Effect of green tea consumption on blood pressure: A meta-analysis of 13 randomized controlled trials (2024)

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Sci Rep. 2014; 4: 6251.

Published online 2014 Sep 1. doi:10.1038/srep06251

PMCID: PMC4150247

PMID: 25176280

Xiaoli Peng,^1,^2,³ Rui Zhou,^2,³ Bin Wang,² Xiaoping Yu,¹ Xiaohong Yang,¹ Kai Liu,^a,² and Mantian Mi^b,²

Author information Article notes Copyright and License information PMC Disclaimer

Associated Data

Supplementary Materials

Abstract

The studies investigating the effects of green tea on blood pressure (BP) have generated inconsistent results. The aim of this study is to quantitatively evaluate the effects of green tea on BP control. PubMed, Embase, and the Cochrane Library (updated to March 2014) were searched for randomized controlled trials evaluating the effects of green tea on BP. Pooled effect of green tea consumption on BP was evaluated using fixed-effects or random-effects model. Thirteen trials comprising a total of 1,367 subjects were included in the current meta-analysis. The overall outcome of the meta-analysis suggested that green tea consumption significantly decrease systolic blood pressure (SBP) level by −1.98 mmHg (95% CI: −2.94, −1.01 mmHg; P < 0.001). Compared with the control group, green tea also showed a significant lowering effect on diastolic blood pressure (DBP) in treatment group (−1.92 mmHg; 95% CI: −3.17, −0.68 mmHg; P = 0.002). Subgroup analyses further suggested that the positive effect of green tea polyphenols on BP was only showed in studies using a low-dose green tea polyphenol, with the long-term intervention duration or ruling out the confounding effects of caffeine. The meta-analysis suggested that green tea consumption had a favorable effect on decrease of BP.

Cardiovascular disease (CVD) is one of the most common public health challenges worldwide. The World Health Organization (WHO) estimates that the cost of not investing in CVD prevention and therapy could amount to as much as $47 trillion worldwide in the next 25 years¹, and the consequences will be more severe in developing countries, given that 80% of cardiovascular deaths occur in low and middle income countries¹. As a major risk factor for cardiovascular disease, hypertension is the most common chronic condition in American adults. Recent studies have shown that two thirds of hypertensives in the United States are undertreated or untreated². It has been demonstrated that even people who are free of hypertension (BP < 140/90 mm Hg) at the age of 55 have a 90% lifetime risk for developing hypertension, according to the Framingham data³. In addition, accumulating evidence suggest that health-promoting lifestyle modifications can improve blood pressure (BP) control and even reduce medication needs⁴. Among the comprehensive lifestyle modifications, dietary adjustment is one of the most effective measures for preventing hypertension. A previous meta-analysis suggested that even small changes in BP caused by dietary modification might have a significant impact on the prevalence of hypertension⁵.

Green tea, derived from the plant Camellia sinensis, is a popular beverage worldwide and the major source of flavonoid intake in the US diet⁶. The most prominent effects of tea on human health have been attributed to green tea, and the health-promoting effects of green tea are mainly attributed to catechins, which belong to a family of compounds known as flavonoid-like polyphenols or flavanols⁷. A recent meta-analysis has revealed that green tea consumption might significantly reduce plasma low density lipoprotein–cholesterol (LDL-C) and total cholesterol concentrations⁸. In addition, our previous meta-analysis demonstrated that green tea may have a favorable effect on glucose control in adults⁹. Therefore, one question is pertinent: does green tea also have beneficial effects on BP? Although Hartley et al. conducted a meta-analysis evaluating the effect of green tea on BP, they only included two RCTs when evaluating the effect of green tea on BP¹⁰, and thus the results of their study might be interpreted with caution. To date, previous randomized controlled trials (RCTs) investigating the effects of green tea consumption on BP have generated inconsistent results. Thus, we conducted the meta-analysis to explore the effects of green tea on BP based on the PRISMA guidelines.

