Elevated Blood Pressure Clinical Trial
Official title:
'Low-salt' Bread as Part of a Pragmatic Reduced-salt Diet for Lowering Blood Pressure in Adults With Elevated Blood Pressure
In the context of public health, reformulation of bread in terms of salt content remains an
important measure to help achieve a reduction in salt intake in the population. Therefore,
the aim of this study was to examine, using a 5-week cross-over design, food-based
intervention trial, the potential for inclusion of 'low-salt' bread as part of a pragmatic
reduced-salt diet on blood pressure (BP) in adults with slightly to moderately elevated BP.
The study consisted of a randomized crossover trial of the effect of reduced-salt intake or
usual-salt intake for 5 weeks on BP (as the primary outcome) in adults with slightly to
moderately elevated BP (seated office systolic BP >120 and <160 mmHg or a diastolic BP >80
and <95 mmHg; identified by a pre-screening phase).
Subjects were randomly assigned to the reduced-salt diet or their usual-salt diet (control)
for 5 weeks, followed by crossover to the alternative dietary regimen for a further 5 weeks.
Subjects randomized to start on the reduced-salt diet were asked to restrict their
consumption of dietary salt using a combination of pragmatic dietary advice as well as the
replacement of bread and a limited number of other foods with equivalent foods which had
lower salt content; these were provided to the participants. At the beginning of the salt
restriction period, a research nutritionist provided the subjects with a list of the common
salt-containing food and were asked to limit the consumption of such, as feasible. The
subjects received in-house prepared 'low-salt (<0.3 g/100 g)' brown or white sliced pan bread
as well as no-salt margarine/butter, and were given luncheon meats with no added salt, if
desired (optional); these were supplied regularly by the research staff. Subjects commencing
the trial on the control diet were allowed to follow their usual diet but were asked to
consume an in-house produced brown or white sliced pan bread equivalent in composition to the
low-salt version but with its more typical salt content (1.2 g/100 g).
Participants met the research staff weekly to receive breads and no-salt margarine/butter as
well as luncheon meats (where applicable), and at these meetings the staff promoted
compliance with the intervention and encouraged completion of the study protocol.
BP and other assessments were made at baseline and at the end of week 5 and week 10.
Brief background and context for the study:
The World Health Organization's Global Action Plan for the Prevention and Control of
Non-Communicable Disease includes a voluntary global target of a 30% relative reduction in
mean population intake of salt/sodium by 2025. Bread and cured/processed meats collectively
contribute anything from about a third upwards of total salt intake of adults in many Western
countries. Reformulation of bread in terms of salt content remains an important measure to
help achieve a reduction in salt intake in the population. Therefore, the aim of this study
was to examine, using a 5-week cross-over design, food-based intervention trial, the
potential for inclusion of 'low-salt' bread as part of a pragmatic reduced-salt diet on blood
pressure (BP) in adults with slightly to moderately elevated BP.
Design:
The study consisted of a randomized crossover trial of the effect of reduced-salt intake or
usual-salt intake for 5 weeks on BP (primary outcome) and biochemical markers of calcium and
bone metabolism as well as plasma lipids (secondary outcomes) in adults with slightly to
moderately elevated BP.
Potential volunteers were screened for BP over 3 weeks preceding the intervention phase of
the trial during which seated office systolic and diastolic BP were measured weekly and those
with systolic BP >120 and <160 mmHg or a diastolic BP >80 and <95 mmHg were considered
eligible.
The dietary intervention phase of the trial was designed in two successive dietary periods,
each of 5 weeks. Subjects were randomly assigned to the reduced-salt diet or their usual-salt
diet (control) for 5 weeks, followed by crossover to the alternative dietary regimen for a
further 5 weeks. At baseline (week 0), the subjects visited the Human Nutrition Studies Unit
within University College Cork in a fasting state and had their BP measured. Prior to the
baseline visit, subjects received instructions on how to collect a 24-h urine sample and were
provided with a suitable container for collection. On the day of the baseline visit, subjects
brought the 24-h urine sample collected from the previous day and deposited it in a cold room
area dedicated for such collections. A blood sample was taken from each subject between 08.30
am and 10.30 am by a trained phlebotomist and anthropometric measures including height and
weight, were taken. A health and lifestyle questionnaire, which assessed physical activity,
general health, smoking status and alcohol consumption was completed by each subject.
Subjects randomized to start on the reduced-salt diet were asked to restrict their
consumption of dietary salt using a combination of pragmatic dietary advice as well as the
replacement of bread and a limited number of other foods with equivalent foods which had
lower salt content; these were provided to the participants. At the beginning of the salt
restriction period, a research nutritionist provided the subjects with a list of the common
salt-containing food and were asked to limit the consumption of such, as feasible. The
subjects received in-house prepared 'low-salt (<0.3 g/100 g)' brown or white sliced pan bread
as well as no-salt margarine/butter, and were given luncheon meats with no added salt, if
desired (optional). Subjects commencing the trial on the control diet were allowed to follow
their usual diet but were asked to consume an in-house produced brown or white sliced pan
bread equivalent in composition to the low-salt version but with its more typical salt
content (1.2 g/100 g).
During the intervention phase, each participant made 2 further visits to the study unit, one
each on the last day of dietary period 1 (week 5) and dietary period 2 (week 10). At these
visits, BP measurements were taken as well as other anthropometric measures, including height
and weight. An overnight fasting blood sample was also taken from each participant between
08.30 am and 10.30 am by a trained phlebotomist, and on each of the visits, the subjects
provided a 24-hour urine sample collected the previous day. Following blood sampling the
participants received their breakfast.
Participants met the research staff weekly to receive breads and no-salt margarine/butter as
well as luncheon meats (where applicable), and at these meetings the staff promoted
compliance with the intervention and encouraged completion of the study protocol.
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