Vol.14  No. 1,  Januray,  2004

Determination of Prevalence of Diabetic Retinopathy & its Relationship to Duration and the age of Onset of Diabetes
Ashish Thapar, Neeraj Arora, Saramma Jaison, SK Chopra

INTRODUCTION
Whilst pouring our knowledge and efforts into the curing of the sick let us not forget that our social conscience would be better served by preventing the sickness. With this statement in mind the dedicated ophthalmologist should make it a part of this practice to participate in research of the preventable cause of blindness.

There is an apparent epidemic of diabetes amongst adult population of disadvantaged communities, both in developing countries and also in the industrialized world.  For every patient who is known to have diabetes, another has the disease unawares (Diabetes 2000 Project Leaflet, 2000).  Thyle, Negrel, Pararajasegram and Dadzie, (1995), in their analysis of WHO Global Data bank on Blindness, said that the survey data on diabetic retinopathy as cause of blindness is too limited to reach an accurate figure. However, it does seem that blinding diabetic eye disease is now the 4th major cause of blindness worldwide, after cataract, glaucoma and trachoma.  Diabetes Mellitus (DM) is one of the leading causes of blindess in the industrialized countries.  It accounts for 10% of all new cases of blindness in the USA (Kahn & Hiller, 1974). In India, the prevalence of retinopathy in diabetic patients has been reported from4-28% and a 6.7% prevalence of retinopathy in patients of NIDDM at initial diagnosis of diabetes.

The affluent urban population of Punjab which has a high rate of DM is a vulnerable group with a high risk of developing retinopathy.  This study was therefore, undertaken to find out the prevalence of diabetic retinopathy in this high risk group and determine its relationship with duration and age of onset of DM.

MATERIAL AND METHODS
This study was conducted on diabetic patients attending the diabetic clinic in the Department of Medicine, Christian Medical College and Hospital, Ludhiana from April 1st 1999 to March 31st 2000.

The following patients were excluded from the study: Patients in whom dilatation of the pupil is contra indicated e.g. angle closure glaucoma. patients with hazy media, thus impairing visualization of the fundus e.g. macular/leucomatous corneal opacities and cataracts.  Small children (10 or less years of age) because of lack of cooperation needed for funds visualization.

A detailed history was elicited from the patients as per the protocol.  A comprehensive ophthalmological examination was carried out.  Visual acuity for distance and near vision was recorded using Snellen's chart and using near vision chart respectively.  Anterior segment examination was done with slit lamp biomicroscope and gonioscopy with goldmann's three mirror gonioscope to detect neovascularisation of iris.  Intraocular pressure was recorded with applanation tonometer.

The pupils of both eyes were dilated with 5-10% Phenylephrine or 1% Tropicamide and/or 1% Cyclopentolate eye drops to achieve maximum pupillary dilatation.  Phenylephrine was avoided in patients with history of systemic hypertension.  A detailed fundus examination of both eyes was made with binocular indirect ophthalmoscope using +20D condensing lens and also with biomicroscopic indirect method using +90D Volk's lens.  Typical diabetic retinopathic changes in patients were documented with fundus photographs and fluorescein angiography.

Classification of diabetic retinopathy was made according to Modified Airlie House Classification (Hykin PG 1996) as follows:

a) Mild Non-Proliferative Diabetic Retinopathy

b) Moderate Non-Proliferative Diabetic Retinopathy

c) Severe Non-Proliferative Diabetic Retinopathy

d) Very Severe Non-Proliferative Diabetic Retinopathy

e) Proliferative Diabetic Retinopathy

f) Maculopathy/Clinically significant Macular Oedema

For statistical analysis, Chi square test was used for comparing the numbers and percentages. Analysis of vAriance (Anova) was used to calculate means.  Student's t-test and F statistics were used for the above purpose.  Non parametric statistics (Mann-Whitney) and Kruskas-Wallis 'H' - Statistics were used wherever required, especially where the distribution of data was not uniform.

The prevalence of diabetic retinopathy was calculated and its relationship to duration of diabetes and the age of onset of the disease was derived and tabulated.

RESULTS
Various studies conducted in India and abroad have reported variable prevalence of diabetic retinopathy.

Khosla, Tiwari & Bajaj 1976                              4-28%

Khosla et al 1976 (Referral retinal clinic)             79.5%

Kahn and Bradley, 1975                                     25%

Shanna 1996 (South Indian diabetic patients)       37%

In the present study the prevalence of diabetic retinopathy was calculated to be 41.6%.  The prevalence of diabetic retinopathy in the present study was expectedly, found to be higher than that amongst the studies in South Indian Population and also more than that seen in most other studies.

Relationship between Prevalence of Diabetic Retinopathy and Duration of diabetes:

Both longitudinal and cross sectional studies show that duration of diabetes mellitus is an excellent predictor of diabetic retinopathy.

