Abstract
Omega-3 fatty acids are potential anti-inflammatory agents that may exert beneficial outcomes in diseases characterised by increased inflammatory profile. The purpose of this study was to comprehensively evaluate the existing research on the effectiveness of n-3 fatty acid supplementation in lowering levels of circulating inflammatory cytokines in patients with heart failure (HF). From the beginning until October 2022, randomised controlled trials (RCTs) were the subject of PubMed, Scopus, Web of Science, and Cochrane Library literature search. Omega-3 fatty acid supplementation vs. placebo were compared in eligible RCTs to see how they affected patients with HF in terms of inflammation, primarily of tumour necrosis factor-alpha (TNF-a), interleukin-6 (IL-6), and c-reactive protein (CRP). A meta-analysis employing the random effects inverse-variance model and standardised mean differences was performed to assess group differences. Ten studies were included in this systematic review and meta-analysis. Our main analysis (k = 5) revealed a beneficial response of n-3 fatty acid supplementation on serum TNF-a (SMD: − 1.13, 95% CI: − 1.75– − 0.50, I2 = 81%, P = 0.0004) and IL-6 levels (k = 4; SMD: − 1.27, 95% CI: − 1.88– − 0.66, I2 = 81%, P < 0.0001) compared to placebo; however, no changes were observed in relation to CRP (k = 6; SMD: − 0.14, 95% CI: − 0.35–0.07, I2 = 0%, P = 0.20). Omega-3 fatty acid supplementation may be a useful strategy for reducing inflammation in patients with HF, but given the paucity of current studies, future studies may increase the reliability of these findings.
Supplementary Information
The online version contains supplementary material available at 10.1007/s10741-023-10327-0.
Keywords: Omega-3, Heart failure, Inflammation, TNF-a, IL-6, CRP
Introduction
Heart failure (HF) is a clinical illness brought on by anatomical and functional myocardial abnormalities that limit ventricular filling or blood ejection [1, 2]. While hemodynamic and neurohormonal responses are triggered to ensure enough tissue perfusion in order to counteract this ventricular dysfunction, their continued activation over the long term results in structural and functional damage [3]. HF is divided in three distinct phenotypes based on left ventricular ejection fraction (LVEF), particularly, reduced (HFrEF; ≤ 40% EF), preserved (HFpEF; ≥ 50% EF), and mid-range (HFmrEF; 41–49% EF) [1, 2]. Differentiation of patients with HF based on LVEF is important due to different underlying aetiologies, demographics, co-morbidities, and response to therapies [4].
In HFrEF, myocardial injury activates the inflammatory responses regulated by the innate and adaptive immune system [5, 6]. The inflammatory responses are described by an initial increase in proinflammatory cytokines and chemokines in conjunction with infiltration of neutrophils and monocytes into the damaged myocardium [6]. Inflammation is considered a critical pathophysiological factor in HF, predicting poor prognosis independent of LVEF [7]. Some notable inflammatory biomarkers in HF include tumour necrosis factor alpha (TNF-a), interleukin 1 (IL-1), interleukin-6 (IL-6), interleukin-8 (IL-8), myeloperoxidase (MPO), inducible nitric oxide synthase (iNOS), and c-reactive protein (CRP) [3]. Several interventional trials have attempted to target or regulate the activity of those inflammatory markers. Indeed, medical treatment has shown promising results to reduce inflammation in people with HF [7], while following a healthy diet has also displayed a beneficial impact [1]. However, whether non-pharmacological interventions such as dietary supplements could benefit patients with HF is currently underexplored.
Attention to the role of n-3 fatty acids in human health and disease has been continuously increased during recent decades. Many clinical and epidemiological studies have shown a positive role for n-3 fatty acids in cardiovascular disease outcomes [8]. More specifically, n-3 fatty acids such as eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) have been reported to modulate the expression of genes involved in the nuclear factor-kappa B (NF-κB) pathway [9]. A recent systematic review and meta-analysis assessed the effect of n-3 fatty acids on left ventricular remodelling in HF [10], indicating that a n-3 dosage of ≥ 600 g/day could decrease serum TNF-a, IL-6, and high sensitivity-CRP (hsCRP) [10]. Nevertheless, the robustness of this systematic review and meta-analysis is questioned due to inflammatory outcomes being secondary outcomes of interest; hence, there was (i) inclusion of non-placebo treated and/or non-randomised controlled studies, (ii) the lack of subgroup analysis based on duration, dose, age, and type of HF, and (iii) the lack of sensitivity analyses.
