Comparison of DNA methylation profiles from saliva in Coeliac disease and non-coeliac disease individuals
BMC Medical Genomics volume 13, Article number: 16 (2020)
Coeliac disease (CD) is a autoimmune disease characterised by mucosal inflammation in the small intestine in response to dietary gluten. Genetic factors play a key role with CD individuals carrying either the HLA-DQ2 or HLA-DQ8 haplotype, however these haplotypes are present in half the general population making them necessary but insufficient to cause CD. Epigenetic modifications, including DNA methylation that can change in response to environmental exposure could help to explain how interactions between genes and environmental factors combine to trigger disease development. Identifying changes in DNA methylation profiles in individuals with CD could help discover novel genomic regions involved in the onset and development of CD.
The Illumina InfiniumMethylation450 Beadchip array (HM450) was used to compare DNA methylation profiles in saliva, in CD and non-CD affected individuals. CD individuals who had been diagnosed at least 2 years previously; were on a GFD; and who were currently asymptomatic; were compared to age and sex-matched non-CD affected healthy controls. Bisulphite pyrosequencing was used to validate regions found to be differentially methylated. These regions were also validated in a second larger cohort of CD and non-CD affected individuals.
Methylation differences within the HLA region at HLA-DQB1 were identified on HM450 but could not be confirmed with pyrosequencing. Significant methylation differences near the SLC17A3 gene were confirmed on pyrosequencing in the initial pilot cohort. Interestingly pyrosequencing sequencing of these same sites within a second cohort of CD and non-CD affected controls produced significant methylation differences in the opposite direction.
Altered DNA methylation profiles appear to be present in saliva in CD individuals. Further work to confirm whether these differences are truly associated with CD is needed.
Coeliac disease (CD) is a chronic autoimmune disease characterised by mucosal inflammation in the small intestine in response to dietary gluten, in genetically susceptible individuals , with the only treatment being a life-long gluten free diet (GFD). It is highly prevalent, affecting approximately 1% of the population worldwide . Clinical presentations can differ between individuals, making it challenging for clinicians to recognise . To complicate matters further, accurate serology and intestinal histopathology for screening and diagnosis, requires active consumption of gluten which can be problematic given the popularity of a GFD, whilst the invasive nature of a gastroscopy carries its own risks.
Genetic factors play a key role as individuals with a family history of CD have a significantly higher likelihood of also developing disease . Individuals with CD carry either the HLA-DQ2 or HLA-DQ8 haplotype. The HLA-DQ2 haplotype is found in 90–95% of patients with CD , while the HLA-DQ8 haplotype is present in approximately 5% of patients . These haplotypes are present in up to 56% of the general population making them necessary but not sufficient for the development of CD . Environmental factors including age at first exposure to gluten, antibiotic and proton pump inhibitor use, and surgeries and trauma have also been associated with CD [8,9,10,11,12]. However, the exact mechanism of how these factors contribute to the development of CD is currently unknown.
Gene-environment interactions are mediated by epigenetic modifications of the genome, and changes to epigenetic profiles can occur in response to changes in the environment . DNA methylation is a type of epigenetic modification that may partially explain how interactions between genes and environmental factors combine to trigger disease development. Altered DNA methylation profiles have been observed in gastrointestinal inflammatory disorders, including CD, autoimmune conditions and cancer [14,15,16]. The identification of DNA methylation profiles that are associated with disease state, offers the potential for discovering new pathways integral to the disease process. DNA methylation profiles associated with disease state are also potential disease biomarkers with utility in disease screening.
DNA methylation profiles unique to CD irrespective of whether individuals are consuming gluten could be a valuable screening tool, particularly if the DNA methylation markers were present in easily an accessible tissue like saliva. Altered DNA methylation profiles have been reported in individuals with CD that were independent of gluten consumption . However, these differences were observed in intestinal mucosal tissue, which require a gastroscopy to obtain tissue. It is unknown whether the differences in DNA methylation profiles are unique to intestinal mucosal tissue or are also present in other tissues. We have previously shown that DNA methylation profiles in saliva correlated well with DNA methylation profiles from intestinal mucosal tissue . The current study compared DNA methylation profiles in saliva from individuals with and without CD, to identify DNA methylation profiles unique to GFD managed CD.
