Assessment of Different Sampling Methods for Measuring and Representing Macular Cone Density Using Flood-Illuminated Adaptive Optics

To describe a standardized flood-illuminated adaptive optics (AO) imaging protocol suitable for the clinical setting and to assess sampling methods for measuring cone density. Cone density was calculated following three measurement protocols: 50 × 50-μm sampling window values every 0.5° along the ho...

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Published inInvestigative ophthalmology & visual science Vol. 56; no. 10; pp. 5751 - 5763
Main Authors Feng, Shu, Gale, Michael J., Fay, Jonathan D., Faridi, Ambar, Titus, Hope E., Garg, Anupam K., Michaels, Keith V., Erker, Laura R., Peters, Dawn, Smith, Travis B., Pennesi, Mark E.
Format Journal Article
LanguageEnglish
Published United States The Association for Research in Vision and Ophthalmology 01.09.2015
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ISSN1552-5783
0146-0404
1552-5783
DOI10.1167/iovs.15-16954

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Abstract To describe a standardized flood-illuminated adaptive optics (AO) imaging protocol suitable for the clinical setting and to assess sampling methods for measuring cone density. Cone density was calculated following three measurement protocols: 50 × 50-μm sampling window values every 0.5° along the horizontal and vertical meridians (fixed-interval method), the mean density of expanding 0.5°-wide arcuate areas in the nasal, temporal, superior, and inferior quadrants (arcuate mean method), and the peak cone density of a 50 × 50-μm sampling window within expanding arcuate areas near the meridian (peak density method). Repeated imaging was performed in nine subjects to determine intersession repeatability of cone density. Cone density montages could be created for 67 of the 74 subjects. Image quality was determined to be adequate for automated cone counting for 35 (52%) of the 67 subjects. We found that cone density varied with different sampling methods and regions tested. In the nasal and temporal quadrants, peak density most closely resembled histological data, whereas the arcuate mean and fixed-interval methods tended to underestimate the density compared with histological data. However, in the inferior and superior quadrants, arcuate mean and fixed-interval methods most closely matched histological data, whereas the peak density method overestimated cone density compared with histological data. Intersession repeatability testing showed that repeatability was greatest when sampling by arcuate mean and lowest when sampling by fixed interval. We show that different methods of sampling can significantly affect cone density measurements. Therefore, care must be taken when interpreting cone density results, even in a normal population.
AbstractList The authors describe a standardized flood-illuminated adaptive optics (AO) imaging protocol suitable for the clinical setting and to assess sampling methods for measuring cone density.
To describe a standardized flood-illuminated adaptive optics (AO) imaging protocol suitable for the clinical setting and to assess sampling methods for measuring cone density.PURPOSETo describe a standardized flood-illuminated adaptive optics (AO) imaging protocol suitable for the clinical setting and to assess sampling methods for measuring cone density.Cone density was calculated following three measurement protocols: 50 × 50-μm sampling window values every 0.5° along the horizontal and vertical meridians (fixed-interval method), the mean density of expanding 0.5°-wide arcuate areas in the nasal, temporal, superior, and inferior quadrants (arcuate mean method), and the peak cone density of a 50 × 50-μm sampling window within expanding arcuate areas near the meridian (peak density method). Repeated imaging was performed in nine subjects to determine intersession repeatability of cone density.METHODSCone density was calculated following three measurement protocols: 50 × 50-μm sampling window values every 0.5° along the horizontal and vertical meridians (fixed-interval method), the mean density of expanding 0.5°-wide arcuate areas in the nasal, temporal, superior, and inferior quadrants (arcuate mean method), and the peak cone density of a 50 × 50-μm sampling window within expanding arcuate areas near the meridian (peak density method). Repeated imaging was performed in nine subjects to determine intersession repeatability of cone density.Cone density montages could be created for 67 of the 74 subjects. Image quality was determined to be adequate for automated cone counting for 35 (52%) of the 67 subjects. We found that cone density varied with different sampling methods and regions tested. In the nasal and temporal quadrants, peak density most closely resembled histological data, whereas the arcuate mean and fixed-interval methods tended to underestimate the density compared with histological data. However, in the inferior and superior quadrants, arcuate mean and fixed-interval methods most closely matched histological data, whereas the peak density method overestimated cone density compared with histological data. Intersession repeatability testing showed that repeatability was greatest when sampling by arcuate mean and lowest when sampling by fixed interval.RESULTSCone density montages could be created for 67 of the 74 subjects. Image quality was determined to be adequate for automated cone counting for 35 (52%) of the 67 subjects. We found that cone density varied with different sampling methods and regions tested. In the nasal and temporal quadrants, peak density most closely resembled histological data, whereas the arcuate mean and fixed-interval methods tended to underestimate the density compared with histological data. However, in the inferior and superior quadrants, arcuate mean and fixed-interval methods most closely matched histological data, whereas the peak density method overestimated cone density compared with histological data. Intersession repeatability testing showed that repeatability was greatest when sampling by arcuate mean and lowest when sampling by fixed interval.We show that different methods of sampling can significantly affect cone density measurements. Therefore, care must be taken when interpreting cone density results, even in a normal population.CONCLUSIONSWe show that different methods of sampling can significantly affect cone density measurements. Therefore, care must be taken when interpreting cone density results, even in a normal population.
