TY - JOUR
T1 - Relation of inflammatory chemokines to insulin resistance and hypoadiponectinemia in coronary artery disease patients
AU - Tretjakovs, Peteris
AU - Jurka, Antra
AU - Bormane, Inga
AU - Mackevics, Vitolds
AU - Balode, Liga
AU - Mikelsone, Indra
AU - Reihmane, Dace
AU - Stukena, Inga
AU - Bahs, Guntis
AU - Aivars, Juris Imants
AU - Pirags, Valdis
N1 - Funding Information:
The study was supported by grant no. 07-VP-8 from the Latvian Council of Science .
Copyright:
Copyright 2010 Elsevier B.V., All rights reserved.
PY - 2009/11
Y1 - 2009/11
N2 - Background: Although many studies have shown that the metabolic syndrome (MS) and type 2 diabetes mellitus (T2DM) both are associated with chronic inflammatory state and are risk factors for coronary artery disease (CAD), it is still unclear which condition is a more important contributor to the increased production of inflammatory chemokines. The purpose of this study was to assess monocyte chemoattractant protein-1 (MCP-1) and interleukin-8 (IL-8) levels and their association with insulin resistance and adiponectin concentrations in CAD patients, who were categorized as having T2DM, MS, or neither. Methods: CAD male patients were categorized into three groups: 24 non-obese patients with T2DM (D), 24 obese patients with MS (M) and 24 patients without T2DM or MS (W). 20 healthy subjects were selected as controls (C). Insulin resistance was assessed by the HOMA-IR method, but serum MCP-1, IL-8, and adiponectin levels were measured by xMAP technology. Results: Serum levels of MCP-1 and IL-8 in D and M groups were increased in comparison with W and C groups (p < 0.001, p < 0.01), but the increase in the M group was significantly higher than that in the D group (p < 0.05, p < 0,001), besides MCP-1 and IL-8 concentrations were correlated with HOMA-IR indexes (r = 0.52; r = 0.49, p < 0.0001) and adiponectin levels (r = - 0.59, p < 0.0001). The M group demonstrated a diminution in the adiponectin level (p < 0.01) and pronounced increase of HOMA-IR in comparison with the other three groups (p < 0.01). Conclusion: Obese CAD patients with MS have a more pronounced increase of MCP-1, IL-8 and HOMA-IR and more decreased adiponectin levels than non-obese CAD patients without MS.
AB - Background: Although many studies have shown that the metabolic syndrome (MS) and type 2 diabetes mellitus (T2DM) both are associated with chronic inflammatory state and are risk factors for coronary artery disease (CAD), it is still unclear which condition is a more important contributor to the increased production of inflammatory chemokines. The purpose of this study was to assess monocyte chemoattractant protein-1 (MCP-1) and interleukin-8 (IL-8) levels and their association with insulin resistance and adiponectin concentrations in CAD patients, who were categorized as having T2DM, MS, or neither. Methods: CAD male patients were categorized into three groups: 24 non-obese patients with T2DM (D), 24 obese patients with MS (M) and 24 patients without T2DM or MS (W). 20 healthy subjects were selected as controls (C). Insulin resistance was assessed by the HOMA-IR method, but serum MCP-1, IL-8, and adiponectin levels were measured by xMAP technology. Results: Serum levels of MCP-1 and IL-8 in D and M groups were increased in comparison with W and C groups (p < 0.001, p < 0.01), but the increase in the M group was significantly higher than that in the D group (p < 0.05, p < 0,001), besides MCP-1 and IL-8 concentrations were correlated with HOMA-IR indexes (r = 0.52; r = 0.49, p < 0.0001) and adiponectin levels (r = - 0.59, p < 0.0001). The M group demonstrated a diminution in the adiponectin level (p < 0.01) and pronounced increase of HOMA-IR in comparison with the other three groups (p < 0.01). Conclusion: Obese CAD patients with MS have a more pronounced increase of MCP-1, IL-8 and HOMA-IR and more decreased adiponectin levels than non-obese CAD patients without MS.
KW - Adiponectin
KW - Chemokines
KW - Coronary artery disease
KW - Insulin resistance
KW - Metabolic syndrome
KW - Type 2 diabetes mellitus
UR - http://www.scopus.com/inward/record.url?scp=70349783826&partnerID=8YFLogxK
U2 - 10.1016/j.ejim.2009.08.004
DO - 10.1016/j.ejim.2009.08.004
M3 - Article
C2 - 19818293
AN - SCOPUS:70349783826
SN - 0953-6205
VL - 20
SP - 712
EP - 717
JO - European Journal of Internal Medicine
JF - European Journal of Internal Medicine
IS - 7
ER -