(Hypertension. 1997;30:163-167.)
© 1997 American Heart Association, Inc.
Articles |
From the First Department of Internal Medicine (Y.H., H.M., G.K.) and Department of Clinical Laboratory Medicine (T.O., R.O., Y.N., M.K.), Hiroshima University School of Medicine (Japan).
Correspondence to Yukihito Higashi, MD, First Department of Internal Medicine, Hiroshima University School of Medicine, 1-2-3 Kasumi, Minami-ku, Hiroshima 734, Japan. E-mail yhigashi{at}mcai.med.hiroshima-u.ac.jp
| Abstract |
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2=6.4;
P=.02; odds ratio, 3.82). These findings suggest that the
NaCl loading blunted the nocturnal decline in blood pressure in
salt-sensitive patients but not in salt-resistant patients.
Key Words: blood pressure monitoring, ambulatory circadian rhythm hypertension, essential sodium
| Introduction |
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Studies have shown that 24-hour ABPM is useful for assessing white coat hypertension,7 episodic hypertension,8 and the effects of antihypertensive agents.9 Individuals with a non-dipper circadian pattern of blood pressure in which the nocturnal decline in blood pressure is diminished or absent have an increased risk of cerebrovascular and cardiovascular complications compared with individuals with a dipper circadian rhythm.10 11 12 13 14 Data on the effects of NaCl intake on diurnal changes in blood pressure, especially nocturnal blood pressure, are limited.
We investigated the effect of NaCl intake and salt sensitivity on the circadian rhythm of blood pressure using 24-hour noninvasive ambulatory blood pressure measurements in 64 Japanese patients with mild to moderate essential hypertension who ate a low NaCl diet (50 mmol/d) for 1 week, and then a high NaCl diet (340 mmol/d) for 1 week.
| Methods |
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Dietary Manipulation of NaCl
Patients did not take any antihypertensive agents for at least 4
weeks before the study. One week before the study subjects were given a
regular diet that contained 170 mmol of NaCl daily to allow the
systemic sodium balance and blood pressure to stabilize. Subjects then
ate a low NaCl diet (50 mmol/d) for 1 week, followed by a
high NaCl diet (340 mmol/d) for 1 week. The NaCl content of
the high NaCl diet was increased by the addition of Slow-Sodium tablets
(10 mmol NaCl per tablet; Mission Pharmaceutical Co) to the diet.
The dietary content of potassium (100 mmol/d) and calcium
(40 mmol/d) was kept constant throughout the study. The
caloric intake was 40 cal/kg daily. Meals were prepared in the
Hiroshima University Hospital kitchen. Rigid compliance to the diet was
confirmed by measuring the 24-hour urinary excretion of sodium,
chloride, and potassium throughout the study.
24-Hour ABPM
ABPM was performed from day 6 to day 7 of each dietary period
using a TM2420 device (AND Co), a noninvasive ambulatory blood pressure
monitor, that was attached to the upper left arm. Blood pressure was
measured by the Korotkoff microphone methods during stepwise
deflations (3.0±1.0 mm Hg/step) of the cuff. The
within-run precision of blood pressure and heart rate measurements was
±4.0 mm Hg and ±5.0%, respectively. The reliability of
this device has been previously confirmed.15 16 Blood
pressure and heart rate measurements were obtained at 30-minute
intervals. A non-dipper pattern was defined as a difference in the mean
blood pressure of less than 10% between the daytime (6 AM
to 9 PM) and nighttime (9 PM to 6
AM) hours. Patients were confined to their ward during the
study and maintained on a regular schedule. They woke at approximately
6 AM and the room light was turned off at 9 PM.
Salt sensitivity was also defined by the percent change in the mean
24-hour blood pressure that resulted between the low NaCl diet (50
mmol/d) and the high NaCl diet (340 mmol/d).
Subjects in whom NaCl loading induced a
10% change in mean blood
pressure were classified as SS, and subjects in whom NaCl loading
induced a <10% change were classified as SR.
Measurement of Clinical Parameters
After a 30-minute rest period, fasting serum concentrations of
total cholesterol, creatinine, glucose, and
electrolytes; the PRA; and the plasma concentration of
norepinephrine were collected in a supine position in a
quiet, dark, and air-conditioned room maintained at a constant
temperature (22°C to 25°C) at 8:30 AM on day 7 of each
dietary period. Blood samples were placed in prechilled tubes
containing EDTA and in polystyrene tubes. After separation, plasma and
serum were stored at -80°C until analysis. Serum
concentrations of total cholesterol,
creatinine, glucose and electrolytes, and urinary
electrolytes were determined by routine chemical methods. The PRA was
measured by a radioimmunoassay. The plasma concentration of
norepinephrine was measured by high-performance
liquid chromatography.
Statistical Analysis
Results are presented as mean±SEM. Baseline
characteristics of the two groups were compared by ANOVA. The
difference in change in parameters between SS and SR
patients was determined by ANCOVA using baseline data as the
covariates. After adjusting for confounders that significantly differed
between SS and SR groups, differences in the distribution of dipper and
non-dipper patterns determined by ABPM between SS and SR patients were
analyzed by the
2 test. A value of
P<.05 was considered statistically significant.
| Results |
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Baseline parameters were similar in the SS and SR patients
during the regular diet (Table 1
).
