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Neuroretinal dysfunction revealed by a flicker electroretinogram correlated with peripheral nerve dysfunction and parameters of atherosclerosis in patients with diabetes

Aims/Introduction Diabetic polyneuropathy (DPN) develops in the early stage of diabetes. However, no common diagnostic protocol has yet been established. Here, to verify that the flicker electroretinogram using a hand‐held device can detect the early dysfunction of the peripheral nervous system in p...

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Published in:Journal of diabetes investigation 2021-07, Vol.12 (7), p.1236-1243
Main Authors: Kawai, Miyuka, Himeno, Tatsuhito, Shibata, Yuka, Hirai, Nobuhiro, Asada‐Yamada, Yuriko, Asano‐Hayami, Emi, Ejima, Yohei, Kasagi, Rina, Nagao, Eriko, Sugiura‐Roth, Yukako, Nakai‐Shimoda, Hiromi, Nakayama, Takayuki, Yamada, Yuichiro, Ishikawa, Takahiro, Morishita, Yoshiaki, Kondo, Masaki, Tsunekawa, Shin, Kato, Yoshiro, Nakamura, Jiro, Kamiya, Hideki
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container_end_page 1243
container_issue 7
container_start_page 1236
container_title Journal of diabetes investigation
container_volume 12
creator Kawai, Miyuka
Himeno, Tatsuhito
Shibata, Yuka
Hirai, Nobuhiro
Asada‐Yamada, Yuriko
Asano‐Hayami, Emi
Ejima, Yohei
Kasagi, Rina
Nagao, Eriko
Sugiura‐Roth, Yukako
Nakai‐Shimoda, Hiromi
Nakayama, Takayuki
Yamada, Yuichiro
Ishikawa, Takahiro
Morishita, Yoshiaki
Kondo, Masaki
Tsunekawa, Shin
Kato, Yoshiro
Nakamura, Jiro
Kamiya, Hideki
description Aims/Introduction Diabetic polyneuropathy (DPN) develops in the early stage of diabetes. However, no common diagnostic protocol has yet been established. Here, to verify that the flicker electroretinogram using a hand‐held device can detect the early dysfunction of the peripheral nervous system in patients with diabetes, we investigated the correlation between the progression of DPN and neuroretinal dysfunction. Materials and Methods In total, 184 participants with type 1 or 2 diabetes underwent a flicker electroretinogram (ERG) using a hand‐held device RETeval™ and nerve conduction study. Participants were also evaluated for intima‐media thickness, ankle‐brachial index, toe brachial index and brachial‐ankle pulse wave velocity. Parameters of the nerve conduction study were used to diagnose the severity according to Baba’s classification. A multiple regression analysis was used to examine the associations of ERG parameters with the severity of DPN categorized by Baba’s classification. Diagnostic properties of the device in DPN were evaluated using a receiver operating characteristic curve. Results A multiple regression model to predict the severity of DPN was generated using ERG. In the model, moderate‐to‐severe DPN was effectively diagnosed (area under the receiver operating characteristic curve 0.692, sensitivity 56.5%, specificity 78.3%, positive predictive value 70.6%, negative predictive value 66.1%, positive likelihood ratio 2.60, negative likelihood ratio 0.56). In the patients without diabetic retinopathy, the implicit time and amplitude in ERG significantly correlated with the parameters of the nerve conduction study, brachial‐ankle pulse wave velocity and intima‐media thickness. Conclusions Electroretinogram parameters obtained by the hand‐held device successfully predict the severity of DPN. The device might be useful to evaluate DPN. The progression of diabetic retinopathy and the dysfunction of neuroretina evaluated using the mydriasis‐free flicker electroretinogram showed a significant correlation. In patients without apparent diabetic retinopathy, the electroretinogram data correlated with parameters indicating vascular dysfunction, and with parameters indicating diabetic polyneuropathy, such as data of a nerve conduction study. Therefore, the electroretinogram data might reflect the neural and vascular impairments of the retina in patients with diabetes. The electroretinogram data were able to be used to predict the severity of diabetic pol
