Cargando…

An Ocular Protein Triad Can Classify Four Complex Retinal Diseases

Retinal diseases generally are vision-threatening conditions that warrant appropriate clinical decision-making which currently solely dependents upon extensive clinical screening by specialized ophthalmologists. In the era where molecular assessment has improved dramatically, we aimed at the identif...

Descripción completa

Detalles Bibliográficos
Autores principales: Kuiper, J. J. W., Beretta, L., Nierkens, S., van Leeuwen, R., ten Dam-van Loon, N. H., Ossewaarde-van Norel, J., Bartels, M. C., de Groot-Mijnes, J. D. F., Schellekens, P., de Boer, J. H., Radstake, T. R. D. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5269719/
https://www.ncbi.nlm.nih.gov/pubmed/28128370
http://dx.doi.org/10.1038/srep41595
_version_ 1782501048270716928
author Kuiper, J. J. W.
Beretta, L.
Nierkens, S.
van Leeuwen, R.
ten Dam-van Loon, N. H.
Ossewaarde-van Norel, J.
Bartels, M. C.
de Groot-Mijnes, J. D. F.
Schellekens, P.
de Boer, J. H.
Radstake, T. R. D. J.
author_facet Kuiper, J. J. W.
Beretta, L.
Nierkens, S.
van Leeuwen, R.
ten Dam-van Loon, N. H.
Ossewaarde-van Norel, J.
Bartels, M. C.
de Groot-Mijnes, J. D. F.
Schellekens, P.
de Boer, J. H.
Radstake, T. R. D. J.
author_sort Kuiper, J. J. W.
collection PubMed
description Retinal diseases generally are vision-threatening conditions that warrant appropriate clinical decision-making which currently solely dependents upon extensive clinical screening by specialized ophthalmologists. In the era where molecular assessment has improved dramatically, we aimed at the identification of biomarkers in 175 ocular fluids to classify four archetypical ocular conditions affecting the retina (age-related macular degeneration, idiopathic non-infectious uveitis, primary vitreoretinal lymphoma, and rhegmatogenous retinal detachment) with one single test. Unsupervised clustering of ocular proteins revealed a classification strikingly similar to the clinical phenotypes of each disease group studied. We developed and independently validated a parsimonious model based merely on three proteins; interleukin (IL)-10, IL-21, and angiotensin converting enzyme (ACE) that could correctly classify patients with an overall accuracy, sensitivity and specificity of respectively, 86.7%, 79.4% and 92.5%. Here, we provide proof-of-concept for molecular profiling as a diagnostic aid for ophthalmologists in the care for patients with retinal conditions.
format Online
Article
Text
id pubmed-5269719
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-52697192017-02-01 An Ocular Protein Triad Can Classify Four Complex Retinal Diseases Kuiper, J. J. W. Beretta, L. Nierkens, S. van Leeuwen, R. ten Dam-van Loon, N. H. Ossewaarde-van Norel, J. Bartels, M. C. de Groot-Mijnes, J. D. F. Schellekens, P. de Boer, J. H. Radstake, T. R. D. J. Sci Rep Article Retinal diseases generally are vision-threatening conditions that warrant appropriate clinical decision-making which currently solely dependents upon extensive clinical screening by specialized ophthalmologists. In the era where molecular assessment has improved dramatically, we aimed at the identification of biomarkers in 175 ocular fluids to classify four archetypical ocular conditions affecting the retina (age-related macular degeneration, idiopathic non-infectious uveitis, primary vitreoretinal lymphoma, and rhegmatogenous retinal detachment) with one single test. Unsupervised clustering of ocular proteins revealed a classification strikingly similar to the clinical phenotypes of each disease group studied. We developed and independently validated a parsimonious model based merely on three proteins; interleukin (IL)-10, IL-21, and angiotensin converting enzyme (ACE) that could correctly classify patients with an overall accuracy, sensitivity and specificity of respectively, 86.7%, 79.4% and 92.5%. Here, we provide proof-of-concept for molecular profiling as a diagnostic aid for ophthalmologists in the care for patients with retinal conditions. Nature Publishing Group 2017-01-27 /pmc/articles/PMC5269719/ /pubmed/28128370 http://dx.doi.org/10.1038/srep41595 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Kuiper, J. J. W.
Beretta, L.
Nierkens, S.
van Leeuwen, R.
ten Dam-van Loon, N. H.
Ossewaarde-van Norel, J.
Bartels, M. C.
de Groot-Mijnes, J. D. F.
Schellekens, P.
de Boer, J. H.
Radstake, T. R. D. J.
An Ocular Protein Triad Can Classify Four Complex Retinal Diseases
title An Ocular Protein Triad Can Classify Four Complex Retinal Diseases
title_full An Ocular Protein Triad Can Classify Four Complex Retinal Diseases
title_fullStr An Ocular Protein Triad Can Classify Four Complex Retinal Diseases
title_full_unstemmed An Ocular Protein Triad Can Classify Four Complex Retinal Diseases
title_short An Ocular Protein Triad Can Classify Four Complex Retinal Diseases
title_sort ocular protein triad can classify four complex retinal diseases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5269719/
https://www.ncbi.nlm.nih.gov/pubmed/28128370
http://dx.doi.org/10.1038/srep41595
work_keys_str_mv AT kuiperjjw anocularproteintriadcanclassifyfourcomplexretinaldiseases
AT berettal anocularproteintriadcanclassifyfourcomplexretinaldiseases
AT nierkenss anocularproteintriadcanclassifyfourcomplexretinaldiseases
AT vanleeuwenr anocularproteintriadcanclassifyfourcomplexretinaldiseases
AT tendamvanloonnh anocularproteintriadcanclassifyfourcomplexretinaldiseases
AT ossewaardevannorelj anocularproteintriadcanclassifyfourcomplexretinaldiseases
AT bartelsmc anocularproteintriadcanclassifyfourcomplexretinaldiseases
AT degrootmijnesjdf anocularproteintriadcanclassifyfourcomplexretinaldiseases
AT schellekensp anocularproteintriadcanclassifyfourcomplexretinaldiseases
AT deboerjh anocularproteintriadcanclassifyfourcomplexretinaldiseases
AT radstaketrdj anocularproteintriadcanclassifyfourcomplexretinaldiseases
AT kuiperjjw ocularproteintriadcanclassifyfourcomplexretinaldiseases
AT berettal ocularproteintriadcanclassifyfourcomplexretinaldiseases
AT nierkenss ocularproteintriadcanclassifyfourcomplexretinaldiseases
AT vanleeuwenr ocularproteintriadcanclassifyfourcomplexretinaldiseases
AT tendamvanloonnh ocularproteintriadcanclassifyfourcomplexretinaldiseases
AT ossewaardevannorelj ocularproteintriadcanclassifyfourcomplexretinaldiseases
AT bartelsmc ocularproteintriadcanclassifyfourcomplexretinaldiseases
AT degrootmijnesjdf ocularproteintriadcanclassifyfourcomplexretinaldiseases
AT schellekensp ocularproteintriadcanclassifyfourcomplexretinaldiseases
AT deboerjh ocularproteintriadcanclassifyfourcomplexretinaldiseases
AT radstaketrdj ocularproteintriadcanclassifyfourcomplexretinaldiseases