Literature DB >> 25778456

Mood Disorders in Systemic Lupus Erythematosus: Results From an International Inception Cohort Study.

John G Hanly1, Li Su2, Murray B Urowitz3, Juanita Romero-Diaz4, Caroline Gordon5, Sang-Cheol Bae6, Sasha Bernatsky7, Ann E Clarke8, Daniel J Wallace9, Joan T Merrill10, David A Isenberg11, Anisur Rahman11, Ellen M Ginzler12, Michelle Petri13, Ian N Bruce14, M A Dooley15, Paul Fortin16, Dafna D Gladman3, Jorge Sanchez-Guerrero3, Kristjan Steinsson17, Rosalind Ramsey-Goldman18, Munther A Khamashta19, Cynthia Aranow20, Graciela S Alarcón21, Barri J Fessler21, Susan Manzi22, Ola Nived23, Gunnar K Sturfelt23, Asad A Zoma24, Ronald F van Vollenhoven25, Manuel Ramos-Casals26, Guillermo Ruiz-Irastorza27, S Sam Lim28, Kenneth C Kalunian29, Murat Inanc30, Diane L Kamen31, Christine A Peschken32, Soren Jacobsen33, Anca Askanase34, Chris Theriault1, Kara Thompson1, Vernon Farewell2.   

Abstract

OBJECTIVE: To examine the frequency, characteristics, and outcome of mood disorders, as well as clinical and autoantibody associations, in a multiethnic/racial, prospective inception cohort of patients with systemic lupus erythematosus (SLE).
METHODS: Patients were assessed annually for mood disorders (4 types, according to the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition) and 18 other neuropsychiatric events. Global disease activity scores (SLE Disease Activity Index 2000 [SLEDAI-2K]), damage scores (Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index [SDI]), and Short Form 36 subscales, mental and physical component summary scores were collected. Time to event, linear and ordinal regressions, and multi-state models were used as appropriate.
RESULTS: Among the 1,827 patients with SLE, 88.9% were female, and 48.9% were Caucasian. The mean ± SD age of the patients was 35.1 ± 13.3 years, disease duration was 5.6 ± 4.8 months, and the length of followup was 4.7 ± 3.5 years. During the course of the study, 863 (47.2%) of the 1,827 patients had 1,627 neuropsychiatric events. Mood disorders occurred in 232 (12.7%) of 1,827 patients, and 98 (38.3%) of 256 mood disorder events were attributed to SLE. The estimated cumulative incidence of any mood disorder after 10 years was 17.7% (95% confidence interval 15.1, 20.2%). A greater risk of mood disorder was associated with concurrent neuropsychiatric events (P ≤ 0.01), and a lower risk was associated with Asian race/ethnicity (P = 0.01) and treatment with immunosuppressive drugs (P = 0.003). Mood disorders were associated with lower mental health and mental component summary scores but not with the SLEDAI-2K, SDI, or lupus autoantibodies. Among the 232 patients with depression, 168 (72.4%) were treated with antidepressants. One hundred twenty-six (49.2%) of 256 mood disorders resolved in 117 (50.4%) of 232 patients.
CONCLUSION: Mood disorders, the second most frequent neuropsychiatric event in patients with SLE, have a negative impact on health-related quality of life and improve over time. The lack of association with global SLE disease activity, cumulative organ damage, and lupus autoantibodies emphasizes the multifactorial etiology of mood disorders and a role for non-lupus-specific therapies.
© 2015, American College of Rheumatology.

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Year:  2015        PMID: 25778456      PMCID: PMC4485527          DOI: 10.1002/art.39111

Source DB:  PubMed          Journal:  Arthritis Rheumatol        ISSN: 2326-5191            Impact factor:   10.995


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