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. 2008 Oct;31(10):1933-8.
doi: 10.2337/dc08-0607. Epub 2008 Jul 7.

Impact of diabetes and its treatment on cognitive function among adolescents who participated in the Diabetes Control and Complications Trial

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Impact of diabetes and its treatment on cognitive function among adolescents who participated in the Diabetes Control and Complications Trial

Gail Musen et al. Diabetes Care. 2008 Oct.

Abstract

Objective: The purpose of this study was to evaluate whether severe hypoglycemia or intensive therapy affects cognitive performance over time in a subgroup of patients who were aged 13-19 years at entry in the Diabetes Control and Complications Trial (DCCT).

Research design and methods: This was a longitudinal study involving 249 patients with type 1 diabetes who were between 13 and 19 years old when they were randomly assigned in the DCCT. Scores on a comprehensive battery of cognitive tests obtained during the Epidemiology of Diabetes Interventions and Complications follow-up study, approximately 18 years later, were compared with baseline performance. We assessed the effects of the original DCCT treatment group assignment, mean A1C values, and frequency of severe hypoglycemic events on eight domains of cognition.

Results: There were a total of 294 reported episodes of coma or seizure. Neither frequency of hypoglycemia nor previous treatment group was associated with decline on any cognitive domain. As in a previous analysis of the entire study cohort, higher A1C values were associated with declines in the psychomotor and mental efficiency domain (P < 0.01); however, the previous finding of improved motor speed with lower A1C values was not replicated in this subgroup analysis.

Conclusions: Despite relatively high rates of severe hypoglycemia, cognitive function did not decline over an extended period of time in the youngest cohort of patients with type 1 diabetes.

Trial registration: ClinicalTrials.gov NCT00360893.

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Figures

Figure 1
Figure 1
Changes in cognitive domains between DCCT baseline cognitive testing and follow-up testing (mean of 18 years after baseline) based on change in Z scores for intensive (□) vs. conventional (▪) treatment groups (A), frequency of severe hypoglycemia (coma or seizure) episodes (no episodes □, 1–5 espisodes ▒, or >5 episodes ▪) (B), and tertiles of mean A1C (<7.9% □, ≤7.9% ▒, or <9.5% ▪) (C). 1, Problem solving; 2, learning; 3, immediate memory; 4, delayed recall; 5, spatial information; 6, attention; 7, psychomotor and mental efficiency; and 8, motor speed. ANCOVA models were used with adjustments for baseline age, sex, years of education, length of follow-up, visual acuity, self-reported sensory loss due to peripheral neuropathy, and the number of interval cognitive tests taken. Neither treatment group nor cumulative number of hypoglycemic episodes influenced performance in any cognitive domain. Higher values of A1C were associated with modest declines in psychomotor and mental efficiency (P < 0.01).

Comment in

References

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