Donate Help Contact The AHA Sign In Home
American Heart Association
Hypertension
Search: search_blue_button Advanced Search
Hypertension. 1997;30:163-167

This Article
Right arrow Abstract Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Higashi, Y.
Right arrow Articles by Kajiyama, G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Higashi, Y.
Right arrow Articles by Kajiyama, G.

(Hypertension. 1997;30:163-167.)
© 1997 American Heart Association, Inc.


Articles

Nocturnal Decline in Blood Pressure Is Attenuated by NaCl Loading in Salt-Sensitive Patients With Essential Hypertension

Noninvasive 24-Hour Ambulatory Blood Pressure Monitoring

Yukihito Higashi; Tetsuya Oshima; Ryoji Ozono; Yukiko Nakano; Hideo Matsuura; Masayuki Kambe; ; Goro Kajiyama

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
up arrowTop
*Abstract
down arrowIntroduction
down arrowMethods
down arrowResults
down arrowDiscussion
down arrowReferences
 
Abstract We investigated the effect of NaCl on the circadian blood pressure rhythm in patients with essential hypertension classified according to the presence or absence of salt sensitivity. We obtained 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, followed by a high NaCl diet (340 mmol/d) for 1 week. Twenty-six patients whose mean blood pressure was increased more than 10% by NaCl loading were classified as salt sensitive. The remaining 38 patients were classified as salt resistant. The nocturnal decline in mean blood pressure was significantly smaller in salt-sensitive patients (8.3±1.0%) than in salt-resistant patients (11.5±0.9%) (P<.05) during a high NaCl diet but was similar in both groups during a low NaCl diet. There was no significant difference in the prevalence of the non-dipper pattern between groups on a low NaCl diet, but the prevalence of the non-dipper pattern was significantly higher in salt-sensitive patients than in salt-resistant patients on a high NaCl diet (0.57 versus 0.26, {chi}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
up arrowTop
up arrowAbstract
*Introduction
down arrowMethods
down arrowResults
down arrowDiscussion
down arrowReferences
 
NaCl has been widely recognized as an important factor in the development of hypertension.1 2 However, excessive amounts of dietary NaCl do not always elevate blood pressure because the pressure response to NaCl loading varies among individuals.3 4 5 Although the role of salt sensitivity in hypertension has not been fully clarified, proposed mechanisms include expansion of fluid volume,6 inappropriate suppression of the renin-angiotensin system,3 4 abnormal response of sympathetic nervous activity,5 6 and the intracellular accumulation of sodium and calcium.3

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
up arrowTop
up arrowAbstract
up arrowIntroduction
*Methods
down arrowResults
down arrowDiscussion
down arrowReferences
 
Subjects
We studied 64 Japanese inpatients with mild to moderate essential hypertension (37 men and 27 women; mean age, 50.6±1.5 years). Office blood pressure measurements were obtained in the outpatient clinic of Hiroshima University School of Medicine. Hypertension was defined in the untreated state as a systolic blood pressure >160 mm Hg and/or a diastolic blood pressure >95 mm Hg in the sitting position on at least three different occasions. Patients had no evidence of advanced target organ damage such as left ventricular hypertrophy, severe retinopathy, or proteinuria. Patients with secondary forms of hypertension were excluded by appropriate clinical and biochemical tests. None of the patients had a history of cardiovascular or cerebrovascular disease, hypercholesterolemia, diabetes mellitus, liver disease, or renal disease. Informed consent for participation was obtained from all subjects.

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 {chi}2 test. A value of P<.05 was considered statistically significant.


*    Results
up arrowTop
up arrowAbstract
up arrowIntroduction
up arrowMethods
*Results
down arrowDiscussion
down arrowReferences
 
Salt-Sensitive and Salt-Resistant Patients
ABPM identified 26 patients as SS (14 men and 12 women; mean age, 54.5±2.3 years) and 38 patients as SR (23 men and 15 women; mean age, 49.4±2.0 years).

