Correlation of Inner Retinal Thickness Evaluated by Spectral-Domain Optical Coherence Tomography and Contrast Sensitivity in Parkinson disease
BACKGROUND:To compare inner retinal layer (IRL) thickness measured by spectral-domain optical coherence tomography (SD-OCT) and contrast sensitivity (CS) in patients with Parkinson disease (PD) and in healthy control (HC) subjects. METHODS:Consecutive patients with and without PD were prospectively...
Saved in:
Published in | Journal of neuro-ophthalmology Vol. 33; no. 2; pp. 137 - 142 |
---|---|
Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Lippincott Williams & Wilkins, Inc
01.06.2013
|
Subjects | |
Online Access | Get full text |
ISSN | 1070-8022 1536-5166 1536-5166 |
DOI | 10.1097/WNO.0b013e31828c4e1a |
Cover
Loading…
Abstract | BACKGROUND:To compare inner retinal layer (IRL) thickness measured by spectral-domain optical coherence tomography (SD-OCT) and contrast sensitivity (CS) in patients with Parkinson disease (PD) and in healthy control (HC) subjects.
METHODS:Consecutive patients with and without PD were prospectively analyzed using SD-OCT and Pelli-Robson CS testing. SD-OCT IRL (ganglion-cell complex) thickness, consisting of the nerve fiber layer, ganglion cell layer, and inner plexiform layer, was segmented using an RTVue Model-RT100 with an EMM5 scan parameter covering a 5.0 × 5.0 mm cube centered on the fovea. Thickness voxel measurements at 0.25-mm intervals at sequential radial distances from the foveola were acquired horizontally and vertically. SD-OCT thickness raw data files were imported and analyzed within MATLAB (version 7.10.0). A database of CS scores and IRL thickness values by foveal location was constructed and statistically evaluated using JMP 10 (SAS Institute, Inc, Cary, NC).
RESULTS:The results were compared between 28 eyes of 14 patients with PD and 28 eyes of 14 HC subjects. Controlling for age, mean CS scores of monocular right and randomized eyes were statistically lower in PD eyes (P < 0.05). IRL was significantly thinner in PD eyes than in HC eyes at several distances from the foveola (P < 0.05). The most numerous and significant thickness differences by diagnosis were located in the superior quadrant at a distance of 1.00–1.75 mm from the foveal center (17 μm; P < 0.01, maximum significant thickness difference and P value). Correlation was demonstrated between monocular CS and IRL thickness by diagnosis at multiple foveal locations for HC eyes as followsnasal quadrant, 0.75–1.00 mm (P < 0.02); temporal quadrant, 0.50–1.00 mm (P < 0.05); superior quadrant, 1.00 mm (P < 0.05); and inferior quadrant, 1.00 mm (P < 0.03). No significant correlation was found between monocular CS and IRL thickness within PD subjects (P > 0.05 for each foveal location measured).
CONCLUSION:CS and foveal IRL thickness are decreased in patients with PD. CS and IRL thickness correlated in HC subjects; however, no such correlation was demonstrated in PD. The functional deficit of dopaminergic interneurons, including amacrine cells, may outstrip the anatomic structural changes in the inner retina of PD patients. Inner retinal atrophic changes may underlie the pathogenesis of CS deficit and IRL thinning in PD. |
---|---|
AbstractList | To compare inner retinal layer (IRL) thickness measured by spectral-domain optical coherence tomography (SD-OCT) and contrast sensitivity (CS) in patients with Parkinson disease (PD) and in healthy control (HC) subjects.BACKGROUNDTo compare inner retinal layer (IRL) thickness measured by spectral-domain optical coherence tomography (SD-OCT) and contrast sensitivity (CS) in patients with Parkinson disease (PD) and in healthy control (HC) subjects.Consecutive patients with and without PD were prospectively analyzed using SD-OCT and Pelli-Robson CS testing. SD-OCT IRL (ganglion-cell complex) thickness, consisting of the nerve fiber layer, ganglion cell layer, and inner plexiform layer, was segmented using an RTVue Model-RT100 with an EMM5 scan parameter covering a 5.0 × 5.0 mm cube centered on the fovea. Thickness voxel measurements at 0.25-mm intervals at sequential radial distances from the foveola were acquired horizontally and vertically. SD-OCT thickness raw data files were imported and analyzed within MATLAB (version 7.10.0). A database of CS scores and IRL thickness values by foveal location was constructed and