Clinical Trial Details
— Status: Completed
Administrative data
NCT number |
NCT03718520 |
Other study ID # |
18-0004 |
Secondary ID |
R21DA043833 |
Status |
Completed |
Phase |
|
First received |
|
Last updated |
|
Start date |
November 7, 2018 |
Est. completion date |
March 31, 2020 |
Study information
Verified date |
October 2021 |
Source |
University of Colorado, Denver |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Observational
|
Clinical Trial Summary
Cannabis is the most commonly used drug by women during pregnancy with an estimated
prevalence of use in Colorado of 5.7%. THC and its metabolites freely cross the placenta and
blood-brain barrier to bind with cannabinoid receptors, disrupting the endogenous cannabinoid
signaling system during a critical period of development of cortical circuitry structure and
function. The density of cannabinoid receptors in the developing brain is high, especially in
the limbic areas and prefrontal lobes. Research in animal models suggests synaptic plasticity
in the prefrontal lobes as well the amygdala and hippocampus are impacted by the prenatal
cannabis exposure; regions associated with both cognitive and emotional control, thus
influencing long-term deficiencies in attention and impulsivity. This pilot study will
collect preliminary data on the structural impact of in utero cannabis exposure on
region-specific morphology and structural connectivity of white matter tracts that connect to
the prefrontal lobes and the limbic regions shortly after birth, before confounding by the
postnatal environment becomes a major influence.
Description:
Cannabis is the most commonly used psychoactive substance among pregnant women, with an
estimated prevalence of use between 5 to 20% in in the United States. Little is known about
the neurodevelopmental consequences for the fetus, particularly in the context of
contemporary cannabis use patterns including high potency strains, cannabinoids and novel
routes of administration. Colorado leads the nation in implementation of legalized medical
and retail marijuana. Coupled with a growing pro-marijuana advocacy movement, marijuana may
be perceived as "safe" to use during pregnancy. The local actions of endocannabinoids are in
place in the placenta during fetal brain development and THC and its metabolites freely pass
the placental barrier and the fetal blood-brain barrier. Furthermore, cannabinoid receptors
appear to be more widespread in the fetal and neonatal prefrontal cortex (PFC) and the limbic
areas (the amygdala and hippocampus) than in the adult brain, thus the in utero period may be
a sensitive period of human brain development during which exogenous cannabinoids could
permanently alter neurodevelopmental processes. Human epidemiologic studies across diverse
populations have reported an emerging theme of deficiencies related to impulse control and
executive functioning among offspring with in utero exposure to cannabis starting in
adolescence. Only rudimentary aspects of executive function are present in infants, thus
evidence of an impact during infancy and the toddler years is sparse, inconsistent and
confounded by the postnatal environment (i.e., daycare, caregiver functioning). Research is
needed to evaluate the proximal impact of in utero cannabis exposure on robust metrics of
neonatal brain morphology and structural integrity of white matter tracts that connect to the
PFC and the limbic regions before the influence of postnatal exposures become a major
confounding influence.
To address this challenge, a pilot prospective pre-birth cohort study will be conducted to
investigate the impact of chronic in utero cannabis exposure by enrolling 110 mother-infant
pairs (50 exposed and 60 unexposed controls) for a neonate neuroimaging scan within 2 weeks
after birth. Chronic in utero cannabis exposure will be quantified using ultra-high
performance liquid chromatography-tandem mass spectrometry (LC-MS) of neonatal meconium. The
associations between in utero cannabis exposure and neural morphological outcomes will be
examined by structural MRI and diffusion tensor imaging (DTI). The central hypothesis is that
in utero cannabis exposure will be associated with alterations in grey and white matter
development in the prefrontal lobe and its connectivity to limbic regions.
Specific Aim 1: To determine the magnitude of the association between in utero exposure to
cannabis and neonate brain morphology and structural connectivity.
Hypothesis: In utero exposure to cannabis (assessed by THC metabolites in meconium) will be
associated with the following neonate brain structural outcomes: (1) Grey matter: reduced
volume in the PFC and limbic regions (i.e. the amygdala, hippocampus); (2) White matter:
reduced structural integrity (assessed by fractional anisotropy) of white matter tracts that
connect to the PFC and the limbic regions including the uncinate fasciculus and the cingulum
bundle. The associations will be independent of other maternal substance use (i.e. tobacco),
postnatal feeding practices (i.e. breastfeeding), socio-demographic characteristics and
maternal mental health.