Key result
Adiponectin in rheumatoid arthritis linked to more favorable lipids but higher blood pressure.
Why the study?
It is unknown whether rheumatoid arthritis changes the influence of adipokines on cardiovascular metabolic risk.
Does rheumatoid arthritis alter the relationship between circulating adipokines (adiponectin, leptin) and cardiovascular metabolic risk factors?
Cross-Sectional (n=277)
Does rheumatoid arthritis alter the relationship between circulating adipokines (adiponectin, leptin) and cardiovascular metabolic risk factors?
p-value: p=<0.05
Rheumatoid arthritis alters the relationship between adiponectin and cardiovascular risk factors, suggesting that adipokine inhibition in RA may not adversely affect overall cardiovascular risk.
RA may modify adiponectin links to lipids and BP; hypothesis-generating for CV effects of adipokine therapies in RA.
Adiponectin and leptin are likely involved in the pathophysiology of rheumatoid arthritis (RA) and therefore potential new therapeutic targets. Adiponectin inhibition could be expected to enhance cardiovascular metabolic risk. However, it is unknown whether RA changes the influence of adipokines on cardiovascular metabolic risk. We determined whether RA impacts on the independent relationships of circulating leptin and adiponectin concentrations with cardiovascular risk factors and carotid intima-media thickness (cIMT) in 277 black African subjects from a developing population; 119 had RA. RA impacted on the relationships of adiponectin concentrations with lipid concentrations and blood pressure, independent of confounders including adiposity (interaction P < 0.05). This translated into an association of adiponectin concentrations with more favorable lipid variables including HDL cholesterol (P = 0.0005), non-HDL cholesterol (P = 0.007), and triglyceride (P = 0.005) concentrations, total cholesterol-HDL cholesterol (P = 0.0002) and triglycerides-HDL cholesterol (P = 0.0003) ratios, and higher systolic (P = 0.0006), diastolic (P = 0.0004), and mean blood pressure (P = 0.0007) in RA but not non-RA subjects. Leptin was not associated with metabolic risk after adjustment for adiposity. The cIMT did not differ by RA status, and adipokine concentrations were unrelated to atherosclerosis. This study suggests that leptin and adiponectin inhibition may not alter overall cardiovascular risk and disease in RA.
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Dessein et al. (2013) conducted a cross-sectional in Rheumatoid arthritis (n=277). Rheumatoid arthritis vs. Non-RA subjects was evaluated on Relationships of circulating leptin and adiponectin concentrations with cardiovascular risk factors and carotid intima-media thickness (p=<0.05). Rheumatoid arthritis modified the association of adiponectin with cardiovascular risk factors, linking it to more favorable lipids but higher blood pressure in RA subjects (interaction P < 0.05).
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