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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Veröffentlicht in:Graefe's archive for clinical and experimental ophthalmology 2008-10, Vol.246 (10), p.1395-1402
Hauptverfasser: Gouras, Peter, Ivert, Lena, Landauer, Noelle, Mattison, Julie A., Ingram, Donald K., Neuringer, Martha
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container_issue 10
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container_title Graefe's archive for clinical and experimental ophthalmology
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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
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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 &amp; 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. 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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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