To describe a standardized flood-illuminated adaptive optics (AO) imaging protocol suitable for the clinical setting and to assess sampling methods for measuring cone density. Cone density was calculated following three measurement protocols: 50 × 50-μm sampling window values every 0.5° along the horizontal and vertical meridians (fixed-interval method), the mean density of expanding 0.5°-wide arcuate areas in the nasal, temporal, superior, and inferior quadrants (arcuate mean method), and the peak cone density of a 50 × 50-μm sampling window within expanding arcuate areas near the meridian (peak density method). Repeated imaging was performed in nine subjects to determine intersession repeatability of cone density. Cone density montages could be created for 67 of the 74 subjects. Image quality was determined to be adequate for automated cone counting for 35 (52%) of the 67 subjects. We found that cone density varied with different sampling methods and regions tested. In the nasal and temporal quadrants, peak density most closely resembled histological data, whereas the arcuate mean and fixed-interval methods tended to underestimate the density compared with histological data. However, in the inferior and superior quadrants, arcuate mean and fixed-interval methods most closely matched histological data, whereas the peak density method overestimated cone density compared with histological data. Intersession repeatability testing showed that repeatability was greatest when sampling by arcuate mean and lowest when sampling by fixed interval. We show that different methods of sampling can significantly affect cone density measurements. Therefore, care must be taken when interpreting cone density results, even in a normal population.
Author Gale, Michael J.
Pennesi, Mark E.
Faridi, Ambar
Garg, Anupam K.
Michaels, Keith V.
Fay, Jonathan D.
Erker, Laura R.
Smith, Travis B.
Feng, Shu
Titus, Hope E.
Peters, Dawn
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References 16650474 - Ophthalmology. 2006 Jun;113(6):1019.e1
20238030 - Adv Exp Med Biol. 2010;664:309-16
22105799 - Am J Ophthalmol. 2012 Apr;153(4):757-68, 768.e1
17429491 - J Opt Soc Am A Opt Image Sci Vis. 2007 May;24(5):1438-47
24148654 - Ophthalmology. 2014 Jan;121(1):234-45
20238033 - Adv Exp Med Biol. 2010;664:333-40
1504026 - Vis Neurosci. 1992 Aug;9(2):169-80
16639019 - Invest Ophthalmol Vis Sci. 2006 May;47(5):2080-92
24246574 - Am J Ophthalmol. 2014 Mar;157(3):558-70.e1-4
23299470 - Invest Ophthalmol Vis Sci. 2013 Feb;54(2):950-61
17591900 - Invest Ophthalmol Vis Sci. 2007 Jul;48(7):3283-91
18499214 - Vision Res. 2008 Nov;48(26):2564-8
24531026 - Am J Ophthalmol. 2014 Jun;157(6):1239-1249.e3
8688716 - BMJ. 1996 Jul 13;313(7049):106
23378739 - Clin Ophthalmol. 2013;7:203-10
22964989 - JAMA Ophthalmol. 2013 Jan;131(1):67-74
23974999 - Retina. 2014 Feb;34(2):421-2
22312577 - Biomed Opt Express. 2012 Feb 1;3(2):225-39
24009995 - Biomed Opt Express. 2013 Jul 12;4(8):1318-31
23550537 - Ophthalmic Physiol Opt. 2013 Jul;33(4):516-26
23929416 - JAMA Ophthalmol. 2013 Oct;131(10):1314-23
24260224 - PLoS One. 2013;8(11):e79447
23620431 - Invest Ophthalmol Vis Sci. 2013 May;54(5):3673-80
23627927 - Ophthalmic Physiol Opt. 2013 Jul;33(4):527-39
