Metabolomics of the Dietary Approaches to Stop Hypertension (DASH) Dietary Pattern
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| ClinicalTrials.gov Identifier: NCT03403166 |
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Recruitment Status :
Completed
First Posted : January 18, 2018
Last Update Posted : January 18, 2018
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| Condition or disease | Intervention/treatment |
|---|---|
| Dietary Modification Blood Pressure | Behavioral: DASH diet Behavioral: Fruits and vegetables diet Behavioral: Control diet |
| Study Type : | Observational |
| Actual Enrollment : | 459 participants |
| Observational Model: | Cohort |
| Time Perspective: | Prospective |
| Official Title: | Metabolomics of the Dietary Approaches to Stop Hypertension (DASH) Dietary Pattern: A Secondary Data Analysis of the DASH Trial |
| Actual Study Start Date : | August 1993 |
| Actual Primary Completion Date : | July 1997 |
| Actual Study Completion Date : | June 2017 |
| Group/Cohort | Intervention/treatment |
|---|---|
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DASH diet
The DASH diet consisted of a high intake of fruits, vegetables, and low-fat dairy products. It included a wide range of sources of protein, such as meat, fish, poultry, nuts, and beans. Sugar-sweetened beverages, desserts, and red meat were restricted. In terms of nutrients, the DASH diet had a high amount of fiber and protein; low amounts of saturated fat, total fat, and cholesterol; and intake of potassium, magnesium, and calcium at levels close to the 75th percentile of U.S. consumption.
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Behavioral: DASH diet
Diet intervention |
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Fruits and vegetables diet
Potassium and magnesium intake was similar to the 75th percentile of U.S. consumption. Fiber intake was high. The fruits and vegetables diet consisted of more fruits and vegetables and fewer snacks and desserts than the control diet, but otherwise was similar to the control diet.
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Behavioral: Fruits and vegetables diet
Diet intervention |
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Control diet
For the control diet, macronutrient intake was similar to average U.S. consumption and intake of potassium, magnesium, and calcium were similar to the 25th percentile of U.S. consumption. Sodium intake was approximately 3 g/day in each diet.
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Behavioral: Control diet
Diet intervention |
- Serum metabolites [ Time Frame: 8 week follow-up visit ]Metabolites were measured using a global, untargeted, metabolomic platform in serum specimens collected at the end of the 8 week diet intervention in the DASH trial. Reverse phase, untargeted ultrahigh-performance liquid chromatography tandem mass spectrometry quantification was used to measure metabolites. Peaks were quantified by calculating the area under the curve. Data were normalized to account for day-to-day instrumental variation. Compounds were identified by comparison to a library of purified standards or recurrent unknown entities and matches were determined based on retention time, mass-to-charge ratio, and chromatographic data. A relative measure of each metabolite (not absolute) is determined. The Metabolon (Durham, NC) platform quantifies over 1,000 compounds representing a broad range of metabolic compounds, including amino acids, carbohydrates, cofactors and vitamins, energy, lipids, nucleotides, peptides, and xenobiotics (chemicals, drugs, and food components).
- Blood pressure [ Time Frame: 8 week follow-up visit ]The change in blood pressure was defined as the blood pressure level at the end of the 8 week diet intervention minus the blood pressure level at baseline.
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| Ages Eligible for Study: | 22 Years to 100 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- Men and women with systolic blood pressure <160 mmHg and diastolic blood pressure 80-95 mmHg
Exclusion Criteria:
- Taking anti-hypertensive medication
- Poorly controlled diabetes mellitus
- Hyperlipidemia
- Cardiovascular event within the past 6 months
- Chronic disease that may interfere with participation
- Pregnancy or lactation
- Body mass index > 35 kg/m2
- Unwilling to stop taking vitamin or mineral supplements or antacids
- Kidney disease
- Consumption of >14 alcoholic beverages per week
- Did not consent to the use of biological specimens
- Did not attend the 8 week follow-up visit
- No serum specimen or insufficient volume of serum specimens in repository
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03403166
| Principal Investigator: | Casey M. Rebholz, PhD, MS, MPH | Johns Hopkins Bloomberg School of Public Health |
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Johns Hopkins Bloomberg School of Public Health |
| ClinicalTrials.gov Identifier: | NCT03403166 |
| Other Study ID Numbers: |
IRB00007383-2 K01DK107782 ( U.S. NIH Grant/Contract ) |
| First Posted: | January 18, 2018 Key Record Dates |
| Last Update Posted: | January 18, 2018 |
| Last Verified: | January 2018 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Hypertension Vascular Diseases Cardiovascular Diseases |

