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International Journal of Hypertension logoLink to International Journal of Hypertension
. 2022 Dec 29;2022:4476905. doi: 10.1155/2022/4476905

The Association between Hypertension and Insomnia: A Bidirectional Meta-Analysis of Prospective Cohort Studies

Dingwei Liu 1, Chao Yu 2, Ke Huang 3, Shawn Thomas 4, Wei Yang 4, Song Liu 5, Jie Kuang 6,
PMCID: PMC9815923  PMID: 36618449

Abstract

Background

Studies on bidirectional associations between hypertension and insomnia are inconclusive. The purpose of this meta-analysis was to systematically review and summarize the current evidence from epidemiological studies that evaluated this relationship.

Materials and Methods

PubMed, Embase, China National Knowledge Infrastructure (CNKI), Wan Fang, and VIP databases were searched for studies published up to May 2021. Prospective cohort studies that reported the relationship between hypertension and insomnia in adults were included. Data were extracted or provided by the authors according to the prevalence rate, incidence rate, unadjusted or adjusted odds ratio (OR), and 95% confidence interval (CI). Heterogeneity was assessed by I2 statistics. ORs were pooled by using random-effects models.

Results

A total of 23 prospective studies were identified. Twenty cohort studies recorded OR-adjusted value with the outcome for hypertension (OR = 1.11, 95% CI: 1.07–1.16; I2 = 83.9%), and three cohort studies reported OR-adjusted value with the outcome for insomnia (OR = 1.20, 95%CI: 1.08–1.32; I2 = 35.1%). Subgroup analysis showed that early morning awakening and composite insomnia were significantly associated with hypertension.

Conclusions

The result indicates a possible bidirectional association between hypertension and insomnia. Early identification and prevention of insomnia in hypertension patients are needed, and vice versa.

1. Introduction

Hypertension affects 26.4% of people worldwide and is considered the main risk factor for mortality [1]. Patients with hypertension commonly complain of insomnia. Hypertension adults have reported an increased risk of insomnia, with a risk ratio of 1.5 to 3.18 [2, 3]. Several studies have reported that adults with hypertension have an increased risk of insomnia. Still, patients with hypertension also suffer from psychological diseases such as anxiety and depression [46], which are risk factors for insomnia. However, there is no systemic evidence available to support this relationship.

Insomnia is the most common sleep disorder and the second most prevalent mental disorder worldwide. It is defined as the occurrence of difficulty initiating sleep (DIS) or difficulty falling asleep (DFA), sleep continuity disturbance (SCD) or difficulty maintaining asleep (DMS), non-restorative sleep (NRS), and early morning awakening (EMA) [79]. About 17%–19% of the US population presented insomnia symptoms [10]. Nearly 15% of the population in China reported insomnia [11].

Insomnia is associated with a variety of mental and physical health problems. In addition, abnormal sleepers may also suffer from cardiovascular disease [12]. Hernandez-Aceituno et al. found that increased use of antihypertensive medications was significantly associated with poor sleep status [13]. Therefore, treating insomnia and ameliorating sleep habits may be crucial to control some chronic diseases [8].

Hypertension and insomnia are major public health issues, and investigations into the association between these diseases have recently attracted broad attention [14]. Li et al. performed a meta-analysis to assess the pooled relative risk (RR) of insomnia on hypertension. The findings suggested that the ultimate RR value was 1.21 (1.10 to 1.33) [15]. However, in various epidemiological studies, this association remains inconsistent [1619], and comprehensive reviews that focus on the bidirectional association between insomnia and hypertension are lacking [20]. Therefore, we conducted a bidirectional systemic review and meta-analysis to determine the association between insomnia and hypertension.

2. Materials and Methods

This meta-analysis was performed according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Two authors (HK and LDW) independently evaluated eligibility, extracted data, and scored the quality of the study included. Disagreements were settled by a discussion until consensus was reached or determined by a third author (KJ).

2.1. Search Strategy

We searched PubMed, Embase, CNKI, Wan Fang, and VIP (up to May 2021). To minimize bias, two authors (HK and LDW) independently performed an online search using the following combination of search terms: “hypertension,” “high blood pressure,” “disorders of initiating and maintaining sleep,” “sleep disturbance,” “sleep disorder,” “sleep quality,” “insomnia,” “agrypnia,” and “sleep maintenance,” to identify published studies evaluating the association between hypertension and insomnia. Additionally, a search of the reference lists of eligible articles was conducted to determine any missed reports.

