The Cognitive and Negative Symptoms in Schizophrenia Trial (CONSIST): The Efficacy of Glutamatergic Agents for Negative Symptoms and Cognitive Impairments
Objective: Patients with schizophrenia frequently present with negative symptoms and cognitive impairments for which no effective treatments are known. Agents that act at the glycine site of the N -methyl- d -aspartic acid (NMDA) glutamatergic receptor have been suggested as promising treatments for...
Saved in:
Published in | The American journal of psychiatry Vol. 164; no. 10; pp. 1593 - 1602 |
---|---|
Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Washington, DC
American Psychiatric Association
01.10.2007
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Objective:
Patients with schizophrenia frequently present with negative symptoms and cognitive impairments for which no effective treatments are known. Agents that act at the glycine site of the
N
-methyl-
d
-aspartic acid (NMDA) glutamatergic receptor have been suggested as promising treatments for moderate to severe negative symptoms and cognitive impairments.
Method:
The Cognitive and Negative Symptoms in Schizophrenia Trial (CONSIST) was a 16-week double-blind, double-dummy, parallel group, randomized clinical trial of adjunctive glycine,
d
-cycloserine, or placebo conducted at four sites in the United States and one site in Israel. The participants were 157 inpatients and outpatients who met DSM-IV criteria for schizophrenia or schizoaffective disorder and retrospective and prospective criteria for moderate to severe negative symptoms without marked positive, depressive, or extrapyramidal symptoms. The primary outcome measures were the average "rate of change" of Scale for the Assessment of Negative Symptoms (SANS) total scores and change in the average cognitive domain z scores.
Results:
There were no significant differences in change in the SANS total score between glycine and placebo subjects or
d
-cycloserine and placebo subjects. A prespecified test for the site-by-treatment-by-time interaction was significant in post hoc tests. One site had greater reduction in the SANS total score for patients receiving
d
-cycloserine relative to patients receiving placebo. A second site had greater reduction in the SANS total score for placebo patients compared with glycine patients. There were no significant differences between glycine and placebo or
d
-cycloserine and placebo subjects on the average cognition z score.
Conclusions:
The study results suggest that neither glycine nor
d
-cycloserine is a generally effective therapeutic option for treating negative symptoms or cognitive impairments. |
---|---|
AbstractList | Patients with schizophrenia frequently present with negative symptoms and cognitive impairments for which no effective treatments are known. Agents that act at the glycine site of the N-methyl-D-aspartic acid (NMDA) glutamatergic receptor have been suggested as promising treatments for moderate to severe negative symptoms and cognitive impairments. The Cognitive and Negative Symptoms in Schizophrenia Trial (CONSIST) was a 16-week double-blind, double-dummy, parallel group, randomized clinical trial of adjunctive glycine, D-cycloserine, or placebo conducted at four sites in the United States and one site in Israel. The participants were 157 inpatients and outpatients who met DSM-IV criteria for schizophrenia or schizoaffective disorder and retrospective and prospective criteria for moderate to severe negative symptoms without marked positive, depressive, or extrapyramidal symptoms. The primary outcome measures were the average "rate of change" of Scale for the Assessment of Negative Symptoms (SANS) total scores and change in the average cognitive domain z scores. There were no significant differences in change in the SANS total score between glycine and placebo subjects or D-cycloserine and placebo subjects. A prespecified test for the site-by-treatment-by-time interaction was significant in post hoc tests. One site had greater reduction in the SANS total score for patients receiving D-cycloserine relative to patients receiving placebo. A second site had greater reduction in the SANS total score for placebo patients compared with glycine patients. There were no significant differences between glycine and placebo or D-cycloserine and placebo subjects on the average cognition z score. The study results suggest that neither glycine nor D-cycloserine is a generally effective therapeutic option for treating negative symptoms or cognitive impairments. OBJECTIVE: Patients with schizophrenia frequently present with negative symptoms and cognitive impairments for which no effective treatments are known. Agents that act at the glycine site of the N-methyl-D-aspartic acid (NMDA) glutamatergic receptor have been suggested as promising treatments for moderate to severe negative symptoms and cognitive impairments. METHOD: The Cognitive and Negative Symptoms in Schizophrenia Trial (CONSIST) was