Circulating E-selectin and tumor necrosis factor-α in extraarticular involvement and joint disease activity in rheumatoid arthritis

Esther G. Corona-Sanchez, Laura Gonzalez-Lopez, Jose F. Muñoz-Valle, Monica Vazquez-Del Mercado, Maria A. Lopez-Olivo, Erika A. Aguilar-Chavez, Mario Salazar-Paramo, Carlos Loaiza-Cardenas, Edith Oregon-Romero, Rosa E. Navarro-Hernandez, Jorge I. Gamez-Nava

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

In this cross-sectional study, we assessed the relationship between circulating TNF-α and E-selectin (sE-selectin) with extraarticular involvement and severity of joint disease in RA. We compared 56 patients who had RA and extraarticular involvement (ExRA) with a group of 84 patients with only articular involvement (non-ExRA). ExRA had higher circulating TNF-α than non-ExRA (32 ± 9 vs. 28 ± 6 pg/mL, P = 0.002). sE-selectin levels did not differ between both groups. sE-selectin correlated with tender joint count (rho = 0.19, P = 0.03), morning stiffness (rho = 0.19, P = 0.03), severity of pain (rho = 0.21, P = 0.02), disease activity (assessed by the patient) (rho = 0.21, P = 0.02), HAQ-DI (rho = 0.29, P = 0.004), and rheumatoid factor titers (rho = 0.31, P = <0.001). Circulating TNF-α had no correlation with sE-selectin or disease activity. We concluded that sE-selectin correlated with severity of joint disease, further follow-up studies should evaluate if sE-selectin is useful as prognosis marker for progression of articular damage.

Original languageEnglish (US)
Pages (from-to)281-286
Number of pages6
JournalRheumatology International
Volume29
Issue number3
DOIs
StatePublished - Jan 2009

Keywords

  • Articular activity
  • Extraarticular involvement
  • Rheumatoid arthritis
  • TNF-α
  • sE-selectin

ASJC Scopus subject areas

  • Rheumatology
  • Immunology and Allergy
  • Immunology

Fingerprint

Dive into the research topics of 'Circulating E-selectin and tumor necrosis factor-α in extraarticular involvement and joint disease activity in rheumatoid arthritis'. Together they form a unique fingerprint.

Cite this