Optimal Frequency of Retinopathy Screening in Adolescents With Type 1 Diabetes: Markov Modeling Approach Based on 30 Years of Data

Author:

Januszewski Andrzej S.1ORCID,Velayutham Vallimayil234,Benitez-Aguirre Paul Z.23,Craig Maria E.235,Cusumano Janine2,Pryke Alison2,Hing Stephen2,Liew Gerald6,Cho Yoon Hi23,Chew Emily Y.7,Jenkins Alicia J.1,Donaghue Kim C.23ORCID

Affiliation:

1. 1National Health and Medical Research Council (NHMRC) Clinical Trials Centre, University of Sydney, Sydney, New South Wales, Australia

2. 2Institute of Endocrinology and Diabetes, The Children’s Hospital at Westmead, Sydney, New South Wales, Australia

3. 3Discipline of Child and Adolescent Health, University of Sydney, Sydney, New South Wales, Australia

4. 4Campbelltown Hospital, Sydney, New South Wales, Australia

5. 5School of Women’s and Children’s Health, University of New South Wales, Sydney, New South Wales, Australia

6. 6Centre for Vision Research, Westmead Institute for Medical Research, University of Sydney, Sydney, New South Wales, Australia

7. 7National Eye Institute, National Institutes of Health, Bethesda, MD

Abstract

OBJECTIVECurrent guidelines recommend biennial diabetic retinopathy (DR) screening commencing at the age of 11 years and after 2–5 years’ duration of type 1 diabetes. Growing evidence suggests less frequent screening may be feasible.RESEARCH DESIGN AND METHODSProspective data were collected from 2,063 youth with type 1 diabetes who were screened two or more times between 1990 and 2019. Baseline (mean ± SD) age was 13.3 ± 1.8 years, HbA1c was 8.6 ± 1.3% (70.1 ± 14.7 mmol/mol), diabetes duration was 5.6 ± 2.8 years, and follow-up time was 4.8 ± 2.8 years. DR was manually graded from 7-field retinal photographs using the Early Treatment Diabetic Retinopathy Study (ETDRS) scale. Markov chain was used to calculate probabilities of DR change over time and hazard ratio (HR) of DR stage transition.RESULTSThe incidence of moderate nonproliferative DR (MNPDR) or worse was 8.6 per 1,000 patient-years. Probabilities of transition to this state after a 3-year interval were from no DR, 1.3%; from minimal DR, 5.1%; and from mild DR, 22.2%, respectively. HRs (95% CIs) for transition per 1% current HbA1c increase were 1.23 (1.16–1.31) from no DR to minimal NPDR, 1.12 (1.03–1.23) from minimal to mild NPDR, and 1.28 (1.13–1.46) from mild to MNPDR or worse. HbA1c alone explained 27% of the transitions between no retinopathy and MNPDR or worse. The addition of diabetes duration into the model increased this value to 31% (P = 0.03). Risk was also increased by female sex and higher attained age.CONCLUSIONSThese results support less frequent DR screening in youth with type 1 diabetes without DR and short duration. Although DR progression to advanced stages is generally slow, higher HbA1c greatly accelerates it.

Publisher

American Diabetes Association

Subject

Advanced and Specialized Nursing,Endocrinology, Diabetes and Metabolism,Internal Medicine

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