2. Current Research on Spirulina
Arterial hypertension is one of the most common health problems in developed countries and is a risk factor for cardiovascular diseases. Numerous studies have shown the positive effect of certain nutrients and dietary interventions on high blood pressure levels
[20]. Diet with natural fruits and vegetables containing antioxidants has a blood pressure-lowering effect
[20]. According to recent studies, lycopene-carotenoid from tomatoes or such nutraceuticals as flavonoids contained in cacao, beetroot with nitrates, garlic, and fish oil, being a source of unsaturated fats, have the potential to improve blood pressure
[20][21].
In this paper, we present the results of a systematic review and meta-analysis which indicated
Spirulina supplementation significant reduction of systolic and diastolic blood pressure. Our meta-analysis focuses on SBP and DBP parameters and not all components of metabolic syndrome, which makes the study comprehensible.
Spirulina is a functional food that might have a beneficial effect on decreasing blood pressure. However, individual RCTs showed some different results regarding blood pressure values between themselves. Martínez-Sámano et al. showed a statistically significant decrease in systolic blood pressure after 12 weeks of
Spirulina supplementation in a dose of 4.5 g per day (
p < 0.05) and no statistically significant changes regarding the diastolic blood pressure
[15]. Miczke et al. confirmed a hypotensive effect of
Spirulina. Significant decreases in SBP and DBP were observed in the
Spirulina group after three months of treatment with 2 g
[16]. Administration of 8 g per day of
Spirulina for 12 weeks showed a significant lowering effect on DBP (
p < 0.021) and no significant effect on SBP in the study by Lee et al.
[17]. Results of the study by Jensen et al. indicated that with a dose of 2.3 g there were no statistically significant differences between
Spirulina and placebo groups regarding SBP and DBP at baseline or after 2 weeks. However, the consumption was associated with a mild reduction in DBP
[18]. In contrast, Moradi et al. claimed that
Spirulina taken 1 g per day by ulcerative colitis patients did not influence blood pressure values (
p > 0.05)
[19].
Discrepancies require further in-depth analyzes. Some other possible confounding factors in assessing the impact of
Spirulina on SBP and DBP, for example, physical activity, diet, and smoking should be taken into consideration. These conflicting outcomes of the studies can depend on the supplementation of different doses of
Spirulina in different periods of time. The fact that no significant hypotensive effect was seen after administration of 1 g of
Spirulina might suggest the role of the appropriate dosage of the supplement to decrease blood pressure. It is worth mentioning that no significant changes in blood pressure parameters were noted in studies, in which the duration of
Spirulina supplementation was below 12 weeks: 2 or 8 weeks, respectively
[18][19]. Studies of 12 weeks of
Spirulina administration showed a significant decrease in at least one component of blood pressure
[15][16][17]. However, our subgroup analysis based on a dose of supplementation indicated that there was no significant difference between dose ≤2 g or >2 g, and subgroup analysis based on “≥12 weeks” or “<12 weeks” duration of
Spirulina intake did not show any difference between subgroups. Meta-analysis results are evidence of greater importance than analysis of particular studies. It is worth highlighting that
Spirulina supplementation resulted in greater SBP lowering in a subgroup of hypertensive patients compared with those with normal blood pressure. It suggests that patients with hypertension might reap greater benefits with
Spirulina supplementation. Both dosage and the duration of supplementation require further studies.
Other non-randomized controlled studies assessing a relationship between
Spirulina intake and blood pressure values showed that 4.5 g per day for 6 weeks had the positive effect on SBP and DBP reduction in a sample of overweight patients
[22]. On the contrary, Mazopakis et al. found no significant changes in SBP and DBP after the intervention of 1 g of
Spirulina per day for 12 weeks in a Cretan population
[23][24].
The mechanism of lowering blood pressure by
Spirulina is partially understood. It was supposed that the high content of potassium in
Spirulina might have a lowering effect on blood pressure
[17]. Phycocyanin, a blue pigment with antioxidant activity from
Spirulina, decreases parameters of blood pressure by strenghtening the expression of endothelial nitric oxide synthase in the aorta after the stimulation of adiponectin
[19][25]. Oxidative stress connected to endothelial damage, contributing to a decrease in nitric oxide synthase (NOs), and decreased vasoconstriction has been reported in hypertension
[15]. In mice, the decameric peptide of
Spirulina platensis decreases blood pressure levels through a PI3K (phosphoinositide-3-kinase)/AKT (serine/threonine kinase Akt)/eNOS (endothelial NO synthase) -dependent mechanism
[26]. Martínez-Sámano et al. proved the antioxidative properties of
Spirulina in SBP—they observed an increase in glutathione peroxidase (GPx) activity and oxidized glutathione (GSSG) concentrations (
p < 0.05)
[15]. Additionally, sVCAM-1, sE-selectin, and endothelin-1 levels—considered as markers of endothelial dysfunction were reduced
[15].
Spirulina improves endothelial function by reducing arterial stiffness index (SI)
[27]. Moreover,
Spirulina contains natural angiotensin I converting enzyme inhibitor (ACEi) peptide. ACEi suppresses the synthesis of angiotensin II that induces the vasoconstriction of blood vessels and the release of aldosterone, resulting in blood pressure increase
[27][28][29]. More studies should be performed to confirm these hypotheses and evaluate the exact mechanism of antihypertensive properties of the substance in humans.
Due to many complications of hypertension, intake of
Spirulina with antioxidant and hypotensive activity might reduce blood pressure, which potentially reduces cardiovascular risk and prevents serious effects such as stroke or heart attack. Moreover, hypertension is frequently associated with diabetes mellitus and metabolic syndrome. Some studies revealed that
Spirulina intake improved glucose and lipid metabolism, reduced oxidative stress, modulated appetite, so it can be considered as a therapeutic nutraceutical not only by reducing blood pressure
[13][25]. According to our analysis,
Spirulina may potentially reduce blood pressure among hypertensive patients. Supplementation of
Spirulina products promoted as “superfoods” is more and more popular due to its health benefits, but recent studies revealed contamination of toxic substances—cyanotoxins, heavy metals, or polycyclic aromatic hydrocarbons (PAHs)
[30][31]. Further research is needed, which doses and forms are the most effective and safe for patients. It is necessary to assess the safety profile of combination therapy consisting of
Spirulina and pharmacotherapy.
The limitations of this meta-analysis were the small number of analyzed RCTs and the lack of possibility to assess publication bias. However, the greatest strength of this paper is the inclusion of two novel studies from 2018 and 2021
[15][19]. The studies were first included in a meta-analysis that broadened the analysis compared with the previous meta-analysis assessing the influence of
Spirulina supplementation on a decrease of blood pressure. In the meta-analysis by Huang H. et al.
Spirulina supplements significantly lowered DBP (weighted mean differences = −7.17 mmHg; 95% CI: −8.57 to −5.78;
p = 0.0001; I
2 = 0%), but not SBP (weighted mean differences = −3.49 mmHg; 95% CI: −7.19 to 0.21;
p = 0.06; I
2 = 50%)
[32]. Differences in included studies might be a reason for different results for SBP compared with our meta-analysis. Yousefi et al. in a systematic review came to similar conclusions to our meta-analysis that additional studies with greater sample sizes and extended durations are needed to establish the hypotensive effect of
Spirulina [33].