About this trial

The proposed pharmacist-led study is a feasibility pilot trial for the management of vascular risk factors of hypertension and hypercholesterolemia in 10 APOE ε4 carriers, 50-75, at-risk for dementia. All participants will receive angiotensin receptor blockers (ARBs) for high blood pressure, and hydrophilic statins (or a non-statin alternative) for high cholesterol over a six-month period.

Eligibility criteria

Qualifiers

APOE ε4 carrier (homozygote or heterozygote)

LDL-C of 100-250 mg/dL

Systolic blood Pressure (SBP) 130-180 mm Hg

Age 50-75 years

Disqualifiers

One minute standing SBP < 110 mm Hg

Arm circumference prevents from accurate BP measurement with use of available devices

Lost weight of > 10% unintendedly (within the past 6 months),

Contraindications to blood pressure and cholesterol lowering medications

Trial design

Treatments tested in this trial

  • Angiotensin Receptor Blockers (ARBs)
  • Hydrophilic Statins or Non-Statin Alternative

Treatment groups

10 Participants
are divided into 1 treatment group

Locations

1
Clinical Sciences Building (CSC)90033, Los AngelesCalifornia, United States

Sponsors and collaborators

University of Southern California

Lead sponsor