Baseline parameters were similar in the SS and SR patients during the regular diet (Table 1Down).


View this table:
[in this window]
[in a new window]
 
Table 1. Clinical Characteristics in SS and SR Patients With a Regular NaCl Diet

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 2Down). 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.


View this table:
[in this window]
[in a new window]
 
Table 2. Clinical Characteristics in SS and SR Patients With Low and High NaCl Diets

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%]; {chi}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 (FigureDown) but not during a low NaCl diet.



View larger version (16K):
[in this window]
[in a new window]
 
Figure 1. Scatterplot showing the relationship between the nocturnal decline in blood pressure during a high NaCl diet (nocturnal BP decline) and the NaCl-induced increase in blood pressure (salt sensitivity).


*    Discussion
up arrowTop
up arrowAbstract
up arrowIntroduction
up arrowMethods
up arrowResults
*Discussion
down arrowReferences
 
The nocturnal decline in blood pressure was attenuated by NaCl loading in SS patients compared with SR patients in the present study. The prevalence of non-dippers was significantly higher in the SS group than in the SR group during a high NaCl diet, whereas there was no significant difference in the frequency of the non-dipper pattern between groups during a low NaCl diet. Our results suggest that the blunted nocturnal decline in blood pressure induced by NaCl loading may be a specific characteristic of SS patients. A recent study showed that a high NaCl diet caused abnormal diurnal changes in blood pressure in spontaneously hypertensive rats but not in Wistar-Kyoto rats.6 These observations suggest that the dietary content of NaCl should be kept fairly constant for assessment of the diurnal blood pressure variation.

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
 
ABPM = ambulatory blood pressure monitoring
PRA = plasma renin activity
SR = salt-resistant
SS = salt-sensitive


*    Acknowledgments
 
This study was supported in part by grants-in-aid for Scientific Research (7407065 and 8457639) from the Ministry of Education, Science and Culture of Japan and a grant from Foundation for Total Health Promotion. The authors thank Sumiko Nakamura for preparing the diets and Yuko Omura for her secretarial assistance.

Received August 18, 1996; first decision October 21, 1996; accepted January 28, 1997.


*    References
up arrowTop
up arrowAbstract
up arrowIntroduction
up arrowMethods
up arrowResults
up arrowDiscussion
*References
 
1. INTERSALT Cooperative Research Group. INTERSALT: an international study of electrolyte excretion and blood pressure: results for 24 hour urinary sodium and potassium excretion. Br Med J. 1988;297:319-354.

2. Campese VM, Romoff MS, Levitan D, Saglikes Y, Friedler RM, Masry SG. Abnormal relationship between Na+ intake and sympathetic nervous system activity in salt-sensitive patients with essential hypertension. Kidney Int. 1982;21:371-378.[Medline] [Order article via Infotrieve]

3. Oshima T, Matsuura H, Kido K, Kajiyama G. Role of cellular calcium in salt sensitivity of patients with essential hypertension. Hypertension. 1988;11:703-707.[Abstract/Free Full Text]

4. Higashi Y, Oshima T, Watanabe M, Matsuura H, Kajiyama G. Renal response to L-arginine in salt-sensitive patients with essential hypertension. Hypertension. 1996;27:643-648.[Abstract/Free Full Text]

5. Weinberger MH, Miller JZ, Luft FC, Grim CE, Fineberg NS. Definition and characteristics of sodium sensitivity and blood pressure resistance. Hypertension. 1986;8(suppl II):II-127-II-134.