a 16-week double-blind, double-dummy, parallel group, randomized clinical trial of adjunctive glycine, D-cycloserine, or placebo conducted at four sites in the United States and one site in Israel. The participants were 157 inpatients and outpatients who met DSM-IV criteria for schizophrenia or schizoaffective disorder and retrospective and prospective criteria for moderate to severe negative symptoms without marked positive, depressive, or extrapyramidal symptoms. The primary outcome measures were the average "rate of change" of Scale for the Assessment of Negative Symptoms (SANS) total scores and change in the average cognitive domain z scores. RESULTS: There were no significant differences in change in the SANS total score between glycine and placebo subjects or D-cycloserine and placebo subjects. A prespecified test for the site-by-treatment-by-time interaction was significant in post hoc tests. One site had greater reduction in the SANS total score for patients receiving D-cycloserine relative to patients receiving placebo. A second site had greater reduction in the SANS total score for placebo patients compared with glycine patients. There were no significant differences between glycine and placebo or D-cycloserine and placebo subjects on the average cognition z score. CONCLUSIONS: The study results suggest that neither glycine nor D-cycloserine is a generally effective therapeutic option for treating negative symptoms or cognitive impairments. Objective: Patients with schizophrenia frequently present with negative symptoms and cognitive impairments for which no effective treatments are known. Agents that act at the glycine site of the N -methyl- d -aspartic acid (NMDA) glutamatergic receptor have been suggested as promising treatments for moderate to severe negative symptoms and cognitive impairments. Method: The Cognitive and Negative Symptoms in Schizophrenia Trial (CONSIST) was a 16-week double-blind, double-dummy, parallel group, randomized clinical trial of adjunctive glycine, d -cycloserine, or placebo conducted at four sites in the United States and one site in Israel. The participants were 157 inpatients and outpatients who met DSM-IV criteria for schizophrenia or schizoaffective disorder and retrospective and prospective criteria for moderate to severe negative symptoms without marked positive, depressive, or extrapyramidal symptoms. The primary outcome measures were the average "rate of change" of Scale for the Assessment of Negative Symptoms (SANS) total scores and change in the average cognitive domain z scores. Results: There were no significant differences in change in the SANS total score between glycine and placebo subjects or d -cycloserine and placebo subjects. A prespecified test for the site-by-treatment-by-time interaction was significant in post hoc tests. One site had greater reduction in the SANS total score for patients receiving d -cycloserine relative to patients receiving placebo. A second site had greater reduction in the SANS total score for placebo patients compared with glycine patients. There were no significant differences between glycine and placebo or d -cycloserine and placebo subjects on the average cognition z score. Conclusions: The study results suggest that neither glycine nor d -cycloserine is a generally effective therapeutic option for treating negative symptoms or cognitive impairments. Patients with schizophrenia frequently present with negative symptoms and cognitive impairments for which no effective treatments are known. Agents that act at the glycine site of the N-methyl-D-aspartic acid (NMDA) glutamatergic receptor have been suggested as promising treatments for moderate to severe negative symptoms and cognitive impairments. The Cognitive and Negative Symptoms in Schizophrenia Trial (CONSIST) was a 16-week double-blind, double-dummy, parallel group, randomized clinical trial of adjunctive glycine, D-cycloserine, or placebo conducted at four sites in the United States and one site in Israel. The participants were 157 inpatients and outpatients who met DSM-IV criteria for schizophrenia or schizoaffective disorder and retrospective and prospective criteria for moderate to severe negative symptoms without marked positive, depressive, or extrapyramidal symptoms. The primary outcome measures were the average "rate of change" of Scale for the Assessment of Negative Symptoms (SANS) total scores and change in the average cognitive domain z scores. There were no significant differences in change in the SANS total score between glycine and placebo subjects or D-cycloserine and placebo subjects. A prespecified test for the site-by-treatment-by-time interaction was significant in post hoc tests. One site had greater reduction in the SANS total score for patients receiving D-cycloserine relative to patients receiving placebo. A second site had greater reduction in the SANS total score for placebo patients compared with glycine patients. There were no