Masked hypertension and cardiovascular outcomes: an updated systematic review and meta-analysis.

BACKGROUND: As many as one-third of individuals with normal office blood pressure (BP) are diagnosed with masked hypertension (HTN) based on ambulatory BP measurements (ABPM). Masked HTN is associated with higher risk of sustained HTN (SH) and increased cardiovascular morbidity.
METHODS: The present study was designed to systematically review cohort studies and assess the effects of masked HTN compared to normotension and SH on cardiovascular events and all-cause mortality. We systematically searched the electronic databases, such as MEDLINE, PubMed, Embase, and Cochrane for prospective cohort studies, which evaluated participants with office and ambulatory and/or home BP.
RESULTS: We included nine studies with a total number of 14729 participants (11245 normotensives, 3484 participants with masked HTN, 1984 participants with white-coat HTN, and 5143 participants with SH) with a mean age of 58 years and follow-up of 9.5 years. Individuals with masked HTN had significantly increased rates of cardiovascular events and all-cause mortality than normotensives and white-coat HTN and had lower rates of cardiovascular events than those with SH (odds ratio 0.61, 95% confidence interval 0.42-0.89; P=0.010; I2=84%). Among patients on antihypertensive treatment, masked HTN was associated with higher rates of cardiovascular events than in those with normotension and white-coat HTN and similar rates of cardiovascular events in those with treated SH.
CONCLUSION: Prompt screening of high-risk individuals with home BP measurements and ABPM, the diagnosis of masked HTN, and the initiation of treatment, may mitigate the adverse cardiovascular effects of masked HTN.

Introduction

Prevalence rates of hypertension (HTN) in the US adult population have increased remarkably over the past two decades but appear to have remained unchanged over the past 10 years, according to data from the National Health and Nutrition Examination Survey (NHANES). HTN contributes to one out of every seven deaths in the US and to nearly half of all cardiovascular disease-related deaths, including stroke. Despite the success of drug therapy in treating HTN and reducing associated adverse cardiovascular effects, the percentage of patients achieving adequate blood pressure (BP) control worldwide remains unacceptably low. Recent data suggest an improvement in the treatment and control of HTN; however, ~48% of those treated are not at a BP goal of <140/90 mmHg in the US.1 These numbers are even higher among hypertensive patients in Europe.2 Importantly, about one-third of hypertensives whose BP levels appear well controlled according to clinic BP measurements have high BP outside the doctor’s office.3,4 The frequency of ambulatory HTN is even higher among patients with chronic kidney disease.5 This phenomenon is called masked HTN or isolated ambulatory HTN and is defined as clinic BP <140/90 mmHg and daytime ambulatory BP ≥135/85 mmHg. An analysis of Dallas Heart Study suggested that in a multiethnic US population, masked HTN was independently associated with increased aortic stiffness, renal injury, and incident cardiovascular events and its prevalence was 17.8%.6 Furthermore, a prospective analysis of the Jackson Heart study cohort of African Americans showed an incidence of masked HTN of 52% and an association with cardiovascular events but not all-cause mortality.7 Moreover, masked HTN was found to be associated with symptoms of end-organ damage such as left ventricular hypertrophy, increased pulse wave velocity, and carotid intima and media thickness.4

To further explore the outcomes of masked HTN both in treated and untreated groups of patient populations, we performed an updated meta-analysis.

Methods

Search strategy

Systematic electronic search was performed on MEDLINE (PubMed interface), Embase, and Cochrane Central Register of Controlled Trials (CENTRAL) with no language limitations. We used the MESH terms “masked hypertension” and “white coat hypertension”. Two reviewers (MP and AB) independently screened titles and abstracts based on inclusion and exclusion criteria. After eliminating irrelevant articles, full-text reports were reviewed. Subsequently, we hand searched all included studies until no further relevant studies were identified. Disagreements between the two reviewers were resolved by the third reviewer. Finally, a total of nine studies have been identified. The electronic search was last updated on September 20, 2017.