The aim of this study was to systematically assess the published literature pertinent to the efficacy of n-3 fatty acid supplementation in reducing the inflammatory cytokine levels of TNF-a, IL-6, and CRP, in patients with HF. A secondary aim was to assess the effect of n-3 fatty acid supplementation on IL-1, intercellular adhesion molecule 1 (ICAM-1), vascular adhesion molecule 1 (VCAM-1), and monocyte chemoattractant protein-1 (MCP-1), which also play a central role in the regulation of inflammatory responses.
Methods
This systematic review and meta-analysis were conducted in accordance with the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines [11]. The protocol was registered in the PROSPERO (International Prospective Register of Systematic Reviews) database (CRD:42,022,367,713).
Search strategy
Two independent reviewers (KP and PG) searched PubMed, Scopus, Web of Science, and the Cochrane library from inception until October 2022. A search strategy involving the following terms was used: “heart failure” OR “ejection fraction” AND “omega-3*” OR “n-3.” A manual search of references cited in the selected articles and published reviews was also performed. Discrepancies in the literature search process were resolved by a third investigator (MI). Studies were included according to the PICOS (Population, Intervention, Comparator, Outcomes, and Study design) process (Table S1). The following inclusion criteria were applied: (1) studies were randomised controlled trials (RCTs); (2) population comprised of patients with HF; (3) intervention group received n-3 supplementation; and (4) control group received a placebo. Studies were excluded if (1) they were not RCTs; and (2) a full text was not available.
Data extraction and risk of bias
Two authors (KP and JM) extracted data independently. Extracted data included the name of first author, country, date of publication, study design, age, sex, type of HF, number of participants, outcomes measured, dose and duration of treatment, and whether dietary intake and serum omega-3 levels were assessed. Disagreements between authors were resolved by a third reviewer (PG). The quality of the included studies was assessed using version 2 of the Cochrane risk-of-bias 2 tool for randomised trials (RoB 2) and evaluated by two independent reviewers (PF and AM). Appraisal of risk of bias using the RoB 2 tool included the assessment of the following domains of bias in RCTs: (1) randomisation process, (2) deviations from intended interventions, (3) missing outcome data, (4) measurement of the outcome, and (5) selection of the reported result. In accordance with the RoB 2 tool scoring system, study quality was defined as low risk of bias, some concerns, or high risk of bias.
Statistical analysis
In this meta-analysis, quantitative data were treated as continuous measurements, and changes in outcomes from baseline to follow-up were compared between groups to calculate mean differences. When units of measurements were inconsistent and could not be converted to units required to be included in the analysis, standardised mean differences were used. Added to this, we combined studies that used both normal and similarly high-sensitivity markers of inflammation (i.e., trials that assessed hsCRP with CRP), considering their identical outcomes. Statistical significance was assessed using the random-effects model and the inverse-variance method. Any changes between baseline and follow-up outcome measurements for which standard deviations were missing were estimated by calculating a correlation coefficient from a known change from the baseline standard deviation derived from a similar study.
Statistical heterogeneity of outcome measurements between different studies was assessed using the overlap of their 95% confidence intervals (95%CIs) and expressed as a measurement of Cochran’s Q (χ2 test) and I2. Data were classified as moderately heterogeneous when I2 values ranged from 50 to 74.9% and as highly heterogeneous when values were 75% and above. Furthermore, sensitivity analysis was performed to evaluate the robustness of reported statistical results by discounting the effects of the HFmrEF and the effects of olive oil as placebo. Subgroup analyses based on age (< 65 years vs. ≥ 65 years), treatment duration (≤ 12 weeks vs. > 12 weeks), dose (low dose < 2 g/day vs. high dose ≥ 2 g/day), and type of HF (acute vs. chronic) were also performed. The meta-analysis of data was synthesised using Cochrane’s Review Manager (RevMan 5.4.1) software.