2.2. Inclusion and Exclusion Criteria

Studies were selected based on the following inclusion criteria: (1) the study design was prospective; (2) participants aged 18 years or older; (3) insomnia diagnosed through any symptoms (DIS, DFA, SCD, NRS, DMS, and EMA) or diagnostic criteria (e.g., DSM-IV/V, ICSD-1/2/3, and ICD-9/10); (4) hypertension diagnosed was based on a current resting systolic blood pressure (SBP) ≥ 140 mmHg and/or diastolic blood pressure (DBP) ≥ 90 mmHg, by self-reported hypertension, or by antihypertensive treatment; (5) included an OR value and a 95% confidence interval or other sufficient results; (6) published in English and Chinese. The exclusion criteria included the following: (1) studies with special populations (e.g., child and pregnancy); (2) letters, comments, reviews, or meta-analyses; and (3) the full text was not available.

2.3. Risk of Bias Assessment

The methodological quality for the included studies was assessed based on the Newcastle-Ottawa Scale (NOS), including the quality of study selection (0–4 points), comparability (0–2 points), and exposure and outcome of study participants. A final score ≥7 is considered a high-quality article [21].

2.4. Data Extraction

Two researchers (HK and LDW) independently extracted the following information from each study: basic information (author, publication time, nationality, source of literature, number of studies, age, and gender), criteria for evaluation of hypertension and insomnia, number of patients and participants, crude, adjusted OR and confidence intervals, and the variables used in multivariate analyses. A maximum level adjustment was selected if adjusted ORs were shown in different adjustment levels.

2.5. Statistical Analysis

The association between hypertension and insomnia was assessed from the following perspectives: (1) the OR of baseline insomnia and risk of incident hypertension in prospective cohort studies; (2) the OR of baseline hypertension and risk of future insomnia in prospective cohort studies. If the studies reported effect size other than OR, the transformation was performed, and unpublished data were collected by contacting the corresponding author if possible. A random-effects model was used to pool the data, and statistical heterogeneity between summary data was evaluated using the I2 statistic. 25%, 50%, and 75% represent low, moderate, and high heterogeneity [22]. Forest plots were used for the graphical display of the results. Funnel plot, Begg's test, and Egger's test were used to assess publication bias. Visual asymmetry in funnel plot or P ≤ 0.05 in Begg's and Egger's tests was considered statistically significant. Subgroup analyses were performed to illustrate the influence of study results' specific characteristics, including age, sex, insomnia type, continent, hypertension assessment, insomnia assessment, and follow-up time. Based on hypertension assessment, studies were divided into different types: SBP ≥ 140 mmHg and/or DBP ≥ 90 mmHg or use of antihypertensive medication and others (self-report or different levels of BP or ICD9/10). For insomnia assessment, studies using sleep questionnaires were defined as “non-clinical insomnia criteria,” and others such as DSM-IV and ICSD-I were defined as “clinical diagnostic criteria.” Sensitivity analyses were conducted to detect the stability of our results by excluding each included study one at a time. Stata version 16.0 (StataCorp, College Station, TX) was used for all statistical analyses. P values were two-sided, and a significance level cutoff of 0.05 was used.

3. Results

3.1. Study Selection and Characteristics

The literature search yielded a total of 14,738 articles. After removing the duplicate articles, 10,409 articles remained. After reviewing the titles and abstracts, articles were excluded for their irrelevance. The remaining 157 articles were identified through full-text screening. One hundred thirty-four articles did not meet the inclusion criteria, and 23 were included. After quality assessment, most studies have shown good quality with scores ranging from 6 to 8.95. 65% (22/23) of the studies' score was ≥6, and 43.48% (10/23) of the studies' score was ≥8. However, three studies did not satisfy the criterion “Demonstration that outcome of interest was not present at start of study.” Two studies [23, 24] did not meet the “Demonstration that outcome of interest was not present at the start of the study” criterion in insomnia predicting incident hypertension. One study [25] did not meet the criterion in hypertension predicting incident insomnia (Supplementary Table 1). The final meta-analysis (Figure 1) included 23 cohort studies (Table 1).

