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Clinical and life style factors related to the nighttime blood pressure, nighttime dipping and their phenotypes in Korean hypertensive patients
Clinical Hypertension volume 29, Article number: 21 (2023)
Abstract
Background
Non-dipping or reverse dipping patterns are known to be associated with adverse cardiovascular prognosis among the general population and clinical cohort. Few large sized studies have explored factors including sleep duration and sleep quality related to nighttime blood pressure (BP) and nocturnal dipping patterns.
Methods
Among 5,360 patients enrolled in Korean multicenter nationwide prospective Registry of ambulatory BP monitoring (KORABP), 981 subjects with complete data on sleep duration, sleep quality assessed using a 4-point Likert scale, and clinical variables were included in the analysis. Phenotypes of nighttime BP pattern were categorized as extreme dipper, dipper, non-dipper, and reverse dipper. Hypertension was defined as a 24-h ambulatory BPs were 130/80 mmHg or higher.
Results
Among 981 subjects, 221 were normotensive, 359 were untreated hypertensive, and 401 were treated hypertensive. Age of the participants were 53.87 ± 14.02 years and 47.1% were female. In overall patients, sleep duration was 431.99 ± 107.61 min, and one to four points of sleep quality were observed in 15.5%, 30.0%, 30.4%, and 24.2%, respectively. Of the 760 hypertensive patients, extreme dipper, dipper, non-dipper, and reverse dipper were observed in 58 (7.63%), 277 (36.45%), 325 (42.76%), and 100 (13.16%), respectively. In multiple linear regression analysis, sleep duration (β = 0.0105, p < 0.001) and sleep quality (β = -0.8093, p < 0.001) were associated with nighttime systolic BP and sleep quality was associated with extent of nighttime systolic BP dipping (β = 0.7622, p < 0.001) in hypertensive patients. In addition, sleep quality showed positive association with dipper pattern (odds ratio [OR] = 1.16, 95% confidence interval [CI] = 1.03–1.30) and showed negative association with reverse dipper pattern (OR = 0.73, 95% CI = 0.62–0.86) in multiple logistic regression analyses.
Conclusion
When adjusted covariates, less sleep duration and poor sleep quality were positively associated with nighttime systolic BP. Additionally, sleep quality was the independent associated factor for dipper and reverse dipper phenotypes. The study also found that male sex, low estimated glomerular filtration rate, high ambulatory BP, low office BP, and poor sleep quality were associated with blunted nighttime SBP dipping.
Introduction
Hypertension is the key risk factor for cardiovascular events and deaths globally [1]. Despite the progress in blood pressure (BP) management strategies, BP control rate remain an unmet challenge for public health [2,3,4]. Difficulties in controlling the BP can be explained by a several factors, including patient related factors, awareness related factors, drug related factors, and lifestyle related factors [5, 6]. Lack of awareness of white-coat and masked which are related to accurate BP monitoring is also important factor hindering optimal BP control [7,8,9]. This is caused by the patients measured their BP only at clinic, so the importance of out-of-office BP measurement through ambulatory BP monitoring (ABPM) or home BP monitoring is emphasized.
Another important residual risk in the management of hypertension is nocturnal hypertension, which can even be a risk factor in patients whose BP are well controlled in daytime. It is well known that nighttime BP and it’s dipping pattern are important for prognosis [8, 10]. However, background factors associated with nighttime BP and dipping patterns of nighttime BP are remain unclear. Previously, few studies have been reported that advanced age, sleep disorder, alcohol consumption, diabetes mellitus, chronic kidney disease, and obstructive sleep apnea might be related with nighttime BP [11,12,13,14]. Dipping patterns of nighttime BP are also related to several factors [15, 16]. Advanced age, obesity, diabetes mellitus, and cardiovascular or renal disease were reported as an associated factor for blunted nocturnal dipping, which are related to poor prognosis [17]. Another important factor related to nighttime BP and it’s dipping pattern are sleep pattern. Disturbance in the quantity or quality of sleep may contribute to the development of nocturnal hypertension [10, 18]. However, there are few studies to investigate the factors related to nighttime BP and nocturnal dipping patterns including sleep duration and sleep quality has been reported [19].
Even though nighttime BP and it’s dipping pattern is known to be important for the prediction for cardiovascular outcomes, the major guidelines have not introduced specific management recommendation for the control of the dipping pattern of nighttime blood pressure. One of the most important barriers to the research for nighttime BP pattern is the poor reproducibility [20]. How to define the sleep time is also an important issue in nighttime BP measurement, given its recognized influence on the dipping patterns of nighttime BP [21]. The aforementioned limitations regarding obtaining nighttime BP, especially during sleep-time BP, may be difficult to overcome in situations where the current "cuff-based" ABPM method is the only widely available method for assessing nighttime BP, even though it can easily disturb sleep [22].