Results

Results of the literature search

Detailed processes of the relevant study selection are shown in Fig. 1. A total of 186 reports were initially identified, and 153 articles were excluded either because of duplication or because they were clearly not relevant to the current meta-analysis after carefully reviewing the titles and abstracts. Thus, 33 articles remained for an in-depth examination. Among these 33 articles, 20 were further excluded for the following reasons: 8 were due to their short duration (<1 day), 6 were due to no data of SBP or DBP, and 6 were discarded because the green tea extract was given as part of a multi-component supplement. Thus, 13 articles were ultimately selected for inclusion in the meta-analysis¹¹^,12^,13^,14^,15^,16^,17^,18^,19^,20^,21^,22^,23.

Study characteristics

A summary of the study characteristics included in the meta-analysis is presented in (Table 1). The total number of subjects included in each study ranged from 22 to 240 subjects. The study duration varied from 3 wk to 3 mo (median: 12 wk). Of the 13 trials included in the current meta-analysis, 9 trials focused on adults with prehypertension, 3 trials selected participants with stage 1 hypertension and one trial investigated subjects with Stage 2 hypertension. Most studies (11 of 13) used parallel design. All studies suggested subjects maintain a usual diet, and one study recommended that subjects maintain their physical activities during the study period. Of the 9 studies ruled out the confounding effect of caffeine on BP, 5 used decaffeinated green tea extract as supplements, 2 used decaffeinated green tea beverage in the intervention group, and 2 used placebo matching caffeine in the control group. And four studies used caffeinated green tea as supplements. The green tea polyphenols content ranged from 208 to 1207 mg/d (median: 582.8 mg/d).

Table 1

Characteristics of 13 randomized controlled trials included in analysis

Source	No. of subjects	Study design	Population	Duration	Tea group	Control group	Jadad score	Type of diet^a
f*ckino, 2005, Japan (11)	66	Parallel	Stage 1 hypertension, overweight, 32–73 y of age	2 mo	DGTB (544 mg polyphenols)	No tea	<4	Usual diet
Diepvens, 2006, Netherlands (12)	46	Parallel	Prehypertension, overweight, 19–57 y of age	87 d	GTE capsule (1,207 mg polyphenols, 236.7 mg caffeine)	Placebo (maltodextrin capsule)	<4	Low-energy diet
Nagao, 2007, Japan (13)	240	Parallel	Prehypertension, obese, 25–55 y of age	12 wk	GTE beverage (582.8 mg polyphenols, 72.3 mg caffeine)	GTE beverage (96 mg catechins, 75.0 mg caffeine)	<4	Usual diet
Hill, 2007, Switzerland (14)	38	Parallel	Prehypertension, overweight/obese, 45–70 y of age	12 wk	DGTE capsule (300 mg polyphenols)	Placebo (lactose capsules)	<4	Usual diet with excise
f*ckino, 2008, Japan (15)	70	Crossover	Stage 1 hypertension, overweight, 32–73 y of age	2 mo	GTE beverage (544 mg polyphenols, 102 mg caffeine)	Water	<4	Usual diet
Nagao, 2009, Japan (16)	43	Parallel	Prehypertension, T2DM, 64.9 ± 1.6 y of age	12 wk	GTE beverage (582.8 mg polyphenols, 72.3 mg caffeine)	GTE beverage (96.3 mg catechins, 75.0 mg caffeine)	<4	Usual diet
Frank, 2009, UK (17)	33	Parallel	Prehypertension, overweight,18–55 y of age	3 wk	GTE Capsule (714 mg polyphenols, 114 mg caffeine)	Placebo (maltodextrin)	<4	Usual diet
Brown, 2009, UK (18)	88	Parallel	Prehypertension, overweight/obese, 40–65 y of age	8 wk	DGTE capsule (800 mg polyphenols)	Placebo (lactose capsules)	≥4	Usual diet
Nantz, 2009, USA (19)	111	Parallel	Prehypertension, overweight, 21–70 y of age	3 mo	DGTB (320 mg polyphenols)	Placebo capsule	≥4	Usual diet
Basu, 2010, USA (20)	22	Parallel	BP < 160/100 mmHg, obesity and metabolic syndrome, 25–63 y of age	8 wk	Green tea beverage (928 mg polyphenols, 8.96 mg caffeine)	Water	<4	Usual diet
Brown, 2011, UK (21)	66	Crossover	Prehypertension, overweight and obese, 40–69 y of age	6 wk	DGTE capsule (800 mg polyphenols)	Placebo (lactose capsules)	≥4	Usual diet
Suliburska, 2012, Poland (22)	46	Parallel	Prehypertension, obese, 30–60 y of age	3 mo	DGTE capsule (208 mg polyphenols)	Placebo capsules (cellulose)	≥4	Usual diet
Bogdanski, 2012, Poland (23)	56	Parallel	Stage 1 hypertension, obese, 30–60 y of age	3 mo	DGTE capsule (208 mg polyphenols)	Placebo capsules (cellulose)	≥4	Usual diet