Figure 1.

Figure 1

Flowchart of the article selection process.

Table 1.

Characteristics of cohort studies in the meta-analysis.

Author Year Country Follow-upyears Sample Age range (or mean age) Insomnia assessment Insomnia type Hypertension assessment Note
Suka et al. [26] 2003 Japan 4 9237 40–55 y Sleep questionnaire DIS, DMS (1) SBP ≥ 140 mmHg and (or) DBP ≥ 90 mmHg Baseline insomnia
(2) Antihypertensive treatment NOS rating: 6
Phillips and Mannino [27] 2007 USA 6 8,757 45–69 y Sleep questionnaire DFA, SCD, NRS (1) SBP ≥ 160 mmHg and (or) DBP ≥ 95 mmHg Baseline insomnia
(2) Antihypertensive treatment NOS rating: 8
Phillips et al. [28] 2009 USA 6 1,419 64–91 y Sleep questionnaire D4FA, EMA, SCD (1) SBP ≥ 140 mmHg and (or) DBP ≥ 90 mmHg Baseline insomnia
(2) Antihypertensive treatment (3) Self-reported hypertension NOS rating: 7
Knutson et al. [29] 2009 USA 5 535 35–45 y Sleep questionnaire DMS (1) SBP≥140 mmHg and (or) DBP ≥ 90 mmHg Baseline insomnia
(2) Antihypertensive treatment NOS rating: 6
Gangwisch et al. [30] 2010 USA 10 4,913 32–86 y Sleep questionnaire DIS, DMS, EMA (1) SBP≥140 mmHg and (or) DBP ≥ 90 mmHg Baseline insomnia
(2) Self-reported hypertension (3) Physician or hospital diagnosis NOS rating: 7
Troxel et al. [31] 2010 USA 3 812 45–74 y Sleep questionnaire DIS, NRS (1) SBP ≥ 130 mmHg and (or) DBP ≥ 85 mmHg Baseline insomnia
(2) Antihypertensive treatment NOS rating: 6
Rod et al. [23] 2011 France 20 16,989 36–52 y Sleep questionnaire DFA, DMS, EMA (1) Self-reported hypertension Baseline insomnia
NOS rating: 6
Fernandez-Mendoza et al. [30] 2012 USA 7.5 786 M = 47.5 y Sleep questionnaire DFA, DMS, EMA, NRS, chronic insomnia (1) SBP ≥ 140 mmHg and (or) DBP ≥ 90 mmHg Baseline insomnia
(2) Self-reported hypertension (3) Antihypertensive treatment NOS rating: 7
Pedraza et al. [31] 2012 USA 3 1,085 ≥75 y Sleep questionnaire DIS, DMS, NRS (1) SBP ≥ 140 mmHg and (or) DBP ≥ 90 mmHg Baseline HTN
(2) Self-reported hypertension
(3) Physician or hospital diagnosis
NOS rating: 6
Singareddy et al. [32] 2012 USA 7.5 1,246 ≥20 y Sleep questionnaire DFA, DMS, EMA, NRS (1) Antihypertensive treatment Baseline HTN
(2) Self-reported hypertension NOS rating: 6
Zhang et al. [19] 2012 China 5.2 2,316 M = 47.5 y DSM-IV, ICSD-1, ICD-10 DIS, DMS, EMA (1) Self-reported hypertension Baseline insomnia
NOS rating: 8
Jaussent et al. [33] 2013 France 6 5,494 65–94 y Sleep questionnaire Eds, DIS, DMS, EMA (1) SBP≥160 mmHg and (or) DBP ≥ 95 mmHg Baseline insomnia
(2) Antihypertensive treatment NOS rating: 6
Haaramo et al. [34] 2014 Finland 5 6,477 40–60 y Sleep questionnaire DFA, DMS (1) Antihypertensive treatment Baseline insomnia
NOS rating: 7
Sivertsen et al. [35] 2014 Norway 11 24,715 20–89 y DSM-IV DMS, DIS, NRS (1) Self-reported hypertension Baseline insomnia
NOS rating: 8
Jackowska and Steptoe [36] 2015 UK 4 3,937 ≥50 y Sleep questionnaire DFA, DMS, EMA (1) SBP ≥ 140 mmHg and (or) DBP ≥ 90 mmHg Baseline insomnia
(2) Antihypertensive treatment NOS rating: 6
Cheng et al. [12] 2015 USA 1 967 M = 43.1 y Sleep questionnaire DFA, DMS (1) Self-reported hypertension Baseline insomnia
NOS rating: 6
Clark et al. [37] 2016 Finland 1 70,049 18–69 y DSM-IV DFA, DMS, EMA, NRS (1) Antihypertensive treatment Baseline insomnia
NOS rating: 8
Leigh et al. [38] 2016 Australia 15 10,721 70–75 y Sleep questionnaire EMA, DIS (1) Self-reported hypertension Baseline HTN
NOS rating: 6
Lin et al. [24] 2016 Taiwan 5 44,559 >20 y 1.ICD-9 DFA, DMS, EMA (1) ICD-9 Baseline insomnia
NOS rating: 7
Dong and Yang [38] 2019 USA 8 18,123 ≥50 y Sleep questionnaire DFA, DMS, EMA, NRS (1) SBP ≥ 140 mmHg and (or) DBP ≥ 90 mmHg Baseline insomnia
(2) Antihypertensive treatment NOS rating: 6
Garbarino and Magnavita [39] 2019 Italy 5 234 M = 36 y Sleep questionnaire DIS, EMA, NRS (1) SBP ≥ 130 mmHg and (or) DBP ≥ 85 mmHg Baseline insomnia NOS rating: 5
Rahim et al. [40] 2020 Canada 12 2,079 35–69 y Sleep questionnaire DIS, DMS, NRS (1) ICD-9, ICD-10 Baseline insomnia NOS rating: 6
Li et al. [41] 2020 USA 6 6,965 18–74 y Women's Health Initiative Insomnia Rating Scale (WHIIRS) NA (1) SBP ≥ 140 mmHg and (or) DBP ≥ 90 mmHg Baseline insomnia NOS rating: 7
(2) Antihypertensive treatment

