Abstract
Purpose
To present the prevalence and determinants of diabetic retinopathy (DR) among more than 40 years old Saudi population.
Methods
A population based survey was conducted in Riyadh district between 2014 and 2017. All Saudi aged >40 years suffering from diabetes and confirmed in the diabetes register of the Primary Health Center (PHC) were the study population. Representative sample was examined. The Best corrected Visual acuity (BCVA), anterior and posterior segment assessment was performed. Digital fundus camera captured the retinal images. DR was graded into No DR, Non-proliferative DR (Mild, Moderate, Severe) and proliferative DR (PDR). Diabetic macular edema (DME) was separately noted. Sight Threatening Diabetic Retinopathy (STDR) included PDR and/or DME.
Results
We examined 890 persons. The age sex adjusted prevalence of DR was 44.7% (95% CI 44.1 – 45.3). The DR among male was significantly higher than in females. [RR = 1.4 (95% CI 1.02 – 1.8)]. The DR in 60 plus population was higher compared to 40 to 60 years old diabetics [RR = 1.64 (95% CI 1.6 – 1.7), P < 0.001]. The crude prevalence of STDR was 12.4% (95% CI 9.1 – 15.7). Among diabetic with DR, bilateral and unilateral Severe Visual Impairment (SVI) rate were 1% and 1.8%. The coverage of retinal laser treatment for STDR was 6.1%.
Conclusions
The DR among diabetics is high among adult Saudi population. Both DR and STDR were more in males. Visual disabilities among DR cases were few. For early detection and timely management the services need urgent attention.
Keywords: Diabetic retinopathy, Sight threatening diabetic retinopathy, Diabetic macular edema, Diabetes, Blindness
Introduction
There are 3.9 million persons with diabetes in the Kingdom of Saudi Arabia (KSA) as per the projections by the International Diabetes Federation (IDF)1 There was rise in the prevalence of diabetes after rapid industrialization in the country. The shift to more sedentary lifestyle along with unhealthy diets and obesity increased the risk of diabetes2. The IDF data was based on glucose tolerance test which is considered to be less suitable for devising public health strategies. Periodically updated information using standard definitions is crucial for the policy planning. The global initiative 'Vision 2020 – The Right to Sight' aims to eliminate avoidable blindness by 2020.3 The member-countries need an evidence base for the prevalence and magnitude of avoidable blindness including DR. Generating a broader and more precise estimate of the prevalence of DR and its relationship with major risk factors, specifically for the sight threatening diabetic retinopathy (STDR), is crucial for planning health promotion and offer optimal clinical management to persons with diabetes.
Studies from different regions of KSA have reported a high prevalence of DR. In a population based study in Taif; a Western region of KSA, researchers reported 36.8% prevalence of DR among persons with diabetes aged 50 years and more.4 In a hospital based study at Madinah; the western region of KSA, DR rate was 36.1%.5 A study in Jazan (southern region of KSA) DR rate was 27.8%.6 The prevalence of DR in urban and rural areas of Al-Hasa; an eastern region of KSA, the DR rates were 28.6% in rural and 30.5% in urban population.7 The prevalence of DR in northern region (Hail) of KSA among 45+ years old persons with diabetes was 28.6%.8 Although the evidence is available in four regions of KSA, to the best of our knowledge, information about community based DR magnitude in the central KSA is not documented.
Based on the population projections using the census 2010 data, the central region of KSA Riyadh governorate has 8 million population that include 4.6 million Saudi nationals. There are 3 million Saudi 40 year and older in Riyadh governorate (excluding capital).9 This population is unique as they have free access to the government hospitals and diabetes centers. Well-developed private hospitals are also accessible to them in Riyadh capital. It will be interesting to study such a population with minimum barriers to avail services and manage DR. Our DR assessment was a component of a population based blindness survey.
We conducted a survey to estimate the age-sex adjusted prevalence of DR and its determinants in 40 year and older people with diabetes.