significant differences between glycine and placebo or D-cycloserine and placebo subjects on the average cognition z score. The study results suggest that neither glycine nor D-cycloserine is a generally effective therapeutic option for treating negative symptoms or cognitive impairments. Patients with schizophrenia frequently present with negative symptoms and cognitive impairments for which no effective treatments are known. Agents that act at the glycine site of the N-methyl-D-aspartic acid (NMDA) glutamatergic receptor have been suggested as promising treatments for moderate to severe negative symptoms and cognitive impairments.OBJECTIVEPatients with schizophrenia frequently present with negative symptoms and cognitive impairments for which no effective treatments are known. Agents that act at the glycine site of the N-methyl-D-aspartic acid (NMDA) glutamatergic receptor have been suggested as promising treatments for moderate to severe negative symptoms and cognitive impairments.The Cognitive and Negative Symptoms in Schizophrenia Trial (CONSIST) was a 16-week double-blind, double-dummy, parallel group, randomized clinical trial of adjunctive glycine, D-cycloserine, or placebo conducted at four sites in the United States and one site in Israel. The participants were 157 inpatients and outpatients who met DSM-IV criteria for schizophrenia or schizoaffective disorder and retrospective and prospective criteria for moderate to severe negative symptoms without marked positive, depressive, or extrapyramidal symptoms. The primary outcome measures were the average "rate of change" of Scale for the Assessment of Negative Symptoms (SANS) total scores and change in the average cognitive domain z scores.METHODThe Cognitive and Negative Symptoms in Schizophrenia Trial (CONSIST) was a 16-week double-blind, double-dummy, parallel group, randomized clinical trial of adjunctive glycine, D-cycloserine, or placebo conducted at four sites in the United States and one site in Israel. The participants were 157 inpatients and outpatients who met DSM-IV criteria for schizophrenia or schizoaffective disorder and retrospective and prospective criteria for moderate to severe negative symptoms without marked positive, depressive, or extrapyramidal symptoms. The primary outcome measures were the average "rate of change" of Scale for the Assessment of Negative Symptoms (SANS) total scores and change in the average cognitive domain z scores.There were no significant differences in change in the SANS total score between glycine and placebo subjects or D-cycloserine and placebo subjects. A prespecified test for the site-by-treatment-by-time interaction was significant in post hoc tests. One site had greater reduction in the SANS total score for patients receiving D-cycloserine relative to patients receiving placebo. A second site had greater reduction in the SANS total score for placebo patients compared with glycine patients. There were no significant differences between glycine and placebo or D-cycloserine and placebo subjects on the average cognition z score.RESULTSThere were no significant differences in change in the SANS total score between glycine and placebo subjects or D-cycloserine and placebo subjects. A prespecified test for the site-by-treatment-by-time interaction was significant in post hoc tests. One site had greater reduction in the SANS total score for patients receiving D-cycloserine relative to patients receiving placebo. A second site had greater reduction in the SANS total score for placebo patients compared with glycine patients. There were no significant differences between glycine and placebo or D-cycloserine and placebo subjects on the average cognition z score.The study results suggest that neither glycine nor D-cycloserine is a generally effective therapeutic option for treating negative symptoms or cognitive impairments.CONCLUSIONSThe study results suggest that neither glycine nor D-cycloserine is a generally effective therapeutic option for treating negative symptoms or cognitive impairments. |
Author | Javitt, Daniel C. Marder, Stephen R. Buchanan, Robert W. Heresco-Levy, Uriel Carpenter, William T. Schooler, Nina R. McMahon, Robert P. Gold, James M. |
Author_xml | – sequence: 1 givenname: Robert W. surname: Buchanan fullname: Buchanan, Robert W. – sequence: 2 givenname: Daniel C. surname: Javitt fullname: Javitt, Daniel C. – sequence: 3 givenname: Stephen R. surname: Marder fullname: Marder, Stephen R. – sequence: 4 givenname: Nina R. surname: Schooler fullname: Schooler, Nina R. – sequence: 5 givenname: James M. surname: Gold fullname: Gold, James M. – sequence: 6 givenname: Robert P. surname: McMahon fullname: McMahon, Robert P. – sequence: 7 givenname: Uriel surname: Heresco-Levy fullname: Heresco-Levy, Uriel – sequence: 8 givenname: William T. surname: Carpenter fullname: Carpenter, William T. |
BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19142090$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/17898352$$D View this record in MEDLINE/PubMed |
