Background Body composition is altered in inflammatory diseases, for example in inflammatory joint diseases, with less muscle mass and more adipose tissue. Metabolic syndrome (MetS) is an increasing global health issue contributing to the cardiovascular disease risk. Low grade inflammation through adipocyte derived adipokines is seen in MetS. Studies have been conducted to evalute the contribution of adipokines to the inflammation of rheumatic diseases and inherent cardioascular risk in established disease.
Objectives To analyse adipokine levels in relation to MetS in patients with newly diagnosed, untreated rheumatoid arthritis (RA), spondyloarthritis (SpA) and undifferentiated arthritis (UA).
Methods Patients with inflammatory joint diseases participating in Northern Savo 2010 study were evaluated for the presence of components of MetS according to the definition by National Cholesterol Education Program Adult Treatment Panel III (NCEP-ATPIII). Adipokines adiponectin, adipsin, leptin and resistin were analysed from plasma samples by enzyme immunoassay.
Results One hundred and seventy-six patients, 47 with RA, 58 with SpA and 71 with UA, were classified according to metabolic condition. When analysing the levels of adiponectin, adipsin, resistin and leptin in various arthritides with MetS present or absent significant differences in leptin in all diagnostic categories, in adipsin in SpA and in adiponectin in UA were recovered.
Of the tested adipokines along with the fulfillment of 0-1 or 2-3 or 4-5 components of NCEP-ATP III adiponectin showed linear decrease in RA and in UA, p=0.037 and <0.001, respectively. In SpA leptin showed linear increase with increasing number of components, p=0.014, and in UA adipsin, resistin and leptin showed a similar trend, p=0.020, 0.028 and <0.001, respectively.
Conclusions Levels of the tested adipokines differed in various arthritis categories along with the metabolic condition suggesting that the inflammatory disease also contributes to the adipokine profiles in patients with rheumatic diseases.
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Disclosure of Interest None declared