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以神经甾体孕烯醇酮为靶点治疗精神分裂症认知和阴性症状的概念验证试验。

Proof-of-concept trial with the neurosteroid pregnenolone targeting cognitive and negative symptoms in schizophrenia.

作者信息

Marx Christine E, Keefe Richard S E, Buchanan Robert W, Hamer Robert M, Kilts Jason D, Bradford Daniel W, Strauss Jennifer L, Naylor Jennifer C, Payne Victoria M, Lieberman Jeffrey A, Savitz Adam J, Leimone Linda A, Dunn Lawrence, Porcu Patrizia, Morrow A Leslie, Shampine Lawrence J

机构信息

Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, NC 27705, USA.

出版信息

Neuropsychopharmacology. 2009 Jul;34(8):1885-903. doi: 10.1038/npp.2009.26. Epub 2009 Apr 1.

Abstract

The neurosteroid pregnenolone and its sulfated derivative enhance learning and memory in rodents. Pregnenolone sulfate also positively modulates NMDA receptors and could thus ameliorate hypothesized NMDA receptor hypofunction in schizophrenia. Furthermore, clozapine increases pregnenolone in rodent hippocampus, possibly contributing to its superior efficacy. We therefore investigated adjunctive pregnenolone for cognitive and negative symptoms in patients with schizophrenia or schizoaffective disorder receiving stable doses of second-generation antipsychotics in a pilot randomized, placebo-controlled, double-blind trial. Following a 2-week single-blind placebo lead-in, patients were randomized to pregnenolone (fixed escalating doses to 500 mg/day) or placebo, for 8 weeks. Primary end points were changes in BACS and MCCB composite and total SANS scores. Of 21 patients randomized, 18 completed at least 4 weeks of treatment (n=9/group). Pregnenolone was well tolerated. Patients receiving pregnenolone demonstrated significantly greater improvements in SANS scores (mean change=10.38) compared with patients receiving placebo (mean change=2.33), p=0.048. Mean composite changes in BACS and MCCB scores were not significantly different in patients randomized to pregnenolone compared with placebo. However, serum pregnenolone increases predicted BACS composite scores at 8 weeks in the pregnenolone group (r(s)=0.81, p=0.022). Increases in allopregnanolone, a GABAergic pregnenolone metabolite, also predicted BACS composite scores (r(s)=0.74, p=0.046). In addition, baseline pregnenolone (r(s)=-0.76, p=0.037), pregnenolone sulfate (r(s)=-0.83, p=0.015), and allopregnanolone levels (r(s)=-0.83, p=0.015) were inversely correlated with improvements in MCCB composite scores, further supporting a possible role for neurosteroids in cognition. Mean BACS and MCCB composite scores were correlated (r(s)=0.74, p<0.0001). Pregnenolone may be a promising therapeutic agent for negative symptoms and merits further investigation for cognitive symptoms in schizophrenia.

摘要

神经甾体孕烯醇酮及其硫酸化衍生物可增强啮齿动物的学习和记忆能力。硫酸孕烯醇酮还能正向调节N-甲基-D-天冬氨酸(NMDA)受体,因此可能改善精神分裂症中假设的NMDA受体功能减退。此外,氯氮平可增加啮齿动物海马体中的孕烯醇酮,这可能是其疗效更佳的原因之一。因此,在一项随机、安慰剂对照、双盲的先导试验中,我们研究了在接受稳定剂量第二代抗精神病药物治疗的精神分裂症或分裂情感性障碍患者中,添加孕烯醇酮对认知症状和阴性症状的影响。经过为期2周的单盲安慰剂导入期后,患者被随机分为接受孕烯醇酮(固定递增剂量至500毫克/天)或安慰剂治疗,为期8周。主要终点是贝克认知评估量表(BACS)和精神分裂症认知功能成套测验(MCCB)综合得分以及阴性症状评定量表(SANS)总分的变化。在随机分组的21例患者中(n = 9/组),18例完成了至少4周的治疗。孕烯醇酮耐受性良好。与接受安慰剂的患者相比,接受孕烯醇酮的患者SANS得分有显著更大的改善(平均变化 = 10.38),而接受安慰剂的患者平均变化 = 2.33,p = 0.048。与安慰剂组相比,随机接受孕烯醇酮的患者BACS和MCCB得分的平均综合变化无显著差异。然而,在孕烯醇酮组中,血清孕烯醇酮升高可预测8周时的BACS综合得分(r(s)=0.81,p = 0.022)。γ-氨基丁酸能孕烯醇酮代谢产物别孕烯醇酮的升高也可预测BACS综合得分(r(s)=0.74,p = 0.046)。此外,基线孕烯醇酮(r(s)= -0.76,p = 0.037)、硫酸孕烯醇酮(r(s)= -0.83,p = 0.015)和别孕烯醇酮水平(r(s)= -0.83,p = 0.015)与MCCB综合得分的改善呈负相关,进一步支持了神经甾体在认知方面可能发挥的作用。BACS和MCCB综合得分均值相关(r(s)=0.74,p<0.0001)。孕烯醇酮可能是治疗阴性症状的一种有前景的治疗药物,对于精神分裂症的认知症状值得进一步研究。

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