TY - JOUR
T1 - Analysis of macular drusen and blood test results in 945 Macaca fascicularis
AU - Nishiguchi, Koji M.
AU - Yokoyama, Yu
AU - Fujii, Yusuke
AU - Fujita, Kosuke
AU - Tomiyama, Yusuke
AU - Kawasaki, Ryo
AU - Furukawa, Toshinori
AU - Ono, Fumiko
AU - Shimozawa, Nobuhiro
AU - Togo, Mutsumi
AU - Suzuki, Michihiro
AU - Nakazawa, Toru
N1 - Funding Information:
The Department of Advanced Ophthalmic Medicine and Department of Retinal Disease Control are endowment departments within Tohoku University Graduate School of Medicine, supported with an unrestricted grant from SENJU Pharmaceutical Co., Ltd and Nidek Co., Ltd, respectively. This does not alter our adherence to PLOS ONE policies on sharing data and materials.
Publisher Copyright:
© 2016 Nishiguchi et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2016/10
Y1 - 2016/10
N2 - Age-dependent formation of macular drusen caused by the focal accumulation of extracellular deposits beneath the retinal pigment epithelium precede the development of agerelated macular degeneration (AMD), one of the leading causes of blindness worldwide. It is established that inflammation contributes to the pathogenesis of drusen and AMD. However, development of a preemptive therapeutic strategy targeting macular drusen and AMD has been impeded by the lack of relevant animal models because most laboratory animals lack macula, an anatomic feature present only in humans and a subset of monkeys. Reportedly, macular drusen and macular degeneration develop in monkeys in an age-dependent manner. In this study, we analyzed blood test results from 945 Macaca fascicularis, 317 with and 628 without drusen. First, a trend test for drusen frequency (the Cochran-Armitage test) was applied to the quartile data for each parameter. We selected variables with an increasing or decreasing trend with higher quartiles at P < 0.05, to which multivariate logistic regression analysis was applied. This revealed a positive association of age (odds ratio [OR]: 1.10 per year, 95% confidence interval [CI]: 1.07-1.12) and white blood cell count (OR: 1.01 per 1 × 103/μl, 95% CI: 1.00-1.01) with drusen. When the monkeys were divided by age, the association between drusen and white blood cell count was only evident in younger monkeys (OR: 1.01 per 1 × 103/μl, 95% CI: 1.00-1.02). In conclusion, age and white blood cell count may be associated with drusen development in M. fascicularis. Systemic inflammation may contribute to drusen formation in monkeys.
AB - Age-dependent formation of macular drusen caused by the focal accumulation of extracellular deposits beneath the retinal pigment epithelium precede the development of agerelated macular degeneration (AMD), one of the leading causes of blindness worldwide. It is established that inflammation contributes to the pathogenesis of drusen and AMD. However, development of a preemptive therapeutic strategy targeting macular drusen and AMD has been impeded by the lack of relevant animal models because most laboratory animals lack macula, an anatomic feature present only in humans and a subset of monkeys. Reportedly, macular drusen and macular degeneration develop in monkeys in an age-dependent manner. In this study, we analyzed blood test results from 945 Macaca fascicularis, 317 with and 628 without drusen. First, a trend test for drusen frequency (the Cochran-Armitage test) was applied to the quartile data for each parameter. We selected variables with an increasing or decreasing trend with higher quartiles at P < 0.05, to which multivariate logistic regression analysis was applied. This revealed a positive association of age (odds ratio [OR]: 1.10 per year, 95% confidence interval [CI]: 1.07-1.12) and white blood cell count (OR: 1.01 per 1 × 103/μl, 95% CI: 1.00-1.01) with drusen. When the monkeys were divided by age, the association between drusen and white blood cell count was only evident in younger monkeys (OR: 1.01 per 1 × 103/μl, 95% CI: 1.00-1.02). In conclusion, age and white blood cell count may be associated with drusen development in M. fascicularis. Systemic inflammation may contribute to drusen formation in monkeys.
UR - http://www.scopus.com/inward/record.url?scp=84992337649&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84992337649&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0164899
DO - 10.1371/journal.pone.0164899
M3 - Article
C2 - 27776188
AN - SCOPUS:84992337649
SN - 1932-6203
VL - 11
JO - PLoS ONE
JF - PLoS ONE
IS - 10
M1 - e0164899
ER -