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(June 2001 – February 2004)
The Chennai Glaucoma Follow-up study
(February 2004 to February 2007)
The Chennai Eye Disease Incidence study
(CEDIS: February 2007- February 2010)
Funded by: The Chennai Willingdon Corporate Foundation
Glaucoma is a potentially blinding disease that affects 66 million persons worldwide. It is the second leading cause of blindness worldwide. The disease is characterized by typical changes in the optic nerve (the nerve that connects the eye to the brain) with associated visual field defects (the area seen by the eye). Since the outer portion of the visual field is the first to be affected and most types of glaucoma are asymptomatic the disease is often diagnosed once significant vision/field has been lost. Therefore, early diagnosis is essential so that treatment to halt/slow progression can be instituted.
Public health planning to develop strategies for early diagnosis and treatment of this disease in the population requires data on the prevalence, distribution and pattern of the disease. Existing data from India suggest that Indians have a different pattern of disease. Recent genetic studies from the West indicate that glaucoma has a hereditary component with specific genes identified from the affected persons. There is a paucity of such data from India . If such data were available it would be possible to identify persons at risk of developing the disease.
The Chennai Glaucoma study is a population-based study, designed with a view to gather information on the prevalence of glaucoma in rural and urban South India . The study, funded by Chennai Willingdon Corporate Foundation, commenced on 2 nd Nov 2000. Clinical work on the rural component started on 15 th June 2001. 7785 persons, above 40 years of age, from rural Tamil Nadu and Chennai city were examined at a special facility created at Sankara Nethralaya. 3924 subjects representing the rural south Indian population participated from 27 contiguous villages of Thiruvallur and Kancheepuram districts of Tamil Nadu. 3850 Urban subjects participated from 5 randomly chosen divisions from Chennai city.
Every patient underwent a detailed ophthalmic evaluation. Ophthalmic examination consisted of the following components/ tests:
(a) Ocular and medical history,
(b) Lensometry (Appasamy LM14 telescopic lensmeter, Chennai , India ) if necessary,
(c) Refraction and recording of best-corrected visual acuity using the Modified ETDRS chart (Light House Low Vision Products, New York , NY , USA ),
(d) Scanning Laser Polarimetry using the NFA GDx (GDx Version 1.0.16, Laser Diagnostic Technologies, San Diego , CA , USA )
(e) Frequency doubling perimetry using the Frequency Doubling Perimeter (Zeiss Humphrey Systems, Dublin , CA , USA )
(f) Corneal pachymetry using the DGH 550 Ultrasonic pachymeter (DGH Technology Inc., Exton , PA , USA )
(g) Slit lamp biomicroscopy, (Zeiss SL 130-Carl Zeiss, Jena , Germany )
(h) Applanation tonometry (Zeiss AT 030 Applanation Tonometer, Carl Zeiss, Jena , Germany )
(i) Gonioscopy, (Sussmann-type 4 mirror hand held gonioscope -Volk Optical Inc, Mentor, Ohio, USA)
(j) Ocular biometry (Alcon ultrasonic biometer - Ocuscan, Alcon laboratories Inc, Fort Worth , TX , USA ).
(k) Grading of lens opacities, (The Lens Opacities Classification System (LOCS II)
(l) Fundus examination, (Indirect ophthalmoscope - Appasamy Associates, Chennai , India )
(m) Optic disc and fundus photography ( Zeiss FF450-plus fundus camera with VISUPAC digital image archiving system - Carl Zeiss, Jena, Germany)
(n) Visual field – White on white ((Zeiss Humphrey Systems, Dublin , CA , USA )
All the abnormal features will be recorded using standard international classifications. Data collection also included assessment of socio-economic status, systemic and ocular history, and ophthalmic examination. In addition a detailed pedigree is taken from those identified to have glaucoma and family members are screened for the disease. Genetic analysis to identify risk factors for glaucoma is also being performed. The project was successfully completed by February 2004. The study has generated 27 peer reviewed publications.
The important findings of the study are:
1) Prevalence of primary open angle glaucoma in the rural population was 1.62%. The prevalence increased with increasing age and 98.5% were unaware that they had the disease.
2) Prevalence of primary angle closure disease (PACG + PAC) in the rural population: 1.58%. An additional 7% were at risk of developing angle closure glaucoma. A few important risk factors were shown to be associated with primary angle closure disease
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Women were at 3 times greater risk thank men |
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Increasing age was a significant risk factor |
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Almost all those with primary angle closure disease were unaware about the disease: |
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The disease was symptomless and only a comprehensive examination would help in timely diagnosis of the disease |
3) Secondary glaucoma also contributes to the burden of blindness in our country. The prevalence of post surgical and pseudoexfoliation glaucoma's have been reported for the rural population.
a. Glaucoma is an important cause of ocular morbidity among those who had underwent cataract surgery (with or without intraocular lens implantation)
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22% were blind in either one or both eyes due to glaucoma |
b. The prevalence of pseudoexfoliation was 3.8% in the rural population
4) Reporting the reasons & risk factors for blindness in the rural population, the study reported that: cataract was the single most important cause of blindness followed by glaucoma.
a. 36% of the rural population were bilaterally blind
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Cataract was responsible in 79%, glaucoma (4.3%), non glaucomatous optic nerve disease (3.42%), cystoid macular edema & corneal scar (2.5% each) |
5) The study also reported the prevalence of refractive errors in the rural south Indian population. Around 49% of the subjects had refractive error.
a. Myopia was the commonest refractive error in the rural population
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27% had myopia (greater than -0.5 diopter power) & 3.7% had high myopia (greater than -5 diopter power) - There was a positive association between nuclear cataract and myopia |
6) Tobacco use was significantly associated with cataract. Use of smokeless tobacco (snuff and/or chewing tobacco) use was strongly associated with cataract.
