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C-reactive protein and glycemic control in adults with diabetes

Dana E King1, Arch G Mainous, Thomas A Buchanan

  • 1Department of Family Medicine, Medical University of South Carolina, Charleston 29425, USA. kingde@musc.edu

Diabetes Care
|April 30, 2003
PubMed

Insights

Poor glycemic control, indicated by high HbA1c levels, is linked to increased C-reactive protein (CRP) in individuals with diabetes. This suggests a connection between blood sugar management and systemic inflammation.

Area of Science:

  • Endocrinology
  • Cardiovascular Disease Research
  • Clinical Chemistry

Background:

  • Poor glycemic control in diabetes is associated with macrovascular complications.
  • C-reactive protein (CRP) is a recognized risk factor for cardiovascular disease.
  • Understanding the relationship between glycemic control and inflammation is crucial for diabetes management.

Purpose of the Study:

  • To investigate the association between HbA1c levels and C-reactive protein (CRP) concentrations.
  • To determine if elevated CRP is linked to poorer glycemic control in a national sample of adults with diabetes.

Main Methods:

  • Utilized data from the National Health and Nutrition Examination Survey III (1988-1994).
  • Analyzed a nationally representative sample of 1,018 noninstitutionalized U.S. adults with diabetes.
  • Stratified participants by HbA1c levels and assessed elevated CRP (>0.30 mg/dl) as the main outcome.

Main Results:

  • Individuals with elevated HbA1c levels (> or =9.0%) showed a significantly higher prevalence of elevated CRP compared to those with low HbA1c (<7%).
  • Adjusted regression analysis revealed that higher HbA1c levels (particularly >9.0% and >11.0%) were significantly associated with an increased likelihood of elevated CRP.
  • HbA1c also predicted elevated CRP when analyzed as a continuous variable.

Conclusions:

  • The likelihood of elevated CRP concentrations rises with increasing HbA1c levels in individuals with diabetes.
  • Findings suggest a significant association between glycemic control and systemic inflammation in established diabetes.
  • This highlights the potential role of inflammation in diabetes-related complications.
Abstract

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