfang
collection PubMed
description Aberrant activation of the Wnt/β-catenin signaling pathway plays a pathogenic role in retinal inflammation and neovascularization. Here, we investigated whether circulating levels of Dickkopf-1 (DKK-1), a specific inhibitor of this pathway, are altered in patients with exudative age-related macular degeneration (AMD). Plasma was obtained from 128 patients with exudative AMD, 46 patients with atrophic AMD and 111 healthy controls. DKK-1 levels in plasma were measured using ELISA, and data analyzed with one-way ANOVA, logistic regression analysis and receiver-operating characteristic analysis (ROC). We found that DKK-1 levels were decreased in exudative AMD patients, compared with healthy controls (P < 0.001) and atrophic AMD patients (P < 0.001). The decrease was more prominent in patients with classic choroidal neovascularization (CNV) than those with occult CNV (P < 0.001). The odds ratio (OR) of exudative AMD was 11.71 (95% CI; 5.24–6.13) for lowest versus upper quartile of DKK-1 levels. For discriminating exudative AMD patients, the optimum diagnostic cutoff of DKK-1 was 583.1 pg/mL with the area under curve (AUC) 0.76 (95% CI, 0.70–0.82; P < 0.001), sensitivity 78.1% and specificity 63.1%. These findings suggested that decreased circulating DKK-1 levels are associated with the development and severity of exudative AMD, and have potential to become a biomarker for exudative AMD.
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spelling pubmed-54306402017-05-15 Decreased Circulating Levels of Dickkopf-1 in Patients with Exudative Age-related Macular Degeneration Qiu, Fangfang Liu, Zhen Zhou, Yueping He, Jia Gong, Songjian Bai, Xue Zeng, Yingxia Liu, Zuguo Ma, Jian-xing Sci Rep Article Aberrant activation of the Wnt/β-catenin signaling pathway plays a pathogenic role in retinal inflammation and neovascularization. Here, we investigated whether circulating levels of Dickkopf-1 (DKK-1), a specific inhibitor of this pathway, are altered in patients with exudative age-related macular degeneration (AMD). Plasma was obtained from 128 patients with exudative AMD, 46 patients with atrophic AMD and 111 healthy controls. DKK-1 levels in plasma were measured using ELISA, and data analyzed with one-way ANOVA, logistic regression analysis and receiver-operating characteristic analysis (ROC). We found that DKK-1 levels were decreased in exudative AMD patients, compared with healthy controls (P < 0.001) and atrophic AMD patients (P < 0.001). The decrease was more prominent in patients with classic choroidal neovascularization (CNV) than those with occult CNV (P < 0.001). The odds ratio (OR) of exudative AMD was 11.71 (95% CI; 5.24–6.13) for lowest versus upper quartile of DKK-1 levels. For discriminating exudative AMD patients, the optimum diagnostic cutoff of DKK-1 was 583.1 pg/mL with the area under curve (AUC) 0.76 (95% CI, 0.70–0.82; P < 0.001), sensitivity 78.1% and specificity 63.1%. These findings suggested that decreased circulating DKK-1 levels are associated with the development and severity of exudative AMD, and have potential to become a biomarker for exudative AMD. Nature Publishing Group UK 2017-04-28 /pmc/articles/PMC5430640/ /pubmed/28455497 http://dx.doi.org/10.1038/s41598-017-01119-2 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Qiu, Fangfang
Liu, Zhen
Zhou, Yueping
He, Jia
Gong, Songjian
Bai, Xue
Zeng, Yingxia
Liu, Zuguo
Ma, Jian-xing
Decreased Circulating Levels of Dickkopf-1 in Patients with Exudative Age-related Macular Degeneration
title Decreased Circulating Levels of Dickkopf-1 in Patients with Exudative Age-related Macular Degeneration
title_full Decreased Circulating Levels of Dickkopf-1 in Patients with Exudative Age-related Macular Degeneration
title_fullStr Decreased Circulating Levels of Dickkopf-1 in Patients with Exudative Age-related Macular Degeneration
title_full_unstemmed Decreased Circulating Levels of Dickkopf-1 in Patients with Exudative Age-related Macular Degeneration
title_short Decreased Circulating Levels of Dickkopf-1 in Patients with Exudative Age-related Macular Degeneration
title_sort decreased circulating levels of dickkopf-1 in patients with exudative age-related macular degeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5430640/
https://www.ncbi.nlm.nih.gov/pubmed/28455497
http://dx.doi.org/10.1038/s41598-017-01119-2
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