Comparison of mfERG waveform components and implicit time measurement techniques for detecting functional change in early diabetic eye disease
This study first compares two methods for measuring first order multifocal electroretinogram (mfERG) implicit time abnormalities in eyes with early diabetic retinopathy. Two analysis methods are used: template stretching (multiplicative scaling) of an 80 msec response epoch and template sliding (cro...
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Veröffentlicht in: | Documenta ophthalmologica 2004-05, Vol.108 (3), p.223-230 |
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description | This study first compares two methods for measuring first order multifocal electroretinogram (mfERG) implicit time abnormalities in eyes with early diabetic retinopathy. Two analysis methods are used: template stretching (multiplicative scaling) of an 80 msec response epoch and template sliding (cross-correlation or additive scaling) of portions of responses containing the major waveform features. The study also compares the relative sensitivities of N1, P1 and N2 implicit time assessed by cross-correlation. The nature of the change in the mfERG waveform associated with diabetes is also assessed. MfERGs were recorded from 15 eyes of 15 individuals with diabetes and early non-proliferative retinopathy and 20 eyes of 20 healthy control subjects of similar age. Implicit time determined by template stretching is more frequently abnormal in the eyes of the diabetic subjects than the implicit time of any of the components assessed by template sliding. This is attributable to the lower variability of the template stretching implicit time measure in normals. Of the components, P1 is most often abnormal in the eyes of individuals with diabetes. Responses recorded from retinal areas with retinopathic signs are more often abnormal than those from other areas. Later components of the response are not delayed more than earlier ones. We conclude that template stretching is a sensitive measurement technique, but that it does not fully capture the effect of diabetes on the first order mfERG well. |
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Two analysis methods are used: template stretching (multiplicative scaling) of an 80 msec response epoch and template sliding (cross-correlation or additive scaling) of portions of responses containing the major waveform features. The study also compares the relative sensitivities of N1, P1 and N2 implicit time assessed by cross-correlation. The nature of the change in the mfERG waveform associated with diabetes is also assessed. MfERGs were recorded from 15 eyes of 15 individuals with diabetes and early non-proliferative retinopathy and 20 eyes of 20 healthy control subjects of similar age. Implicit time determined by template stretching is more frequently abnormal in the eyes of the diabetic subjects than the implicit time of any of the components assessed by template sliding. This is attributable to the lower variability of the template stretching implicit time measure in normals. Of the components, P1 is most often abnormal in the eyes of individuals with diabetes. Responses recorded from retinal areas with retinopathic signs are more often abnormal than those from other areas. Later components of the response are not delayed more than earlier ones. We conclude that template stretching is a sensitive measurement technique, but that it does not fully capture the effect of diabetes on the first order mfERG well.</description><identifier>ISSN: 0012-4486</identifier><identifier>EISSN: 1573-2622</identifier><identifier>DOI: 10.1007/s10633-004-8745-z</identifier><identifier>PMID: 15573946</identifier><identifier>CODEN: DOOPAA</identifier><language>eng</language><publisher>Dordrecht: Springer</publisher><subject>Adult ; Aged ; Associated diseases and complications ; Biological and medical sciences ; Diabetes Complications - diagnosis ; Diabetes. Impaired glucose tolerance ; Diabetic Retinopathy - diagnosis ; Electroretinography - methods ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Humans ; Medical sciences ; Middle Aged ; Ophthalmology ; Retina - pathology ; Retinopathies ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Surgery of the eye and orbit ; Time Factors</subject><ispartof>Documenta ophthalmologica, 2004-05, Vol.108 (3), p.223-230</ispartof><rights>2004 INIST-CNRS</rights><rights>Copyright (c) 2004 Kluwer Academic Publishers</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c385t-9bfae495a13ab6ee0eaf3e54cca3661ac9ef38583ba4259ceec0d5601a3554303</citedby><cites>FETCH-LOGICAL-c385t-9bfae495a13ab6ee0eaf3e54cca3661ac9ef38583ba4259ceec0d5601a3554303</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16216645$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15573946$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SCHNECK, Marilyn E</creatorcontrib><creatorcontrib>BEARSE, Marcus A</creatorcontrib><creatorcontrib>YING HAN</creatorcontrib><creatorcontrib>BAREZ, Shirin</creatorcontrib><creatorcontrib>JACOBSEN, Carl</creatorcontrib><creatorcontrib>ADAMS, Anthony J</creatorcontrib><title>Comparison of mfERG waveform components and implicit time measurement techniques for detecting functional change in early diabetic eye disease</title><title>Documenta ophthalmologica</title><addtitle>Doc Ophthalmol</addtitle><description>This study first compares two methods for measuring first order multifocal electroretinogram (mfERG) implicit time abnormalities in eyes with early diabetic retinopathy. Two analysis methods are used: template stretching (multiplicative scaling) of an 80 msec response epoch and template sliding (cross-correlation or additive scaling) of portions of responses containing the major waveform features. The study also compares the relative sensitivities of N1, P1 and N2 implicit time assessed by cross-correlation. The nature of the change in the mfERG waveform associated with diabetes is also assessed. MfERGs were recorded from 15 eyes of 15 individuals with diabetes and early non-proliferative retinopathy and 20 eyes of 20 healthy control subjects of similar age. Implicit time determined by template stretching is more frequently abnormal in the eyes of the diabetic subjects than the implicit time of any of the components assessed by template sliding. This is attributable to the lower variability of the template stretching implicit time measure in normals. Of the components, P1 is most often abnormal in the eyes of individuals with diabetes. Responses recorded from retinal areas with retinopathic signs are more often abnormal than those from other areas. Later components of the response are not delayed more than earlier ones. We conclude that template stretching is a sensitive measurement technique, but that it does not fully capture the effect of diabetes on the first order mfERG well.</description><subject>Adult</subject><subject>Aged</subject><subject>Associated diseases and complications</subject><subject>Biological and medical sciences</subject><subject>Diabetes Complications - diagnosis</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Diabetic Retinopathy - diagnosis</subject><subject>Electroretinography - methods</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Ophthalmology</subject><subject>Retina - pathology</subject><subject>Retinopathies</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. 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Impaired glucose tolerance</topic><topic>Diabetic Retinopathy - diagnosis</topic><topic>Electroretinography - methods</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Ophthalmology</topic><topic>Retina - pathology</topic><topic>Retinopathies</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Surgery of the eye and orbit</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SCHNECK, Marilyn E</creatorcontrib><creatorcontrib>BEARSE, Marcus A</creatorcontrib><creatorcontrib>YING HAN</creatorcontrib><creatorcontrib>BAREZ, Shirin</creatorcontrib><creatorcontrib>JACOBSEN, Carl</creatorcontrib><creatorcontrib>ADAMS, Anthony J</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Documenta ophthalmologica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SCHNECK, Marilyn E</au><au>BEARSE, Marcus A</au><au>YING HAN</au><au>BAREZ, Shirin</au><au>JACOBSEN, Carl</au><au>ADAMS, Anthony J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of mfERG waveform components and implicit time measurement techniques for detecting functional change in early diabetic eye disease</atitle><jtitle>Documenta ophthalmologica</jtitle><addtitle>Doc Ophthalmol</addtitle><date>2004-05-01</date><risdate>2004</risdate><volume>108</volume><issue>3</issue><spage>223</spage><epage>230</epage><pages>223-230</pages><issn>0012-4486</issn><eissn>1573-2622</eissn><coden>DOOPAA</coden><abstract>This study first compares two methods for measuring first order multifocal electroretinogram (mfERG) implicit time abnormalities in eyes with early diabetic retinopathy. Two analysis methods are used: template stretching (multiplicative scaling) of an 80 msec response epoch and template sliding (cross-correlation or additive scaling) of portions of responses containing the major waveform features. The study also compares the relative sensitivities of N1, P1 and N2 implicit time assessed by cross-correlation. The nature of the change in the mfERG waveform associated with diabetes is also assessed. MfERGs were recorded from 15 eyes of 15 individuals with diabetes and early non-proliferative retinopathy and 20 eyes of 20 healthy control subjects of similar age. Implicit time determined by template stretching is more frequently abnormal in the eyes of the diabetic subjects than the implicit time of any of the components assessed by template sliding. This is attributable to the lower variability of the template stretching implicit time measure in normals. Of the components, P1 is most often abnormal in the eyes of individuals with diabetes. Responses recorded from retinal areas with retinopathic signs are more often abnormal than those from other areas. Later components of the response are not delayed more than earlier ones. We conclude that template stretching is a sensitive measurement technique, but that it does not fully capture the effect of diabetes on the first order mfERG well.</abstract><cop>Dordrecht</cop><pub>Springer</pub><pmid>15573946</pmid><doi>10.1007/s10633-004-8745-z</doi><tpages>8</tpages></addata></record> |
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subjects | Adult Aged Associated diseases and complications Biological and medical sciences Diabetes Complications - diagnosis Diabetes. Impaired glucose tolerance Diabetic Retinopathy - diagnosis Electroretinography - methods Endocrine pancreas. Apud cells (diseases) Endocrinopathies Humans Medical sciences Middle Aged Ophthalmology Retina - pathology Retinopathies Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Surgery of the eye and orbit Time Factors |
title | Comparison of mfERG waveform components and implicit time measurement techniques for detecting functional change in early diabetic eye disease |
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