Participant recruitment, selection criteria and data collection
Recruitment was carried out between April 2014 and August 2017. Individuals were recruited at the annual Gluten-Free Expos in Sydney and Melbourne, Australia. Following written informed consent, individuals were asked questions regarding their socio-demographic characteristics, health and disease status, as previously described  (Additional file 1). Saliva samples were collected from all participants using the Oragene DNA OG500 self-collection kits (DNA Genotek, Canada). The study was approved by the Western Sydney University Research Ethics Committee (approval number H10513) and the Macquarie University Human Ethics Committee (approval number 5201700199) and was carried out in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki and its later amendments.
Pilot cohort: Illumina Infinium HumanMethylation450 Beadchip (HM450) array
The pilot cohort consisted of n = 59 individuals consisting of CD individuals and non-affected controls. CD status was confirmed via endoscopy reports. For inclusion, these individuals had a CD diagnosis that was more than 2 years old, adhered to a strict gluten free diet since diagnosis; were free of any associated symptoms; and carried at least one HLA-DQ2 or DQ8 haplotype. For non-affected controls, these individuals reported no family history of CD, and were age (± 3 years) and sex matched to the CD group. Non-affected controls were free of any associated symptoms; carried at least one HLA-DQ2 or DQ8 haplotype and were negative for CD using the Simtomax® CD assay, a point-of-care test that detects antibodies against deamidated gliadin peptides (HealthScreen Solutions, AUS). This is a commercially available screening tool that has a negative predictive value of 99.1% .
Secondary cohort: validation group to confirm any methylation differences
An additional n = 221 CD cases and non-affected controls were recruited to enable validation of any differentially methylated CpG sites identified in the pilot cohort. These individuals were defined as having CD if they fulfilled the following criteria: had been diagnosed with CD via duodenal biopsy by a gastrointestinal specialist; were currently on a gluten free diet; and carried at least one HLA-DQ2 or HLA-DQ8 haplotype. Individuals were classified as non-affected controls if they reported not having CD or CD associated symptoms and were not on a gluten-free diet (GFD). For all individuals, body mass index (BMI) was analysed as a categorical variable according to World Health Organization guidelines . Alcohol consumption was categorised into zero, 1–2, and 3–7 standard drinks per week. Smoking status was dichotomised into never smoked and having ever smoked. Participants reported if they had ever been clinically diagnosed with cancer, asthma, or any of the following autoimmune conditions: Type 1 diabetes mellitus; Autoimmune thyroid disease; Rheumatoid arthritis; Lupus; Addison’s disease; Dermatitis herpetiformis; Alopecia, Autoimmune Hepatitis, Multiple Sclerosis, Sjogren’s syndrome or Psoriasis. Data from each autoimmune condition variable was combined to generate the variable ‘other autoimmune conditions’ as the prevalence of each individual condition was low. Individuals with missing data; who were current smokers; or reported a history of cancer were excluded.
DNA extraction and HLA genotyping
Whole saliva was collected from all participants. Saliva (2 ml) was collected using the Oragene DNA OG500 self-collection kits (DNA Genotek, Canada). Genomic DNA was extracted as per the Oragene prep-IT L2P (DNA Genotek, Canada) protocol, and purified using the Qiagen DNA mini kit (Qiagen, Germany) and samples were stored at − 20 °C until analysis. All samples were genotyped for the CD susceptibility haplotypes HLA-DQ2 and HLA-DQ8 using TaqMan SNP genotyping assays (Life Technologies, AUS): C_11409965_10, C_29315313_10, C_58662585_10, C_29817179_10, and a custom designed assay for rs4713586, as previously described .