Methods
A population based cross-sectional survey was conducted in Riyadh governorate of KSA between 2013 and 2017. The Institutional Research board at our institute approved this study (P-1309). This study adhered to the guidelines of the Declaration of Helsinki. The survey targeted all Saudi aged 40 years and older who were residents during the study period of Riyadh governorate (except capital) region. We excluded capital city because it is part of population based blindness survey that focused only the area outside capital. There were 400 PHCs in this area and of them, seven PHCs were randomly selected. Each of 400 PHC had equal opportunity to be included in the survey. The family list that were resident of the catchment area of the PHC was referred for randomly selecting families for including in the present survey. The patients visiting PHC were not included in the survey. For logistic ease and periodic calibration of equipment, a separate area of PHC was used to conduct this survey. Among survey participants, history about diabetes and medications for diabetes was inquired. They were confirmed by review of the diabetes registry at the PHC. All persons with diabetes in the catchment area are registered, offered free of cost medications and are referred for their annual assessment by diabetologist and ophthalmologist for DR screening. PHC doctors use Diabetes Canada Clinical Practice Guidelines that include fasting plasma glucose of ≥7.0 mmol/L, a 2-hour plasma glucose value in a 75 g oral glucose tolerance test of ≥11.1 mmol/L or a glycated hemoglobin (A1C) of ≥6.5%.10
For calculation of the sample size among population of 100,000 Saudi persons with diabetes in the study area of Riyadh governorate, we assumed that the prevalence of DR in 40 above population would be 21.6%.11 To achieve 95% confidence interval (CI), 5% acceptable error margin and 1.5% design effect, we needed 391 persons with diabetes. So we examined randomly selected 395 persons with diabetes in this study.
The staff of selected PHCs liaised with the community, informed them about timing of survey. The survey team comprised of one optometrist, one ophthalmologist and one clinical coordinator In the PHC, two rooms were allotted for the survey activities. In one room, optometrist gathered demographic information and conducted vision testing. In the second room, ophthalmologist did a thorough eye examination using slit lamp bio-microscope (Topcon, USA), Tonopen (Medtronics, USA) and Gonioscopy(G-4 mirror, Volk, USA). Retina evaluation was first done by slit lamp biomicroscope using +90D double aspherical lens (Volk, USA) and then binocular indirect ophthalmoscopy using 20 DCC Aspherical lens (Nikon, Japan) after dilating the pupils. To obtain digital retinal images, non-mydriatic fundus camera (Topcon Corp., Tokyo, Japan) was used. These images were evaluated by three retina specialists. The survey team visited the PHC twice a week for DR screening. An informed verbal consent was obtained. Examination procedure included Visual Acuity (VA) assessment in appropriate light using the WHO recommended tumbling “E” chart. VA for distance as presented and pinhole correction was tested for each eye. Cases in need of urgent intervention and/or further serious investigations were advised and referred to receive appropriate eye care.
The DR and Diabetic Macular edema (DME) were graded separately. The severity of DR was defined according to the Early Treatment Diabetic Retinopathy study (ETDRS).12 They included ‘No DR’, ‘Mild Non Proliferative Diabetic Retinopathy (NPDR) (only micro-aneurysm), Moderate NPDR (Micro-aneurysms present but not having changes suggestive of severe NPDR) and Severe NPDR (More than 20 intra-retinal hemorrhages in each of four quadrants or definite venous beading in two quadrants or Prominent intra-retinal microvascular abnormalities (IRMA) in one quadrant but no signs of proliferative retinopathy). Proliferative Diabetic Retinopathy (PDR) was defined as presence of neovascularization and/or vitreous/pre-retinal hemorrhage. DME was defined as the presence of retinal thickness and/or hard exudates in posterior pole.12 Moderate Visual impairment (MVI) was defined as distance vision ‘< 20/60 to ≥20/200’. Severe Visual Impairment (SVI) was define as distance vision ‘< 20/200 to ≥20/400’.4
Data were collected on pretested data collection forms and then transferred to the spreadsheet of Microsoft excel®. For univariate analysis, we used parametric method of Statistical Package for Social Sciences (SPSS-24) (IBM, Chicago, USA). The population of persons with diabetes were calculated for both age-groups and gender as per the census 2010 projected for 2013 and diabetes rate applied to the surveyed population. The rates of DR and/or DME were calculated in each subgroup as crude rate. Accordingly, the persons with DR were projected among persons with diabetes. In view of disproportionate representation of subgroups in examined sample compared to population of diabetes in the study area, we estimated age-sex adjusted prevalence rates for different stages of DR, presented as the percentage proportions and their 95% confidence intervals (95% CI). The rates were also presented for both genders and different age groups. The variations in rates in subgroups were validated using two sided p values and chi-square values. A value of <0.05 was considered as statistically significant.