To overcome this limitation, it is still important to investigate the factors related to nighttime BP and it’s dipping pattern because considerations of those factors could improve the reproducibility of nighttime BP parameters. In this study, using the data from Korean Registry for ABPM (KORABP) in which lifestyle factors such as regular physical exercise, smoking and alcohol habit, and questionnaire for subjective sleep quality during ABPM were included, the factors associated with nighttime BP and it’s dipping patterns were analyzed.
Methods
Study population
This study was conducted using data from KORABP registry, a multicenter observational registry that aims to determine the prognostic threshold of ambulatory BP for predicting clinical outcomes in Korean hypertensive patients referred to secondary or tertiary hospitals as detailed in the previous report [23]. Among data for 5,360 patients available in the second version of the KORABP database, 981 subjects (221 normotensives and, 760 hypertensives) with complete data for questionnaire, laboratory and clinical data were analyzed [24].
Blood pressure measurements
Office BP was measured by physicians or nurses using an upper arm cuff oscillometric BP device (A&D, UA-767, Tokyo, Japan) after the participants had rested for 5 min the sitting position. Two measurements were taken at 1 min intervals, and the average was used to define office systolic BP (SBP) and diastolic BP (DBP).
ABPM was carried out with a validated automatic oscillometric method device that passed the Association for the Advancement of Medical Instrumentation (AAMI) or the European Society of Hypertension (ESH) validation protocol for 15–30 min intervals during the daytime and 30–60 min intervals during the nighttime as reported previously [25]. Raw data files of ABPM were defined as valid when at least 20 readings during daytime and at least 7 readings during nighttime were available, after omitting erroneous reading according to the following criteria: 1) SBP < 70 mmHg or > 250 mmHg, 2) DBP < 40 mmHg or > 150 mmHg, and 3) pulse pressure < 20 mmHg or > 150 mmHg [26].
Definition of hypertension
Hypertension was defined when a patient was taking antihypertensive drug therapy or when 24-h BPs were 130/80 mmHg or higher. Hypertension by office BPs was defined as office BPs were 140/90 mmHg or higher [27].
Assessment of physical activity, smoking and alcohol habits
The questionnaire used for Korean National Health and Nutrition Survey to examine physical activity, smoking and alcohol habits were used. Regular physical activity was defined as 3 or more structured exercise of moderate intensity or higher per week. Smoking was defined as current smoker and alcohol drinking was defined as current drinking at least one time per month. Alcohol intake at the day of ABPM was not collected [28].
Assessment of sleep duration and quality
Sleep duration was defined by the time from the stating of sleep and the time of awakening by the patient’s diary. Sleep quality was assessed by the questions of “How was the sleep last night?” and the response was choosing one of four Likert scales, 1-point for hardly sleep, 2-points for poor sleep, 3-points for not so bad, and 4-points for very good.
Definition of nighttime blood pressure and nocturnal dipping pattern
Nighttime SBP dipping was defined as decrease in SBP during sleep compared to that during daytime. Nighttime BP was defined by average BP during actual sleep time. Daytime was defined as the time interval from 8am to 9 pm. Average BP was calculated using the number of readings and the weighting for the measurement interval between readings. Twenty-four-hour BP was defined as nighttime BP x actual sleeping duration/24 + daytime BP x (24 minus actual sleep duration)/24. Nighttime BP by narrow fixed interval method was defined by average BP from midnight to 5AM and nighttime BP during deep sleep was defined by the average BP between the time of 2 h after sleep and the time of 1 h before awakening. We sub-classified the patients according to the percentage of nighttime SBP decline as follows: extreme dippers if the nighttime SBP reduction was 20% at least; dippers if the fall was 10% at least but < 20%; non-dippers if the fall was 0% at least but < 10%; and the reverse dippers if it was < 0% [29].
Clinical data
Clinical data were obtained using a web-based electronic data capture system that included electronic case report forms from the KORABP registry database. The following characteristics were collected: age, gender, height, weight, and medical history including the diagnosis of hypertension, diabetes, dyslipidemia, myocardial infarction, coronary artery disease, and stroke, along with data on treatment for any of the above conditions. The following laboratory data were collected: fasting glucose level, total cholesterol, and creatinine. Dyslipidemia was defined from the records based on the diagnosis of dyslipidemia, the use of statins, or total cholesterol levels ≥ 240 mg/dL. Diabetes mellitus was defined based on past medical history, fasting blood glucose level was 126 mg/dl or higher or hemoglobin A1C was 6.5% or higher. Estimated glomerular filtration rate (eGFR) was calculated using the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) formula.