The Wisconsin Epidemiological study on diabetic retinopathy, 1984 found that in patients with insulin dependent diabetes melliltus, prevalence of diabetic retinopathy varied from 2% in patients with < 2 years of diabetes to 98% in patients with 10 or more years of diabetes.  In a study amongst diabetic patients in the Joslin Clinic, 1975, the prevalence of diabetic retinopathy was 7% in patients with diabetes for <10 years, 26% in patients with 10 to 14 years of diabetes and 63% in patients with diabetes for 15 or more years.

In a study among patients with noninsulin dependent diabetes mellitus, Yanko et al (1983), found that the prevalence of diabetic retinopathy 11 to 13 years after the onset of diabetes was 26% and after 16 or more years, it was 63%.

In India Mohan, Vijayprabha and Roma, (1996) in their study of vascular complications in South Indians with non insulin dependent  diabetes, found that as the duration of diabetes increased, the prevalence of diabetic retinopathy also increased.  After 25 years of diabetes the prevalence of diabetic retinopathy was found to be 52%.

The present study made the following observations:

Duration

Prevalence of Diabetic Retinopathy

<6 months

3.4%

7-12 months

25%

<1-5 years

30%

6-10 years

58%

11-20 years

68.3%

>20 years

80%

It was hence concluded that as the duration of diabetes mellitus increased, the prevalence of diabetic retinopathy also increased (P<0.05).

It has also been seen in various studies that the prevalence of more severe grades of diabetic retinopathy increases as the 'duration of diabetes increases.  Sharma (1996) found that no retinopathy was found in patients with mean duration of diabetes 4.8 years or less.  Background diabetic retinopathy was found in patients with mean duration of diabetes 9.4 years, preproliferative diabetic retinopathy in patients with mean duration of diseases 10.4 years and proliferative diabetic retinopathy in patients with mean duration of diabetes 12.4 years.

In the present study the following observations were made:

1.    The prevalence of all grades of diabetic retinopathy increased as the duration of diabetes increased.

Duration of diabetes

Proliferative Diabetic retinopathy

7-12 months

0%

<1-5 years

2.3%

6-10 years

6.6%

11-20 years

11.7%

Thus it was seen that there was a significant relationship between the duration of diabetes and severity of diabetic retinopathy (p<0.05).  The prevalence of clinically significant macular oedema in different studies was compared and its relationship to duration of diabetes studied.

Gupta and Chandrasekhar, (1998), reported that as the duration of diabetes increased, the risk of developing clinically significant macular oedema also increased.

The following observations were made in the present study:

1.    Prevalence of clinically significant macular oedema in the population group studied was 8.8% (22/250).

2.    Of the 22 patients with clinically significant macular oedema, the frequency was as follows:

Duration of diabetes

Clinically significant macular oedema

7-12 months

4.5%

<1-5 years

18.2%

6-10 years

31.8%

11-20 years

45.5%

From the above observations, we can conclude that the risk of developing clinically signifiant macular oedema increases significantly as the duration of diabetes increases (0<0.5).

Relationship between Prevalence of Diabetic Retinopathy and age of onset of Diabetes:

According to the Wisconsin Epidemiological Study of Diabetic Retinopathy 1989 the older onset diabetic patients with less than 2 years of disease had higher rates of diabetic retinopathy (25% in those taking insulin and 20% in those not taking insulin) than among younger onset diabetic (2%).

Jerneld and Peep, (1986), found that the highest prevalence of diabetic retinopathy was found amongst patients with age of onset of diabetes less than 20 years and the lowest when diabetes was diagnosed after the age of 60 years.  Also, prevalence of proliferative diabetic retinopathy was 28% in patients with age of onset of diabetes less than 20 years and 5% in patients with age of onset more than 60 years.  Caird et al (1969), however estimated that the risk of blindness for a given duration of diabetes increases with the age of the patient at the time of diagnosis of disease.

Thus we can see that there have been discrepancies in the prevalence of diabetic retinopathy according to the age of onset of diabetes in different studies.

The present study made the following observations;

  1. The prevalence and severity of diabetic retinopathy is highest when the age of onset of diabetes is 20 years or less. This result is similar to that found in Wisconsin Epidemiological study of diabetic retinopathy, 1989. However, the number of such patients was only 10 out of 250, hence this result cannot be statistically significant.

  2. Prevalence and severity of diabetic retinopathy in patients with age of onset of diabetes 21 years or more increase as the age of onset of diabetes increases.

  3. Relationship between age of onset of diabetes and clinically significant macular oedema was not found to be significant.

  4. Other risk variables studied were:

  1. Gener- for a given duration of diabetes no significant relationship existed between sex and prevalence of diabetic retinopathy.