Results
Search results
Our initial literature search tallied 964 publications. After the exclusion of 187 duplicates, 777 unique publications were screened. Overall, 751 publications were marked as ineligible, while full-text screening of the remaining 26 publications resulted in 14 eligible RCTs examining n-3 fatty acid supplementation on patients with HF. Finally, 11 RCTs were included in the systematic review and meta-analysis [12-22], for which one could not be included in our meta-analysis due to inadequate data [22]. Regarding the excluded studies, one study was missing baseline values, one study used coadministration of n-3 with glutamine, and one study used no treatment as control (Fig. 1).
Fig. 1.
Flowchart of the literature search
Characteristics of the included studies
A comprehensive description of the included studies is presented in Table 1.
Table 1.
Study and participant characteristics of the included studies in the meta-analysis
| Study year | Country | Study design | Total | Omega-3 | Placebo | Treatment dose (g/day) | Treatment duration | Control group | Outcomes | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| n (M/F) | Age | n (M/F) | Age | n (M/F) | Age | |||||||
| Palomas 2021 | Spain | Double-blind RCT | 43 (31/12) | 75.5 (8.7) | 20 (14/6) | 76 (7.7) | 23 (17/6) | 75 (9.6) | 4 | 4 weeks | Placebo (gelatin) | CRP |
| Oikonomou 2018 | Greece | Double-blind cross-over trial | 31 (23/8) | 66.5 (5.5) | 15 (11/4) | 66 (4) | 16 (12/4) | 67 (7) | 2 | 8 weeks (× 2) + 6-week washout period | Placebo (olive oil) | hsCRP |
| Wurm 2018 | Austria | Double-blind RCT | 40 (34/6) | 59.7 (8.0) |
1 g: 12 (10/2) 4 g: 12 (12/0) |
1 g: 59 (54–63) 4 g: 64 (58–66) |
16 (12/4) | 56 (46–63) | 1 or 4 | 12 weeks | Placebo | CRP |
| Makarewicz-Wujec 2017 | Poland | Double-blind RCT | 30 (26/4) | 64.56 (1.06) | 15 (13/2) | 67.5 (0.7) | 15 (13/2) | 62.06 (1.41) | 1 | 12 weeks | Placebo (corn oil) |
hsCRP MCP-1 |
| Heydari 2016 | USA | Double-blind RCT | 358 (288/70) | 180 (148/32) | 60 (10) | 178 (140/38) | 58 (10) | 4 | 6 months | Placebo (corn oil) | hsCRP | |
| Moertl 2011 | Austria | Double-blind RCT | 43 (37/6) | 58.7 (9.8) | 1 g: 14 (12/2), 4 g: 13 (13/0) | 1 g: 59 (7), 4 g: 61.9 (9.6) | 16 (12/4) | 55.1 (12.7) | 1 or 4 | 12 weeks | Placebo (gelatin) |
TNF-a IL-6 |
| Nodari 2011 | USA | Double-blind RCT | 133 (120/13) | 62.5 (10.0) | 67 (64/3) | 61 (11) | 66 (56/10) | 64 (9) | 2 | 12 months | Placebo (olive oil) |
TNF-a IL-6 IL-1 |
| Eschen 2010 | Italy | Double-blind RCT | 138 (118/20) | 59.5 (9.0) | 69 (57/12) | 58 (10) | 69 (61/8) | 61 (8) | 0.9 | 24 weeks | Placebo (olive oil) |
hsCRP ICAM-1 VCAM-1 |
| Nodari 2009 | Italy | Double-blind RCT | 44 (40/4) | 62.96 (10.29) | 22 (21/1) | 61.09 (11.22) | 22 (19/3) | 64.82 (9.46) | 1 | 6 months | Placebo (olive oil) |
TNF-a IL-6 IL-1 |
| Zhao 2009 | China | Single-blind RCT | 75 (55/20) | 72.5 (8.0) | 38 (27/11) | 74 (6) | 37 (28/9) | 71 (10) | 2 | 3 months | Placebo |
TNF-a IL-6 hsCRP ICAM-1 VCAM-1 |
| Mehra 2006 | USA | Double-blind RCT | 14 (12/2) | 60.5 (7.5) | 7 (6/1) | 59 (7) | 7 (6/1) | 61 (8) | 8 | 18 weeks | Placebo (corn oil) |
TNF-a IL-1 |
CRP c-reactive protein, hsCRP high-sensitivity c-reactive protein, ICAM-1 intercellular adhesion molecule 1, IL interleukin, MCP-1 monocyte chemoattractant protein-1, TNF-a tumour necrosis factor-alpha, VCAM-1 vascular cell adhesion molecule 1
Values are expressed as mean ± SD
Risk of bias assessment
Of the included studies, four studies were classified as having overall some concerns [12, 16, 20, 21], due to unclear description of randomisation process, and as to whether participants were aware of the intervention. In one study [21], the intervention group was comprised of patients with greater body mass index compared to controls. In addition, in the same study, there was no clear description on blinding of the investigators [21]. The rest of the studies were identified having low risk [13–15, 17–19, 22]. A detailed traffic light plot is presented in Table S2.
