Epigenetic mechanisms have been suggested to play a role in the genetic regulation of pathways related to inflammation. Therefore, we aimed to systematically review studies investigating the association between DNA methylation and histone modifications with circulatory inflammation markers in blood. Five bibliographic databases were screened until 21 November of 2017. We included studies conducted on humans that examined the association between epigenetic marks (DNA methylation and/or histone modifications) and a comprehensive list of inflammatory markers. Of the 3,759 identified references, 24 articles were included, involving, 17,399 individuals. There was suggestive evidence for global hypomethylation but better-quality studies in the future have to confirm this. Epigenome-wide association studies (EWAS) (n=7) reported most of the identified differentially methylated genes to be hypomethylated in inflammatory processes. Candidate genes studies reported 18 differentially methylated genes related to several circulatory inflammation markers. There was no overlap in the methylated sites investigated in candidate gene studies and EWAS, except for TMEM49, which was found to be hypomethylated with higher inflammatory markers in both types of studies. The relation between histone modifications and inflammatory markers was assessed by one study only. This review supports an association between epigenetic marks and inflammation, suggesting hypomethylation of the genome. Important gaps in the quality of studies were reported such as inadequate sample size, lack of adjustment for relevant confounders, and failure to replicate the findings. While most of the studies have been focused on C-reactive protein, further efforts should investigate other inflammatory markers.

1. Introduction

Inflammation is a critical response to pathogens and injuries in the human body. Specifically, chronic low-grade inflammation plays a key role in the pathogenesis of chronic conditions and diseases like obesity, diabetes mellitus, and cardiovascular disease [13]. A better understanding of factors that contribute to the development of inflammation and its consequences on disease is essential to improve prevention strategies in inflammation-related disorders.

Genome-wide association studies have identified several genetic variants associated with inflammatory markers such as C-reactive protein, the most widely studied marker [4, 5], but the explained variance is relatively small. In addition, nongenetic factors such as smoking and dietary behaviours have been shown to exhibit a strong influence on the inflammatory response [6, 7]. Emerging evidence suggests that epigenetic processes, reflecting changes in gene expression that occur without sequence mutations, may offer opportunities to understand the pathophysiology of inflammation processes. The role of epigenetic determinants is increasingly being recognized as a link between environmental factors and disease risk. Moreover, epigenetic modifications are also involved in differentiation of the immune cells, a key component of the inflammatory process. Epigenetics is defined as a group of chemical modifications of the DNA sequence, which could be affected by external factors such as BMI, smoking, and inflammation and can be transmitted from one generation of cells to the others [8]. The molecular basis of epigenetic mechanisms is complex and comprises DNA methylation, modifications of histones, and gene regulation by noncoding RNAs [9]. Unlike genetic variation, epigenetic modifications are dynamic and potentially reversible and, therefore, could be modified by lifestyle and other therapeutic approaches.

Until now, a comprehensive and systematic appraisal of the current literature on the role of epigenetic modifications in inflammation measured by levels of inflammatory markers is missing. Therefore, we aimed to identify and synthetize all available evidence conducted in humans and quantify the association of two of the major epigenetic modifications, DNA methylation, and histone modifications, with circulation inflammatory markers in blood.

2. Materials and Methods

This review was conducted and reported using a predefined protocol and in accordance with the PRISMA [10] and MOOSE [11] guidelines (Supplement Material S1 and S2). We sought studies published before 21 November of 2017 (date last searched) in five electronic databases: Embase.com, Medline (Ovid), Web-of-Science, Cochrane Central, and Google Scholar. We did the search with the help of an experienced medical information specialist. In databases where a thesaurus was available (Embase and Medline), articles were searched by thesaurus terms, title and/or abstract and in other databases, only by title and/or abstract. The search combined terms related to the exposure (e.g., epigenetic, hypomethylation, hypermethylation, DNA methylation, and histone acetylation) and outcome (e.g., inflammation, C-reactive protein, and cytokine). We did not apply any language restriction, but we restricted the search to studies on humans alive. The full search strategies of all databases are provided in Supplement Material S3. The study identification also included manual search, based on the screening of the citations of the relevant studies.

