Drusenoid maculopathy in rhesus monkeys (Macaca mulatta): effects of age and gender
Purpose To compare drusenoid maculopathy in monkeys with human age-related macular degeneration, and evaluate the influence of age, gender and caloric restriction. Methods Examination by indirect ophthalmoscopy, slit-lamp biomicroscopy and fundus photography, including in some cases fluorescein angi...
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creator | Gouras, Peter Ivert, Lena Landauer, Noelle Mattison, Julie A. Ingram, Donald K. Neuringer, Martha |
description | Purpose
To compare drusenoid maculopathy in monkeys with human age-related macular degeneration, and evaluate the influence of age, gender and caloric restriction.
Methods
Examination by indirect ophthalmoscopy, slit-lamp biomicroscopy and fundus photography, including in some cases fluorescein angiography, was performed on 61 male and 60 female rhesus macaques of ages 10–39 years. Fifty-four of the monkeys were maintained on a calorically restricted diet (approximately 30% lower than control levels) and 67 on an approximately ad libitum diet for 2–19 years, with all other environmental factors held constant. Maculopathies were graded on a 5-point scale and the effects of age, sex, and diet on prevalence and severity were examined. The retinas of six monkeys with macular drusen, 19–28 years old, were examined histologically.
Results
Rhesus monkeys showed a high prevalence (61%) of drusenoid maculopathy. The prevalence and severity of the maculopathy increased with age (
p
= 0.012). Fully half of all monkeys aged 10–12 years had some detectable degree of drusen. This high prevalence in young adulthood indicates that drusen develop much earlier in rhesus monkeys than in humans, who develop early maculopathy most rapidly at 50–60 years of age, even when correcting for the 3-fold difference in lifespan. No neovascularization or geographic atrophy was found. Females had a higher prevalence and severity than males (
p
= 0.019). Calorically restricted monkeys had a slightly lower prevalence and severity at 10–12 years than controls, but the difference was not statistically significant. This is an on-going project, and differences between the caloric restricted and ad-lib groups may emerge as the animals age. Some monkeys developed severe maculopathy in their 20s, with others unaffected in their 30s. The histology of drusen resembled those in human retina.
Conclusion
Drusenoid maculopathy is common in rhesus monkeys, even in young adult life. Half of the rhesus monkeys examined have drusen at a much younger age than in humans. Severity of maculopathy was greater in female monkeys, a gender difference not consistently found in humans. No differences were detected due to caloric restriction, but a definitive test of this intervention will require a larger sample, longer period of observation, and/or an earlier institution of caloric restriction. Genetic factors are implied because with similar environments, some monkeys are affected at an early age, while older on |
doi_str_mv | 10.1007/s00417-008-0910-8 |
format | Article |