Results
We examined 890 persons aged 40 years and more in seven clusters. The population demographics of projected persons with diabetes and persons with DR in the study area is given in Table 1. There were 133 (33.7%) DR cases in at least one eye of 395 persons with diabetes. As many as 13,151 DR cases are projected in 29,419 possible persons with diabetes in the study area.
Table 1.
Projected population demographics of diabetes and diabetic retinopathy in central KSA excluding capital city.
| Age groups | Diabetic population in central KSA excluding capital city |
Diabetic retinopathy population in central KSA excluding capital city |
||||||
|---|---|---|---|---|---|---|---|---|
| Male | Female | Total | Proportion | Male | Female | Total | Proportion | |
| 40–49 years | 3592 | 5933 | 9525 | 32.4 | 1724 | 902 | 2626 | 20.0 |
| 50–59 years | 4894 | 5730 | 10,624 | 36.1 | 2677 | 2740 | 5417 | 41.2 |
| 60–69 years | 2807 | 3088 | 5895 | 20.0 | 1460 | 2451 | 3911 | 29.7 |
| 70 years+ | 1350 | 2025 | 3375 | 11.5 | 1002 | 195 | 1197 | 9.1 |
| Total | 12,643 | 16,776 | 29,419 | 100 | 6863 | 6288 | 13,151 | 100 |
The number and proportion of persons with DM and DR among examined participants are given in Table 2.
Table 2.
Comparison of diabetes & diabetic retinopathy population in central KSA excluding capital city.
| Age group in years | Profile of persons with diabetes(DM)-[A] |
Profile of persons with diabetic retinopathy (DR)-[B] |
Proportion of DR cases to DM cases. [B/A] |
||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Male | Female | Total | Proportion | Male | Female | Total | Proportion | Male | Female | Total | |
| 40–49 years | 42 | 49 | 91 | 23.0 | 10 | 12 | 22 | 16.6 | 0.24 | 0.24 | 0.24 |
| 50–59 years | 60 | 69 | 129 | 32.7 | 18 | 21 | 39 | 29.3 | 0.3 | 0.3 | 0.3 |
| 60–69 years | 61 | 44 | 105 | 26.6 | 28 | 17 | 45 | 33.8 | 0.46 | 0.39 | 0.43 |
| 70 years+ | 45 | 25 | 70 | 17.7 | 24 | 3 | 27 | 20.3 | 0.56 | 0.12 | 0.39 |
| Total | 208 | 187 | 395 | 100 | 80 | 53 | 133 | 100 | 0.38 | 0.28 | 0.37 |
The age-sex adjusted prevalence of DR among Saudi person with diabetes aged 40 years and more residing in Riyadh governorate (except the capital) was 44.7% (95% CI 44.1–45.3). The adjusted prevalence rates of DR in both genders and age-groups of persons with DM are given in Table 3.
Table 3.
Age and Sex adjusted prevalence of diabetes and diabetic retinopathy in central KSA excluding capital city.
| Age group in years | Age and sex adjusted prevalence of persons with diabetes |
Age and sex adjusted prevalence of persons with DR |
||||||
|---|---|---|---|---|---|---|---|---|
| M | F | T | 95% CI | M | F | T | 95% CI | |
| 40–49 years | 18.1 | 31.2 | 24.5 | 24.1–24.9 | 48 | 15.2 | 27.6 | 26.7–28.5 |
| 50–59 years | 44.1 | 54.9 | 49.3 | 48.7–50.0 | 54.7 | 47.8 | 51.0 | 50.0–52.0 |
| 60–69 years | 52.5 | 59.8 | 56.1 | 55.2–57.1 | 52.0 | 79.4 | 66.3 | 65.1–67.5 |
| 70 years+ | 32.7 | 51.0 | 41.7 | 40.6–42.7 | 74.2 | 9.6 | 35.5 | 33.9–37.1 |
| Total | 31.3 | 43.4 | 37.2 | 36.9–37.6 | 54.3 | 37.5 | 44.7 | 44.1–45.3 |
The prevalence of DR of our study was compared with that published in other Gulf countries Table 4.
