Task-related fMRI responses to a nicotinic acetylcholine receptor partial agonist in schizophrenia: A randomized trial

被引:9
作者
Barch, Deanna M. [1 ,3 ,9 ]
Marder, Stephen R. [2 ,10 ]
Harms, Michael P. [3 ]
Jarskog, L. Fredrik [4 ]
Buchanan, Robert W. [5 ]
Cronenwett, Will [6 ]
Chen, Li-Shiun [3 ]
Weiss, Markus [7 ]
Maguire, Ralph P. [7 ]
Pezous, Nicole [7 ]
Feuerbach, Dominik [7 ]
Lopez-Lopez, Cristina [7 ]
Johns, Donald R. [7 ]
Behrje, Rhett B. [7 ]
Gomez-Mancilla, Baltazar [7 ,8 ]
机构
[1] Washington Univ, Dept Psychol, St Louis, MO 63130 USA
[2] Univ Calif Los Angeles, Semel Inst Neurosci, Los Angeles, CA USA
[3] Washington Univ, Sch Med, Dept Psychiat, St Louis, MO 63110 USA
[4] Univ N Carolina, Dept Psychiat, Chapel Hill, NC USA
[5] Univ Maryland, Sch Med, Dept Psychiat, Maryland Psychiat Res Ctr, Baltimore, MD 21201 USA
[6] Northwestern Univ, Feinberg Sch Med, Dept Psychiat & Behav Sci, Chicago, IL 60611 USA
[7] Novartis Pharma AG, Basel, Switzerland
[8] McGill Univ, Dept Neurol & Neurosurg, Montreal, PQ, Canada
[9] Washington Univ, Sch Med, Dept Radiol, St Louis, MO 63110 USA
[10] VA Desert Pacific Mental Illness Res Educ & Clin, Los Angeles, CA USA
关键词
AQW051; Clinical trial; Functional magnetic resonance imaging; Nicotinic acetylcholine receptor (nAChR); Schizophrenia; WORKING-MEMORY; IMAGING BIOMARKERS; ACTIVATION; COGNITION; DEFICITS; HEALTHY;
D O I
10.1016/j.pnpbp.2016.06.013
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: AQW051, an alpha 7-nicotinic acetylcholine receptor partial agonist, enhanced cognitive function in rodent models of learning and memory. This study evaluated brain activation during performance of a working memory task (WMT) and an episodic memory task (EMT), and the effect of AQW051 on task-related brain activation and performance in subjects with schizophrenia. Methods: This was a double-blind, randomized, placebo-controlled, multicenter, 2-period cross-over trial (NCT00825539) in participants with chronic, stable schizophrenia. Participants, stratified according to smoking status, were randomized (1: 1: 1: 1: 1: 1) to 1 of 6 sequence groups that determined the study drug dose (AQW051 7.5 mg, 50 mg or 100 mg) and order of administration versus placebo. The primary outcome was brain activation in a priori target regions of interest (ROIs) during performance of the WMT and EMT, measured using functional magnetic resonance imaging. The effect of AQW051 on task-related (EMT and WMT) brain activation and performance was also assessed, as were safety and tolerability. Results: Overall, 60 of 68 enrolled participants completed the study (AQW051 then placebo: 7.5 mg n = 9; 50 mg n = 11; 100 mg n = 10. Placebo then AQW051: 7.5 mg n = 10; 50 mg n = 11; 100 mg n = 9). Significant task-related brain activation (5% significance level) was observed with placebo. During the WMT, a medium effect size was observed in the inferior prefrontal cortex with AQW051 100 mg versus placebo (0.431; p = 0.105). During the EMT encoding phase, a large effect size was observed in the anterior hippocampus (0.795; p = 0.007) and a medium effect size in the posterior hippocampus (0.476; p = 0.079) with AQW051 7.5 mg. No other medium/large effect sizes were observed with any dose on either task. Effects on brain activation were generally not associated with changes in cognitive performance. AQW051 was well tolerated with an acceptable safety profile. Conclusions: Overall, no consistent effects of AQW051 on brain regions involved in the performance of aWMT or EMT were observed; however, this study presents a model for evaluating potential response to pharmacological interventions for cognitive impairment in schizophrenia. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:66 / 75
页数:10
相关论文
共 30 条
[1]  
[Anonymous], NEUROPSYCHOPHARMACOL
[2]   Working Memory Encoding and Maintenance Deficits in Schizophrenia: Neural Evidence for Activation and Deactivation Abnormalities [J].
