Changes in serum adipokines profile and insulin resistance in patients with rheumatoid arthritis treated with anti-TNF-α

被引:28
作者
Corrado, Addolorata [1 ]
Colia, Ripalta [1 ]
Rotondo, Cinzia [1 ]
Sanpaolo, Eliana [1 ]
Cantatore, Francesco Paolo [1 ]
机构
[1] Univ Foggia, Dept Med & Surg Sci, Rheumatol Clin, Foggia, Italy
关键词
Adipokines; rheumatoid arthritis; TNF-alpha insulin resistance; insulin sensitivity; atherogenic index; NECROSIS-FACTOR-ALPHA; HIGH-DENSITY-LIPOPROTEIN; LIPID PROFILE; METABOLIC SYNDROME; INFLAMMATION; THERAPY; RISK; CHOLESTEROL; ATHEROSCLEROSIS; TOFACITINIB;
D O I
10.1080/03007995.2019.1654988
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Rheumatoid arthritis (RA) is a chronic inflammatory joint disease characterized by an altered glucose and lipid metabolism. Tumor necrosis factor alpha (TNF-alpha) is involved in the pathogenesis of both RA and metabolic syndrome. This study evaluated the effects of anti-TNF-alpha agents (adalimumab, etanercept, infliximab) on lipid and glucose metabolism in patients with RA. Methods: A total of 33 RA, biological therapy-naive patients were recruited. Changes in Disease Activity, Body Mass Index, resistin, leptin and adiponectin serum levels, lipid profile, atherogenic index, insulin sensitivity index, and insulin resistance index were evaluated at baseline and after anti-TNF-alpha treatments. Results: Anti-TNF-alpha treatment was effective in reducing disease activity. An inverse relationship between disease activity and adiponectin levels was found, whereas leptin and resistin levels directly correlated with disease activity. TNF-alpha therapy significantly reduced leptin, resistin, and increased adiponectin. TNF-alpha inhibition resulted in a reduction of atherogenic index and insulin resistance index while increased insulin sensitivity index. Conclusion: Anti-TNF-alpha agents could have a crucial role in modifying the impact of lipid profile and glucose levels dysregulation in RA patients. TNF-alpha inhibition may be a potential strategy for the prevention of metabolic syndrome and could play a role in the reduction of cardiovascular risk in RA.
引用
收藏
页码:2197 / 2205
页数:9
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