Key Takeaways
- Diabetic retinopathy (DR) affects approximately 1 in 3 people with diabetes.
- In the US, about 8 million people aged 40 and older have DR.
- Globally, DR is responsible for 2.6% of total blindness.
- Duration of diabetes >15 years increases DR risk by 5-fold.
- Poor glycemic control (HbA1c >8%) doubles DR risk.
- Hypertension increases DR risk by 2.5 times.
- Nonproliferative DR (NPDR) first stage with microaneurysms.
- Mild NPDR: microaneurysms only, asymptomatic.
- Moderate NPDR: venous beading, hemorrhages.
- Annual dilated eye exams recommended for screening.
- Fundus photography detects 90% of referable DR.
- Optical coherence tomography (OCT) gold standard for DME.
- Panretinal photocoagulation (PRP) standard for PDR.
- Anti-VEGF injections reduce DME by 50% thickness.
- Focal laser for CSME improves vision +2 lines in 70%.
Diabetic retinopathy is common but early control can prevent most cases.
Clinical Stages and Symptoms
- Nonproliferative DR (NPDR) first stage with microaneurysms.
- Mild NPDR: microaneurysms only, asymptomatic.
- Moderate NPDR: venous beading, hemorrhages.
- Severe NPDR: 4-2-1 rule (hemorrhages, IRMA, venous loops).
- Proliferative DR (PDR): neovascularization on disc or elsewhere.
- Diabetic macular edema (DME) occurs in 7-10% of DR cases.
- Blurred vision common in 50% of symptomatic DR.
- Floaters indicate vitreous hemorrhage in PDR.
- Sudden vision loss from tractional retinal detachment.
- 20/20 vision possible in early DR, progresses to legal blindness.
- Cotton wool spots represent nerve fiber infarcts.
- Hard exudates near macula cause metamorphopsia.
- Neovascularization of iris (rubeosis) in advanced PDR.
- Asymptomatic until macular involvement in 70% cases.
- Color vision defects in 30% moderate NPDR.
- Night blindness from peripheral ischemia.
- Relative afferent pupillary defect in severe cases.
- Intraretinal microvascular abnormalities (IRMA) pre-PDR sign.
- Clinically significant macular edema (CSME) defined by ETDRS.
- Flame hemorrhages superficial, dot-blot deep.
- Vitreous hemorrhage obscures fundus in 15% PDR.
- Traction macular hole in 5% advanced DR.
- Sectoral laser scars from focal treatment.
Clinical Stages and Symptoms Interpretation
Diagnosis and Screening
- Annual dilated eye exams recommended for screening.
- Fundus photography detects 90% of referable DR.
- Optical coherence tomography (OCT) gold standard for DME.
- Fluorescein angiography shows leakage in 80% CSME.
- Ultra-widefield imaging covers 200 degrees retina.
- AI screening sensitivity 97% for referable DR.
- Visual acuity testing ETDRS chart standard.
- Slit-lamp biomicroscopy for anterior segment neovasc.
- IOP measurement for neovascular glaucoma risk.
- Stereoscopic fundus exam classifies NPDR levels.
- Telemedicine screening reaches 70% more patients.
- HbA1c correlates with DR severity staging.
- Contrast sensitivity testing detects early dysfunction.
- Microperimetry maps macular sensitivity loss.
- B-scan ultrasound for vitreous hemorrhage extent.
- ETDRS 7-field stereo photos for clinical trials.
- teleretinal screening specificity 95%.
- Pupillary response abnormal in 20% advanced DR.
- Dark adaptometry prolonged in ischemia.
- Fundus autofluorescence shows RPE damage.
- Laser Doppler flowmetry measures retinal blood flow.
Diagnosis and Screening Interpretation
Prevalence and Incidence
- Diabetic retinopathy (DR) affects approximately 1 in 3 people with diabetes.
- In the US, about 8 million people aged 40 and older have DR.
- Globally, DR is responsible for 2.6% of total blindness.
- Prevalence of DR in type 1 diabetes is around 35-40% after 10 years.
- In type 2 diabetes, DR prevalence reaches 60-80% after 20 years.
- 1.02 billion people worldwide have DR in 2020 estimates.
- In India, DR prevalence among diabetics is 17.6%.
- UKPDS study: 25% of newly diagnosed type 2 diabetics had DR.
- Annual incidence of DR in type 1 diabetes is 2.6%.
- In Australia, 28.5% of diabetics have some DR.
- DR prevalence in Hispanic diabetics in US is 42%.
- In China, 26.5% of type 2 diabetics have DR.