Table 4.
Comparison of prevalence of DR in gulf countries.
| # | Country | Author | Year | Sample | Age (year) | Site of survey | Outcome | Refs. |
|---|---|---|---|---|---|---|---|---|
| 1 | KSA | Yasir et al. | 2017 | 395 | >40 | Community | DR 44.7%, STDR: 12.4% | Current |
| 2 | Qatar | Elshafei et al. | 2011 | 540 | >40 | Community | DR 23.5%, STDR: 5.6% | 15 |
| 3 | Oman | Khandekar et al. | 2003 | 2249 | adult | Registry based | DR: 14.4% | 17 |
| 4 | Iran | Maroufizadeh et al. | 2017 | 23 729 | all ages | Meta-analysis | DR: 41.9% | 19 |
| 5 | Jordan | Rabiu MM et al. | 2015 | 1040 | >50 | Community | DR: 48.4% | 13 |
| 6 | UAE | Al Maskari et al. | 2007 | 513 | all ages | Hospital based | DR: 19%, STDR: 5.5% | 16 |
| 7 | Yemen | Bamashmus et al. | 2009 | 350 | all ages | Hospital based | DR: 54.9%, STDR: 22% | 14 |
| 8 | Kuwait | Al-Adsani | 2007 | 165 | adult | Diabetic clinic | DR: 40%, STDR: 20.6% | 20 |
| 9 | Bahrain | Al-Alawi et al. | 2012 | 17,490 | all ages | PHC based | DR: 20%, STDR: 7.4% | 18 |
| 10 | KSA | Al-Rubeaan | 2015 | 50,464 | 25 + | Registry based | DR: 19.7%, STDR: 10.6% | 11 |
| 11 | KSA | Ahmed | 2016 | 401 | 20–90 yr | Diabetic center | DR: 36.4%, STDR: 18.8% | 23 |
| 12 | KSA | Hajar et al. | 2015 | 740 | >50 | Community | DR: 27.8%, STDR: 5.7% | 6 |
| 13 | KSA | Al-Ghamdi et al | 2012 | 612 | >50 | Community | DR; 36.8, STDR: 17.5% | 4 |
Graphical presentation of persons with and without diabetes among examined persons in the study area is given in Fig. 1.
Fig. 1.
Distribution of persons by diabetes status among examined Saudi population aged 40 years and more in catchment areas of seven Primary Health centers of Riyadh Governorate (except capital).
Of the 395 DM cases, 49 had sight threatening diabetic retinopathy (STDR) (PDR and/or DME). The prevalence of STDR was 12.4% (95% CI 9.1–15.7). There could be as many as 1800 cases of STDR among persons with diabetes in the study area. The distribution of cases of different DR grades is shown in Fig. 2. The STDR in males was 6.3% (95% CI 4.1–8.5) and 4.7% (95% CI 2.5–6.9) in females. The STDR rate was similar in males and females.
Fig. 2.
Distribution of persons with diabetic retinopathy (DR) by grade among persons with diabetes aged 40 years and older residing in catchment areas of seven Primary Health centers of Riyadh Governorate (except capital). DME – Diabetic macular edema. NPDR – Non-proliferative diabetic retinopathy. PDR – Proliferative diabetic retinopathy. No DR – no diabetic retinopathy.
The risk of DR among male was significantly higher than that of females. [Relative Risk (RR) 1.4 (95% CI 1.02–1.8), P < 0.001]. The prevalence of DR in age-group 60 years and more was higher compared to age groups 40 to 60 [RR 1.64 (95% CI 1.6–1.7), P < 0.001].
There were four persons with STDR and SVI, seven persons with NPDR + DME and one of them with SVI in one eye. Thus among DM cases with DR, the rate of bilateral SVI was 1% and unilateral SVI was 1.8%.
