Vitreal Cytokine Profile Differences Between Eyes With Epiretinal Membranes or Macular Holes
Cytokines play an important role in cell signaling in inflammatory and repair processes, also within the posterior segment of the eye. These molecules are thus implicated in the pathophysiology of several vitreoretinal diseases. In the present study, we compared vitreal cytokine profiles in patients...
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Veröffentlicht in: | Investigative ophthalmology & visual science 2016-11, Vol.57 (14), p.6320-6326 |
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description | Cytokines play an important role in cell signaling in inflammatory and repair processes, also within the posterior segment of the eye. These molecules are thus implicated in the pathophysiology of several vitreoretinal diseases. In the present study, we compared vitreal cytokine profiles in patients with idiopathic epiretinal membranes (ERMs) and idiopathic full-thickness macular holes (MHs) without epiretinal membranes.
Native vitreal humor was collected during elective pars plana vitrectomy for the treatment of macular pathologies (group 1: ERM; group 2: MH) from patients without any other ocular or systemic disease. The concentrations of 43 chemokines and cytokines were measured in parallel by multiplex beads analysis. Intergroup comparisons were conducted using the Mann-Whitney U test and Bonferroni's correction, at a level of significance of P < 0.0012.
Vitreal samples from 31 patients with ERMs (group 1) and from 30 with MHs (group 2) were analyzed. For 12 of the tested cytokines (GM-CSF, MCP-1, MIF, CCL15, CCL20, CCL17, CX3CL1, CXCL10, CXCL16, and TGF-β-1, -2, and -3), no intergroup differences were revealed; for the other 31, the concentrations were higher in the ERM than in the MH group (P < 0.0012 in each case).
The vitreal levels of 72% of the tested cytokines were higher in ERM than in MH. This indicates that even in the absence of clinical markers, activation of inflammatory and profibrotic mechanisms is implicated in the progression of ERMs. Although frequently used as such in the past, eyes with ERMs should be considered with caution as a healthy control group. |
doi_str_mv | 10.1167/iovs.16-20657 |
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Native vitreal humor was collected during elective pars plana vitrectomy for the treatment of macular pathologies (group 1: ERM; group 2: MH) from patients without any other ocular or systemic disease. The concentrations of 43 chemokines and cytokines were measured in parallel by multiplex beads analysis. Intergroup comparisons were conducted using the Mann-Whitney U test and Bonferroni's correction, at a level of significance of P < 0.0012.
Vitreal samples from 31 patients with ERMs (group 1) and from 30 with MHs (group 2) were analyzed. For 12 of the tested cytokines (GM-CSF, MCP-1, MIF, CCL15, CCL20, CCL17, CX3CL1, CXCL10, CXCL16, and TGF-β-1, -2, and -3), no intergroup differences were revealed; for the other 31, the concentrations were higher in the ERM than in the MH group (P < 0.0012 in each case).
The vitreal levels of 72% of the tested cytokines were higher in ERM than in MH. This indicates that even in the absence of clinical markers, activation of inflammatory and profibrotic mechanisms is implicated in the progression of ERMs. Although frequently used as such in the past, eyes with ERMs should be considered with caution as a healthy control group.</description><identifier>ISSN: 1552-5783</identifier><identifier>EISSN: 1552-5783</identifier><identifier>DOI: 10.1167/iovs.16-20657</identifier><identifier>PMID: 27893098</identifier><language>eng</language><publisher>United States</publisher><subject>Aged ; Biomarkers - metabolism ; Cytokines - metabolism ; Epiretinal Membrane - diagnosis ; Epiretinal Membrane - metabolism ; Epiretinal Membrane - surgery ; Female ; Follow-Up Studies ; Humans ; Male ; Prospective Studies ; Retinal Perforations - diagnosis ; Retinal Perforations - metabolism ; Tomography, Optical Coherence ; Visual Acuity ; Vitrectomy ; Vitreous Body - diagnostic imaging ; Vitreous Body - metabolism</subject><ispartof>Investigative ophthalmology & visual science, 2016-11, Vol.57 (14), p.6320-6326</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c332t-c2b40416314cb6faeab3d8eb906147ac8a7cf2f033705d1cf0708726dc7101c53</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27893098$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zandi, Souska</creatorcontrib><creatorcontrib>Tappeiner, Christoph</creatorcontrib><creatorcontrib>Pfister, Isabel B</creatorcontrib><creatorcontrib>Despont, Alain</creatorcontrib><creatorcontrib>Rieben, Robert</creatorcontrib><creatorcontrib>Garweg, Justus G</creatorcontrib><title>Vitreal Cytokine Profile Differences Between Eyes With Epiretinal Membranes or Macular Holes</title><title>Investigative ophthalmology & visual science</title><addtitle>Invest Ophthalmol Vis Sci</addtitle><description>Cytokines play an important role in cell signaling in inflammatory and repair processes, also within the posterior segment of the eye. These molecules are thus implicated in the pathophysiology of several vitreoretinal diseases. In the present study, we compared vitreal cytokine profiles in patients with idiopathic epiretinal membranes (ERMs) and idiopathic full-thickness macular holes (MHs) without epiretinal membranes.