- 90% of DR cases can be prevented or delayed with control.
- In Europe, DR affects 22-39% of diabetics.
- Incidence of proliferative DR (PDR) is 3-5% per year in uncontrolled.
- 4.2 million Americans aged 40+ have DR.
- Vision-threatening DR affects 1.5 million US adults.
- In Africa, DR prevalence is 15-20% among diabetics.
- DCCT trial: Intensive control reduced DR incidence by 76%.
- 103 million projected DR cases by 2045 globally.
- In Japan, DR in 29.3% of type 2 diabetics.
- South Korea: 15.6% DR prevalence in diabetics.
- Brazil: 28% DR in type 2 diabetes.
- Egypt: 40.3% DR prevalence.
- Singapore: 35% any DR in diabetics.
- Canada: 29% DR prevalence.
- Mexico: 30.5% DR in diabetics.
- Turkey: 27.8% prevalence.
- Iran: 32.6% DR rate.
- Saudi Arabia: 36.4% in type 2.
Prevalence and Incidence Interpretation
Risk Factors and Etiology
- Duration of diabetes >15 years increases DR risk by 5-fold.
- Poor glycemic control (HbA1c >8%) doubles DR risk.
- Hypertension increases DR risk by 2.5 times.
- Smoking raises DR progression risk by 1.8-fold.
- Dyslipidemia (high triglycerides) associated with 1.7x DR risk.
- Nephropathy present in 40% of PDR cases.
- Type 1 diabetes patients have higher PDR risk than type 2.
- Obesity increases DR incidence by 1.3-fold.
- Anemia correlates with severe DR in 25% cases.
- Pregnancy increases DR progression by 20-60%.
- Male gender has 1.2x higher DR prevalence.
- African Americans have 1.5x DR risk vs whites.
- Insulin use associated with 2x DR risk in type 2.
- Sleep apnea increases DR odds by 1.4.
- High BMI (>30) raises severe DR by 30%.
- Hyperglycemia primary driver, VEGF upregulation.
- AGEs (advanced glycation end-products) contribute to pathogenesis.
- Oxidative stress key in endothelial damage.
- Inflammation markers (CRP) elevated in DR.
- Genetic factors account for 20-30% heritability.
- ACE gene polymorphisms increase risk by 1.5x.
- Poor prenatal glycemic control in GDM raises offspring DR risk.
- Chronic kidney disease stage 3+ triples DR severity.
- Alcohol consumption >30g/day increases risk 1.2x.
- Statin use may reduce DR progression by 25%.
- Rapid HbA1c lowering can worsen DR temporarily (early worsening).
Risk Factors and Etiology Interpretation
Treatment, Management, and Prognosis
- Panretinal photocoagulation (PRP) standard for PDR.
- Anti-VEGF injections reduce DME by 50% thickness.
- Focal laser for CSME improves vision +2 lines in 70%.
- Vitrectomy success 85% for tractional detachment.
- Intensive glycemic control slows DR progression 50%.
- Ranibizumab monthly gains +7.2 ETDRS letters.
- Aflibercept superior for persistent DME.
- Corticosteroid implants (Ozurdex) for pseudophakic eyes.
- PRP reduces severe vision loss by 90% in PDR.
- 5-year risk of blindness <1% with treatment.
- Aspirin does not increase vitreous hemorrhage risk.
- Bevacizumab off-label reduces neovasc rapidly.
- Pars plana vitrectomy within 1 month for VH.
- Blood pressure <130/80 mmHg halves progression.
- Faricimab dual angiopoietin-VEGF inhibitor promising.
- 10% recurrence after successful vitrectomy.
- Lipid control with fenofibrate slows progression 30%.
- Untreated PDR leads to blindness in 50% within 5 years.
- DME treatment improves vision in 60-70% cases.
- Gene therapy trials for VEGF suppression ongoing.
- Stem cell therapy experimental for retinal repair.
- Navigation-guided laser reduces treatment spots 40%.
- Pregnancy management: 45% progression, treat aggressively.
Treatment, Management, and Prognosis Interpretation
Sources & References
- Reference 1NEInei.nih.govVisit source
- Reference 2CDCcdc.govVisit source
- Reference 3WHOwho.intVisit source
- Reference 4PUBMEDpubmed.ncbi.nlm.nih.govVisit source
- Reference 5DIABETESJOURNALSdiabetesjournals.orgVisit source
- Reference 6JAMANETWORKjamanetwork.comVisit source
- Reference 7AAOaao.orgVisit source
- Reference 8ADAada.orgVisit source






