Original paper

DOI: 10.5603/OJ.2023.0015

Diabetic retinopathy among diabetic patients seen at tertiary care centre in Andaman and Nicobar Islands

Shipra Gupta1Sutapa Das1Abhishek Onkar2Tushar Vashisht3
1Department of Ophthalmology, ANIIMS, Port Blair, India
2 Department of Ophthalmology, AIIMS, Deoghar, India
3Department of Pharmacology, ANIIMS, Port Blair, India

Corresponding author:

Dr Tushar Vashisht, Department of Pharmacology, ANIIMS, Port Blair, India, tel: 9915183172; e-mail: vashisht.tushar@gmail.com

This article is available in open access under Creative Common Attribution-Non-Commercial-No Derivatives 4.0 International (CC BY-NC-ND 4.0) license, allowing to download articles and share them with others as long as they credit the authors and the publisher, but without permission to change them in any way or use them commercially

ABSTRACT
Background: The objective of this study was to evaluate the presence of diabetic retinopathy (DR) in patients with diabetes mellitus (DM) in a tertiary health care centre in Andaman and Nicobar Islands and attempt to establish history-based risk factors.
Material and methods: This cross-sectional study was conducted in a hospital over a year. Detailed ocular examinations for diabetic retinopathy were performed on 600 diabetes mellitus patients.
Results: A total of 600 individuals with diabetes were screened. 40% were males, and 60% were females. DR prevalence in the entire data set was 18.67% (p = 0.001). Males (p = 0.011), patients with diabetes with a history of more 5 five years (p = 0.008), people aged 61 to 70 (p = 0.001), and those with poorly controlled diabetes with glycated haemoglobin (HbA1c) values > 5 % (p = 0.001) all had a higher prevalence of DR.
Conclusions: The study identified the prevalence of DR in Andaman and Nicobar Islands, raising awareness among DM patients for the need of regular ocular examination.
Key words: diabetic retinopathy (DR); diabetes mellitus (DM); prevalence
Ophthalmol J 2023; Vol. 8, 68–71

Introduction

India is on track to become the world’s diabetes capital. Diabetes mellitus (DM) had impacted 31.7 million persons in India by 2000, according to the World Heath Organization (WHO). This population is expected to climb to 79.4 million by 2030, the highest of any country globally. Almost two-thirds patients with type 2 DM (T2DM) and nearly all with type 1 (T1DM) are likely to develop diabetic retinopathy (DR) over time [1–3]. Because retinopathy frequently goes undiscovered until vision loss occurs, early detection, timely treatment, and adequate care can protect or delay vision loss [4].

The widespread prevalence of DR also places a significant financial and public health burden on the national healthcare system. This highlights the importance of epidemiological research on diabetes-related complications in those with diabetes. Despite the ramifications of this condition and the rising prevalence of diabetes in India, there are few precise estimates of the prevalence of DR in India, and no such published statistics are currently available in the Andaman and Nicobar Islands. We want to know what the prevalence of diabetes is and how it relates to age, gender, diabetes duration, and diabetes control utilising HBA1c levels. The initiative served as the first Island attempt to address the issue of DR blindness.

Material and methods

This was a cross-sectional study conducted from January 2019 to January 2020 in a tertiary care hospital.

Six hundred DM patients from the eye outpatient department (OPD) were chosen. Prior clearance from the Institutional Ethics Committee (IEC) was obtained. Detailed history and ocular examination for DR were performed. Written informed consent was obtained from each patient before the study. A structured protocol was used for documenting the patient’s assessment. All questions for eliciting history were asked of the patient in their native language. For clinical examination, standard techniques and equipment were employed; retinal evaluation was performed with a direct/indirect ophthalmoscope or a 90D lens on a slit lamp. The present study did not consider retinopathy grading or the presence of macular oedema.

Statistical methods

The prevalence of DR in the study population was calculated, and the Chi-Square test was used to analyse relationships with gender, age, diabetes duration, and diabetes control as measured by HBA1c levels.

Results

The overall prevalence of DR in our entire study data set was (18.67%; p = 0.001) as depicted in Table 1. Among 600 patients, 40% were males and 60% were females, and the prevalence of DR was higher in males (20%; p = 0.011) than in females (17.78%; p = 0.003) (Tab. 1). Table 2 depicts the proportion of DR patients by age group.

Table 1. Prevalence and frequency distribution of patients with diabetes and diabetic retinopathy (DR)

Total

Percentage

With DR

Percentage

p-value

Total

600

100

112

18.67

0.001

Males

240

40

48

20

0.011

Females

360

60

64

17.78

0.003

Table 2. Diabetic retinopathy distribution according to age group

Age of the patient

No. of patients with diabetes

No. of patients with DR

Percentage (%) of patients with DR

p-value

2130

15

1

6.67

0.062

3140

29

3

10.34

0.001

4150

133

18

13.53

0.001

5160

178

37

20.79

0.001

6170

196

46

23.47

0.001

≥ 71

49

7

14.29

0.001

Total

600

112

18.67

0.001

Approximately 84.5% of those screened were aged 40 to 70 (Tab. 2). Table 3 shows that the prevalence of DR was more in the duration of DM more than 10 years (26.80%; p = 0.008), and over half of patients had diabetes more than 10 years. The prevalence of DR was significantly more in patients with poor control of diabetes checked via HBA1c levels of > 5 % (p = 0.001) (Tab. 4).

