忧郁乐观症患者至少能对负面反应表示最差

W. Sondermann
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摘要

背景/目的:本研究旨在探讨抑郁和焦虑症状对银屑病患者依那西普治疗临床疗效的预测价值。方法:85例接受依那西普治疗6个月的银屑病患者被纳入前瞻性队列研究。在第0个月(M0)、M1、M3和M6时评估银屑病面积和严重程度指数(PASI)评分,并在每次就诊时评估相应的PASI 75/90反应。此外,采用医院焦虑抑郁量表(HADS)在M0、M1、M3和M6阶段评估焦虑和抑郁症状。结果:银屑病患者抑郁症状与女性(p = 0.004)、病程较长(p = 0.018)、PASI评分较高(p < 0.001)相关,焦虑症状与女性(p = 0.017)、银屑病患者体表面积较大(p = 0.049)、PASI评分较高(p = 0.017)相关。依那西普治疗后,与M0相比,M1、M3和M6时hads -抑郁(HADS-D)和hads -焦虑(HADS-A)评分均下降(p均< 0.001)。最重要的是,与基线非抑郁患者相比,基线抑郁患者在M3 (p = 0.014)和M6 (p = 0.005)时的PASI 75反应率较低,M6时的PASI 90反应率较低(p = 0.045)。此外,多变量logistic回归分析显示,基线时的抑郁症状是银屑病患者在M6时PASI 75反应(p = 0.048)和PASI 90反应(p = 0.048)达到较低可能性的独立预测因素。然而,没有观察到基线焦虑症状与PASI 75/90反应的相关性。结论:基线抑郁症状独立预测依那西普治疗银屑病患者的临床反应较差。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Depressive Psoriasis-Patienten können ein schlechteres Ansprechen auf Etanercept zeigen
Background/Aims: This study aimed to investigate the predicting values of depression and anxiety symptoms for clinical response to etanercept treatment in psoriasis patients. Methods: A total of 85 psoriasis patients who received 6 months of etanercept treatment were consecutively enrolled in this prospective cohort study. The Psoriasis Area and Severity Index (PASI) score was evaluated at month 0 (M0), M1, M3, and M6, and the corresponding PASI 75/90 response at each visit was assessed. Also, anxiety and depression symptoms were assessed by the Hospital Anxiety and Depression Scale (HADS) at M0, M1, M3, and M6. Results: Depression symptoms were observed to correlate with female gender (p = 0.004), longer disease duration (p = 0.018), and higher PASI score (p < 0.001), and anxiety symptoms were seen to be associated with female gender (p = 0.017), larger psoriasis-affected body surface area (p = 0.049), and higher PASI score (p = 0.017) in psoriasis patients. After etanercept treatment, HADS-Depression (HADS-D) and HADS-Anxiety (HADS-A) scores were both decreased at M1, M3, and M6 (all p < 0.001) compared with M0. Most importantly, baseline depressed patients presented with a lower PASI 75 response rate at M3 (p = 0.014) and M6 (p = 0.005), and a reduced PASI 90 response rate at M6 (p = 0.045) compared with baseline non-depressed patients. Furthermore, multivariate logistic regression analyses revealed that depression symptoms at baseline were an independent predictive factor for the lower possibility of both PASI 75 response (p = 0.048) and PASI 90 response (p = 0.048) achievements at M6 in psoriasis patients. However, no correlation of baseline anxiety symptoms with PASI 75/90 responses was observed. Conclusion: Depression symptoms at baseline independently predict a worse clinical response to etanercept treatment in psoriasis patients.
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