Of the 49 cases of STDR, three STDR (2 DME and 1 PDR + DME) patients had undergone retinal laser procedure in the past (based on participant’s feedback). Thus, the coverage of retinal laser for STDR was 3/49 = 6.1% in the study area. Among these three STDR cases, one person had bilateral PDR + DME while two patients had unilateral DME and no PDR. There were two cases of DR who had history of intravitreal injection.
Discussion
About 45% of Saudi persons with diabetes aged 40+ years and residing in the Riyadh governorate (except the capital) had DR. One in eight DM patients had severe vision loss. Older age-group and male gender were associated with higher prevalence of DR. The coverage of laser treatment of STDR was very low.
This study is unique since the population based survey for blinding eye diseases including DR was undertaken perhaps for the first time in the central semi-urban areas of Saudi Arabia. Recommendations based on this study would be useful in improving eye care of persons with diabetes not only of the study area but other semi-urban areas of the Kingdom.
Prevalence of DR in our study was high and matched with that found in other gulf countries. UAE, Qatar, Oman and Bahrein had lower DR rates whereas the prevalence of DR in northern Jordan and Yemen were similar to our study.13, 14, 15, 16, 17, 18 While inferring the variation in DR rates, it should be noted that some studies were hospital-based,14, 16, 17, 20 while other were community based.13, 15 In addition, the ages of the target population also differed.
The projected DM and DR cases in the study area is a matter of concern for the health care providers since annual DR screening of such large number of cases will be a mammoth task. There is an urgent need for organized program approach to strengthen the DR screening. The ophthalmic services also need to look at available resources and plan for timely management of DR & STDR so as to avoid visual disabilities.
In our study, fewer male DM cases were enrolled compared to female DM cases but the magnitude of DR was higher in males than females. The STDR rate was although similar, the proportion of cases of STDR in males was slightly more than that in females. This is unusual because the demography of KSA suggests that the proportion of male and female is equal.9 The national registry for Saudi persons with diabetes revealed higher rate in female compared to males.11 Higher rates of DR in males in our study implies that females have lesser risk of DR. One of the reasons for this gender variation could be due to female hormones being protective in development of DR. The researchers of Los Angeles study also confirmed this hypothesis and recommended investigating sex-specific etiologies of DM type 2 and its association to the complications.21 Male gender dominance for DR was noted in other studies at KSA and in Finland.11, 22 The gender preponderance of male with DR conflicts with other studies, some having equal rates in both sexes.15 Other studies showed higher DR rates in females.13 In developing countries, females face barriers for accessing the health services.24 This could result in higher prevalence of DR and STDR in females compared to males. The diabetic patients of our study area have easy, free of cost access to eye care services therefore such barriers are less likely to be responsible for high DR rates and observed gender disparity.
DR was higher in older age-groups in our study. This was also noted in Qatar.15 Perhaps age is a proxy indicator for the duration of diabetes. It develops in nearly all persons with type1 diabetes and in more than 77% of those with type 2 diabetes, who survive over 20 years with the disease.25, 26
The severe visual disabilities among DR cases in our study were few. In northern Jordan also the vision loss among DR patients was low.13 In contrast, a study in Yemen, rate of visual disabilities among DR cases was high.14 It seems that when DR screening is undertaken in the community, the visual disabilities are fewer. But if it is done for diabetes patients in the hospital, visual disabilities are in large numbers.
The diabetes control program in the study area is likely to have 29,000 persons with diabetes that need primary prevention and annual DR screening. This means one ophthalmologist will have to screen 112 patients per working day throughout the year just to address the backlog. Tele-screening should be thought of as the modern mode of early detection of DR and refer STDR cases for urgent management.27 There could be as many as 1800 STDR cases in the study area that need urgent of pan retinal photocoagulation (PRP) and selected cases with DME will need intravitreal anti VEGF injections.28 The ophthalmic services should be strengthened with adequate resources to manage these cases.
There were few limitations in our study. This being a cross-sectional study, the risk factors for DR and STDR should be considered as trends and need further longitudinal studies to confirm. It was part of a major survey for estimating the magnitude of visual disabilities and hence DR and STDR could not be associated to the known diabetes related risk factors like poor glycemic control, hypertension and longer duration of diabetes.
