Effects of Nebivolol on Skeletal Muscle During Exercise in Hypertensive Patients

The University of Texas System (UT)

Status and phase: Completed; Phase 4

Conditions: Hypertension

Treatments: Procedure: Endothelial cell collection; Procedure: Microvascular perfusion assessment using Definity; Drug: Metoprolol succinate; Drug: Nebivolol; Procedure: Non-invasive measurement of Cardiac Output (CO)

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT01501929

Bystolic MD52

Details and patient eligibility

About

The purpose of this study is to determine if Nebivolol improves microvascular perfusion in skeletal muscle during exercise in hypertensive patients and whether this improvement is accompanied by reduction in vascular oxidative stress or increased endothelial nitric oxide synthase (eNOS) expression in humans.

Full description

In 32 untreated stage 1 hypertensive subjects, the investigators will measure blood pressure; noninvasive cardiac output by thoracic electrical bioimpedance (Bioz, Cardio Dynamics); forearm mediated vasodilation (FMD), which is a non-invasive assessment of endothelial function; collect venous endothelial cells; and measure microvascular perfusion using an Octafluoropropane microbubble contrast agent (Definity).

To obtain FMD, the brachial artery will be imaged using ultrasound. After a clear picture has been obtained, the cuff on the same arm will be inflated until it is tight for five minutes. During and following this, the subject's arm will continue to be imaged to monitor maximal increase in the brachial artery diameter.

To collect endothelial cells, a thin wire will be inserted in the vein to collect cells from the inner lining of the vein. The cells collected will be processed and stained for several proteins involved in endothelial cell function, using immunofluorescent technique.

To assess the microvascular perfusion in the skeletal muscle, a contrast agent (Definity) will be administered at baseline and after 5 minutes of rhythmic hand grip exercise at 30% of maximal voluntary contraction.

The investigators will then randomize our subjects to receive 12 weeks of Metoprolol or Nebivolol, using a cross over design. There will be a 4 week washout period between the two treatments. During the washout period, subjects will be followed after 2 weeks of drug withdrawal. Subjects found to have BP > 140/90 mmHg then, will be started on hydrochlorothiazide (HCTZ) at 25 mg once daily. Then subjects will be asked to return in 2 weeks. At that time HCTZ will be stopped if started in the earlier visit, and subject will be switched to the remaining treatment (Nebivolol or Metoprolol). Then, the investigators will assess microvascular perfusion in the skeletal muscle at rest and during handgrip exercise, endothelial function (FMD), and changes in endothelial cell protein expression after 12 weeks of Nebivolol and after 12 weeks of Metoprolol treatment in the same subjects.

Enrollment: 32 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Men and women with stage I primary untreated hypertension (BP between 140-159/90-99 mmHg)
• Age 18-65

Exclusion criteria

• Congestive heart failure
• Coronary artery disease
• Left ventricular hypertrophy by echocardiography or ECG
• History of stroke
• Average blood pressure >159/99 mmHg
• Bradycardia with a resting heart rate <55 bpm
• Chronic kidney disease with a serum creatinine > 1.4 mg/dL
• Asthma or chronic obstructive pulmonary disease
• Women who are pregnant or planning to become pregnant
• Hypersensitivity to beta blockers, hydrochlorothiazide, or Definity
• Any history of substance abuse (other than tobacco)
• Concomitant drug treatment which raises endogenous nitric oxide levels, including nitrates or phosphodiesterase V inhibitors (Viagra, Levitra)
• History of symptomatic bradycardia or heart block
• Patients with Right-to-left, bidirectional, or transient right-to-left cardiac shunts
• Hypersensitivity to perflutren, blood, blood products or albumin.

Trial design

Primary purpose: Diagnostic

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: None (Open label)

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32 participants in 2 patient groups

Initial treatment with metoprolol

Active Comparator group

Description:

The subject will be started on metoprolol succinate (Toprol XL) 100-300mg daily, which he/she will continue for a period of 12 weeks. Following the 12-week treatment period, the procedures listed below will be performed. After completion of the study procedures, the medication will be discontinued. If necessary, 2 weeks after drug withdrawal, subjects will be started on HCTZ if BP \> 140/90 mmHg and will continue HCTZ for a 2-week period, after which the subject will be transitioned to nebivolol (Bystolic) 5-20mg daily, which he or she will continue for a period of 12 weeks. Following the 12-week treatment period, the procedures listed below will be performed. After completion of the study procedures, the medication will be discontinued.

Treatment:

Procedure: Microvascular perfusion assessment using Definity

Procedure: Non-invasive measurement of Cardiac Output (CO)

Drug: Nebivolol

Drug: Metoprolol succinate

Procedure: Endothelial cell collection

Initial treatment with nebivolol

Active Comparator group

Description:

The subject will be started on nebivolol (Bystolic) 5-20mg daily, which he or she will continue for a period of 12 weeks. Following the 12-week treatment period, the procedures listed below will be performed. After completion of the study procedures, the medication will be discontinued. If necessary, 2 weeks after drug withdrawal, subject will be started on HCTZ if BP \> 140/90 mmHg and will continue HCTZ for a 2-week period, after which the subject will be transitioned to metoprolol succinate (Toprol XL) 100-300mg daily, which he or she will continue for a period of 12 weeks. Following the 12-week treatment period, the procedures listed below will be performed. After completion of the study procedures, the medication will be discontinued.

Treatment:

Procedure: Microvascular perfusion assessment using Definity

Procedure: Non-invasive measurement of Cardiac Output (CO)

Drug: Nebivolol

Drug: Metoprolol succinate

Procedure: Endothelial cell collection