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Metabolic Effects of Antihypertensive Drugs on People With Metabolic Syndrome (The MEAD Study)

Metabolic Effects of Antihypertensive Drugs

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00887510
Acronym
MEAD
Enrollment
24
Registered
2009-04-24
Start date
2007-05-31
Completion date
2009-11-30
Last updated
2014-06-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension

Keywords

Metabolic Syndrome, High Blood Pressure, Abdominal Obesity, Impaired Glucose Tolerance

Brief summary

High blood pressure, also referred to as hypertension, is a blood pressure level of 140/90 mm Hg or higher. Along with lifestyle changes, various medications are currently used to treat people with hypertension. Some of these medications, however, may affect the way the body handles sugar, essentially preventing the body from breaking down sugar and predisposing people to developing diabetes. People who have metabolic syndrome-a condition primarily characterized by an increased waist measurement, abnormal blood lipid levels, hypertension, and high blood sugar levels-are already at risk of developing diabetes. In these people, taking the antihypertensive medications that prevent sugar breakdown may further increase their risk of diabetes. The purpose of this study is to gain an understanding of how people with metabolic syndrome respond to antihypertensive medications that alter the body's ability to break down sugar.

Detailed description

Treatment for hypertension includes lifestyle changes and medications. Examples of some antihypertensive medications include diuretics, beta-blockers, angiotensin-converting enzyme (ACE) inhibitors, angiotensin receptor blockers (ARBs), and vasodilators. Mounting research suggests that certain antihypertensive medications, such as thiazide diuretics, are associated with metabolic disturbances that result in increased glucose intolerance, while other antihypertensive medications, such as ACE inhibitors and ARBs, appear to improve insulin sensitivity and glucose metabolism. The influence of these medications may be especially critical in people with metabolic syndrome, who are already at risk of developing glucose intolerance and diabetes. The purpose of this study is to gain an understanding of how people with metabolic syndrome respond to antihypertensive medications that alter the body's ability to break down sugar. The long-term goal of the study is to determine the best antihypertensive medications for people who have both metabolic syndrome and hypertension so as to prevent or delay the onset of diabetes in this population. Participation in this study will last 18 weeks and involve four study visits. Participants will be randomly assigned to initially receive 6 weeks of treatment with either hydrochlorothiazide (HCTZ), which is a thiazide diuretic, or trandolapril, which is an ACE inhibitor. Both medications are FDA-approved for treating hypertension. After 6 weeks of treatment, if participants' blood pressure levels are not too low, they will add the second medication so that they are taking both HCTZ and trandolapril for the next 6 weeks, until Week 12. At Week 12, again if participants' blood pressure levels are not too low, they will then take only the second medication for the last 6 weeks. The four study visits will occur at baseline and after each of the three 6-week treatment periods (Weeks 6, 12, and 18). All study visits will include blood pressure and pulse measurements, urine and blood sampling, oral glucose tolerance testing, and questions about diet and exercise habits. The first and last study visits will also include a physical examination and a medical history review. Some of the blood collected during the first study visit will be used for genetic testing. There will be no follow-up visits.

Interventions

DRUGHydrochlorothiazide

25 mg tablet once daily for 6 weeks Other Names: HCTZ

4 mg tablet once daily for 6 weeks

Sponsors

National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH
University of Florida
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Hypertension, defined as systolic blood pressure greater than or equal to 130 but less than 160 mm Hg and diastolic blood pressure greater than or equal to 85 but less than 110 mm Hg * Must have any two of the following criteria: 1. Abdominal obesity, defined as a waist circumference greater than 40 inches in men and greater than 35 inches in women 2. High-density lipoprotein (HDL) cholesterol level of less than 40 mg/dL in men and less than 50 mg/dL in women 3. Fasting triglycerides greater than or equal to 150 mg/dL 4. Fasting glucose level of 100-125 mg/dL

Exclusion criteria

* Significant hypertension (greater than 160/110 mm Hg) * Isolated systolic hypertension * Diseases requiring treatment with diuretics or angiotensin-converting enzyme (ACE) inhibitors * Cardiovascular disease (history of heart attack, stroke, heart failure) * Hypersensitivity to HCTZ or ACE inhibitor * Type 1 or type 2 diabetes * Hypokalemia * Peri-menopause (symptom onset within 1 year) * Pregnant or breastfeeding * Secondary causes of hypertension * Current use of antihypertensive medications known to affect glucose homeostasis (e.g., diuretics, beta blockers, corticosteroids, ACE inhibitors, angiotensin receptor blockers \[ARBs\])

Design outcomes

Primary

MeasureTime frameDescription
Change in Oral Glucose Tolerance Test (OGTT) Area Under Curve (AUC) After Addition of Trandolapril to Hydrochlorothiazide (HCTZ) Compared With Change in OGTT AUC After Addition of HCTZ to TrandolaprilOGTT AUC measured over 120 minutes after receiving study intervention for 18-24 weeks.Comparing the change in OGTT AUC rand 1 visit4-visit 3 with rand 2 visit 3-2. This allows for understanding the effects of addition of trandolapril to 12 weeks of HCTZ compared with addition of HCTZ to 12 weeks of trandolapril. This is the primary outcome of the study.