Study selection

We included randomized clinical trials, prospective and retrospective observational studies published as original articles in peer-reviewed scientific journals. The population studied was patients who were treated for masked HTN, white-coat HTN, normotension, or sustained HTN (SH). We excluded nonhuman studies, incorrect comparator studies, single-arm noncomparative studies, and review articles. We did not restrict eligibility based on study outcomes.

Data extraction and quality

The data were independently extracted by two authors (MP and AB) using standardized protocol and data extraction form. Disagreements were resolved by discussion with the third reviewer, and consensus was reached after discussion. We extracted data on outcome measures, study characteristics, such as study design, year of study, study population, sample size, and follow-up duration, and patient characteristics, such as baseline demographic and clinical characteristics.

Assessment of outcomes

Our primary outcome measure was composite cardiovascular events. Secondary outcome measures were all-cause mortality and stroke.

Risk of bias

Cochrane’s risk of bias tool has been used in order to assess the individual risk of bias of each study.19–21 Two authors (MP and AB) independently assessed the risk of bias and quality of studies in each eligible trial. The criteria used for the risk of bias assessment were adequate sequence generation, allocation concealment, blinding of participants, research personnel and outcome assessors, personnel and outcome assessors, incomplete outcome data, and selective outcome reporting. Low-quality studies had two or more quality assessment criteria qualified as high or unclear risk of bias.

Data analysis, summary measures, and synthesis of results

Systematic review and meta-analysis were done in compliance with the Cochrane Collaboration and the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) Statement.19–21 Meta-analyses were performed by using the Review Manager (RevMan) Version 5.3 (Nordic Cochrane Centre, The Cochrane Collaboration, 2012, Copenhagen, Denmark). Chi-square test of heterogeneity and I2 statistic of inconsistency were used to assess the heterogeneity between studies. I2 values of 25, 50, and 75% were considered as low, moderate, and high heterogeneities, respectively.22 A significant heterogeneity was considered if P<0.05 or I2 statistics >25%. Pooled effect of intervention was measured using odds ratio (OR) or standardized mean difference (SMD) with 95% confidence interval (CI). Mantel–Haenszel fixed-effects model was used to estimate the pooled effect measure if the heterogeneity is <25%. In case of significant heterogeneity between studies, DerSimonian and Laird23 random-effects model was used. Reported values are two tailed, and hypothesis testing results were considered statistically significant at P<0.05. Sensitivity analyses were performed by eliminating each study at a time to assess the influence of any included study on the results and the robustness of results. Significant heterogeneity between the studies was further explored using subgroup analyses. The small study effect, including publication bias, was tested using the visual estimation of funnel plot for asymmetry and Egger’s regression test.24,25 If visual asymmetry funnel plot was found, then nonparametric trim and fill method of Duvall and Tweedie was performed to add studies that appeared to be missing.26

Results

Study characteristics

Electronic search of scientific literature identified 1553 articles. After deduplication, screening of titles and abstracts, and full-text review based on inclusion and exclusion criteria, nine studies were identified and included in the meta-analysis.6,7,16,27–32 The characteristics of each study are shown in Table 1.

Table 1

Study characteristics

Study	Study design	Sample size				Mean follow-up (years)
		Masked HTN	Normotension	White-coat HTN	Sustained HTN
Björklund et al (2003)27	Prospective observational study	82	188		308	5.9
Fagard et al (2005)28	Prospective observational study	31	136	87	105	10.9
Mancia et al (2006)29	Prospective observational study	184	909	242	528	12.3
Hansen et al (2006)30	Prospective observational study	211	859	159	471	12.8
Pierdomenico et al (2008)31	Prospective observational study	120	471			6.6
Stergiou et al (2014)16	Prospective observational study	636	3312	925	1585	8.3
Asayama et al (2014)32	Prospective observational study	1612	4176	515	1934	11.1
Booth et al (2016)7	Prospective observational study	385	353			8.5
Tientcheu et al (2017)6	Prospective observational study	256	865	56	212	9.5

Abbreviation: HTN, hypertension.