doi_str_mv 10.1111/jdi.13465
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However, no common diagnostic protocol has yet been established. Here, to verify that the flicker electroretinogram using a hand‐held device can detect the early dysfunction of the peripheral nervous system in patients with diabetes, we investigated the correlation between the progression of DPN and neuroretinal dysfunction. Materials and Methods In total, 184 participants with type 1 or 2 diabetes underwent a flicker electroretinogram (ERG) using a hand‐held device RETeval™ and nerve conduction study. Participants were also evaluated for intima‐media thickness, ankle‐brachial index, toe brachial index and brachial‐ankle pulse wave velocity. Parameters of the nerve conduction study were used to diagnose the severity according to Baba’s classification. A multiple regression analysis was used to examine the associations of ERG parameters with the severity of DPN categorized by Baba’s classification. Diagnostic properties of the device in DPN were evaluated using a receiver operating characteristic curve. Results A multiple regression model to predict the severity of DPN was generated using ERG. In the model, moderate‐to‐severe DPN was effectively diagnosed (area under the receiver operating characteristic curve 0.692, sensitivity 56.5%, specificity 78.3%, positive predictive value 70.6%, negative predictive value 66.1%, positive likelihood ratio 2.60, negative likelihood ratio 0.56). In the patients without diabetic retinopathy, the implicit time and amplitude in ERG significantly correlated with the parameters of the nerve conduction study, brachial‐ankle pulse wave velocity and intima‐media thickness. Conclusions Electroretinogram parameters obtained by the hand‐held device successfully predict the severity of DPN. The device might be useful to evaluate DPN. The progression of diabetic retinopathy and the dysfunction of neuroretina evaluated using the mydriasis‐free flicker electroretinogram showed a significant correlation. In patients without apparent diabetic retinopathy, the electroretinogram data correlated with parameters indicating vascular dysfunction, and with parameters indicating diabetic polyneuropathy, such as data of a nerve conduction study. Therefore, the electroretinogram data might reflect the neural and vascular impairments of the retina in patients with diabetes. The electroretinogram data were able to be used to predict the severity of diabetic polyneuropathy.</description><identifier>ISSN: 2040-1116</identifier><identifier>EISSN: 2040-1124</identifier><identifier>DOI: 10.1111/jdi.13465</identifier><identifier>PMID: 33210835</identifier><language>eng</language><publisher>Japan: John Wiley &amp; Sons, Inc</publisher><subject>Aged ; Ankle ; Ankle Brachial Index ; Arteriosclerosis ; Atherosclerosis ; Atherosclerosis - complications ; Atherosclerosis - physiopathology ; Carotid Intima-Media Thickness ; Classification ; Creatinine ; Diabetes ; Diabetes mellitus (insulin dependent) ; Diabetes Mellitus, Type 1 - complications ; Diabetes Mellitus, Type 1 - physiopathology ; Diabetes Mellitus, Type 2 - complications ; Diabetes Mellitus, Type 2 - physiopathology ; Diabetic neuropathies ; Diabetic Neuropathies - diagnosis ; Diabetic