CHENNAI GLAUCOMA FOLLOW-UP STUDY (Feb 2004 to Feb 2007)
A cohort of normal subjects from the urban subset of the Chennai Glaucoma Study and those who had been diagnosed to have primary glaucoma, ocular hypertension, primary angle closure suspects were followed up for a period of three years at six monthly intervals. All subjects underwent a comprehensive ocular examination during each visit.
THE CHENNAI EYE DISEASE INCIDENCE STUDY (CEDIS: Feb 2007- Feb 2010)
This is a population based Incidence study. All subjects who had participated in the Chennai glaucoma study (2001-2004) from both the rural and urban arm will undergo a repeat history and detailed ophthalmic examination. The incidence of new diseases from the baseline and changes from the first examination will be studied
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Determinants of glaucoma awareness and knowledge in urban Chennai.
Sathyamangalam RV, Paul PG, George R, Baskaran M, Hemamalini A, Madan RV, Augustian J, Prema R, Lingam V.
Indian J Ophthalmol. 2009 Sep-Oct;57(5):355-60.
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Comparison of Humphrey MATRIX and Swedish interactive threshold algorithm standard strategy in detecting early glaucomatous visual field loss.
Prema R, George R, Hemamalini A, Sathyamangalam Ve R, Baskaran M, Vijaya L.
Indian J Ophthalmol. 2009 May-Jun;57(3):207-11.
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Agreement between two Goldmann type applanation tonometers.
George R, Arvind H, Baskaran M, Ramesh SV, Raju P, Vijaya L.
Indian J Ophthalmol. 2008 Nov-Dec;56(6):516-7.
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Prevalence of retinitis pigmentosa in South Indian population aged above 40 years.
Sen P, Bhargava A, George R, Ve Ramesh S, Hemamalini A, Prema R, Kumaramanickavel G, Vijaya L.
Ophthalmic Epidemiol. 2008 Jul-Aug;15(4):279-81.
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Lower threshold estimates at the onset of automated perimetry causing artefacts in perimetrically naive subjects.Preetha MM, George R, Ve RS, Raju P, Vijaya L.
Ophthalmic Physiol Opt. 2008 Sep;28(5):492-6.
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Neural rim characteristics of healthy South Indians: the Chennai Glaucoma Study.
Arvind H, George R, Raju P, Ve RS, Mani B, Kannan P, Vijaya L.
Invest Ophthalmol Vis Sci. 2008 Aug;49(8):3457-64. Epub 2008 Apr 17.
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Prevalence of idiopathic macular hole in adult rural and urban south Indian population.
Sen P, Bhargava A, Vijaya L, George R.
Clin Experiment Ophthalmol. 2008 Apr;36(3):257-60.
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Association of non-synonymous single nucleotide polymorphisms in the LOXL1 gene with pseudoexfoliation syndrome in India.
Ramprasad VL, George R, Soumittra N, Sharmila F, Vijaya L, Kumaramanickavel G.
Mol Vis. 2008 Feb 9;14:318-22.
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Comparison of refractive errors and factors associated with spectacle use in a rural and urban South Indian population.
Prema R, George R, Sathyamangalam Ve R, Hemamalini A, Baskaran M, Kumaramanickavel G, Catherine M, Vijaya L.
Indian J Ophthalmol. 2008 Mar-Apr;56(2):139-44.
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First World Glaucoma day, March 6, 2008: tackling glaucoma challenges in India.
George R, Vijaya L.
Indian J Ophthalmol. 2008 Mar-Apr;56(2):97-8. No abstract available.
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Agreement between clinical estimates and planimetric measures of vertical cup:disc ratio.
Arvind H, George R, Raju P, Ramesh SV, Mani B, Kannan P, Vijaya L.
Clin Experiment Ophthalmol. 2007 Dec;35(9):881-2. No abstract available.
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Prevalence of primary angle-closure disease in an urban south Indian population and comparison with a rural population. The Chennai Glaucoma Study.
Vijaya L, George R, Arvind H, Baskaran M, Ve Ramesh S, Raju P, Kumaramanickavel G, McCarty C.
Ophthalmology. 2008 Apr;115(4):655-660.e1. Epub 2007 Sep 17.
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Prevalence of primary open-angle glaucoma in an urban south Indian population and comparison with a rural population. The Chennai Glaucoma Study.
Vijaya L, George R, Baskaran M, Arvind H, Raju P, Ramesh SV, Kumaramanickavel G, McCarty C.