statistically evaluated using JMP 10 (SAS Institute, Inc, Cary, NC).METHODSConsecutive patients with and without PD were prospectively analyzed using SD-OCT and Pelli-Robson CS testing. SD-OCT IRL (ganglion-cell complex) thickness, consisting of the nerve fiber layer, ganglion cell layer, and inner plexiform layer, was segmented using an RTVue Model-RT100 with an EMM5 scan parameter covering a 5.0 × 5.0 mm cube centered on the fovea. Thickness voxel measurements at 0.25-mm intervals at sequential radial distances from the foveola were acquired horizontally and vertically. SD-OCT thickness raw data files were imported and analyzed within MATLAB (version 7.10.0). A database of CS scores and IRL thickness values by foveal location was constructed and statistically evaluated using JMP 10 (SAS Institute, Inc, Cary, NC).The results were compared between 28 eyes of 14 patients with PD and 28 eyes of 14 HC subjects. Controlling for age, mean CS scores of monocular right and randomized eyes were statistically lower in PD eyes (P < 0.05). IRL was significantly thinner in PD eyes than in HC eyes at several distances from the foveola (P < 0.05). The most numerous and significant thickness differences by diagnosis were located in the superior quadrant at a distance of 1.00-1.75 mm from the foveal center (17 μm; P < 0.01, maximum significant thickness difference and P value). Correlation was demonstrated between monocular CS and IRL thickness by diagnosis at multiple foveal locations for HC eyes as follows: nasal quadrant, 0.75-1.00 mm (P < 0.02); temporal quadrant, 0.50-1.00 mm (P < 0.05); superior quadrant, 1.00 mm (P < 0.05); and inferior quadrant, 1.00 mm (P < 0.03). No significant correlation was found between monocular CS and IRL thickness within PD subjects (P > 0.05 for each foveal location measured).RESULTSThe results were compared between 28 eyes of 14 patients with PD and 28 eyes of 14 HC subjects. Controlling for age, mean CS scores of monocular right and randomized eyes were statistically lower in PD eyes (P < 0.05). IRL was significantly thinner in PD eyes than in HC eyes at several distances from the foveola (P < 0.05). The most numerous and significant thickness differences by diagnosis were located in the superior quadrant at a distance of 1.00-1.75 mm from the foveal center (17 μm; P < 0.01, maximum significant thickness difference and P value). Correlation was demonstrated between monocular CS and IRL thickness by diagnosis at multiple foveal locations for HC eyes as follows: nasal quadrant, 0.75-1.00 mm (P < 0.02); temporal quadrant, 0.50-1.00 mm (P < 0.05); superior quadrant, 1.00 mm (P < 0.05); and inferior quadrant, 1.00 mm (P < 0.03). No significant correlation was found between monocular CS and IRL thickness within PD subjects (P > 0.05 for each foveal location measured).CS and foveal IRL thickness are decreased in patients with PD. CS and IRL thickness correlated in HC subjects; however, no such correlation was demonstrated in PD. The functional deficit of dopaminergic interneurons, including amacrine cells, may outstrip the anatomic structural changes in the inner retina of PD patients. Inner retinal atrophic changes may underlie the pathogenesis of CS deficit and IRL thinning in PD.CONCLUSIONCS and foveal IRL thickness are decreased in patients with PD. CS and IRL thickness correlated in HC subjects; however, no such correlation was demonstrated in PD. The functional deficit of dopaminergic interneurons, including amacrine cells, may outstrip the anatomic structural changes in the inner retina of PD patients. Inner retinal atrophic changes may underlie the pathogenesis of CS deficit and IRL thinning in PD. To compare inner retinal layer (IRL) thickness measured by spectral-domain optical coherence tomography (SD-OCT) and contrast sensitivity (CS) in patients with Parkinson disease (PD) and in healthy control (HC) subjects. Consecutive patients with and without PD were prospectively analyzed using SD-OCT and Pelli-Robson CS testing. SD-OCT IRL (ganglion-cell complex) thickness, consisting of the nerve fiber layer, ganglion cell layer, and inner plexiform layer, was segmented using an RTVue Model-RT100 with an EMM5 scan parameter covering a 5.0 × 5.0 mm cube centered on the fovea. Thickness voxel measurements at 0.25-mm intervals at sequential radial distances from the foveola were acquired