Espadaler Jordi, Tuson Miquel, Lopez-Ibor Jose Miguel, Lopez-Ibor Franciso, Lopez-Ibor Maria Ines
1Innovation Department,AB-Biotics SA,Barcelona,Spain.
2Center Dr. Lopez-Ibor SA,Madrid,Spain.
CNS Spectr. 2017 Aug;22(4):315-324. doi: 10.1017/S1092852915000711. Epub 2016 Apr 21.
We investigated the association between clinical outcome and the recommendations of a pharmacogenetic test (Neuropharmagen) in patients with a variety of psychiatric conditions whose previous treatment regimen had failed.
This retrospective, naturalistic, multicenter study included adult psychiatric patients (depression, psychosis, anxiety, bipolar, etc.) who had been seen at 3 private clinics. All patients had received pharmacogenetic testing (Neuropharmagen) and were classified depending on whether or not their post-test treatment regimen followed the test recommendations. Clinical severity was assessed with the Clinical Global Impression of Severity (CGI-S) at baseline (pre-test) and 3-month follow-up, and adverse events were recorded.
182 patients were available for analysis. After multivariate adjustment, patients whose treatment followed the test recommendations had odds of improvement about 4 times greater than patients whose treatment did not follow the recommendations (adjusted OR=3.86, 95%CI 1.36-10.95; p=0.011). Importantly, psychiatric diagnosis did not significantly affect the odds of improvement. Also, in the subpopulation with baseline CGI-S score >3 (N=170), the rate of stabilization at follow-up (defined as CGI-S≤3) was significantly higher in patients whose treatment followed the pharmacogenetic recommendations (p=0.033). There was no apparent difference in the incidence of adverse events (6 patients in each group).
Non-drug naïve patients whose treatment followed the recommendations of pharmacogenetic testing were more likely to improve their condition than patients whose treatment did not. These results are consistent with previous clinical research on depressed patients, and this study also suggests that this benefit can be extended to psychiatric conditions other than depression.
我们调查了在多种精神疾病患者中,临床结局与药物遗传学检测(Neuropharmagen)建议之间的关联,这些患者既往的治疗方案均告失败。
这项回顾性、自然主义的多中心研究纳入了在3家私人诊所就诊的成年精神科患者(抑郁症、精神病、焦虑症、双相情感障碍等)。所有患者均接受了药物遗传学检测(Neuropharmagen),并根据检测后治疗方案是否遵循检测建议进行分类。在基线(检测前)和3个月随访时,使用临床总体严重程度印象量表(CGI-S)评估临床严重程度,并记录不良事件。
182例患者可供分析。经过多变量调整后,治疗遵循检测建议的患者病情改善的几率比治疗未遵循建议的患者高约4倍(调整后的OR=3.86,95%CI 1.36-10.95;p=0.011)。重要的是,精神科诊断对改善几率没有显著影响。此外,在基线CGI-S评分>3的亚组(N=170)中,治疗遵循药物遗传学建议的患者在随访时病情稳定的比例(定义为CGI-S≤3)显著更高(p=0.033)。不良事件的发生率在两组中没有明显差异(每组6例患者)。
治疗遵循药物遗传学检测建议的非初治患者比治疗未遵循建议的患者更有可能改善病情。这些结果与先前关于抑郁症患者的临床研究一致,并且这项研究还表明这种益处可以扩展到抑郁症以外的精神疾病。