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Diabetes Care, Vol 23, Issue 8 1084-1091, Copyright © 2000 by American Diabetes Association
Effect of pregnancy on microvascular complications in the diabetes control and complications trial. The Diabetes Control and Complications Trial Research Group
OBJECTIVE: To assess the effect of pregnancy on the development and
progression of retinopathy and microalbuminuria in type 1 diabetes.
RESEARCH DESIGN AND METHODS: We conducted longitudinal analyses of the
Diabetes Control and Complications Trial (DCCT), a multicenter controlled
clinical trial that compared intensive treatment with conventional diabetes
therapy and studied 180 women who had 270 pregnancies and 500 women who did
not become pregnant during an average of 6.5 years of follow-up. Women
assigned to the conventional treatment group were changed to intensive
therapy if they were planning pregnancy or as soon as possible after
conception. Fundus photography was performed every 6 months, and the
urinary albumin excretion rate (AER) was measured annually. RESULTS:
Compared with nonpregnant women, pregnant women had a 1.63-fold greater
risk of any worsening of retinopathy from before to during pregnancy (P
< 0.05) in the intensive treatment group; the risk was 2.48-fold greater
for pregnant vs. not pregnant women in the conventional group (P <
0.001). In the conventional group, the odds of > or =3-step progression
from the baseline retinopathy level was >2.9-fold among pregnant vs. not
pregnant women (P = 0.003). The odds ratio (OR) peaked during the second
trimester (OR = 4.26, P = 0.001) and persisted as long as 12 months
postpregnancy (OR = 2.87, P = 0.005). The level of AER during pregnancy in
the intensive group, but not in the conventional group, was significantly
elevated from the level at baseline, albeit in the normal range. Although
individual patients had transient worsening of retinopathy during
pregnancy, even to the proliferative level, at the end of the DCCT, mean
levels of retinopathy and albuminuria in subjects who had become pregnant
were similar to those in subjects who had not become pregnant within each
treatment group. CONCLUSIONS: Pregnancy in type 1 diabetes induces a
transient increase in the risk of retinopathy; increased ophthalmologic
surveillance is needed during pregnancy and the first year postpartum. The
long-term risk of progression of early retinopathy and albumin excretion,
however, does not appear to be increased by pregnancy.

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Copyright © 2000 by the American Diabetes Association.
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