Faglige interesser
- Kjønnsforskjeller i psykisk helse
- Psykisk helse hos ungdom
- Utviklingspsykopatologi
- Samspill mellom genetikk og miljøfaktorer i utvikling av psykiske lidelser
Forskning
I PhD-prosjektet mitt undersøker jeg årsakene til at forekomsten av depresjon er høyere hos jenter enn gutter, blant annet ved å studere kjønnsspesifikke utviklingsveier til depresjon hos ungdom. PhD-prosjektet er tilknyttet forskningsgruppen TRACE ved PROMENTA. Prosjektet "Utviklingsveier til depresjon hos jenter" er finansiert av stiftelsen DAM og gjennomføres i samarbeid med Sanitetskvinnene og FREMSAM.
Undervisning
Bakgrunn
- Utdannet psykolog (cand.psychol.) ved Universitetet i Oslo (2023)
- Vitenskapelig assistent i forskningsgruppen Nevrokognitiv utvikling ved psykologisk institutt, UiO (2022)
- Forskningsassistent ved Folkehelseinstituttet, avdeling for barns helse og utvikling (2018-2021)
Emneord:
PROMENTA
Publikasjoner
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Kraft, Brage; MacSweeney, Niamh Anne; Page, Christian Magnus; Lyle, Robert; Tsotsi, Stella & Ulset, Vidar Sandsaunet
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(2026).
The effect of prenatal maternal stress on adolescent internalizing symptoms and the genetic moderation of executive functioning and prefrontal cortex.
Psychological Medicine.
ISSN 0033-2917.
56.
doi:
10.1017/S0033291726105431.
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Background: Prenatal maternal stress is a known risk factor for later emotional problems, yet not all exposed offspring develop psychopathology. Executive functioning and prefrontal cortex structure and activity may buffer these effects, but it remains unclear whether genetic predis positions in these domains moderate associations with adolescent internalizing symptoms.
Methods: We examined 3,111 adolescents (1,881 females, 1,230 males). Prenatal stress was measured via a cumulative index across four domains. Internalizing symptoms were self reported at ages 14 and 16. Genetic predisposition for executive functioning was indexed using a polygenic score (PGS) derived from adult samples, applied here to estimate genetic predis position for executive functioning in adolescence. We also estimated a prefrontal cortex PGS based on cortical thickness and activation in six prefrontal regions, with a composite index derived from the first principal axis summarizing these measures.
Results: Higher prenatal stress was significantly associated with more internalizing symptoms in adolescence. Female sex and maternal genetic risk for internalizing symptoms were also associated with higher symptom levels. Neither genetic disposition for executive functioning nor prefrontal cortex moderated this association overall. However, a weak interaction emerged at age 16, indicating that a genetic disposition for higher executive functioning was associated with greater internalizing symptoms under high stress exposure.
Conclusions: Prenatal maternal stress predicted increased adolescent internalizing symptoms, with limited evidence for moderation by genetic predisposition for executive functioning. Higher genetic potential for executive functioning may confer increased sensitivity to early stress under certain developmental conditions.
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Publisert
14. aug. 2025 10:41
- Sist endret
14. aug. 2025 12:20