Statistical analyses
Data were expressed as mean ± standard deviation or number with percentage, as appropriate. Clinical characteristics were described according to the hypertension status and antihypertensive medication status. In addition, clinical characteristics according to the nocturnal dipping pattern in hypertensive patients were also described. The difference among groups in the continuous variables was tested with ANOVA and Scheffe post-hoc multiple comparison test. The difference of the distribution among the group in the categorical variables was tested using the Chi-square test. The factors associated with nighttime SBP and the extent of nighttime SBP dipping were explored using multiple linear regression analyses including independent variables such as age, sex, regular physical activity which was defined as 3 or more moderate intensity exercise per week, body mass index (BMI), current smoking, alcohol drinking, antihypertensive medication status, medical histories of diabetes mellitus and dyslipidemia, medical history of cardiovascular disease such as coronary artery disease, stroke, and heart failure, total cholesterol, eGFR, 24-h mean SBP, office SBP, sleep duration, and sleep quality. The factors associated with nighttime dipping less than 10% and each nocturnal dipping pattern, i.e., dipper, non-dipper, reverse dipper, and extreme dipper were explored using generalized linear models including the relevant covariates such as, age, sex, regular physical activity, BMI, current smoking, alcohol drinking, antihypertensive medication status, medical histories of diabetes mellitus and dyslipidemia, medical history of cardiovascular disease such as coronary artery disease, stroke, and heart failure, eGFR, 24-h mean SBP, office SBP, sleep duration, and sleep quality. Analyses were also performed using different definitions of nighttime BP, i.e., mean BP without time weighting, mean BP with narrow fixed time interval method, and mean BP during deep sleep were described. McNemar’s test and Cochran’s Q test were used to compare the proportion of each dipping pattern between different definitions of nighttime BP. P value < 0.05 was considered as statistically significant. RStudio ver 1.1.414 and R ver 4.2.1 were used for the statistical analysis.
Results
Clinical characteristics
Among the 981 patients, 221 were normotensive, 359 were untreated hypertensive and, 401 were treated hypertensive. In overall patients, sleep duration was 431.99 ± 107.61 min, and one to four points of sleep quality were observed in 15.5%, 30.0%, 30.4%, and 24.2%, respectively. Clinical characteristics of the study patients according to the hypertension status and antihypertensive medication status were summarized in Table 1. There were no significant differences among the groups of normotensive, untreated hypertensive, and treated hypertensive, in terms of sex, regular physical activity, alcohol drinking, sleep duration and sleep quality. There were significant differences in the age, BMI, comorbidities, laboratory findings, office and ambulatory BPs. BPs and frequency of comorbidities were generally higher in hypertensive patients. In the nocturnal dipping pattern, the proportion of extreme dipper and non-dipper significantly differed between the groups, but there were no differences in the proportion of dipper and reverse dipper.
Comparison of characteristics according to the nocturnal dipping pattern in hypertensive patients
As shown in Table 2, among the group of nocturnal dipping patterns in hypertensive patients, there were significant differences in the age, sex, proportion of participants taking antihypertensive drugs, medical history of myocardial infarction and stroke, laboratory findings such as low eGFR (< 60 ml/min/1.73m2), and BPs such as 24-h mean SBP and DBP, daytime mean DBP, and nighttime SBP and DBP. There were significant differences in sleep quality between the groups, while there was no difference in sleep duration between the groups.
Relationship between sleep duration and sleep quality with nighttime blood pressure and nighttime systolic blood pressure dipping
As shown in Table 3, sleep duration (β = 0.0105, p < 0.001) and sleep quality (β = -0.8093, p < 0.001) were significantly associated with nighttime SBP in multiple linear regression analysis. In addition, sleep quality was also significantly associated with extent of nighttime SBP dipping (β = 0.7622, p < 0.001), but sleep duration was not associated with extent of nighttime SBP dipping (β = -0.0036, p = 0.081) (Table 4). Age, sex, SBP, smoking status, and total cholesterol were also associated factors for nighttime SBP and extent of nighttime SBP dipping. Since there is a possibility that office SBP and 24-h mean SBP are not independent of each other, we excluded each from the model and analyzed them separately. Table S1 showed the association of other variables with nighttime SBP dipping was consistent in both models. However, in the analysis performed excluding 24-h SBP, office SBP did not show significant association with nighttime SBP dipping.
Associated factor for nighttime systolic blood pressure dipping less than 10 percent
Table 5 showed the significant associated factors associated with less than 10 percent nighttime SBP which was analyzed using multiple logistic regression analysis with consideration of relevant variables. The result showed that male sex (odds ratio [OR] for female sex = 0.72, 95% confidence interval [CI] = 0.56–0.94), low eGFR (< 60 ml/min/1.73m2) (OR = 1.55, 95% CI = 1.06–2.30), high ambulatory BP (≥ 130/80 mmHg) (OR = 1.76, 95% CI = 1.33–2.33), low office BP (≥ 140/90 mmHg) (OR = 0.56, 95% CI = 0.41–0.75), and poor sleep quality (OR = 0.84, 95% CI = 0.75–0.94) were significant factors associated with nighttime SBP dipping less than 10 percent.