Table 3. Diabetic retinopathy (DR) distribution in relation to duration of diabetes mellitus (DM)

Duration of diabetes

Total patients

DR patients

Percentage (%)

p-value

< 5 years

70

5

7.14

0.481

510 years

224

25

11.16

0.030

> 10 years

306

82

26.80

0.008

Table 4. Diabetic retinopathy (DR) distribution in relation to control of diabetes mellitus (DM) checked via glycated haemoglobin (HbA1c) levels

HbA1c levels (%)

Percentage (%)

p-value

04

2.94

0.114

59

19.72

0.001

> 10

19.29

0.001

Discussion

One of the most severe microvascular consequences of DM, DR, is a significant contributor to irreversible vision loss in working-age individuals (20–74 years). The severity of hyperglycemia, the prevalence of hypertension, and the length of DM are all widely recognised as key risk factors for developing DR [5, 6]. In the present study, the prevalence of DR was 18.67% which was similar to that observed by Rema et al. (17.6%), Raman et al. (18.1%) studies done in the southern states of India and Gadkari et al. (21.7%) study conducted pan India [7–9]. We found a correlation between the length of DM and the emergence of DR and that the proportion of patients with DR increases as DM persists longer. Our research showed that DR emerged in 26.80% of patients after 10 years of DM, and in 7.14% of the population as early as 5 years of DM. This finding confirmed the notion that the most frequent predictor of the severity of DR is the duration of DM [10, 11]. In contrast to a study that indicated the overall age-standardized prevalence of DR to be 34.6% with a mean age of 58 years [12], our research discovered that 20.79% of patients with retinopathy fell into the 51–60 age range.

The prevalence of DR was found to considerably increase with an increase in glycated haemoglobin levels, based upon findings from the Chennai Urban, Rural Epidemiology Study (CURES) eye study [13]. In the present study, DR prevalence was significantly higher in patients with poor control of diabetes checked via HbA1c levels of > 5 % (p = 0.001). Therefore, our findings are consistent with earlier reports that found a strong and significant link between DR and inadequate DM control. The number of patients with DR progressively grew along with the fraction of HbA1c.

According to the UK Prospective Diabetes Study (UKPDS), the level of glycemic control was more crucial than anti-diabetic medication for preventing retinopathy [6].

In this study, we found that men were more impacted by DR than women were. The LALES study showed that men had a 50% higher chance of developing diabetes than women (p = 0.006) [14]. In a similar vein, the UKPDS 50 study found that women had a decreased relative risk of DR advancement (p = 0.0016) [15].

It was unable to distinguish between patients with T2DM and T1DM in the self-reported data set for both our study and those carried out by other ophthalmic facilities. Studies that had access to all of the patient’s medical records could distinguish between those with T1DM and T2DM. The prevalence between the two subsets has been found to differ considerably. According to the UK National Diabetic Retinopathy Screening Service, those with T1DMs had a 56.0% prevalence of any DR, whereas people with T2DM had a 30.3% prevalence [16]. Most study participants had their retinas examined by a doctor; however, there was no photographic documentation. The National Diabetic Retinopathy Screening Service in the United Kingdom and the United States uses photographic documentation as a standard procedure. Retinal fundus imaging (photography) is considered to have advantages in improved standardisation, permanent keeping documentation, and accurate reporting by a reading centre; disadvantages include the expense of the image and related technology. According to research by Gadkari et al., low-cost options such a smartphone and portable retinal cameras that transmit data through cellular networks are efficient [17].

The critical merits of our study were the inclusion of both genders, the broad age range of patients seen, taking into account their HbA1c levels, and the detailed examination of critical clinical data from the previous year. Notably, because the study was carried out in a tertiary care institution, our results may be very applicable to clinical practice. Through our study, we intended to educate people with diabetes on the benefits of routine and early ocular examination.

Conclusion

In the Andaman and Nicobar Islands, this was the first research of its kind. The study helped determine the prevalence of DR in the population and create awareness among diabetic patients of the need for regular ocular examination. This study helped to develop a bridge between medicine and ophthalmology in treating diabetic patients.

Conflict of interest

None declared.

Funding

None declared.