BookMark | eNqFkstqGzEUhkVJaZy0rxBEoaVd2NVlLprSTTBpagjJwi50J85oJFtmRppIMwX3Ufq0nYmdBELBK3HQ95_rf4ZOnHcaoQtKZpTm2RdoWzuDbTtjhOQzkhFBeSpeoQlNeTrNGRMnaEIIYdMi5b9O0VmM2yEkPGdv0CnNRSF4yibo72qj8dyvne3sb43BVfhWr-EhWO6atvNNxNbhpdrYP77dBO0s4FWwUONP87vb5WK5-vwVj1mujLEK1A57g6_rvoMGOh3WVuHLtXZdxMaH_yQfSz43sGhasKEZ-bfotYE66neH9xz9_H61mv-Y3txdL-aXN1NISd5NlcmrEpIqNwBZBSknig3bKErDK10mpMpSQ0UiuMhZlnKlSqqI0VoVKiWiIvwcfdznbYO_73XsZGOj0nUNTvs-ykxwWiQsOwoyklCWsWQA378At74PbhhCsgEqBCnYAF0coL5sdCXbYBsIO_l4mwH4cAAgKqhNAKdsfOYKmjBSjP1_23Mq-BiDNlLZbliyd10AW0tK5GgZOVpGDpaRo2Xko2UGefZC_lThmJDvhQ__TxMeUf0DrSPY_w |
CODEN | AJPSAO |
CitedBy_id | crossref_primary_10_1016_j_schres_2013_08_020 crossref_primary_10_1016_j_euroneuro_2012_09_008 crossref_primary_10_3928_00485713_20180308_01 crossref_primary_10_1176_appi_focus_18309 crossref_primary_10_1016_j_nicl_2022_103119 crossref_primary_10_1038_npp_2011_181 crossref_primary_10_1016_j_biopsych_2010_09_052 crossref_primary_10_1038_npp_2008_200 crossref_primary_10_1152_jn_00481_2016 crossref_primary_10_1016_j_jpsychires_2017_11_004 crossref_primary_10_1038_nrd3893 crossref_primary_10_1517_14656566_2016_1149164 crossref_primary_10_1586_ern_12_60 crossref_primary_10_1517_14728214_13_3_479 crossref_primary_10_2217_npy_11_58 crossref_primary_10_1016_j_schres_2018_02_003 crossref_primary_10_1093_schbul_sbu151 crossref_primary_10_1016_j_psychres_2015_08_040 crossref_primary_10_1016_j_pscychresns_2009_03_004 crossref_primary_10_1111_bph_13919 crossref_primary_10_3109_15622975_2015_1117654 crossref_primary_10_1517_14728214_2011_556112 crossref_primary_10_3390_bs12030060 crossref_primary_10_5042_mhrj_2010_0368 crossref_primary_10_3390_molecules24203709 crossref_primary_10_1002_brb3_1383 crossref_primary_10_3390_biom10060947 crossref_primary_10_1038_npp_2010_129 crossref_primary_10_1016_j_schres_2012_10_001 crossref_primary_10_1016_j_euroneuro_2015_04_014 crossref_primary_10_1093_schbul_sbq002 crossref_primary_10_1007_s00406_015_0596_y crossref_primary_10_1177_0269881114565806 crossref_primary_10_1002_hup_2758 crossref_primary_10_1016_j_chc_2008_06_010 crossref_primary_10_1016_j_euroneuro_2009_02_004 crossref_primary_10_1016_j_schres_2012_02_018 crossref_primary_10_1016_j_psychres_2018_09_006 crossref_primary_10_1517_13543784_2016_1121995 crossref_primary_10_1016_j_schres_2012_02_014 crossref_primary_10_1016_j_schres_2016_02_014 crossref_primary_10_1038_s41537_018_0064_6 crossref_primary_10_1073_pnas_1113793109 crossref_primary_10_1016_j_schres_2011_01_011 crossref_primary_10_1038_npp_2010_156 crossref_primary_10_1038_s41398_024_03221_2 crossref_primary_10_1016_j_pbb_2011_03_011 crossref_primary_10_1038_s41398_022_02253_w crossref_primary_10_3371_CSRP_4_3_6 crossref_primary_10_1016_j_pnpbp_2016_02_008 crossref_primary_10_1111_j_1751_7893_2009_00142_x crossref_primary_10_3389_fpsyt_2021_514579 crossref_primary_10_1016_S0140_6736_21_01730_X crossref_primary_10_1016_j_biopsych_2010_08_024 crossref_primary_10_3389_fpsyt_2019_00093 crossref_primary_10_1002_j_2051_5545_2008_tb00181_x crossref_primary_10_1097_JCP_0000000000001388 crossref_primary_10_2217_npy_11_35 crossref_primary_10_1007_s40263_014_0146_6 crossref_primary_10_1017_S1092852914000601 crossref_primary_10_31887_DCNS_2010_12_3_jcoyle crossref_primary_10_1093_ijnp_pyae066 crossref_primary_10_1016_j_pbb_2011_08_023 crossref_primary_10_1159_000494495 crossref_primary_10_1038_mp_2012_47 crossref_primary_10_1093_schbul_sbp125 crossref_primary_10_1017_S1748232107000134 crossref_primary_10_1002_jclp_20614 crossref_primary_10_1111_bcp_12015 crossref_primary_10_1016_j_schres_2010_10_023 crossref_primary_10_1016_j_schres_2019_01_024 crossref_primary_10_1007_s00213_013_3260_0 crossref_primary_10_1097_JCP_0000000000001397 crossref_primary_10_1016_j_bbr_2010_09_030 crossref_primary_10_1016_j_pnpbp_2024_110991 crossref_primary_10_1016_j_talanta_2015_03_032 crossref_primary_10_1007_s00213_014_3643_x crossref_primary_10_1016_j_schres_2016_05_014 crossref_primary_10_1038_s41386_023_01560_0 crossref_primary_10_5402_2012_427267 crossref_primary_10_1177_0269881118822157 crossref_primary_10_1016_j_schres_2016_05_015 crossref_primary_10_1371_journal_pone_0214314 crossref_primary_10_1097_JCP_0b013e318204825b crossref_primary_10_1093_schbul_sbt143 crossref_primary_10_1111_bdi_12202 crossref_primary_10_3390_biom12070909 crossref_primary_10_1016_j_psychres_2015_05_039 crossref_primary_10_1016_j_tips_2010_05_004 crossref_primary_10_1038_s41537_019_0090_z crossref_primary_10_1016_j_neubiorev_2017_04_005 crossref_primary_10_1007_s00702_020_02284_x crossref_primary_10_1007_s12640_010_9210_2 crossref_primary_10_1016_j_biopsych_2010_10_015 crossref_primary_10_1016_j_schres_2013_01_001 crossref_primary_10_1038_s41398_020_00875_6 crossref_primary_10_1186_s12888_019_2306_1 crossref_primary_10_1177_0269881119889296 crossref_primary_10_1186_s13020_023_00746_4 crossref_primary_10_1113_JP280875 