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Rheumatoid arthritis and major depression: Effects of antidepressant therapy on markers of inflammation

机译:类风湿关节炎和严重抑郁症:抗抑郁药对炎症标志物的影响

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摘要

Purpose. Evidence exists of systemic inflammation in both rheumatoid arthritis (RA) and major depression (MD). However, little is known about the effects of antidepressants on systemic inflammation. The purpose of this study was to examine the effects of effective antidepressant treatment on inflammatory immune markers (Tumor Necrosis Factor alpha---TNF-alpha, Interleukin-1 Receptor Antagonist---IL-1Ra, and C-reactive protein---CRP) in persons with combined RA and MD. Methods. This was a secondary analysis of a study in which subjects (n = 54) with RA received cognitive-behavioral and pharmacologic treatment for MD (Parker et al., 2003) and on-going rheumatology care. The current study focused on a subset of subjects (n = 38) treated for 15 months with sertraline. Serum TNF-alpha, IL-1Ra, and CRP levels; depression (Hamilton Depression Rating Scale), RA health status, and joint disease activity were obtained at baseline and following 15 months of antidepressant treatment with sertraline. Serum TNF-alpha and IL-1Ra levels were obtained by enzyme-linked immunosorbent assay; Serum CRP levels were obtained by high sensitivity CRP chemiluminescent immunoassay. Results. Following 15 months of antidepressant treatment, significant reductions were noted for depression severity (p = .001); 87% of subjects had at least a 50% reduction in depression severity scores. There was a near significant (p = .06) decrease in serum TNF-alpha levels; while serum IL-1Ra and CRP levels remained unchanged (p = .62, p = .97, respectively). Baseline serum TNF-alpha and IL-1Ra levels predicted the amount of reduction in depression severity (R2 =35, p =.002). Subjects with lower baseline serum levels of the inflammatory cytokine TNF-alpha had greater reductions in depression severity scores; subjects with higher baseline serum levels of the anti-inflammatory cytokine IL-1Ra had greater reductions in depression severity scores. Conclusions . This study provides preliminary evidence that baseline serum TNF-alpha and IL-1Ra levels in persons with RA and MD predict the amount of improvement in depression severity with antidepressant treatment. Serum TNF-alpha levels decreased following antidepressant treatment. These findings support the importance of vigilance in monitoring for and successfully managing MD in persons with RA.
机译:目的。有证据表明类风湿关节炎(RA)和重度抑郁症(MD)都存在全身性炎症。然而,关于抗抑郁药对全身性炎症的作用知之甚少。这项研究的目的是检查有效的抗抑郁药治疗对炎性免疫标记物(肿瘤坏死因子α--TNF-α,白介素1受体拮抗剂--IL-1Ra和C反应蛋白- CRP)用于RA和MD合并患者。方法。这是一项研究的二级分析,其中患有RA的受试者(n = 54)接受了MD的认知行为和药物治疗(Parker等,2003)和持续的风湿病治疗。目前的研究集中于舍曲林治疗15个月的一组受试者(n = 38)。血清TNF-α,IL-1Ra和CRP水平;在基线和舍曲林抗抑郁药治疗15个月后获得了抑郁(汉密尔顿抑郁评估量表),RA健康状况和关节疾病活动。酶联免疫吸附法检测血清TNF-α和IL-1Ra水平。血清CRP水平通过高灵敏度CRP化学发光免疫分析获得。结果。经过15个月的抗抑郁药治疗,抑郁症严重程度明显降低(p = 0.001); 87%的受试者的抑郁严重程度评分降低了至少50%。血清TNF-α水平下降了近显着(p = .06)。而血清IL-1Ra和CRP水平保持不变(分别为p = 0.62,p = 0.97)。基线血清TNF-α和IL-1Ra水平可预测抑郁症严重程度的减轻程度(R2 = 35,p = .002)。炎症细胞因子TNF-α的基线血清水平较低的受试者抑郁症严重程度得分的降低幅度更大。抗炎细胞因子IL-1Ra的基线血清水平较高的受试者抑郁症严重程度评分的降低幅度更大。结论。这项研究提供了初步的证据,即RA和MD患者的基线血清TNF-α和IL-1Ra水平预测了抗抑郁药治疗可降低抑郁严重程度。抗抑郁药治疗后血清TNF-α水平下降。这些发现支持了警惕在监测和成功治疗RA患者中MD的重要性。

著录项

  • 作者

    Johnston, Sandra K.;

  • 作者单位

    University of Washington.;

  • 授予单位 University of Washington.;
  • 学科 Immunology.;Nursing.
  • 学位 Ph.D.
  • 年度 2004
  • 页码 160 p.
  • 总页数 160
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 11:43:50

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