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The Relationship between Carotid Intima-Media Thickness and Ocular Circulation in Type-2 Diabetes
Purpose. To compare clinical findings, including ocular blood flow and intima-media thickness (IMT) of the carotid artery, in mild nonproliferative diabetic retinopathy (NPDR) and no diabetic retinopathy (NDR) patients, and to determine risk factors contributing to mild NPDR. Methods. In 129 subject...
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Published in: | Journal of ophthalmology 2019-01, Vol.2019 (2019), p.1-8 |
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description | Purpose. To compare clinical findings, including ocular blood flow and intima-media thickness (IMT) of the carotid artery, in mild nonproliferative diabetic retinopathy (NPDR) and no diabetic retinopathy (NDR) patients, and to determine risk factors contributing to mild NPDR. Methods. In 129 subjects (129 eyes) with type-2 diabetes patients and mild NPDR or NDR, standard statistical techniques were used to determine associations between clinical findings, including diabetes duration, blood levels of creatinine and hemoglobin A1c (HbA1c), central macular thickness (CMT; measured with optical coherence tomography), mean blur rate (MBR; measured with laser speckle flowgraphy), and ultrasound-measured carotid IMT. Results. Diabetes duration, IMT, and CMT were significantly higher in the mild NPDR patients than the NDR patients (P=0.004, P=0.004, and P=0.003, respectively), while conversely, MBR in the overall optic nerve head (MBR-A) was lower in the mild NPDR patients. Furthermore, a logistic regression analysis showed that diabetes duration (OR, 1.11; P=0.006), diastolic blood pressure (OR, 0.93; P=0.025), heart rate (OR, 1.07; P=0.004), IMT (OR, 8.65; P=0.005), and CMT (OR, 1.03; P=0.007) were independent contributing factors to mild NPDR. Spearman’s rank correlation test also showed that IMT was negatively correlated with MBR-A (P=0.011). Conclusions. Increased IMT showed a close association with ocular ischemia in patients with type-2 diabetes and contributed to the presence of mild NPDR. These findings suggest that IMT may be an early biomarker of mild NPDR. |
doi_str_mv | 10.1155/2019/3421305 |
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To compare clinical findings, including ocular blood flow and intima-media thickness (IMT) of the carotid artery, in mild nonproliferative diabetic retinopathy (NPDR) and no diabetic retinopathy (NDR) patients, and to determine risk factors contributing to mild NPDR. Methods. In 129 subjects (129 eyes) with type-2 diabetes patients and mild NPDR or NDR, standard statistical techniques were used to determine associations between clinical findings, including diabetes duration, blood levels of creatinine and hemoglobin A1c (HbA1c), central macular thickness (CMT; measured with optical coherence tomography), mean blur rate (MBR; measured with laser speckle flowgraphy), and ultrasound-measured carotid IMT. Results. Diabetes duration, IMT, and CMT were significantly higher in the mild NPDR patients than the NDR patients (P=0.004, P=0.004, and P=0.003, respectively), while conversely, MBR in the overall optic nerve head (MBR-A) was lower in the mild NPDR patients. Furthermore, a logistic regression analysis showed that diabetes duration (OR, 1.11; P=0.006), diastolic blood pressure (OR, 0.93; P=0.025), heart rate (OR, 1.07; P=0.004), IMT (OR, 8.65; P=0.005), and CMT (OR, 1.03; P=0.007) were independent contributing factors to mild NPDR. Spearman’s rank correlation test also showed that IMT was negatively correlated with MBR-A (P=0.011). Conclusions. Increased IMT showed a close association with ocular ischemia in patients with type-2 diabetes and contributed to the presence of mild NPDR. These findings suggest that IMT may be an early biomarker of mild NPDR.