Omega-3 supplementation and TNF-a
Our main analysis (k = 5) revealed a significant impact of n-3 fatty acid supplementation to lower TNF-a levels compared to placebo, showing a high degree of heterogeneity (SMD: − 1.13, 95% CI: − 1.75– − 0.50, I2 = 81%, P = 0.0004) (Fig. 2). Subgroup analysis showed a significant change by lower dose (k = 3; SMD: − 1.20, 95% CI: − 1.98– − 0.43, I2 = 86%, P = 0.002), but not using higher doses (k = 2; SMD: − 1.07, 95% CI: − 2.54–0.41, I2 = 75%, P = 0.16) (Fig. S1). In addition, longer treatment duration (k = 4; SMD: − 1.31, 95% CI: − 2.00– − 0.62, I2 = 80%, P = 0.0002) (Fig. S2) and being below 65 years of age (k = 4; SMD: − 1.29, 95% CI: − 2.00– − 0.59, I2 = 77%, P = 0.0003) (Fig. S3) were significant contributors in lowering TNF-a levels compared to placebo.
Fig. 2.
Effect of n-3 fatty acid supplementation on TNF-a levels in patients with HF
Omega-3 supplementation and IL-6
Our main analysis (k = 4) revealed a significant impact of n-3 supplementation on suppressing IL-6 levels compared to placebo with a high degree of heterogeneity (SMD: − 1.27, 95% CI: − 1.88– − 0.66, I2 = 81%, P < 0.0001) (Fig. 3). Subgroup analysis showed a significant change by lower dose (k = 3; SMD: − 1.37, 95% CI: − 2.15– − 0.60, I2 = 86%, P = 0.0005) (Fig. S4), longer treatment duration (k = 3; SMD: − 1.37, 95% CI: − 2.15– − 0.60, I2 = 86%, P = 0.0005) (Fig. S5), and patients below 65 years of age (k = 3; SMD: − 1.50, 95% CI: − 2.05– − 0.95, I2 = 64%, P < 0.0001) (Fig. S6).
Fig. 3.
Effect of n-3 fatty acid supplementation on IL-6 levels in patients with HF
Omega-3 supplementation and CRP
Our main analysis (k = 6) showed no significant differences between n-3 supplementation and placebo on CRP, analysing studies with low degree of heterogeneity (SMD: − 0.14, 95% CI: − 0.35–0.07, I2 = 0%, P = 0.20) (Fig. 4). Subgroup analysis showed no significant changes by lower (k = 4; SMD: − 0.12, 95% CI: − 0.36–0.11, I2 = 0%, P = 0.31) or higher dose (k = 2; SMD: − 0.19, 95% CI: − 0.62–0.25, I2 = 0%, P = 0.40) (Fig. S7), type of acute (k = 3; SMD: − 0.14, 95% CI: − 0.52–0.23, I2 = 0%, P = 0.46) or chronic HF (k = 3; SMD: − 0.14, 95% CI: − 0.39–0.11, I2 = 0%, P = 0.29) (Fig. S8), and patients 65 years of age and above (k = 5; SMD: − 0.17, 95% CI: − 0.44–0.10, I2 = 0%, P = 0.22) (Fig. S9). Sensitivity analysis based on LVEF > 40% (one study had a mean of 42%) and a concerning risk for bias [21] did not alter the findings of the main analysis (k = 5; SMD: − 0.15, 95% CI: − 0.37–0.07, I2 = 0%, P = 0.18) (Fig. S10). Likewise, exclusion of two studies due to having olive oil as placebo [15, 20] showed no changes (k = 4; SMD: − 0.15, 95% CI: − 0.44–0.14, I2 = 0%, P = 0.32) (Fig. S11).
