David J. Williamson , Keith H. Nuechterlein , Todd Tishler , Joseph Ventura , Benjamin M. Ellingson , Ibrahim Turkoz , Richard S.E. Keefe , Larry Alphs
{"title":"认知表现测试分数在矩阵共识认知电池上的分散:一个不同的视角","authors":"David J. Williamson , Keith H. Nuechterlein , Todd Tishler , Joseph Ventura , Benjamin M. Ellingson , Ibrahim Turkoz , Richard S.E. Keefe , Larry Alphs","doi":"10.1016/j.scog.2022.100270","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><p>Persons with schizophrenia exhibit greater neurocognitive test score dispersion. Here, we seek to characterize dispersion on the Neurocognitive Composite subtests of the Measurement of Treatment Research to Improve Cognition in Schizophrena Consensus Cognitive Battery (MCCB) and determine the relative effects of different antipsychotic formulations on dispersion and mean performance.</p></div><div><h3>Method</h3><p>In this post hoc analysis of the DREaM study (<span>NCT02431702</span><svg><path></path></svg>), which compared treatment with paliperidone palmitate (PP) long-acting injectable with oral antipsychotic (OAP) treatment over 18 months, dispersion in MCCB neurocognitive subtest performance was calculated for each participant by visit (test occasion).</p></div><div><h3>Results</h3><p>Over 18 months, mean neurocognitive performance improved in a manner consistent with the expected effects of practice in both groups (<em>p</em> < 0.05); this improvement was observed during the first 9 months (PP: <em>p</em> < 0.05, OAP: <em>p</em> < 0.001), followed by stable performance over the second 9 months (PP: <em>p</em> = 0.821, OAP: <em>p</em> = 0.375). Rates of change did not differ between groups (treatment-by-visit interaction: <em>p</em> = 0.548). In contrast, analyses of dispersion focusing on contrasts between baselines and end points of the first and second 9 months revealed different patterns. Over the first 9 months, dispersion in both groups lessened to a similar extent. However, over the second 9 months, dispersion remained stable in the PP group, whereas neurocognitive performance became significantly more variable in the OAP group (<em>p</em> < 0.01).</p></div><div><h3>Conclusion</h3><p>Dispersion of neurocognitive test scores provides a different index of cognitive change than that provided by composite scores. Long-term maintenance of therapeutic levels provided by PP over time may limit (relative to oral AP) the extent to which cognitive performance becomes more variable.</p></div>","PeriodicalId":38119,"journal":{"name":"Schizophrenia Research-Cognition","volume":null,"pages":null},"PeriodicalIF":2.3000,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/10/08/main.PMC9468588.pdf","citationCount":"1","resultStr":"{\"title\":\"Dispersion of cognitive performance test scores on the MATRICS Consensus Cognitive Battery: A different perspective\",\"authors\":\"David J. Williamson , Keith H. Nuechterlein , Todd Tishler , Joseph Ventura , Benjamin M. Ellingson , Ibrahim Turkoz , Richard S.E. Keefe , Larry Alphs\",\"doi\":\"10.1016/j.scog.2022.100270\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objective</h3><p>Persons with schizophrenia exhibit greater neurocognitive test score dispersion. Here, we seek to characterize dispersion on the Neurocognitive Composite subtests of the Measurement of Treatment Research to Improve Cognition in Schizophrena Consensus Cognitive Battery (MCCB) and determine the relative effects of different antipsychotic formulations on dispersion and mean performance.</p></div><div><h3>Method</h3><p>In this post hoc analysis of the DREaM study (<span>NCT02431702</span><svg><path></path></svg>), which compared treatment with paliperidone palmitate (PP) long-acting injectable with oral antipsychotic (OAP) treatment over 18 months, dispersion in MCCB neurocognitive subtest performance was calculated for each participant by visit (test occasion).