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帕罗西汀治疗轻度抑郁的2型糖尿病患者的生活质量和代谢状况:一项双盲随机安慰剂对照的6个月试验。

Quality of life and metabolic status in mildly depressed patients with type 2 diabetes treated with paroxetine: a double-blind randomised placebo controlled 6-month trial.

作者信息

Paile-Hyvärinen Maria, Wahlbeck Kristian, Eriksson Johan G

机构信息

National Public Health Institute, Mannerheimintie, Helsinki, Finland.

出版信息

BMC Fam Pract. 2007 Jun 15;8:34. doi: 10.1186/1471-2296-8-34.

Abstract

BACKGROUND

Depression is prevalent in people with type 2 diabetes and affects both glycaemic control and overall quality of life. The aim of this investigator-initiated trial was to evaluate the effect of the antidepressant paroxetine on quality of life, metabolic control, and mental well-being in mildly depressed diabetics aged 50-70 years.

METHODS

We randomised 49 mildly depressed primary care outpatients with non-optimally controlled diabetes to a 6-month double-blind treatment with either paroxetine 20 mg per day or matching placebo. Primary efficacy measurements were quality of life and glycaemic control. The primary global outcome of the study was defined as a 10 points improvement in the SF-36 quality of life score. The primary metabolic outcome of the study was defined as a 0.8%-units decrease in glycosylated haemoglobin A1c(GHbA1c). Psychiatric symptoms were assessed with the Hospital Anxiety and Depression Scale.

RESULTS

Six patients withdrew their consent before starting medication and six dropped out later in the study. We performed analysis of covariance with the baseline value as a covariate. Quality of life and glycaemic control as well as symptoms of depression and anxiety improved in both groups over the 6-month study period. After three months of treatment we found a statistically significant difference between the two treatment groups in GHbA1c (mean difference = 0.59%-units, p = 0.018) and in SF-36 score (mean difference = 11.0 points, p = 0.039). However, at the end of the study, no statistically significant differences between the treatment groups were observed. No severe adverse events occurred.

CONCLUSION

This pragmatic study of primary care patients did not confirm earlier preliminary findings indicating a beneficial effect of paroxetine on glycaemic control. The study indicates that in pragmatic circumstances any possible benefit from administration of paroxetine in diabetic patients with sub-threshold depression is likely to be modest and of short duration. Routine antidepressant prescription for patients with diabetes and sub-threshold depressive symptoms is not indicated.

TRIAL REGISTRATION

Current controlled trials ISRCTN55819922.

摘要

背景

抑郁症在2型糖尿病患者中普遍存在,且会影响血糖控制和总体生活质量。这项研究者发起的试验旨在评估抗抑郁药帕罗西汀对50至70岁轻度抑郁糖尿病患者生活质量、代谢控制及心理健康的影响。

方法

我们将49例糖尿病控制不佳的轻度抑郁初级保健门诊患者随机分为两组,分别接受为期6个月的每日20毫克帕罗西汀或匹配安慰剂的双盲治疗。主要疗效指标为生活质量和血糖控制。该研究的主要总体结局定义为SF-36生活质量评分提高10分。该研究的主要代谢结局定义为糖化血红蛋白A1c(GHbA1c)降低0.8个百分点。采用医院焦虑抑郁量表评估精神症状。

结果

6例患者在开始用药前撤回同意书,6例在研究后期退出。我们以基线值作为协变量进行协方差分析。在为期6个月的研究期间,两组患者的生活质量、血糖控制以及抑郁和焦虑症状均有所改善。治疗三个月后,我们发现两个治疗组在GHbA1c(平均差值 = 0.59个百分点,p = 0.018)和SF-36评分(平均差值 = 11.0分,p = 0.039)方面存在统计学显著差异。然而,在研究结束时,未观察到治疗组之间存在统计学显著差异。未发生严重不良事件。

结论

这项针对初级保健患者的实用性研究未证实早期初步研究结果,即帕罗西汀对血糖控制有有益作用。该研究表明,在实际情况下,帕罗西汀用于轻度抑郁糖尿病患者可能带来的任何益处可能都很有限且持续时间较短。不建议对有亚阈值抑郁症状的糖尿病患者常规开具抗抑郁药处方。

试验注册号

现行对照试验ISRCTN55819922

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dde/1914073/9fa807e6ce2b/1471-2296-8-34-1.jpg

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