Factors associated with cognitive dysfunction in treatment-responsive and -resistant schizophrenia: A pilot cross-sectional study
Cognitive dysfunction is a core feature of schizophrenia. Although treatment-resistant schizophrenia (TRS) exhibits wide-ranging neuropsychological deficits, factors defining cognitive prognosis in TRS are unclear. We aimed to clarify the association between cognitive dysfunction and factors, such a...
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Veröffentlicht in: | Journal of psychiatric research 2024-10, Vol.178, p.228-235 |
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creator | Suzuki, Yuhei Watanabe, Kenya Kanno-Nozaki, Keiko Horikoshi, Sho Ichinose, Mizue Hirata, Yoichiro Kobayashi, Yuri Takeuchi, Satoshi Osonoe, Kouichi Hoshino, Shuzo Miura, Itaru |
description | Cognitive dysfunction is a core feature of schizophrenia. Although treatment-resistant schizophrenia (TRS) exhibits wide-ranging neuropsychological deficits, factors defining cognitive prognosis in TRS are unclear. We aimed to clarify the association between cognitive dysfunction and factors, such as plasma concentrations of clozapine (CLZ), N-desmethylclozapine (NDMC), and homovanillic acid (HVA), due to differences in antipsychotic responses in patients with schizophrenia.
This pilot cross-sectional study included 60 Japanese patients (35 with TRS and 25 with non-CLZ antipsychotic responders (AR)). Cognitive function was evaluated using the Brief Assessment of Cognition Short Form (BAC-SF). Plasma concentrations of HVA, CLZ, and NDMC were analyzed by high-performance liquid chromatography.
The cognitive performance of patients with AR was better than that of patients with TRS in all tasks. No significant cognitive differences were detected between the CLZ responders and non-responders. The severity of negative and extrapyramidal symptoms was found to be potentially negatively associated with BAC-SF composite and several subtest scores. In patients with TRS, chlorpromazine equivalents and the CLZ/NDMC ratio were identified as factors negatively associated with Digit Sequencing and the Symbol Coding subtest scores of the BAC-SF, respectively.
Our study suggests that patients with TRS experience worse cognitive dysfunction than those with AR, and CLZ responsiveness in TRS may be not associated with cognitive dysfunction. Additionally, higher chlorpromazine equivalents and the CLZ/NDMC ratio may be associated with severity of cognitive dysfunction in patients with TRS. Further studies are required to clarify the relationship between treatment response and cognitive dysfunction in schizophrenia. |
doi_str_mv | 10.1016/j.jpsychires.2024.08.012 |
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This pilot cross-sectional study included 60 Japanese patients (35 with TRS and 25 with non-CLZ antipsychotic responders (AR)). Cognitive function was evaluated using the Brief Assessment of Cognition Short Form (BAC-SF). Plasma concentrations of HVA, CLZ, and NDMC were analyzed by high-performance liquid chromatography.
The cognitive performance of patients with AR was better than that of patients with TRS in all tasks. No significant cognitive differences were detected between the CLZ responders and non-responders. The severity of negative and extrapyramidal symptoms was found to be potentially negatively associated with BAC-SF composite and several subtest scores. In patients with TRS, chlorpromazine equivalents and the CLZ/NDMC ratio were identified as factors negatively associated with Digit Sequencing and the Symbol Coding subtest scores of the BAC-SF, respectively.