Ophthalmology. 2008 Apr;115(4):648-654.e1. Epub 2007 Jul 30.
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Transforming growth factor beta-1 -509C>T polymorphism in Indian patients with primary open angle glaucoma.
Sripriya S, George R, Arvind H, Baskaran M, Raju P, Ramesh SV, Karthiyayini T, Vijaya L, Kumaramanickavel G.
Mol Diagn Ther. 2007;11(3):151-4.
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Population norms for frequency doubling perimetry with uncorrected refractive error.
Ramesh SV, George R, Soni PM, Palaniappan L, Raju P, Paul PG, Ramsathish S, Vijaya L.
Optom Vis Sci. 2007 Jun;84(6):496-504.
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Molecular genetic analysis of a consanguineous south Indian family with congenital glaucoma: relevance of genetic testing and counseling.
Ramprasad VL, George RJ, Sripriya S, Nirmaladevi J, Vijaya L, Kumaramanickavel G.
Ophthalmic Genet. 2007 Mar;28(1):17-24.
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Gender variation in ocular biometry and ultrasound biomicroscopy of primary angle closure suspects and normal eyes.
Ramani KK, Mani B, Ronnie G, Joseph R, Lingam V.
J Glaucoma. 2007 Jan;16(1):122-8.
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OPTN gene: profile of patients with glaucoma from India.
Sripriya S, Nirmaladevi J, George R, Hemamalini A, Baskaran M, Prema R, Ve Ramesh S, Karthiyayini T, Amali J, Job S, Vijaya L, Kumaramanickavel G.
Mol Vis. 2006 Jul 24;12:816-20.
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Influence of tobacco use on cataract development.
Raju P, George R, Ve Ramesh S, Arvind H, Baskaran M, Vijaya L.
Br J Ophthalmol. 2006 Nov;90(11):1374-7. Epub 2006 Jul 12.
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Prevalence and causes of blindness in the rural population of the Chennai Glaucoma Study.
Vijaya L, George R, Arvind H, Baskaran M, Raju P, Ramesh SV, Paul PG, Kumaramanickavel G, McCarty C.
Br J Ophthalmol. 2006 Apr;90(4):407-10.
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Prevalence of angle-closure disease in a rural southern Indian population.
Vijaya L, George R, Arvind H, Baskaran M, Paul PG, Ramesh SV, Raju P, Kumaramanickavel G, McCarty C.
Arch Ophthalmol. 2006 Mar;124(3):403-9.
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Prevalence of open-angle glaucoma in a rural south Indian population.
Vijaya L, George R, Paul PG, Baskaran M, Arvind H, Raju P, Ramesh SV, Kumaramanickavel G, McCarty C.
Invest Ophthalmol Vis Sci. 2005 Dec;46(12):4461-7.
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Genetic homogeneity for inherited congenital microcoria loci in an Asian Indian pedigree.
Ramprasad VL, Sripriya S, Ronnie G, Nancarrow D, Saxena S, Hemamalini A, Kumar D, Vijaya L, Kumaramanickavel G.
Mol Vis. 2005 Nov 3;11:934-40.
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A comparison of participants and non-participants in the Chennai Glaucoma Study-rural population.
Paul PP, George RJ, Arvind H, Raj M, Augustian, Ramesh SV, Sriram P, Kumaramanickavel G, McCarthy C, Vijaya L.
Ophthalmic Epidemiol. 2005 Apr;12(2):125-35.
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Glaucoma in aphakia and pseudophakia in the Chennai Glaucoma Study.
Arvind H, George R, Raju P, Ramesh SV, Baskaran M, Paul PG, McCarty C, Vijaya L.
Br J Ophthalmol. 2005 Jun;89(6):699-703.
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Effect of cataract surgery with intraocular lens implant on frequency doubling perimetry.
Arvind H, George R, Baskaran M, Raju P, Ramesh SV, Paul PG, Vijaya L.
Curr Eye Res. 2005 Feb;30(2):123-8. Erratum in: Curr Eye Res. 2005 Nov;30(11):1033.
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Low frequency of myocilin mutations in Indian primary open-angle glaucoma patients.
Sripriya S, Uthra S, Sangeetha R, George RJ, Hemamalini A, Paul PG, Amali J, Vijaya L, Kumaramanickavel G.
Clin Genet. 2004 Apr;65(4):333-7.
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Pseudoexfoliation in South India.
Arvind H, Raju P, Paul PG, Baskaran M, Ramesh SV, George RJ, McCarty C, Vijaya L.
Br J Ophthalmol. 2003 Nov;87(11):1321-3.
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Methods and design of the Chennai Glaucoma Study.
Arvind H, Paul PG, Raju P, Baskaran M, George R, Balu S, Sripriya S, Ramesh SV, Mukesh BN, Vijaya L, Kumaramanickavel G, McCarty C.
Ophthalmic Epidemiol. 2003 Dec;10(5):337-48.
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Ocular biometry in occludable angles and angle closure glaucoma: a population based survey.
George R, Paul PG, Baskaran M, Ramesh SV, Raju P, Arvind H, McCarty C, Vijaya L.
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