Patient characteristics

A total number of 14729 participants (11245 normotensives, 3484 participants with masked HTN, 1984 participants with white-coat HTN, and 5143 participants with SH) were included in the meta-analysis. The mean age of the study population was 58 years. Other baseline demographics and clinical characteristics are shown in Table 2. The mean follow-up duration was 9.5 years. Clinic and ambulatory mean BP measurements are shown in Table 3.

Table 2

Baseline clinical characteristics

Study	Age (mean, years)				Males (%)				BMI (mean, kg/m2)				Smokers (%)				DM (%)
	Masked HTN	Normo-tension	White-coat HTN	Sustained HTN	Masked HTN	Normo-tension	White-coat HTN	Sustained HTN	Masked HTN	Normo-tension	White-coat HTN	Sustained HTN	Masked HTN	Normo-tension	White-coat HTN	Sustained HTN	Masked HTN	Normo-tension	White-coat HTN	Sustained HTN
Björklund et al27	70	70		70	100	100		100	26	25		26	22	21		22	5	6		15
Fagard et al28	68	69	70	72	55	48	28	35	28	27	27	28	29	26	8	12	0	4	10	12
Mancia et al29	53	44	52	60	68	43	53	58	26	24	27	28	42	27	24	21
Hansen et al30	55	53	60	60	63	45	41	63	26	24	26	27	52	50	22	38	3	1	1	4
Pierdomenico et al31	50	50			57	44			26	26			30	19
Stergiou et al16	65	60	62	66	54	37	43	46	26	24	25	27	26	17	15	18	16	8	10	13
Asayama et al32	53	46	59	61	63	45	54	67	26	24	26	27	37	31	19	27	7	4	8	9
Booth et al7	60	57			37	21			31	31			12	7			31	17
Tientcheu et al6	47	40	49	50	47	44	42	46	31	28	31	32	30	26	27	32	17	7	21	21

Abbreviations: BMI, body mass index; DM, diabetes mellitus; HTN, hypertension.

Table 3

Clinic and ambulatory blood pressure measurements

Study	Clinic BP (mmHg)				Ambulatory BP (mmHg)				Normal ambulatory BP
	Masked HTN	Normotension	White-coat HTN	Sustained HTN	Masked HTN	Normotension	White-coat HTN	Sustained HTN
Björklund et al27	129/77	126/76		155/87	145/80 (daytime)	124/73 (daytime)		151/84 (daytime)	Daytime <135/85
					115/64 (nighttime)	106/62 (nighttime)		127/69 (nighttime)
Fagard et al28	128/75	123/72	154/80	163/83	140/84 (daytime)	120/73 (daytime)	126/72 (daytime)	145/83 (daytime)	Daytime <135/85
Mancia et al29	126/81	118/77	140/90	157/94	134/84	111/70	120/75	146/86	Home <135/83
Hansen et al30	126/82	117/77	144/90	148/92	139/84 (daytime)	123/74 (daytime)	129/77 (daytime) 112/63	145/87 (daytime)	Daytime <135/85
					115/67 (nighttime)	106/60 (nighttime)	(nighttime) 124/73	125/71 (nighttime)
					133/79 (24 hours)	118/70 (24 hours)	(24 hours)	139/82 (24 hours)
Pierdomenico et al31	133/82	129/80			135/85 (daytime)	124/77 (daytime)			Daytime <135/85
					118/71 (nighttime)	110/65 (nighttime)
					130/81 (24 hours)	120/74 (24 hours)
Stergiou et al16	128/76	122/73	149/86	157/89	142/84	118/71	124/75	149/85	24 hours <135/85
Asayama et al32	126/79	117/73	148/86	157/92	139/85 (daytime)	121/74 (daytime)	128/77 (daytime) 110/63	147/87 (daytime)	Daytime <135/85
					121/70 (nighttime)	104/60 (nighttime)	(nighttime) 121/72	128/73 (nighttime)	nighttime <120/70
					133/80 (24 hours)	115/69 (24 hours)	(24 hours)	141/83 (24 hours)	24 hours <130/80
Booth et al7	123/75	117/74			134/80 (daytime)	119/72 (daytime)			Daytime <135/85
					127/72 (nighttime)	107/61 (nighttime)			nighttime <120/70
					131/77 (24 hours)	114/68 (24 hours)			24 hours <130/80
Tientcheu et al6	141/87	117/74	123/76	154/92	127/79	118/74	146/88	153/91	24 hours <135/85

Abbreviations: BP, blood pressure; HTN, hypertension.