Our study suggests that patients with TRS experience worse cognitive dysfunction than those with AR, and CLZ responsiveness in TRS may be not associated with cognitive dysfunction. Additionally, higher chlorpromazine equivalents and the CLZ/NDMC ratio may be associated with severity of cognitive dysfunction in patients with TRS. Further studies are required to clarify the relationship between treatment response and cognitive dysfunction in schizophrenia.</description><identifier>ISSN: 0022-3956</identifier><identifier>ISSN: 1879-1379</identifier><identifier>EISSN: 1879-1379</identifier><identifier>DOI: 10.1016/j.jpsychires.2024.08.012</identifier><identifier>PMID: 39163661</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adult ; Antipsychotic Agents - pharmacology ; Clozapine ; Clozapine - analogs & derivatives ; Clozapine - pharmacology ; Cognitive Dysfunction - drug therapy ; Cognitive Dysfunction - etiology ; Cognitive Dysfunction - physiopathology ; Cognitive function ; Cross-Sectional Studies ; Female ; Homovanillic Acid - blood ; Humans ; Male ; Middle Aged ; Pilot Projects ; Psychiatric Status Rating Scales ; Schizophrenia ; Schizophrenia - blood ; Schizophrenia - complications ; Schizophrenia - drug therapy ; Schizophrenia - physiopathology ; Schizophrenia, Treatment-Resistant - blood ; Schizophrenia, Treatment-Resistant - drug therapy ; Therapeutic drug monitoring ; Treatment-resistant ; Ultra-treatment-resistant</subject><ispartof>Journal of psychiatric research, 2024-10, Vol.178, p.228-235</ispartof><rights>2024 Elsevier Ltd</rights><rights>Copyright © 2024 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c319t-8b3c2189654cd5b3e962c5083a0f2ed0ccd8c9d6e6e1d4681f9b3f80f31295f53</cites><orcidid>0000-0002-2133-5809 ; 0009-0007-1830-460X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0022395624004618$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39163661$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Suzuki, Yuhei</creatorcontrib><creatorcontrib>Watanabe, Kenya</creatorcontrib><creatorcontrib>Kanno-Nozaki, Keiko</creatorcontrib><creatorcontrib>Horikoshi, Sho</creatorcontrib><creatorcontrib>Ichinose, Mizue</creatorcontrib><creatorcontrib>Hirata, Yoichiro</creatorcontrib><creatorcontrib>Kobayashi, Yuri</creatorcontrib><creatorcontrib>Takeuchi, Satoshi</creatorcontrib><creatorcontrib>Osonoe, Kouichi</creatorcontrib><creatorcontrib>Hoshino, Shuzo</creatorcontrib><creatorcontrib>Miura, Itaru</creatorcontrib><title>Factors associated with cognitive dysfunction in treatment-responsive and -resistant schizophrenia: A pilot cross-sectional study</title><title>Journal of psychiatric research</title><addtitle>J Psychiatr Res</addtitle><description>Cognitive dysfunction is a core feature of schizophrenia. Although treatment-resistant schizophrenia (TRS) exhibits wide-ranging neuropsychological deficits, factors defining cognitive prognosis in TRS are unclear. We aimed to clarify the association between cognitive dysfunction and factors, such as plasma concentrations of clozapine (CLZ), N-desmethylclozapine (NDMC), and homovanillic acid (HVA), due to differences in antipsychotic responses in patients with schizophrenia.
This pilot cross-sectional study included 60 Japanese patients (35 with TRS and 25 with non-CLZ antipsychotic responders (AR)). Cognitive function was evaluated using the Brief Assessment of Cognition Short Form (BAC-SF). Plasma concentrations of HVA, CLZ, and NDMC were analyzed by high-performance liquid chromatography.
The cognitive performance of patients with AR was better than that of patients with TRS in all tasks. No significant cognitive differences were detected between the CLZ responders and non-responders. The severity of negative and extrapyramidal symptoms was found to be potentially negatively associated with BAC-SF composite and several subtest scores. In patients with TRS, chlorpromazine equivalents and the CLZ/NDMC ratio were identified as factors negatively associated with Digit Sequencing and the Symbol Coding subtest scores of the BAC-SF, respectively.
