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Diabetic Retinopathy & Medical Retina - aioseducation

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70th AIOC Proceedings, Cochin 2012<br />

thus, early intervention can be undertaken at an appropriate time to prevent<br />

further progression of the disease, before it reaches an irreversible stage.<br />

REFERENCES<br />

1. Klein R, Klein BEK, Moss SE. The Winconsin Epidemiological Study of <strong>Diabetic</strong><br />

<strong>Retinopathy</strong>, III:Prevalence and risk of diabetic retinopathy when age of diagonosis<br />

is 30 or more years. Arch Ophthalmol 1984;102:527-32.<br />

2. Liech E, gardener TW, Barber AJ. <strong>Retina</strong>l neurodegeneration:early pathology in<br />

diabetes. ClinExpOphthalmol 2000;28: 3-8<br />

3. Barber AJ. A new view of diabetic retinopathy: a neurodegenerative disease of the<br />

eye. Prog Neuropsychopharmol Biol Psychiatry 2003;27:283-90.<br />

4. Lopes de Faria,Russ H Costa VP. <strong>Retina</strong>l Fibre layer loss in patients with type 1<br />

diabetes mellitus without retinopathy. Br J Ophthalmol 2002;86:725-8.<br />

5. Nakazawa T, Takahashi H, Nishijima K. Pitavastatin prevents NMDA-induced<br />

retinal ganglion cell death by suppressing leukocyte recruitment. J Neaurochemistry<br />

2007;100:1018-31.<br />

6. Coupland SG: A comparison of oscillatory potential and pattern electroretinogram<br />

measures in diabetic retinopathy. Doc Ophthalmol 1987;66:207–18.<br />

7. Chen H, Zhang M, Huang S, Wu D. The photopic negative response of flash ERG in<br />

nonproliferative diabetic retinopathy. Doc Ophthalmol 2008;117:129-35.<br />

Investigation into The Levels of VEGF, PEDF and<br />

Other Biochemical Parameters in <strong>Diabetic</strong><br />

<strong>Retinopathy</strong><br />

Dr. Mohammad Arif Mulla, Dr. Gopal Lingam, Dr. Angayarkanni N.,<br />

Dr. Kaviarasan<br />

To determine the levels of vascular endothelial growth factor (VEGF),<br />

cytokines, pigment epithelium derived factor (PEDF), along with other<br />

biochemical parameters in the patients with diabetes, non-proliferative<br />

diabetic retinopathy (NPDR), proliferative diabetic retinopathy (PDR) and<br />

compared with age-matched controls<br />

MATERIALS AND METHODS<br />

Study Design: Patients aged between 40-65 years with type II diabetes, NPDR<br />

and PDR and Macular hole (MH) patients as control were included in this<br />

study.<br />

This study was carried out after receiving ethical approval from the<br />

institutional ethics committee.<br />

880

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