Masked HTN versus normotension

Composite cardiovascular events

Composite cardiovascular events occurred in 12.3% of patients with masked HTN and 5.1% of patients with normotension. The frequency of cardiovascular events was significantly higher in patients with masked HTN (OR 2.91, 95% CI 2.54–3.33; P<0.00001; I2=17%, Figure 1A). No significant heterogeneity was seen among studies.

Figure 1

Masked HTN versus normotension – whole cohort.

Notes: (A) Composite cardiovascular events. (B) All-cause mortality.

Abbreviations: CI, confidence interval; HTN, hypertension; M–H, Mantel–Haenszel.

All-cause mortality

All-cause death occurred in 15.8% of patients with masked HTN and 7.8% of patients with normotension. The risk of all-cause mortality was significantly higher in patients with masked HTN (OR 2.65, 95% CI 2.18–3.23; P<0.00001; I2=0%, Figure 1B) without significant heterogeneity among studies.

Masked HTN versus white-coat HTN

Composite cardiovascular events were encountered in 12.8% of patients with masked HTN and 10.8% of patients with white-coat HTN, and the risk of cardiovascular events was significantly higher in patients with masked HTN (OR 1.38, 95% CI 1.04–1.83; P=0.02; I2=41%, Figure 2A) with significant heterogeneity among studies.

Figure 2

Masked HTN versus white-coat HTN – whole cohort.

Notes: (A) Composite cardiovascular events. (B) All-cause mortality.

Abbreviations: CI, confidence interval; HTN, hypertension; M–H, Mantel–Haenszel.

The rates of all-cause mortality were significantly elevated in patients with masked HTN (OR 1.71, 95% CI 1.34–2.19; P<0.0001; I2=0%, Figure 2B) without significant heterogeneity among studies.

Masked HTN versus SH

Composite cardiovascular events occurred in 12.7% of patients with masked HTN and 19.3% of patients with SH. We found significantly lower risk of cardiovascular events in patients with masked HTN compared with patients with SH (OR 0.61, 95% CI 0.42–0.89; P=0.010; I2=84%, Figure 3A). However, significant heterogeneity was presented among the included studies.

Figure 3

Masked HTN versus sustained HTN – whole cohort.

Notes: (A) Composite cardiovascular events. (B) All-cause mortality.

Abbreviations: CI, confidence interval; HTN, hypertension; M–H, Mantel–Haenszel.

We did not identify significant differences in the all-cause mortality rates between patients with masked and SH (OR 1.00, 95% CI 0.44–2.26; P=1.0; I2=90%, Figure 3B). Significant heterogeneity was found among the included studies.

Patients without treatment

Masked HTN versus normotension – untreated patients

Composite cardiovascular events

We observed significantly higher rates of cardiovascular events in patients with masked HTN (OR 3.10, 95% CI 2.50–3.83; P<0.00001; I2=4%, Figure 4A) without significant heterogeneity among studies.

Figure 4

Masked HTN versus normotension – untreated.

Notes: (A) Composite cardiovascular events. (B) All-cause mortality.

Abbreviations: CI, confidence interval; HTN, hypertension; M–H, Mantel–Haenszel.

All-cause mortality

All-cause death occurred in 10.3% of patients with masked HTN and 3.5% of patients with normotension. The risk of all-cause mortality was significantly higher in patients with masked HTN (OR 3.12, 95% CI 2.24–4.35; P<0.00001; I2=28%, Figure 4B) without significant heterogeneity among studies.

