Generalized neurocognitive impairment in individuals at ultra‐high risk for psychosis: The possible key role of slowed processing speed
Abstract Objective Widespread neurocognitive impairment is well‐established in individuals at ultra‐high risk (UHR) for developing psychoses, but it is unknown whether slowed processing speed may underlie impairment in other neurocognitive domains, as found in schizophrenia. The study delineated dom...
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Wiley
2021-03-01
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Series: | Brain and Behavior |
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Online Access: | https://doi.org/10.1002/brb3.1962 |
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author | Lasse Randers Jens Richardt Møllegaard Jepsen Birgitte Fagerlund Dorte Nordholm Kristine Krakauer Carsten Hjorthøj Birte Glenthøj Merete Nordentoft |
author_facet | Lasse Randers Jens Richardt Møllegaard Jepsen Birgitte Fagerlund Dorte Nordholm Kristine Krakauer Carsten Hjorthøj Birte Glenthøj Merete Nordentoft |
author_sort | Lasse Randers |
collection | DOAJ |
description | Abstract Objective Widespread neurocognitive impairment is well‐established in individuals at ultra‐high risk (UHR) for developing psychoses, but it is unknown whether slowed processing speed may underlie impairment in other neurocognitive domains, as found in schizophrenia. The study delineated domain functioning in a UHR sample and examined if neurocognitive slowing might account for deficits across domains. Methods The cross‐sectional study included 50 UHR individuals with no (n = 38) or minimal antipsychotic exposure (n = 12; mean lifetime dose of haloperidol equivalent = 17.56 mg; SD = 13.04) and 50 matched healthy controls. Primary analyses compared group performance across neurocognitive domains before and after covarying for processing speed. To examine the specificity of processing speed effects, post hoc analyses examined the impact of the other neurocognitive domains and intelligence as covariates. Results UHR individuals exhibited significant impairment across all neurocognitive domains (all ps ≤ .010), with medium to large effect sizes (Cohen's ds = −0.53 to −1.12). Only processing speed used as covariate eliminated significant between‐group differences in all other domains, reducing unadjusted Cohen's d values with 68% on average, whereas the other domains used as covariates averagely reduced unadjusted Cohen's d values with 20% to 48%. When covarying each of the other domains after their shared variance with speed of processing was removed, all significant between‐group domain differences remained (all ps ≤ .024). Conclusion Slowed processing speed may underlie generalized neurocognitive impairment in UHR individuals and represent a potential intervention target. |
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id | doaj.art-332e81dbf8fe4b33b36d3db500b99bf4 |
institution | Directory Open Access Journal |
issn | 2162-3279 |
language | English |
last_indexed | 2024-12-16T17:55:47Z |
publishDate | 2021-03-01 |
publisher | Wiley |
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series | Brain and Behavior |
spelling | doaj.art-332e81dbf8fe4b33b36d3db500b99bf42022-12-21T22:22:10ZengWileyBrain and Behavior2162-32792021-03-01113n/an/a10.1002/brb3.1962Generalized neurocognitive impairment in individuals at ultra‐high risk for psychosis: The possible key role of slowed processing speedLasse Randers0Jens Richardt Møllegaard Jepsen1Birgitte Fagerlund2Dorte Nordholm3Kristine Krakauer4Carsten Hjorthøj5Birte Glenthøj6Merete Nordentoft7Copenhagen Research Center for Mental Health ‐ CORE Mental Health Center Copenhagen Copenhagen University Hospital Copenhagen DenmarkCopenhagen Research Center for Mental Health ‐ CORE Mental Health Center Copenhagen Copenhagen University Hospital Copenhagen DenmarkCenter for Clinical Intervention and Neuropsychiatric Schizophrenia Research (CINS) Mental Health Center Glostrup Copenhagen University Hospital Glostrup DenmarkCopenhagen Research Center for Mental Health ‐ CORE Mental Health Center Copenhagen Copenhagen University Hospital Copenhagen DenmarkCopenhagen Research Center for Mental Health ‐ CORE Mental Health Center Copenhagen Copenhagen University Hospital Copenhagen DenmarkCopenhagen Research Center for Mental Health ‐ CORE Mental Health Center Copenhagen Copenhagen University Hospital Copenhagen DenmarkCenter for Clinical Intervention and Neuropsychiatric Schizophrenia Research (CINS) Mental Health Center Glostrup Copenhagen University Hospital Glostrup DenmarkCopenhagen Research Center for Mental Health ‐ CORE Mental Health Center Copenhagen Copenhagen University Hospital Copenhagen DenmarkAbstract Objective Widespread neurocognitive impairment is well‐established in individuals at ultra‐high risk (UHR) for developing psychoses, but it is unknown whether slowed processing speed may underlie impairment in other neurocognitive domains, as found in schizophrenia. The study delineated domain functioning in a UHR sample and examined if neurocognitive slowing might account for deficits across domains. Methods The cross‐sectional study included 50 UHR individuals with no (n = 38) or minimal antipsychotic exposure (n = 12; mean lifetime dose of haloperidol equivalent = 17.56 mg; SD = 13.04) and 50 matched healthy controls. Primary analyses compared group performance across neurocognitive domains before and after covarying for processing speed. To examine the specificity of processing speed effects, post hoc analyses examined the impact of the other neurocognitive domains and intelligence as covariates. Results UHR individuals exhibited significant impairment across all neurocognitive domains (all ps ≤ .010), with medium to large effect sizes (Cohen's ds = −0.53 to −1.12). Only processing speed used as covariate eliminated significant between‐group differences in all other domains, reducing unadjusted Cohen's d values with 68% on average, whereas the other domains used as covariates averagely reduced unadjusted Cohen's d values with 20% to 48%. When covarying each of the other domains after their shared variance with speed of processing was removed, all significant between‐group domain differences remained (all ps ≤ .024). Conclusion Slowed processing speed may underlie generalized neurocognitive impairment in UHR individuals and represent a potential intervention target.https://doi.org/10.1002/brb3.1962at‐risk mental stateclinical high riskcognitionneuropsychologyschizophrenia |
spellingShingle | Lasse Randers Jens Richardt Møllegaard Jepsen Birgitte Fagerlund Dorte Nordholm Kristine Krakauer Carsten Hjorthøj Birte Glenthøj Merete Nordentoft Generalized neurocognitive impairment in individuals at ultra‐high risk for psychosis: The possible key role of slowed processing speed Brain and Behavior at‐risk mental state clinical high risk cognition neuropsychology schizophrenia |
title | Generalized neurocognitive impairment in individuals at ultra‐high risk for psychosis: The possible key role of slowed processing speed |
title_full | Generalized neurocognitive impairment in individuals at ultra‐high risk for psychosis: The possible key role of slowed processing speed |
title_fullStr | Generalized neurocognitive impairment in individuals at ultra‐high risk for psychosis: The possible key role of slowed processing speed |
title_full_unstemmed | Generalized neurocognitive impairment in individuals at ultra‐high risk for psychosis: The possible key role of slowed processing speed |
title_short | Generalized neurocognitive impairment in individuals at ultra‐high risk for psychosis: The possible key role of slowed processing speed |
title_sort | generalized neurocognitive impairment in individuals at ultra high risk for psychosis the possible key role of slowed processing speed |
topic | at‐risk mental state clinical high risk cognition neuropsychology schizophrenia |
url | https://doi.org/10.1002/brb3.1962 |
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