Fig. 4.
Effect of n-3 fatty acid supplementation on CRP levels in patients with HF
Due to inadequate data for which one study provided only the differences between the treatment vs. placebo [22], levels of CRP followed a decreasing trend following a 4 g daily dose of omega-3 supplementation (− 25% vs. placebo), albeit no statistically significant differences occurred.
Omega-3 supplementation and IL-1, ICAM-1, and vICAM-1
Our main analysis (k = 3) showed no significant differences between n-3 supplementation and placebo on IL-1, using RCTs of high degree of heterogeneity (SMD: − 0.94, 95% CI: − 2.66–0.78, I2 = 95%, P = 0.28) (Fig. S12). Additionally, similar results were found regarding ICAM-1 and vICAM-1 (k = 2) (SMD: − 0.19, 95% CI: − 0.95–0.56, I2 = 86%, P = 0.61) (Fig. S13). Subgroup analysis based on lower n-3 dose showed a significant reduction of IL-1 compared to placebo, although a high degree of heterogeneity was identified (k = 2; SMD: − 1.81, 95% CI: − 3.23– − 0.40, I2 = 92%, P = 0.01) (Fig. S14).
Discussion
In this study, we reviewed RCTs investigating the effect of n-3 fatty acid supplementation on alleviating inflammatory cytokine levels in patients with HF. Our main analysis revealed that n-3 fatty acid supplementation suppresses circulating TNF-a and IL-6 levels. Subgroup analyses identified a beneficial effect of supplementation in patients aged < 65 years, longer treatment duration (> 12 weeks), and lower dose (< 2 g/day), in both cytokines. There was no significant effect of n-3 fatty acid supplementation on serum CRP, IL-1, ICAM-1, and VCAM-1.
Findings from subgroup analyses
Our subgroup analysis based on the dose of n-3 fatty acid supplementation showed that lower dose (< 2 g/day) led to a significant suppression of TNF-a and IL-6, while a higher dose (≥ 2 g/day) did not. Although a biological rationale behind this finding has not been explored, we speculate that the high 95% CIs and SD values of the low number (k = 2) of studies and sample size included in this subgroup analysis could explain these contrasting results. In the study by Moertl et al. (2011), the authors utilised a lower dose of n-3 supplementation (1 g/day) in 14 participants, showing statistically similar findings (P = 0.17), with a minor clinical difference compared to the higher dose of 4 g/day (P = 0.07) (1 g/day—pre: 2.6 (2.4–3.29) to post: 2.4 (1.9–2.5) pg/mL; 4 g/day—pre: 2.1 (1.6–2.6) to post: 1.5 (0.1–2.1) pg/mL; n = 13) [19]. It may be more illuminating to determine whether a larger number of studies demonstrating that high n-3 doses have a negligible impact on TNF-a could yield a statistically significant result in a future meta-analysis or whether a biological mechanism of increased doses could negate its efficacy in lowering this inflammatory marker.
From previous studies, mechanistically, n-3 fatty acids displace arachidonic acid on cell membranes and produce eicosanoids that are deemed anti-inflammatory [23]. N-3 fatty acids also downregulate the expression of cyclooxygenase (COX); a key enzyme in production of pro-inflammatory cytokines by inhibition of NF-kB signalling [24]. Previous research has also showed that n-3 fatty acid supplementation has resulted in lower levels of inflammatory cell infiltration and fibrosis in cardiac tissue in murine models [25] and has augmented the polarisation of the anti-inflammatory M2 macrophage, resulting in cardiac remodelling [25, 26].
