Transdiagnostic subgroups of cognitive impairment in early affective and psychotic illness.
Transdiagnostic subgroups of cognitive impairment in early affective and psychotic illness.
复制标题
早期情感性和精神性疾病中认知障碍的跨诊断亚群。
DOI:
10.1038/s41386-023-01729-7
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发表时间:
2024-02
影响因子:
7.6
通讯作者:
Kambeitz-Ilankovic, Lana
中科院分区:
文献类型:
--
作者:
Wenzel, Julian;Badde, Luzie;Haas, Shalaila S.;Bonivento, Carolina;Van Rheenen, Tamsyn E.;Antonucci, Linda A.;Ruef, Anne;Penzel, Nora;Rosen, Marlene;Lichtenstein, Theresa;Lalousis, Paris Alexandros;Paolini, Marco;Stainton, Alexandra;Dannlowski, Udo;Romer, Georg;Brambilla, Paolo;Wood, Stephen J.;Upthegrove, Rachel;Borgwardt, Stefan;Meisenzahl, Eva;Salokangas, Raimo K. R.;Pantelis, Christos;Lencer, Rebekka;Bertolino, Alessandro;Kambeitz, Joseph;Koutsouleris, Nikolaos;Dwyer, Dominic B.;Kambeitz-Ilankovic, Lana
Cognitively impaired and spared patient subgroups were identified in psychosis and depression, and in clinical high-risk for psychosis (CHR). Studies suggest differences in underlying brain structural and functional characteristics. It is unclear whether cognitive subgroups are transdiagnostic phenomena in early stages of psychotic and affective disorder which can be validated on the neural level. Patients with recent-onset psychosis (ROP; N = 140; female = 54), recent-onset depression (ROD; N = 130; female = 73), CHR (N = 128; female = 61) and healthy controls (HC; N = 270; female = 165) were recruited through the multi-site study PRONIA. The transdiagnostic sample and individual study groups were clustered into subgroups based on their performance in eight cognitive domains and characterized by gray matter volume (sMRI) and resting-state functional connectivity (rsFC) using support vector machine (SVM) classification. We identified an impaired subgroup (NROP = 79, NROD = 30, NCHR = 37) showing cognitive impairment in executive functioning, working memory, processing speed and verbal learning (all p < 0.001). A spared subgroup (NROP = 61, NROD = 100, NCHR = 91) performed comparable to HC. Single-disease subgroups indicated that cognitive impairment is stronger pronounced in impaired ROP compared to impaired ROD and CHR. Subgroups in ROP and ROD showed specific symptom- and functioning-patterns. rsFC showed superior accuracy compared to sMRI in differentiating transdiagnostic subgroups from HC (BACimpaired = 58.5%; BACspared = 61.7%, both: p < 0.01). Cognitive findings were validated in the PRONIA replication sample (N = 409). Individual cognitive subgroups in ROP, ROD and CHR are more informative than transdiagnostic subgroups as they map onto individual cognitive impairment and specific functioning- and symptom-patterns which show limited overlap in sMRI and rsFC. German Clinical Trials Register (DRKS). Clinical trial registry URL: https://www.drks.de/drks_web/. Clinical trial registry number: DRKS00005042.
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影响因子:
6.9
作者:
Burdick KE;Russo M;Frangou S;Mahon K;Braga RJ;Shanahan M;Malhotra AK
通讯作者:
Malhotra AK
影响因子:
3.4
作者:
HALL, RCW
通讯作者:
HALL, RCW
影响因子:
1.8
作者:
Hennig, Christian
通讯作者:
Hennig, Christian
影响因子:
3
作者:
ELIASON, MJ;RICHMAN, LC
通讯作者:
RICHMAN, LC
影响因子:
25.8
作者:
Fusar-Poli, Paolo;Borgwardt, Stefan;Bechdolf, Andreas;Addington, Jean;Riecher-Rossler, Anita;Schultze-Lutter, Frauke;Keshavan, Matcheri;Wood, Stephen;Ruhrmann, Stephan;Seidman, Larry J.;Valmaggia, Lucia;Cannon, Tyrone;Velthorst, Eva;De Haan, Lieuwe;Cornblatt, Barbara;Bonoldi, Ilaria;Birchwood, Max;McGlashan, Thomas;Carpenter, William;McGorry, Patrick;Klosterkotter, Joachim;McGuire, Philip;Yung, Alison
通讯作者:
Yung, Alison