Neuropathies - etiology ; Diabetic neuropathy ; Diabetic retinopathy ; Diabetic Retinopathy - diagnosis ; Diabetic Retinopathy - etiology ; Edema ; Electroretinography ; Electroretinography - instrumentation ; Electroretinography - methods ; Female ; Humans ; Kinases ; Laboratories ; Male ; Medical personnel ; Middle Aged ; Multiple regression analysis ; Nerve conduction ; Nervous system ; Neural Conduction - physiology ; Original ; Patients ; Peripheral nerves ; Peripheral Nerves - physiopathology ; Point‐of‐care testing ; Polyneuropathy ; Predictive Value of Tests ; Pulse Wave Analysis ; Retinopathy ; ROC Curve ; Severity of Illness Index ; Skin ; Velocity</subject><ispartof>Journal of diabetes investigation, 2021-07, Vol.12 (7), p.1236-1243</ispartof><rights>2020 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley &amp; Sons Australia, Ltd</rights><rights>2020 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley &amp; Sons Australia, Ltd.</rights><rights>2021. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c5885-4905d7ac132ab22c4507b2abf07342700c1bcde87462f8dccd0bff43758733c3</cites><orcidid>0000-0003-0558-3404 ; 0000-0002-5677-1125 ; 0000-0002-3008-292X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2552762999/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2552762999?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,883,11549,25740,27911,27912,36999,37000,44577,46039,46463,53778,53780,74881</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33210835$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kawai, Miyuka</creatorcontrib><creatorcontrib>Himeno, Tatsuhito</creatorcontrib><creatorcontrib>Shibata, Yuka</creatorcontrib><creatorcontrib>Hirai, Nobuhiro</creatorcontrib><creatorcontrib>Asada‐Yamada, Yuriko</creatorcontrib><creatorcontrib>Asano‐Hayami, Emi</creatorcontrib><creatorcontrib>Ejima, Yohei</creatorcontrib><creatorcontrib>Kasagi, Rina</creatorcontrib><creatorcontrib>Nagao, Eriko</creatorcontrib><creatorcontrib>Sugiura‐Roth, Yukako</creatorcontrib><creatorcontrib>Nakai‐Shimoda, Hiromi</creatorcontrib><creatorcontrib>Nakayama, Takayuki</creatorcontrib><creatorcontrib>Yamada, Yuichiro</creatorcontrib><creatorcontrib>Ishikawa, Takahiro</creatorcontrib><creatorcontrib>Morishita, Yoshiaki</creatorcontrib><creatorcontrib>Kondo, Masaki</creatorcontrib><creatorcontrib>Tsunekawa, Shin</creatorcontrib><creatorcontrib>Kato, Yoshiro</creatorcontrib><creatorcontrib>Nakamura, Jiro</creatorcontrib><creatorcontrib>Kamiya, Hideki</creatorcontrib><title>Neuroretinal dysfunction revealed by a flicker electroretinogram correlated with peripheral nerve dysfunction and parameters of atherosclerosis in patients with diabetes</title><title>Journal of diabetes investigation</title><addtitle>J Diabetes Investig</addtitle><description>Aims/Introduction Diabetic polyneuropathy (DPN) develops in the early stage of diabetes. However, no common diagnostic protocol has yet been established. Here, to verify that the flicker electroretinogram using a hand‐held device can detect the early dysfunction of the peripheral nervous system in patients with diabetes, we investigated the correlation between the progression of DPN and neuroretinal dysfunction. Materials and Methods In total, 184 participants with type 1 or 2 diabetes underwent a flicker electroretinogram (ERG) using a hand‐held device RETeval™ and nerve conduction study. Participants were also evaluated for intima‐media thickness, ankle‐brachial index, toe brachial index and brachial‐ankle pulse wave velocity. Parameters of the nerve conduction study were used to diagnose the severity according to Baba’s classification. A multiple regression