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Abbreviations: DGTB, Decaffeinated green tea beverage; DGTE, decaffeinated green tea extract; EGCG, epigallocatechin gallat; GTE, green tea extract; T2DM, type 2 diabetes mellitus.

^aA usual diet was similar to a conventional diet; a low-energy diet contained less amounts of energy than a usual diet.

Data quality

Study quality was assessed by using the Jadad scale and the results were varied. Five trials¹⁸^,19^,21^,22^,23 were classified as high quality (Jadad score of ≥4) and the remaining 8 trials were low quality (Jadad score of <4). All of the high-quality RCTs reported the use of random number generation or randomization list performed by an independent statistician, and 2 studies used an adequate allocation concealment conducted by a third-party manufacture. Details related to the dropouts were reported in all high quality trials.

Effect of green tea consumption on blood pressure

As shown in Fig. 2, a significant reduction in SBP was observed in subjects supplemented with green tea (−1.98 mmHg; 95% CI, −2.94 to −1.01 mmHg; P < 0.001) when compared with control subjects. The mean difference in DBP was reported in 13 trials and was found to be significantly different (−1.92 mmHg; 95% CI, −3.17 to −0.68 mmHg; P = 0.002; Fig. 3). In addition, no significant differences were detected when we used the different model to pooling the data (Supplementary Fig. S1 and Fig. S2 online).

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Figure 2

Table 2

Subgroup analyses of blood pressure (BP) stratified by previously defined study characteristics

	Systolic blood pressure (SBP)					Diastolic blood pressure (DBP)
			Test of heterogeneity					Test of heterogeneity
Variables	No. of trials	Net change (95% CI)	P	I²,%	P	No. of trials	Net change (95% CI)	P	I²,%	P
BP status
Stage 1hypertension	3	−3.52 (−5.61, −1.43)^a	0.30	16.2	0.001	3	−4.30 (−5.99, −2.60)^a	0.81	<0.001	<0.001
		−3.56 (−5.65, −1.47)^b			0.006		−4.30 (−5.99, −2.60)^b			<0.001
Prehypertension	9	−1.57 (−2.66, −0.48)^a	0.56	<0.001	0.005	9	−1.33 (−2.11, −0.56)^a	0.05	49.3	0.001
		−1.57 (−2.66, −0.48)^b			0.005		−1.96 (−3.53, −0.39)^b			0.012
Study design
Parallel	11	−2.82 (−3.95, −1.69)^a	0.95	<0.001	<0.001	11	−2.52 (−3.33, −1.70)^a	0.29	15.9	<0.001
		−2.82 (−3.95, −1.69)^b			<0.001		−2.39 (−3.37, −1.41)^b			<0.001
Crossover	2	0.31 (−1.54, 2.16)^a	0.97	<0.001	0.743	2	0.05 (−1.33, 1.43)^a	0.04	76.0	0.942
		0.31 (−1.54, 2.16)^b			0.743		−2.20 (−8.49, 4.10)^b			0.494
Type of intervention
Trials ruling out confounding effect of caffeine	9	−2.00 (−2.99, −1.01)^a	0.19	28.8	<0.001	9	−1.84 (−2.56, −1.12)^a	0.01	63.0	<0.001
		−2.04 (−3.31, −0.77)^b			0.002		−1.89 (−3.24, −0.54)^b			0.006
Trials using green tea contained caffeine	4	−1.55 (−5.84, 2.75)^a	0.89	<0.001	0.481	4	−2.16 (−5.36, 1.05)^a	0.23	30.5	0.187
		−1.55 (−5.84, 2.75)^b			0.481		−2.15 (−6.06, 1.76)^b			0.281
Duration
<12 wk (low median)	5	−0.44 (−1.97, 1.09)^a	0.59	<0.001	0.575	5	−0.79 (−1.90, 0.32)^a	0.02	65.3	0.161
		−0.44 (−1.97, 1.09)^b			0.575		−1.60 (−4.16, 0.96)			0.220
≥12 wk (low median)	8	−2.98 (−4.21, −1.74)^a	0.91	<0.001	<0.001	8	−2.57 (−3.48, −1.66)^a	0.29	17.2	<0.001
		−2.98 (−4.21, −1.74)^b			<0.001		−2.43 (−3.54, −1.32)^b			<0.001
Green tea polyphenols dose
<582.8 mg/d (low median)	6	−2.87 (−4.23, −1.51)^a	0.55	<0.001	<0.001	6	−3.19 (−4.20, −2.18)^a	0.44	<0.001	<0.001
		−2.87 (−4.23, −1.51)^b			<0.001		−3.19 (−4.20, −2.18)^b			<0.001
≥582.8 mg/d (high median)	7	−1.08 (−2.44, 0.29)^a	0.60	<0.001	0.122	7	−0.60 (−1.58, 0.37)^a	0.23	25.9	0.227
		−1.08 (−2.44, 0.29)^b			0.122		−0.79 (−2.11, 0.54)^b			0.244
Jadad score
Low (<4)	8	−1.76 (−3.92, 0.40)^a	0.97	<0.001	0.110	8	−1.17 (−2.67, 0.32)^a	0.47	<0.001	0.125
		−1.76 (−3.92, 0.40)^b			0.110		−1.17 (−2.67, 0.32)^b			0.125
High (≥4)	5	−2.03 (−3.10, −0.96)^a	0.04	60.7	<0.001	5	−2.04 (−2.84, −1.25)^a	0.001	78.1	<0.001
		−2.15 (−3.94, −0.36)^b			0.019		−2.20 (−4.06, −0.35)^b			0.020