DBP = diastolic blood pressure; DFA, difficulty falling asleep; DIS, difficulty initiating sleep; DMS, difficulty maintaining sleep; DSM, Diagnostic and Statistical Manual of Mental Disorders; EMA, early morning awakening; HTN = hypertension; ICSD, International Classification of Sleep Disorders; ICD, International Classification of Diseases; NA = not available; NOS = Newcastle-Ottawa Scale; NRS, non-restorative sleep; SBP = systolic blood pressure.

3.2. Cohort Studies of Baseline Insomnia Predicting the Risk of Hypertension

The association between samples with insomnia at baseline and incident hypertension was investigated in twenty studies, with a total of 242,415 participants. Table 1 summarizes the basic characteristics of these studies. Of the 20 studies, hypertension was identified by measured blood pressure, self-reported hypertension, or antihypertensive treatment. Sleep questionnaire was used in four studies for diagnosing insomnia; one study used the Women's Health Initiative Insomnia Rating Scale (WHIIRS), and four studies used DSM-IV, ICSD-1, and ICD-9/10 instead. Seventeen studies were conducted in North America or Europe and three in Asia. The follow-up ranges from 1 to 20 years.

The result was OR = 1.11 (95% CI: 1.07–1.16) with high heterogeneity (I2 = 83.9%, P  < 0.001) detected (Figure 2). Publication bias was found in the funnel plot (Supplementary Figure 1(a)) and confirmed by Egger's test (P = 0.01) but not in Begg's test (P = 0.347). We further performed subgroup analyses (Table 2). The association between insomnia and hypertension were significant in the age subgroups (40−60 vs. < 40 y: OR=1.10, 95% CI: 1.05−1.15, I2 = 85.2%, P < 0.001; >60 vs. < 40 y: OR=1.12, 95% CI: 1.09−1.16, I2 = 0%, P < 0.810). In male (the proportion of males in each study <40%) (OR = 1.10, 95%CI: 1.03–1.17, I2 = 81.0%, P < 0.001) and male (the proportion of males in each study: 40%–60%) (OR = 1.12, 95%CI: 1.08–1.15, I2 = 15.4%, P = 0.294) groups, we also found an association between insomnia and incident hypertension. Studies in North America (OR = 1.07, 95%CI: 1.01–1.13, I2 = 79.1%, P < 0.001) and Europe (OR = 1.14, 95%CI: 1.04–1.25, I2 = 72.5%, P = 0.001) found that insomnia was significantly associated with increased risk of hypertension, while studies in Asia did not. However, in Asia, the estimate was based on only three studies. More studies are needed to get more accurate values. The subgroup that included the insomnia subtype found that early morning awakening (EMA) (OR = 1.13, 95%CI: 1.07–1.20, I2 = 0%, P = 0.566) and composite insomnia (OR = 1.12, 95%CI: 1.06–1.17, I2 = 79.9%, P < 0.001) were associated with incident hypertension. In the subgroup of insomnia assessment, non-clinical insomnia criteria (OR = 1.12, 95%CI: 1.07–1.17, I2 = 86.3%, P < 0.001) showed an association between insomnia and incident hypertension. As for hypertension