horizontally and vertically. SD-OCT thickness raw data files were imported and analyzed within MATLAB (version 7.10.0). A database of CS scores and IRL thickness values by foveal location was constructed and statistically evaluated using JMP 10 (SAS Institute, Inc, Cary, NC). The results were compared between 28 eyes of 14 patients with PD and 28 eyes of 14 HC subjects. Controlling for age, mean CS scores of monocular right and randomized eyes were statistically lower in PD eyes (P < 0.05). IRL was significantly thinner in PD eyes than in HC eyes at several distances from the foveola (P < 0.05). The most numerous and significant thickness differences by diagnosis were located in the superior quadrant at a distance of 1.00-1.75 mm from the foveal center (17 μm; P < 0.01, maximum significant thickness difference and P value). Correlation was demonstrated between monocular CS and IRL thickness by diagnosis at multiple foveal locations for HC eyes as follows: nasal quadrant, 0.75-1.00 mm (P < 0.02); temporal quadrant, 0.50-1.00 mm (P < 0.05); superior quadrant, 1.00 mm (P < 0.05); and inferior quadrant, 1.00 mm (P < 0.03). No significant correlation was found between monocular CS and IRL thickness within PD subjects (P > 0.05 for each foveal location measured). CS and foveal IRL thickness are decreased in patients with PD. CS and IRL thickness correlated in HC subjects; however, no such correlation was demonstrated in PD. The functional deficit of dopaminergic interneurons, including amacrine cells, may outstrip the anatomic structural changes in the inner retina of PD patients. Inner retinal atrophic changes may underlie the pathogenesis of CS deficit and IRL thinning in PD. BACKGROUND:To compare inner retinal layer (IRL) thickness measured by spectral-domain optical coherence tomography (SD-OCT) and contrast sensitivity (CS) in patients with Parkinson disease (PD) and in healthy control (HC) subjects. METHODS:Consecutive patients with and without PD were prospectively analyzed using SD-OCT and Pelli-Robson CS testing. SD-OCT IRL (ganglion-cell complex) thickness, consisting of the nerve fiber layer, ganglion cell layer, and inner plexiform layer, was segmented using an RTVue Model-RT100 with an EMM5 scan parameter covering a 5.0 × 5.0 mm cube centered on the fovea. Thickness voxel measurements at 0.25-mm intervals at sequential radial distances from the foveola were acquired horizontally and vertically. SD-OCT thickness raw data files were imported and analyzed within MATLAB (version 7.10.0). A database of CS scores and IRL thickness values by foveal location was constructed and statistically evaluated using JMP 10 (SAS Institute, Inc, Cary, NC). RESULTS:The results were compared between 28 eyes of 14 patients with PD and 28 eyes of 14 HC subjects. Controlling for age, mean CS scores of monocular right and randomized eyes were statistically lower in PD eyes (P < 0.05). IRL was significantly thinner in PD eyes than in HC eyes at several distances from the foveola (P < 0.05). The most numerous and significant thickness differences by diagnosis were located in the superior quadrant at a distance of 1.00–1.75 mm from the foveal center (17 μm; P < 0.01, maximum significant thickness difference and P value). Correlation was demonstrated between monocular CS and IRL thickness by diagnosis at multiple foveal locations for HC eyes as followsnasal quadrant, 0.75–1.00 mm (P < 0.02); temporal quadrant, 0.50–1.00 mm (P < 0.05); superior quadrant, 1.00 mm (P < 0.05); and inferior quadrant, 1.00 mm (P < 0.03). No significant correlation was found between monocular CS and IRL thickness within PD subjects (P > 0.05 for each foveal location measured). CONCLUSION:CS and foveal IRL thickness are decreased in patients with PD. CS and IRL thickness correlated in HC subjects; however, no such correlation was demonstrated in PD. The functional deficit of dopaminergic interneurons, including amacrine cells, may outstrip the anatomic structural changes in the inner retina of PD patients. Inner retinal atrophic changes may underlie the pathogenesis of CS deficit and IRL thinning in PD. |
Author | Shrier, Eric Ding, Yin Bodis-Wollner, Ivan Adam, Christopher R. Glazman, Sofya |
AuthorAffiliation | Departments of Ophthalmology (ES) and Neurology (SG, IV-B), College of Medicine (CRA), SUNY-Downstate Medical Center, Brooklyn, New York; SUNY Eye Institute (ES, IV-B), Brooklyn, New York; and Department of Electrical Engineering (YD), Polytechnic Institute of NYU, Brooklyn, New York |
