The effect of atorvastatin therapy on tumour necrosis factor-α and vascular adhesion molecules in patients with type 2 diabetes mellitus with no prior history of coronary heart disease

We examined the effect of atorvastatin (and placebo) on tumour necrosis factor (TNF)α, soluble vascular cell adhesion molecule-1 (sVCAM-1) and soluble intercellular cell adhesion molecule-1 (sICAM-1) in patients with type 2 diabetes without prior cardiovascular disease (CVD) and investigated whether...

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Main Authors: Soedamah-Muthu, S, Charlton-Menys, V, Bao, W, Schalkwijk, C, Da Stehouwer, C, Colhoun, H, Betteridge, D, Durrington, P, Hitman, G, Neil, H, Livingstone, S, Fuller, J, Demicco, D, Preston, G
Format: Journal article
Language:English
Published: 2011
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author Soedamah-Muthu, S
Charlton-Menys, V
Bao, W
Schalkwijk, C
Da Stehouwer, C
Colhoun, H
Betteridge, D
Durrington, P
Hitman, G
Neil, H
Livingstone, S
Fuller, J
Demicco, D
Preston, G
author_facet Soedamah-Muthu, S
Charlton-Menys, V
Bao, W
Schalkwijk, C
Da Stehouwer, C
Colhoun, H
Betteridge, D
Durrington, P
Hitman, G
Neil, H
Livingstone, S
Fuller, J
Demicco, D
Preston, G
author_sort Soedamah-Muthu, S
collection OXFORD
description We examined the effect of atorvastatin (and placebo) on tumour necrosis factor (TNF)α, soluble vascular cell adhesion molecule-1 (sVCAM-1) and soluble intercellular cell adhesion molecule-1 (sICAM-1) in patients with type 2 diabetes without prior cardiovascular disease (CVD) and investigated whether adhesion molecules were associated with incident CVD. Baseline and follow-up concentrations of TNFα, sVCAM-1 and sICAM-1 were measured in patients from the Collaborative AtoRvastatin Diabetes Study (CARDS). Patients had a mean age of 61 years (standard deviation = 8) and 70% were men. TNFα 2.20 pg/mL (1.82-2.86), sVCAM-1 865 ng/mL (729-1059) and sICAM-1 619 ng/mL (533-753) concentrations (median, interquartile range 25, 75%) were similar at baseline in atorvastatin (given values) and placebo groups and not significantly different at 2 years. The multivariable hazard ratios for the associations between sVCAM-1 and sICAM-1 (doubling the concentration) and CVD were, 0.82 (95% confidence interval (CI) 0.66-1.0) and 0.59 (95% CI 0.50-0.71), respectively. In conclusion atorvastatin had no significant effect on TNFα, sVCAM-1 or sICAM-1 levels in type 2 diabetic patients without a prior history of CVD compared with placebo. In addition, both sVCAM-1 and sICAM-1 concentrations were associated with a decreased risk of CVD. © SAGE Publications 2011.
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spelling oxford-uuid:a641d9b4-b933-48c2-8857-4f2aa37b041b2022-03-27T02:45:56ZThe effect of atorvastatin therapy on tumour necrosis factor-α and vascular adhesion molecules in patients with type 2 diabetes mellitus with no prior history of coronary heart diseaseJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:a641d9b4-b933-48c2-8857-4f2aa37b041bEnglishSymplectic Elements at Oxford2011Soedamah-Muthu, SCharlton-Menys, VBao, WSchalkwijk, CDa Stehouwer, CColhoun, HBetteridge, DDurrington, PHitman, GNeil, HLivingstone, SFuller, JDemicco, DPreston, GWe examined the effect of atorvastatin (and placebo) on tumour necrosis factor (TNF)α, soluble vascular cell adhesion molecule-1 (sVCAM-1) and soluble intercellular cell adhesion molecule-1 (sICAM-1) in patients with type 2 diabetes without prior cardiovascular disease (CVD) and investigated whether adhesion molecules were associated with incident CVD. Baseline and follow-up concentrations of TNFα, sVCAM-1 and sICAM-1 were measured in patients from the Collaborative AtoRvastatin Diabetes Study (CARDS). Patients had a mean age of 61 years (standard deviation = 8) and 70% were men. TNFα 2.20 pg/mL (1.82-2.86), sVCAM-1 865 ng/mL (729-1059) and sICAM-1 619 ng/mL (533-753) concentrations (median, interquartile range 25, 75%) were similar at baseline in atorvastatin (given values) and placebo groups and not significantly different at 2 years. The multivariable hazard ratios for the associations between sVCAM-1 and sICAM-1 (doubling the concentration) and CVD were, 0.82 (95% confidence interval (CI) 0.66-1.0) and 0.59 (95% CI 0.50-0.71), respectively. In conclusion atorvastatin had no significant effect on TNFα, sVCAM-1 or sICAM-1 levels in type 2 diabetic patients without a prior history of CVD compared with placebo. In addition, both sVCAM-1 and sICAM-1 concentrations were associated with a decreased risk of CVD. © SAGE Publications 2011.
spellingShingle Soedamah-Muthu, S
Charlton-Menys, V
Bao, W
Schalkwijk, C
Da Stehouwer, C
Colhoun, H
Betteridge, D
Durrington, P
Hitman, G
Neil, H
Livingstone, S
Fuller, J
Demicco, D
Preston, G
The effect of atorvastatin therapy on tumour necrosis factor-α and vascular adhesion molecules in patients with type 2 diabetes mellitus with no prior history of coronary heart disease
title The effect of atorvastatin therapy on tumour necrosis factor-α and vascular adhesion molecules in patients with type 2 diabetes mellitus with no prior history of coronary heart disease
title_full The effect of atorvastatin therapy on tumour necrosis factor-α and vascular adhesion molecules in patients with type 2 diabetes mellitus with no prior history of coronary heart disease
title_fullStr The effect of atorvastatin therapy on tumour necrosis factor-α and vascular adhesion molecules in patients with type 2 diabetes mellitus with no prior history of coronary heart disease
title_full_unstemmed The effect of atorvastatin therapy on tumour necrosis factor-α and vascular adhesion molecules in patients with type 2 diabetes mellitus with no prior history of coronary heart disease
title_short The effect of atorvastatin therapy on tumour necrosis factor-α and vascular adhesion molecules in patients with type 2 diabetes mellitus with no prior history of coronary heart disease
title_sort effect of atorvastatin therapy on tumour necrosis factor α and vascular adhesion molecules in patients with type 2 diabetes mellitus with no prior history of coronary heart disease
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