首页> 外文期刊>Journal of clinical psychopharmacology >Evaluation of platelet activation in depressed patients with ischemic heart disease after paroxetine or nortriptyline treatment.
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Evaluation of platelet activation in depressed patients with ischemic heart disease after paroxetine or nortriptyline treatment.

机译:帕罗西汀或去甲替林治疗后的缺血性心脏病抑郁患者的血小板活化评估。

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This study investigated the effects of antidepressant treatment on platelet activation in depressed patients with ischemic heart disease (IHD). Plasma levels of platelet alpha-granule release products beta-thromboglobulin (BTG) and platelet factor 4 (PF4) were measured in 17 depressed patients with IHD who were treated in a 6-week, double-blind trial with either paroxetine (10 patients) or nortriptyline (7 patients). Baseline measurements of BTG and PF4 were significantly elevated in both drug treatment groups before the initiation of antidepressant therapy compared with those of healthy control subjects. In the paroxetine group, mean PF4 and BTG levels significantly decreased from these elevated baseline values within 1 week of treatment and remained low at 3- and 6-week measurements. In contrast, the nortriptyline group did not exhibit a significant decrease in PF4 or BTG plasma levels after 1, 3, or 6 weeks of treatment. Therefore, platelet activation in depressed patients with IHD seems to be inhibited by the selective serotonin reuptake inhibitor paroxetine. The effect of paroxetine on PF4 and BTG plasma levels suggests that it may reduce platelet aggregation in vivo and may positively impact IHD-related mortality in this population.
机译:这项研究调查了抗抑郁药治疗对缺血性心脏病(IHD)抑郁症患者血小板活化的影响。在17例IHD抑郁症患者中进行了血浆α-颗粒释放产物β-血栓球蛋白(BTG)和血小板因子4(PF4)的血浆水平测定,这些患者在一项为期6周的双盲试验中接受了帕罗西汀的治疗(10例)或去甲替林(7例)。与健康对照组相比,在开始抗抑郁治疗之前,两个药物治疗组中BTG和PF4的基线测量值均显着升高。在帕罗西汀组中,平均PF4和BTG水平在治疗1周内从这些升高的基线值开始显着降低,而在3周和6周的测量中仍然较低。相反,去甲替林组在治疗1、3或6周后并未表现出PF4或BTG血浆水平的明显降低。因此,抑郁症的IHD患者的血小板活化似乎被选择性5-羟色胺再摄取抑制剂帕罗西汀抑制。帕罗西汀对PF4和BTG血浆水平的影响表明,它可能会降低体内的血小板聚集,并可能对该人群中与IHD相关的死亡率产生积极影响。

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