Figure 1 showed the predictive OR curves for the continuous relationship between age, ambulatory SBP, office SBP, sleep quality and odds of nighttime SBP dipping less than 10 percent. The result showed that age and ambulatory SBP had a positive linear relationship with the odds of nighttime SBP dipping less than 10 percent. On the other hand, office SBP and sleep quality exhibited a negative linear relationship with the odds of nighttime SBP dipping less than 10 percent.
Associated factor for each nocturnal dipping pattern
Table 6 showed the associated factors for each nocturnal dipping pattern which was analyzed by multiple logistic regression analysis. Taking antihypertensive drugs (OR = 1.91, 95% CI = 1.18–3.09) is the independent factor for extreme dipper. Contrarily, medical history of diabetes mellitus (OR = 0.53, 95% CI = 0.27–0.97) and high ambulatory BP (≥ 130/80 mmHg) (OR = 0.48, 95% CI = 0.29–0.80) are inversely associated with extreme dipper. In addition, low ambulatory BP (OR = 0.68, 95% CI = 0.51–0.90), high office BP (OR = 1.73, 95% CI = 1.27–2.36), and better sleep quality (OR = 1.16, 95% CI = 1.03–1.30) were significant factors associated for dipper.
In non-dipper pattern, male sex was significant associated factor (OR for female sex = 0.74, 95% CI = 0.58–0.96). High ambulatory BP (≥ 130/80 mmHg) was also significant associated factor for non-dipper (OR = 1.51, 95% CI = 1.15–2.00), but low office BP (≥ 140/90 mmHg) was not. In addition, low eGFR (< 60 ml/min/1.73m2) (OR = 2.30, 95% CI = 1.47–3.54) and poor sleep quality (OR = 0.73, 95% CI = 0.62–0.86) were significant associated factors for reverse dipper. Contrary to dipper, high office BP (≥ 140/90 mmHg) was significant associated factor for reverse dipper (OR = 1.81, 95% CI = 1.23–2.64), but high ambulatory BP (≥ 130/80 mmHg) was not. Sleep duration was not associated with all of nocturnal dipping pattern.
Comparison among the different definitions of nighttime BP
BP patterns and comparisons of the proportion of dipping patterns according to different definitions of nighttime BP are summarized in Tables S2 and S3. The extent of nighttime SBP according to the time weighted actual sleep time method, non-time weighted actual sleep time method, narrow fixed interval method, and deep sleep method were 8.81 ± 7.94%, 9.27 ± 8.22%, 8.95 ± 8.97%, and 10.35 ± 9.44%, respectively. When nighttime BP was defined according to non-time weighting method, the proportions of extreme dipper, dipper, non-dipper, and reverse dipper were 8.55%, 37.76%, 45.52%, and 13.55%, respectively. The proportions extreme dipper, dipper, non-dipper, and reverse dipper were 10.26%, 35.00%, 37.37%, and 16.32% in the definition according to the narrow fixed interval method, and 14.34%, 36.71%, 31.32%, and 13.82% in the definition according to the deep sleep method (overall p-value = 0.005).
Table S4 showed comparison of factors related to dipping less than 10 percent in hypertensive patients according to the different definitions of nighttime BP. Low eGFR (< 60 ml/min/1.73m2), low office BP (≥ 140/90 mmHg), and poor sleep quality were factors consistently showed significant association with dipping less than 10 percent. Age, sex, and medical history of dyslipidemia showed significant associations according to some definitions of nighttime BPs. Sleep duration was independent associated factor for dipping less than 10 percent only when nighttime BP was defined by non-time weighting method.
Discussions
In this study, we demonstrated that sleep quality was significantly associated with nighttime SBP and extent of nighttime SBP dipping. Also, better sleep quality was independently associated with dipper and poor sleep quality was independently associated with reverse dipper. In addition, associated factor for nighttime SBP and extent of nighttime SBP dipping were age, sex, SBP, smoking status, and total cholesterol. Furthermore, male sex, low eGFR, high ambulatory BP, low office BP, and poor sleep quality were significant associated factors for nighttime SBP dipping less than 10 percent. It is very well known that non-dipper or reverse dipper is associated with poor cardiovascular prognosis [30, 31], and the association between nighttime dipping and cardiovascular prognosis could be non-linear or J shape as suggested by the association between extreme dipper and cardiovascular prognosis [32]. However, there are few studies reporting the epidemiologic features and associated factor for nighttime dipping and/or the phenotype of nighttime BP pattern [23]. In our study, clinical characteristics and associated factor for nighttime BP and nocturnal dipping pattern were demonstrated in a relatively large-sized study population.