assessment, significant associations were found both in SBP ≥ 140 mmHg and/or DBP ≥ 90 mmHg or use of the antihypertensive medication group (OR = 1.21, 95%CI: 1.10–1.33, I2 = 86.9%,P < 0.001) and other (self-report or different levels of BP or ICD9/10) group (OR = 1.04, 95%CI: 1.01–1.08, I2 = 66.3%, P = 0.001). Sensitivity analyses were then performed, and the results showed that the estimated ORs were still statistically significant (Supplementary Figure 2(a)). We also drew a forest plot after excluding two studies [23, 24] that did not satisfy the “Demonstration that outcome of interest was not present at the start of the study” criterion (Supplementary Figure 3(a)). The figure shows that excluding the two studies does not influence the main results. We have also plotted the effect size against follow-up time to confirm there is no link between the two (Supplementary Figure 4(a)).

Figure 2.

Figure 2

Forest plots of insomnia predicting incident hypertension. Squares represent the study-specific relative risk. Diamonds represent the summary relative risks (SRRs). Horizontal lines represent 95% confidence intervals (CIs).

Table 2.

Subgroup analyses of the association between insomnia and hypertension.

No. of reports OR (95% CI) Pvalue for heterogeneity I 2 (%)
Subgroup analyses
Age
 <40 1 2.89 (0.76–11.07)
 40–60 14 1.10 (1.05–1.15) <0.001 85.2
 >60 5 1.12 (1.09–1.16) 0.810 0
Sex1
 Male (<40%) 6 1.10 (1.03–1.17) <0.001 81.0
 Male (40%–60%) 12 1.12 (1.08–1.15) 0.294 15.4
 Male (>60%) 2 1.40 (0.78–2.52) <0.001 97
Continent
 North America 10 1.07 (1.01–1.13) <0.001 79.1
 Asia 3 1.40 (0.94–2.08) 0.011 77.9
 Europe 7 1.14 (1.04–1.25) 0.001 72.5
Follow-up time
 >5 11 1.06 (1.02–1.10) <0.001 81.9
 ≤5 9 1.27 (1.12–1.43) 0.008 55.6
Insomnia subtype2
 DIS/DFA 4 1.26 (0.87–1.84) 0.004 77.9
 DMS 4 1.17 (0.89–1.55) 0.001 83.0
 EMA 2 1.13 (1.07–1.20) 0.566 0
 NRS 1 1.39 (0.78–2.48)
 Composite insomnia 15 1.12 (1.06–1.17) <0.001 79.9
Hypertension assessment
 SBP ≥ 140 mmHg and/or DBP ≥ 90 mmHg or use of antihypertensive medication 9 1.21 (1.10–1.33) <0.001 86.9
 Others (self-report or different levels of BP or ICD9/10) 11 1.04 (1.01–1.08) 0.001 66.3
Insomnia assessment
 Clinical diagnostic criteria 3 1.03 (0.91–1.17) 0.448 0
 Non-clinical insomnia criteria 17 1.12 (1.07–1.17) <0.001 86.3

CI, confidence interval; OR, odds ratio. HTN, hypertension; BP, blood pressure; EMA: early morning awakening; DMS, difficulty maintaining sleep; DIS; difficulty initiating sleep; DFA; difficulty falling asleep; NRS; non-restorative sleep. 1The variable “sex” was used as a continuous variable (according to the proportion of males in each study). 2One study provided data on DMS and DIS/DFA. Two studies provided data on DMS, DIS/DFA, and EMA. One study provided data on DIS/DFA and NRS. One study provided data only on DMS. Therefore, there are 26 reports from 20 studies.

