65 OBESITY, DIABETES, AND INSULIN RESISTANCE: RELATION TO ELEVATED C-REACTIVE PROTEIN LEVELS IN AFRICAN AMERICANS. Issue 1 (1st January 2007)
- Record Type:
- Journal Article
- Title:
- 65 OBESITY, DIABETES, AND INSULIN RESISTANCE: RELATION TO ELEVATED C-REACTIVE PROTEIN LEVELS IN AFRICAN AMERICANS. Issue 1 (1st January 2007)
- Main Title:
- 65 OBESITY, DIABETES, AND INSULIN RESISTANCE: RELATION TO ELEVATED C-REACTIVE PROTEIN LEVELS IN AFRICAN AMERICANS.
- Authors:
- Taylor, J. K.
Taylor, H. A.
Benjamin, E. J.
Rotimi, C. N.
Sarpong, D. F.
Wilson, J. G.
Samdarshi, T.
Steffes, M. W.
Fox, E. R. - Abstract:
- Abstract : Purpose: Elevated C-reactive protein (CRP) has been strongly related to obesity, diabetes (DM), and insulin resistance (IR) in predominantly white non-Hispanic cohorts. There is limited information on systemic inflammation in African Americans. Methods: The study cohort consisted of 5, 202 participants (55 ± 13 years, 64% female) who presented for Jackson Heart Study Exam 1 (2001-2004). The contribution of traditional risk factors to the variability of CRP was tested using a stepwise regression model. We evaluated the relation of obesity, DM and IR to CRP among participants using analysis of variance. Results: In the stepwise regression, the amount of variability in CRP explained by clinical covariates was 23%. BMI explained 57% of the variability of CRP due to traditional risk factors. The mean CRP for participants was 1.4 mg/L for those nonobese without IR, 3.2 mg/L for those obese without IR, 2.2 mg/L for those nonobese with IR, 4.0 mg/L for those obese with IR, 1.9 mg/L for those nonobese with DM, and 4.1 mg/L for those obese with DM. CRP was significantly higher for obese participants compared with nonobese participants regardless of IR or DM status ( p < .0001). For both obese and nonobese participants, CRP was significantly higher in nondiabetics with IR compared with nondiabetics without IR ( p < .0001). CRP was significantly higher in diabetics compared with nondiabetics without IR ( p < .0001). Conclusions: In this large population-based cohort ofAbstract : Purpose: Elevated C-reactive protein (CRP) has been strongly related to obesity, diabetes (DM), and insulin resistance (IR) in predominantly white non-Hispanic cohorts. There is limited information on systemic inflammation in African Americans. Methods: The study cohort consisted of 5, 202 participants (55 ± 13 years, 64% female) who presented for Jackson Heart Study Exam 1 (2001-2004). The contribution of traditional risk factors to the variability of CRP was tested using a stepwise regression model. We evaluated the relation of obesity, DM and IR to CRP among participants using analysis of variance. Results: In the stepwise regression, the amount of variability in CRP explained by clinical covariates was 23%. BMI explained 57% of the variability of CRP due to traditional risk factors. The mean CRP for participants was 1.4 mg/L for those nonobese without IR, 3.2 mg/L for those obese without IR, 2.2 mg/L for those nonobese with IR, 4.0 mg/L for those obese with IR, 1.9 mg/L for those nonobese with DM, and 4.1 mg/L for those obese with DM. CRP was significantly higher for obese participants compared with nonobese participants regardless of IR or DM status ( p < .0001). For both obese and nonobese participants, CRP was significantly higher in nondiabetics with IR compared with nondiabetics without IR ( p < .0001). CRP was significantly higher in diabetics compared with nondiabetics without IR ( p < .0001). Conclusions: In this large population-based cohort of African Americans, we found that among traditional risk factors, BMI contributed the greatest to the variability of CRP. DM and IR were also significantly related to CRP. … (more)
- Is Part Of:
- Journal of investigative medicine. Volume 55:Issue 1(2007)
- Journal:
- Journal of investigative medicine
- Issue:
- Volume 55:Issue 1(2007)
- Issue Display:
- Volume 55, Issue 1 (2007)
- Year:
- 2007
- Volume:
- 55
- Issue:
- 1
- Issue Sort Value:
- 2007-0055-0001-0000
- Page Start:
- S257
- Page End:
- S257
- Publication Date:
- 2007-01-01
- Subjects:
- Clinical medicine -- Periodicals
Medicine -- Research -- Periodicals
Medicine
Research -- United States
Clinical medicine
Medicine -- Research
Periodicals
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- 1081-5589
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