ABSTRACT
Objectives: To assess the prevalence and risk factors of diabetic retinopathy (DR) in patients with type 2 diabetes mellitus (T2DM) of different risks, based on the level of glycated hemoglobin (HbA1c).
Methods: A cross-sectional study was conducted in in the chronic illness clinics in Saudi Arabia between January 2019 and February 2020. Data were extracted from 428 T2DM patients’ medical records and random sampling were carried out using a ratio of 1:3, matched for gender and duration of DM. Patients with HbA1c level ≥9% were classified as ‘high-risk’ and HbA1c ≤7% as ‘low-risk’. Retinopathy was confirmed by an ophthalmologist using fundus photography.
Results: The prevalence of DR in high-risk patient was 88.1% and 22.1% in low-risk patients. The prevalence of macular oedema was higher in the high-risk compared to low-risk patients (15.8% versus 4.9%, p<0.001). Patients’ mean age was 61±11 years and duration of diabetes was 13±7 years. Hemoglobin A1c and low-density lipoprotein (LDL) levels were significantly higher in high-risk patients (p<0.0001) in bivariate but not multivariate analysis.
Conclusion: High HbA1c and LDL levels were associated with DR risk. Further multicentre studies involving large samples are required to assess the risk factors associated with DR progression.
Diabetes is a common chronic disease associated with micro- and macro- vascular complications. The global burden of diabetes has been rising, mainly type 2 (T2DM), it is anticipated to reach 578 million cases by 2030, compared with 463 million cases in 2019.1 In respect of prevalence and incidence of diabetes in the Kingdom of Saudi Arabia, the International Diabetes Federation (IDF) ranked Saudi Arabia among one of the highest countries in the Middle East and North Africa.2
Diabetic retinopathy (DR) is a common diabetic complication, a recent pooled prevalence rates showed 18.5% for any retinopathy among diabetic patients. Non-proliferative diabetic retinopathy (NPDR) estimated to be 15.1% and proliferative diabetic retinopathy (PDR) 1%.3
Diabetic retinopathy ranked as the third leading cause for visual impairment and blindness worldwide following cataract and glaucoma.4 It is estimated that DR accounts for 4.8% of cases of blindness (37 million) worldwide, particularly in individuals aged 50 years and older.4 The prevalence of retinopathy in Saudi Arabia was aligned between 28.1% and 45.7%, whereas vision-threatening diabetic retinopathy (VTDR) ranged between 4.5% and 17.5% in diabetic patients.5
Long standing poor glycemic levels beside uncontrolled of other metabolic and clinical parameters are always associated with the severity of DR.6 Therefore, DR is associated globally with hyperglycemia, hyperlipidemia, hypertension, obesity, and duration of diabetes.4 In Saudi Arabia, poor glycemic control, older age, longer diabetic duration, and the presence of other diabetic complications such as nephropathy and neuropathy have been associated with DR.7,8 However, data on DR risk factors in Saudi Arabia are limited with conflicting findings.6,8
The aim of this study is to assess the prevalence and risk factors of DR in patients with T2DM of different risks, based on the level of glycemic control.
Methods
A cross-sectional study was conducted at chronic illness clinic (CIC) between January 2019 and February 2020. The study design was approved by the local Institutional Review Board. The study was conducted according to the principles of Helsinki Declaration. We used PubMed and advanced Google scholar during search.
The current study was targeting patients with T2DM managed at the CIC, a primary healthcare canter in Riyadh, Saudi Arabia. Patients age ≥18 years with T2DM (diagnosis confirmed at least 2 years prior to enrolment) and recent (≤1 year) measurements of glycated hemoglobin (HbA1c) and retinal examination were included. Patients were excluded if they had diagnosis of T1DM, pregnancy, complications involving immunosuppression or collagenopathy, missing or incomplete data (more than 20%), out of date (>1 year) data, or inability or unwillingness to manage their illness and comply with medical advice.
A structural study data collection form was designs to extract data from medical records of the included patients. These included demographic and clinical characteristics; such as age, gender, body mass index (BMI), blood pressure, smoking status, duration of diabetes, use of medications, laboratory parameters, and ophthalmology screening results closest in time to HbA1c results. A random sample was chosen from the CIC patients in a ratio of 1:3; 101 high-risk patients and 327 low-risk patients matched on gender and diabetes duration. Patients with HbA1c level ≥9% were classified as ‘high-risk’, and patients with an HbA1c ≤7% as ‘low-risk’.9 Patients were classified as non-proliferative (NPDR) or proliferative DR (PDR), with or without macular oedema (MO) or clinically significant MO (CSMO), based on the international clinical disease severity criteria.10
Ophthalmological evaluation
Assessment of DR and MO was performed using slit lamp examination and color fundus photographs obtained through dilated pupils. All examinations were performed by trained ophthalmologists who were unaware of the patients’ medical conditions, and their findings were confirmed by a fundus specialist.
