Literature DB >> 10685798

Determinants of health status in fibromyalgia: a comparative study with systemic lupus erythematosus.

D Da Costa1, P L Dobkin, M A Fitzcharles, P R Fortin, A Beaulieu, M Zummer, J L Senécal, J R Goulet, E Rich, D Choquette, A E Clarke.   

Abstract

OBJECTIVE: To compare perceived health status in women with fibromyalgia (FM) and systemic lupus erythematosus (SLE) using the Medical Outcomes Study (MOS) Short Form Health Survey (SF-36); and to identify determinants of physical and mental health in each patient group.
METHODS: A cross sectional study of 46 women with FM (mean age 48.13 yrs, SD 9.40) and 59 women with SLE (mean age 42.36 yrs, SD 11.31). Patients with FM were recruited from a rheumatology clinic and a rheumatology practice, while patients with SLE were recruited from 4 rheumatology clinics. Clinical examination determined disease activity (by Systemic Lupus Activity Measure) in SLE and a tender point count was used for FM. Patients completed questionnaires assessing health status (SF-36), stress (Hassles), social support (Social Support Questionnaire 6), and coping (Coping Inventory for Stressful Situations).
RESULTS: Patients with FM reported more impairment on the following SF-36 subscales: physical function (p < 0.001), role physical (p < 0.001), bodily pain (p < 0.001), and vitality (p < 0.001). Physical component summary scores were also significantly lower (p < 0.001) for the FM group. Four hierarchical regression analyses were computed to determine factors related to physical and mental health in each patient group, with the following variables in the equation: age, income, disease activity (Step 1), hassles (Step 2), emotional and task coping, and social support (Step 3). Better physical health in FM was related to higher income (R2 = 0.17, p < 0.05). In the SLE group, better physical health was associated with younger age, less disease activity, and lower hassles (R2 = 0.37, p < 0.0001). Worse mental health among women with FM was associated with more hassles, more emotional coping, and less satisfaction with social support (R2 = 0.64, p < 0.0001), while lower income, higher hassles, and more emotional coping were linked to worse mental health in SLE (R2 = 0.46, p < 0.0001).
CONCLUSION: Health related quality of life (HRQL) is impaired among women with FM and SLE, with FM patients reporting greater impairment along several dimensions. Enhancing the HRQL of patients with FM and SLE requires targeting specific modifiable psychosocial factors.

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Year:  2000        PMID: 10685798

Source DB:  PubMed          Journal:  J Rheumatol        ISSN: 0315-162X            Impact factor:   4.666


  25 in total

1.  Cytokine balance and behavioral intervention; findings from the Peer Approaches to Lupus Self-Management (PALS) project.

Authors:  Edith M Williams; J Madison Hyer; Ramakrishnan Viswanathan; Trevor D Faith; Leonard Egede; Jim C Oates; Gailen D Marshall
Journal:  Hum Immunol       Date:  2017-07-14       Impact factor: 2.850

2.  A Comparison of Fibromyalgia Symptoms in Patients with Healthy versus Depressive, Low and Reactive Affect Balance Styles.

Authors:  Loren L Toussaint; Ann Vincent; Samantha J McAllister; Terry H Oh; Afton L Hassett
Journal:  Scand J Pain       Date:  2014-07-01

Review 3.  Quality-of-life measurements versus disease activity in systemic lupus erythematosus.

Authors:  Adnan N Kiani; Michelle Petri
Journal:  Curr Rheumatol Rep       Date:  2010-08       Impact factor: 4.592

4.  Improvement of coping abilities in patients with systemic lupus erythematosus: a prospective study.

Authors:  M Haupt; S Millen; M Jänner; D Falagan; R Fischer-Betz; M Schneider
Journal:  Ann Rheum Dis       Date:  2005-04-13       Impact factor: 19.103

5.  Meta-analysis reveals a lack of association between a common catechol-O-methyltransferase (COMT) polymorphism val¹⁵⁸met and fibromyalgia.

Authors:  Lei Zhang; Junwei Zhu; Yong Chen; Jianning Zhao
Journal:  Int J Clin Exp Pathol       Date:  2014-12-01

6.  Disability in valued life activities among individuals with systemic lupus erythematosus.

Authors:  Patricia Katz; Anne Morris; Laura Trupin; Jinoos Yazdany; Edward Yelin
Journal:  Arthritis Rheum       Date:  2008-04-15

7.  The impact of Fibromyalgia on health-related quality of life in patients according to age.

Authors:  Ricardo Pereira Campos; Maria Isabel Vázquez
Journal:  Rheumatol Int       Date:  2012-11-15       Impact factor: 2.631

8.  Predictors of self-reported health-related quality of life in systemic lupus erythematosus.

Authors:  Adnan N Kiani; Vibeke Strand; Hong Fang; Jawali Jaranilla; Michelle Petri
Journal:  Rheumatology (Oxford)       Date:  2013-05-16       Impact factor: 7.580

9.  Health-related quality of life measured by the Short Form 36 (SF-36) in systemic sclerosis: correlations with indexes of disease activity and severity, disability, and depressive symptoms.

Authors:  Elisabetta Danieli; Paolo Airò; Lorenzo Bettoni; Massimo Cinquini; Chiara M Antonioli; Ilaria Cavazzana; Franco Franceschini; Roberto Cattaneo
Journal:  Clin Rheumatol       Date:  2004-08-06       Impact factor: 2.980

Review 10.  Fibromyalgia in systemic lupus erythematosus: prevalence and clinical implications.

Authors:  Dan Buskila; Joseph Press; Mahmoud Abu-Shakra
Journal:  Clin Rev Allergy Immunol       Date:  2003-08       Impact factor: 8.667

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