Masked HTN versus white-coat HTN – untreated patients

Composite cardiovascular events occurred in 11.9% of patients with masked HTN and 9.6% of patients with white-coat HTN with significantly higher risk of cardiovascular events in patients with masked HTN (OR 1.33, 95% CI 1.01–1.75; P=0.04; I2 = 3%, Figure 5A) without significant heterogeneity among studies.

Figure 5

Masked HTN versus white-coat HTN – untreated.

Notes: (A) Composite cardiovascular events. (B) All-cause mortality.

Abbreviations: CI, confidence interval; HTN, hypertension; M–H, Mantel–Haenszel.

All-cause mortality occurred in 10.7% of patients with masked HTN and 8.5% of patients with white-coat HTN. The risk of all-cause mortality was nonsignificantly higher in patients with masked HTN (OR 1.62, 95% CI 1.01–2.60; P=0.05; I2=41%, Figure 5B).

Masked HTN versus SH – untreated patients

Composite cardiovascular events were reported in 11.9% of patients with masked HTN and 16.7% of patients with SH. The risk of cardiovascular events was significantly lower in patients with masked HTN compared with patients with SH (OR 0.68, 95% CI 0.53–0.86; P=0.001; I2=20%, Figure 6A) without significant heterogeneity among studies.

Figure 6

Masked HTN versus sustained HTN – untreated.

Notes: (A) Composite cardiovascular events. (B) All-cause mortality.

Abbreviations: CI, confidence interval; HTN, hypertension; M–H, Mantel–Haenszel.

All-cause mortality occurred in 10.7% of patients with masked HTN and 12.6% of patients with SH. No significant difference was found in the all-cause mortality rates between patients with masked and SH (OR 0.88, 95% CI 0.33–2.37; P=0.80; I2=89%, Figure 6B).

Patients on treatment

Masked HTN versus normotension – treated patients

Composite cardiovascular events were found in 27.9% of patients with masked HTN and 15.5% of patients with normotension with significantly higher rates of cardiovascular events in patients with masked HTN (OR 2.03, 95% CI 1.52–2.72; P<0.00001; I2=0%, Figure 7A). No significant heterogeneity was observed between the studies.

Figure 7

Masked HTN versus normotension – treated.

Notes: (A) Composite cardiovascular events. (B) All-cause mortality.

Abbreviations: CI, confidence interval; HTN, hypertension; M–H, Mantel–Haenszel.

All-cause mortality occurred in 15.2% of patients with masked HTN and 10.4% of patients with normotension. The risk of all-cause mortality was significantly higher in patients with masked HTN (OR 1.44, 95% CI 1.03–2.01; P=0.03; I2=0%, Figure 7B) without significant heterogeneity among studies.

Masked HTN versus white-coat HTN – treated patients

Composite cardiovascular events were reported in 27.9% of patients with masked HTN and 19.4% of patients with white-coat HTN with significantly higher risk of cardiovascular events in patients with masked HTN (OR 1.64, 95% CI 1.20–2.25; P=0.002; I2=0%, Figure 8A). No significant heterogeneity was found between the studies.

Figure 8

Masked HTN versus white-coat HTN – treated.

Notes: (A) Composite cardiovascular events. (B) All-cause mortality.

Abbreviations: CI, confidence interval; HTN, hypertension; M–H, Mantel–Haenszel.

All-cause mortality occurred in 21.0% of patients with masked HTN and 17.3% of patients with white-coat HTN. No significant difference was found in the rates of all-cause mortality between the patients with masked and white-coat HTN (OR 1.03, 95% CI 0.55–1.90; P=0.94; I2=39%, Figure 8B).

Masked HTN versus SH – treated patients

We did not find significant differences in the risk of cardiovascular events between patients with masked and SH (OR 1.08, 95% CI 0.71–1.65; P=0.72; I2=45%, Figure 9A) with significant heterogeneity among studies.

Figure 9

Masked HTN versus sustained HTN – treated.

Notes: (A) Composite cardiovascular events. (B) All-cause mortality.

Abbreviations: CI, confidence interval; HTN, hypertension; M–H, Mantel–Haenszel.