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^aThe result was obtained from a fixed-effects model.

^bThe result was obtained from a random-effects model.

The results of meta-regression analysis did not observe a significant dose-responsive effect between green tea and SBP (P for trend = 0.14) or DBP (P for trend = 0.16). And the sensitivity analyses showed that the pooled effects of green tea on BP were not altered when the analyses were limited to high-quality studies and after imputation using a correlation coefficient of 0.5. Moreover, systematically removing each trial during the sensitivity analyses did not significantly change the overall observed effects of green tea on BP.

Publication bias

Funnel plots (Supplementary Fig. S3 and Fig. S4 online) and Egger's tests showed no significant publication bias in the current meta-analyses of SBP and DBP (Egger's test: P = 0.62 and 0.81).

Discussion

Our meta-analysis showed that green tea consumption significantly lowered BP and this effect was not altered when we pooled the data according to BP status. Significant reductions in SBP and DBP were only observed in the low-dose green tea polyphenols, the long-term duration, parallel-design RCTs, high-quality trials subgroups or when the confounding effect of caffeine was removed.

A previous meta-analysis of observational studies demonstrated that 1 cup/d of green tea was associated with a 10% decrease in the risk of developing coronary artery diseases²⁴. A large population-based, prospective cohort study also found that an average of 2 cups/d of green tea intake significantly decreased the mortality risk of CVD²⁵. The overall result of the current meta-analysis and its subgroup analyses consistently suggested that green tea had a significant lowering effect on BP, which might partially explain the favorable effects of green tea on CVD.

