Introduction
Among patients diagnosed with hypertension, only 13.8% were considered controlled [
1], and more than 9 million people die each year from hypertension-related diseases [
2]. The most severe risk of hypertension is its complications, elevated systolic and diastolic blood pressures are strongly associated with cardiovascular disease risk [
3,
4]. A follow-up study of 23,272 patients in the National Health and Nutrition Examination Survey (NHANES) showed that more than 50% of patients who died of coronary heart disease and stroke combined with hypertension [
5], Population-based Atherosclerosis Risk in Communities (ARIC) study shows 25% of cardiovascular events are associated with hypertension [
6]. However, despite a large number of hypertensive patients and the horrible complications it causes, the treatment of hypertension remains unsatisfactory. Unlike other diseases, hypertension has no apparent symptoms; in other words, hypertension is a so-called silent disease, so fewer patients will request treatment at an early stage or fail to follow prescriptions carefully [
7]. Corrao et al. reported that more than 40% of patients would not continue initiating drug therapy within 1 year [
8], about 10% of patients forget to take their daily medications [
9]. It is therefore not surprising that exploring additional and complementary therapies for hypertension [
10].
Aspirin is widely used for the secondary prevention of cardiovascular disease with positive effects [
11‐
13]. In some secondary prevention studies, aspirin has been found to reduce the incidence of myocardial infarction and ischemic stroke [
14‐
16]. However, previous studies mainly focused on the preventive effects of aspirin, and few studies have focused on the effects of aspirin on blood pressure [
17]. There has been a lack of reliable evidence on whether taking aspirin affects blood pressure. Does it lower blood pressure and work in conjunction with other anti-hypertensive medications, or does it have no effect on blood pressure, or is it even more likely to cause fluctuations in blood pressure when taken over a long period? Some studies have found no relationship between aspirin and blood pressure [
18‐
22], while Hermida et al. reported that taking aspirin at bedtime lowered blood pressure [
23‐
28]. In their study, untreated hypertensive patients taking aspirin at bedtime reduced SBP and DBP by 6 mmHg and 4 mmHg, respectively. In conclusion, it remains uncertain what effect aspirin has on blood pressure, and therefore, studies are necessary to clarify the relationship between aspirin and blood pressure.
Methods
This study was designed and carried out with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) criteria [
29]. The protocol was registered in PROSPERO. (PROSPERO 2022
CRD42022346453).
Eligibility criteria
Inclusion and exclusion criteria were based on population, interventions, comparisons, outcomes (PICO) criteria.
Studies meeting the following criteria will be included: (1) Participants should be at least 18 years old and diagnosed with hypertension (defined as systolic blood pressure greater than 140 mmHg or diastolic blood pressure greater than 90 mmHg, or both), their blood pressure was measured by validation techniques, receiving other anti-hypertensive medications was not restricted during the study period. (2) Participants in the intervention group should take aspirin, and the control group should take placebo or no treatment at all. (3) The study should report BP reduction as an outcome.
Studies with the following characteristics will be excluded: (1) Reviews, case reports and, conference abstracts. (2) Studies with less than 50 participants. (3) Literature for which experimental data were not available. (4) Articles for which full text was not available. (5) Non-clinical studies, such as in vivo or in vitro experiments. (6) Non-RCTs, including cohort studies and case-control trials. (7) Studies written in languages other than English.
After reading the title and abstract of the article, articles that met the inclusion criteria and did not conflict with the exclusion criteria will be read in full. Articles that had been read in full and meet the criteria will undergo data extraction. All publications were screened independently by two authors (Li, Xu), any disagreements were resolved after discussions between the two authors or by consulting a third reviewer.
Search strategy
We searched the following databases for relevant papers: PubMed, Cochrane Library, Scopus, Embase, and Medline. We also searched the clinical research registry websites ClinicalTrials (clinicaltrials.gov) and ICTRP (trialsearch.who.int) to ensure no pertinent studies were missed. Searches were conducted up to September 2023.
We utilized a data extraction form based on the Data Extraction Form of the Cochrane Review Group (Cochrane Collaboration) and modified some of its items to suit our study. The data extraction form mainly included the following: age, gender, race, country, blood pressure, intervention method, intervention duration, and primary outcomes. Two authors (Li, Xu) collected the data independently, and any disagreements were resolved through discussions between the two authors or by consulting a third reviewer.
Quality assessment
As only RCTs were included, we used the Cochrane Collaboration’s Risk of Bias tool to assess study quality [
30]. We used the Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) criteria to assess the quality of evidence.
Statistical analysis
We used Stata17 and Review Manager 5.4 software for data synthesis, with mean difference (MD) selected as the Effect Magnitude Indices for continuous variables (e.g., blood pressure reduction). For studies with more than one intervention group, we combined all intervention groups into one group as recommended by the Cochrane Handbook for the Systematic Review of Interventions [
31]. Higgin’s I
2 statistics and Cochran’s Q test were used to detect statistical heterogeneity between various studies [
32]. When I
2 > 50%, a random-effects model was used to evaluate the pooled results; otherwise, a fixed-effects model was used to analyze the pooled results. We used meta-regression to identify any possible sources of heterogeneity. A prespecified subgroup analysis was conducted according to [
33] duration of intervention (>3 months vs. <3 months), time of aspirin administration (morning vs. evening), co-administration of other medications (co-administration of other medications vs. aspirin only), and type of control (placebo vs. no treatment). A sensitivity analysis was performed to assess the combined data’s stability and to pinpoint the cause of any heterogeneity. Begg’s and Egger’s linear regression tests were used to investigate publication bias [
34].
