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      Retinal Vascular Geometry Predicts Incident Renal Dysfunction in Young People With Type 1 Diabetes

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          Abstract

          OBJECTIVE

          To examine the relationship between retinal vascular geometry parameters and development of incident renal dysfunction in young people with type 1 diabetes.

          RESEARCH DESIGN AND METHODS

          This was a prospective cohort study of 511 adolescents with type 1 diabetes of at least 2 years duration, with normal albumin excretion rate (AER) and no retinopathy at baseline while attending an Australian tertiary-care hospital. AER was quantified using three overnight, timed urine specimen collections and early renal dysfunction was defined as AER >7.5 μg/min. Retinal vascular geometry (including length-to-diameter ratio [LDR] and simple tortuosity [ST]) was quantified from baseline retinal photographs. Generalized estimating equations were used to examine the relationship between incident renal dysfunction and baseline venular LDR and ST, adjusting for age, diabetes duration, glycated hemoglobin (A1C), blood pressure (BP), BMI, and cholesterol.

          RESULTS

          Diabetes duration at baseline was 4.8 (IQR 3.3–7.5) years. After a median 3.7 (2.3–5.7) years follow-up, 34% of participants developed incident renal dysfunction. In multivariate analysis, higher retinal venular LDR (odds ratio 1.7, 95% CI 1.2–2.4; quartile 4 vs. 1–3) and lower venular ST (1.6, 1.1–2.2; quartile 1 vs. 2–4) predicted incident renal dysfunction.

          CONCLUSIONS

          Retinal venular geometry independently predicted incident renal dysfunction in young people with type 1 diabetes. These noninvasive retinal measures may help to elucidate early mechanistic pathways for microvascular complications. Retinal venular geometry may be a useful tool to identify individuals at high risk of renal disease early in the course of diabetes.

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          Most cited references22

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          The case for intrarenal hypertension in the initiation and progression of diabetic and other glomerulopathies.

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            Optimality principles in arterial branching.

            M. Zamir (1976)
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              Alterations in Retinal Microvascular Geometry in Young Type 1 Diabetes

              OBJECTIVE To describe retinal microvascular geometric parameters in young patients with type 1 diabetes. RESEARCH DESIGN AND METHODS Patients with type 1 diabetes (aged 12–20 years) had clinical assessments and retinal photography following standardized protocol at a tertiary-care hospital in Sydney. Retinal microvascular geometry, including arteriolar and venular tortuosity, branching angles, optimality deviation, and length-to-diameter ratio (LDR), were measured from digitized photographs. Associations of these geometric characteristics with diabetes duration, A1C level, systolic blood pressure (SBP), and other risk factors were assessed. RESULTS Of 1,159 patients enrolled, 944 (81.4%) had gradable photographs and 170 (14.7%) had retinopathy. Older age was associated with decreased arteriolar (P = 0.024) and venular (P = 0.002) tortuosity, and female subjects had larger arteriolar branching angle than male subjects (P = 0.03). After adjusting for age and sex, longer diabetes duration was associated with larger arteriolar branching angle (P ≤ 0.001) and increased arteriolar optimality deviation (P = 0.018), higher A1C was associated with increased arteriolar tortuosity (>8.5 vs. ≤8.5%, P = 0.008), higher SBP was associated with decreased arteriolar LDR (P = 0.002), and higher total cholesterol levels were associated with increased arteriolar LDR (P = 0.044) and decreased venular optimality deviation (P = 0.044). These associations remained after controlling for A1C, retinal vessel caliber, and retinopathy status and were seen in subjects without retinopathy. CONCLUSIONS Key diabetes-related factors affect retinal microvascular geometry in young type 1 diabetes, even in those without evidence of retinopathy. These early retinal alterations may be markers of diabetes microvascular complications.
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                Author and article information

                Journal
                Diabetes Care
                diacare
                dcare
                Diabetes Care
                Diabetes Care
                American Diabetes Association
                0149-5992
                1935-5548
                March 2012
                10 February 2012
                : 35
                : 3
                : 599-604
                Affiliations
                [1] 1The Children’s Hospital at Westmead, Westmead, Australia
                [2] 2Discipline of Paediatrics and Child Health, The University of Sydney, Sydney, Australia
                [3] 3Centre for Eye Research Australia, Royal Victorian Eye and Ear Hospital, University of Melbourne, East Melbourne, Victoria, Australia
                [4] 4Department of Ophthalmology, Faculty of Medicine, Gadjah Mada University, Yogyakarta, Indonesia
                [5] 5School of Women’s and Children’s Health, University of New South Wales, Kensington, New South Wales, Australia
                [6] 6Department of Medicine, St. Vincent’s Hospital, University of Melbourne, Melbourne, Australia and
                [7] 7Singapore Eye Research Institute, National University of Singapore, Queenstown, Singapore
                Author notes
                Corresponding author: Kim C. Donaghue, kimd@ 123456chw.edu.au .
                Article
                1177
                10.2337/dc11-1177
                3322713
                22250064
                f22d6a08-5504-478d-995c-8d41593be7b5
                © 2012 by the American Diabetes Association.

                Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.

                History
                : 21 June 2011
                : 28 November 2011
                Categories
                Original Article
                Pathophysiology/Complications

                Endocrinology & Diabetes
                Endocrinology & Diabetes

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