analysis was used to examine the associations of ERG parameters with the severity of DPN categorized by Baba’s classification. Diagnostic properties of the device in DPN were evaluated using a receiver operating characteristic curve. Results A multiple regression model to predict the severity of DPN was generated using ERG. In the model, moderate‐to‐severe DPN was effectively diagnosed (area under the receiver operating characteristic curve 0.692, sensitivity 56.5%, specificity 78.3%, positive predictive value 70.6%, negative predictive value 66.1%, positive likelihood ratio 2.60, negative likelihood ratio 0.56). In the patients without diabetic retinopathy, the implicit time and amplitude in ERG significantly correlated with the parameters of the nerve conduction study, brachial‐ankle pulse wave velocity and intima‐media thickness. Conclusions Electroretinogram parameters obtained by the hand‐held device successfully predict the severity of DPN. The device might be useful to evaluate DPN. The progression of diabetic retinopathy and the dysfunction of neuroretina evaluated using the mydriasis‐free flicker electroretinogram showed a significant correlation. In patients without apparent diabetic retinopathy, the electroretinogram data correlated with parameters indicating vascular dysfunction, and with parameters indicating diabetic polyneuropathy, such as data of a nerve conduction study. Therefore, the electroretinogram data might reflect the neural and vascular impairments of the retina in patients with diabetes. The electroretinogram data were able to be used to predict the severity of diabetic polyneuropathy.</description><subject>Aged</subject><subject>Ankle</subject><subject>Ankle Brachial Index</subject><subject>Arteriosclerosis</subject><subject>Atherosclerosis</subject><subject>Atherosclerosis - complications</subject><subject>Atherosclerosis - physiopathology</subject><subject>Carotid Intima-Media Thickness</subject><subject>Classification</subject><subject>Creatinine</subject><subject>Diabetes</subject><subject>Diabetes mellitus (insulin dependent)</subject><subject>Diabetes Mellitus, Type 1 - complications</subject><subject>Diabetes Mellitus, Type 1 - physiopathology</subject><subject>Diabetes Mellitus, Type 2 - complications</subject><subject>Diabetes Mellitus, Type 2 - physiopathology</subject><subject>Diabetic neuropathies</subject><subject>Diabetic Neuropathies - diagnosis</subject><subject>Diabetic Neuropathies - etiology</subject><subject>Diabetic neuropathy</subject><subject>Diabetic retinopathy</subject><subject>Diabetic Retinopathy - diagnosis</subject><subject>Diabetic Retinopathy - etiology</subject><subject>Edema</subject><subject>Electroretinography</subject><subject>Electroretinography - instrumentation</subject><subject>Electroretinography - methods</subject><subject>Female</subject><subject>Humans</subject><subject>Kinases</subject><subject>Laboratories</subject><subject>Male</subject><subject>Medical personnel</subject><subject>Middle Aged</subject><subject>Multiple regression analysis</subject><subject>Nerve conduction</subject><subject>Nervous system</subject><subject>Neural Conduction - physiology</subject><subject>Original</subject><subject>Patients</subject><subject>Peripheral nerves</subject><subject>Peripheral Nerves - physiopathology</subject><subject>Point‐of‐care testing</subject><subject>Polyneuropathy</subject><subject>Predictive Value of Tests</subject><subject>Pulse Wave Analysis</subject><subject>Retinopathy</subject><subject>ROC Curve</subject><subject>Severity of Illness