References

  1. Wild S, Roglic G, Green A, et al. Global prevalence of diabetes: estimates for the year 2000 and projections for 2030. Diabetes Care. 2004; 27(5): 10471053, doi: 10.2337/diacare.27.5.1047, indexed in Pubmed: 15111519.
  2. World Health Organization 2006. Prevention of blindness from diabetes mellitus: report of a WHO consultation in Geneva, Switzerland, 911 November 2005. https://apps.who.int/iris/handle/10665/43576 (2006).
  3. Aravind Eye Care System. Guidelines for the Comprehensive Management of Diabetic Retinopathy in India. A Vision 2020 the right to sight India publication. July, 2008. https://www.iapb.org/wp-content/uploads/Guidelines-for-the-Comprehensive-Management-of-DR-in-India.pdf.
  4. Looker HC, Nyangoma SO, Cromie D, et al. Scottish Diabetic Retinopathy Screening Collaborative, Scottish Diabetes Research Network Epidemiology Group. Diabetic retinopathy at diagnosis of type 2 diabetes in Scotland. Diabetologia. 2012; 55(9): 23352342, doi: 10.1007/s00125-012-2596-z, indexed in Pubmed: 22688348.
  5. Nathan DM, Genuth S, Lachin J, et al. Diabetes Control and Complications Trial Research Group. The effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin-dependent diabetes mellitus. N Engl J Med. 1993; 329(14): 977986, doi: 10.1056/NEJM199309303291401, indexed in Pubmed: 8366922.
  6. Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33). UK Prospective Diabetes Study (UKPDS) Group. Lancet. 1998; 352(9131): 837853, indexed in Pubmed: 9742976.
  7. Rema M, Premkumar S, Anitha B, et al. Prevalence of diabetic retinopathy in urban India: the Chennai Urban Rural Epidemiology Study (CURES) eye study, I. Invest Ophthalmol Vis Sci. 2005; 46(7): 23282333, doi: 10.1167/iovs.05-0019, indexed in Pubmed: 15980218.
  8. Raman R, Rani PK, Reddi Rachepalle S, et al. Prevalence of diabetic retinopathy in India: Sankara Nethralaya Diabetic Retinopathy Epidemiology and Molecular Genetics Study report 2. Ophthalmology. 2009; 116(2): 311318, doi: 10.1016/j.ophtha.2008.09.010, indexed in Pubmed: 19084275.
  9. Gadkari SS, Maskati QB, Nayak BK. Prevalence of diabetic retinopathy in India: The All India Ophthalmological Society Diabetic Retinopathy Eye Screening Study 2014. Indian J Ophthalmol. 2016; 64(1): 3844, doi: 10.4103/0301-4738.178144, indexed in Pubmed: 26953022.
  10. Bamashmus MA, Gunaid AA, Khandekar RB. Diabetic retinopathy, visual impairment and ocular status among patients with diabetes mellitus in Yemen: a hospital-based study. Indian J Ophthalmol. 2009; 57(4): 293298, doi: 10.4103/0301-4738.53055, indexed in Pubmed: 19574698.
  11. Rani PK, Raman R, Chandrakantan A, et al. Risk factors for diabetic retinopathy in self-reported rural population with diabetes. J Postgrad Med. 2009; 55(2): 9296, doi: 10.4103/0022-3859.48787, indexed in Pubmed: 19550052.
  12. Yau JWY, Rogers SL, Kawasaki R, et al. Meta-Analysis for Eye Disease (META-EYE) Study Group. Global prevalence and major risk factors of diabetic retinopathy. Diabetes Care. 2012; 35(3): 556564, doi: 10.2337/dc11-1909, indexed in Pubmed: 22301125.
  13. Pradeepa R, Anitha B, Mohan V, et al. Risk factors for diabetic retinopathy in a South Indian Type 2 diabetic population--the Chennai Urban Rural Epidemiology Study (CURES) Eye Study 4. Diabet Med. 2008; 25(5): 536542, doi: 10.1111/j.1464-5491.2008.02423.x, indexed in Pubmed: 18346159.
  14. Varma R, Macias GL, Torres M, et al. Los Angeles Latino Eye Study Group. Biologic risk factors associated with diabetic retinopathy: the Los Angeles Latino Eye Study. Ophthalmology. 2007; 114(7): 13321340, doi: 10.1016/j.ophtha.2006.10.023, indexed in Pubmed: 17306879.
  15. Stratton IM, Kohner EM, Aldington SJ, et al. UKPDS 50: risk factors for incidence and progression of retinopathy in Type II diabetes over 6 years from diagnosis. Diabetologia. 2001; 44(2): 156163, doi: 10.1007/s001250051594, indexed in Pubmed: 11270671.
  16. Thomas RL, Dunstan FD, Luzio SD, et al. Prevalence of diabetic retinopathy within a national diabetic retinopathy screening service. Br J Ophthalmol. 2015; 99(1): 6468, doi: 10.1136/bjophthalmol-2013-304017, indexed in Pubmed: 25091950.
  17. Gadkari S. The Pune diabetic retinopathy awareness and screening model. J Clin Ophthalmol Res. 2015; 3(1): 23, doi: 10.4103/2320-3897.149352.

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