Secondary

MeasureTime frameDescription
Change in Total Adiponectin Level After Addition of Trandolapril to HCTZ Compared With Change in Adiponectin After Addition of HCTZ to TrandolaprilOver the course of 18 weeksComparing the change in adiponectin: rand 1 visit4-visit 3 with rand 2 visit 3-2. This allows for understanding the effects of addition of trandolapril to 12 weeks of HCTZ compared with addition of HCTZ to 12 weeks of trandolapril.

Countries

United States

Participant flow

Recruitment details

Patients were enrolled from the University of Florida Shands healthcare system between May 2007 and June 2009.

Pre-assignment details

24 participants recruited; 24 randomized, 61 excluded (61 did not meet inclusion criteria)

Participants by arm

ArmCount
Thiazide First
Participants will receive 25 mg of hydrochlorothiazide (HCTZ) each day for 6 weeks, followed by 25 mg of HCTZ every day plus 4 mg of trandolapril each day for 6 weeks, followed by 4 mg trandolapril each day for 6 weeks.
12
Trandolapril First
Participants will receive 4 mg of trandolapril each day for 6 weeks, followed by 4 mg of trandolapril for 6 weeks plus 25 mg of HCTZ each day for 6 weeks, followed by 25 mg of HCTZ each day for 6 weeks.
12
Total24

Baseline characteristics

CharacteristicThiazide FirstTrandolapril FirstTotal
Age, Continuous43.4 years
STANDARD_DEVIATION 9.6
45.7 years
STANDARD_DEVIATION 10.6
44.5 years
STANDARD_DEVIATION 10.1
Region of Enrollment
United States
12 participants12 participants24 participants
Sex: Female, Male
Female
6 Participants6 Participants12 Participants
Sex: Female, Male
Male
6 Participants6 Participants12 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
0 / 120 / 12
serious
Total, serious adverse events
1 / 120 / 12

Outcome results

Primary

Change in Oral Glucose Tolerance Test (OGTT) Area Under Curve (AUC) After Addition of Trandolapril to Hydrochlorothiazide (HCTZ) Compared With Change in OGTT AUC After Addition of HCTZ to Trandolapril

Comparing the change in OGTT AUC rand 1 visit4-visit 3 with rand 2 visit 3-2. This allows for understanding the effects of addition of trandolapril to 12 weeks of HCTZ compared with addition of HCTZ to 12 weeks of trandolapril. This is the primary outcome of the study.

Time frame: OGTT AUC measured over 120 minutes after receiving study intervention for 18-24 weeks.

ArmMeasureValue (MEAN)Dispersion
Thiazide FirstChange in Oral Glucose Tolerance Test (OGTT) Area Under Curve (AUC) After Addition of Trandolapril to Hydrochlorothiazide (HCTZ) Compared With Change in OGTT AUC After Addition of HCTZ to Trandolapril-472 minutes*mg/dlStandard Deviation 2064
Trandolapril FirstChange in Oral Glucose Tolerance Test (OGTT) Area Under Curve (AUC) After Addition of Trandolapril to Hydrochlorothiazide (HCTZ) Compared With Change in OGTT AUC After Addition of HCTZ to Trandolapril1571 minutes*mg/dlStandard Deviation 2256
Secondary

Change in Total Adiponectin Level After Addition of Trandolapril to HCTZ Compared With Change in Adiponectin After Addition of HCTZ to Trandolapril

Comparing the change in adiponectin: rand 1 visit4-visit 3 with rand 2 visit 3-2. This allows for understanding the effects of addition of trandolapril to 12 weeks of HCTZ compared with addition of HCTZ to 12 weeks of trandolapril.

Time frame: Over the course of 18 weeks

ArmMeasureValue (MEAN)Dispersion
Thiazide FirstChange in Total Adiponectin Level After Addition of Trandolapril to HCTZ Compared With Change in Adiponectin After Addition of HCTZ to Trandolapril-1.36 mcg/mlStandard Deviation 0.96
Trandolapril FirstChange in Total Adiponectin Level After Addition of Trandolapril to HCTZ Compared With Change in Adiponectin After Addition of HCTZ to Trandolapril0.42 mcg/mlStandard Deviation 1.11

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026