fullrecord | <record><control><sourceid>proquest_swepu</sourceid><recordid>TN_cdi_swepub_primary_oai_swepub_ki_se_562724</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1549295271</sourcerecordid><originalsourceid>FETCH-LOGICAL-c571t-2d8d2c4db3b258378ec951b472e959e6f5d472c292de57a3dad6b6a5f1513a223</originalsourceid><addsrcrecordid>eNp1kU1v1DAQhi1ERZfCD-CCLA4IDgZ_xLHTAxIqUJCKOABSb5ZjT3bTJvZiJ6D99_Vqo5YiIR88mnnmHXtehJ4x-oZRqt5mSiumCKWa0IZRoh-gFauEJIryy4doRRVnRAt-eYwe53xFCy4ke4SOmVa0EZqt0PcPac4QYu_xaN08xK2dNjvcB5w2kOeMxxiuYZfxq6_WlYPHebDTZF-fYug6cFPGscN2DdgGj9cQPKQn6KizQ4any32Cfn76-OPsM7n4dv7l7P0FcVKxiXCvPXeVb0XLpRZKg2skayvFoZEN1J30JXa84R6kssJbX7e1lR2TTFjOxQkiB938B7Zza7apH23amWh7s6SuSwRG1lzxqvDvDnypjOAdhCnZ4V7b_UroN2YdfxteBES1H_hyEUjx1wx5MmOfHQyDDRDnbOpG8oo1e_DFP-BVnFMoyzBcUKW1lrJA7AC5FHNO0N2-hFGz99cc_DXFX7P31-jS8_zvL9x1LIYWgC87KaWwhnQ3-f-qN9u2sX4</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>230788855</pqid></control><display><type>article</type><title>Drusenoid maculopathy in rhesus monkeys (Macaca mulatta): effects of age and gender</title><source>MEDLINE</source><source>SpringerLink Journals (MCLS)</source><source>SWEPUB Freely available online</source><creator>Gouras, Peter ; Ivert, Lena ; Landauer, Noelle ; Mattison, Julie A. ; Ingram, Donald K. ; Neuringer, Martha</creator><creatorcontrib>Gouras, Peter ; Ivert, Lena ; Landauer, Noelle ; Mattison, Julie A. ; Ingram, Donald K. ; Neuringer, Martha</creatorcontrib><description>Purpose
To compare drusenoid maculopathy in monkeys with human age-related macular degeneration, and evaluate the influence of age, gender and caloric restriction.
Methods
Examination by indirect ophthalmoscopy, slit-lamp biomicroscopy and fundus photography, including in some cases fluorescein angiography, was performed on 61 male and 60 female rhesus macaques of ages 10–39 years. Fifty-four of the monkeys were maintained on a calorically restricted diet (approximately 30% lower than control levels) and 67 on an approximately ad libitum diet for 2–19 years, with all other environmental factors held constant. Maculopathies were graded on a 5-point scale and the effects of age, sex, and diet on prevalence and severity were examined. The retinas of six monkeys with macular drusen, 19–28 years old, were examined histologically.
Results
Rhesus monkeys showed a high prevalence (61%) of drusenoid maculopathy. The prevalence and severity of the maculopathy increased with age (
p
= 0.012). Fully half of all monkeys aged 10–12 years had some detectable degree of drusen. This high prevalence in young adulthood indicates that drusen develop much earlier in rhesus monkeys than in humans, who develop early maculopathy most rapidly at 50–60 years of age, even when correcting for the 3-fold difference in lifespan. No neovascularization or geographic atrophy was found. Females had a higher prevalence and severity than males (
p
= 0.019). Calorically restricted monkeys had a slightly lower prevalence and severity at 10–12 years than controls, but the difference was not statistically significant. This is an on-going project, and differences between the caloric restricted and ad-lib groups may emerge as the animals age. Some monkeys developed severe maculopathy in their 20s, with others unaffected in their 30s. The histology of drusen resembled those in human retina.