Index</subject><subject>Skin</subject><subject>Velocity</subject><issn>2040-1116</issn><issn>2040-1124</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqFkstuEzEUQEcIRKvQBT-ALLGBRVq_ZsbZIKG2QFAFm-4tP64Th8k42J5U-ST-sm4mRAQJ4YVt2cfHvr63ql4TfElKu1pZf0kYb-pn1TnFHE8Jofz5cU6as-oipRUujQnRNO3L6owxSrBg9Xn16xsMMUTIvlcdsrvkht5kH3oUYQuqA4v0DinkOm9-QETQgcmHA2ER1RqZECN0Khfywecl2kD0myXEoushbuFEqnqLNqocgwwxoeCQyoUNyXRPvU_I9wXIHvqcRp_1Shc6vapeONUluDiMk-r-0-399Zfp3ffP8-uPd1NTC1FP-QzXtlWGMKo0pYbXuNVl6nDLOG0xNkQbC6LlDXXCGmOxdo6zthYtY4ZNqvmotUGt5Cb6tYo7GZSX-4UQF1LF7Mt7JdPCMcWUqU3DgQvtRAsaK0Kdpka3xfVhdG0GvQZrSlDlW06kpzu9X8pF2EpBG85LvibVu4Mghp8DpCzXPhnoOtVDGJKkJQhOCOezgr79C12FIZakFqquadvQ2ew_FJ8RSun-2vcjZUpOUgR3fDLB8qnoZCk6uS-6wr75M8Yj-bvECnA1Ag--g92_TfLrzXxUPgKFauWy</recordid><startdate>202107</startdate><enddate>202107</enddate><creator>Kawai, Miyuka</creator><creator>Himeno, Tatsuhito</creator><creator>Shibata, Yuka</creator><creator>Hirai, Nobuhiro</creator><creator>Asada‐Yamada, Yuriko</creator><creator>Asano‐Hayami, Emi</creator><creator>Ejima, Yohei</creator><creator>Kasagi, Rina</creator><creator>Nagao, Eriko</creator><creator>Sugiura‐Roth, Yukako</creator><creator>Nakai‐Shimoda, Hiromi</creator><creator>Nakayama, Takayuki</creator><creator>Yamada, Yuichiro</creator><creator>Ishikawa, Takahiro</creator><creator>Morishita, Yoshiaki</creator><creator>Kondo, Masaki</creator><creator>Tsunekawa, Shin</creator><creator>Kato, Yoshiro</creator><creator>Nakamura, Jiro</creator><creator>Kamiya, Hideki</creator><general>John Wiley &amp; Sons, Inc</general><general>John Wiley and Sons Inc</general><general>Wiley</general><scope>24P</scope><scope>WIN</scope><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>3V.</scope><scope>7T5</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-0558-3404</orcidid><orcidid>https://orcid.org/0000-0002-5677-1125</orcidid><orcidid>https://orcid.org/0000-0002-3008-292X</orcidid></search><sort><creationdate>202107</creationdate><title>Neuroretinal dysfunction revealed by a flicker electroretinogram correlated with peripheral nerve dysfunction and parameters of atherosclerosis in patients with diabetes</title><author>Kawai, Miyuka ; Himeno, Tatsuhito ; Shibata, Yuka ; Hirai, Nobuhiro ; Asada‐Yamada, Yuriko ; Asano‐Hayami, Emi ; Ejima, Yohei ; Kasagi, Rina ; Nagao, Eriko ; Sugiura‐Roth, Yukako ; Nakai‐Shimoda, Hiromi ; Nakayama, Takayuki ; Yamada, Yuichiro ; Ishikawa, Takahiro ; Morishita, Yoshiaki ; Kondo, Masaki ; Tsunekawa, Shin ; Kato, Yoshiro ; Nakamura, Jiro ; Kamiya, Hideki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5885-4905d7ac132ab22c4507b2abf07342700c1bcde87462f8dccd0bff43758733c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Aged</topic><topic>Ankle</topic><topic>Ankle Brachial Index</topic><topic>Arteriosclerosis</topic><topic>Atherosclerosis</topic><topic>Atherosclerosis - complications</topic><topic>Atherosclerosis - physiopathology</topic><topic>Carotid Intima-Media Thickness</topic><topic>Classification</topic><topic>Creatinine</topic><topic>Diabetes</topic><topic>Diabetes mellitus (insulin dependent)</topic><topic>Diabetes Mellitus, Type 1 - complications</topic><topic>Diabetes Mellitus, Type 1 - physiopathology</topic><topic>Diabetes Mellitus, Type 2 - complications</topic><topic>Diabetes Mellitus, Type 2 - physiopathology</topic><topic>Diabetic neuropathies</topic><topic>Diabetic Neuropathies - diagnosis</topic><topic>Diabetic Neuropathies - etiology</topic><topic>Diabetic neuropathy</topic><topic>Diabetic retinopathy</topic><topic>Diabetic Retinopathy - diagnosis</topic><topic>Diabetic Retinopathy - etiology</topic><topic>Edema</topic><topic>Electroretinography</topic><topic>Electroretinography - instrumentation</topic><topic>Electroretinography - methods</topic><topic>Female</topic><topic>Humans</topic><topic>Kinases</topic><topic>Laboratories</topic><topic>Male</topic><topic>Medical personnel</topic><topic>Middle Aged</topic><topic>Multiple regression analysis</topic><topic>Nerve conduction</topic><topic>Nervous system</topic><topic>Neural Conduction - physiology</topic><topic>Original</topic><topic>Patients</topic><topic>Peripheral nerves</topic><topic>Peripheral Nerves - physiopathology</topic><topic>Point‐of‐care testing</topic><topic>Polyneuropathy</topic><topic>Predictive Value of Tests</topic><topic>Pulse Wave Analysis</topic><topic>Retinopathy</topic><topic>ROC Curve</topic><topic>Severity of Illness Index</topic><topic>Skin</topic><topic>Velocity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kawai, Miyuka</creatorcontrib><creatorcontrib>Himeno, Tatsuhito</creatorcontrib><creatorcontrib>Shibata, Yuka</creatorcontrib><creatorcontrib>Hirai, Nobuhiro</creatorcontrib><creatorcontrib>Asada‐Yamada, Yuriko</creatorcontrib><creatorcontrib>Asano‐Hayami, Emi</creatorcontrib><creatorcontrib>Ejima, Yohei</creatorcontrib><creatorcontrib>Kasagi, Rina</creatorcontrib><creatorcontrib>Nagao, Eriko</creatorcontrib><creatorcontrib>Sugiura‐Roth, Yukako</creatorcontrib><creatorcontrib>Nakai‐Shimoda, Hiromi</creatorcontrib><creatorcontrib>Nakayama, Takayuki</creatorcontrib><creatorcontrib>Yamada, Yuichiro</creatorcontrib><creatorcontrib>Ishikawa, Takahiro</creatorcontrib><creatorcontrib>Morishita, Yoshiaki</creatorcontrib><creatorcontrib>Kondo, Masaki</creatorcontrib><creatorcontrib>Tsunekawa, Shin</creatorcontrib><creatorcontrib>Kato, Yoshiro</creatorcontrib><creatorcontrib>Nakamura, Jiro</creatorcontrib><creatorcontrib>Kamiya, Hideki</creatorcontrib><collection>Wiley-Blackwell Open Access Collection</collection><collection>Wiley Online Library Open Access</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>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content 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><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of diabetes investigation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kawai, Miyuka</au><au>Himeno, Tatsuhito</au><au>Shibata, Yuka</au><au>Hirai, Nobuhiro</au><au>Asada‐Yamada, Yuriko</au><au>Asano‐Hayami, Emi</au><au>Ejima, Yohei</au><au>Kasagi, Rina</au><au>Nagao, Eriko</au><au>Sugiura‐Roth, Yukako</au><au>Nakai‐Shimoda, Hiromi</au><au>Nakayama, Takayuki</au><au>Yamada, Yuichiro</au><au>Ishikawa, Takahiro</au><au>Morishita, Yoshiaki</au><au>Kondo, Masaki</au><au>Tsunekawa, Shin</au><au>Kato, Yoshiro</au><au>Nakamura, Jiro</au><au>Kamiya, Hideki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neuroretinal dysfunction revealed by a flicker electroretinogram correlated with peripheral nerve dysfunction and parameters of atherosclerosis in patients with diabetes</atitle><jtitle>Journal of diabetes investigation</jtitle><addtitle>J Diabetes Investig</addtitle><date>2021-07</date><risdate>2021</risdate><volume>12</volume><issue>7</issue><spage>1236</spage><epage>1243</epage><pages>1236-1243</pages><issn>2040-1116</issn><eissn>2040-1124</eissn><abstract>Aims/Introduction Diabetic polyneuropathy (DPN) develops in the early stage of diabetes. However, no common diagnostic protocol has yet been established. Here, to verify that the flicker electroretinogram using a hand‐held device can detect the early dysfunction of the peripheral nervous system in patients with diabetes, we investigated the correlation between the progression of DPN and neuroretinal dysfunction. Materials and Methods In total, 184 participants with type 1 or 2 diabetes underwent a flicker electroretinogram (ERG) using a