Previous studies reported that age, sleep disorder, alcohol consumption, and various comorbidities such as diabetes mellitus and chronic kidney disease can affect to nighttime BP [11, 12, 18]. In our study, the nighttime SBP dipping was positively associated with younger age, female sex, higher office SBP, smoking, higher total cholesterol, and lower 24-h mean SBP. Younger age, higher office SBP, and smoking can be explained by the increased daytime activity or stress and/or responsiveness to the stress during daytime, which can be relieved by sleep or rest. In particular, smoking showed positive trend with extreme dipper and negative trend with reverse dipper in Table 6. These findings can be explained by the possibility that smoking can increase daytime BP level thus increasing nighttime SBP dipping [33]. Nighttime SBP dipping is defined by 24-h BP, so the association between office BP and nighttime SBP dipping is relatively weak. As shown in Table 4 and Table S1, interpretation should be cautious as the association between office SBP and nighttime SBP dipping may vary depending on whether 24-h mean SBP is adjusted or not.
In our study, the difference between daytime and nighttime SBP was similar between untreated hypertensive patients and treated hypertensive patients, therefore nighttime SBP dipping was similar in both groups. In addition, taking antihypertensive drug was not independent factor for nighttime SBP and extent of nighttime SBP dipping. This finding suggests that antihypertension medication itself does not have effect on improvement of non-dipper or reverse dipper pattern. One interesting finding was that taking antihypertensive drug was associated with extreme dipper pattern. Little is known about the factors associated with extreme dippers, so further studies are needed on this finding.
More than a half of the patients were non-dipper or reverse dipper in our study. This prevalence is much higher than that in the general population. For example, in the Ohasama study population in Japan, the prevalence of non-dipper or reverse dipper was only 16% [34]. However, in a study conducted with subjects had high BP in office, the prevalence of non-dipper or reverse dipper was 41% to 52.8%, which is similar with our results [17]. Previous studies reported that non-dipper was associated with obesity, aging, autonomic dysfunction, and overt cardiovascular and renal disease [17, 35]. However, in our study, these factors did not show significant association with non-dipper or reverse dipper phenotype, except for low eGFR (< 60 ml/min/1.73m2) which showed significant association with reverse dipper.
From a clinical point of view, it is unclear whether non-dipper and reverse dipper are distinct phenotypes. When we combine these two patterns and analyze them in Table 5, male sex, low eGFR, high ambulatory BP, low office BP, and poor sleep quality were independent associated factor for nighttime dipping less than 10 percent. In addition, when analyzed using different definitions of nighttime BP, only low eGFR, low office BP, and poor sleep quality were consistently associated factors for nighttime dipping less than 10 percent. Moreover, low eGFR (< 60 ml/min/1.73m2) was significantly associated with reverse dipper in our study. This finding was consistent with the previous study [36], and may suggest the clinical importance of accompanying chronic kidney disease in hypertensive patients. In our study, age was associated with extent of nighttime SBP dipping, but was not associated with non-dipper or reverse dipper patterns. It is still controversial whether non-dipper is related to age itself or to factors such as sleep quality and arterial stiffness, which increase with aging [37, 38].
In our study, as shown in Table 6, hypertension by office BP and sleep quality are closely associated with both dipper and reverse dipper. This finding is important for the following reasons. First, recent findings suggest that sleep quality is not affected by ABPM and that poor sleep quality could be associated with hypertension itself regardless of the non-dipper or dipper pattern [39]. Second, regarding the poor sleep quality, sleep apnea syndrome has been spotlighted recently [40]. For extreme dipper, for which there is a controversy regarding the clinical implications as a prognostic factor or as a marker for morning surge [41], sleep quality could be an important confounding variable. Nocturnal hypertension has been long known to be associated with cardiovascular prognosis without any breakthrough, and has not been utilized for clinical applications. To address this challenge, our study showed that sleep quality could be another path to understanding the unfavorable patterns of nighttime BP.
There is insufficient evidence to support the preference for any specific definition of sleep time in ABPM [42]. In our study, when nighttime BP is defined by actual sleep time, male sex, low eGFR, high ambulatory BP, low office BP, and poor sleep quality were associated factor blunted nighttime SBP dipping. But the dipping patterns themselves are affected by the different method to define sleep time.
