Associations of age, sex and body mass index to brain [11C]-UCB-J PET in first episode psychosis patients and healthy controls
Rimpiläinen, Salla (2025-03-05)
Associations of age, sex and body mass index to brain [11C]-UCB-J PET in first episode psychosis patients and healthy controls
Rimpiläinen, Salla
(05.03.2025)
Julkaisu on tekijänoikeussäännösten alainen. Teosta voi lukea ja tulostaa henkilökohtaista käyttöä varten. Käyttö kaupallisiin tarkoituksiin on kielletty.
suljettu
Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2025031217405
https://urn.fi/URN:NBN:fi-fe2025031217405
Tiivistelmä
Psychotic disorders are a complex, multifactorial group of disorders that are caused
by both genetic and environmental factors. Although the underlying biochemical mechanisms are
poorly understood, disturbed neuronal connectivity and altered synaptic density have been proposed
to play key roles in the etiology of this group of severe illnesses. For example, post-mortem and
animal studies show evidence of a lowered synaptic density in psychosis patients and schizophrenia
animal models. Recent advancements in radiotracer development presents to us the opportunity to
investigate synapses in vivo; [11C]-UCB-J is a rather new radiotracer used in positron emission
tomography (PET) imaging. It targets a ubiquitously expressed synaptic vesicle protein 2A (SV2A)
in the human brain. This has been proposed to represent synaptic density. However, common
demographic variables, such as age, can plausibly confound these measurements of synaptic
density. We researched associations of relevant demographic factors age, sex, BMI and injected
dose to [11C]-UCB-J binding in first episode psychosis patients (FEP) and healthy controls. This
study broadens our knowledge of the possible pitfalls and confounding factors in clinical studies
using [11C]-UCB-J and PET.
by both genetic and environmental factors. Although the underlying biochemical mechanisms are
poorly understood, disturbed neuronal connectivity and altered synaptic density have been proposed
to play key roles in the etiology of this group of severe illnesses. For example, post-mortem and
animal studies show evidence of a lowered synaptic density in psychosis patients and schizophrenia
animal models. Recent advancements in radiotracer development presents to us the opportunity to
investigate synapses in vivo; [11C]-UCB-J is a rather new radiotracer used in positron emission
tomography (PET) imaging. It targets a ubiquitously expressed synaptic vesicle protein 2A (SV2A)
in the human brain. This has been proposed to represent synaptic density. However, common
demographic variables, such as age, can plausibly confound these measurements of synaptic
density. We researched associations of relevant demographic factors age, sex, BMI and injected
dose to [11C]-UCB-J binding in first episode psychosis patients (FEP) and healthy controls. This
study broadens our knowledge of the possible pitfalls and confounding factors in clinical studies
using [11C]-UCB-J and PET.