Our study was in semi-urban area adjoining to a large city; Riyadh with very good health services both at government and private sector. We believe that population with easy access if have such status of DM and DR, other far places are likely to have more barriers and challenges. Such studies if carried out in other areas of the Kingdom, the outcomes would complement the findings of the present study and guide the National eye health care planners for improving ophthalmic services for persons with diabetes.
Conflict of interest
The authors declared that there is no conflict of interest.
Footnotes
Peer review under responsibility of Saudi Ophthalmological Society, King Saud University.
References
- 1.IDF Diabetes Atlas – 8th ed. Available from <http://www.diabetesatlas.org/> [accessed on 25/1/2019].
- 2.Qidwai W., Ashfaq T. Imminent epidemic of diabetes mellitus in Pakistan: issues and challenges for health care providers. JLUMHS. 2010;9(03):112. [Google Scholar]
- 3.VISION 2020. The right to sight. Available from <https://www.who.int/blindness/Vision2020_report.pdf?ua=1> [accessed on 25/2/2019].
- 4.Al Ghamdi A.H., Rabiu M., Hajar S., Yorston D., Kuper H., Polack S. Rapid assessment of avoidable blindness and diabetic retinopathy in Taif, Saudi Arabia. Brit J Ophthalmol. 2012;96(9):1168–1172. doi: 10.1136/bjophthalmol-2012-301874. [DOI] [PubMed] [Google Scholar]
- 5.El-Bab M.F., Shawky N., Al-Sisi A., Akhtar M. Retinopathy and risk factors in diabetic patients from Al-Madinah Al-Munawarah in the Kingdom of Saudi Arabia. Clin Ophthalmol (Auckland, NZ) 2012;6:269. doi: 10.2147/OPTH.S27363. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Hajar S., Al Hazmi A., Wasli M., Mousa A., Rabiu M. Prevalence and causes of blindness and diabetic retinopathy in Southern Saudi Arabia. Saudi Med J. 2015;36(4):449. doi: 10.15537/smj.2015.4.10371. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Khan A.R., Wiseberg J.A., Lateef Z.A., Khan S.A. Prevalence and determinants of diabetic retinopathy in Al Hasa region of Saudi Arabia: primary health care centre based cross-sectional survey, 2007–2009. Middle East African J ophthalmol. 2010;17(3):257. doi: 10.4103/0974-9233.65502. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Alshaya A.K., Alsayegh A.K., Alshaya H.K. The common complications and comorbidities among saudi diabetic patients in Northern Saudi Arabia. Open J Endocrine Metabolic Dis. 2017;7(07):151. [Google Scholar]
- 9.Ministry of Health, Statistical book (table 1-3, page 30), (Table 1, page 29). Available from <https://www.moh.gov.sa/en/Ministry/Statistics/book/Documents/Statistical-Yearbook-1437H.pdf> [accessed on 27/9/2018].
- 10.Goldenberg R., Punthakee Z. Definition, classification and diagnosis of diabetes, prediabetes and metabolic syndrome. Can J Diabetes. 2013;37:S8–S11. doi: 10.1016/j.jcjd.2013.01.011. [DOI] [PubMed] [Google Scholar]
- 11.Al-Rubeaan K., Abu El-Asrar A.M., Youssef A.M. Diabetic retinopathy and its risk factors in a society with a type 2 diabetes epidemic: a S audi N ational D iabetes R egistry-based study. Acta Ophthalmol. 2015;93(2):e140–e147. doi: 10.1111/aos.12532. [DOI] [PubMed] [Google Scholar]
- 12.Wilkinson C.P., Ferris F.L., 3rd, Klein R.E. Global Diabetic Retinopathy Project Group. Proposed international clinical diabetic retinopathy and diabetic macular edema disease severity scales. Ophthalmology. 2003;110(9):1677–1682. doi: 10.1016/S0161-6420(03)00475-5. [DOI] [PubMed] [Google Scholar]
- 13.Rabiu M.M., Al Bdour M.D., Abu Ameerh M.A., Jadoon M.Z. Prevalence of blindness and diabetic retinopathy in northern Jordan. Eur J Ophthalmol. 2015;25(4):320–327. doi: 10.5301/ejo.5000557. [DOI] [PubMed] [Google Scholar]