Information about study selection and inclusion criteria, data extraction process, and risk of bias assessment is described in Supplement Material S4.

3. Results

After deduplication, we identified 3,759 potentially relevant citations. Based on the title and abstract, 3,679 studies were excluded due to inappropriate exposure (gene mutations, gene polymorphism, and microRNA), inappropriate outcome (autoimmune diseases, cancer, and inflammation-related diseases such as asthma), or both. We also excluded investigations conducted in mice or rats (n=298). Additionally, we excluded studies that reported methylation levels in inflamed body areas or inflamed cells without quantitative investigation with inflammation markers, as well as studies that assessed methylation changes before and after immunotherapy. The final set of 80 studies were considered for full-text assessment. Of these, 24 unique studies met our eligibility criteria and were included in this review. The other 56 articles were excluded for reasons shown in Figure 1.

3.1. Characteristics of the Included Studies

Detailed characteristics of the included studies are summarized in Tables 13. All included studies were of cross-sectional design, except one study of prospective design [12]. Overall, 17,399 individuals were participating in these studies. Nine studies included participants from the USA, three studies from China, three studies from Canada, and the rest included participants from Brazil, Colombia, India, Ireland, Germany, Greece, Mexico, Spain, and Sweden. One of the studies [13] included participants from different cohorts such as USA, UK, Italy, Germany, and Netherlands. The majority (n=23) of studies assessed epigenetic signatures in blood, whereas other assessed epigenetic marks in tumour specimens (glioblastomas).

Of the 24 studies included, four studies assessed only global DNA methylation, eleven studies assessed only DNA methylation in specific candidate genes, and seven studies used genome-wide approaches. One additional study examined both global DNA methylation and methylation in specific candidate genes [14]. Only one study assessed histone modification in relation to inflammation markers [15].

The most studied marker was C-reactive protein (CRP), which was evaluated in 17 studies. Interleukins like IL-4, IL-6, IL-8, IL-9, IL-10, and IL-18 were evaluated in 11 studies. TNF-α was assessed in three studies, fibrinogen was assessed in two studies, and other markers such as VCAM, ICAM, VEFG, COX2, leptin, TNFR2, C-CAM1, alpha interferon, and TGF-β were assessed one single time. Nine studies were judged at medium risk of bias whereas the rest were at high risk of bias.

3.2. Global DNA Methylation and Inflammatory Markers

Five studies examined the association between global DNA methylation and inflammatory markers in blood samples (Table 1). Four of these studies assessed methylation in long-interspersed nuclear element (LINE-1). A large portion of methylation sites within the genome are found in these repeat sequences and transposable elements and correlate well with total genomic methylation content. From the four studies, two [14, 16] reported no association between global DNA methylation and CRP levels, while the other two showed lower methylation to be related with higher CRP levels [17, 18].

One study [16], in addition to CRP levels, also evaluated the association of global DNA methylation at LINE-1 with VCAM-1 and ICAM-1 and reported an inverse association with VCAM-1 but no association with ICAM-1. One study quantified global DNA methylation by measuring the amount of methylated cytokines in the sample (5 mc) relative to global cytidine (5mC + dC) in a positive control and found no association between global DNA methylation and IL-6 serum levels [19].

3.3. Gene-Specific DNA Methylation and Inflammatory Markers

Twelve studies examined the relation of inflammatory markers with methylation sites in, or near, candidate genes (Table 2). One study measured DNA methylation in tumour specimens [20], whereas the other studies used blood samples to assess the DNA methylation.

Of the twelve studies, eight did not report any level of adjustment or control for confounders, one of them controlled for age and sex [21], and the others controlled for these two confounders plus additional ones such as diet and race [14, 22, 23]. Of the twelve studies, three focused solely on CRP as outcome, one solely on interleukins, and one solely on leptin and the others assessed a set of inflammatory markers including interleukins, TNF-α, and fibrinogen.

