A normative chart for cognitive development in a genetically selected population
dc.contributor.author | Fiksinski, Ania | |
dc.contributor.author | Bearden, Carrie | |
dc.contributor.author | Bassett, Anne | |
dc.contributor.author | Kahn, René | |
dc.contributor.author | Zinkstok, Janneke | |
dc.contributor.author | Hooper, Stephen R | |
dc.contributor.author | Tempelaar, Wanda | |
dc.contributor.author | McDonald, Donna | |
dc.contributor.author | Swillen, Ann | |
dc.contributor.author | Emanuel, Beverly | |
dc.contributor.author | Morrow, Bernice | |
dc.contributor.author | Gur, Raquel | |
dc.contributor.author | Chow, Eva | |
dc.contributor.author | Van den Bree, Marianne | |
dc.contributor.author | Vermeesch, Joris | |
dc.contributor.author | Warren, Stephen | |
dc.contributor.author | Owen, Michael | |
dc.contributor.author | Van Amelsvoort, Therese | |
dc.contributor.author | Eliez, Stephan | |
dc.contributor.author | Gothelf, Doron | |
dc.contributor.author | Arango, Celso | |
dc.contributor.author | Kates, Wendy | |
dc.contributor.author | Simon, Tony | |
dc.contributor.author | Murphy, Kieran | |
dc.contributor.author | Repetto, Gabriela | |
dc.contributor.author | Heine, Damian | |
dc.contributor.author | Vicari, Stefano | |
dc.contributor.author | Cubells, Joseph | |
dc.contributor.author | Armando, Marco | |
dc.contributor.author | Philip, Nicole | |
dc.contributor.author | Campbell, Linda | |
dc.contributor.author | García, Sixto | |
dc.contributor.author | Schneider, Maude | |
dc.contributor.author | Shashi, Vandana | |
dc.contributor.author | 22q11DS International Consortium on Brain and Behavior | |
dc.contributor.author | Vorstman, Jacob | |
dc.contributor.author | Breetvelt, Elemi | |
dc.date.accessioned | 2022-03-30T13:26:16Z | |
dc.date.available | 2022-03-30T13:26:16Z | |
dc.date.issued | 2021 | |
dc.description.abstract | Certain pathogenic genetic variants impact neurodevelopment and cause deviations from typical cognitive trajectories. Understanding variant-specific cognitive trajectories is clinically important for informed monitoring and identifying patients at risk for comorbid conditions. Here, we demonstrate a variant-specific normative chart for cognitive development for individuals with 22q11.2 deletion syndrome (22q11DS). We used IQ data from 1365 individuals with 22q11DS to construct variant-specific normative charts for cognitive development (Full Scale, Verbal, and Performance IQ). This allowed us to calculate Z-scores for each IQ datapoint. Then, we calculated the change between first and last available IQ assessments (delta Z-IQ-scores) for each individual with longitudinal IQ data (n = 708). We subsequently investigated whether using the variant-specific IQ-Z-scores would decrease required sample size to detect an effect with schizophrenia risk, as compared to standard IQ-scores. The mean Z-IQ-scores for FSIQ, VIQ, and PIQ were close to 0, indicating that participants had IQ-scores as predicted by the normative chart. The mean delta-Z-IQ-scores were equally close to 0, demonstrating a good fit of the normative chart and indicating that, as a group, individuals with 22q11DS show a decline in IQ-scores as they grow into adulthood. Using variant-specific IQ-Z-scores resulted in 30% decrease of required sample size, as compared to the standard IQ-based approach, to detect the association between IQ-decline and schizophrenia (p < 0.01). Our findings suggest that using variant-specific normative IQ data significantly reduces required sample size in a research context, and may facilitate a more clinically informative interpretation of IQ data. This approach allows identification of individuals that deviate from their expected, variant-specific, trajectory. This group may be at increased risk for comorbid conditions, such as schizophrenia in the case of 22q11DS. | es |
dc.description.version | Versión publicada | es |
dc.identifier.citation | Fiksinski AM, Bearden CE, Bassett AS, Kahn RS, Zinkstok JR, Hooper SR, Tempelaar W, McDonald-McGinn D, Swillen A, Emanuel B, Morrow B, Gur R, Chow E, van den Bree M, Vermeesch J, Warren S, Owen M, van Amelsvoort T, Eliez S, Gothelf D, Arango C, Kates W, Simon T, Murphy K, Repetto G, Suner DH, Vicari S, Cubells J, Armando M, Philip N, Campbell L, Garcia-Minaur S, Schneider M, Shashi V; 22q11DS International Consortium on Brain and Behavior, Vorstman J, Breetvelt EJ. A normative chart for cognitive development in a genetically selected population. Neuropsychopharmacology. 2021 Mar 29. doi: 10.1038/s41386-021-00988-6 | es |
dc.identifier.uri | https://doi.org/10.1038/s41386-021-00988-6 | es |
dc.identifier.uri | http://hdl.handle.net/11447/5854 | |
dc.language.iso | en | es |
dc.subject | Adolescent | es |
dc.subject | Age Factors | es |
dc.subject | Child | es |
dc.subject | Cognition Disorders / complications | es |
dc.subject | Cognition Disorders / psychology | es |
dc.subject | Humans | es |
dc.subject | Intelligence Tests | es |
dc.subject | Neuropsychological Tests | es |
dc.subject | Psychotic Disorders / complications | es |
dc.subject | Psychotic Disorders / psychology | es |
dc.subject | Cognitive development | es |
dc.title | A normative chart for cognitive development in a genetically selected population | es |
dc.type | Article | es |
dcterms.source | Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology | es |
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