Conclusion
Drusenoid maculopathy is common in rhesus monkeys, even in young adult life. Half of the rhesus monkeys examined have drusen at a much younger age than in humans. Severity of maculopathy was greater in female monkeys, a gender difference not consistently found in humans. No differences were detected due to caloric restriction, but a definitive test of this intervention will require a larger sample, longer period of observation, and/or an earlier institution of caloric restriction. Genetic factors are implied because with similar environments, some monkeys are affected at an early age, while older ones are not.</description><identifier>ISSN: 0721-832X</identifier><identifier>EISSN: 1435-702X</identifier><identifier>DOI: 10.1007/s00417-008-0910-8</identifier><identifier>PMID: 18709381</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Age Factors ; Animals ; Caloric Restriction ; Female ; Fluorescein Angiography ; Humans ; Macaca mulatta ; Macular Degeneration - diagnosis ; Macular Degeneration - epidemiology ; Macular Degeneration - veterinary ; Male ; Medicine ; Medicine & Public Health ; Monkey Diseases - diagnosis ; Monkey Diseases - epidemiology ; Ophthalmology ; Ophthalmoscopy ; Photography ; Prevalence ; Retinal Disorders ; Retinal Drusen - diagnosis ; Retinal Drusen - epidemiology ; Retinal Drusen - veterinary ; Sex Factors</subject><ispartof>Graefe's archive for clinical and experimental ophthalmology, 2008-10, Vol.246 (10), p.1395-1402</ispartof><rights>Springer-Verlag 2008</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c571t-2d8d2c4db3b258378ec951b472e959e6f5d472c292de57a3dad6b6a5f1513a223</citedby><cites>FETCH-LOGICAL-c571t-2d8d2c4db3b258378ec951b472e959e6f5d472c292de57a3dad6b6a5f1513a223</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00417-008-0910-8$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00417-008-0910-8$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,309,310,314,550,776,780,785,786,881,23909,23910,25118,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18709381$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:117561168$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Gouras, Peter</creatorcontrib><creatorcontrib>Ivert, Lena</creatorcontrib><creatorcontrib>Landauer, Noelle</creatorcontrib><creatorcontrib>Mattison, Julie A.</creatorcontrib><creatorcontrib>Ingram, Donald K.</creatorcontrib><creatorcontrib>Neuringer, Martha</creatorcontrib><title>Drusenoid maculopathy in rhesus monkeys (Macaca mulatta): effects of age and gender</title><title>Graefe's archive for clinical and experimental ophthalmology</title><addtitle>Graefes Arch Clin Exp Ophthalmol</addtitle><addtitle>Graefes Arch Clin Exp Ophthalmol</addtitle><description>Purpose
To compare drusenoid maculopathy in monkeys with human age-related macular degeneration, and evaluate the influence of age, gender and caloric restriction.
Methods
Examination by indirect ophthalmoscopy, slit-lamp biomicroscopy and fundus photography, including in some cases fluorescein angiography, was performed on 61 male and 60 female rhesus macaques of ages 10–39 years. Fifty-four of the monkeys were maintained on a calorically restricted diet (approximately 30% lower than control levels) and 67 on an approximately ad libitum diet for 2–19 years, with all other environmental factors held constant. Maculopathies were graded on a 5-point scale and the effects of age, sex, and diet on prevalence and severity were examined. The retinas of six monkeys with macular drusen, 19–28 years old, were examined histologically.
Results
Rhesus monkeys showed a high prevalence (61%) of drusenoid maculopathy. The prevalence and severity of the maculopathy increased with age (
p
= 0.012). Fully half of all monkeys aged 10–12 years had some detectable degree of drusen. This high prevalence in young adulthood indicates that drusen develop much earlier in rhesus monkeys than in humans, who develop early maculopathy most rapidly at 50–60 years of age, even when correcting for the 3-fold difference in lifespan. No neovascularization or geographic atrophy was found. Females had a higher prevalence and severity than males (
p
= 0.019). Calorically restricted monkeys had a slightly lower prevalence and severity at 10–12 years than controls, but the difference was not statistically significant. This is an on-going project, and differences between the caloric restricted and ad-lib groups may emerge as the animals age. Some monkeys developed severe maculopathy in their 20s, with others unaffected in their 30s. The histology of drusen resembled those in human retina.