Discussion
Some hypertensive patients need to take aspirin for a long time to prevent cardiovascular events, so it is natural to wonder whether aspirin affects blood pressure and the effect of antihypertensive drugs. Aspirin blocks TXA2 and promotes nitric oxide synthesis, which may lead to vasodilation, reduced peripheral vascular resistance, and lower blood pressure [
36]. Some studies have also found that aspirin inhibits COX-1 and COX-2. Inhibition of COX-1 leads to vasoconstriction, which in turn leads to increased blood pressure [
38]. In addition, some studies have shown that different dosing times or drug interactions can also affect blood pressure [
28,
39,
40]. Because of conflicting findings from previous studies, we conducted this meta-analysis and systematic review to clarify what effect aspirin would have on patients with hypertension.
Our study found that aspirin did not change blood pressure levels, either SBP (MD = -0.78, 95% CI: − 2.41, 0.84) or DBP (MD = -0.86, 95% CI: − 2.14, 0.42). We found no significant difference between subgroups after subgroup analysis for factors such as administration time, follow-up, type of control, and concomitant treatment with other medications. However, caution should be exercised in interpreting the findings due to the few included studies. Although some studies have reported that different administration times, especially at bedtime, can lower blood pressure [
27,
28], our study showed no significant difference between taking aspirin at bedtime and in the morning. However, the pooled results for the different subgroups do show contrasting trends, and perhaps with more studies included, this difference will be statistically significant. Patients with hypertension often have other co-morbidities that require them to take multiple medications simultaneously. Subgroup analysis showed that concomitant administration of other drugs does not change the result, which could indicate that aspirin does not interfere with other medications, which is consistent with the findings of Johnson et al. [
41]. The rest of the subgroup analyses also showed no significant differences between groups. Begg’s test and Egger’s test showed no significant publication bias. However, the publication bias test is not very reliable due to the small number of included studies [
34]. Sensitivity analysis showed that the pooled results were not affected by any single studies, and after removing individual studies, the conclusions remained consistent with the main study findings.
In fact, despite some controversy, most people agree that aspirin does not affect blood pressure [
20,
21,
42,
43], and our study simply provides more compelling evidence to dispel some of the concerns in clinical practice. Aspirin, primarily used as an antiplatelet drug, may affect blood pressure through certain pathways. For example, it can inhibit the synthesis of the vasodilators PGI2 and PGE2 by blocking COX-1 and COX-2 and causing sodium and water retention [
44]. Aspirin can also act in the vascular endothelium to inhibit the expression of pro-inflammatory cytokines and the adhesion of leukocytes, increasing the generation of nitric oxide, which ultimately leads to vasodilatation. This effect becomes more potent as thromboxane A2 and prostaglandins decrease [
45‐
47]. We hypothesized that perhaps it is this delicate balance that led to the results of our study, namely that taking aspirin did not affect blood pressure. On the other hand, the effects mentioned above are limited and indirect because aspirin cannot directly affect the mechanisms that regulate blood pressure, which may explain why no blood pressure fluctuations were observed in patients taking aspirin. Our findings are also consistent with some recent studies; for example, in the study by Mirabito Colafella et al., they found that aspirin does not affect vascular function [
48]. In a study by Dong et al., they found that aspirin has no significant effect on the gut microbiota of spontaneously hypertensive rats, and alterations in the gut microbiota may be associated with hypertension [
49].
Subgroup analyses of different dosing times showed no significant difference in the antihypertensive effect when administered in the morning versus in the afternoon or at bedtime. However, due to the small number of participants in the bedtime dosing subgroup, this conclusion may not be as reliable, especially since some studies did propose that different dosing times result in different antihypertensive effects [
50]. Since the secretion of nitric oxide, prostaglandins, angiotensin II, and angiotensin-converting enzyme has a circadian rhythm, different administration times may produce different effects [
51,
52]. However, whether these differences are sufficient to alter blood pressure levels remains uncertain. Therefore, we believe there is a need for more trials focusing on this variable.
Limitations
This study also has some limitations. First, most of the included studies had small sample sizes or low study quality, which would lead to unstable and less credible results. Second, the number of included studies was also small, so the assessment of publication bias may lack accuracy, and the overall results may also lack statistical significance. Finally, most of the included studies did not use placebo as a control. Since 20–24% of long-term changes in blood pressure are attributable to the placebo effect [
53], the lack of placebo may cause a misinterpretation of the study results.
Future directions
Our findings reduce some of the uncertainty in clinical practice and the process of developing guidelines. Clinicians may not have to worry about whether prescribing aspirin to patients with controlled hypertension will cause blood pressure fluctuations. As aspirin is widely used for secondary prevention of cardiovascular disease, this study may lead to updates in some guidelines. In conclusion, our systematic review and meta-analysis summarizes the results of global studies and draws compelling conclusions about whether aspirin affects blood pressure.
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