In total, eight studies assessed CRP as inflammatory marker. Overall, these studies found higher levels of CRP to be associated with higher degree of methylation of SOCS-1 [24], LY86 [22], and EEF2 [25] and higher levels of CRP to be associated with lower degree of methylation of AIM2 [26], IL-6 [27], and IL-6 promoter gene [21]. One additional study that examined methylation levels of IL-6 promoter and CRP reported no association [14]. In addition, no association was found between methylation status of F2RL3 in peripheral blood cells and CRP levels.

Five studies evaluated the association of gene-specific DNA methylation with IL-6. They found higher degree of methylation of MGMT, RARβ, RASSF1A, and CDH13 in tumour specimens and of SOCS-1 in peripheral blood with higher levels of IL-6, while others found less degree of methylation of USP2, TMEM49, SMAD3, DTNB, and IL-6 promoter with higher levels of IL-6. Other interleukins such as IL-8, IL-10, and IL-18 were only evaluated once [20, 23, 28]. No significant correlation was found for IL-8, whereas for IL-10 and IL-18 inverse association was found with DNA methylation in IL-10 promoter and F2RL3, respectively (Table 2).

Two studies evaluated leptin as outcome, showing contradictory results. One reported inverse association between leptin levels and Leptin Receptor methylation [25], whereas the other reported no association between Leptin promoter and leptin levels [29].

Two studies assessed the association of DNA methylation and TNFα levels. Higher levels of methylation of EEF2 [25] and SOCS-1 [24] were found with higher levels of TNFα.

Additionally, six studies reported the association between methylation at different genes (MGMT, RARβ, RASSF1A, CDH13, USP2, TMEM49, EEF2, COL18A1, IL4I1, LEPR, PLAGL1, IFRD1, MAPKAPK2, PPARGC1B, SMAD3, DTNB, LY86, and F2RL3) with levels of several inflammatory markers other than CRP and interleukins (VEGF, VCAM1, C-CAM1, COX-2, sTNFR2, and fibrinogen) (Supplement Table 1).

3.4. Epigenome-Wide Analysis and Inflammatory Markers

Seven studies investigated differentially methylated regions in the genome in a hypothesis-free approach. Six of them adjusted at least for age and sex. Of these six, four adjusted additionally for BMI, smoking, and/or other confounders. All of the studies used blood samples to assess DNA methylation.

One study assessed 121 biomarkers related with inflammation, cancer, and cardiovascular disease [30] and five studies assessed CRP. The remaining two studies evaluated TNF and interleukins such as IL-1β, IL-6, IL-8, and IL-10 [31, 32] (Table 3).

Three out of seven studies used replication to validate their findings: two of them [13, 33] used external validations and one [34] internal validation.

The identified genes were enriched by pathways such as atherosclerosis, IL-6, IL-9, IL-8, growth hormone, and JAK/STAT signalling pathways.

Among the genes reported to be differentially methylated, SOCS3 and BCL3 were found to be significantly hypomethylated in two studies [13, 33]. BCL3 was no longer significant in the replication cohort, whereas SOCS3 remained significant after replication.

3.5. Histone Modifications and Inflammatory Markers

Only one study examined the association between histone modifications and inflammatory markers [15]. The authors assessed levels of acetylated histone H4 in the peripheral blood mononuclear cells of Chronic Obstructive Pulmonary Disease (COPD) patients and reported higher acetylation levels in patients with higher IL-8 levels and in patients with lower IL-4 levels.

4. Discussion

This is the first attempt to summarize current literature on the role of epigenetic marks in chronic inflammation. There is suggestive evidence for hypomethylation of overall genome in inflammatory processes, but better-quality studies have to confirm these results. Histone modification and inflammatory markers are scarcely investigated. Given the complexity and variability of proteins involved in the inflammation network, most of the studies focused on exploring CRP levels with few studies on IL-6 and fewer investigations on IL-8, IL-10, IL-18, VEGF, Cox-2, TNF-α, sTNFR2, leptin, and fibrinogen levels. The largest epigenome-wide association study up to date found AIM2 and SOCS3 to be top genes related to CRP levels in whole blood.