Limitations in our study need to be mentioned. Firstly, the association is only cross-sectional so that the mechanism and/or causality behind the association are unknown. Secondly, our data is registry data. Therefore, laboratory data were collected at the physician’s discretion according to own usual standards of care. However, the participating patient population was large enough to explore the cross-sectional relationship, and the result from multiple linear regression analysis is quite consistent with multiple logistic regression analyses. Thirdly, even though the four-point Likert scale for the questionnaire determining sleep quality is adopted for this study, this scale was not validated using gold standard polysomnography and is therefore quite subjective.
Conclusions
In conclusion, based on the data from KORABP registry, extent of nighttime SBP dipping was associated with age, sex, SBP, smoking status, total cholesterol, and sleep quality. Moreover, blunted nighttime SBP dipping was associated with male sex, low eGFR, high ambulatory BP, low office BP, and poor sleep quality. In addition, it was found that better sleep quality was associated with dipper and poor sleep quality was associated with reverse dipper.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Abbreviations
- BP:
-
Blood pressure
- ABPM:
-
Ambulatory blood pressure monitoring
- KORABP:
-
Korean Registry for Ambulatory Blood Pressure Monitoring
- SBP:
-
Systolic blood pressure
- DBP:
-
Diastolic blood pressure
- AAMI:
-
Association for the Advancement of Medical Instrumentation
- ESH:
-
European Society of Hypertension
- eGFR:
-
Estimated glomerular filtration rate
- CKD-EPI:
-
Chronic Kidney Disease Epidemiology Collaboration
- BMI:
-
Body mass index
- OR:
-
Odds ratio
- CI:
-
Confidence interval
References
Organization WH. A global brief on hypertension: silent killer, global public health crisis: World Health Day 2013. In.: World Health Organization; 2013.
Parati G, Lombardi C, Pengo M, Bilo G, Ochoa JE. Current challenges for hypertension management: From better hypertension diagnosis to improved patients’ adherence and blood pressure control. Int J Cardiol. 2021;331:262–9.
Kim HC, Cho SMJ, Lee H, Lee HH, Baek J, Heo JE. Korea hypertension fact sheet 2020: analysis of nationwide population-based data. Clin Hypertens. 2021;27(1):8.
NCD Risk Factor Collaboration (NCD-RisC). Worldwide trends in hypertension prevalence and progress in treatment and control from 1990 to 2019: a pooled analysis of 1201 population-representative studies with 104 million participants. Lancet (London, England). 2021;398(10304):957–80.
Elnaem MH, Mosaad M, Abdelaziz DH, Mansour NO, Usman A, Elrggal ME, Cheema E. Disparities in Prevalence and Barriers to Hypertension Control: A Systematic Review. Int J Environ Res Public Health. 2022;19(21):14571.
Ostchega Y, Zhang G, Hughes JP, Nwankwo T. Factors Associated With Hypertension Control in US Adults Using 2017 ACC/AHA Guidelines: National Health and Nutrition Examination Survey 1999–2016. Am J Hypertens. 2018;31(8):886–94.
Ihm SH, Park JH, Kim JY, Kim JH, Kim KI, Lee EM, Lee HY, Park S, Shin J, Kim CH. Home blood pressure monitoring: a position statement from the Korean Society of Hypertension Home Blood Pressure Forum. Clin Hypertens. 2022;28(1):38.
Asayama K, Fujiwara T, Hoshide S, Ohkubo T, Kario K, Stergiou GS, Parati G, White WB, Weber MA, Imai Y. Nocturnal blood pressure measured by home devices: evidence and perspective for clinical application. J Hypertens. 2019;37(5):905–16.
Zanchetti A. Challenges of hypertension and hypertension treatment. J Hypertens. 2014;32(10):1917–8.
Cho MC. Clinical Significance and Therapeutic Implication of Nocturnal Hypertension: Relationship between Nighttime Blood Pressure and Quality of Sleep. Korean Circ J. 2019;49(9):818–28.
Hornstrup BG, Gjoerup PH, Wessels J, Lauridsen TG, Pedersen EB, Bech JN. Nocturnal blood pressure decrease in patients with chronic kidney disease and in healthy controls - significance of obstructive sleep apnea and renal function. Int J Nephrol Renovasc Dis. 2018;11:279–90.
Kim Y-S, Davis SCAT, Stok WJ, van Ittersum FJ, van Lieshout JJ. Impaired nocturnal blood pressure dipping in patients with type 2 diabetes mellitus. Hypertens Res. 2019;42(1):59–66.
Lattanzi S, Brigo F, Silvestrini M. Obstructive sleep apnea syndrome and the nocturnal blood pressure profile. J Clin Hypertens (Greenwich). 2018;20(6):1036–8.
O’Brien E. Dipping Comes of Age. Hypertension. 2009;53(3):446–7.
Kastarinen H, Vasunta RL, Ukkola O, Kesäniemi YA. Glomerular filtration rate is related to dipping pattern in ambulatory blood pressure monitoring–a cross-sectional population-based study. J Hum Hypertens. 2010;24(4):247–53.