crossref_primary_10_1016_j_psc_2012_06_008 crossref_primary_10_1093_schbul_sbt158 crossref_primary_10_1097_JCP_0000000000000720 crossref_primary_10_1016_j_cpr_2009_01_001 crossref_primary_10_1093_schbul_sbx192 crossref_primary_10_1017_S1461145709990939 crossref_primary_10_1097_JCP_0000000000001253 crossref_primary_10_1016_j_psiq_2011_10_010 crossref_primary_10_1001_jamapsychiatry_2018_2475 crossref_primary_10_1016_j_biopsych_2016_11_014 crossref_primary_10_1016_j_biopsych_2007_09_017 crossref_primary_10_1517_14656566_2015_1032248 crossref_primary_10_1108_AMHID_10_2015_0049 crossref_primary_10_1016_j_pnpbp_2019_02_001 crossref_primary_10_1016_j_schres_2012_10_012 crossref_primary_10_1016_j_ddstr_2008_10_001 crossref_primary_10_1016_j_schres_2023_04_010 crossref_primary_10_1097_FBP_0b013e32833a5bcb crossref_primary_10_1016_j_ebiom_2019_11_029 crossref_primary_10_1080_15504263_2018_1549764 crossref_primary_10_3389_fpsyt_2014_00032 crossref_primary_10_1016_S2215_0366_15_00098_X crossref_primary_10_1007_s11055_022_01284_6 crossref_primary_10_1016_j_biopsych_2008_06_011 crossref_primary_10_1186_s12888_017_1410_3 crossref_primary_10_1093_schbul_sbw193 crossref_primary_10_1016_j_schres_2011_06_001 crossref_primary_10_1016_j_jpsychires_2012_03_015 crossref_primary_10_1007_s00213_016_4291_0 crossref_primary_10_1093_ijnp_pyv102 crossref_primary_10_1016_j_schres_2008_06_003 crossref_primary_10_1016_j_drudis_2009_05_002 crossref_primary_10_1016_j_pharmthera_2015_06_008 crossref_primary_10_17116_jnevro202112108137 crossref_primary_10_1016_j_bpsc_2018_02_002 crossref_primary_10_1186_s12974_014_0151_1 crossref_primary_10_4062_biomolther_2012_20_1_001 crossref_primary_10_1517_14728220802507852 crossref_primary_10_1016_j_neuropharm_2013_08_038 crossref_primary_10_1016_j_schres_2015_04_008 crossref_primary_10_1590_S0100_879X2009001100002 crossref_primary_10_1002_wps_20026 crossref_primary_10_1038_s41398_021_01477_6 crossref_primary_10_5455_bcp_20140918102748 crossref_primary_10_1007_s00213_019_5188_5 crossref_primary_10_1016_j_acthis_2020_151531 crossref_primary_10_1038_s41380_024_02645_y crossref_primary_10_3389_fnins_2021_641047 crossref_primary_10_3390_biomedicines13030540 crossref_primary_10_1016_j_jpba_2017_02_052 crossref_primary_10_1038_mp_2015_28 crossref_primary_10_1016_j_pnpbp_2021_110436 crossref_primary_10_1016_j_euroneuro_2013_10_010 crossref_primary_10_1038_s41398_021_01540_2 crossref_primary_10_1093_schbul_sbs012 crossref_primary_10_1517_13543784_2014_933806 crossref_primary_10_1007_s15016_022_9404_x crossref_primary_10_2174_1570159X18666200303104235 crossref_primary_10_1002_brb3_978 crossref_primary_10_1002_syn_20760 crossref_primary_10_1111_j_1744_6163_2012_00333_x crossref_primary_10_1016_j_jchromb_2015_04_040 crossref_primary_10_1254_fpj_136_128 crossref_primary_10_1016_j_bmcl_2013_01_006 crossref_primary_10_1097_YCO_0b013e328329cd73 crossref_primary_10_1007_s00213_008_1302_9 crossref_primary_10_1016_j_jpsychires_2013_01_011 crossref_primary_10_1016_j_psiq_2010_01_005 crossref_primary_10_1016_S2215_0366_18_30050_6 crossref_primary_10_1016_j_psychres_2016_07_018 crossref_primary_10_1007_s00213_010_1802_2 crossref_primary_10_1016_j_psychres_2019_06_041 crossref_primary_10_1016_S0013_7006_16_30010_0 crossref_primary_10_2165_11586650_000000000_00000 crossref_primary_10_1016_j_euroneuro_2008_06_005 crossref_primary_10_1111_j_1399_5618_2009_00716_x crossref_primary_10_1073_pnas_1208494109 crossref_primary_10_1097_01_PSYPHR_0000433989_65396_2b crossref_primary_10_1016_j_jpsychires_2018_07_006 crossref_primary_10_1177_20451253221110014 crossref_primary_10_1016_j_biopsych_2024_08_019 crossref_primary_10_1016_j_biopsych_2008_09_017 crossref_primary_10_1007_s40501_024_00324_x crossref_primary_10_1016_j_schres_2014_12_026 crossref_primary_10_1016_j_neuropharm_2019_05_009 crossref_primary_10_1016_j_schres_2014_01_016 crossref_primary_10_1586_14737175_2014_864237 crossref_primary_10_1586_14737175_9_1_55 crossref_primary_10_3390_ijms22094467 crossref_primary_10_1016_j_euroneuro_2012_03_006 crossref_primary_10_1016_j_ebiom_2024_105045 crossref_primary_10_1017_S0033291715000306 crossref_primary_10_1016_j_schres_2014_04_037 crossref_primary_10_1016_j_schres_2017_02_027 crossref_primary_10_3389_fpsyt_2017_00177 crossref_primary_10_2174_1568026619666191011095341 crossref_primary_10_1016_j_schres_2023_07_010 crossref_primary_10_1016_j_brainres_2014_01_050 crossref_primary_10_1016_j_schres_2011_05_004 crossref_primary_10_1042_CS20170964 crossref_primary_10_1017_S1461145713000928 crossref_primary_10_1093_schbul_sbr153 crossref_primary_10_1016_j_schres_2018_04_025 crossref_primary_10_3390_jcm11123255 crossref_primary_10_1093_schbul_sbw046 crossref_primary_10_1097_YCO_0000000000000152 crossref_primary_10_1038_clpt_2011_154 crossref_primary_10_1016_j_schres_2020_02_012 crossref_primary_10_1097_WNF_0b013e31816f2795 crossref_primary_10_1177_1049731509355812 crossref_primary_10_1038_mp_2015_68 crossref_primary_10_1177_0269881110391123 