All-cause death occurred in 21.0% of patients with masked HTN and 17.1% of patients with SH without significant differences in the risk of all-cause mortality between the patients with masked and SH (OR 0.92, 95% CI 0.26–3.22; P=0.90; I2=85%, Figure 9B). Significant heterogeneity was observed between studies.

Assessment of risk of bias

Cochrane’s risk of bias tool suggested low-to-moderate risk of bias in all studies. Assessment of individual components of Cochrane’s risk of bias tool in all trials showed low risk of bias in case of sequence generation, blinding of outcome assessment, incomplete outcome data, and selective outcome reporting.

Discussion

The salient findings of our meta-analysis can be summarized as follows: 1) the composite cardiovascular events and all-cause mortality were significantly higher in patients with masked HTN compared with patients with normotension and white-coat HTN; 2) composite cardiovascular events were significantly lower in patients with masked HTN compared with patients with SH; however, no significant difference was seen in all-cause mortality between the two groups; 3) similar results were observed in the sub-group analysis of patients who are untreated; and 4) in the sub-group of patients who received antihypertensive treatment, no significant difference was observed in composite cardiovascular events and all-cause mortality between the patients with masked and SH. Among treated patients, masked HTN was associated with higher rates of cardiovascular events compared with normotension and white-coat HTN.

Early identification and diagnosis of masked HTN with 24-hour ambulatory BP measurements (ABPM) and home BP measurements (HBPM) are important. Although HMBP lacks night-time measurement and may misclassify some masked HTN patients as normotensives, ABPM may have limited tolerability, affordability, and availability particularly in the US. Despite the limited sensitivity and specificity of HBPM in diagnosis of masked HTN,8 there is available evidence from the Finn-Home study that HBPM is superior to office BP in predicting cardiovascular risk and that HBPM should be used to screen for masked HTN in prehypertensive patients according to office BP.9 Therefore, a diagnosis of masked HTN can be based on HBPM and should be confirmed by ABPM before initiation of antihypertensive therapy.

Population cohort studies have suggested that among patients with masked HTN, one-third progresses to SH and one-third regresses to normotension in 5 years.10 Delayed diagnosis of masked HTN is related to high prevalence of hypertensive target organ damage in both treated and untreated patients with masked HTN.4 Work- and home-related stress, smoking, age, sedentary lifestyle, and sleep disturbances have been identified as risk factors for masked HTN.11–14 It is suggested that masked HTN can be classified into masked daytime HTN and masked nocturnal HTN.15 Based on findings from the Jackson Heart study in blacks, nocturnal masked HTN is more frequent with the prevalence of 48.2 versus 28.2% prevalence of day-time masked HTN. The International Database of Home Blood Pressure in Relation to Cardiovascular Outcomes (IDHOCO) study demonstrated that masked HTN is more prevalent in treated hypertensive patients than in untreated individuals as anti-hypertensive treatment results in greater disproportional reduction of office BP than ABPM.16,17 Noncompliance with medication, except just prior to office visits and morning peak levels of medications that coincide with office visits, may explain these observations. As emphasized in the International Database on Ambulatory Blood Pressure in Relation to Cardiovascular Outcomes (IDACO) study, antihypertensive treatment leads to a transformational change from SH to masked uncontrolled HTN and finally to sustained normotension. However, the risk of converted normotensives remains higher than that of normotensive individuals.18

Our findings are consistent with prior population-based studies such as the Dallas Heart Study and the Jackson Heart Study, which showed increased incidence of cardiovascular events in patients with masked HTN compared to patients with normotension, suggesting the malignant nature of masked HTN.6,7 Pooled analysis of 12 different populations from IDACO performed by Asayama et al32 showed similar findings. In contrast to the Jackson Heart Study, we found a significant increase in all-cause mortality in patients with masked HTN compared to patients with normotension. However, the Jackson Heart Study had small sample size with predominantly African American population.7 Our findings are consistent with large multiple population-based study performed by Stergiou et al,16 further potentiating the nature of masked HTN. Prior studies showed inconsistent results in cardiovascular outcomes between the patients with masked HTN and white-coat HTN.16,32 We found significant increase in composite cardiovascular events and all-cause mortality in patients with masked HTN compared to patients with white-coat HTN, which is similar to the study reported by Stergiou et al.16