</description><identifier>ISSN: 2090-004X</identifier><identifier>EISSN: 2090-0058</identifier><identifier>DOI: 10.1155/2019/3421305</identifier><identifier>PMID: 30915237</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Age ; Analysis ; Atherosclerosis ; Biomarkers ; Blood pressure ; Carotid arteries ; Creatinine ; Diabetes ; Diabetic retinopathy ; Glaucoma ; Glucose ; Glycosylated hemoglobin ; Heart beat ; Medical research ; Medicine, Experimental ; Risk factors ; Type 2 diabetes ; Ultrasonic imaging ; Vascular endothelial growth factor ; Veins & arteries</subject><ispartof>Journal of ophthalmology, 2019-01, Vol.2019 (2019), p.1-8</ispartof><rights>Copyright © 2019 Kohei Ichinohasama et al.</rights><rights>COPYRIGHT 2019 John Wiley & Sons, Inc.</rights><rights>Copyright © 2019 Kohei Ichinohasama et al. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright © 2019 Kohei Ichinohasama et al. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c701t-9c6c7dcc8dd6409cbf72a10c1dbf6df32672f8c3f04e27e459286e8faefecb5a3</citedby><cites>FETCH-LOGICAL-c701t-9c6c7dcc8dd6409cbf72a10c1dbf6df32672f8c3f04e27e459286e8faefecb5a3</cites><orcidid>0000-0003-0642-793X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2407640545/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2407640545?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30915237$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Ahmadieh, Hamid</contributor><contributor>Hamid Ahmadieh</contributor><creatorcontrib>Nakazawa, Toru</creatorcontrib><creatorcontrib>Katagiri, Hideki</creatorcontrib><creatorcontrib>Kondo, Keiichi</creatorcontrib><creatorcontrib>Sawada, Shojiro</creatorcontrib><creatorcontrib>Yasuda, Masayuki</creatorcontrib><creatorcontrib>Ito, Azusa</creatorcontrib><creatorcontrib>Kunikata, Hiroshi</creatorcontrib><creatorcontrib>Ichinohasama, Kohei</creatorcontrib><creatorcontrib>Satake, Chihiro</creatorcontrib><title>The Relationship between Carotid Intima-Media Thickness and Ocular Circulation in Type-2 Diabetes</title><title>Journal of ophthalmology</title><addtitle>J Ophthalmol</addtitle><description>Purpose. To compare clinical findings, including ocular blood flow and intima-media thickness (IMT) of the carotid artery, in mild nonproliferative diabetic retinopathy (NPDR) and no diabetic retinopathy (NDR) patients, and to determine risk factors contributing to mild NPDR. Methods. In 129 subjects (129 eyes) with type-2 diabetes patients and mild NPDR or NDR, standard statistical techniques were used to determine associations between clinical findings, including diabetes duration, blood levels of creatinine and hemoglobin A1c (HbA1c), central macular thickness (CMT; measured with optical coherence tomography), mean blur rate (MBR; measured with laser speckle flowgraphy), and ultrasound-measured carotid IMT. Results. Diabetes duration, IMT, and CMT were significantly higher in the mild NPDR patients than the NDR patients (P=0.004, P=0.004, and P=0.003, respectively), while conversely, MBR in the overall optic nerve head (MBR-A) was lower in the mild NPDR patients. Furthermore, a logistic regression analysis showed that diabetes duration (OR, 1.11; P=0.006), diastolic blood pressure (OR, 0.93; P=0.025), heart rate (OR, 1.07; P=0.004), IMT (OR, 8.65; P=0.005), and CMT (OR, 1.03; P=0.007) were independent contributing factors to mild NPDR. Spearman’s rank correlation test also showed that IMT was negatively correlated with MBR-A (P=0.011). Conclusions. Increased IMT showed a close association with ocular ischemia in patients with type-2 diabetes and contributed to the presence of mild NPDR. These findings suggest that IMT may be an early biomarker of mild NPDR.