</p></div><div><h3>Results</h3><p>Over 18 months, mean neurocognitive performance improved in a manner consistent with the expected effects of practice in both groups (<em>p</em> < 0.05); this improvement was observed during the first 9 months (PP: <em>p</em> < 0.05, OAP: <em>p</em> < 0.001), followed by stable performance over the second 9 months (PP: <em>p</em> = 0.821, OAP: <em>p</em> = 0.375). Rates of change did not differ between groups (treatment-by-visit interaction: <em>p</em> = 0.548). In contrast, analyses of dispersion focusing on contrasts between baselines and end points of the first and second 9 months revealed different patterns. Over the first 9 months, dispersion in both groups lessened to a similar extent. However, over the second 9 months, dispersion remained stable in the PP group, whereas neurocognitive performance became significantly more variable in the OAP group (<em>p</em> < 0.01).</p></div><div><h3>Conclusion</h3><p>Dispersion of neurocognitive test scores provides a different index of cognitive change than that provided by composite scores. Long-term maintenance of therapeutic levels provided by PP over time may limit (relative to oral AP) the extent to which cognitive performance becomes more variable.</p></div>\",\"PeriodicalId\":38119,\"journal\":{\"name\":\"Schizophrenia Research-Cognition\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2022-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/10/08/main.PMC9468588.pdf\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Schizophrenia Research-Cognition\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S221500132200035X\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"PSYCHIATRY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Schizophrenia Research-Cognition","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S221500132200035X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PSYCHIATRY","Score":null,"Total":0}
引用次数: 1
摘要
目的:精神分裂症患者表现出更大的神经认知测试分数分散性。在这里,我们试图在改善精神分裂症共识认知电池(MCCB)认知的治疗研究测量的神经认知复合子测试中表征离散度,并确定不同抗精神病药物配方对离散度和平均表现的相对影响。方法对DREaM研究(NCT02431702)进行事后分析,比较长效注射棕榈酸帕利哌酮(PP)与口服抗精神病药(OAP)治疗超过18个月的时间,通过访问(测试地点)计算每个参与者MCCB神经认知亚测试成绩的离散度。结果18个月后,两组患者的平均神经认知能力均得到改善,与预期的练习效果一致(p <0.05);在前9个月观察到这种改善(PP: p <0.05, OAP: p <0.001),其次是第二个9个月的稳定表现(PP: p = 0.821, OAP: p = 0.375)。两组之间的变化率没有差异(就诊治疗交互作用:p = 0.548)。相比之下,对第一和第二个9个月的基线和终点的差异进行的分散分析显示了不同的模式。在前9个月,两组的分散程度相似。然而,在接下来的9个月里,PP组的离散度保持稳定,而OAP组的神经认知表现变得明显更加多变(p <0.01)。结论神经认知测验分数离散度与复合分数提供的认知变化指标不同。长期维持PP提供的治疗水平可能会限制(相对于口服AP)认知表现变得更可变的程度。
Dispersion of cognitive performance test scores on the MATRICS Consensus Cognitive Battery: A different perspective
Objective
Persons with schizophrenia exhibit greater neurocognitive test score dispersion. Here, we seek to characterize dispersion on the Neurocognitive Composite subtests of the Measurement of Treatment Research to Improve Cognition in Schizophrena Consensus Cognitive Battery (MCCB) and determine the relative effects of different antipsychotic formulations on dispersion and mean performance.
Method
In this post hoc analysis of the DREaM study (NCT02431702), which compared treatment with paliperidone palmitate (PP) long-acting injectable with oral antipsychotic (OAP) treatment over 18 months, dispersion in MCCB neurocognitive subtest performance was calculated for each participant by visit (test occasion).
Results
Over 18 months, mean neurocognitive performance improved in a manner consistent with the expected effects of practice in both groups (p < 0.05); this improvement was observed during the first 9 months (PP: p < 0.05, OAP: p < 0.001), followed by stable performance over the second 9 months (PP: p = 0.821, OAP: p = 0.375). Rates of change did not differ between groups (treatment-by-visit interaction: p = 0.548). In contrast, analyses of dispersion focusing on contrasts between baselines and end points of the first and second 9 months revealed different patterns. Over the first 9 months, dispersion in both groups lessened to a similar extent. However, over the second 9 months, dispersion remained stable in the PP group, whereas neurocognitive performance became significantly more variable in the OAP group (p < 0.01).
Conclusion
Dispersion of neurocognitive test scores provides a different index of cognitive change than that provided by composite scores. Long-term maintenance of therapeutic levels provided by PP over time may limit (relative to oral AP) the extent to which cognitive performance becomes more variable.