Our study suggests that patients with TRS experience worse cognitive dysfunction than those with AR, and CLZ responsiveness in TRS may be not associated with cognitive dysfunction. Additionally, higher chlorpromazine equivalents and the CLZ/NDMC ratio may be associated with severity of cognitive dysfunction in patients with TRS. Further studies are required to clarify the relationship between treatment response and cognitive dysfunction in schizophrenia.</description><subject>Adult</subject><subject>Antipsychotic Agents - pharmacology</subject><subject>Clozapine</subject><subject>Clozapine - analogs & derivatives</subject><subject>Clozapine - pharmacology</subject><subject>Cognitive Dysfunction - drug therapy</subject><subject>Cognitive Dysfunction - etiology</subject><subject>Cognitive Dysfunction - physiopathology</subject><subject>Cognitive function</subject><subject>Cross-Sectional Studies</subject><subject>Female</subject><subject>Homovanillic Acid - blood</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Pilot Projects</subject><subject>Psychiatric Status Rating Scales</subject><subject>Schizophrenia</subject><subject>Schizophrenia - blood</subject><subject>Schizophrenia - complications</subject><subject>Schizophrenia - drug therapy</subject><subject>Schizophrenia - physiopathology</subject><subject>Schizophrenia, Treatment-Resistant - blood</subject><subject>Schizophrenia, Treatment-Resistant - drug therapy</subject><subject>Therapeutic drug monitoring</subject><subject>Treatment-resistant</subject><subject>Ultra-treatment-resistant</subject><issn>0022-3956</issn><issn>1879-1379</issn><issn>1879-1379</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU9v1DAQxS1ERZeWr4B85JLgP4nX5laqFpAqcWnPlteesF5l7eBxipYb35xst8CR02ik37w3M48QylnLGVfvd-1uwoPfxgLYCia6lumWcfGCrLhem4bLtXlJVowJ0UjTq3PyGnHHGFsL3r0i59JwJZXiK_Lr1vmaC1KHmH10FQL9EeuW-vwtxRofgYYDDnPyNeZEY6K1gKt7SLVZzKec8Mi4FOixj1hdqhSX1X7maVsgRfeBXtEpjrlSXzJig_Ck5UaKdQ6HS3I2uBHhzXO9IA-3N_fXn5u7r5--XF_dNV5yUxu9kV5wbVTf-dBvJBglfM-0dGwQEJj3QXsTFCjgoVOaD2YjB80GyYXph15ekHcn3ank7zNgtfuIHsbRJcgzWslMz9ddz-SC6hP6tHCBwU4l7l05WM7sMQC7s_8CsMcALNN2CWAZffvsMm_2EP4O_vn4Anw8AbDc-hihWPQRkoewaPlqQ47_d_kNR4agcQ</recordid><startdate>202410</startdate><enddate>202410</enddate><creator>Suzuki, Yuhei</creator><creator>Watanabe, Kenya</creator><creator>Kanno-Nozaki, Keiko</creator><creator>Horikoshi, Sho</creator><creator>Ichinose, Mizue</creator><creator>Hirata, Yoichiro</creator><creator>Kobayashi, Yuri</creator><creator>Takeuchi, Satoshi</creator><creator>Osonoe, Kouichi</creator><creator>Hoshino, Shuzo</creator><creator>Miura, Itaru</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-2133-5809</orcidid><orcidid>https://orcid.org/0009-0007-1830-460X</orcidid></search><sort><creationdate>202410</creationdate><title>Factors associated with cognitive dysfunction in treatment-responsive and -resistant schizophrenia: A pilot cross-sectional study</title><author>Suzuki, Yuhei ; Watanabe, Kenya ; Kanno-Nozaki, Keiko ; Horikoshi, Sho ; Ichinose, Mizue ; Hirata, Yoichiro ; Kobayashi, Yuri ; Takeuchi, Satoshi ; Osonoe, Kouichi ; Hoshino, Shuzo ; Miura, Itaru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c319t-8b3c2189654cd5b3e962c5083a0f2ed0ccd8c9d6e6e1d4681f9b3f80f31295f53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adult</topic><topic>Antipsychotic Agents - pharmacology</topic><topic>Clozapine</topic><topic>Clozapine - analogs & derivatives</topic><topic>Clozapine - pharmacology</topic><topic>Cognitive Dysfunction - drug therapy</topic><topic>Cognitive Dysfunction - etiology</topic><topic>Cognitive Dysfunction - physiopathology</topic><topic>Cognitive function</topic><topic>Cross-Sectional Studies</topic><topic>Female</topic><topic>Homovanillic Acid - blood</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Pilot Projects</topic><topic>Psychiatric Status Rating Scales</topic><topic>Schizophrenia</topic><topic>Schizophrenia - blood</topic><topic>Schizophrenia - complications</topic><topic>Schizophrenia - drug therapy</topic><topic>Schizophrenia - physiopathology</topic><topic>Schizophrenia, Treatment-Resistant - blood</topic><topic>Schizophrenia, Treatment-Resistant - drug therapy</topic><topic>Therapeutic drug