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Default mode network in young people with familial risk for psychosis – The Oulu Brain and Mind Study




AlaotsikkoThe Oulu Brain and Mind Study

TekijätTuomas Jukuri, Vesa Kiviniemi, Juha Nikkinen, Jouko Miettunen, Pirjo Mäki, Erika Jääskeläinen, Sari Mukkala, Jenni Koivukangas, Tanja Nordström, Anja Taanila, Irma Moilanen, Markus Heinimaa, Jennifer H Barnett, Peter B Jones, Graham K Murray, Juha Veijola

KustantajaElsevier BV

Julkaisuvuosi2013

JournalSchizophrenia Research

Numero sarjassa2

Vuosikerta143

Numero2

Aloitussivu239

Lopetussivu245

Sivujen määrä7

ISSN0920-9964

DOIhttps://doi.org/10.1016/j.schres.2012.11.020


Tiivistelmä
Objective

The default mode network (DMN) is active in the brain at rest and de-activated during cognitive tasks. Abnormal function in the DMN has been reported in people with schizophrenia but it is not known whether this applies also to people with a familial risk for psychosis (FR). We compared the activity of the DMN between FR participants and controls.


Methods

We conducted a resting state functional MRI (R-fMRI) in 72 young adults without psychosis and with a history of psychosis in one or both parents (FR group) and 72 age matched controls without parental psychosis, and without current psychosis or a current prodromal syndrome. Both groups were drawn from the Northern Finland Birth Cohort 1986 (Oulu Brain and Mind study). Parental psychosis was established using the Finnish hospital discharge register. We pre-processed R-fMRI data using independent component analysis followed by a dual regression approach to assess differences between the groups. The FR vs. Control group differences were assessed using non-parametric permutation tests utilizing threshold-free cluster enhancement and correcting for multiple comparisons (p<0.05).


Results

FR participants demonstrated significantly lower activity compared with controls in the posterior cingulate cortex, the central node of the DMN. The size of the region was 41mm3.


Conclusion

The activity of the DMN differed between FR and control groups. This suggests that familial risk for psychotic disorders may be mediated through genetic effects on connectivity in the posterior cingulate cortex.



Last updated on 2024-26-11 at 22:55