Plasma Cytokines, Metabolic Syndrome, and Atherosclerosis in Humans. Issue 1 (1st January 2007)
- Record Type:
- Journal Article
- Title:
- Plasma Cytokines, Metabolic Syndrome, and Atherosclerosis in Humans. Issue 1 (1st January 2007)
- Main Title:
- Plasma Cytokines, Metabolic Syndrome, and Atherosclerosis in Humans
- Authors:
- Reilly, Muredach P.
Rohatgi, Anand
McMahon, Kimberly
Wolfe, Megan L.
Pinto, Shailesh C.
Rhodes, Thomas
Girman, Cynthia
Rader, Daniel J. - Abstract:
- Abstract : Background: Interleukin-6 (IL-6) and tumor necrosis factor α (TNF-α) integrate inflammatory and adipose signaling but also have direct vascular effects. We hypothesized that plasma levels of IL-6 and soluble tumor necrosis factor α receptor 2 (sol-TNFR2) would be related to coronary atherosclerosis beyond established risk factors and the metabolic syndrome. Methods: We examined the association of IL-6 and sol-TNFR2 with metabolic syndrome, C-reactive protein (CRP), and coronary artery calcification (CAC) in 875 asymptomatic participants in the Study of Inherited Risk of Coronary Atherosclerosis. Results: IL-6 levels were 56% higher ( p < .001) and sol-TNFR2 levels 16% higher ( p < .001) in subjects with metabolic syndrome compared with those without. Both cytokines were associated with CAC beyond age, gender, Framingham risk scores, family history, metabolic syndrome, and CRP (odds ratio and 95% confidence interval of higher CAC for 1 SD increase in log-transformed cytokine levels: 1.23 [1.06-1.43], p = .006 for IL-6 and 1.15 [1.01-1.31], p = .04 for sol-TNFR2). In fact, cytokine levels were independently associated with CAC scores in the subgroup with metabolic syndrome and were additive to the homeostasis model assessment of insulin resistance in predicting CAC. Conclusions: Plasma IL-6 and sol-TNFR2 levels were independently associated with CAC, suggesting a role in integrating innate immune and adipose signaling in promoting atherosclerosis and cardiovascularAbstract : Background: Interleukin-6 (IL-6) and tumor necrosis factor α (TNF-α) integrate inflammatory and adipose signaling but also have direct vascular effects. We hypothesized that plasma levels of IL-6 and soluble tumor necrosis factor α receptor 2 (sol-TNFR2) would be related to coronary atherosclerosis beyond established risk factors and the metabolic syndrome. Methods: We examined the association of IL-6 and sol-TNFR2 with metabolic syndrome, C-reactive protein (CRP), and coronary artery calcification (CAC) in 875 asymptomatic participants in the Study of Inherited Risk of Coronary Atherosclerosis. Results: IL-6 levels were 56% higher ( p < .001) and sol-TNFR2 levels 16% higher ( p < .001) in subjects with metabolic syndrome compared with those without. Both cytokines were associated with CAC beyond age, gender, Framingham risk scores, family history, metabolic syndrome, and CRP (odds ratio and 95% confidence interval of higher CAC for 1 SD increase in log-transformed cytokine levels: 1.23 [1.06-1.43], p = .006 for IL-6 and 1.15 [1.01-1.31], p = .04 for sol-TNFR2). In fact, cytokine levels were independently associated with CAC scores in the subgroup with metabolic syndrome and were additive to the homeostasis model assessment of insulin resistance in predicting CAC. Conclusions: Plasma IL-6 and sol-TNFR2 levels were independently associated with CAC, suggesting a role in integrating innate immune and adipose signaling in promoting atherosclerosis and cardiovascular risk. Measurement of their levels may facilitate cardiovascular risk prediction and targeting of therapeutic strategies. … (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:
- 26
- Page End:
- 35
- Publication Date:
- 2007-01-01
- Subjects:
- atherosclerosis -- cytokines -- metabolic syndrome
Clinical medicine -- Periodicals
Medicine -- Research -- Periodicals
Medicine
Research -- United States
Clinical medicine
Medicine -- Research
Periodicals
616.075 - Journal URLs:
- http://journals.lww.com/jinvestigativemed/pages/default.aspx ↗
http://jim.bmj.com/ ↗
https://journals.sagepub.com/home/IMJ ↗
http://journals.lww.com ↗ - DOI:
- 10.2310/6650.2007.06013 ↗
- Languages:
- English
- ISSNs:
- 1081-5589
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5008.010000
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