monitoring</topic><topic>Treatment-resistant</topic><topic>Ultra-treatment-resistant</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Suzuki, Yuhei</creatorcontrib><creatorcontrib>Watanabe, Kenya</creatorcontrib><creatorcontrib>Kanno-Nozaki, Keiko</creatorcontrib><creatorcontrib>Horikoshi, Sho</creatorcontrib><creatorcontrib>Ichinose, Mizue</creatorcontrib><creatorcontrib>Hirata, Yoichiro</creatorcontrib><creatorcontrib>Kobayashi, Yuri</creatorcontrib><creatorcontrib>Takeuchi, Satoshi</creatorcontrib><creatorcontrib>Osonoe, Kouichi</creatorcontrib><creatorcontrib>Hoshino, Shuzo</creatorcontrib><creatorcontrib>Miura, Itaru</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of psychiatric research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Suzuki, Yuhei</au><au>Watanabe, Kenya</au><au>Kanno-Nozaki, Keiko</au><au>Horikoshi, Sho</au><au>Ichinose, Mizue</au><au>Hirata, Yoichiro</au><au>Kobayashi, Yuri</au><au>Takeuchi, Satoshi</au><au>Osonoe, Kouichi</au><au>Hoshino, Shuzo</au><au>Miura, Itaru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Factors associated with cognitive dysfunction in treatment-responsive and -resistant schizophrenia: A pilot cross-sectional study</atitle><jtitle>Journal of psychiatric research</jtitle><addtitle>J Psychiatr Res</addtitle><date>2024-10</date><risdate>2024</risdate><volume>178</volume><spage>228</spage><epage>235</epage><pages>228-235</pages><issn>0022-3956</issn><issn>1879-1379</issn><eissn>1879-1379</eissn><abstract>Cognitive dysfunction is a core feature of schizophrenia. Although treatment-resistant schizophrenia (TRS) exhibits wide-ranging neuropsychological deficits, factors defining cognitive prognosis in TRS are unclear. We aimed to clarify the association between cognitive dysfunction and factors, such as plasma concentrations of clozapine (CLZ), N-desmethylclozapine (NDMC), and homovanillic acid (HVA), due to differences in antipsychotic responses in patients with schizophrenia.
This pilot cross-sectional study included 60 Japanese patients (35 with TRS and 25 with non-CLZ antipsychotic responders (AR)). Cognitive function was evaluated using the Brief Assessment of Cognition Short Form (BAC-SF). Plasma concentrations of HVA, CLZ, and NDMC were analyzed by high-performance liquid chromatography.
The cognitive performance of patients with AR was better than that of patients with TRS in all tasks. No significant cognitive differences were detected between the CLZ responders and non-responders. The severity of negative and extrapyramidal symptoms was found to be potentially negatively associated with BAC-SF composite and several subtest scores. In patients with TRS, chlorpromazine equivalents and the CLZ/NDMC ratio were identified as factors negatively associated with Digit Sequencing and the Symbol Coding subtest scores of the BAC-SF, respectively.
Our study suggests that patients with TRS experience worse cognitive dysfunction than those with AR, and CLZ responsiveness in TRS may be not associated with cognitive dysfunction. Additionally, higher chlorpromazine equivalents and the CLZ/NDMC ratio may be associated with severity of cognitive dysfunction in patients with TRS. Further studies are required to clarify the relationship between treatment response and cognitive dysfunction in schizophrenia.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>39163661</pmid><doi>10.1016/j.jpsychires.2024.08.012</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-2133-5809</orcidid><orcidid>https://orcid.org/0009-0007-1830-460X</orcidid></addata></record> |
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subjects | Adult Antipsychotic Agents - pharmacology Clozapine Clozapine - analogs & derivatives Clozapine - pharmacology Cognitive Dysfunction - drug therapy Cognitive Dysfunction - etiology Cognitive Dysfunction - physiopathology Cognitive function Cross-Sectional Studies Female Homovanillic Acid - blood Humans Male Middle Aged Pilot Projects Psychiatric Status Rating Scales Schizophrenia Schizophrenia - blood Schizophrenia - complications Schizophrenia - drug therapy Schizophrenia - physiopathology Schizophrenia, Treatment-Resistant - blood Schizophrenia, Treatment-Resistant - drug therapy Therapeutic drug monitoring Treatment-resistant Ultra-treatment-resistant |
title | Factors associated with cognitive dysfunction in treatment-responsive and -resistant schizophrenia: A pilot cross-sectional study |
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