Proof-of-Concept Trial with the Neurosteroid Pregnenolone Targeting Cognitive and Negative Symptoms in Schizophrenia

被引:150
作者
Marx, Christine E. [1 ,2 ]
Keefe, Richard S. E.
Buchanan, Robert W. [3 ]
Hamer, Robert M. [4 ]
Kilts, Jason D. [2 ]
Bradford, Daniel W.
Strauss, Jennifer L. [2 ]
Naylor, Jennifer C. [2 ]
Payne, Victoria M. [2 ]
Lieberman, Jeffrey A. [5 ]
Savitz, Adam J. [6 ]
Leimone, Linda A. [2 ]
Dunn, Lawrence
Porcu, Patrizia [4 ]
Morrow, A. Leslie [4 ]
Shampine, Lawrence J. [2 ]
机构
[1] Duke Univ, Med Ctr, Dept Psychiat & Behav Sci, Durham VA Med Ctr, Durham, NC 27705 USA
[2] Vet Affairs Midatlantic Mental Illness Res Educ &, Durham, NC USA
[3] Univ Maryland, Maryland Psychiat Res Ctr, Baltimore, MD 21201 USA
[4] Univ N Carolina, Dept Psychiat, Chapel Hill, NC USA
[5] Columbia Univ, Dept Psychiat, Coll Phys & Surg, New York, NY USA
[6] Cornell Univ, Dept Psychiat, Weill Med Coll, New York, NY 10021 USA
关键词
schizophrenia; negative symptoms; cognitive symptoms; neurosteroid; pregnenolone; allopregnanolone; TRAUMATIC BRAIN-INJURY; D-ASPARTATE RECEPTOR; HIGH-DOSE GLYCINE; MICROTUBULE-ASSOCIATED PROTEIN-2; CYCLOSERINE ADJUVANT THERAPY; STEROID-HORMONE METABOLITES; LINKED-IMMUNOSORBENT-ASSAY; NEUROACTIVE STEROIDS; D-SERINE; BENZODIAZEPINE-RECEPTOR;
D O I
10.1038/npp.2009.26
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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. Neuropsychopharmacology (2009) 34, 1885-1903; doi: 10.1038/npp.2009.26; published online 1 April 2009
引用
收藏
页码:1885 / 1903
页数:19
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