Subedi Ananta, Magder Laurence S, Petri Michelle
Department of Medicine, Thomas Jefferson University Hospital, 833 Chestnut Street, Suite 701, Philadelphia, PA, 19107, USA.
Department of Epidemiology and Public Health, University of Maryland, 660 West Redwood Street, Baltimore, MD, 21201, USA.
Rheumatol Int. 2015 Oct;35(10):1687-92. doi: 10.1007/s00296-015-3265-6. Epub 2015 Apr 3.
Leukopenia is a common manifestation of SLE. Addition of immunosuppressive therapy in a SLE patient who is already leukopenic is a clinical concern. It could worsen leukopenia, increase the risk of infection, or both. The aim of this study was to analyze the immediate effect of mycophenolate mofetil on the white blood cell count and the rate of infection in SLE patients. Two hundred and forty-four patients within the Hopkins Lupus Cohort who were newly started on mycophenolate mofetil were included in the study. The white blood cell count and interval infection history on the day mycophenolate mofetil was started were compared with the white blood cell count and interval infection history at the next visit. The study was based on 244 patients who began taking mycophenolate mofetil in the cohort. The study population included 47 % African Americans, 44 % Caucasians, and 9 % other ethnicities. There was a slight but not statistically significant increase in the white blood cell count (6.63 vs. 7.01), after starting mycophenolate mofetil. Patients with a baseline white blood cell count <3000/mm(3) did have a statistically significant increase in the white blood cell count after starting mycophenolate mofetil (2.57 vs. 5.13, P = 0.0047). We also found a statistically significant increase in the risk of bacterial infection (but not viral infection) after starting mycophenolate mofetil (4 vs. 9 %, P = 0.0036). Leukopenia does not worsen with mycophenolate mofetil. However, mycophenolate mofetil appears to slightly increase the rate of bacterial (but not viral) infection.
白细胞减少是系统性红斑狼疮(SLE)的常见表现。在已经存在白细胞减少的SLE患者中加用免疫抑制治疗是一个临床关注点。这可能会使白细胞减少加重,增加感染风险,或两者兼而有之。本研究的目的是分析霉酚酸酯对SLE患者白细胞计数和感染率的即时影响。霍普金斯狼疮队列中244例新开始使用霉酚酸酯的患者纳入本研究。将开始使用霉酚酸酯当天的白细胞计数和期间感染史与下次就诊时的白细胞计数和期间感染史进行比较。该研究基于队列中开始服用霉酚酸酯的244例患者。研究人群包括47%的非裔美国人、44%的白种人和9%的其他种族。开始使用霉酚酸酯后,白细胞计数有轻微但无统计学意义的升高(6.63对7.01)。基线白细胞计数<3000/mm³的患者在开始使用霉酚酸酯后白细胞计数有统计学意义的升高(2.57对5.13,P = 0.0047)。我们还发现开始使用霉酚酸酯后细菌感染风险有统计学意义的升高(但病毒感染无升高)(4%对9%,P = 0.0036)。霉酚酸酯不会使白细胞减少加重。然而,霉酚酸酯似乎会轻微增加细菌(而非病毒)感染率。