Anticevic, Alan ;
Repovs, Grega ;
Barch, Deanna M. .
SCHIZOPHRENIA BULLETIN, 2013, 39 (01) :168-178
[3]  
Barch D.M., 2000, NEUROIMAGE, V11, pS193, DOI DOI 10.1016/S1053-8119(00)91126-1
[4]   Abnormal parietal cortex activation during working memory in schizophrenia: Verbal phonological coding disturbances versus domain-general executive dysfunction [J].
Barch, Deanna M. ;
Csernansky, John G. .
AMERICAN JOURNAL OF PSYCHIATRY, 2007, 164 (07) :1090-1098
[5]   CNTRICS Imaging Biomarkers Selection: Working Memory [J].
Barch, Deanna M. ;
Moore, Holly ;
Nee, Derek E. ;
Manoach, Dara S. ;
Luck, Steven J. .
SCHIZOPHRENIA BULLETIN, 2012, 38 (01) :43-52
[6]   Abnormal regulation of high affinity nicotinic receptors in subjects with schizophrenia [J].
Breese, CR ;
Lee, MJ ;
Adams, CE ;
Sullivan, B ;
Logel, J ;
Gillen, KM ;
Marks, MJ ;
Collins, AC ;
Leonard, S .
NEUROPSYCHOPHARMACOLOGY, 2000, 23 (04) :351-364
[7]   Imaging Biomarkers for Treatment Development for Impaired Cognition: Report of the Sixth CNTRICS Meeting: Biomarkers Recommended for Further Development [J].
Carter, Cameron S. ;
Barch, Deanna M. .
SCHIZOPHRENIA BULLETIN, 2012, 38 (01) :26-33
[8]   Cognitive Neuroscience Treatment Research to Improve Cognition in Schizophrenia II: Developing Imaging Biomarkers to Enhance Treatment Development for Schizophrenia and Related Disorders [J].
Carter, Cameron S. ;
Barch, Deanna M. ;
Bullmore, Edward T. ;
Breiling, James ;
Buchanan, Robert W. ;
Butler, Pamela ;
Cohen, Jonathan D. ;
Geyer, Mark ;
Gollub, Randy ;
Green, Michael F. ;
Jaeger, Judith ;
Krystal, John H. ;
Moore, Holly ;
Nuechterlein, Keith ;
Robbins, Trevor ;
Silverstein, Steven ;
Smith, Edward E. ;
Strauss, Milton ;
Wykes, Til .
BIOLOGICAL PSYCHIATRY, 2011, 70 (01) :7-12
[9]   Temporal dynamics of brain activation during a working memory task [J].
Cohen, JD ;
Perlstein, WM ;
Braver, TS ;
Nystrom, LE ;
Noll, DC ;
Jonides, J ;
Smith, EE .
NATURE, 1997, 386 (6625) :604-608
[10]   AQW051, a novel, potent and selective α7 nicotinic ACh receptor partial agonist: pharmacological characterization and phase I evaluation [J].
Feuerbach, Dominik ;
Pezous, Nicole ;
Weiss, Markus ;
Shakeri-Nejad, Kasra ;
Lingenhoehl, Kurt ;
Hoyer, Daniel ;
Hurth, Konstanze ;
Bilbe, Graeme ;
Pryce, Christopher R. ;
McAllister, Kevin ;
Chaperon, Frederique ;
Kucher, Klaus ;
Johns, Donald ;
Blaettler, Thomas ;
Lopez Lopez, Cristina .
BRITISH JOURNAL OF PHARMACOLOGY, 2015, 172 (05) :1292-1304