Illumina Infinium HumanMethylation450 BeadChip analysis
Genomic DNA (500 ng) was treated with sodium bisulphite using the EZ DNA methylation kit (Zymo Research, CA, USA), as per the manufacturers protocol. Bisulphite converted genomic DNA was hybridized to the Illumina Infinium HumanMethylation450 BeadChip (Illumina, San Diego, CA), using the Illumina supplied reagents. Samples were randomly allocated across array chips (mix of CD and control samples on each array). Amplification, hybridization, washing, labelling and scanning of the array was performed by the Australian Genome Research Facility (AGRF) a commercial fee for service provider. Illumina’s GenomeStudio v2011.1 with Methylation module 1.9.0 software, with the default Illumina settings and the Illumina HumanMethylation450 15,017,482 v.1.2 manifest file, was used in the generation of data. Raw IDAT files containing signal intensities for each probe were extracted using Illumina GenomeStudio software and imported into RStudio using the methylumi and minfi packages. Data from samples passing initial quality filtering have been deposited into the Gene Expression Ominibus (GSE119078). Multi-dimensional scaling (MDS) plots of variably methylated probes on the sex chromosomes were used to confirm that the predicted sex matches the reported sex for each participant. Data quality control and processing steps were conducted using the methylumi and wateRmelon packages . The pfilter function was used to discard samples with a detection p-value > 0.01 in at least 1% samples and/or a bead count less than 3 in 5% of samples. Data was normalised using the dasen function . Probes targeting sites on sex chromosomes, non-CpG targeting probes, those that containing a SNP with minor allele frequency > 1% within 5 bp of the single base extension site , and cross hybridising probes  were removed from all analyses.
Saliva contains a mixture of different cell types, and cell-type proportions may differ across individuals. Surrogate variable analysis using the sva package was used to identify potential sources of variation, including cell type heterogeneity within samples and potential batch effects  . sva using the “leek” method identified 3 surrogate variables that were then adjusted for in subsequent analysis.
Analyses were performed to test differences in DNA methylation between individuals with CD and healthy controls at the individual probe level. To model the effect of sample-specific variables, linear regression for each probe using age, sex and CD status as independent variables were performed using the limma package . Prior to analysis, the log2 ratio of β-values was calculated and denoted as M-values which were used for statistical analyses, while β-values were used for interpretation of the results. P-values were adjusted for multiple testing according to the false discovery rate (FDR) procedure of Benjamini Hochberg. Significantly differentially methylated probes (DMPs) were selected using a cut-off of a |β| difference of ≥5% and an adjusted p < 0.05. The DMRcate package  was then used to identify significantly differentially methylated regions (DMRs) (p < 0.05, minimum cpg sites = 2) between CD and healthy control samples, as previously described .
Functional annotation analysis and gene ontology (GO) enrichment analysis was performed using the missMethyl package . The gometh function (prior.prob. = TRUE) was used to test GO enrichment for significant CpGs. In addition, the gometh function was used to perform pathway enrichment analysis based on the Kyoto Encyclopedia of Genes and Genomes (KEGG) classification databases to identify significant pathways. Following this, the topGO or topKEGG function of the limma package was used to identify the most significant GO terms and KEGG pathways. In addition, Database for Annotation, Visualization and Integrated Discovery (DAVID version 6.8) Bioinformatics Resources web-based software tool was used to perform functional annotation analysis and GO enrichment analysis. Gene identifiers were uploaded, and functional annotation analysis was performed, against the human reference genome (GRCh37/hg19) using a Benjamini-Hochberg multiple-test adjustment threshold of p < 0.05. Pathway enrichment analysis based on the protein annotation through evolutionary relationship and KEGG classification databases was used to identify significant pathways.
Sanger sequencing and Bisulphite pyrosequencing
CpG sites within genes that mapped to DMRs with a mean |Δβ| > 5% were further investigated. The UCSC genome browser was used to investigate whether known DNA variants were present in and around the CpG sites of interest. In cases where known DNA variants (single nucleotide polymorphisms SNPs) were reported that may alter the CpG site, and thus methylation status, DNA sequencing was used to determine whether underlying DNA variation was responsible for differences in methylation. All sequencing assays were performed by AGRF (Additional file 2: Table S1). Samples from across the methylation profile (high vs low) were sequenced. Forward and reverse sequences were provided to us by AGRF, and sequences were analysed using Sequencer v.5.4 (Genecodes,USA).
