Cannabis Effects on Brain Morphology in Aging
| Status: | Active, not recruiting |
|---|---|
| Conditions: | Psychiatric |
| Therapuetic Areas: | Psychiatry / Psychology |
| Healthy: | No |
| Age Range: | 60 - 80 |
| Updated: | 7/5/2018 |
| Start Date: | January 2013 |
| End Date: | December 2018 |
Effects of Heavy Adolescent Cannabis Use on Brain Morphology in Aging
Marijuana (Cannabis sativa) is the most widely used illicit drug worldwide, with 17.4 million
Americans reporting past month use in 2010 and 4.6 million meeting criteria for dependence,
underscoring the public health importance of understanding the biological implications of
use. How heavy cannabis use affects brain structure and cognitive performance in late life is
unknown. The ongoing maturation in the adolescent brain, including the developmental
circuitry underlying memory performance and executive control puts the adolescent brain at
high risk for detrimental effects of heavy cannabis use. With the aging of the 'baby boomer'
generation, many people who used cannabis heavily as adolescents are now entering their
senior years when age-related cognitive decline may begin. Cannabis use doubled in less than
a decade during the 1970's when 38% of those surveyed in the U.S. Survey on Drug Abuse
reported using cannabis and 12% of those users reported using cannabis more than 20 times a
month. Understanding how heavy, early cannabis use may affect neurobiological and cognitive
outcomes is of high importance for this aging population, which is already at risk for memory
and cognitive deficits in aging. Because cannabis use appears to have a primary effect within
the hippocampus, the main structure for memory and the structure affected most by age-related
memory impairments and pre-clinical Alzheimer's disease, we expect that the effects of
chronic cannabis use may be greatest during aging. To our knowledge, no study has
investigated the long-term effects of adolescent cannabis use on hippocampal morphology and
cognitive performance in an aging population.
Investigators will investigate hippocampal integrity and cognitive performance using
high-resolution magnetic resonance imaging (MRI), diffusion tensor imaging (DTI) and
neuropsychological testing in an aging population of subjects (55-70 years old) who used
cannabis more than 20 times a month for at least a year during adolescence. Investigators
will compare data collected from heavy cannabis users to subjects who did not use cannabis
but are matched for age, gender, education, light tobacco and light alcohol use. Finally,
because family history and genetic risk are known to accelerate hippocampal morphology and
memory decline in aging, the investigators will investigate whether possession of the APOE ε4
variant in heavy cannabis users is synergistically related to thinner hippocampal cortex and
white matter deficits.
Americans reporting past month use in 2010 and 4.6 million meeting criteria for dependence,
underscoring the public health importance of understanding the biological implications of
use. How heavy cannabis use affects brain structure and cognitive performance in late life is
unknown. The ongoing maturation in the adolescent brain, including the developmental
circuitry underlying memory performance and executive control puts the adolescent brain at
high risk for detrimental effects of heavy cannabis use. With the aging of the 'baby boomer'
generation, many people who used cannabis heavily as adolescents are now entering their
senior years when age-related cognitive decline may begin. Cannabis use doubled in less than
a decade during the 1970's when 38% of those surveyed in the U.S. Survey on Drug Abuse
reported using cannabis and 12% of those users reported using cannabis more than 20 times a
month. Understanding how heavy, early cannabis use may affect neurobiological and cognitive
outcomes is of high importance for this aging population, which is already at risk for memory
and cognitive deficits in aging. Because cannabis use appears to have a primary effect within
the hippocampus, the main structure for memory and the structure affected most by age-related
memory impairments and pre-clinical Alzheimer's disease, we expect that the effects of
chronic cannabis use may be greatest during aging. To our knowledge, no study has
investigated the long-term effects of adolescent cannabis use on hippocampal morphology and
cognitive performance in an aging population.
Investigators will investigate hippocampal integrity and cognitive performance using
high-resolution magnetic resonance imaging (MRI), diffusion tensor imaging (DTI) and
neuropsychological testing in an aging population of subjects (55-70 years old) who used
cannabis more than 20 times a month for at least a year during adolescence. Investigators
will compare data collected from heavy cannabis users to subjects who did not use cannabis
but are matched for age, gender, education, light tobacco and light alcohol use. Finally,
because family history and genetic risk are known to accelerate hippocampal morphology and
memory decline in aging, the investigators will investigate whether possession of the APOE ε4
variant in heavy cannabis users is synergistically related to thinner hippocampal cortex and
white matter deficits.
Inclusion Criteria
- Subjects will be 60 heavy users or non-users between 60-80 years of age
- Participants who used marijuana during adolescence. Current marijuana usage not
allowed and subjects must complete urine screening at the time of inclusion.
Exclusion Criteria
- Major psychiatric disorders, such bipolar disorder or schizophrenia as revealed by the
Structured Clinical Interview for DSM-IV Disorders (100) and exclude for confounding
psychiatric conditions
- Evidence of untreated depression as determined by a HAM-D Score of >12 (17-item
version) or untreated anxiety by a score of > 8 on the Hamilton Anxiety Scale
- Evidence of neurologic or other physical illness that could produce cognitive
deterioration.
- Volunteers with a history of TIAs, carotid bruits, or lacunae on MRI scan will be
excluded
- History of myocardial infarction within the previous year or unstable cardiac disease
- Uncontrolled hypertension (systolic BP > 170 or diastolic BP > 100)
- History of significant liver disease
- Clinically significant pulmonary disease, diabetes, or cancer
- Because medications can affect cognitive functioning, subjects needing medicines that
could influence psychometric test results will be excluded. These include: centrally
active beta-blockers, narcotics, clonidine, anti-Parkinsonian medications, systemic
corticosteroids, benzodiazepines, medications with significant cholinergic or
anticholinergic effects, anticonvulsants, or warfarin, and any affecting the serotonin
system, which may affect neuropsychological test results.
- Current diagnosis or history of alcoholism or dependence on any illicit drugs other
than marijuana.
- Use of any investigational drugs within the previous month or longer, depending on
drug half-life.
- Contraindication for MRI scan (e.g. metal in body, claustrophobia).
We found this trial at
1
site
Los Angeles, California 90095
Principal Investigator: Alison Burggren, Ph.D.
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