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Ann Intern Med. 2009 Dec 15;151(12):854-60. doi: 10.7326/0003-4819-151-12-200912150-00005.

Comorbidity affects the relationship between glycemic control and cardiovascular outcomes in diabetes: a cohort study.

Author information

  • 1University of California Irvine, Irvine, California, USA. sgreenfi@uci.edu

Abstract

BACKGROUND:

Recent studies have shown mixed results regarding the effectiveness of intensive glucose-lowering therapy in reducing risk for cardiovascular events.

OBJECTIVE:

To determine whether attaining hemoglobin A(1c) (HbA(1c)) targets of 6.5% or less or 7.0% or less for glycemic control at baseline provides differential benefits for patients with high versus low-to-moderate levels of comorbidity.

DESIGN:

5-year longitudinal observational study of patients with type 2 diabetes. Patients were categorized into high and low-to-moderate comorbidity subgroups by using the Total Illness Burden Index (TIBI), a validated patient-reported measure of comorbidity.

SETTING:

101 diabetes outpatient clinics and 103 general practitioners' clinics in Italy.

PATIENTS:

2613 (83%) of 3074 patients with type 2 diabetes, sampled randomly from diabetes outpatient clinic rosters and recruited consecutively from general practitioners' clinics, who completed the baseline questionnaire.

MEASUREMENTS:

TIBI score, total mortality, and incident cardiovascular events. Hazard ratios (HRs) were adjusted for age and sex.

RESULTS:

Attaining an HbA(1c) level of 6.5% or less at baseline was associated with lower 5-year incidence of cardiovascular events in the low-to-moderate comorbidity subgroup (adjusted HR, 0.60 [95% CI, 0.42 to 0.85]; P = 0.005) but not in the high comorbidity subgroup (adjusted HR, 0.92 [CI, 0.68 to 1.25]; P = 0.61; P for subgroup by HbA(1c) interaction = 0.048). Similarly, attaining a baseline HbA(1c) level of 7.0% predicted fewer cardiovascular events in the low-to-moderate comorbidity subgroup (adjusted HR, 0.61 (CI, 0.44 to 0.83; P = 0.001) but not in the high comorbidity subgroup (adjusted HR, 0.88 [CI, 0.66 to 1.17]; P = 0.38; P for subgroup by HbA(1c) interaction = 0.093).

LIMITATIONS:

The observational nature of the study does not allow causal inference. The length of the data collection period was limited. Information on clinical management was not available.

CONCLUSION:

Patients with the high levels of comorbidity common in type 2 diabetes may receive diminished cardiovascular benefit from intensive blood glucose control. Comorbidity should be considered when tailoring glucose-lowering therapy in patients with type 2 diabetes.

PRIMARY FUNDING SOURCE:

Pfizer of Italy.

Comment in

PMID:
20008761
[PubMed - indexed for MEDLINE]
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