Native vitreal humor was collected during elective pars plana vitrectomy for the treatment of macular pathologies (group 1: ERM; group 2: MH) from patients without any other ocular or systemic disease. The concentrations of 43 chemokines and cytokines were measured in parallel by multiplex beads analysis. Intergroup comparisons were conducted using the Mann-Whitney U test and Bonferroni's correction, at a level of significance of P < 0.0012.
Vitreal samples from 31 patients with ERMs (group 1) and from 30 with MHs (group 2) were analyzed. For 12 of the tested cytokines (GM-CSF, MCP-1, MIF, CCL15, CCL20, CCL17, CX3CL1, CXCL10, CXCL16, and TGF-β-1, -2, and -3), no intergroup differences were revealed; for the other 31, the concentrations were higher in the ERM than in the MH group (P < 0.0012 in each case).
The vitreal levels of 72% of the tested cytokines were higher in ERM than in MH. This indicates that even in the absence of clinical markers, activation of inflammatory and profibrotic mechanisms is implicated in the progression of ERMs. Although frequently used as such in the past, eyes with ERMs should be considered with caution as a healthy control group.</description><subject>Aged</subject><subject>Biomarkers - metabolism</subject><subject>Cytokines - metabolism</subject><subject>Epiretinal Membrane - diagnosis</subject><subject>Epiretinal Membrane - metabolism</subject><subject>Epiretinal Membrane - surgery</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Male</subject><subject>Prospective Studies</subject><subject>Retinal Perforations - diagnosis</subject><subject>Retinal Perforations - metabolism</subject><subject>Tomography, Optical Coherence</subject><subject>Visual Acuity</subject><subject>Vitrectomy</subject><subject>Vitreous Body - diagnostic imaging</subject><subject>Vitreous Body - metabolism</subject><issn>1552-5783</issn><issn>1552-5783</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkE1PwzAMhiMEYmNw5Ipy5NIRJ23THWEMhrQJDnxckKo0dUSgbUbSgvbv6WAgTrblx6-sh5BjYGOAVJ5Z9xHGkEacpYncIUNIEh4lMhO7__oBOQjhlTEOwNk-GXCZTQSbZEPy_Ghbj6qi03Xr3myD9M47Yyukl9YY9NhoDPQC20_Ehs7W_fBk2xc6W1mPrW36yyXWhVdNv3GeLpXuKuXp3FUYDsmeUVXAo20dkYer2f10Hi1ur2-m54tIC8HbSPMiZjGkAmJdpEahKkSZYTFhKcRS6UxJbbhhQkiWlKANkyyTPC21BAY6ESNy-pO78u69w9DmtQ0aq6r_ynUhhyyORSJi4D0a_aDauxA8mnzlba38OgeWb4TmG6E5pPm30J4_2UZ3RY3lH_1rUHwBM4Nx0Q</recordid><startdate>20161101</startdate><enddate>20161101</enddate><creator>Zandi, Souska</creator><creator>Tappeiner, Christoph</creator><creator>Pfister, Isabel B</creator><creator>Despont, Alain</creator><creator>Rieben, Robert</creator><creator>Garweg, Justus G</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20161101</creationdate><title>Vitreal Cytokine Profile Differences Between Eyes With Epiretinal Membranes or Macular Holes</title><author>Zandi, Souska ; Tappeiner, Christoph ; Pfister, Isabel B ; Despont, Alain ; Rieben, Robert ; Garweg, Justus G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c332t-c2b40416314cb6faeab3d8eb906147ac8a7cf2f033705d1cf0708726dc7101c53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Aged</topic><topic>Biomarkers - metabolism</topic><topic>Cytokines - metabolism</topic><topic>Epiretinal Membrane - diagnosis</topic><topic>Epiretinal Membrane - metabolism</topic><topic>Epiretinal Membrane - surgery</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Male</topic><topic>Prospective Studies</topic><topic>Retinal Perforations - diagnosis</topic><topic>Retinal Perforations - metabolism</topic><topic>Tomography, Optical Coherence</topic><topic>Visual Acuity</topic><topic>Vitrectomy</topic><topic>Vitreous Body - diagnostic imaging</topic><topic>Vitreous Body - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zandi, Souska</creatorcontrib><creatorcontrib>Tappeiner, Christoph</creatorcontrib><creatorcontrib>Pfister, Isabel B</creatorcontrib><creatorcontrib>Despont, Alain</creatorcontrib><creatorcontrib>Rieben, Robert</creatorcontrib><creatorcontrib>Garweg, Justus G</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Investigative ophthalmology & visual science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zandi, Souska</au><au>Tappeiner, Christoph</au><au>Pfister, Isabel B</au><au>Despont, Alain</au><au>Rieben, Robert</au><au>Garweg, Justus G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Vitreal Cytokine Profile Differences Between Eyes With Epiretinal Membranes or Macular Holes</atitle><jtitle>Investigative ophthalmology & visual science</jtitle><addtitle>Invest Ophthalmol Vis Sci</addtitle><date>2016-11-01</date><risdate>2016</risdate><volume>57</volume><issue>14</issue><spage>6320</spage><epage>6326</epage><pages>6320-6326</pages><issn>1552-5783</issn><eissn>1552-5783</eissn><abstract>Cytokines play an important role in cell signaling in inflammatory and repair processes, also within the posterior segment of the eye. These molecules are thus implicated in the pathophysiology of several vitreoretinal diseases. In the present study, we compared vitreal cytokine profiles in patients with idiopathic epiretinal membranes (ERMs) and idiopathic full-thickness macular holes (MHs) without epiretinal membranes.
Native vitreal humor was collected during elective pars plana vitrectomy for the treatment of macular pathologies (group 1: ERM; group 2: MH) from patients without any other ocular or systemic disease. The concentrations of 43 chemokines and cytokines were measured in parallel by multiplex beads analysis. Intergroup comparisons were conducted using the Mann-Whitney U test and Bonferroni's correction, at a level of significance of P < 0.0012.
Vitreal samples from 31 patients with ERMs (group 1) and from 30 with MHs (group 2) were analyzed. For 12 of the tested cytokines (GM-CSF, MCP-1, MIF, CCL15, CCL20, CCL17, CX3CL1, CXCL10, CXCL16, and TGF-β-1, -2, and -3), no intergroup differences were revealed; for the other 31, the concentrations were higher in the ERM than in the MH group (P < 0.0012 in each case).
The vitreal levels of 72% of the tested cytokines were higher in ERM than in MH. This indicates that even in the absence of clinical markers, activation of inflammatory and profibrotic mechanisms is implicated in the progression of ERMs. Although frequently used as such in the past, eyes with ERMs should be considered with caution as a healthy control group.</abstract><cop>United States</cop><pmid>27893098</pmid><doi>10.1167/iovs.16-20657</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Biomarkers - metabolism Cytokines - metabolism Epiretinal Membrane - diagnosis Epiretinal Membrane - metabolism Epiretinal Membrane - surgery Female Follow-Up Studies Humans Male Prospective Studies Retinal Perforations - diagnosis Retinal Perforations - metabolism Tomography, Optical Coherence Visual Acuity Vitrectomy Vitreous Body - diagnostic imaging Vitreous Body - metabolism |
title | Vitreal Cytokine Profile Differences Between Eyes With Epiretinal Membranes or Macular Holes |
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