6. Calhoun DA, Zhu S, Wyss M, Oparil S. Diurnal blood pressure variation and dietary salt in spontaneously hypertensive rats. Hypertension. 1994;24:1-7.[Abstract/Free Full Text]

7. Verdecchia P, Schillaci G, Boldrini F, Zampi I, Porcellati C. Variability between current definitions of `normal' ambulatory blood pressure: implications in the assessment of white coat hypertension. Hypertension. 1992;20:555-562.[Abstract/Free Full Text]

8. Mann S, Altman DG, Raftery EB, Bannister R. Circadian variation of blood pressure in autonomic failure. Circulation. 1983;68:477-483.[Abstract/Free Full Text]

9. Neutel JM, Smith DH, Ram CV, Kaplan NM, Papademetriou V, Fagan TC, Lefkowitz MP, Kazempour MK, Weber MA. Application of ambulatory blood pressure monitoring in differentiating between antihypertensive agents. Am J Med. 1993;94:181-187.[Medline] [Order article via Infotrieve]

10. O'Brien E, Sherdan J, O'Malley K. Dippers and non-dippers. Lancet. 1988;2:397. Letter.[Medline] [Order article via Infotrieve]

11. Shimada K, Kawamoto A, Matsubayashi K, Nishinaga M, Kimura S, Ozawa T. Diurnal blood pressure variations and silent cerebrovascular damage in elderly patients with hypertension. J Hypertens. 1992;10:875-878.[Medline] [Order article via Infotrieve]

12. Parati G, Pomidossi G, Albini F, Malaspina D, Mancia G. Relationship of 24-hour blood pressure mean and variability to severity of target-organ damage in hypertension. J Hypertens. 1987;5:93-98.[Medline] [Order article via Infotrieve]

13. Sihm I, Schroeder AP, Aalkjer C, Holm M, Morn B, Mulvany M, Thygesen K, Lederballe O. The relation between peripheral vascular structure, left ventricular hypertrophy, and ambulatory blood pressure in essential hypertension. Am J Hypertens. 1995;8:987-996.[Medline] [Order article via Infotrieve]

14. Verdecchia P, Schillaci G, Guerrieri M, Gatteschi C, Benemio G, Boldrini F, Porcellati C. Circadian blood pressure changes and left ventricular hypertrophy in essential hypertension. Circulation. 1990;81:528-536.[Abstract/Free Full Text]

15. White WB, Pickering TG, Morganroth J, James GD, McCabe EJ, Moucha O, Hunter H. A multicenter evaluation of the A&D TM-2420 ambulatory blood pressure recorder. Am J Hypertens. 1991;4:890-896.[Medline] [Order article via Infotrieve]

16. Hoegholm A, Eidemak I, Kristensen KS, Bang LE, Madsen NH. Clinical evaluation of the Takeda Medical (A&D) TM 2420 ambulatory blood pressure monitor: practical experience and comparison with direct and indirect measurements. Scand J Clin Lab Invest. 1992;52:261-268.[Medline] [Order article via Infotrieve]

17. Inoue I, Matsuura H, Matsumoto K, Otsuki T, Shingu T, Yuasa A, Kido K, Kajiyama G. Effect of sodium chloride on ambulatory blood pressure monitoring in patients with essential hypertension: importance of intracelluar sodium and calcium concentration. Ther Res. 1989;10:2293-2297.

18. Littler WA, Watson RD, Stallard TJ. Circadian variation of blood pressure. Lancet. 1978;1:995-996.

19. Watson RD, Hamilton CA, Reid JL, Littler WA. Changes in plasma norepinephrine, blood pressure, and heart rate during physical activity in hypertensive man. Hypertension. 1979;1:341-346.[Abstract/Free Full Text]

20. Imai Y, Abe K, Munakata M, Sakuma H, Hashimoto J, Imai K, Sekino H, Yoshinaga K. Circadian blood pressure variations under different pathophysiological conditions. J Hypertens. 1990;8(suppl 7):S125-S132.