Statistical analysis
The collected data were transferred and analyzed using SPSS Statistics for Windows, version 26 (IBM Corp., Armonk, N.Y., USA).11 Descriptive statistics, such as means, standard deviations were used to summarize age, BMI, SBP, DBP, low-density lipoprotein (LDL), albumin to creatinine ratio, diabetes duration and estimated glomerular filtration rate compared between the 2 groups. Percentages were used to summarize gender, smoking status, ACEi and ARB use, statin use. Also, the type and prevalence of DR among study participants; DR, NPDR, PDR, MO and CSMO. Chi squared tests were used to test the associations between different variables across high risk and low risk patients. Adjusted logistic models were used to identify the risk factors that associated with diabetic retinopathy. P-values <0.05 were considered significant. The adjusted odds ratios (aORs) with 95% confidence interval were reported to describe the strength of these associations. Sample size calculation was conducted using sample size will be calculated using Raosoft sample size calculator a trademark (confidence level of 95%, margin of error of 5%, and response of distribution 50%).12
Results
A total of 428 participants were included in the study. One hundred and one (23.6%) patient were considered high-risk group. As shown in Table 1, the prevalence of DR was 88.1% in the high-risk patients, 22.1% in low-risk patients, and 37.6% in all patients. Among the low-risk patients, 68 (94.4%) of the patients were classified as NPDR while only 4 (5.6%) were classified as PDR. Among the high-risk patients, 74 (83.1%) of the patients were classified as NPDR, while 15 (16.9%) were classified as PDR. The prevalence of MO and CSMO were higher in the high-risk compared to low-risk patients (15.8% versus 4.9%, p<0.001 for MO and 7.9% versus 0.6%, p<0.001 for CSMO).
- Type and prevalence of diabetic retinopathy among study participants (N=428).
Table 2 showed the demographic and clinical characteristics of the patients by risk groups. The female patients were 65.1%, mean age was 61±11 years, and the mean duration of disease was 13±7years. Among all variables in Table 2, only mean LDL values were significantly different between groups, being higher in high-risk patients (p<0.001). Table 3 shows the multivariate analysis for the factors that are potentially associated with DR by risk group. None of the examined factors were independently associated with DR in either group. Also, there were no difference between the adjusted odds ratio between the 2 groups.
- Comparison of baseline demographics and clinical characteristics of the participants (N=428).
- Multivariate analysis for the factors that are potentially associated with diabetic retinopathy by risk group.
Discussion
This cross-sectional study examined the prevalence of DR in a total of 428 high- and low- risk T2DM patients, stratified based on HbA1c levels >9 and ≤7 respectively, who were treated at a primary healthcare canter. The prevalence of DR was 88.1% (p<0.001) in the high-risk patients, 22.1% (p<0.001) in low-risk patients, and 37.6% in all patients. The overall DR prevalence in the current study was comparable to previous studies estimating DR between 28.1% and 45.7% of diabetic patients in Saudi Arabia.5,7 Additionally, the observed higher prevalence in high-risk patients was similar the prevalence estimated by Magliah et al6 in Jeddah, Saudi Arabia where DR was diagnosed of high-risk diabetic patients in 86.8% and of low-risk diabetic patients in 13.2%.
In the present study, the total numbers of MO case was 32 (7.5%) and CSMO case was 10 (2.3%) (p<0.001). However, Martinell et al13 reported an MO prevalence of 11% at the time of DM diagnosis in a Swedish population. These discrepancies in prevalence between studies might be accounted by genetic differences between populations; for example, Tan et al14 have shown that individual of Malays and Chinese descent are less likely to develop DR and MO compared to Indian and Singapore.
Glycated hemoglobin A1c and LDL levels in the current study were strongly associated with DR risk in the bivariate analysis (p<0.001). The observed strong association of DR with HbA1c was consistent in all previous local6,7 and international studies.4 Evidence shows that an increased rate of DR is more closely associated to LDL than to other lipid profile parameters, such as high-density lipoprotein, total cholesterol, or triglycerides.15 Therefore, IDF recommends glycemic control and lipid profile management to delay DR progression.2 This can be achieved by patient compliance with recommended medications and scheduled visits.
Study limitations
The current study used a comprehensive data for DR prevalence and risk factors. Nevertheless, some limitations are acknowledged. Being a single primary care centre, the generalisability should be limited to similar population. In addition, data on BMI, smoking status, and ACE inhibitors and ARBs use were missing from several patient records, which might have affected the results. Despite reporting the MO prevalence in our study, we were unable to account for its classification due to the lack of relevant data.
In conclusion, among a sample of patients with an average 13 years of T2DM managed at a primary care centre in Saudi Arabia, the prevalence of DR was 88.1% in the high-risk patients, 22.1% in low-risk patients, and 37.6% in all patients. High HbA1c and LDL levels were associated with higher DR risk. Larger multicentre studies with longitudinal data may be required to assess the risk factors associated with DR progression.
Acknowledgment
The authors would like to thank Dr. Farooq A. Bodla for his help in performing ophthalmology screening, Ms. Reuof A. Bushnag and Ms. Jancy Thomson for their help in recruiting participants, data collection and providing technical help. We also would like to thank Elsevier (www.elsevier.com) for English language editing.
Footnotes
Disclosure. Authors have no conflict of interests, and the work was not supported or funded by any drug company.
- Received January 7, 2021.
- Accepted April 19, 2021.
- Copyright: © Saudi Medical Journal
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