The
Diabetes Control and Complications Trial (DCCT, 1983-1993) showed that intensive therapy (mean HbA1c 7.2%) compared
with conventional therapy (mean HbA1c 9.0%) markedly reduced the risks
of retinopathy, nephropathy and neuropathy, and these reductions in
complications were entirely attributable, statistically, to the difference in
mean HbA1c levels. The DCCT cohort has been followed in the Epidemiology of
Diabetes Interventions and Complications study (EDIC, 1994 to date).
<p>Early in EDIC, mean HbA1c levels in the former
intensively and conventionally treated groups converged. Nevertheless, the
beneficial effects of DCCT intensive versus conventional therapy on
microvascular complications not only persisted but increased during EDIC. The
differences in complications during EDIC were wholly explained, statistically,
by differences between groups in HbA1c levels during DCCT. These observations give rise to the concept of
metabolic memory. Subsequent similar findings from the UKPDS gave rise to a
similar concept, which they called the legacy effect. </p>
<p>In
this report, we present the evidence to support metabolic memory as both a
biological and epidemiological phenomenon, and discuss potential underlying
mechanisms. We also compare metabolic memory and the legacy effect and conclude
that the two are likely biologically similar, with comparable effects on
long-term outcomes.</p>
<p>The long-term influence of metabolic memory on the
risk of micro- and macrovascular complications supports the implementation of
intensive therapy, with the goal of maintaining near normal levels of glycemia,
as early and as long as safely possible in order to limit the risk of
complications.</p>
Effect of pregnancy on microvascular complications in the diabetes control and complications trial. The Diabetes Control and Complications Trial Research Group