Conclusion
Drusenoid maculopathy is common in rhesus monkeys, even in young adult life. Half of the rhesus monkeys examined have drusen at a much younger age than in humans. Severity of maculopathy was greater in female monkeys, a gender difference not consistently found in humans. No differences were detected due to caloric restriction, but a definitive test of this intervention will require a larger sample, longer period of observation, and/or an earlier institution of caloric restriction. Genetic factors are implied because with similar environments, some monkeys are affected at an early age, while older ones are not.</description><subject>Age Factors</subject><subject>Animals</subject><subject>Caloric Restriction</subject><subject>Female</subject><subject>Fluorescein Angiography</subject><subject>Humans</subject><subject>Macaca mulatta</subject><subject>Macular Degeneration - diagnosis</subject><subject>Macular Degeneration - epidemiology</subject><subject>Macular Degeneration - veterinary</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Monkey Diseases - diagnosis</subject><subject>Monkey Diseases - epidemiology</subject><subject>Ophthalmology</subject><subject>Ophthalmoscopy</subject><subject>Photography</subject><subject>Prevalence</subject><subject>Retinal Disorders</subject><subject>Retinal Drusen - diagnosis</subject><subject>Retinal Drusen - epidemiology</subject><subject>Retinal Drusen - veterinary</subject><subject>Sex Factors</subject><issn>0721-832X</issn><issn>1435-702X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>D8T</sourceid><recordid>eNp1kU1v1DAQhi1ERZfCD-CCLA4IDgZ_xLHTAxIqUJCKOABSb5ZjT3bTJvZiJ6D99_Vqo5YiIR88mnnmHXtehJ4x-oZRqt5mSiumCKWa0IZRoh-gFauEJIryy4doRRVnRAt-eYwe53xFCy4ke4SOmVa0EZqt0PcPac4QYu_xaN08xK2dNjvcB5w2kOeMxxiuYZfxq6_WlYPHebDTZF-fYug6cFPGscN2DdgGj9cQPKQn6KizQ4any32Cfn76-OPsM7n4dv7l7P0FcVKxiXCvPXeVb0XLpRZKg2skayvFoZEN1J30JXa84R6kssJbX7e1lR2TTFjOxQkiB938B7Zza7apH23amWh7s6SuSwRG1lzxqvDvDnypjOAdhCnZ4V7b_UroN2YdfxteBES1H_hyEUjx1wx5MmOfHQyDDRDnbOpG8oo1e_DFP-BVnFMoyzBcUKW1lrJA7AC5FHNO0N2-hFGz99cc_DXFX7P31-jS8_zvL9x1LIYWgC87KaWwhnQ3-f-qN9u2sX4</recordid><startdate>20081001</startdate><enddate>20081001</enddate><creator>Gouras, Peter</creator><creator>Ivert, Lena</creator><creator>Landauer, Noelle</creator><creator>Mattison, Julie A.</creator><creator>Ingram, Donald K.</creator><creator>Neuringer, Martha</creator><general>Springer-Verlag</general><general>Springer Nature B.V</general><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>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>ADTPV</scope><scope>BNKNJ</scope><scope>BVBDO</scope><scope>D8T</scope></search><sort><creationdate>20081001</creationdate><title>Drusenoid maculopathy in rhesus monkeys (Macaca mulatta): effects of age and gender</title><author>Gouras, Peter ; Ivert, Lena ; Landauer, Noelle ; Mattison, Julie A. ; Ingram, Donald K. ; Neuringer, Martha</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c571t-2d8d2c4db3b258378ec951b472e959e6f5d472c292de57a3dad6b6a5f1513a223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Age Factors</topic><topic>Animals</topic><topic>Caloric Restriction</topic><topic>Female</topic><topic>Fluorescein Angiography</topic><topic>Humans</topic><topic>Macaca mulatta</topic><topic>Macular Degeneration - diagnosis</topic><topic>Macular Degeneration - epidemiology</topic><topic>Macular Degeneration - veterinary</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Monkey Diseases - diagnosis</topic><topic>Monkey Diseases - epidemiology</topic><topic>Ophthalmology</topic><topic>Ophthalmoscopy</topic><topic>Photography</topic><topic>Prevalence</topic><topic>Retinal Disorders</topic><topic>Retinal Drusen - diagnosis</topic><topic>Retinal Drusen - epidemiology</topic><topic>Retinal Drusen - veterinary</topic><topic>Sex Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gouras, Peter</creatorcontrib><creatorcontrib>Ivert, Lena</creatorcontrib><creatorcontrib>Landauer, Noelle</creatorcontrib><creatorcontrib>Mattison, Julie A.</creatorcontrib><creatorcontrib>Ingram, Donald K.</creatorcontrib><creatorcontrib>Neuringer, Martha</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Conference</collection><collection>SwePub Conference full text</collection><collection>SWEPUB Freely available online</collection><jtitle>Graefe's archive for clinical and experimental ophthalmology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gouras, Peter</au><au>Ivert, Lena</au><au>Landauer, Noelle</au><au>Mattison, Julie A.</au><au>Ingram, Donald K.</au><au>Neuringer, Martha</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Drusenoid maculopathy in rhesus monkeys (Macaca mulatta): effects of age and gender</atitle><jtitle>Graefe's archive for clinical and experimental ophthalmology</jtitle><stitle>Graefes Arch Clin Exp Ophthalmol</stitle><addtitle>Graefes Arch Clin Exp Ophthalmol</addtitle><date>2008-10-01</date><risdate>2008</risdate><volume>246</volume><issue>10</issue><spage>1395</spage><epage>1402</epage><pages>1395-1402</pages><issn>0721-832X</issn><eissn>1435-702X</eissn><abstract>Purpose
To compare drusenoid maculopathy in monkeys with human age-related macular degeneration, and evaluate the influence of age, gender and caloric restriction.
