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Retinal Vascular Caliber and Risk of
Retinopathy in Young Patients With Type 1 Diabetes
Alibrahim
E, Donaghue KC, Rogers S, Hing S, Jenkins AJ, Chan A, Wong TY. Ophthalmology. 2006;113:1499-1503.
In the Diabetes
Control and Complications Trial, 10% of patients with good glycemic control
(A1C ≤6.87%) developed diabetic retinopathy (DR), but 43% of patients
with poor glycemic control (A1C ≥9.49%) did not. This suggests that
although A1C is an important predictor for the incidence and progression of DR,
it does not fully explain the risk. In adults, retinal vascular caliber
measured from fundus photographs has been associated with the risk of DR, diabetic
nephropathy, and cardiovascular mortality. The Wisconsin Epidemiologic Study of
Diabetic Retinopathy showed that larger arteriolar and venular calibers (AC and
VC, respectively) predicted the progression of DR and the incidence of proliferative
diabetic retinopathy (PDR) but not the incidence of nonproliferative diabetic
retinopathy (NPDR). The purpose of this Australian case-control study was to
determine whether similar associations between retinal vascular caliber and DR
risk exist in children and adolescents with type 1 diabetes.
Cases and
controls were identified from among 668 patients, ages 12-20 years, who had had
a baseline retinal exam between 1990 and 2002; there were 172 patients who
developed DR in this cohort who had had at least 1 follow-up retinal exam
before age 20. Age- and gender-matched controls (n = 180) were randomly
selected from among patients who did not develop DR after at least 2 years of
follow-up (3 clinic visits). The median follow-up times for cases and controls
were 3.1 years and 3.6 years, respectively. Retinal vascular caliber was
assessed from 7-field stereo fundus photographs taken according to the Beaver
Dam Eye Study protocol, which takes into account variations in AC and VC with
the pulse,1 and graded according to Early
Treatment Diabetic Retinopathy Study standards. AC, VC, and the ratio of AC to VC
(A:V) were calculated for both eyes of all patients. Baseline photographs from
21 patients were ungradable, so results were computed from 166 cases and 165
controls. Cases and controls did not differ by any clinical parameter at
baseline. Baseline A1C was slightly higher in cases (8.7 ± 1.4%) than in
controls (8.5 ± 1.1%) but not significantly (P = .178). However, retinal AC was significantly larger among cases
than among controls (AC = 6.3 μm, P
= .004). Retinal VC was larger, but not significantly, among cases than among controls
(P = .312). A:V was significantly
larger in cases than in controls (0.63 ± 0.05 vs 0.61 ± 0.04, P = .011).
After
controlling for age, gender, duration of diabetes, A1C, blood pressure, body
mass index, and pubertal stage, the odds ratio for developing mild DR increased
by 1.38 (P = .014) and 1.44 (P = .006) for each standard deviation
increase in A:V and AC, respectively. No cases developed moderate or severe
NPDR or any PDR. There was considerable overlap of retinal vascular caliber
measurements between cases and controls; however, if these results are
supported by future studies, patients with a large AC may be referred for more
frequent retinal exams and more aggressive management of other risk factors for
DR. These measures might include a lower A1C target.
Reference
1. Wong TY, Knudtson MD, Klein R, et al. Computer-assisted measurement of
retinal vessel diameters in the Beaver Dam Eye Study: methodology, correlation
between eyes, and effect of refractive errors. Ophthalmology. 2004;111:1183-1190.
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