Consistent with this meta-analysis, a recent meta-analysis also found that green tea consumption could improve both SBP and DBP control²⁶. Another meta-analysis suggested that green tea intervention had a favorable effect on SBP, but failed to lower the DBP level²⁷. Contrary to the two studies, this meta-analysis improved the design of the subgroup analyses and investigated the potential influence of more confounding factors such as caffeine, intervention duration of green tea consumption, and study quality on the overall results of the meta-analysis. Our subgroup analyses showed that green tea consumption significantly decreased BP in subjects with Stage 1 hypertension or prehypertension, and the beneficial effects of green tea on lowering BP were more prominent in subjects with Stage 1 hypertension. In addition, the subgroup analyses based on the parallel-design RCTs and high-quality study indicated that green tea has a significant lowering effect on BP. Consistent with the study, in vivo studies have revealed that green tea extract can significantly reduce the increase of BP and enhance endothelial function in hypertensive rats²⁸^,29^,30. The mechanism underlying the beneficial effect of green tea on BP control may involve the following aspects: 1) Green tea extract can maintain vascular tone by balancing vasoconstricting substances, including angiotensin II (Ang-II), prostaglandins, endothelin-1 (ET-1), and vasodilating substances, such as prostacyclin and various endothelium-derived hyperpolarizing factors (EDHFs)³¹^,32^,33^,34. 2) Green tea can improve ventricular function and exert beneficial effects via increasing nitric oxide (NO) production from endothelium in PI3-kinase dependent pathways²⁹. Green tea extract is also capable of regulating eNOS activation and ROS production, thereby increasing the production of NO³⁵. 3) Green tea is able to reduce oxidative stress and manage the generation of ROS by inhibiting pro-oxidant enzymes and inducing antioxidant enzymes. Green tea catechins also function circuitously by inhibiting the nuclear factor-kappa B, redox-sensitive transcription factors, and activator protein-1 responsible for oxidative stress³⁶^,37^,38. Moreover, green tea catechins can induce an anti-inflammatory effect by suppression of several inflammatory factors, such as cytokines, adhesion molecules, and nuclear factor-kappa B³⁵^,39.

We observed a significant reduction of SBP and DBP in the studies with a low-dose green tea polyphenols consumption subgroup and the subgroup of long-term intervention. Meanwhile, our study indicates that green tea intake has a significant lowering BP effect only in the trials designed to rule out the confounding effects of caffeine when we stratify the studies according to the type of intervention. This finding may partially explain why a high-dose of green tea consumption did not reduce BP, since a higher dose of green tea contains more caffeine and regular caffeine intake might increase BP, as reported by Noordzij et al⁴⁰ in their meta-analysis. Additionally, a previous cohort study including 1017 US males with a median age of 33 years suggested that drinking coffee was associated with BP increase and the risk of hypertension⁴¹. Despite its potential BP-increasing effect, coffee drinking appeared not to be related to coronary events in a prospective study that included over 45 000 US male⁴². Therefore, the effects of high-dose green tea containing caffeine on cardiovascular disease events need to be further evaluated by more high-quality and large sample size studies. Finally, a significant reduction in BP was found in the high Jadad score subgroup that possessed less bias, but was not shown in the low Jadad score subgroup.

Although the relatively larger number of pooled participants provides stronger statistical power to evaluate the treatment effect, this meta-analysis has several inevitable limitations. First, of the 13 studies, 5 studies were high-quality RCTs, whereas the remaining 8 studies were of low quality. The slight inconsistent results of the subgroup analyses conducted to explore the effects of green tea on BP may be attributed to the differences in study quality and an overall limited number of high-quality studies. The 2010 Consolidated Standard of Reporting Trials (CONSORT) is used worldwide to improve the reporting of RCTs, and also provides the professional guidance on the study design and conducting⁴³. To improve the study qualities, future RCTs should be conducted in accordance with the CONSORT statement, and particularly provide the enough information on the five items in Jadad scoring criterion which are essential for subsequent quality evaluation in the meta-analysis. Second, BP was not the primary outcome in part of the RCTs selected in this meta-analysis and the null findings of secondary outcomes may not be published. Third, the results of meta-regression analysis did not show a significant dose-responsive effect between green tea and SBP or DBP. Therefore, it is difficult to determine the optimal dose for a dietary program as part of a health policy aimed at improving hypertension health. In addition, most of the selected studies (11 of 13) did not report the information on sample size calculation. We could not directly evaluate the rationality of sample sizes in these studies, because the appropriate sample size for the RCT is based on the power calculation, α value, SD value and expected difference according to the specific study design⁴⁴. The investigators should properly calculate sample sizes before starting the future RCTs and report the details in the publication.