Methods
Examination by indirect ophthalmoscopy, slit-lamp biomicroscopy and fundus photography, including in some cases fluorescein angiography, was performed on 61 male and 60 female rhesus macaques of ages 10–39 years. Fifty-four of the monkeys were maintained on a calorically restricted diet (approximately 30% lower than control levels) and 67 on an approximately ad libitum diet for 2–19 years, with all other environmental factors held constant. Maculopathies were graded on a 5-point scale and the effects of age, sex, and diet on prevalence and severity were examined. The retinas of six monkeys with macular drusen, 19–28 years old, were examined histologically.
Results
Rhesus monkeys showed a high prevalence (61%) of drusenoid maculopathy. The prevalence and severity of the maculopathy increased with age (
p
= 0.012). Fully half of all monkeys aged 10–12 years had some detectable degree of drusen. This high prevalence in young adulthood indicates that drusen develop much earlier in rhesus monkeys than in humans, who develop early maculopathy most rapidly at 50–60 years of age, even when correcting for the 3-fold difference in lifespan. No neovascularization or geographic atrophy was found. Females had a higher prevalence and severity than males (
p
= 0.019). Calorically restricted monkeys had a slightly lower prevalence and severity at 10–12 years than controls, but the difference was not statistically significant. This is an on-going project, and differences between the caloric restricted and ad-lib groups may emerge as the animals age. Some monkeys developed severe maculopathy in their 20s, with others unaffected in their 30s. The histology of drusen resembled those in human retina.
Conclusion
Drusenoid maculopathy is common in rhesus monkeys, even in young adult life. Half of the rhesus monkeys examined have drusen at a much younger age than in humans. Severity of maculopathy was greater in female monkeys, a gender difference not consistently found in humans. No differences were detected due to caloric restriction, but a definitive test of this intervention will require a larger sample, longer period of observation, and/or an earlier institution of caloric restriction. Genetic factors are implied because with similar environments, some monkeys are affected at an early age, while older ones are not.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>18709381</pmid><doi>10.1007/s00417-008-0910-8</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; SpringerLink Journals (MCLS); SWEPUB Freely available online |
subjects | Age Factors Animals Caloric Restriction Female Fluorescein Angiography Humans Macaca mulatta Macular Degeneration - diagnosis Macular Degeneration - epidemiology Macular Degeneration - veterinary Male Medicine Medicine & Public Health Monkey Diseases - diagnosis Monkey Diseases - epidemiology Ophthalmology Ophthalmoscopy Photography Prevalence Retinal Disorders Retinal Drusen - diagnosis Retinal Drusen - epidemiology Retinal Drusen - veterinary Sex Factors |
title | Drusenoid maculopathy in rhesus monkeys (Macaca mulatta): effects of age and gender |
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