4.1. Global DNA Methylation

There were either no or an inverse association of inflammatory markers such as CRP, VCAM-1, and ICAM-1 in whole blood. Because we identified only a small number of studies, we cannot make any firm inferences on the overall hypomethylation of the genome due to inflammation. Moreover, populations were hardly comparable as two of the studies were conducted on children while the others on adults. As global DNA hypomethylation has become the hallmark of most human cancers, stroke, and heart disease [3538], the need to measure this epigenetic signature has become more essential. Global methylation would enable the ability to associate, for example, LINE-1 or 5-mdC levels, with correlative factors such as patient history or clinical outcome. The observed hypomethylation could lead to activation of dormant repeat elements and the subsequent aberrant expression of associated genes or may contribute to genomic instability and increased mutation rates. More intense efforts in studies investigating global DNA methylation through different methodologies such as Alu repeats and LUMA can hold future prospects for guiding risk stratification in individuals with high levels of inflammatory markers at an increased risk of chronic diseases.

4.2. EWAS vs. Candidate Gene Approaches

Ligthart et al. identified and validated 58 CpG sites located in 45 unique loci in whole blood among 12,974 individuals of European and African descent [13]. The top signal near AIM2 gene was found to be inversely associated with gene expression levels and with lower CRP levels. AIM2 is a key regulator of human innate immune response implicated in defence mechanism against bacterial and viral pathogens [39, 40]. Several of these hits including cg18181703 (SOCS3), cg06126421 (TUBB), and cg05575921 (AHRR) were associated with future incidence of coronary heart disease and smoking [13], whereas two other CpGs were recently identified in an EWAS of type 2 diabetes [41]. The gene SOCS3, suppressor of cytokine signalling 3, plays a pivotal role in the innate immune system as a regulator of cytokine signalling along the JAK/STAT pathway and was previously reported to have an important role in the processes of atherosclerosis [42]. Moreover, another epigenome-wide association study conducted among 1,741 individuals of European descent reported SOCS3, among others, to be significantly associated with systemic CRP levels, not only in peripheral blood tissue, but also in human liver tissue [33].

Given the reported association of CRP levels and these cardiometabolic clinical outcomes, it seems that inflammation-related epigenetic features may explain part of the observed associations reported in epidemiology. However, the results should be interpreted with caution, as the association of CRP and DNA methylation were not adjusted for these factors. Most of the replicated CpG sites reported in the study of Lighart et al. were associated with different cardiometabolic phenotypes (body mass index, fasting glucose, fasting insulin, triglycerides, total cholesterol, and HDL-cholesterol), highlighting the evidence of a pleiotropic network of epigenetics across various phenotypes. This information is promising as it holds new insights into shared epigenetic mechanisms and provides opportunities to link the inflammation processes with clinical outcomes. Moreover, two large cohorts (KORA and GENOA) observed hypomethylation to be related with higher levels of CRP [33, 43]. The latter, reported a similar trend of hypomethylation among individuals of older age and suggested that these patterns of modifications of DNA methylation on CpG islands between aging and inflammatory markers may indicate shared molecular mechanisms underlying chronic diseases through epigenetic changes [43].

Differentially methylated genes associated with CRP levels and other inflammatory markers did not directly overlap with the genes identified from previously reported genome-wide association studies influencing CRP levels and other biomarkers. The nonoverlap between GWAS and EWAS identified genes shows that clinical phenotypes are being influenced by different molecular mechanism, all of them important to explain phenotypical variation. Most of the identified genes are involved in common inflammation pathways related to cancer, rheumatic diseases, and gastrointestinal pathologies [24, 27]. Nevertheless, candidate gene approaches have less stringent criteria to assign significance on the expense of a narrower focus on genes. This might explain the absence of reproducibility of results in the reviewed epigenome-wide association studies, except for TMEM49, which was found to be inversely associated with sTNFR2 and IL-6 levels in the candidate gene approach study of Smith et al, and shared the same direction of association with CRP levels, in the EWAS study of Lighart et al.