In the pilot cohort, pyrosequencing assays were performed on 6 CpG sites within the HLADQB1 (1 CpG), SLC17A3 (3 CpG) and ZFYVE19 (2 CpG) genes to confirm the methylation status of these CpG sites. These sites were selected as they did not contain underlying DNA variations, had |Δβ| > 5% at the CpG site; and primers to enable accurate amplification for pyrosequencing could be designed (Additional file 2: Table S2). All pyrosequencing assays were designed, optimised, performed, and analysed by AGRF (Additional file 2). Percentage methylation at the select CpG sites for each sample were provided to us by AGRF. CpG sites that were confirmed as being differentially methylated in the pilot cohort, were then quantified in the second larger validation cohort using the same pyrosequencing assays.
For description of participant’s demographic and clinical characteristics, mean and standard deviation (SD) were used for continuous variables with normal distribution, and proportions were used for categorical variables. A logistic regression model was applied to the demographic parameters with CD status, adjusted for age and sex. Independent T- tests were used to compare DNA methylation levels between CD cases and non-affected controls for sites measured via pyrosequencing.
The pilot cohort comprised of saliva samples obtained from 31 CD individuals (12 male) and 28 controls (13 male), matched for sex and age. The mean age of individuals with CD was 42 ± 15 years old and healthy controls was 37 ± 14 years old. For CD individuals, a family history of CD was reported in 39% of the group, and the mean length of time since diagnosis was 8.7 ± 6.5 years and ranged from 2.1 to 26.2 years. All individuals were Caucasian and no significant differences in BMI, smoking status, and alcohol consumption between the two groups was observed. The frequency of another autoimmune condition was higher in individuals with CD compared to controls (45.2% vs 17.9%). Demographic information is summarised in Table 1.
DNA methylation was quantified using the Illumina Infinium HumanMethylation450 Beadchip (HM450). Following quality control, pre-processing and normalisation, all 31 CD and 28 control samples were used for analysis. A total of 20 differentially methylated positions (DMPs) were identified (adj. p value < 0.05), 9 hypermethylated and 11 hypomethylated, between CD and controls, after adjusting for age, sex and are shown in Table 2. Region analysis of DNA methylation across adjacent probes did not identify any regions that were differentially methylated using a Bonferroni adjusted p-value < 0.05. Using the criteria of an unadjusted p < 0.05 and mean |Δβ| ≥ 5%, 351 regions 147 hypermethylated and 204 hypomethylated, that mapped to 334 unique annotated genes were identified. The top regions are summarised in Table 3. Functional annotation analysis of genes that mapped to these regions did not identify any terms that were significantly enriched (Bonferroni adj. p value < 0.05), however the top 10 terms identified by DAVID included Type 1 diabetes mellitus (non-adjusted p = 0.02), autoimmune thyroid disease (non-adjusted p = 0.04) and rheumatoid arthritis (non-adjusted p = 0.03).
CpG sites within the SET and MYND domain containing 3 (SMYD3) gene, the solute carrier family 17 member 3 (SLC17A3) gene, the zinc finger FYVE-type containing 19 (ZFYVE19) gene, the major histocompatibility complex, class II, DP beta 1 (HLADPB1) gene and the major histocompatibility complex class II DQ beta I (HLADQB1) were selected for further investigation based on the magnitude of mean DNA methylation difference across all CpG sites within the region (Fig. 1).
Underlying DNA variants can cause disruption of methylation at CpG sites resulting in bi or tri modal methylation patterns (~ 0%, ~ 50% and ~ 100%). The tri modal pattern of DNA methylation observed at the cg04798314 (SYMD3) and cg14373797 (HLA-DPB1) sites (Fig. 2) is indicative of underlying DNA variants disrupting the CpG site. Known DNA polymorphisms at these sites were identified using the UCSC genome browser. The rs201044038 polymorphism in SMYD3 results in the insertion of a thymine (T) between the cytosine and guanine leading to the loss of the cg4798314 site and subsequent methylation. The population frequency of rs201044038 is unknown and was not excluded during the initial methylation pre-processing when probes within known variants with a minor allele frequency greater than 1% were removed. Similarly, the rs9276 variant in HLADPB1 results in a substitution of a guanine leading to a loss of the cg14373797 site and loss of methylation. No DNA variants were reported at the CpG sites within HLADQB1, SLC17A3 and ZFYVE19.