In conclusion, this meta-analysis indicates that green tea consumption significantly lowers BP. The significant decrease of BP in low-dose green tea subgroup, long-term intervention duration subgroup or the subgroup ruling out the confounding effects of caffeine needs to be evaluated by more high-quality RCTs specifically designed to evaluate the effects of green tea on BP.

Methods

Search strategy

PubMed (updated to March 2014; http://www.ncbi.nlm.nih.gov/pubmed/), Embase (updated to March 2014; http://www.embase.com/), the Cochrane Library (updated to March 2014; http://www.cochrane.org/) database, and reference lists and reviews were searched for RCTs examining the effects of green tea on BP in humans. The structured search strategies used the following terms: green tea, green tea extract, catechin, catechins, EGCG, camellia sinensis, or tea polyphenols [All Fields] which were paired with blood pressure [All Fields]. The searching was restricted to the reports of randomized controlled trials conducted in human subjects.

Study selection

Studies were included in the meta-analysis if they met the following criteria: 1) subjects ingested green tea beverage or extract for ≥1 wk; 2) the study was a RCT conducted in human subjects with either a parallel or crossover design; 3) the baseline and endpoint values for systolic blood pressure (SBP), diatolic blood pressure (DBP), or their difference with either SD, SEM or 95% CI were available for each group in the study; 4) the green tea or green tea extract was not given as part of a multi-component supplement; 5) the study used a concurrent control group for green tea or green tea extract treatment group and the only difference between the control and treatment group was green tea or green tea extract.

Data extraction and quality assessment

The data were collected by using a standardized and pre-piloted data extraction form that included the following categories: 1) study characteristics including authors, publication year, sample size, study design, study duration, dose, type of intervention and type of diet; 2) population information including age and baseline health status; and 3) net changes in SBP or DBP.

The quality of RCTs was evaluated by using the following criteria: 1) randomization (the study was described as randomized); 2) double blinding (participant masking and researcher masking); 3) reporting the number of withdrawals and reasons for withdrawal; 4) allocation concealment; and 5) generation of random numbers (using computer, random numbers table, shuffled cards or tossed coins, etc). RCTs scored one point for each area addressed in the study design with a possible score ranging between 0 and 5 (highest level of quality)⁴⁵. The studies that received a score of ≥4 were deemed to be of high quality, whereas those that received a score of <4 were considered low quality.

Statistical analysis

Our meta-analysis was performed using STATA (Version 11; StataCorp, College Station, TX). The treatment effects were defined as weighted mean difference and 95% CIs calculated for net changes in BP values. The statistic heterogeneity was assessed by using Cochran's test (P < 0.1). The I² statistic was also calculated, and an I² > 50% indicated significant heterogeneity across studies⁴⁶. A random-effects model was used if significant heterogeneity was shown among the trials. Otherwise, the results were obtained from a fixed-effects model. To provide more information on the data synthesis, we showed the results calculated from both the two models.

We excluded percent changes in mean and SD values when we extracted data for the meta-analysis. SD values were calculated from standard errors, 95% CIs, P values, or t-statistics when they were not directly available. In addition, change-from-baseline SD values were imputed as suggested by Follmann et al⁴⁷, assuming a correlation coefficient of 0.5.

Publication bias was assessed with funnel plots and Egger's test. Previously defined subgroup analyses were performed to examine the potential source of heterogeneity within these studies and included BP status, study design, type of intervention, duration, green tea polyphenol dose, and Jadad score. Additional sensitivity analyses were also performed according to the Handbook for Systematic Review of Interventions of Cochrane software (Version 5.0.2; The Cochrane Collaboration, Oxford, United Kingdom).

Author Contributions

Conceived and designed the experiments: X.L.P., K.L. and M.T.M. Analyzed the data: X.L.P., R.Z. and K.L. Contributed reagents/materials/analysis tools: X.L.P., K.L., R.Z., X.P.Y., X.H.Y. and M.T.M. Wrote the first draft of the manuscript: X.L.P., R.Z. and K.L. Reviewed, edited and approved the manuscript: X.L.P., R.Z., B.W., K.L. and M.T.M.

Supplementary Material

Supplementary Information:

Supplementary information

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Acknowledgments

This study was supported by the “12th Five year Plan” for National Key Technology Research and Development Program (grant number: 2012BAI35B02).

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