Prevalence of masked HTN was found to be significantly high. Patients with masked HTN were 18% of population sample in the Dallas Heart Study.6 Similar results were seen in the pooled analysis of IDACO performed by Asayama et al.32 The Jackson Heart Study showed even higher prevalence patients with masked HTN.7 Furthermore, >50% of these patient populations were untreated.6,7 The increased incidence of cardiovascular events and mortality in patients with masked HTN compared to patients with white-coat HTN are most likely due to the fact that the significant number of masked HTN patients being untreated. Subgroup analysis of patients treated with antihypertensives showed no significant difference in morality between the patients with masked HTN and white-coat HTN, suggesting that the patients with masked HTN who are successfully treated will have better outcomes. However, the cardiovascular events and mortality continued to be significantly high in patients with masked HTN compared to patients with normotension.

Based on current results, treating patients with masked HTN might prevent cardiovascular events and decrease the mortality. The two important issues to be addressed before treating the patients with masked HTN are how to diagnose masked HTN and what should be the target BP. Diagnosis can be made by ambulatory or home BP monitoring both in untreated and treated patients.33 However, identifying the patients to be screened is a more difficult task in untreated patients with masked HTN compared to treated patients with masked uncontrolled HTN. The main obstacle is diagnosing masked HTN in untreated population with normal office BP. ABPM and HBPM should have a complimentary role in the diagnosis and management of masked HTN. Patients with pre-HTN according to office BP, at high risk (diabetes, obstructive sleep apnea, and smoking), or evidence of target organ damage (chronic kidney disease and left ventricular hypertrophy) and normal office BP should be screened with HBPM.33–35 Nighttime and daytime BP recordings with ABPM may better define cardiovascular risk and guide treatment, as it prevents incomplete treatment of uncontrolled masked HTN.

Treating patients with masked HTN showed significant reductions in systolic BP; however, no significant difference was seen in end organ effects such as left ventricular mass index.36 Furthermore, there are no studies addressing the effect of treating masked HTN on clinic outcomes. Aggressive risk factors’ modification such as obesity, diabetes, and sleep apnea would be an important step in preventing the adverse effects associated with masked HTN.33 Although HBPM rather than office BP measurements are more effective in guiding adjustments of antihypertensive medications to goal daytime BP, ~25% of patients will be undertreated with this strategy due to the persistence of nocturnal HTN. Therefore, after reaching the daytime BP goal with HBPM, ABPM can establish whether escalation of antihypertensive treatment is required for the treatment of masked uncontrolled nocturnal HTN.

Limitations

There are some limitations to the interpretation of our data analysis. First, publication bias may still exist despite our best efforts to conduct a comprehensive search and despite the lack of statistical evidence for the existence of bias. Second, any meta-analysis based on the pooling of data from different cohorts with different inclusion criteria, different designs and populations, variable follow-up duration with differing attrition rates, and not being unified in definition and validation of endpoints in individual trials presents challenges. Moreover, our main endpoint, CVD events, was defined differently in most of the studies. Finally, the fact that some studies used ABPM and others used HBPM to define masked HTN may also increase the heterogeneity and affect the validity of the study.

The findings of our meta-analysis are in accordance with the findings of previous meta-analyses.37,38 Compared with previous works, our study is more comprehensive as it included slightly higher number of studies and analyzed not only cardiovascular events but also all-cause mortality as endpoints.

Conclusion

In this large meta-analysis of 14729 patients, the cardiovascular morbidity and mortality associated with masked HTN is higher than normotension and white-coat HTN but significantly lower than SH. Among treated patients, masked HTN and SH were associated with similar rates of cardiovascular events and mortality. Future studies should focus on the benefit of early screening and identification of patients with masked HTN and also evaluate BP treatment goals for these patients based on HBPM and ABPM.