crossref_primary_10_1016_j_ejphar_2012_02_033 crossref_primary_10_3390_ijms251910668 crossref_primary_10_3389_fpsyt_2018_00091 crossref_primary_10_1002_syn_20842 crossref_primary_10_1007_s00213_016_4318_6 crossref_primary_10_1016_j_psychres_2009_11_008 crossref_primary_10_1016_j_schres_2013_07_026 crossref_primary_10_1111_j_1476_5381_2011_01638_x crossref_primary_10_1002_hup_2384 crossref_primary_10_1016_j_psychres_2013_03_020 crossref_primary_10_1007_s11920_008_0056_8 crossref_primary_10_2147_NDT_S225643 crossref_primary_10_1016_j_pbb_2011_03_023 crossref_primary_10_1016_j_coph_2014_12_004 crossref_primary_10_1038_npp_2017_176 crossref_primary_10_1124_pr_109_002451 crossref_primary_10_1038_npp_2009_26 crossref_primary_10_1007_s40263_023_01022_7 crossref_primary_10_1007_s12035_020_01875_9 crossref_primary_10_1176_ps_2009_60_11_1468 crossref_primary_10_1192_bjp_bp_111_107359 crossref_primary_10_5455_bcp_20140626063115 crossref_primary_10_1176_appi_psychotherapy_20180036 crossref_primary_10_1016_j_bcp_2024_116298 crossref_primary_10_1016_j_clinthera_2023_07_002 crossref_primary_10_1016_j_neubiorev_2009_08_002 crossref_primary_10_31887_DCNS_2010_12_3_jkane crossref_primary_10_1007_s00213_008_1278_5 crossref_primary_10_1176_ps_2008_59_9_958 crossref_primary_10_3389_fpsyt_2018_00537 crossref_primary_10_3389_fpsyt_2021_742058 crossref_primary_10_1097_HRP_0000000000000101 crossref_primary_10_1007_s00702_022_02487_4 crossref_primary_10_1007_s11326_011_0149_6 crossref_primary_10_1007_s00702_020_02292_x crossref_primary_10_1016_j_bcp_2011_02_003 crossref_primary_10_1038_s41398_018_0104_z crossref_primary_10_1016_j_bpsc_2024_09_001 crossref_primary_10_1586_ecp_12_57 crossref_primary_10_1155_2012_275957 crossref_primary_10_1016_j_pmip_2019_02_001 crossref_primary_10_1017_S0033291715000069 crossref_primary_10_1007_s00213_018_4997_2 crossref_primary_10_1177_0269881120965937 crossref_primary_10_3389_fnsyn_2014_00028 crossref_primary_10_1016_j_biopsych_2013_07_026 crossref_primary_10_3371_CSRP_BOMU_012513 crossref_primary_10_1016_j_nbd_2012_10_025 crossref_primary_10_1038_npp_2010_101 crossref_primary_10_1097_NMD_0000000000000782 crossref_primary_10_1155_2017_2875904 crossref_primary_10_1016_j_schres_2017_01_028 crossref_primary_10_1038_npp_2015_120 crossref_primary_10_1016_j_schres_2018_03_037 crossref_primary_10_1016_j_pbb_2010_11_009 crossref_primary_10_1007_s11065_009_9103_4 crossref_primary_10_1016_j_eurpsy_2009_09_006 crossref_primary_10_1016_j_biopsych_2012_05_009 crossref_primary_10_1124_mol_109_059865 crossref_primary_10_1016_j_schres_2008_09_020 crossref_primary_10_2165_11585350_000000000_00000 |
Cites_doi | 10.1176/ajp.148.10.1301 10.1097/00002826-199619050-00008 10.1093/schbul/sbi035 10.1176/ajp.151.8.1234 10.1016/0893-133X(94)00131-I 10.1176/ajp.153.12.1628 10.1016/j.biopsych.2003.09.012 10.1016/j.biopsych.2004.12.037 10.1001/archpsyc.56.1.29 10.1016/j.biopsych.2005.06.032 10.1097/00004850-199605002-00002 10.1016/0165-1781(89)90153-4 10.1017/S1461145701002590 10.1016/S0893-133X(99)00122-0 10.1016/S0006-3223(03)00707-8 10.1093/schbul/sbi007 10.1093/schbul/sbi004 10.1001/archpsyc.56.1.21 10.1016/S0006-3223(98)00279-0 10.1093/jschbul/sbi001 10.1176/ajp.156.11.1822 10.1080/01621459.1997.10473627 10.1001/archpsyc.1995.03950240016004 10.1016/S0010-440X(61)80033-3 10.1176/ajp.153.3.321 10.1001/archpsyc.1982.04290070020005 10.1001/archpsyc.1994.03950030035004 10.1093/schbul/sbj053 10.1146/annurev.pharmtox.42.082701.160735 10.1038/sj.npp.1300313 10.1097/00004714-199002000-00027 10.1016/j.biopsych.2006.04.005 10.1016/j.schres.2004.03.013 10.1192/bjp.169.5.610 10.1097/01.yco.0000214340.14131.bd 10.1002/sim.1837 10.1007/s00213-004-2032-2 10.1016/S0006-3223(96)00311-3 10.1111/j.1600-0447.1970.tb02066.x 10.1007/BF01276429 10.1176/ajp.152.5.815 10.1016/j.schres.2004.05.005 |
ContentType | Journal Article |
Copyright | 2007 INIST-CNRS Copyright American Psychiatric Association Oct 2007 |
Copyright_xml | – notice: 2007 INIST-CNRS – notice: Copyright American Psychiatric Association Oct 2007 |
DBID | AAYXX CITATION IQODW CGR CUY CVF ECM EIF NPM K9. NAPCQ 7TK 7X8 |
DOI | 10.1176/appi.ajp.2007.06081358 |
DatabaseName | CrossRef Pascal-Francis Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed ProQuest Health & Medical Complete (Alumni) Nursing & Allied Health Premium Neurosciences Abstracts MEDLINE - Academic |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) ProQuest Health & Medical Complete (Alumni) Nursing & Allied Health Premium Neurosciences Abstracts MEDLINE - Academic |
DatabaseTitleList | ProQuest Health & Medical Complete (Alumni) Neurosciences Abstracts MEDLINE MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1535-7228 |
EndPage | 1602 |
ExternalDocumentID | 1360500971 17898352 19142090 10_1176_appi_ajp_2007_06081358 10.1176/appi.ajp.2007.06081358 |
Genre | Research Support, U.S. Gov't, Non-P.H.S Multicenter Study Comparative Study Randomized Controlled Trial Journal Article Research Support, N.I.H., Extramural |