3.3. Cohort Studies of Baseline Hypertension Predicting the Risk of Insomnia

The samples with hypertension at baseline and incident insomnia were investigated in three studies, including 13,052 participants, as shown in Table 1. Of the three studies, hypertension was identified by SBP and (or) DBP ≥ 140/90, self-reported hypertension, or antihypertensive treatment. Sleep questionnaires were used in three studies for diagnosing insomnia. Two studies were conducted in the USA and one in Australia. The follow-up ranges from 3 to 15 years. Three reported ORs were included in the pooled result. The result was OR = 1.20 (95% CI: 1.08–1.32) with low heterogeneity detected (I2 = 35.1%, P = 0.214) (Figure 3). However, the pooled OR and 95% CI were based on only three studies, which will affect the results. We drew a funnel plot (Supplementary Figure 1(b)) to show the general condition of each study and performed Begg's and Egger's tests to identify the publication bias. No publication bias was found by Begg's (P = 1.000) and Egger's test (P = 0.332). Sensitivity analyses showed that the estimated ORs were still statistically significant (Supplementary Figure S2(b)). We also drew a forest plot after excluding one study [25] that did not satisfy the “Demonstration that outcome of interest was not present at the start of the study” criterion (Supplementary Figure S3(b)). The figure shows that excluding the study does not influence the main results. We have also plotted the effect size against follow-up time to confirm there is no link between the two (Supplementary Figure 4(b)).

Figure 3.

Figure 3

Forest plots of hypertension predicting incident insomnia. Squares represent the study-specific relative risk. Diamonds represent the summary relative risks (SRRs). Horizontal lines represent 95% confidence intervals (CIs).

4. Discussion

It is the first meta-analysis to investigate the bidirectional association between insomnia and hypertension as far as we know. This meta-analysis indicated a likely bidirectional association between insomnia and hypertension in the prospective cohort studies.

Our results suggested that insomnia and hypertension are significantly related. We collected adjusted ORs to test their association, and we found that the OR of insomnia predicting hypertension was 1.11 (95%CI: 1.07–1.16), and the OR of hypertension predicting insomnia risk was 1.20 (95% CI: 1.08–1.32). When stratified by insomnia assessment, we found an association only between insomnia diagnosed by non-clinical criteria and hypertension, not with insomnia diagnosed by clinical criteria. Studies that used non-clinical criteria, such as sleep questionnaires, may have a higher sensitivity to detect missed sleep issues when collecting only doctor-reported medical diagnoses. In addition, composite insomnia and early morning awakening were found to be significantly associated with hypertension, consistent with the previous meta-analysis [42]. It is also worth noting that we found a more substantial effect in using SBP ≥ 140 mmHg and/or DBP ≥ 90 mmHg or antihypertensive medication group (OR = 1.21, 95%CI: 1.10–1.33) compared with the other group (self-report or different levels of BP or ICD9/10) (OR = 1.04, 95%CI: 1.01–1.08). The reason may be that some patients tended not to report hypertension without knowing the diagnostic criteria, so patients with hypertension can be classified as not hypertensive [43]. Using different levels of BP may decrease the number of people diagnosed with hypertension. As for gender difference, men with insomnia were more likely to suffer from hypertension than women [38].

