Literature DB >> 24497416

Changes in quality of life in the first 5 years of disease in a multicenter cohort of patients with systemic lupus erythematosus.

M Urowitz1, D D Gladman, D Ibañez, J Sanchez-Guerrero, S C Bae, C Gordon, P R Fortin, A Clarke, S Bernatsky, J G Hanly, D J Wallace, D Isenberg, A Rahman, J Merrill, E Ginzler, G S Alarcón, B Fessler, M Khamashta, K Steinsson, M Petri, M Dooley, I N Bruce, S Manzi, G Sturfelt, O Nived, R Ramsey-Goldman, A Zoma, P Maddison, K Kalunian, R van Vollenhoven, C Aranow, J Romero Diaz, T Stoll.   

Abstract

OBJECTIVE: The Medical Outcomes Study Short Form 36 (SF-36) is recommended to assess quality of life (QOL) in systemic lupus erythematosus (SLE). The aim of the current study was to assess QOL over time in the first 5 years of a multicenter inception cohort of patients with SLE.
METHODS: An inception SLE cohort was assembled according to a standardized protocol between 2000 and 2012. In addition to clinical and laboratory assessments, patients completed the SF-36 at yearly intervals. Only patients who had ≥5 completed QOL questionnaires were included in these analyses. Generalized estimating equation models were run separately for each of the 8 subscales and for the physical and mental component summary scores, adjusting for repeated measures by patients.
RESULTS: A total of 495 patients were included. The mean ± SD disease duration at the first visit was 5.3 ± 4.1 months. The mean ± SD age at enrollment was 35.8 ± 13.2 years. All 8 subscales and the 2 summary scores showed improvement in the first 2 years from enrollment. Between years 2 and 5, none of the subscales or summary scores showed any change. Minimum clinically important improvement was achieved by 35-56% of the patients and was influenced by demographic and disease factors.
CONCLUSION: Unlike late-stage lupus, where QOL is stable over time, in patients with early disease, all subscales improve in early followup up to 2 years. Therefore, the SF-36 may be a sensitive outcome measure in early disease in patients with SLE.
Copyright © 2014 by the American College of Rheumatology.

Entities:  

Mesh:

Year:  2014        PMID: 24497416     DOI: 10.1002/acr.22299

Source DB:  PubMed          Journal:  Arthritis Care Res (Hoboken)        ISSN: 2151-464X            Impact factor:   4.794


  17 in total

1.  Associations between illness duration and health-related quality of life in specified mental and physical chronic health conditions: results from a population-based survey.

Authors:  Lucy Busija; Jeretine Tan; Kerrie M Sanders
Journal:  Qual Life Res       Date:  2017-05-12       Impact factor: 4.147

2.  An evaluation of health-related quality of life in patients with systemic lupus erythematosus using PROMIS and Neuro-QoL.

Authors:  Jin-Shei Lai; Jennifer L Beaumont; Sally E Jensen; Karen Kaiser; David L Van Brunt; Amy H Kao; Shih-Yin Chen
Journal:  Clin Rheumatol       Date:  2016-11-15       Impact factor: 2.980

Review 3.  Patient-Reported Outcomes in Systemic Lupus Erythematosus.

Authors:  Mary Mahieu; Susan Yount; Rosalind Ramsey-Goldman
Journal:  Rheum Dis Clin North Am       Date:  2016-03-17       Impact factor: 2.670

4.  Differential impact of systemic lupus erythematosus and rheumatoid arthritis on health-related quality of life.

Authors:  Benjamin Chaigne; Axel Finckh; Deshire Alpizar-Rodriguez; Delphine Courvoisier; Camillo Ribi; Carlo Chizzolini
Journal:  Qual Life Res       Date:  2017-03-11       Impact factor: 4.147

5.  The Avise Lupus Test and Cell-bound Complement Activation Products Aid the Diagnosis of Systemic Lupus Erythematosus.

Authors:  James Mossell; John A Goldman; Derren Barken; Roberta Vezza Alexander
Journal:  Open Rheumatol J       Date:  2016-10-31

6.  Failure to achieve lupus low disease activity state (LLDAS) six months after diagnosis is associated with early damage accrual in Caucasian patients with systemic lupus erythematosus.

Authors:  Matteo Piga; Alberto Floris; Giulia Cappellazzo; Elisabetta Chessa; Mattia Congia; Alessandro Mathieu; Alberto Cauli
Journal:  Arthritis Res Ther       Date:  2017-11-10       Impact factor: 5.156

7.  Neuropsychiatric symptoms in systemic lupus erythematosus: impact on quality of life.

Authors:  R C Monahan; L J J Beaart-van de Voorde; G M Steup-Beekman; C Magro-Checa; T W J Huizinga; J Hoekman; A A Kaptein
Journal:  Lupus       Date:  2017-02-22       Impact factor: 2.911

8.  Impact of disease activity on health-related quality of life in systemic lupus erythematosus - a cross-sectional analysis of the Swiss Systemic Lupus Erythematosus Cohort Study (SSCS).

Authors:  Benjamin Chaigne; Carlo Chizzolini; Thomas Perneger; Marten Trendelenburg; Uyen Huynh-Do; Eric Dayer; Thomas Stoll; Johannes von Kempis; Camillo Ribi
Journal:  BMC Immunol       Date:  2017-03-28       Impact factor: 3.615

9.  Longitudinal analysis of quality of life in patients with undifferentiated connective tissue diseases.

Authors:  Michele Iudici; Rosaria Irace; Antonella Riccardi; Giovanna Cuomo; Serena Vettori; Gabriele Valentini
Journal:  Patient Relat Outcome Meas       Date:  2017-02-02

10.  Association of age with health-related quality of life in a cohort of patients with systemic lupus erythematosus: the Georgians Organized Against Lupus study.

Authors:  Laura Plantinga; S Sam Lim; C Barrett Bowling; Cristina Drenkard
Journal:  Lupus Sci Med       Date:  2016-07-19
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