AuthorAffiliation_xml | – name: Departments of Ophthalmology (ES) and Neurology (SG, IV-B), College of Medicine (CRA), SUNY-Downstate Medical Center, Brooklyn, New York; SUNY Eye Institute (ES, IV-B), Brooklyn, New York; and Department of Electrical Engineering (YD), Polytechnic Institute of NYU, Brooklyn, New York |
Author_xml | – sequence: 1 givenname: Christopher surname: Adam middlename: R. fullname: Adam, Christopher R. organization: Departments of Ophthalmology (ES) and Neurology (SG, IV-B), College of Medicine (CRA), SUNY-Downstate Medical Center, Brooklyn, New York; SUNY Eye Institute (ES, IV-B), Brooklyn, New York; and Department of Electrical Engineering (YD), Polytechnic Institute of NYU, Brooklyn, New York – sequence: 2 givenname: Eric surname: Shrier fullname: Shrier, Eric – sequence: 3 givenname: Yin surname: Ding fullname: Ding, Yin – sequence: 4 givenname: Sofya surname: Glazman fullname: Glazman, Sofya – sequence: 5 givenname: Ivan surname: Bodis-Wollner fullname: Bodis-Wollner, Ivan |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/23612240$$D View this record in MEDLINE/PubMed |
BookMark | eNqNkctuFDEQRS0URB7wBwh5yaaDX_1ih4YAkSIGkUEsLbe7TJtx243tTjQ_wTdjSLLJioVll3xulereU3TkgweEXlJyTknfvvn-eXtOBkI5cNqxTgug6gk6oTVvqpo2zVF5k5ZUHWHsGJ2m9JMQwgnrn6FjxhvKmCAn6PcmxAhOZRs8DgZfeg8Rf4VsvXJ4N1m995ASvrhRblUZRjwc8PUCOkflqvdhVtbj7ZKtLvgmTBDBa8C7MIcfUS3TASs_lg9f-JTxNfhks72x-YCL8IuKe-tTGT3aBCrBc_TUKJfgxf19hr59uNhtPlVX24-Xm3dXlRa06yveCaJMz6DuB2UYA9qNugXF2uJIZzShtaZa99rU1HSGibqvG0HVOLDigdD8DL2-67vE8GuFlOVskwbnlIewJkl5zYnglDQFfXWPrsMMo1yinVU8yAcPC_D2DtAxpBTBSG3zP0PLztZJSuTfwGQJTD4OrIjFI_FD__-T3QaXIaa9W28hygmUy5MsQQvKWVuxIiNNKatySM__AFeArJg |
CitedBy_id | crossref_primary_10_1186_s41983_021_00421_1 crossref_primary_10_1016_j_jns_2019_06_009 crossref_primary_10_1111_ene_15896 crossref_primary_10_3389_fncel_2017_00091 crossref_primary_10_1007_s10072_020_04289_6 crossref_primary_10_31083_j_jin2203056 crossref_primary_10_1371_journal_pone_0074439 crossref_primary_10_1007_s00702_020_02224_9 crossref_primary_10_1016_j_neubiorev_2016_01_002 crossref_primary_10_1002_mds_26533 crossref_primary_10_1186_s12920_021_01005_x crossref_primary_10_1007_s00417_018_3957_1 crossref_primary_10_1007_s00401_018_01956_z crossref_primary_10_1038_srep03921 crossref_primary_10_1212_WNL_0000000000006157 crossref_primary_10_1016_j_parkreldis_2024_107229 crossref_primary_10_1016_j_parkreldis_2016_10_006 crossref_primary_10_1097_ICU_0000000000000000 crossref_primary_10_1177_201010581402300112 crossref_primary_10_3389_fnins_2020_00921 crossref_primary_10_1097_WNO_0000000000000203 crossref_primary_10_1186_s40478_016_0346_z crossref_primary_10_1136_bmjopen_2015_009658 crossref_primary_10_1007_s10792_021_02133_0 crossref_primary_10_3389_fnins_2021_726476 crossref_primary_10_1136_practneurol_2020_002824 crossref_primary_10_1016_j_parkreldis_2020_11_025 crossref_primary_10_1002_mds_27454 crossref_primary_10_1016_j_parkreldis_2015_09_015 crossref_primary_10_1016_j_parkreldis_2016_07_004 crossref_primary_10_1167_tvst_13_4_3 crossref_primary_10_1097_OPX_0000000000001650 crossref_primary_10_1002_mds_28182 crossref_primary_10_1038_nrneurol_2014_79 crossref_primary_10_1016_j_exer_2021_108693 crossref_primary_10_1016_j_preteyeres_2018_02_002 crossref_primary_10_1007_s10792_018_0934_y crossref_primary_10_1093_texcom_tgab042 crossref_primary_10_1002_mds_27728 crossref_primary_10_3389_fnins_2020_567129 crossref_primary_10_3389_fneur_2017_00710 crossref_primary_10_1097_OPX_0000000000001449 crossref_primary_10_1016_j_ymgmr_2021_100767 crossref_primary_10_1002_mds_25741 crossref_primary_10_1007_s00702_014_1214_2 crossref_primary_10_1177_2040622319882205 crossref_primary_10_1007_s13760_020_01274_w crossref_primary_10_1186_s12886_016_0216_2 crossref_primary_10_3389_fnins_2021_799526 crossref_primary_10_3389_fnagi_2022_832768 crossref_primary_10_1016_j_preteyeres_2020_100938 crossref_primary_10_1016_j_parkreldis_2015_08_002 crossref_primary_10_1371_journal_pone_0123229 crossref_primary_10_3389_fneur_2020_577362 crossref_primary_10_1002_mds_25896 crossref_primary_10_1167_jov_24_4_5 crossref_primary_10_5664_jcsm_8212 crossref_primary_10_1097_WNO_0000000000000505 crossref_primary_10_3389_fneur_2017_00701 crossref_primary_10_1364_JOSAA_382042 crossref_primary_10_1002_ana_25897 |