Moreover, while our subgroup analysis demonstrated a significant reduction in TNF-a and IL-6 in trials with longer treatment duration (> 12 weeks), only one study included in our main analysis followed a shorter term duration (≤ 12 weeks) [19]. In particular, this study revealed a significant reduction of IL-6 with 4 g/day of n-3 fatty acid supplementation, although a non-significant but decreasing trend with 1 g/day. Albeit these findings may support a higher dose to reduce IL-6 levels, the same study found a non-significant decrease in TNF-a utilising a higher dose (4 g/day). Therefore, in spite of the low sample size in this study, it is worth stating that the non-statistically significant result in the subgroup analysis utilising higher doses of n-3 fatty acids may had also been impacted by insufficient treatment duration.
Our subgroup analysis based on age showed a reduction of serum TNF-a and IL-6 in patients with HF aged < 65 years. However, there was only one RCT demonstrating a significant decrease in serum TNF-a and IL-6 in patients ≥ 65 years following 3 months of 2 g/day n-3 fatty acid supplementation [13], and as such, these results cannot be extrapolated in patients aged ≥ 65 years. Interestingly, longitudinal research in patients with HF above 65 years has demonstrated that ageing is a significant contributor to higher levels of inflammatory markers and is linked to a greater risk of HF development [27]. Therefore, further clinical trials are required to explore whether patients aged ≥ 65 years would experience similar reductions in TNF-a and IL-6.
Strengths and limitations
To our knowledge, this is the first meta-analysis of RCTs with the main aim to investigate the effect of n-3 fatty acid supplementation on pro-inflammatory cytokines in patients with HF. HF in patients aged < 65 years may have a different aetiology compared to their older counterparts [28] and, hence, different response to the anti-inflammatory effects of n-3 fatty acids. Therefore, our results may be represented more accurately in patients with HF aged < 65 years, given that middle-aged (i.e., < 65 years) and older (i.e., ≥ 65 years) patients with HF may display similar cardiac remodelling during disease progression but differing inflammatory profiles [29]. In addition, our analysis was limited by a small number of available RCTs to draw conclusions pertinent to lower vs. higher dose and shorter vs. longer treatment duration. Hence, the results from subgroup analyses should be interpreted with caution due to the limited number of studies (i.e., k = 3 for lower dose, and k = 2 for higher dose; regarding TNF-a).
Conclusion
This systematic review and meta-analysis demonstrated the potential of n-3 fatty acid supplementation to suppress markers of inflammation in patients with HF. Whether these results may be applicable to only lower doses, longer treatment duration, and patients aged < 65 years have yet to be investigated, concerning the limited research around this field. Supplementation with n-3 fatty acids is an inexpensive non-pharmacological agent; hence, more research on the topic could yield prominent findings pertaining to HF treatment by mediating patients’ inflammatory response.
Supplementary Information
Below is the link to the electronic supplementary material.
Acknowledgements
The authors acknowledge support from Dunhill Medical Trust.
Author contributions
Study concept and design: K.P. and M.I. Acquisition of data: K.P. and J.M. Analysis and interpretation of data: K.P. and A.T. Statistical analysis: K.P. and P.G. Drafting of the manuscript: K.P., A.T., and J.M. Critical revision of the manuscript for important intellectual content: P.F., A.M., and M.I.
Availability of data and materials
The authors confirm that the data supporting the findings of this study are available within the article and/or its supplementary materials.
Declarations
Ethical approval
This work required no ethical approval.
Conflict of interest
The authors declare no competing interests.
Footnotes
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Contributor Information
Konstantinos Prokopidis, Email: k.prokopidis@liverpool.ac.uk.
Atiporn Therdyothin, Email: a.therdyothin@liverpool.ac.uk.
Panagiotis Giannos, Email: panagiotis.giannos19@imperial.ac.uk.
Jordi Morwani-Mangnani, Email: j.morwani_mangnani@lumc.nl.
Panagiotis Ferentinos, Email: p.ferentinos@leedsbeckett.ac.uk.
Alexandros Mitropoulos, Email: alexandros.mitropoulos@shu.ac.uk.
Masoud Isanejad, Email: m.isanejad@liverpool.ac.uk.
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Data Availability Statement
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