GrantInformation_xml | – fundername: NIMH NIH HHS grantid: 5 R01 MH59750 – fundername: NIMH NIH HHS grantid: 5 R01 MH69807 – fundername: NIMH NIH HHS grantid: P30 MH06850 – fundername: NIMH NIH HHS grantid: 5 R01 MH59687 – fundername: NIMH NIH HHS grantid: 5 R01 MH59784 |
GroupedDBID | --- --Z -DZ -~X .55 .GJ 08P 0WA 1CY 1HT 1KJ 1QT 23M 2QL 2WC 354 3O- 4.4 41~ 53G 5GY 5RE 6J9 6TJ 7K8 85S 8F7 8R4 8R5 AAAHA AAIKC AAJMC AAJWC AAKAS AAMNW AAQQT AAWTL AAWTO AAYJJ ABIVO ABPPZ ABZEH ACBMB ACGFO ACGOD ACHQT ACNCT ADBBV ADCOW ADZCM AENEX AERZD AETEA AFAZI AFFDN AFFNX AFMIJ AFOSN AGHSJ AGNAY AHJKT AHMBA AI. AIZTS ALMA_UNASSIGNED_HOLDINGS ASUFR BAJDF BAWUL BCR BENPR BKOMP BLC CS3 DIK E3Z EBS EJD EX3 F20 F5P F8P FA8 FJW G0H G8K GOZPB GRPMH HF~ HZ~ J5H L7B LPU LXL LXN MVM N4W N9A NEJ NHB OHT OK1 OVD P-O P2P PEA PQQKQ Q.- Q2X RAY RWL RXW RYA S10 SJN SKT TAE TEORI TR2 TWZ UBC UHB UKR ULE UPT UQL VH1 VVN WH7 WHG WOQ WOW X4V X6Y X7M XJT XOL XSW XZL YCJ YFH YOC YQI YQJ YRY YSK YWH YXB YYQ YZZ ZCA ZGI ZHY ZKB ZRR ZXP ZY1 ~A~ ~G0 ~X8 AAYXX ABDPE ADGHP ADMHG CITATION H13 08R AAPBV AAUGY ABPTK AKALU IQODW ZA5 CGR CUY CVF ECM EIF NPM K9. NAPCQ 7TK 7X8 |
ID | FETCH-LOGICAL-a507t-cf7dba4d7faa6da530c20819bf3deb40d65f18483872653ccb1c0feec9c508d03 |
ISSN | 0002-953X |
IngestDate | Fri Jul 11 02:30:50 EDT 2025 Thu Jul 10 18:44:18 EDT 2025 Sun Jun 29 14:36:26 EDT 2025 Mon Jul 21 06:04:56 EDT 2025 Sun Oct 22 16:09:37 EDT 2023 Tue Jul 01 01:51:32 EDT 2025 Thu Apr 24 23:06:58 EDT 2025 Wed Jul 24 08:10:55 EDT 2024 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 10 |
Keywords | Psychosis Schizophrenia Cognition Cognitive disorder Negative symptom |
Language | English |
License | CC BY 4.0 |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-a507t-cf7dba4d7faa6da530c20819bf3deb40d65f18483872653ccb1c0feec9c508d03 |
Notes | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 14 ObjectType-Article-1 ObjectType-Feature-2 content type line 23 ObjectType-Undefined-3 |
PMID | 17898352 |
PQID | 220498092 |
PQPubID | 40661 |
PageCount | 10 |
ParticipantIDs | proquest_miscellaneous_68319426 proquest_miscellaneous_20412624 proquest_journals_220498092 pubmed_primary_17898352 pascalfrancis_primary_19142090 crossref_citationtrail_10_1176_appi_ajp_2007_06081358 crossref_primary_10_1176_appi_ajp_2007_06081358 appi_journals_10_1176_appi_ajp_2007_06081358 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2007-10-01 |
PublicationDateYYYYMMDD | 2007-10-01 |
PublicationDate_xml | – month: 10 year: 2007 text: 2007-10-01 day: 01 |
PublicationDecade | 2000 |
PublicationPlace | Washington, DC |
PublicationPlace_xml | – name: Washington, DC – name: United States – name: Washington |
PublicationTitle | The American journal of psychiatry |
PublicationTitleAlternate | Am J Psychiatry |
PublicationYear | 2007 |
Publisher | American Psychiatric Association |
Publisher_xml | – name: American Psychiatric Association |
References | p_49 p_46 p_47 p_48 (p_39) 2003; 64 Westfall PH (p_41) 1999 p_42 p_43 Malhotra AK (p_13) 1994 p_44 p_40 p_2 p_1 p_4 p_34 p_3 p_6 p_36 p_5 p_37 p_7 p_9 First MB (p_33) 1997 p_30 p_32 p_27 p_28 Deutch SI (p_8) 1989; 12 p_29 p_23 p_24 p_25 p_26 p_20 p_21 p_22 Overall JE (p_35) 1962; 10 p_16 p_17 Guy W (p_38) 1976 p_18 Buchanan RW (p_45) 2005; 31 p_19 p_12 p_14 p_15 Tsai G (p_31) 1999; 156 p_10 p_11 p_50 |
References_xml | – ident: p_7 doi: 10.1176/ajp.148.10.1301 – ident: p_23 doi: 10.1097/00002826-199619050-00008 – ident: p_6 doi: 10.1093/schbul/sbi035 – ident: p_47 doi: 10.1176/ajp.151.8.1234 – ident: p_14 doi: 10.1016/0893-133X(94)00131-I – ident: p_25 doi: 10.1176/ajp.153.12.1628 – ident: p_27 doi: 10.1016/j.biopsych.2003.09.012 – ident: p_30 doi: 10.1016/j.biopsych.2004.12.037 – ident: p_17 doi: 10.1001/archpsyc.56.1.29 – volume: 64 start-page: 2 year: 2003 ident: p_39 publication-title: J Clin Psychiatry – ident: p_28 doi: 10.1016/j.biopsych.2005.06.032 – ident: p_1 doi: 10.1097/00004850-199605002-00002 – ident: p_37 doi: 10.1016/0165-1781(89)90153-4 – ident: p_19 doi: 10.1017/S1461145701002590 – ident: p_43 doi: 10.1016/S0893-133X(99)00122-0 – ident: p_18 doi: 10.1016/S0006-3223(03)00707-8 – ident: p_3 doi: 10.1093/schbul/sbi007 – ident: p_5 doi: 10.1093/schbul/sbi004 – ident: p_21 doi: 10.1001/archpsyc.56.1.21 – ident: p_29 doi: 10.1016/S0006-3223(98)00279-0 – ident: p_4 doi: 10.1093/jschbul/sbi001 – volume: 156 start-page: 1822 year: 1999 ident: p_31 publication-title: Am J Psychiatry doi: 10.1176/ajp.156.11.1822 – ident: p_40 doi: 10.1080/01621459.1997.10473627 – ident: p_9 doi: 10.1001/archpsyc.1995.03950240016004 – ident: p_12 doi: 10.1016/S0010-440X(61)80033-3 – volume-title: Va year: 1994 ident: p_13 – ident: p_2 doi: 10.1176/ajp.153.3.321 – ident: p_34 doi: 10.1001/archpsyc.1982.04290070020005 – ident: p_11 doi: 10.1001/archpsyc.1994.03950030035004 – volume-title: Hochberg Y: Multiple Comparisons and Multiple Tests Using the SAS System year: 1999 ident: p_41 – volume-title: Williams J: Structural Clinical Interview for