Loading…

The feet in systemic lupus erythematosus; are we underestimating their involvement and functional impact?

To evaluate biomechanical and ultrasound (US) abnormalities in SLE patients as compared with controls and to assess the relationship between these abnormalities and SLE activity. Fifty-four consecutive female patients with SLE with and without foot pain and 60 female controls (30 with foot pain and...

Full description

Saved in:
Bibliographic Details
Published in:Clinical and experimental rheumatology 2016-07, Vol.34 (4), p.609-617
Main Authors: Morales-Lozano, Rosario, Martínez-Barrio, Julia, González-Fernández, María Luz, López-Longo, Francisco Javier, Ovalles-Bonilla, Juan Gabriel, Valor, Lara, Janta, Iustina, Nieto, Juan Carlos, Hernández-Flórez, Diana, González, Carlos M, Monteagudo, Indalecio, Garrido, Jesús, Carreño, Luis, Naredo, Esperanza
Format: Article
Language:English
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:To evaluate biomechanical and ultrasound (US) abnormalities in SLE patients as compared with controls and to assess the relationship between these abnormalities and SLE activity. Fifty-four consecutive female patients with SLE with and without foot pain and 60 female controls (30 with foot pain and 30 without foot pain) were recruited. SLE activity was assessed by the Systemic Lupus Erythematosus Disease Activity Index (SLEDAI). SLE patients and controls blindly underwent a comprehensive podiatric, biomechanical and US evaluation of the feet. US assessment included detection of B-mode synovitis, tenosynovitis, enthesopathy, bone changes and synovial, tenosynovial and entheseal power Doppler (PD) signal. Thirty-one (57.4%) SLE patients had bilateral foot pain and 5 (9.3%) had unilateral foot pain. Metatarsalgia was the most common location for pain but without significant difference between groups (p=0.284). Toe joint deformities were significantly more common in SLE feet as compared with control feet (p
ISSN:0392-856X
1593-098X