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Comorbidity and Glycemic Control in Patients With Type 2 Diabetes
Imad M. El-Kebbi, MD;
David C. Ziemer, MD;
Curtiss B. Cook, MD;
Christopher D. Miller, MD;
Daniel L. Gallina, MD;
Lawrence S. Phillips, MD
Arch Intern Med. 2001;161:1295-1300.
Background It is commonly believed that good glycemic control is hard to achieve
in patients with diabetes mellitus and concurrent chronic illnesses.
Objective To determine the impact of comorbidity on glycemic control at presentation
and subsequent follow-up in patients with type 2 diabetes.
Methods We studied 654 consecutive patients who presented to a diabetes clinic
in 1997. Comorbidity was rated using the Chronic Disease Score (CDS) index,
which is a validated, weighted score that takes into account the patient's
age, sex, and classes of medications. Univariate and multivariate linear regressions
were used to determine the contribution of age, body mass index (calculated
as weight in kilograms divided by the square of height in meters), diabetes
duration, type of therapy, and CDS to initial hemoglobin A1c (HbA1c) level. A similar analysis was performed for the 169 patients with
follow-up HbA1c levels 6 months after presentation.
Results Patients were 90% African American, and 66% female, with average age
of 53 years. Average diabetes duration was 5 years; body mass index, 33; HbA1c level, 8.8%; and CDS, 1121 (range, 232-7953). At presentation, patients
with higher CDSs tended to be older and to have a lower HbA1c level,
but multivariate linear regression showed that receiving pharmacological therapy,
younger age, and having a lower C-peptide level were the only significant
contributors to HbA1c level. In the 169 follow-up patients, presenting
characteristics were not significantly different from those of the full cohort:
average initial HbA1c level was 8.8%; CDS, 1073. Their HbA1c level at 6 months averaged 7.5% and the CDS had no significant impact
on their follow-up HbA1c level.
Conclusion Comorbidity does not appear to limit achievement of good glycemic control
in patients with type 2 diabetes.
From the Division of Endocrinology and Metabolism, Department of Medicine,
Emory University School of Medicine, Atlanta, Ga.
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