</description><subject>Age</subject><subject>Analysis</subject><subject>Atherosclerosis</subject><subject>Biomarkers</subject><subject>Blood pressure</subject><subject>Carotid arteries</subject><subject>Creatinine</subject><subject>Diabetes</subject><subject>Diabetic retinopathy</subject><subject>Glaucoma</subject><subject>Glucose</subject><subject>Glycosylated hemoglobin</subject><subject>Heart beat</subject><subject>Medical research</subject><subject>Medicine, Experimental</subject><subject>Risk factors</subject><subject>Type 2 diabetes</subject><subject>Ultrasonic imaging</subject><subject>Vascular endothelial growth factor</subject><subject>Veins & arteries</subject><issn>2090-004X</issn><issn>2090-0058</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNks1rFDEYhwdRbKm9eZYBQQSdNp-TmYtQ1q-FSkFW8BYyyZud1NlkTWYs_e_NdtdtVzyYHBKSJ0-Sl19RPMfoDGPOzwnC7TllBFPEHxXHBLWoQog3j_dz9v2oOE3pGuVGMeMcPS2OKGoxJ1QcF2rRQ_kVBjW64FPv1mUH4w2AL2cqhtGZcu5Ht1LVFzBOlYve6R8eUiqVN-WVngYVy5mLm8nGUDpfLm7XUJHyvVNZBelZ8cSqIcHpbjwpvn38sJh9ri6vPs1nF5eVFgiPVatrLYzWjTE1Q63urCAKI41NZ2tjKakFsY2mFjEgAhhvSVNDYxVY0B1X9KSYb70mqGu5jvnR8VYG5eTdQohLqeLo9ACy6TATwhrRWc5AsKarEe26TnDbgtY8u95tXeupW4HR4MeohgPp4Y53vVyGXzI_nRBcZ8HrnSCGnxOkUa5c0jAMykOYkiS4bXiNmhZl9OVf6HWYos-lkoQhkY2c8XtqqfIHnLch36s3UnlRE4oFRYRl6uwfVO4GVk4HD9bl9YMDrx4c6EENY5_CMN2l4RB8uwV1DClFsPtiYCQ3UZSbKMpdFDP-4mEB9_Cf4GXgzRbonTfqxv2nDjIDVt3TuOGMtPQ3VLHt1Q</recordid><startdate>20190101</startdate><enddate>20190101</enddate><creator>Nakazawa, Toru</creator><creator>Katagiri, Hideki</creator><creator>Kondo, Keiichi</creator><creator>Sawada, Shojiro</creator><creator>Yasuda, Masayuki</creator><creator>Ito, Azusa</creator><creator>Kunikata, Hiroshi</creator><creator>Ichinohasama, Kohei</creator><creator>Satake, Chihiro</creator><general>Hindawi Publishing Corporation</general><general>Hindawi</general><general>John Wiley & Sons, Inc</general><general>Hindawi Limited</general><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</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>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/0000-0003-0642-793X</orcidid></search><sort><creationdate>20190101</creationdate><title>The Relationship between Carotid Intima-Media Thickness and Ocular Circulation in Type-2 Diabetes</title><author>Nakazawa, Toru ; Katagiri, Hideki ; Kondo, Keiichi ; Sawada, Shojiro ; Yasuda, Masayuki ; Ito, Azusa ; Kunikata, Hiroshi ; Ichinohasama, Kohei ; Satake, Chihiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c701t-9c6c7dcc8dd6409cbf72a10c1dbf6df32672f8c3f04e27e459286e8faefecb5a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Age</topic><topic>Analysis</topic><topic>Atherosclerosis</topic><topic>Biomarkers</topic><topic>Blood pressure</topic><topic>Carotid arteries</topic><topic>Creatinine</topic><topic>Diabetes</topic><topic>Diabetic retinopathy</topic><topic>Glaucoma</topic><topic>Glucose</topic><topic>Glycosylated hemoglobin</topic><topic>Heart beat</topic><topic>Medical research</topic><topic>Medicine, Experimental</topic><topic>Risk factors</topic><topic>Type 2 diabetes</topic><topic>Ultrasonic imaging</topic><topic>Vascular endothelial growth factor</topic><topic>Veins & arteries</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nakazawa, Toru</creatorcontrib><creatorcontrib>Katagiri, Hideki</creatorcontrib><creatorcontrib>Kondo, Keiichi</creatorcontrib><creatorcontrib>Sawada, Shojiro</creatorcontrib><creatorcontrib>Yasuda, Masayuki</creatorcontrib><creatorcontrib>Ito, Azusa</creatorcontrib><creatorcontrib>Kunikata, Hiroshi</creatorcontrib><creatorcontrib>Ichinohasama, Kohei</creatorcontrib><creatorcontrib>Satake, Chihiro</creatorcontrib><collection>الدوريات العلمية والإحصائية - e-Marefa Academic and Statistical Periodicals</collection><collection>معرفة - المحتوى العربي الأكاديمي المتكامل - e-Marefa Academic Complete</collection><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & 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</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>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 ophthalmology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nakazawa, Toru</au><au>Katagiri, Hideki</au><au>Kondo, Keiichi</au><au>Sawada, Shojiro</au><au>Yasuda, Masayuki</au><au>Ito, Azusa</au><au>Kunikata, Hiroshi</au><au>Ichinohasama, Kohei</au><au>Satake, Chihiro</au><au>Ahmadieh, Hamid</au><au>Hamid Ahmadieh</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Relationship between Carotid Intima-Media Thickness and Ocular Circulation in Type-2 Diabetes</atitle><jtitle>Journal of ophthalmology</jtitle><addtitle>J Ophthalmol</addtitle><date>2019-01-01</date><risdate>2019</risdate><volume>2019</volume><issue>2019</issue><spage>1</spage><epage>8</epage><pages>1-8</pages><issn>2090-004X</issn><eissn>2090-0058</eissn><abstract>Purpose. To compare clinical findings, including ocular blood flow and intima-media thickness (IMT) of the carotid artery, in mild nonproliferative diabetic retinopathy (NPDR) and no diabetic retinopathy (NDR) patients, and to determine risk factors contributing to mild NPDR. Methods. In 129 subjects (129 eyes) with type-2 diabetes patients and mild NPDR or NDR, standard statistical techniques were used to determine associations between clinical findings, including diabetes duration, blood levels of creatinine and hemoglobin A1c (HbA1c), central macular thickness (CMT; measured with optical coherence tomography), mean blur rate (MBR; measured with laser speckle flowgraphy), and ultrasound-measured carotid IMT. Results. Diabetes duration, IMT, and CMT were significantly higher in the mild NPDR patients than the NDR patients (P=0.004, P=0.004, and P=0.003, respectively), while conversely, MBR in the overall optic nerve head (MBR-A) was lower in the mild NPDR patients. Furthermore, a logistic regression analysis showed that diabetes duration (OR, 1.11; P=0.006), diastolic blood pressure (OR, 0.93; P=0.025), heart rate (OR, 1.07; P=0.004), IMT (OR, 8.65; P=0.005), and CMT (OR, 1.03; P=0.007) were independent contributing factors to mild NPDR. Spearman’s rank correlation test also showed that IMT was negatively correlated with MBR-A (P=0.011). Conclusions. Increased IMT showed a close association with ocular ischemia in patients with type-2 diabetes and contributed to the presence of mild NPDR. These findings suggest that IMT may be an early biomarker of mild NPDR.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>30915237</pmid><doi>10.1155/2019/3421305</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-0642-793X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Age Analysis Atherosclerosis Biomarkers Blood pressure Carotid arteries Creatinine Diabetes Diabetic retinopathy Glaucoma Glucose Glycosylated hemoglobin Heart beat Medical research Medicine, Experimental Risk factors Type 2 diabetes Ultrasonic imaging Vascular endothelial growth factor Veins & arteries |
title | The Relationship between Carotid Intima-Media Thickness and Ocular Circulation in Type-2 Diabetes |
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