  2. Treatment: 80.4% patients on irregular treatment had diabetic retinopathy only, 34.2% patients on regular treatment had the same (p<0.05).  Also, it was found that patients on insulin or combined treatment were at a greater risk of developing retinopathy than on oral hypoglycaemics alone.

  3. Positive family history,  d) Hypertension and  e) diabetic nephropathy were found to be strongly associated with the prevalence and severity of diabetic retinopathy.

CONCLUSION
Of the 250 patients examined, 104 had diabetic retinopathy.  The prevalence of diabetic retinopathy was hence calculated to be 41.6% which is higher then that found in most other studies, leading us to conclude that the urban population of Punjab is indeed at a considerably higher risk of developing diabetic retinopathy.

The prevalence of diabetic retinopathy was seen to increase as the duration of diabetes increased.

Prevalence of diabetic retinopathy was found to be high in patients with age onset of diabetes 20 years or less (60%).  All these patients had insulin dependent diabetes mellitus.  From the age of onset of diabetes 21 years onwards, the prevalence of diabetic retinopathy gradually increased as the age of onset increased.

However, it was also seen that the increase in prevalence and severity of diabetic retinopathy was much steeper with increasing duration of diabetes than with increase in age of onset of diabetes.  Duration of diabetes mellitus therefore, remains the best predictor of prevalence and severity of diabetic retinopathy.

Patients with 11-20 years duration of diabetes and age of onset of diabetes 31-40 years were seen to have the highest prevalence of diabetic retinopathy and hence form a high risk group, which required regular monitoring.

We would like to emphasis that ignorance of patients about diabetes and its complications was identified as the most important contributor towards higher prevalence of diabetic retinopathy.

Patient education, physician and primary health care personnel orientation, application of research, comprehensive ophthalmological examination, mass media utilization and prompt referrals would go a long way in curbing the menace of this blinding diabetic eye disease.

REFERENCES

  1. Diabetes 2000 Project Leaflet. Elimination of preventable blindness form diabetes by the year 2000. Am Academy Ophthalmol USA 1996.

  2. Thyle B, Negrel AD, Prarajasegaram R and Dadzieky. Global data on blindness, Bull WHO 1995; 73(1): 115-121.

  3. Kahn HA, Hiller R. Blindness caused by Diabetic Retinopathy. Am J Ophthalmol 1974; 78:58.

  4. Khosla Pk, Tewari HK and Bajaj JS. A study of diabetic retinopathy in India: Epidemiology, biochemical correlates and treatment with xenon arc photocoagulation. Proc. IX congress of International Diabetic Federation, N Delhi, 1976; 629.

  5. Ramachandran A, Snehlatha C, Vijay Y et al. Diabetic retinopathy at the time of diagnosis of NIDDM in South Indian Subjects.  Diabetes Res Clin Pract 1996; 32:III.

  6. Hykin PG. Diabetic Retinopathy: Clinical features and management. Community Eye health 1996; 9 (20): 58-62.

  7. Kahn HA, Bradley RF. Prevalence of Diabetic Retinopathy : age, sex and duration of diabetes. Br J Ophthalmol 1975;59:345

  8. Sharma RA. Diabetic eye disease in Southern India Community Eye Health 1996; 9 (20): 56-58.

  9. Klein R, Klein BEK, Moss SE et al.  The WESDR II : Prevalence and risk of diabetic retinopathy when age at diagnosis is less than 30 years. Arch Ophthalmol 1984; 102: 520-526.

  10. Yanko L, Goldbourt U, Michaelson IC et al. Prevalence and 15- year incidence of retinopathy and associated characteristics in middle aged and elderly diabetic men. Br J Ophthalmol 1983;67: 759-765.

  11. Mohan Y, Vijayprabya R and Roma M. Vascular complications in long term South Indian NIDDM of over 25 years duration. Diabetes Res Clin Pract 1996; 31:133.

  12. Gupta DK, Chandrasekhar N. Diabetic Maculopathy, North Zone J of Ophthalmol, 1998, 8 (2): 15-22.

  13. Klein R, Klein BEK, Moss SE et al. The WESDR III prevalence and risk of diabetic retinopathy when age at diagnosis 30 or more years. Arch Ophthalmol 1989; 102:527-532.

  14. Jerneld B, Algvere P. Relationship of duration and onset of Diabetes Mellitus to Prevalence of Diabetic Retinopathy. Am J Ophthalmol 1986; 102: 431-437.

  15. Caird FI, Pirie A, Ramsell TG. Diabetes and the eye, Oxford Blackwell Scientific Publications 1968, 1-7.


Address for Correspondence

Dr. Ashish Thapar, Deptt. of Ophthalmology,
Christian Medical College, Ludhiana


  Copyright © 2004-05 North Zone Ophthalmological Society India. All rights reserved.
Powered by Indmedica.com - India's Largest Medical Portal