Cites_doi | 10.1007/BF01946404 10.1007/s10633-007-9091-8 10.5301/EJO.2010.1318 10.1212/WNL.40.11.1710 10.1016/j.visres.2004.06.009 10.1212/01.wnl.0000280584.64363.83 10.1212/WNL.45.12.2143 10.1016/S0042-6989(00)00036-5 10.1007/BF01186992 10.1212/01.wnl.0000294876.49861.dc 10.1136/bjo.87.7.899 10.1016/S0022-510X(99)00204-X 10.1068/p170315 10.1111/j.1755-3768.1979.tb00517.x 10.1136/bjo.69.1.51 10.1001/archneur.1995.00540340109020 10.1002/mds.1099 10.1001/archopthalmol.2011.1576 10.1016/0168-5597(95)00169-7 10.1093/brain/110.2.415 10.1093/brain/111.1.131 10.1093/brain/110.6.1675 10.1002/1097-0185(20001001)260:2<124::AID-AR20>3.0.CO;2-D 10.1016/j.ophtha.2011.10.010 10.1001/archophthalmol.2009.106 10.1007/s00702-009-0292-z 10.1017/S0952523800002303 10.1136/bjo.2007.131094 10.1023/B:DOOP.0000019487.88486.0a 10.1155/2012/728457 10.1016/0166-2236(90)90113-O 10.1093/brain/101.4.661 10.1016/0042-6989(94)90248-8 10.1016/S0042-6989(97)00129-6 |
ContentType | Journal Article |
Copyright | 2013 Lippincott Williams & Wilkins, Inc. |
Copyright_xml | – notice: 2013 Lippincott Williams & Wilkins, Inc. |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 7X8 |
DOI | 10.1097/WNO.0b013e31828c4e1a |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed MEDLINE - Academic |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic MEDLINE |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1536-5166 |
EndPage | 142 |
ExternalDocumentID | 23612240 10_1097_WNO_0b013e31828c4e1a 00041327-201306000-00009 |
Genre | Randomized Controlled Trial Research Support, Non-U.S. Gov't Journal Article |
GroupedDBID | --- .GJ .Z2 0R~ 2V- 53G 5GY 5RE 5VS AAAAV AAHPQ AAIQE AARTV AASCR AAYEP ABASU ABBUW ABDIG ABJNI ABPXF ABVCZ ABXRP ABXVJ ABZAD ABZZY ACDDN ACEWG ACGFO ACGFS ACILI ACNCT ACWDW ACWRI ACXJB ACXNZ ADBBV ADFPA ADGGA ADHPY ADNKB AE3 AE6 AEETU AENEX AFBFQ AFDTB AFUWQ AHQNM AHRYX AHVBC AINUH AJCLO AJIOK AJNWD AJNYG AJZMW AKCTQ ALKUP ALMA_UNASSIGNED_HOLDINGS ALMTX AMJPA AMKUR AMNEI AOHHW AOQMC BAWUL BQLVK BS7 C45 CS3 DIK DIWNM DU5 DUNZO E.X E3Z EBS EEVPB EJD EX3 F2K F2L F5P FCALG FL- GNXGY GQDEL H0~ HLJTE HZ~ IKREB IN~ IPNFZ JK3 JK8 K8S KD2 KMI L-C N~M O9- OCUKA ODA OK1 OL1 OLG OLV OLZ OPUJH ORVUJ OUVQU OVD OVDNE OXXIT P-K P2P R58 RIG RLZ S4R S4S TEORI TR2 TSPGW V2I W3M WOQ WOW X3V X3W YFH ZFV ZZMQN AAFWJ AAYXX CITATION CGR CUY CVF ECM EIF NPM 7X8 |
ID | FETCH-LOGICAL-c4189-3840af92e59baf22e18dc7ea270b08fc015c1cc9cf51f8f24595641adb20034c3 |
ISSN | 1070-8022 1536-5166 |
IngestDate | Thu Jul 10 23:30:25 EDT 2025 Thu Apr 03 06:56:58 EDT 2025 Tue Jul 01 03:16:28 EDT 2025 Thu Apr 24 23:09:06 EDT 2025 Fri May 16 03:44:05 EDT 2025 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 2 |
Language | English |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c4189-3840af92e59baf22e18dc7ea270b08fc015c1cc9cf51f8f24595641adb20034c3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Undefined-3 |
PMID | 23612240 |
PQID | 1353043106 |
PQPubID | 23479 |
PageCount | 6 |
ParticipantIDs | proquest_miscellaneous_1353043106 pubmed_primary_23612240 crossref_citationtrail_10_1097_WNO_0b013e31828c4e1a crossref_primary_10_1097_WNO_0b013e31828c4e1a wolterskluwer_health_00041327-201306000-00009 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2013-June 2013-06-00 2013-Jun 20130601 |
PublicationDateYYYYMMDD | 2013-06-01 |
PublicationDate_xml | – month: 06 year: 2013 text: 2013-June |
PublicationDecade | 2010 |
PublicationPlace | United States |
PublicationPlace_xml | – name: United States |
PublicationTitle | Journal of neuro-ophthalmology |
PublicationTitleAlternate | J Neuroophthalmol |
PublicationYear | 2013 |
Publisher | Lippincott Williams & Wilkins, Inc |
Publisher_xml | – name: Lippincott Williams & Wilkins, Inc |
