E. Moskalets et al., ASSOCIATION OF BLINDNESS TO INTENSIFICATION OF GLYCEMIC CONTROL IN INSULIN-DEPENDENT DIABETES-MELLITUS, Journal of diabetes and its complications, 8(1), 1994, pp. 45-50
Intensive glycemic control (IGC) in previously hyperglycemic insulin-d
ependent diabetes mellitus (IDDM) patients is associated with a decrea
sed long-term risk of progression of diabetic retinopathy (DR); up to
12 months after institution of IGC, however, the risk of progression o
f DR transiently increases. In an observational study, a cohort of 122
patients with IDDM was followed prospectively for changes in glycosyl
ated hemoglobin (HbA1, normal <8%) and in DR 0-12 months after institu
tion of IGC. In six of these patients (women, mean age 24 years, durat
ion of diabetes 14.3 years, with incipent nephropathy and retinopathy)
a total of seven eyes went blind after 6-12 months of IGC, despite la
ser coagulation treatment. From the whole sample, a control groups of
eight patients (six women) was set up, matched for age, duration of ID
DM, degree of retinopathy, visual acuity, blood pressure, and microalb
uminuria, with preserved vision after 12 months of IGC. In the case pa
tients, the mean (95% confidence interval) initial HbA1 was 14.9% (13.
8%-16.1%), versus 13.4% (12.4%-14.4%) in the control patients (p < 0.0
5). The mean HbA1 decrements after 4 months of IGC, were 3.0% (1.9%-4.
1%) in the cases, and 2.1% (1.2%-3.0%) in the controls (NS); and after
12 months, the respective decrements were 4.9% (2.4%-7.4%) in the cas
es versus 2.0% (0.5%-3.5%) in the controls (p = 0.04). In conclusion,
IGC with a decrement of >2% per year is associated with a high risk of
progression of antecedent diabetic retinopathy to blindness in IDDM p
atients with an extremely high initial HbA1. Such patients should, the
refore, be excluded from diabetes treatment programs aiming at immedia
te IGC.