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Long-term Glycemic Control and Dementia Risk in Type 1 Diabetes. | LitMetric

Long-term Glycemic Control and Dementia Risk in Type 1 Diabetes.

Diabetes Care

Department of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, CA.

Published: November 2018

Objective: Individuals with type 1 diabetes have experienced an increase in life expectancy, yet it is unknown what level of glycemic control is ideal for maintaining late-life brain health. We investigated the association of long-term glycemic control with dementia in older individuals with type 1 diabetes.

Research Design And Methods: We followed 3,433 members of a health care system with type 1 diabetes, aged ≥50 years, from 1996 to 2015. Repeated measurements of hemoglobin A (HbA), dementia diagnoses, and comorbidities were ascertained from health records. Cox proportional hazards models were fit to evaluate the association of time-varying glycemic exposure with dementia, with adjustment for age, sex, race/ethnicity, baseline health conditions, and frequency of HbA measurement.

Results: Over a mean follow-up of 6.3 years, 155 individuals (4.5%) were diagnosed with dementia. Patients with ≥50% of HbA measurements at 8-8.9% (64-74 mmol/mol) and ≥9% (≥75 mmol/mol) had 65% and 79% higher risk of dementia, respectively, compared with those with <50% of measurements exposed (HbA 8-8.9% adjusted hazard ratio [aHR] 1.65 [95% CI 1.06, 2.57] and HbA ≥9% aHR 1.79 [95% CI 1.11, 2.90]). By contrast, patients with ≥50% of HbA measurements at 6-6.9% (42-52 mmol/mol) and 7-7.9% (53-63 mmol/mol) had a 45% lower risk of dementia (HbA 6-6.9% aHR 0.55 [95% CI 0.34, 0.88] and HbA 7-7.9% aHR 0.55 [95% CI 0.37, 0.82]).

Conclusions: Among older patients with type 1 diabetes, those with majority exposure to HbA 8-8.9% and ≥9% had increased dementia risk, while those with majority exposure to HbA 6-6.9% and 7-7.9% had reduced risk. Currently recommended glycemic targets for older patients with type 1 diabetes are consistent with healthy brain aging.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6196833PMC
http://dx.doi.org/10.2337/dc18-0073DOI Listing

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