Full metadata record
DC Field | Value | Language |
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dc.contributor.author | 배상철 | - |
dc.date.accessioned | 2019-07-17T07:27:09Z | - |
dc.date.available | 2019-07-17T07:27:09Z | - |
dc.date.issued | 2019-02 | - |
dc.identifier.citation | ARTHRITIS & RHEUMATOLOGY, v. 71, NO. 2, Page. 281-289 | en_US |
dc.identifier.issn | 2326-5191 | - |
dc.identifier.issn | 2326-5205 | - |
dc.identifier.uri | https://onlinelibrary.wiley.com/doi/full/10.1002/art.40764 | - |
dc.identifier.uri | https://repository.hanyang.ac.kr/handle/20.500.11754/107565 | - |
dc.description.abstract | Objective To determine, in a large, multiethnic/multiracial, prospective inception cohort of patients with systemic lupus erythematosus (SLE), the frequency, attribution, clinical, and autoantibody associations with lupus psychosis and the short- and long-term outcomes as assessed by physicians and patients. Methods Patients were evaluated annually for 19 neuropsychiatric (NP) events including psychosis. Scores on the Systemic Lupus Erythematosus Disease Activity Index 2000, the Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index, and the Short Form 36 (SF-36) were recorded. Time to event and linear regressions were used as appropriate. Results Of 1,826 SLE patients, 88.8% were female and 48.8% were Caucasian. The mean +/- SD age was 35.1 +/- 13.3 years, the mean +/- SD disease duration was 5.6 +/- 4.2 months, and the mean +/- SD follow-up period was 7.4 +/- 4.5 years. There were 31 psychotic events in 28 of 1,826 patients (1.53%), and most patients had a single event (26 of 28 [93%]). In the majority of patients (20 of 25 [80%]) and events (28 of 31 [90%]), psychosis was attributed to SLE, usually either in the year prior to or within 3 years of SLE diagnosis. Positive associations (hazard ratios [HRs] and 95% confidence intervals [95% CIs]) with lupus psychosis were previous SLE NP events (HR 3.59 [95% CI 1.16-11.14]), male sex (HR 3.0 [95% CI 1.20-7.50]), younger age at SLE diagnosis (per 10 years) (HR 1.45 [95% CI 1.01-2.07]), and African ancestry (HR 4.59 [95% CI 1.79-11.76]). By physician assessment, most psychotic events resolved by the second annual visit following onset, in parallel with an improvement in patient-reported SF-36 summary and subscale scores. Conclusion Psychosis is an infrequent manifestation of NPSLE. Generally, it occurs early after SLE onset and has a significant negative impact on health status. As determined by patient and physician report, the short- and long-term outlooks are good for most patients, although careful follow-up is required. | en_US |
dc.description.sponsorship | Dr. Hanly’s work was supported by the Canadian Institutes of Health Research (grant MOP-88526). Drs. Su and Farewell’s work was supported by the UK Medical Research Council (grant MC_UU_00002/8). Dr. Gordon’s work was supported by Lupus UK, the Sandwell and West Birmingham Hospitals NHS Trust, and the NIHR/Wellcome Trust Birmingham Clinical Research Facility. Dr. Bae’s work was supported in part by the Bio & Medical Technology Development Program of the National Research Foundation, funded by the Ministry of Science & ICT of the Republic of Korea (grant NRF-2017M3A9B4050335). Dr. Bernatsky’s work and the Montreal General Hospital Lupus Clinic were supported in part by the Singer Family Fund for Lupus Research. Drs. Isenberg and Rahman’s work was supported by the NIHR University College London Hospitals Biomedical Research Center. Dr. Bruce’s work was supported by Arthritis Research UK, the NIHR Biomedical Research Unit Funding Scheme, the NIHR Manchester Biomedical Research Centre, and the NIHR/Wellcome Trust Clinical Research Facility at Central Manchester Foundation Trust. Dr. Petri’s work and the Hopkins Lupus Cohort were supported by the NIH (grants AR-43727 and AR-69572). Dr. Dooley’s work was supported by the NIH (grant RR-00046). Dr. Ramsey-Goldman’s work was supported by the NIH (grants 5UL-1TR-001422-02 [formerly 8UL- 1TR-000150], UL-1RR-025741, K24-AR-02318, and P60-AR-064464 [formerly P60-AR-48098]). Dr. Ruiz-Irastorza’s work was supported by the Department of Education, Universities, and Research of the Basque Government. Dr. Jacobsen’s work was supported by the Danish Rheumatism Association (grant A3865) and the Novo Nordisk Foundation (grant A05990). | en_US |
dc.language.iso | en | en_US |
dc.publisher | WILEY | en_US |
dc.subject | NEUROPSYCHIATRIC EVENTS | en_US |
dc.subject | STEROID PSYCHOSIS | en_US |
dc.subject | ANTIPHOSPHOLIPID ANTIBODIES | en_US |
dc.subject | PROTEIN-S | en_US |
dc.subject | PREVALENCE | en_US |
dc.subject | DIAGNOSIS | en_US |
dc.subject | ASSOCIATION | en_US |
dc.subject | VALIDATION | en_US |
dc.subject | CRITERIA | en_US |
dc.subject | CLASSIFICATION | en_US |
dc.title | Psychosis in Systemic Lupus Erythematosus: Results From an International Inception Cohort Study | en_US |
dc.type | Article | en_US |
dc.relation.no | 2 | - |
dc.relation.volume | 71 | - |
dc.identifier.doi | 10.1002/art.40764 | - |
dc.relation.page | 281-289 | - |
dc.relation.journal | ARTHRITIS & RHEUMATOLOGY | - |
dc.contributor.googleauthor | Hanly, John G. | - |
dc.contributor.googleauthor | Li, Qiuju | - |
dc.contributor.googleauthor | Su, Li | - |
dc.contributor.googleauthor | Urowitz, Murray B. | - |
dc.contributor.googleauthor | Gordon, Caroline | - |
dc.contributor.googleauthor | Bae, Sang-Cheol | - |
dc.contributor.googleauthor | Romero-Diaz, Juanita | - |
dc.contributor.googleauthor | Sanchez-Guerrero, Jorge | - |
dc.contributor.googleauthor | Bernatsky, Sasha | - |
dc.contributor.googleauthor | Clarke, Ann E. | - |
dc.relation.code | 2019003214 | - |
dc.sector.campus | S | - |
dc.sector.daehak | COLLEGE OF MEDICINE[S] | - |
dc.sector.department | DEPARTMENT OF MEDICINE | - |
dc.identifier.pid | scbae | - |
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