21. Tanaka T, Natsume T, Shibata H, Nozawa K, Kojima S, Tsuchiya M, Ashida T, Ikeda M. Circadian rhythm of blood pressure in primary aldosteronism and renovascular hypertension analysis by cosinor method. Jpn Circ J. 1983;47:788-794.[Medline] [Order article via Infotrieve]

22. Rath W, Schrader J, Guhlke U, Buhr SH, Haupt A, Kramer A, Kuhn W. 24-hour ambulatory blood pressure measurements in normotensive pregnancy and in preeclampsia. Klin Wochenschr. 1990;68:768-773.[Medline] [Order article via Infotrieve]

23. Baumgart P, Walger P, Gemen S, von Eiff M, Raidt H, Rahn KH. Blood pressure elevation during the night in chronic renal failure, hemodialysis and after renal transplantation. Nephron. 1991;57:293-298.[Medline] [Order article via Infotrieve]

24. Oshima T, Matsuura H, Kido K, Matsumoto K, Shingu T, Otsuki T, Inoue I, Kajiyama G. Factors determining sodium chloride sensitivity of patients with essential hypertension: evaluation by multivariate analysis. J Hypertens. 1989;7:223-227.[Medline] [Order article via Infotrieve]

25. Brandenberger G, Follenius M, Simon C, Ehrhart J, Libert JP. Nocturnal oscillations in plasma renin activity and REM-NREM sleep cycles in humans: a common regulatory mechanism? Sleep. 1989;11:242-250.

26. Verdecchia P, Porcellati C, Schillaci G, Borgioni C, Ciucci A, Battistelli M, Guerrieri M, Gatteschi C, Zampi I, Santucci A, Santucci C, Reboldi G. Ambulatory blood pressure: an independent predictor of prognosis in essential hypertension. Hypertension. 1994;24:793-801.[Abstract/Free Full Text]

27. Verdecchia P, Schillaci G, Porcellati C. Dippers versus non-dippers. J Hypertens. 1991;9(suppl 8):S42-S44.

28. Schmieder RE, Rockstroh JK, Aepfelbacher F, Schulze B, Messerli FH. Gender-specific cardiovascular adaptation due to circadian blood pressure variations in essential hypertension. Am J Hypertens. 1995;8:1160-1166.[Medline] [Order article via Infotrieve]




This article has been cited by other articles:


Home page
J. Appl. Physiol.Home page
R. D. Rudic and D. J. Fulton
Pressed for time: the circadian clock and hypertension
J Appl Physiol, October 1, 2009; 107(4): 1328 - 1338.
[Abstract] [Full Text] [PDF]


Home page
HypertensionHome page
A. Sachdeva and A. B. Weder
Nocturnal Sodium Excretion, Blood Pressure Dipping, and Sodium Sensitivity
Hypertension, October 1, 2006; 48(4): 527 - 533.
[Full Text] [PDF]


Home page
J Am Coll CardiolHome page
Y. Higashi, K. Nakagawa, M. Kimura, K. Noma, K. Hara, S. Sasaki, C. Goto, T. Oshima, K. Chayama, and M. Yoshizumi
Circadian variation of blood pressure and endothelial function in patients with essential hypertension: a comparison of dippers and non-dippers
J. Am. Coll. Cardiol., December 4, 2002; 40(11): 2039 - 2043.
[Abstract] [Full Text] [PDF]


Home page
HypertensionHome page
M. Suzuki, Y. Kimura, M. Tsushima, and Y. Harano
Association of Insulin Resistance With Salt Sensitivity and Nocturnal Fall of Blood Pressure
Hypertension, April 1, 2000; 35(4): 864 - 868.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
T. Uzu and G. Kimura
Diuretics Shift Circadian Rhythm of Blood Pressure From Nondipper to Dipper in Essential Hypertension
Circulation, October 12, 1999; 100(15): 1635 - 1638.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
P. Li, S. H. Sur, R. E. Mistlberger, and M. Morris
Circadian blood pressure and heart rate rhythms in mice
Am J Physiol Regulatory Integrative Comp Physiol, February 1, 1999; 276(2): R500 - R504.
[Abstract] [Full Text] [PDF]


This Article
Right arrow Abstract Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Higashi, Y.
Right arrow Articles by Kajiyama, G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Higashi, Y.
Right arrow Articles by Kajiyama, G.