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Correlation between markers of renal function and sight-threatening diabetic retinopathy in type 2 diabetes: a longitudinal study in an Indian clinic population
  1. Ramachandran Rajalakshmi1,
  2. Coimbatore Subramanian Shanthi Rani2,
  3. Ulagamathesan Venkatesan3,
  4. Ranjit Unnikrishnan4,
  5. Ranjit Mohan Anjana4,
  6. Saravanan Jeba Rani5,
  7. Ganesan UmaSankari2,
  8. Sobha Sivaprasad6,7,
  9. Rajiv Raman8,
  10. Viswanathan Mohan4
  1. 1Ophthalmology, Madras Diabetes Research Foundation and Dr. Mohan’s Diabetes Specialities Centre, Chennai, Tamil Nadu, India
  2. 2Epidemiology, Madras Diabetes Research Foundation, Chennai, Tamil Nadu, India
  3. 3Biostatistics, Madras Diabetes Research Foundation, Chennai, Tamil Nadu, India
  4. 4Diabetology, Madras Diabetes Research Foundation and Dr. Mohan’s Diabetes Specialities Centre, Chennai, Tamil Nadu, India
  5. 5Data Management, Madras Diabetes Research Foundation, Chennai, Tamil Nadu, India
  6. 6University College London, London, UK
  7. 7NIHR Moorfields Biomedical Research Centre, Moorfields Eye Hospital NHS Foundation Trust, London, UK
  8. 8Vitreo-Retina Services, Vision Research Foundation, Chennai, Tamil Nadu, India
  1. Correspondence to Dr Viswanathan Mohan; drmohans{at}diabetes.ind.in

Abstract

Introduction Previous epidemiological studies have reported on the prevalence of diabetic kidney disease (DKD) and diabetic retinopathy (DR) from India. The aim of this study is to evaluate the effect of DKD on the development of new-onset DR and sight-threatening diabetic retinopathy (STDR) in Asian Indians with type 2 diabetes (T2D).

Research design and methods The study was done on anonymized electronic medical record data of people with T2D who had undergone screening for DR and renal work-up as part of routine follow-up at a tertiary care diabetes center in Chennai, South India. The baseline data retrieved included clinical and biochemical parameters including renal profiles (serum creatinine, estimated glomerular filtration rate (eGFR) and albuminuria). Grading of DR was performed using the modified Early Treatment Diabetic Retinopathy Study grading system. STDR was defined as the presence of proliferative diabetic retinopathy (PDR) and/or diabetic macular edema. DKD was defined by the presence of albuminuria (≥30 µg/mg) and/or reduction in eGFR (<60 mL/min/1.73 m2). Cox regression analysis was used to evaluate the hazard ratio (HR) for DR and STDR.

Results Data of 19 909 individuals with T2D (mean age 59.6±10.2 years, mean duration of diabetes 11.1±12.1 years, 66.1% male) were analyzed. At baseline, DR was present in 7818 individuals (39.3%), of whom 2249 (11.3%) had STDR. During the mean follow-up period of 3.9±1.9 years, 2140 (17.7%) developed new-onset DR and 980 individuals with non-proliferative DR (NPDR) at baseline progressed to STDR. Higher serum creatinine (HR 1.5, 95% CI 1.3 to 1.7; p<0.0001), eGFR <30 mL/min/1.73 m2 (HR 4.9, 95% CI 2.9 to 8.2; p<0.0001) and presence of macroalbuminuria >300 µg/mg (HR 3.0, 95% CI 2.4 to 3.8; p<0.0001) at baseline were associated with increased risk of progression to STDR.

Conclusions DKD at baseline is a risk factor for progression to STDR. Physicians should promptly refer their patients with DKD to ophthalmologists for timely detection and management of STDR.

  • retinopathy
  • kidney
  • Asian Indians
  • type 2 diabetes
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Footnotes

  • Contributors Conceived and designed the study: RRaj, SS, VM. Wrote the manuscript: RRaj, CSSR. Data retrieval: SJR. Data cleansing and analysis: GU, CSSR. Statistical analysis: UV. Helped in revising the manuscript for important intellectual content: VM, RU, RMA, SS, RRN. Read and approved the final manuscript: RRaj, CSSR, UV, GU, SJR, RU, RMA, SS, RRN, VM.

  • Funding This study, within the ORNATE India project, was funded by the Global Challenges Research Fund (GCRF) UK Research and Innovation (UKRI) (MR/P207881/1). The research was supported by the NIHR Biomedical Research Centre at Moorfields Eye Hospital NHS Foundation Trust.

  • Competing interests None declared.

  • Patient consent for publication Not required.

  • Ethics approval This study was approved by the Institutional Ethical Committee of Madras Diabetes Research Foundation (Reg No ECR/194/Inst/TN/2013/RR-16).

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data availability statement All data relevant to the study are included in the article or uploaded as supplementary information. Additional data are available upon reasonable request.