Cerebral Small Vessel Diseases Clinical Trial
Official title:
The Effect of Tadalafil on Cerebral Large Arteries in Stroke Patients
In a double blind placebo-controlled cross-over study the effect of tadalafil on blood flow velocity in the large arteries of the brain, cortical brain oxygenation, peripheral endothelial function, and endothelial biomarkers will be tested in patients with lacunar stroke caused by cerebral small vessel disease.
Stroke frequently causes death and decreased function in the everyday life, and the disease
has a great human and economic impact. Cerebral small vessel disease (SVD) is the underlying
cause of 25 % of all ischemic cerebral strokes and it can further lead to vascular cognitive
impairment (VCI), disability and in some cases vascular dementia (VaD). It is well known that
cerebral blood flow (CBF) is reduced in VCI. To be able to improve the blood flow in the
vasculature of white and gray matter is therefore desirable in slowing the pathology of VCI.
The nitric oxide-cGMP vasodilator pathways has been shown to be impaired in endothelial
dysfunction which is seen in SVD.This study targets this well-established mechanism of action
by use of a compound selectively inhibiting the breakdown of cGMP, the PDE5 inhibitor
tadalafil.
The overall hypothesis is that chronic PDE5 inhibition with tadalafil will lessen the
severity and progression of vascular brain lesions via augmentation of cerebral blood flow in
the deep brain areas. The specific primary hypothesis for the current project is that PDE5
inhibition with a single dose of tadalafil (Cialis®) will, in contrast to placebo,
temporarily change the blood flow in the large blood vessels in the brain and change cortical
brain oxygenation in patients with cerebral small vessel disease measured with Transcranial
Doppler and near-infrared spectroscopy (NIRS). The secondary hypothesis is that tadalafil
will improve the peripheral endothelial function measured as improved blood vessel response
in the fingers after a brief occlusion of the arm's blood supply measured with EndoPAT2000.
In addition there will be a change of endothelial function biomarkers in the blood after a
single dose of tadalafil, and these changes are consistent with the measured peripheral and
central blood vessel function.
In regulation of cerebral artery flow and neuronal signalling nitric oxide (NO) and cGMP act
as key molecules. In animal models, selective inhibitors of the cGMP degrading PDE5,
sildenafil and tadalafil, have been reported to improve the associated symptoms of
endothelial dysfunction and stroke recovery. Pre-clinical studies support a CBF-enhancing
action of PDE5 inhibitors in cerebrovascular disease while human studies to date have been
limited to sildenafil and have not specifically addressed effects on CBF in people with SVD.
Tadalafil (Cialis®; Eli Lilly) is widely prescribed for erectile dysfunction in men. It is
also registered for regular daily use at a dose of 40 mg for pulmonary hypertension and 5 mg
for benign prostatic hyperplasia. The side effects of tadalafil is well-known and the
medicine is usually well tolerated. Tadalafil was chosen over other PDE5 inhibitors (such as
sildenafil, Viagra®) due to it's potency, plasma half-life, selectivity for PDE5, and
documented brain penetration.
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