4.3. Histone Modification

This review demonstrated that evidence involving inflammation and histone modification mechanisms are inexistent. Histone modifications are another epigenetic mark that play a pivotal role in the epigenetic regulation of transcription and other functions in cells. In addition, histone modifications have been linked to other inflammatory-related disorders, such as dyslipidaemia, obesity, diabetes, cancer, and cardiovascular disease [4446]. Future studies on histone modifications and inflammation markers might shed light on their functional role in chronic diseases and might provide novel target therapies for inflammatory conditions.

4.4. Bias, Confounding, and Tissue Specificity

There is quite ample evidence showing differential DNA methylation differing by ethnicity [47]. Therefore, it is recommended that studies investigating epigenetics of genes related to inflammation should replicate their findings in diverse populations. The largest to date epigenome-wide association study investigating DNA methylation and CRP levels used as discovery set a large European population (n = 8,863) and sought transethnic replication in African Americans (n = 4,111) [13]. As in genetic studies, the importance of replication of the significant findings in epigenetic association studies is a paramount in order to prevent false-positive results [48, 49].

Unlike genetic association studies that are less prone to confounding, epigenetic signatures throughout the genome are highly labile due to temporal or spatial factors affecting DNA such as age, gender, demographics, lifestyle, comorbidities, and medication use. It has been shown that methylation investigations harbour new information in explaining the variation of complex traits such as inflammation characterized by a strong influence of environment [4, 13, 50]. Inflammatory markers such as CRP, one of the most studied, are affected by both genetic and environmental factors. Therefore, controlling for confounders in epigenetic studies is crucial. In our review, the majority of our studies (62.5%) were classified as low quality largely explained by the lack of proper adjustment in the statistical models. While epigenome-wide studies controlled for life-style factors such as smoking, alcohol consumption, and BMI, candidate-gene approach studies were heavily suffering from incomplete adjustments.

Most of the inflammatory markers, and especially the ones of the acute phase, are predominantly synthesized in liver cells and hepatocytes and are regulated via transcription factors such as STAT3, C/EBP family members, and NF-kappa B by the proinflammatory cytokines IL-6 and IL-1β [51, 52]. Nevertheless, extrahepatic expression to a lesser degree has been reported for adipose tissue and blood cells [52]. DNA methylation profiles have been commonly studied in whole blood due to the easy access to the biological samples. Environmental exposure signatures such as smoking, alcohol, and other conditions involving the circulatory system and the immune response are well reflected in whole blood. This tissue is primarily composed of leukocytes, a key component of the human immune system and, therefore, highly relevant to systematic inflammation. However, since peripheral blood constitutes a heterogeneous admixture of different cell populations, it is possible that the results reflect inflammation-related DNA methylation changes that influence a single cell type component of blood cells. Adjusting for measured or estimated blood cell proportions, or future studies conducted in cell specific tissues, would help to rule out presence of any residual confounding caused by white blood cell distribution.

4.5. Causality and Study Designs

In the last years, the GWAS have resulted in the identification of many genetic variants that are associated with clinical traits and diseases. However, together, these variants explain only a small fraction of the variability. It has been suggested that epigenetics might hold promise to uncover the rest of the missing heritability. Moreover, it has been commonly hypothesized that epigenetic signatures are a cause for disease, rather than consequence. With the current evidence, it is unclear if epigenetic variation is causal to these inflammatory markers. In a recent study of Ahsan et al, the authors investigated the genetic and epigenetic influence in a large set of disease-related inflammatory markers [30]. Combining results of GWAS/EWAS in around 1,069 individuals and employing a complex bidirectional model to asses causality between genetic variation-DNA methylation-inflammation markers, it was concluded that DNA methylation has a limited direct effect on inflammatory markers. It reflects the underlying pattern of genetic variants, environmental exposures or secondary effect of the disease pathogenesis. In line with recent evidence, rather than a cause, DNA methylation seems to be a consequence of clinical traits, such as BMI [53].