References | Bodis-Wollner (R22-9-20210126) 2011; 52 Ikeda (R16-9-20210126) 1994; 34 Witkovsky (R17-9-20210126) 2004; 108 de Rijk (R2-9-20210126) 1995; 45 Bodis-Wollner (R20-9-20210126) 1987; 110 Harnois (R15-9-20210126) 1990; 31 Ross (R28-9-20210126) 1985; 69 Leung (R33-9-20210126) 2012; 119 Djamgoz (R14-9-20210126) 1997; 37 Mestre (R6-9-20210126) 1990; 40 Trenkwalder (R3-9-20210126) 1995; 52 Bodis-Wollner (R7-9-20210126) 1978; 101 Schutte (R13-9-20210126) 1991; 20 Derefeldt (R26-9-20210126) 1979; 57 Reader (R40-9-20210126) 1986; 42 Bodis-Wollner (R38-9-20210126) 2011; 52 Shrier (R42-9-20210126) 2012; 2012 Knight (R29-9-20210126) 2012; 130 Regan (R41-9-20210126) 1987; 110 Valenti (R11-9-20210126) 2007; 69 Aaker (R36-9-20210126) 2010; 4 Altintas (R35-9-20210126) 2008; 1116 Crassini (R25-9-20210126) 1988; 17 Gao (R30-9-20210126) 1992; 33 Bodis-Wollner (R44-9-20210126) 2009; 116 Watson (R21-9-20210126) 1990; 4 La Morgia (R37-9-20210126) 2013; 20 Inzelberg (R34-9-20210126) 2004; 44 Moschos (R39-9-20210126) 2011; 21 Elliott (R27-9-20210126) 1987; 7 Harman (R31-9-20210126) 2000; 260 Bodis-Wollner (R43-9-20210126) 1990; 13 Tagliati (R8-9-20210126) 1996; 100 Ghilardi (R19-9-20210126) 1988; 111 Alamouti (R23-9-20210126) 2003; 87 Shulman (R4-9-20210126) 2001; 16 Rodnitzky (R5-9-20210126) 1998; 5 Pieri (R9-9-20210126) 2000; 172 Hajee (R10-9-20210126) 2009; 127 Pulicken (R12-9-20210126) 2007; 69 Eriksson (R24-9-20210126) 2009; 93 Jonas (R32-9-20210126) 1992; 33 Wink (R18-9-20210126) 2000; 40 |
References_xml | – volume: 4 start-page: 1427 year: 2010 ident: R36-9-20210126 article-title: Detection of retinal changes in Parkinsons disease with spectral-domain optical coherence tomography. publication-title: Clin Ophthalmol – volume: 33 start-page: 1 year: 1992 ident: R30-9-20210126 article-title: Aging of the human retina. Differential loss of neurons and retinal pigment epithelial cells. publication-title: Invest Ophthalmol Vis Sci – volume: 42 start-page: 1242 year: 1986 ident: R40-9-20210126 article-title: Dopamine in the visual cortex of the cat. publication-title: Experientia doi: 10.1007/BF01946404 – volume: 1116 start-page: 137 year: 2008 ident: R35-9-20210126 article-title: Correlation between retinal morphological and functional findings and clinical severity in Parkinsons Disease. publication-title: Doc Ophthalmol doi: 10.1007/s10633-007-9091-8 – volume: 21 start-page: 24 year: 2011 ident: R39-9-20210126 article-title: Morphologic changes and functional retinal impairment in patients with Parkinson disease without visual loss. publication-title: Eur J Ophthalmol doi: 10.5301/EJO.2010.1318 – volume: 40 start-page: 1710 year: 1990 ident: R6-9-20210126 article-title: Spatiotemporal contrast sensitivity differs in normal aging and Parkinsons disease. publication-title: Neurology doi: 10.1212/WNL.40.11.1710 – volume: 44 start-page: 2793 year: 2004 ident: R34-9-20210126 article-title: Retinal nerve fiber layer thinning in Parkinson disease. publication-title: Vision Res doi: 10.1016/j.visres.2004.06.009 – volume: 69 start-page: 1060 year: 2007 ident: R11-9-20210126 article-title: Neuroimaging of retinal nerve fiber layer in AD using optical coherence tomography. publication-title: Neurology doi: 10.1212/01.wnl.0000280584.64363.83 – volume: 7 start-page: 415 year: 1987 ident: R27-9-20210126 article-title: Contrast sensitivity decline with ageing: a neural or optical phenomenon Ophthalmic Physiol Opt. – volume: 45 start-page: 2143 year: 1995 ident: R2-9-20210126 article-title: Prevalence of Parkinsons disease in the elderly: the Rotterdam Study. publication-title: Neurology doi: 10.1212/WNL.45.12.2143 – volume: 31 start-page: 2473 year: 1990 ident: R15-9-20210126 article-title: Decreased dopamine in the retinas of patients with Parkinsons disease. publication-title: Invest Ophthalmol Vis Sci – volume: 40 start-page: 1937 year: 2000 ident: R18-9-20210126 article-title: A model of the parkinsonian visual system: support for the dark adaptation hypothesis. publication-title: Vision Res doi: 10.1016/S0042-6989(00)00036-5 – volume: 20 start-page: 195 year: 1991 ident: R13-9-20210126 article-title: Dopaminergic interplexiform cells and centrifugal fibres in the Xenopus retina. publication-title: J Neurocytol doi: 10.1007/BF01186992 – volume: 33 start-page: 2012 year: 1992 ident: R32-9-20210126 article-title: Human optic nerve fiber count and optic disc size. publication-title: Invest Ophthalmol Vis Sci – volume: 69 start-page: 2085 year: 2007 ident: R12-9-20210126 article-title: Optical coherence tomography and disease subtype in multiple sclerosis. publication-title: Neurology doi: 10.1212/01.wnl.0000294876.49861.dc – volume: 87 start-page: 899 year: 2003 ident: R23-9-20210126 article-title: Retinal thickness decreases with age: an OCT study. publication-title: Br J Ophthalmol doi: 10.1136/bjo.87.7.899 – volume: 172 start-page: 7 year: 2000 ident: R9-9-20210126 article-title: Decreased color discrimination and contrast sensitivity in Parkinsons disease. publication-title: J Neurol Sci doi: 10.1016/S0022-510X(99)00204-X – volume: 20 start-page: 198 year: 2013 ident: R37-9-20210126 article-title: Loss of temporal retinal nerve fibers in Parkinson disease: a mitochondrial pattern Eur J Neurol. – volume: 17 start-page: 315 year: 1988 ident: R25-9-20210126 article-title: Age-related changes in contrast sensitivity in central and peripheral retina. publication-title: Perception doi: 10.1068/p170315 – volume: 57 start-page: 679 year: 1979 ident: R26-9-20210126 article-title: Age variations in normal human contrast sensitivity. publication-title: Acta Ophthalmol (Copenh) doi: 10.1111/j.1755-3768.1979.tb00517.x – volume: 69 start-page: 51 year: 1985 ident: R28-9-20210126 article-title: Effect of age on contrast sensitivity function: uniocular and binocular findings. publication-title: Br J Ophthalmol doi: 10.1136/bjo.69.1.51 – volume: 52 start-page: 1017 year: 1995 ident: R3-9-20210126 article-title: Starnberg trial on epidemiology of parkinsonism and hypertension in the elderly. Prevalence of Parkinsons disease and related disorders assessed by a door-to-door survey of inhabitants older than 65 years. publication-title: Arch Neurol doi: 10.1001/archneur.1995.00540340109020 – volume: 16 start-page: 507 year: 2001 ident: R4-9-20210126 article-title: Comorbidity of the nonmotor symptoms of Parkinsons disease. publication-title: Mov Disord doi: 10.1002/mds.1099 – volume: 130 start-page: 312 year: 2012 ident: R29-9-20210126 article-title: Effect of race, age, and axial length on optic nerve head parameters and retinal nerve fiber layer thickness measured by Cirrus HD-OCT. publication-title: Arch Ophthalmol doi: 10.1001/archopthalmol.2011.1576 – volume: 100 start-page: 1 year: 1996 ident: R8-9-20210126 article-title: The pattern electroretinogram in Parkinsons disease reveals lack of retinal spatial tuning. publication-title: Electroencephalogr Clin Neurophysiol doi: 10.1016/0168-5597(95)00169-7 – volume: 110 start-page: 415 year: 1987 ident: R41-9-20210126 article-title: Orientation-selective visual loss in patients with Parkinsons disease. publication-title: Brain doi: 10.1093/brain/110.2.415 – volume: 111 start-page: 131 year: 1988 ident: R19-9-20210126 article-title: Spatial frequency dependent abnormalities of the pattern electroretinogram and visual evoked potentials in a parkinsonian monkey model. publication-title: Brain doi: 10.1093/brain/111.1.131 – volume: 52 start-page: 6660 year: 2011 ident: R38-9-20210126 article-title: Remodeling of the fovea in Parkinson disease. publication-title: Invest Ophthalmol Vis Sci – volume: 110 start-page: 1675 year: 1987 ident: R20-9-20210126 article-title: Visual dysfunction in Parkinsons disease. Loss in spatiotemporal contrast sensitivity. publication-title: Brain doi: 10.1093/brain/110.6.1675 – volume: 260 start-page: 124 year: 2000 ident: R31-9-20210126 article-title: Neuronal density in the human retinal ganglion cell layer from 16-77 years. publication-title: Anat Rec doi: 10.1002/1097-0185(20001001)260:2<124::AID-AR20>3.0.CO;2-D – volume: 119 start-page: 731 year: 2012 ident: R33-9-20210126 article-title: Retinal nerve fiber layer imaging with spectral-domain optical coherence tomography: a prospective analysis of age- related loss. publication-title: Ophthalmology doi: 10.1016/j.ophtha.2011.10.010 – volume: 127 start-page: 737 year: 2009 ident: R10-9-20210126 article-title: Inner retinal layer thinning in Parkinson disease. publication-title: Arch Ophthalmol doi: 10.1001/archophthalmol.2009.106 – volume: 116 start-page: 1493 year: 2009 ident: R44-9-20210126 article-title: Retinopathy in Parkinson disease. publication-title: J Neural Transm doi: 10.1007/s00702-009-0292-z – volume: 52 start-page: 6660 year: 2011 ident: R22-9-20210126 article-title: Remodeling of the fovea in Parkinson disease. publication-title: Invest Ophthalmol Vis Sci – volume: 4 start-page: 147 year: 1990 ident: R21-9-20210126 article-title: Gain, noise, and contrast sensitivity of linear visual neurons. publication-title: Vis Neurosci doi: 10.1017/S0952523800002303 – volume: 93 start-page: 1448 year: 2009 ident: R24-9-20210126 article-title: Macular thickness decreases with age in normal eyes: a study on the macular thickness map protocol in the Stratus OCT. publication-title: Br J Ophthalmol doi: 10.1136/bjo.2007.131094 – volume: 108 start-page: 17 year: 2004 ident: R17-9-20210126 article-title: Dopamine and retinal function. publication-title: Doc Ophthalmol doi: 10.1023/B:DOOP.0000019487.88486.0a – volume: 2012 start-page: 728457 year: 2012 ident: R42-9-20210126 article-title: Intraocular asymmetry of foveal thickness in Parkinson disease. publication-title: J Ophthalmol doi: 10.1155/2012/728457 – volume: 13 start-page: 296 year: 1990 ident: R43-9-20210126 article-title: Visual deficits related to dopamine deficiency in experimental animals and Parkinsons disease patients. publication-title: Trends Neurosci doi: 10.1016/0166-2236(90)90113-O – volume: 101 start-page: 661 year: 1978 ident: R7-9-20210126 article-title: Measurements of visual evoked potentials in Parkinsons disease. publication-title: Brain doi: 10.1093/brain/101.4.661 – volume: 34 start-page: 2629 year: 1994 ident: R16-9-20210126 article-title: Electrophysiological signs of retinal dopamine deficiency in recently diagnosed Parkinsons disease and a follow up study. publication-title: Vision Res doi: 10.1016/0042-6989(94)90248-8 – volume: 5 start-page: 102 year: 1998 ident: R5-9-20210126 article-title: Visual dysfunction in Parkinsons disease. publication-title: Clin Neurosci – volume: 37 start-page: 3509 year: 1997 ident: R14-9-20210126 article-title: Neurobiology of retinal dopamine in relation to degenerative states of the tissue. publication-title: Vision Res doi: 10.1016/S0042-6989(97)00129-6 |
SSID | ssj0003029 |
Score | 2.261372 |
Snippet | BACKGROUND:To compare inner retinal layer (IRL) thickness measured by spectral-domain optical coherence tomography (SD-OCT) and contrast sensitivity (CS) in... To compare inner retinal layer (IRL) thickness measured by spectral-domain optical coherence tomography (SD-OCT) and contrast sensitivity (CS) in patients with... |
SourceID | proquest pubmed crossref wolterskluwer |
SourceType | Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 137 |
SubjectTerms | Aged Analysis of Variance Contrast Sensitivity - physiology Female Functional Laterality Humans Male Middle Aged Parkinson Disease - complications Parkinson Disease - diagnosis Perceptual Disorders - diagnosis Perceptual Disorders - etiology Retina - pathology Tomography, Optical Coherence |
Title | Correlation of Inner Retinal Thickness Evaluated by Spectral-Domain Optical Coherence Tomography and Contrast Sensitivity in Parkinson disease |
URI | https://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=fulltext&D=ovft&AN=00041327-201306000-00009 https://www.ncbi.nlm.nih.gov/pubmed/23612240 https://www.proquest.com/docview/1353043106 |
Volume | 33 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3bbtQwELWWIiEQQtxZbjISb1UgcS6bPFblUkAtD7SiPEW24yirZjerblao_Qj-gH9lxrGdbLeIy0u0yia2lHMyHk9mzhDyEtbYRKo49jhTKWxQUuHxkGO0KRCwfIZJIrDeef8g2TuKPh7Hx6PRz0HW0qoVr-T5pXUl_4MqnANcsUr2H5B1g8IJ-A34whEQhuNfYbyLrTVq5_TpNlrbWJaoU8irqTzRhswoene-pi6tPOW1VzQzPoX7Fq0RCamM4mzbzIyOtSl6w_jvst1eYq67aTYBN2K9tC4dW_vIs-nnasVMr1lUbcXr2VoUf6fo6DhQOOgTGL9U2EzP2mrncJseLN-mjtXva35u47hNecaHgQzdVMIGMpQ1vokXB10XFmudO5kMw0I2MLVBJxazsQR00sJfDz73MV6WykgFfHg5ALmYaVqg-gz6Nf2C6NIU7V9XyFUGuxC0-28-fHILfeizzFZjZpPXl02JWtNmkHXHZ2M3c4Pc_N5ggsTyRNdHDLycw9vkloGN7nRcu0NGan6XXNs3CRj3yI8B5WhTUk05aihHHeWooxwVZ_QC5aihHHWUoz3lKFCOWsrRAeVgKuooRw3l7pOjd28Pd_c809LDk1GQZl6YRj4vM6biTPCSMRWkhZwozibw5NJSgnMqAykzWcZBmZYsimH_HgW8EJhEGcnwAdmaN3P1CHPy-CQUBZOocclFLDi4wjCKFDLLJFNjEtrnnUujd49tV-rc5l0AYPlFwMbEc3ctOr2XP1z_wkKZg2HGr218rprVMseGMqhc5Sdj8rDD2I1oOQGzrYGed8XPmBECziWbePie-IlRf_Czx78d6Qm53r9TT8lWe7pSz8BdbsVzTdpfPu3FVg |
linkProvider | Flying Publisher |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Correlation+of+inner+retinal+thickness+evaluated+by+spectral-domain+optical+coherence+tomography+and+contrast+sensitivity+in+Parkinson+disease&rft.jtitle=Journal+of+neuro-ophthalmology&rft.au=Adam%2C+Christopher+R&rft.au=Shrier%2C+Eric&rft.au=Ding%2C+Yin&rft.au=Glazman%2C+Sofya&rft.date=2013-06-01&rft.eissn=1536-5166&rft.volume=33&rft.issue=2&rft.spage=137&rft_id=info:doi/10.1097%2FWNO.0b013e31828c4e1a&rft_id=info%3Apmid%2F23612240&rft.externalDocID=23612240 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1070-8022&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1070-8022&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1070-8022&client=summon |