DSM-IV Axis Disorders (SCID) year: 1997 ident: p_33 – ident: p_44 doi: 10.1093/schbul/sbj053 – volume: 31 start-page: 5 year: 2005 ident: p_45 – ident: p_10 doi: 10.1146/annurev.pharmtox.42.082701.160735 – ident: p_48 doi: 10.1038/sj.npp.1300313 – ident: p_15 doi: 10.1097/00004714-199002000-00027 – ident: p_32 doi: 10.1016/j.biopsych.2006.04.005 – ident: p_26 doi: 10.1016/j.schres.2004.03.013 – ident: p_16 doi: 10.1192/bjp.169.5.610 – ident: p_46 doi: 10.1097/01.yco.0000214340.14131.bd – volume: 12 start-page: 1013 year: 1989 ident: p_8 publication-title: Clin Neuropharmacol – ident: p_42 doi: 10.1002/sim.1837 – ident: p_50 doi: 10.1007/s00213-004-2032-2 – ident: p_22 doi: 10.1016/S0006-3223(96)00311-3 – ident: p_36 doi: 10.1111/j.1600-0447.1970.tb02066.x – start-page: 534 volume-title: Md year: 1976 ident: p_38 – volume: 10 start-page: 799 year: 1962 ident: p_35 publication-title: Gorham DR: The Brief Psychiatric Rating Scale. Psychol Rep – ident: p_24 doi: 10.1007/BF01276429 – ident: p_20 doi: 10.1176/ajp.152.5.815 – ident: p_49 doi: 10.1016/j.schres.2004.05.005 |
SSID | ssj0000372 |
Score | 2.4274936 |
Snippet | Objective:
Patients with schizophrenia frequently present with negative symptoms and cognitive impairments for which no effective treatments are known. Agents... Patients with schizophrenia frequently present with negative symptoms and cognitive impairments for which no effective treatments are known. Agents that act at... OBJECTIVE: Patients with schizophrenia frequently present with negative symptoms and cognitive impairments for which no effective treatments are known. Agents... |
SourceID | proquest pubmed pascalfrancis crossref appi |
SourceType | Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 1593 |
SubjectTerms | Adolescent Adult Adult and adolescent clinical studies Biological and medical sciences Cognition & reasoning Cognition Disorders - diagnosis Cognition Disorders - drug therapy Cognition Disorders - psychology Cycloserine - therapeutic use Double-Blind Method Excitatory Amino Acid Agents - therapeutic use Female Follow-Up Studies Glycine - therapeutic use Humans Hypotheses Male Medical sciences Middle Aged Neuropsychological Tests - statistics & numerical data Patients Placebos Psychiatric Status Rating Scales - statistics & numerical data Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Psychoses Psychotic Disorders - drug therapy Psychotic Disorders - psychology Psychotropic drugs Receptors, N-Methyl-D-Aspartate - drug effects Receptors, N-Methyl-D-Aspartate - physiology Schizophrenia Schizophrenia - diagnosis Schizophrenia - drug therapy Schizophrenic Psychology Severity of Illness Index Studies Treatment Outcome |
Title | The Cognitive and Negative Symptoms in Schizophrenia Trial (CONSIST): The Efficacy of Glutamatergic Agents for Negative Symptoms and Cognitive Impairments |
URI | http://dx.doi.org/10.1176/appi.ajp.2007.06081358 https://www.ncbi.nlm.nih.gov/pubmed/17898352 https://www.proquest.com/docview/220498092 https://www.proquest.com/docview/20412624 https://www.proquest.com/docview/68319426 |
Volume | 164 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1bb9MwFLa2ISEkQNwpg-EHkEAlW-IkdszbVAYraEWindhb5Vw8FdG06lIk-Cn8Wo5vSco6jfESVXF9ac-X43Pic76D0ItAghlN88yjPCJelArm8UQWXgBeHMmIZgBR0RYDengcfTyJTzY2b7WilpZVupv9WptX8j9ShXsgV5UlewXJ1oPCDfgM8oUrSBiu_yzjXh3_o16BD4pTw-Q9_DmdV7OpjnYdtgPruiNdp0Md3n4eDPvD0UvCXejFgeKTUPXfwYL8AAsXYM4WC9CN3f1TnQmnYhLPT6EmbpbRBwUzWUwdR5SzfEdNCkvZ5qtYDbc2mRUqG9meT-nA7-7X3TrSR_yw51kmOb7bq5uOxCK3ZcRM6Fr3S91myEZN62BSCtfk3newOnKuaqUYuA3CFDM5B-VG2fNYlxuGrc7pd1W91-ajuw3A8Kg7pPstfQ7GXtiyDQKq08PX7DtMEy7PVf7ht7llxqRgboWGmP4vTu_LumyiawTcHlWR413_U2NZhIw4d079MJvxDiPtrR8H7AzVsGJz3ZyLM3j8panbcrFjpQ2s0R1023pGeN_A_C7aKMp76PqRjf24j34DgnANMwygww6K2EERT0q8gnas0Y5fWay_fovVKA7neCbxCs6xwTkGnK8ZXE3ZLKCF8wfo-P3BqHfo2coingD_p_IyyfJURDmTQtBcxKEPagls41SGeZFGfk5jGSRREiaM0DjMsjTIfFkUGc_Aocn98CHaKmdl8RjhUCY-5STIWU7BuYk449SXAZU5eEIiDDrojRLB2D5YZ2PtdTM61ndBYqoQLBs7iXVQ7EQ1zixLvyoW8_3Sfnt1v7nhqbm0x84KEppuPIiIz_0O2nbQaFZPiB_xxOekg57XrbAjqWNGURazJXxFUfhREl38DZrAxg-uQQc9Mohr5mYJVz7hk6v9a9voRqMqnqKtarEsnoGzUKU7-gn6A9hSEmc |
linkProvider | Flying Publisher |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=The+Cognitive+and+Negative+Symptoms+in+Schizophrenia+Trial+%28CONSIST%29%3A+The+Efficacy+of+Glutamatergic+Agents+for+Negative+Symptoms+and+Cognitive+Impairments&rft.jtitle=The+American+journal+of+psychiatry&rft.au=Buchanan%2C+Robert+W.&rft.au=Javitt%2C+Daniel+C.&rft.au=Marder%2C+Stephen+R.&rft.au=Schooler%2C+Nina+R.&rft.date=2007-10-01&rft.pub=American+Psychiatric+Association&rft.issn=0002-953X&rft.eissn=1535-7228&rft.volume=164&rft.issue=10&rft.spage=1593&rft.epage=1602&rft_id=info:doi/10.1176%2Fappi.ajp.2007.06081358&rft.externalDocID=10.1176%2Fappi.ajp.2007.06081358 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0002-953X&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0002-953X&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0002-953X&client=summon |