ABSTRACT
In recent years, cannabis, and its constituents (delta-9 tetrahydrocannabinol [THC] and cannabidiol [CBD]) have
been promoted as natural remedies, with chronic disease patients as prominent marketing targets.
Consequently, adults with underlying medical conditions are more likely to use cannabis compared to adults
without medical conditions. This is alarming given that evidence for therapeutic benefits or potential risks related
to cannabis use is generally lacking. Additionally, the impact of cannabis use on the clinical course of chronic
diseases, which could be significant, is unknown. Here, we propose to recruit a prospective cohort of adult
patients with early-stage high blood pressure (BP). This sizable population (30% of all United States adults) are
at a heightened risk for cardiovascular disease (CVD). We will recruit patients from primary care clinics in
Michigan, where cannabis is legal for adult consumption, and use data from detailed questionnaires, physical
exams and biospecimen collections across the 30-month study to a) characterize cannabis use trajectories
among patients, b) estimate the association between cannabis use trajectories and cardiovascular risk status
and c) estimate the association between cannabis use trajectories and underlying mechanisms of CVD including
systemic inflammation, platelet aggregation and arterial vasospasm. We hypothesize that persistent or
escalating high THC cannabis smoking trajectories will predict worsened cardiovascular risk status in patients
with high BP compared to other use trajectories (e.g., high CBD, oral ingestion, cessation) or non-use.
Epidemiological studies on the cardiovascular health effects of cannabis are scarce, their results are mixed, and
they lack cannabis and CVD measurements proposed here. We will study the cardiovascular health effects of
cannabis use while accounting for cannabis potency and route of administration. Existing research relied heavily
on controlled laboratory studies, conducted using NIDA-supplied cannabis that differs from cannabis used in the
real world. Hence, generalizability and applicability to human health remain uncertain. We will adapt a mobile
pharmacology laboratory approach to assess the potency of cannabis products available to patients in Michigan.
This proposal is important and timely given the recent changes in cannabis policies. In 2018, Michigan became
the first state in the Midwest to legalize cannabis for recreational use. On the other hand, CVD is the leading
cause of death in Michigan and the state rank poorly relative to other states. Characterizing cannabis use
trajectories and how they relate to cardiovascular health over time is essential for cannabis policies, to identify
which trajectories are associated with fewer or greater cardiovascular risks and communicate these risks and
harm reduction strategies to the public. Our results will also inform medical cannabis recommendations, not only
for patients with high BP, but for a diverse group of patients who need cannabis for the management of anorexia,
pain, anxiety, or sleep problems, and are at increased risk of CVD (e.g., patients with HIV, depression, post-
traumatic stress disorder and neuropathies).