Title: Proof-of-concept randomized controlled trial of pregnenolone in schizophrenia
year: 2014
Journal: Psychopharmacology (Berl)
Volume: 231
Issue: 17
Pages: 3647-62
Epubdate: 18/07/2014
date: Sep
Alternate Journal: Psychopharmacology
ISSN: 0033-3158
DOI: 10.1007/s00213-014-3673-4
Accession Number: 25030803
Abstract: RATIONALE: Preclinical and clinical data suggest that pregnenolone may be a promising therapeutic in schizophrenia. Pregnenolone is neuroprotective and enhances learning and memory, myelination, and microtubule polymerization. Treatment with pregnenolone elevates allopregnanolone (a neurosteroid that enhances GABAA receptor responses) and pregnenolone sulfate (a positive NMDA receptor modulator). Pregnenolone could thus potentially mitigate GABA dysregulation and/or NMDA receptor hypofunction in schizophrenia via metabolism to other neurosteroids. OBJECTIVE: The objective of this study is to conduct a randomized controlled trial of adjunctive pregnenolone in schizophrenia. METHODS: Following a placebo lead-in, 120 participants were randomized to pregnenolone or placebo for 8 weeks (Institute for Mental Health, Singapore). Primary endpoints were changes in MATRICS Consensus Cognitive Battery (MCCB) composite scores (cognitive symptoms), UCSD Performance-based Skills Assessment-Brief (UPSA-B) composite scores (functional capacity), and Scale for Assessment of Negative Symptoms (SANS) total scores (negative symptoms). A modified intent-to-treat analysis approach was utilized. RESULTS: No significant changes compared to placebo were demonstrated in composite MCCB scores. In contrast, participants randomized to pregnenolone (n = 56) demonstrated greater improvements in functional capacity (UPSA-B composite changes) compared to placebo (n = 55), p = 0.03. Pregnenolone was also superior to placebo in the communication subscale of the UPSA-B (p < 0.001). Serum pregnenolone changes post-treatment were correlated with UPSA-B composite score changes in females (r s = 0.497, p < 0.042, n = 17) but not in males. Mean total SANS scores were very low at baseline and did not improve further post-treatment. Pregnenolone was well-tolerated. CONCLUSIONS: Pregnenolone improved functional capacity in participants with schizophrenia, but did not improve cognitive symptoms over an 8-week treatment period. Neurosteroid changes correlated with functional improvements in female participants. Neurosteroid interventions may exhibit promise as new therapeutic leads for schizophrenia.
Notes: 1432-2072
Marx, Christine E
Lee, Jimmy
Subramaniam, Mythily
Rapisarda, Attilio
Bautista, Dianne C T
Chan, Edwin
Kilts, Jason D
Buchanan, Robert W
Wai, Eu Pui
Verma, Swapna
Sim, Kang
Hariram, Jayaraman
Jacob, Rajesh
Keefe, Richard S E
Chong, Siow Ann
Journal Article
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.
Germany
Psychopharmacology (Berl). 2014 Sep
231(17):3647-62. doi: 10.1007/s00213-014-3673-4. Epub 2014 Jul 17.
URI: https://open-access.imh.com.sg/handle/123456789/4724
Authors Address: Psychiatry & Behavioral Sciences, Duke University Medical Center, Durham, NC, USA, christine.marx@duke.edu.
Translated author: NLM
Translated title: eng
Appears in Collections:2014

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