hand‐held device RETeval™ and nerve conduction study. Participants were also evaluated for intima‐media thickness, ankle‐brachial index, toe brachial index and brachial‐ankle pulse wave velocity. Parameters of the nerve conduction study were used to diagnose the severity according to Baba’s classification. A multiple regression analysis was used to examine the associations of ERG parameters with the severity of DPN categorized by Baba’s classification. Diagnostic properties of the device in DPN were evaluated using a receiver operating characteristic curve. Results A multiple regression model to predict the severity of DPN was generated using ERG. In the model, moderate‐to‐severe DPN was effectively diagnosed (area under the receiver operating characteristic curve 0.692, sensitivity 56.5%, specificity 78.3%, positive predictive value 70.6%, negative predictive value 66.1%, positive likelihood ratio 2.60, negative likelihood ratio 0.56). In the patients without diabetic retinopathy, the implicit time and amplitude in ERG significantly correlated with the parameters of the nerve conduction study, brachial‐ankle pulse wave velocity and intima‐media thickness. Conclusions Electroretinogram parameters obtained by the hand‐held device successfully predict the severity of DPN. The device might be useful to evaluate DPN. The progression of diabetic retinopathy and the dysfunction of neuroretina evaluated using the mydriasis‐free flicker electroretinogram showed a significant correlation. In patients without apparent diabetic retinopathy, the electroretinogram data correlated with parameters indicating vascular dysfunction, and with parameters indicating diabetic polyneuropathy, such as data of a nerve conduction study. Therefore, the electroretinogram data might reflect the neural and vascular impairments of the retina in patients with diabetes. The electroretinogram data were able to be used to predict the severity of diabetic polyneuropathy.</abstract><cop>Japan</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>33210835</pmid><doi>10.1111/jdi.13465</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-0558-3404</orcidid><orcidid>https://orcid.org/0000-0002-5677-1125</orcidid><orcidid>https://orcid.org/0000-0002-3008-292X</orcidid><oa>free_for_read</oa></addata></record>
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subjects Aged
Ankle
Ankle Brachial Index
Arteriosclerosis
Atherosclerosis
Atherosclerosis - complications
Atherosclerosis - physiopathology
Carotid Intima-Media Thickness
Classification
Creatinine
Diabetes
Diabetes mellitus (insulin dependent)
Diabetes Mellitus, Type 1 - complications
Diabetes Mellitus, Type 1 - physiopathology
Diabetes Mellitus, Type 2 - complications
Diabetes Mellitus, Type 2 - physiopathology
Diabetic neuropathies
Diabetic Neuropathies - diagnosis
Diabetic Neuropathies - etiology
Diabetic neuropathy
Diabetic retinopathy
Diabetic Retinopathy - diagnosis
Diabetic Retinopathy - etiology
Edema
Electroretinography
Electroretinography - instrumentation
Electroretinography - methods
Female
Humans
Kinases
Laboratories
Male
Medical personnel
Middle Aged
Multiple regression analysis
Nerve conduction
Nervous system
Neural Conduction - physiology
Original
Patients
Peripheral nerves
Peripheral Nerves - physiopathology
Point‐of‐care testing
Polyneuropathy
Predictive Value of Tests
Pulse Wave Analysis
Retinopathy
ROC Curve
Severity of Illness Index
Skin
Velocity
title Neuroretinal dysfunction revealed by a flicker electroretinogram correlated with peripheral nerve dysfunction and parameters of atherosclerosis in patients with diabetes
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