8082844 - Graefes Arch Clin Exp Ophthalmol. 1994 Jun;232(6):361-7
23044944 - Arch Ophthalmol. 2012 Oct;130(10):1301-8
19037393 - J Opt Soc Am A Opt Image Sci Vis. 2008 Dec;25(12):3021-9
23765342 - JAMA Ophthalmol. 2013 Sep;131(9):1207-15
21833357 - Biomed Opt Express. 2011 Aug 1;2(8):2189-201
23949236 - JAMA Ophthalmol. 2013 Oct;131(10):1363-4
23696695 - Clin Ophthalmol. 2013;7:859-64
22504330 - Optom Vis Sci. 2012 May;89(5):632-43
24298413 - Biomed Opt Express. 2013 Oct 18;4(11):2527-39
19997159 - Opt Express. 2009 Oct 26;17(22):19382-400
23621343 - Curr Eye Res. 2013 Jul;38(7):709-21
21436275 - Invest Ophthalmol Vis Sci. 2011 Jun;52(7):4757-64
22727285 - J Cataract Refract Surg. 2012 Jul;38(7):1147-55
21724911 - Invest Ophthalmol Vis Sci. 2011 Sep;52(10):7376-84
23928676 - Retina. 2014 Mar;34(3):546-57
23492950 - Retina. 2013 Sep;33(8):1630-9
25190651 - Invest Ophthalmol Vis Sci. 2014 Oct;55(10):6381-97
22959359 - Am J Ophthalmol. 2012 Dec;154(6):987-1001.e1
21057346 - Optom Vis Sci. 2010 Dec;87(12):930-41
21559146 - Biomed Opt Express. 2011 Apr 26;2(5):1351-8
2324310 - J Comp Neurol. 1990 Feb 22;292(4):497-523
23465268 - Am J Ophthalmol. 2013 Jun;155(6):1045-1057.e4
24183341 - Ophthalmology. 2014 Feb;121(2):545-51
18552378 - Invest Ophthalmol Vis Sci. 2008 Oct;49(10):4679-87
17429482 - J Opt Soc Am A Opt Image Sci Vis. 2007 May;24(5):1364-72
23908179 - Invest Ophthalmol Vis Sci. 2013;54(8):5836-47
23538574 - Retina. 2013 Sep;33(8):1640-9
23615345 - Retina. 2013 Sep;33(8):1650-8
24049715 - Transl Vis Sci Technol. 2013 Feb;2(2):4
17429481 - J Opt Soc Am A Opt Image Sci Vis. 2007 May;24(5):1358-63
21320953 - Arch Ophthalmol. 2011 Jun;129(6):703-8
23276813 - Exp Eye Res. 2013 Mar;108:1-9
23717484 - PLoS One. 2013;8(5):e63786
References_xml – reference: 20238033 - Adv Exp Med Biol. 2010;664:333-40
– reference: 23765342 - JAMA Ophthalmol. 2013 Sep;131(9):1207-15
– reference: 23717484 - PLoS One. 2013;8(5):e63786
– reference: 19997159 - Opt Express. 2009 Oct 26;17(22):19382-400
– reference: 24049715 - Transl Vis Sci Technol. 2013 Feb;2(2):4
– reference: 16650474 - Ophthalmology. 2006 Jun;113(6):1019.e1
– reference: 22964989 - JAMA Ophthalmol. 2013 Jan;131(1):67-74
– reference: 8082844 - Graefes Arch Clin Exp Ophthalmol. 1994 Jun;232(6):361-7
– reference: 24246574 - Am J Ophthalmol. 2014 Mar;157(3):558-70.e1-4
– reference: 23949236 - JAMA Ophthalmol. 2013 Oct;131(10):1363-4
– reference: 23465268 - Am J Ophthalmol. 2013 Jun;155(6):1045-1057.e4
– reference: 24009995 - Biomed Opt Express. 2013 Jul 12;4(8):1318-31
– reference: 23928676 - Retina. 2014 Mar;34(3):546-57
– reference: 8688716 - BMJ. 1996 Jul 13;313(7049):106
– reference: 24148654 - Ophthalmology. 2014 Jan;121(1):234-45
– reference: 23276813 - Exp Eye Res. 2013 Mar;108:1-9
– reference: 23696695 - Clin Ophthalmol. 2013;7:859-64
– reference: 23974999 - Retina. 2014 Feb;34(2):421-2
– reference: 23621343 - Curr Eye Res. 2013 Jul;38(7):709-21
– reference: 17591900 - Invest Ophthalmol Vis Sci. 2007 Jul;48(7):3283-91
– reference: 23044944 - Arch Ophthalmol. 2012 Oct;130(10):1301-8
– reference: 23538574 - Retina. 2013 Sep;33(8):1640-9
– reference: 18499214 - Vision Res. 2008 Nov;48(26):2564-8
– reference: 22312577 - Biomed Opt Express. 2012 Feb 1;3(2):225-39
– reference: 24298413 - Biomed Opt Express. 2013 Oct 18;4(11):2527-39