Although our study confirmed that insomnia was associated with an increase in hypertension occurrence, the mechanism behind it was not fully elucidated. Generally, insomnia affects blood pressure through 3 pathways. (1) Psychogenic pathways: insomnia leads to mental changes, mainly manifested as anxiety [42], depression [38], and so on. The sympathetic nervous system becomes overactive leading to peripheral vasoconstriction and blood pressure increase. (2) Neurogenic pathway: it was found that the activity of the sympathetic nervous system (SNS) increased in insomnia patients, which would lead to a series of hypertension events [44, 45]. (3) Humoral pathway: insomnia has been proven to increase the release of pulsatile cortisol by affecting its rhythm [46]. In addition, insomnia causes stress dysregulation [47], which is a potential cause of high hypothalamic-pituitary-adrenal (HPA) reactivity [48]. The renin-angiotensin-aldosterone system (RAAS) was also activated along with the HPA axis [49]. In addition, insomnia is a pathological state accompanied by inflammation, oxidative stress, and endothelial dysfunction [47], which may be the potential mechanism of hypertension [50]. At the same time, the melatonin secretion of patients with hypertension could be disturbed [47], circadian rhythm would change, and sleep disorders would occur [8, 47]. Indeed, these mechanisms may interact with subsequent pathological conditions. Besides, nocturnal hypertension may also be a likely link between insomnia and increased blood pressure, which may be triggered by specific triggers (OSA episode, arousal, rapid-eye-movement sleep, and nocturia). However, few studies investigate the biological plausibility between hypertension and insomnia. The exact mechanism between hypertension and insomnia still needs further elucidation.

This meta-analysis has several strengths and limitations to address. The primary strength is that this is the first meta-analysis that comprehensively examines the bidirectional association of insomnia and hypertension based on a comprehensive literature search of studies. Our meta-analysis provided more reliable results in cohort studies with a larger number of studies than the previous meta-analysis. In addition, our study quantifies the bidirectional association in detail, which was stratified according to factors such as gender, continents, hypertension assessment, and different types of insomnia. Insomnia assessment based on formal criteria was first considered in the current studies, which helps to shed new light on the exact effect of different criteria. However, there are still some limitations in this study. First, the heterogeneity is high in some analyses of insomnia and hypertension. By subgroup analysis, different types of hypertension assessment and insomnia subtypes might be the source of the heterogeneity. Secondly, some studies failed to control potential confounders such as psychological symptoms, age, or gender, although most studies adjusted several factors. Thirdly, publication bias of baseline insomnia and risk of hypertension was found in the funnel plot and identified by Egger's test (P=0.01). Three studies have different hypertension assessments than most included studies, which may be why they are outside the confidence interval of the funnel plot. Fourth, our analyses did not consider the effect of sleep time on hypertension because insomnia patients often have abnormal sleep time, which could bias our research results. Finally, the results of baseline hypertension predicting the risk of insomnia were based on only three studies, which will affect the stability of the meta-analysis. So, there is an increasing demand for high-quality research in the future.

5. Conclusions

In summary, our study shows that there may be a statistically significant bidirectional association between hypertension and insomnia. Early morning awakening and composite insomnia are potential risk factors for hypertension, while baseline hypertension also serves as a risk factor for insomnia. An assessment of insomnia may be beneficial for patients with hypertension, and treatment for hypertension may include improving sleep quality in those patients who show significant clinical symptoms of insomnia.

Acknowledgments

This study was supported by the National Natural Science Foundation of China (no. 82160645), Natural Science Foundation of Jiangxi Province (20212ACB206019, 20212BAB206091, and 20212BAG70029), and Fund Project of the Second Affiliated Hospital of Nanchang University (2021efyA01 and 2021YNFY2024).

Data Availability

The data used to support the findings of this study are available from the corresponding author upon reasonable request.

Ethical Approval

This article does not contain any studies with human participants performed by any of the authors.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Authors' Contributions

All authors were involved in the study design and preparation of the manuscript. Dingwei Liu and Chao Yu contributed equally to this study.

Supplementary Materials

Supplementary Materials

Supplementary Table 1: quality assessment of included studies. Supplementary Figure 1: funnel plot with pseudo-95% confidence limits. Supplementary Figure 2: sensitivity analysis of the relationship between insomnia and hypertension. Supplementary Figure 3: funnel plot after excluding studies. Supplementary Figure 4: the correlation between follow-up time and effect size.

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplementary Materials

Supplementary Table 1: quality assessment of included studies. Supplementary Figure 1: funnel plot with pseudo-95% confidence limits. Supplementary Figure 2: sensitivity analysis of the relationship between insomnia and hypertension. Supplementary Figure 3: funnel plot after excluding studies. Supplementary Figure 4: the correlation between follow-up time and effect size.

Data Availability Statement

The data used to support the findings of this study are available from the corresponding author upon reasonable request.


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