Amah G, Ouardani R, Pasteur-Rousseau A, Voicu S, Safar ME, Kubis N, Bonnin P. Extreme-Dipper Profile, Increased Aortic Stiffness, and Impaired Subendocardial Viability in Hypertension. Am J Hypertens. 2017;30(4):417–26.
de la Sierra A, Redon J, Banegas JR, Segura J, Parati G, Gorostidi M, de la Cruz JJ, Sobrino J, Llisterri JL, Alonso J, et al. Prevalence and factors associated with circadian blood pressure patterns in hypertensive patients. Hypertension. 2009;53(3):466–72.
Ulmer CS, Calhoun PS, Bosworth HB, Dennis MF, Beckham JC. Nocturnal blood pressure non-dipping, posttraumatic stress disorder, and sleep quality in women. Behav Med. 2013;39(4):111–21.
Imai Y, Nishiyama A, Ohkubo T, Tsuji I, Nagai K, Kikuchi N, Satoh H, Hisamichi S. Factors affecting the nocturnal decrease in blood pressure: a community-based study in Ohasama. J Hypertens. 1997;15(8):827–38.
Mancia G, Facchetti R, Bombelli M, Quarti-Trevano F, Cuspidi C, Grassi G. Short- and Long-Term Reproducibility of Nighttime Blood Pressure Phenotypes and Nocturnal Blood Pressure Reduction. Hypertension. 2021;77(5):1745–55.
Slusniene A, Navickas P, Stankus A, Lauceviciene I, Ryliskyte L, Laucevicius A. Defining the nocturnal period in 24-h ambulatory blood pressure monitoring: a comparison of three methods. Blood Press Monit. 2021;26(3):207–14.
Agarwal R, Light RP. The effect of measuring ambulatory blood pressure on nighttime sleep and daytime activity–implications for dipping. Clin J Am Soc Nephrol. 2010;5(2):281–5.
Yi JE, Shin J, Ihm SH, Kim JH, Park S, Kim KI, Kim WS, Pyun WB, Kim YM, Kim SK. Not nondipping but nocturnal blood pressure predicts left ventricular hypertrophy in the essential hypertensive patients: the Korean Ambulatory Blood Pressure multicenter observational study. J Hypertens. 2014;32(10):1999–2004; discussion 2004.
Kim HJ, Shin JH, Lee Y, Kim JH, Hwang SH, Kim WS, Park S, Rhee SJ, Lee EM, Ihm SH, et al. Clinical features and predictors of masked uncontrolled hypertension from the Korean Ambulatory Blood Pressure Monitoring Registry. Korean J Intern Med. 2021;36(5):1102–14.
Shin J, Kario K, Chia YC, Turana Y, Chen CH, Buranakitjaroen P, Divinagracia R, Nailes J, Hoshide S, Siddique S, et al. Current status of ambulatory blood pressure monitoring in Asian countries: A report from the HOPE Asia Network. J Clin Hypertens (Greenwich). 2020;22(3):384–90.
Staessen J, Fagard R, Lijnen P, Thijs L, van Hoof R, Amery A. Ambulatory blood pressure monitoring in clinical trials. J Hypertens Suppl. 1991;9(1):S13-19.
Lee HY, Shin J, Kim GH, Park S, Ihm SH, Kim HC, Kim KI, Kim JH, Lee JH, Park JM, et al. 2018 Korean Society of Hypertension Guidelines for the management of hypertension: part II-diagnosis and treatment of hypertension. Clin Hypertens. 2019;25:20.
Kim S, Choi S, Kim J, Park S, Kim YT, Park O, Oh K. Trends in health behaviors over 20 years: findings from the 1998–2018 Korea National Health and Nutrition Examination Survey. Epidemiol Health. 2021;43:e2021026.
Kario K, Hoshide S, Chia YC, Buranakitjaroen P, Siddique S, Shin J, Turana Y, Park S, Tsoi K, Chen CH, et al. Guidance on ambulatory blood pressure monitoring: A statement from the HOPE Asia Network. J Clin Hypertens (Greenwich). 2021;23(3):411–21.
Kim BK, Kim YM, Lee Y, Lim YH, Shin J. A reverse dipping pattern predicts cardiovascular mortality in a clinical cohort. J Korean Med Sci. 2013;28(10):1468–73.
Yano Y, Kario K. Nocturnal blood pressure and cardiovascular disease: a review of recent advances. Hypertens Res. 2012;35(7):695–701.
Kario K, Matsuo T, Kobayashi H, Imiya M, Matsuo M, Shimada K. Nocturnal fall of blood pressure and silent cerebrovascular damage in elderly hypertensive patients. Advanced silent cerebrovascular damage in extreme dippers. Hypertension. 1996;27(1):130–5.