All of the included studies in this systematic review were of cross-sectional design, except for one [47], meaning that both epigenetic signatures and outcomes were measured at the same time. This design challenges further inferences concerning causal relation, a typical vulnerability of epigenetic studies. In longitudinal cohort designs, repeated measurements for both inflammatory markers and dynamic methylation changes could improve our knowledge of the directionality of events. Furthermore, statistical approaches like Mendelian Randomization, in which genetic variants are used as proxies for DNA methylation and the outcome of interest, offer new opportunity to investigate the directionality of evidence from cross-sectional data [54]. The identification, directionality, and molecular pathways underlying the relation between epigenetic signatures and inflammatory markers represent promising targets for future functional studies.

4.6. Epigenetic Screening

In the last years, many advances in technologies related to measurements of epigenetic signatures have been developed to respond to the fast-growing pace of the field [55]. These techniques allow the investigation of DNA methylation either on candidate genes or on the whole-genome level. However, as the number of genes of interest increases along with the number of tissues of relevance, investigating the role of DNA methylation in different clinical traits could be very costly and time consuming. Progressing to more cost-effective solutions, high-throughput technologies have open new opportunities for epigenome-wide investigations in large-scale screening such as in population-based cohort studies. Furthermore, gene-specific assays such as bisulfite conversion provide a quick and efficient result for epigenetic investigations requiring relatively low DNA input with minimum DNA loss [56, 57]. Cloning, the gold standard method for gene-specific DNA methylation studies, followed by Sanger sequencing is another technological option [58]. Although the time for the procedure has been significantly reduced, the sequencing step might introduce several sources of errors [55, 59]. Another technique, pyrosequencing, represents a high throughput quantitative method used for bisulfite sequencing [60, 61]. This technique, which can be used for both DNA methylation and genetic variation (single nucleotide polymorphism) analysis, takes less time than cloning providing accurate reads within each run. Yet, optimal DNA quality is important to avoid misreads of pyrosequencing [55]. Mass spectrometry assay, on the other side, is a tool that can be used for the discovery and quantification of DNA methylation sites based on difference in fragments weights that have been cleaved depending on the methylation status [59]. This technology is highly sensitive and has the ability to sequence reads up to 600 bp, which is considerably longer than other methods. Quantitative Polymerase Chain Reaction (qPCR) arrays are another alternative of methylation quantification techniques operating on fluorophore-labelled probes that emit fluorescence when bound to a complementary DNA sequence. This method might not be ideal for regions with multiple CpG sites because many probes need to be created, resulting rather costly. However, if a region is characterized by a few CpGs, qPCR method might provide a simple and relatively inexpensive way to conclude a high-powered study [55].

Other chip techniques for epigenetic studies, in particular for histone modifications, include chromatin immunoprecipitation (ChIP), methylated DNA immunoprecipitation (MeDIP) platforms, and methyl-binding protein immunoprecipitation platforms. A major limitation to these techniques in epigenome-wide analysis is the quality of the antibody, which plays an important role in the proper enrichment of DNA. In general, the immunoprecipitation techniques require the availability of large sample volumes and only measure relative enrichment of epigenetic markers.

