Functional disability is related to serum chemerin levels in rheumatoid arthritis

Adipokines, especially chemerin, can interact with cytokines and other molecules in inflammation. To date, there is insufficient information regarding a possible correlation between functional disability and chemerin and other pro-inflammatory molecules in rheumatoid arthritis (RA). To identify the association of functional disability with serum chemerin and other pro-inflammatory molecules, including other adipokines, cytokines and E-selectin, in patients with RA. Cross-sectional study. Assessment: disease activity (DAS28-ESR) and functional disability (HAQ-DI). We compared the adipokines (chemerin, leptin, adiponectin, resistin, and visfatin), cytokines (TNF-α, IL-6, IL-1β, and IL-18) and E-selectin levels between RA with functional disability and RA non-disabled patients. Of 82 patients with RA, 43 (52%) had functional disability. The RA with functional disability group had higher chemerin (140 vs. 112 ng/mL, p = 0.007) than the non-disabled RA group. Chemerin correlated with the HAQ-DI (rho = 0.27, p = 0.02) and DAS28-ESR (rho = 0.21, p = 0.05). Severe activity correlated with IL-6 (rho = 0.33, p = 0.003) and E-selectin (rho = 0.23, p = 0.03) but not with disability. No other pro-inflammatory molecules correlated with HAQ-DI. High chemerin levels were associated with functional disability in RA, whereas no other molecules correlated with loss of function. These results encourage further studies assessing new roles of chemerin as a marker of impairment in RA.
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Maria Luisa Vazquez-Villegas #, Jorge I Gamez-Nava #, A Miriam Saldaña-Cruz, Alfredo Celis, Esther N Sanchez-Rodriguez, Edsaul Emilio Perez-Guerrero, Melissa Ramirez-Villafaña, Cesar Arturo Nava-Valdivia, Betsabe Contreras-Haro, Jose C Vasquez-Jimenez, Juan M Ponce-Guarneros, Ana K Barocio-Ramirez, Sergio Cerpa-Cruz, Miriam F Alcaraz-Lopez, Laura Gonzalez-Lopez

  • Sci Rep
  • 4.6
  • 2021 Apr 16;11(1):8360.
  • Human
  • 抗体芯片
  • 运动系统
  • 运动系统
  • 关节炎
  • Adiponectin,FGF basic,M-CSF,Angiopoietin-1,FGF-19,MIF,Angiopoietin-2,Fibrinogen,Myeloperoxidase,Angiopoietin-like 2,Growth Hormone,Nidogen-1/Entactin,Angiopoietin-like 3,HGF,Oncostatin M,BAFF/BLyS,ICAM-I,Pappalysin-1/PAPP-A,BMP-4,IGFBP-2,PBEF/Visfatin,Cathepsin D,IGFBP-3,PCSK9,Cathepsin L,IGFBP-4,Pentraxin-3,Cathepsin S,IGFBP-6,Pref-1/DLK-1/FA1,CCL2/MCP-1,IGFBP-rp1/IGFBP-7,RAGE,CCL5/RANTES,IL-1 beta,Resistin,Chemerin,IL-6,Serpin A12,Complement Factor D,IL-10,Serpin A8/AGT,C-Reactive Protein,IL-11,Serpin E1/PAI-1,CXCL8/IL-8,LAP (TGF-ß1),TIMP-1,DPPIV/CD26,Leptin,TIMP-3,Endocan,LIF,TNF-alpha,EN-RAGE,Lipocalin-2/NGAL,VEGF,Fetuin B

相关货号

LXAH058-1

Abstract

Adipokines, especially chemerin, can interact with cytokines and other molecules in inflammation. To date, there is insufficient information regarding a possible correlation between functional disability and chemerin and other pro-inflammatory molecules in rheumatoid arthritis (RA). To identify the association of functional disability with serum chemerin and other pro-inflammatory molecules, including other adipokines, cytokines and E-selectin, in patients with RA. Cross-sectional study. Assessment: disease activity (DAS28-ESR) and functional disability (HAQ-DI). We compared the adipokines (chemerin, leptin, adiponectin, resistin, and visfatin), cytokines (TNF-α, IL-6, IL-1β, and IL-18) and E-selectin levels between RA with functional disability and RA non-disabled patients. Of 82 patients with RA, 43 (52%) had functional disability. The RA with functional disability group had higher chemerin (140 vs. 112 ng/mL, p = 0.007) than the non-disabled RA group. Chemerin correlated with the HAQ-DI (rho = 0.27, p = 0.02) and DAS28-ESR (rho = 0.21, p = 0.05). Severe activity correlated with IL-6 (rho = 0.33, p = 0.003) and E-selectin (rho = 0.23, p = 0.03) but not with disability. No other pro-inflammatory molecules correlated with HAQ-DI. High chemerin levels were associated with functional disability in RA, whereas no other molecules correlated with loss of function. These results encourage further studies assessing new roles of chemerin as a marker of impairment in RA.
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