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Effects of Dietary NaCl on Clinical Characteristics
During a low NaCl diet, there were no significant differences in
parameters between the SS and the SR patients except for
the PRA, which was higher in SR patients than in SS patients
(P<.05) (Table 2
). During a
high NaCl diet, body weight (P<.01) and urinary sodium
excretion (P<.001) increased significantly and the PRA
(P<.01) decreased significantly in all patients. Mean blood
pressures during a high NaCl diet were significantly higher in SS
patients than in SR patients. The percent change in mean blood pressure
at night was smaller in the SS group than in the SR group during a high
NaCl diet (8.3±1.0% versus 11.5±0.9%, P<.05) but was
similar in both groups during a low NaCl diet.
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Prevalence of Dipper and Non-Dipper Types
A non-dipper pattern was observed in 13 (50%) of 26 SS patients
and in 10 (26%) of 38 SR patients during the regular diet. There was
no significant difference in the frequency of the non-dipper pattern
between groups during a low NaCl diet (SS patients: 12/26 [46%]
versus SR patients: 12/38 [32%]). The frequency of the non-dipper
pattern was significantly higher in SS patients than in SR patients
during a high NaCl diet (15/26 [57%] versus 10/38 [26%];
2=6.4; P=.02; odds ratio, 3.82).
The NaCl-induced increase in blood pressure was correlated with the
nocturnal decline in blood pressure during a high NaCl diet
(Figure
) but not during a low NaCl
diet.
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| Discussion |
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Although the mechanism of the blunted nocturnal decline in blood pressure in SS patients during a high NaCl diet remains unclear, there are a number of potential explanations. Studies have shown that factors that regulate blood pressure, such as sympathetic nervous activity,2 5 body fluid volume,5 PRA,3 4 intracellular sodium and free calcium metabolism,3 17 renal hemodynamics,4 and nitric oxide production,4 are altered by changes in the dietary intake of NaCl. Because these factors also contribute to a circadian rhythm of blood pressure, the NaCl-induced changes in these factors may account for the difference in the change in nocturnal decline in blood pressure.
Previous studies have shown that abnormalities in autonomic nervous system function, especially in sympathetic nervous activity, inhibit the nocturnal decline in blood pressure.18 19 20 Studies have suggested that sympathetic nervous activity dysfunction is increased by a high NaCl diet in SS patients2 5 and by NaCl-induced hypertension in animal models,6 resulting in an increase in blood pressure. However, the plasma concentrations of norepinephrine as one of the indexes of sympathetic nervous system were similar in SS and SR patients during low and high NaCl diets. Therefore, the difference in blood pressure between SS and SR patients could not be explained by the different sympathetic nerve activity. Because we did not measure the plasma concentration of norepinephrine during the nighttime or throughout 24 hours, in the present study we could not determine whether an abnormal response of sympathetic nervous activity in SS patients may have been responsible for the absence of the nocturnal decline in blood pressure during a high NaCl diet. Further study is needed to clarify the diurnal blood pressure in response to NaCl intake and the autonomic nervous system.
The nocturnal decline in blood pressure is diminished in the presence of diseases that cause expansion of fluid volume, such as primary aldosteronism,21 toxemia of pregnancy,22 and renal failure.23 SS patients and rats are not able to prevent excessive fluid volume expansion in response to a high NaCl intake, suggesting that the natriuretic and diuretic responses may be impaired in the salt sensitivity, resulting in an increase in blood pressure. These findings suggest that an increase in body fluid volume may be a mechanism of the diminished nocturnal decline in blood pressure during a high NaCl diet. In the present study, however, changes in body weight, as indexes of changes in extracellular fluid volume, by NaCl loading were similar in SS and SR patients, in agreement with our previous report.24 Thus, changes in extracellular fluid volume by NaCl loading may not contribute to this mechanism in patients with essential hypertension.
The renin-angiotensin-aldosterone system may also play a role in the regulation of diurnal blood pressure. Brandenberger et al25 demonstrated that a nighttime decrease in renin secretion contributed to the nocturnal reduction in blood pressure. The suppression of the renin-angiotensin-aldosterone system by NaCl loading may lead to the reduction in the diurnal variation of blood pressure. The suppression of PRA induced by a high NaCl diet was significantly smaller in SS patients than in SR patients. This inappropriate suppression of the renin-angiotensin system in SS patients may have contributed to the decreased nocturnal decline in blood pressure.
The non-dipper pattern has been defined in various ways: as a mean
nocturnal blood pressure
10% of the average daytime blood pressure,
a mean nocturnal blood pressure that is
10 mm Hg of the
average daytime blood pressure, and a nocturnal increase in mean blood
pressure compared with the average daytime blood pressure. The
prevalence of non-dipper pattern tended to be higher in the present
study with all three diets (regular NaCl: 40.6%; low NaCl: 37.5%;
high NaCl: 39.1%) than in previous reports (17.1% to
40%).15 16 26 27 28 A study using more rigid criteria (a
decrease in systolic/diastolic pressure <10/5
mm Hg from daytime to nighttime) found a 17% prevalence of the
non-dipper pattern,15 but studies based on criteria
similar to those used in the present study found rates of
prevalence of 25% to 35%.16 26 27 The higher prevalence
of the non-dipper pattern in the present study may have been
related to the inpatient setting. In many studies, ABPM is performed on
an outpatient basis, and thus differences in daytime activity may
contribute to variations in blood pressure. Patients in the present
study followed the same daily routine, which may have reduced the
influence of daytime activity in blood pressure.
In conclusion, the decline in nocturnal blood pressure was attenuated by NaCl loading in SS patients, resulting in an increased prevalence of the non-dipper pattern in these subjects. This abnormal diurnal blood pressure variation in response to a NaCl diet may be a common characteristic of SS patients.
| Selected Abbreviations and Acronyms |
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| Acknowledgments |
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Received August 18, 1996; first decision October 21, 1996; accepted January 28, 1997.
| References |
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