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Cognitive functioning throughout adulthood and illness stages in individuals with psychotic disorders and their unaffected siblings.

Eva VelthorstJosephine MollonRobin M MurrayLieuwe de HaanInez Myin GermeysDavid C GlahnCelso ArangoEls van der VenMarta Di FortiMiguel BernardoSinan GuloksuzPhilippe DelespaulGisela MezquidaSilvia AmorettiJulio BobesPilar A SaizMaría Paz García-PortillaJosé Luis SantosEstela Jiménez-LópezJulio SanjuanEduardo J AguilarManuel ArrojoAngel CarracedoGonzalo LópezJavier González-PeñasMara ParelladaE Cem AtbasogluMeram Can SakaAlp ÜçokKöksal AlptekinBerna AkdedeTolga BinbayVesile AltınyazarHalis UlaşBerna YalınçetinGüvem Gümüş-AkayBurçin Cihan BeyazHaldun SoygürEylem Şahin CankurtaranSemra Ulusoy KaymakNadja P MaricMarina M MihaljevicSanja Andric PetrovicTijana MirjanicCristina Marta Del BenLaura FerraroCharlotte Gayer-AndersonPeter B JonesHannah E JongsmaJames Bowes KirkbrideCaterina La CasciaAntonio LasalviaSarah TosatoPierre Michel LlorcaPaulo Rossi MenezesCraig MorganDiego QuattroneMarco MenchettiJean-Paul SeltenAndrei SzökeIlaria TarriconeAndrea TortelliPhilip McGuireLucia ValmaggiaMatthew J KemptonMark van der GaagAnita Riecher-RösslerRodrigo Affonseca BressanNeus Barrantes-VidalBarnaby NelsonPatrick McGorryChristos PantelisMarie-Odile KrebsStephan RuhrmannGabriele SachsBart P F RuttenJim van OsBehrooz Z AlizadehTherese van AmelsvoortAgna A Bartels-VelthuisRichard BruggemanNico J van BeverenJurjen J LuykxWiepke CahnClaudia J P SimonsRene S KahnFrederike SchirmbeckRuud van Winkelnull nullAbraham Reichenberg
Published in: Molecular psychiatry (2021)
Important questions remain about the profile of cognitive impairment in psychotic disorders across adulthood and illness stages. The age-associated profile of familial impairments also remains unclear, as well as the effect of factors, such as symptoms, functioning, and medication. Using cross-sectional data from the EU-GEI and GROUP studies, comprising 8455 participants aged 18 to 65, we examined cognitive functioning across adulthood in patients with psychotic disorders (n = 2883), and their unaffected siblings (n = 2271), compared to controls (n = 3301). An abbreviated WAIS-III measured verbal knowledge, working memory, visuospatial processing, processing speed, and IQ. Patients showed medium to large deficits across all functions (ES range = -0.45 to -0.73, p < 0.001), while siblings showed small deficits on IQ, verbal knowledge, and working memory (ES = -0.14 to -0.33, p < 0.001). Magnitude of impairment was not associated with participant age, such that the size of impairment in older and younger patients did not significantly differ. However, first-episode patients performed worse than prodromal patients (ES range = -0.88 to -0.60, p < 0.001). Adjusting for cannabis use, symptom severity, and global functioning attenuated impairments in siblings, while deficits in patients remained statistically significant, albeit reduced by half (ES range = -0.13 to -0.38, p < 0.01). Antipsychotic medication also accounted for around half of the impairment in patients (ES range = -0.21 to -0.43, p < 0.01). Deficits in verbal knowledge, and working memory may specifically index familial, i.e., shared genetic and/or shared environmental, liability for psychotic disorders. Nevertheless, potentially modifiable illness-related factors account for a significant portion of the cognitive impairment in psychotic disorders.
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