Ohta Y, Kawano Y, Hayashi S, Iwashima Y, Yoshihara F, Nakamura S. Effects of cigarette smoking on ambulatory blood pressure, heart rate, and heart rate variability in treated hypertensive patients. Clin Exp Hypertens. 2016;38(6):510–3.
Ohkubo T, Imai Y, Tsuji I, Nagai K, Watanabe N, Minami N, Kato J, Kikuchi N, Nishiyama A, Aihara A, et al. Relation between nocturnal decline in blood pressure and mortality. The Ohasama Study. Am J Hypertens. 1997;10(11):1201–7.
Dauphinot V, Gosse P, Kossovsky MP, Schott A-M, Rouch I, Pichot V, Gaspoz J-M, Roche F, Barthelemy J-C. Autonomic nervous system activity is independently associated with the risk of shift in the non-dipper blood pressure pattern. Hypertens Res. 2010;33(10):1032–7.
An HR, Park S, Yoo TH, Kang SW, Ryu JH, Lee YK, Yu M, Ryu DR, Kim SJ, Kang DH, et al. Non-dipper status and left ventricular hypertrophy as predictors of incident chronic kidney disease. J Korean Med Sci. 2011;26(9):1185–90.
Camafort M, Chung W-J, Shin J-H. Role of ambulatory blood pressure monitoring in elderly hypertensive patients. Clin Hypertens. 2022;28(1):22.
Lee HT, Park JK, Choi SY, Choi BY, Kim MK, Mori M, Yamori Y, Lim YH, Shin J. Mediating effects of nocturnal blood pressure and morning surge on the contributions of arterial stiffness and sodium intake to morning blood pressure: A path analysis. Blood Press. 2016;25(1):28–35.
Sherwood A, Hill LK, Blumenthal JA, Hinderliter AL. The Effects of Ambulatory Blood Pressure Monitoring on Sleep Quality in Men and Women With Hypertension: Dipper vs. Nondipper and Race Differences. Am J Hypertens. 2019;32(1):54–60.
Yeghiazarians Y, Jneid H, Tietjens JR, Redline S, Brown DL, El-Sherif N, Mehra R, Bozkurt B, Ndumele CE, Somers VK. Obstructive Sleep Apnea and Cardiovascular Disease: A Scientific Statement From the American Heart Association. Circulation. 2021;144(3):e56–67.
Kario K, Shimada K. Risers and extreme-dippers of nocturnal blood pressure in hypertension: antihypertensive strategy for nocturnal blood pressure. Clin Exp Hypertens. 2004;26(2):177–89.
Nolde JM, Hillis GS, Atkins E, Von Huben A, Marschner S, Chan J, Reid CM, Nelson MR, Figtree G, Chalmers J, et al. Impact of various night-time period definitions on nocturnal ambulatory blood pressure. J Hypertens. 2022;40(11):2271–9.
Acknowledgements
We wish to thank the Working Group of Blood Pressure Monitoring in Korean Society of Hypertension for managing the registry data construction.
Funding
This study was sponsored by Korean Society of Hypertension, South Korea.
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BSK was responsible for drafting the article, and was a major contributor in writing the manuscript. JHK and WK were responsible for data collection. WSK and SP were responsible for data analysis. SJL and JYK were responsible for data interpretation. EML and SHI were responsible for manuscript preparation. WBP and J-HS were responsible for study design. JH was responsible for conceptualization, study design, and manuscript preparation. All authors read and approved the final manuscript.
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The study was conducted in compliance with the Helsinki Declaration, and the study protocol was approved by the clinical research ethics committee in each hospital involved, including Hanyang University Seoul Hospital (HYUH IRB No. 2009-R-12). Written informed consent was obtained from all participants.
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Additional file 1:
Table S1. Additional multiple linear regression analysis performed by excluding 24-hour mean SBP and Office SBP for the factor associated with extent of nighttime systolic blood pressure dipping in hypertensive patients. Table S2. Blood pressure patterns according to the different definitions of nighttime blood pressure. Table S3. Comparisons of the proportion of dipping patterns according to the different definitions of nighttime blood pressure. Table S4. Multiple logistic regression analysis for the factors associated with nighttime dipping less than 10 percent in hypertensive patients according to the different definitions of nighttime blood pressure.
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Kim, B.S., Kim, J.H., Kim, W. et al. Clinical and life style factors related to the nighttime blood pressure, nighttime dipping and their phenotypes in Korean hypertensive patients. Clin Hypertens 29, 21 (2023). https://doi.org/10.1186/s40885-023-00241-w
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DOI: https://doi.org/10.1186/s40885-023-00241-w