– reference: 17429491 - J Opt Soc Am A Opt Image Sci Vis. 2007 May;24(5):1438-47
– reference: 17429481 - J Opt Soc Am A Opt Image Sci Vis. 2007 May;24(5):1358-63
– reference: 21057346 - Optom Vis Sci. 2010 Dec;87(12):930-41
– reference: 23550537 - Ophthalmic Physiol Opt. 2013 Jul;33(4):516-26
– reference: 23620431 - Invest Ophthalmol Vis Sci. 2013 May;54(5):3673-80
– reference: 19037393 - J Opt Soc Am A Opt Image Sci Vis. 2008 Dec;25(12):3021-9
– reference: 24183341 - Ophthalmology. 2014 Feb;121(2):545-51
– reference: 22105799 - Am J Ophthalmol. 2012 Apr;153(4):757-68, 768.e1
– reference: 2324310 - J Comp Neurol. 1990 Feb 22;292(4):497-523
– reference: 24531026 - Am J Ophthalmol. 2014 Jun;157(6):1239-1249.e3
– reference: 23615345 - Retina. 2013 Sep;33(8):1650-8
– reference: 21559146 - Biomed Opt Express. 2011 Apr 26;2(5):1351-8
– reference: 18552378 - Invest Ophthalmol Vis Sci. 2008 Oct;49(10):4679-87
– reference: 21724911 - Invest Ophthalmol Vis Sci. 2011 Sep;52(10):7376-84
– reference: 23492950 - Retina. 2013 Sep;33(8):1630-9
– reference: 23908179 - Invest Ophthalmol Vis Sci. 2013;54(8):5836-47
– reference: 16639019 - Invest Ophthalmol Vis Sci. 2006 May;47(5):2080-92
– reference: 23299470 - Invest Ophthalmol Vis Sci. 2013 Feb;54(2):950-61
– reference: 22504330 - Optom Vis Sci. 2012 May;89(5):632-43
– reference: 22959359 - Am J Ophthalmol. 2012 Dec;154(6):987-1001.e1
– reference: 25190651 - Invest Ophthalmol Vis Sci. 2014 Oct;55(10):6381-97
– reference: 23378739 - Clin Ophthalmol. 2013;7:203-10
– reference: 23627927 - Ophthalmic Physiol Opt. 2013 Jul;33(4):527-39
– reference: 24260224 - PLoS One. 2013;8(11):e79447
– reference: 21833357 - Biomed Opt Express. 2011 Aug 1;2(8):2189-201
– reference: 22727285 - J Cataract Refract Surg. 2012 Jul;38(7):1147-55
– reference: 21320953 - Arch Ophthalmol. 2011 Jun;129(6):703-8
– reference: 20238030 - Adv Exp Med Biol. 2010;664:309-16
– reference: 1504026 - Vis Neurosci. 1992 Aug;9(2):169-80
– reference: 21436275 - Invest Ophthalmol Vis Sci. 2011 Jun;52(7):4757-64
– reference: 23929416 - JAMA Ophthalmol. 2013 Oct;131(10):1314-23
– reference: 17429482 - J Opt Soc Am A Opt Image Sci Vis. 2007 May;24(5):1364-72
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Snippet To describe a standardized flood-illuminated adaptive optics (AO) imaging protocol suitable for the clinical setting and to assess sampling methods for...
The authors describe a standardized flood-illuminated adaptive optics (AO) imaging protocol suitable for the clinical setting and to assess sampling methods...
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StartPage 5751
SubjectTerms Adolescent
Adult
Aged
Cell Count
Female
Humans
Lighting - methods
Macula Lutea - physiology
Male
Middle Aged
Multidisciplinary Ophthalmic Imaging
Ophthalmoscopy - methods
Optical Phenomena
Photography - methods
Reproducibility of Results
Retinal Cone Photoreceptor Cells - cytology
Retinal Cone Photoreceptor Cells - physiology
Visual Fields - physiology
Young Adult
Title Assessment of Different Sampling Methods for Measuring and Representing Macular Cone Density Using Flood-Illuminated Adaptive Optics
URI https://www.ncbi.nlm.nih.gov/pubmed/26325414
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