- 14.Bamashmus M.A., Gunaid A.A., Khandekar R.B. Diabetic retinopathy, visual impairment and ocular status among patients with diabetes mellitus in Yemen: a hospital-based study. Indian J Ophthalmol. 2009;57(4):293. doi: 10.4103/0301-4738.53055. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Elshafei M., Gamra H., Khandekar R., Hashimi M.A., Pai A., Ahmed M.F. Prevalence and determinants of diabetic retinopathy among persons≥ 40 years of age with diabetes in Qatar: a community-based survey. Eur J Ophthalmol. 2011;21(1):39–47. doi: 10.5301/ejo.2010.2699. [DOI] [PubMed] [Google Scholar]
- 16.Al-Maskari F., El-Sadig M. Prevalence of diabetic retinopathy in the United Arab Emirates: a cross-sectional survey. BMC Ophthalmol. 2007;7(1):11. doi: 10.1186/1471-2415-7-11. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Khandekar R., Al Lawatii J., Mohammed A.J., Al Raisi A. Diabetic retinopathy in Oman: a hospital based study. Br J Ophthalmol. 2003;87(9):1061–1064. doi: 10.1136/bjo.87.9.1061. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Al Alawi E., Ahmed A.A. Screening for diabetic retinopathy: the first telemedicine approach in a primary care setting in Bahrain. MEAJO. 2012;19(3):295–298. doi: 10.4103/0974-9233.97928. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Maroufizadeh S., Almasi-Hashiani A., Hosseini M., Sepidarkish M., Samani R.O. Prevalence of diabetic retinopathy in Iran: a systematic review and Meta-analysis. Int J Ophthalmol. 2017;10(5):782. doi: 10.18240/ijo.2017.05.21. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Al-Adsani A.M. Risk factors for diabetic retinopathy in Kuwaiti type 2 diabetic patients. SMJ. 2007;28(4):579–583. [PubMed] [Google Scholar]
- 21.Ding E.L., Song Y., Malik V.S., Liu S. Sex differences of endogenous sex hormones and risk of type 2 diabetes: a systematic review and meta-analysis. JAMA. 2006;295(11):1288–1299. doi: 10.1001/jama.295.11.1288. [DOI] [PubMed] [Google Scholar]
- 22.Harjutsalo V., Maric C., Forsblom C. Sex-related differences in the long-term risk of microvascular complications by age at onset of type 1 diabetes. Diabetologia. 2011;54(8):1992–1999. doi: 10.1007/s00125-011-2144-2. [DOI] [PubMed] [Google Scholar]
- 23.Ahmed R.A., Khalil S.N., Al-Qahtani M.A. Diabetic retinopathy and the associated risk factors in diabetes type 2 patients in Abha, Saudi Arabia. JFCM. 2016;23(1):18. doi: 10.4103/2230-8229.172225. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Baru R., Acharya A., Acharya S., Kumar A.S., Nagaraj K. Inequities in access to health services in India: caste, class and region. Econ Polit Weekly. 2010;18:49–58. [Google Scholar]
- 25.Voigt M., Schmidt S., Lehmann T. Prevalence and progression rate of diabetic retinopathy in type 2 diabetes patients in correlation with the duration of diabetes. Exp Clin Endocrinol Diabetes. 2018;126(09):570–576. doi: 10.1055/s-0043-120570. [DOI] [PubMed] [Google Scholar]
- 26.World Health Organization. Prevention of blindness from diabetes mellitus. p. 8. Available from <https://apps.who.int/iris/bitstream/handle/10665/43576/924154712X_eng.pdf?sequence=1&isAllowed=y> [accessed on 25/1/2019].
- 27.Silva P.S., Cavallerano J.D., Aiello L.M., Aiello L.P. Telemedicine and diabetic retinopathy: moving beyond retinal screening. Arch Ophthalmol. 2011;129(2):236–242. doi: 10.1001/archophthalmol.2010.365. [DOI] [PubMed] [Google Scholar]
- 28.Bandello F., Lattanzio R., Zucchiatti I., Del Turco C. Pathophysiology and treatment of diabetic retinopathy. Acta Diabetol. 2013;50(1):1–20. doi: 10.1007/s00592-012-0449-3. [DOI] [PubMed] [Google Scholar]