Concerning large-scale epigenetic analysis, the most widely used platforms, as shown from our review, are from Illumina. Illumina methylation profiling is based on bisulfite converted DNA genotyping [62]. For example, The Illumina Infinium HumanMethylation27 (27,000 CpG site) and Human-Methylation450 Bead (450,000 CpG sites) arrays provide genome-wide coverage, featuring methylation status at CpG islands, CpG shores, non-CpG sites, promoter regions, 5′ UTR, 3′ UTR, and gene bodies. More recent platforms, such as Infinium MethylationEPIC BeadChip Kit, have increased the number of interrogated sites to more than 850,000 CpGs across the genome at single-nucleotide resolution for only of 250 ng DNA as input quantity [63]. Moreover, TruSeq Methyl Capture EPIC Library Prep Kit, is another option that combines whole-genome bisulfite sequencing with methylation arrays that can support both screening and biomarker discovery studies targeting over 3.3 million CpGs [64]. These technologies rapidly produce a large amount of data at relatively low costs and are mostly preferred in population studies. On the other hand, epigenome-wide sequencing is another technology that is holding high hopes for future discoveries in the field of epigenetics. Currently, its widespread use is hampered by the high costs and computation burden of the analysis.

4.7. Clinical Implications

Understanding the epigenomic regulation of loci related to inflammatory markers might hold the possibility of discovering attractive targets for controlling inflammatory processes and, consequently, improving therapeutic interventions for chronic diseases that share in their aetiology, inflammatory-related pathophysiology. The identified epigenetic patterns may be used not only in functional studies to provide further insights into molecular mechanisms of inflammatory processes but also in biomarker studies using whole blood to improve the prediction of inflammation-related clinical disorders or events.

5. Conclusions

Current evidence suggests a potential role of epigenetics on the level of inflammatory markers in blood. Studies reporting on the association of inflammation with global DNA methylation show a hypomethylation trend. However, this evidence is not conclusive. Further studies are recommended to explore this relation. Moreover, studies on the role of histone modifications in inflammation markers are scarce. While most of the studies have been focused on CRP, reporting replicated genes across cohorts such as SOCS3, further efforts should focus on other biomarkers of the inflammatory cascade such as interleukins. Most importantly, given the systemic nature of inflammation, validation of the methylation sites among different tissues is paramount. The identified and reported genes so far involve epigenetics of inflammation with cardiometabolic factors, but also cancer and rheumatic diseases highlighting the potential of these regions as translational targets in the future. Given that we observed a lack of high quality investigations included in this review, we recommend future studies to improve some of the most urging factors such as an appropriate study design. This might be done by involving repeated measurements or with a prospective design that would allow drawing insights on one of the most important drawbacks of epigenetic data, assessing the directionality of the effects. Another important aspect to improve is to increase the sample size in order to provide adequate power and to perform proper adjustment of analysis to account for the role of environment on both epigenetics and inflammation. Lastly, the identified genes need to be validated in functional (in vitro and in vivo) studies in order to draw valuable and conclusive insights into the epigenetic mechanisms of inflammatory markers.

Conflicts of Interest

The authors declare that there is no conflict of interest regarding the publication of this paper.

Authors’ Contributions

The contributions of the authors were as follows: Valentina Gonzalez-Jaramillo, Eliana Portilla-Fernandez, and Marija Glisic screened title/abstract. Valentina Gonzalez-Jaramillo obtained full text, determined eligibility of articles, and participated in data extraction. Valentina Gonzalez-Jaramillo and Eliana Portilla-Fernandez assessed the quality of the included studies. Eliana Portilla-Fernandez participated in data synthesis/analysis and interpretation of the data. Valentina Gonzalez-Jaramillo, Eliana Portilla-Fernandez, and Jana Nano drafted the final manuscript. All authors contributed to the critical revision of the manuscript and approved the final version.


This project was completed thanks to grant funded by Metagenics Inc.

Supplementary Materials

Supplement Material S1: PRISMA guidelines checklist for reporting systematic reviews. Supplement Material S2: MOOSE guidelines checklist for reporting systematic reviews. Supplement Material S3: Search strategy. It provides a full description of the search strategies of all databases used in this systematic review. Supplement Material S4: Methods. It describes information about study selection and inclusion criteria, data extraction process, and risk of bias assessment. Supplement Table 1: Methylation of genes among candidate-gene approach studies. (Supplementary Materials)