DNA sanger sequencing to genotype the rs201044038 and rs9276 polymorphisms within the pilot cohort found the frequency of rs201044038 was significantly lower in CD individuals when compared to non-affected controls (57% vs 96%, p = 0.002), while the frequency of rs9276 was significantly higher in CD individuals when compared to non-affected controls (52% vs 4%, p < 0.001). Individuals who were heterozygous or homozygous for the rs246668601 or the rs9276 variants had reduced or no methylation at these sites.
Bisulphite pyrosequencing was used to validate 6 CpG sites within the HLADQB1, SLC17A3 and ZFYVE19 genes within the pilot cohort. Three sites near the SLC17A3 gene were confirmed as being differentially methylated between CD and control individuals (Fig. 3a). Pyrosequencing did not confirm methylation differences for the two sites within ZFYVE19 gene, cg13045913 (6.7% vs 4.9%, p = 0.17) and cg25498107 (20.3% vs 16.3%, p = 0.21). The cg10982913 in HLADQB1 could not be validated due to the large number of polymorphisms within the region.
We subsequently recruited an additional n = 202 individuals, 139 CD and 63 controls to determine whether the methylation differences near SLC17A3 could be replicated in a larger dataset (validation cohort). Within the validation cohort, the mean age of individuals with CD was 44.8 ± 15 years old and healthy controls was 40.5 ± 15 years old. There were significantly more females in the CD group (p < 0.001) and a higher proportion of CD individuals reported having been diagnosed with another autoimmune condition. No significant difference in age, BMI, family history of CD, or lifestyle factors was observed between CD and nob-affected controls in this cohort (Table 4).
Pyrosequencing of the three cg sites near the SLC17A3 region in the validation cohort (n = 202) found significant differences in methylation between CD and controls (Fig. 3b). Interestingly, the direction of the methylation differences between the groups was in the opposite direction to that seen in the initial cohort, with methylation at all three sites lower in CD compared with controls in the larger cohort.
Genotyping of the SYMD3 variant rs201044038 in the validation cohort found no difference in the frequency between the CD and unaffected controls (71.4% vs 76.7%, p = 0.40). While the frequency of the rs9276 variant in the HLADPB1 gene was found to be higher in the CD group (33.1% vs 16.4%, p = 0.006).
CD is a chronic autoimmune condition that can be challenging to recognise and diagnose. It has a known genetic component with CD individuals carrying either the HLA-DQ2 or HLA-DQ8 haplotype. However, these haplotypes are present in up to 56% of the general population making them necessary but not sufficient for the development of CD . Environmental factors have been reported to play a role in triggering CD in genetically susceptible individuals however the exact mechanism of how they contribute to disease development is unknown. Changes in DNA methylation may help to explain how environmental triggers can induce disease development. To our knowledge this is the first study to investigate DNA methylation in oral mucosa cells from saliva in individuals with managed CD and healthy controls. Our preliminary findings identified DNA methylation differences in the HLA region near the SLC17A3 gene.
Altered DNA methylation profiles in CD have been previously reported. That study compared DNA methylation profiles from intestinal mucosal biopsy samples in individuals with active and GFD treated CD, with non-CD individuals . They analysed the duodenal mucosa by separating the epithelial and immune cell populations of the biopsy samples and found a cell-type specific methylation signature with the epithelial methylome being characterised by the loss of CpG island boundaries and altered gene expression. DMPs were found at 43 sites in the epithelial fraction and 310 sites in immune fraction, of which genes within the HLA region were differentially methylated in both cell populations .
Methylation differences within and around the HLA region were also identified on array in our study (Table 3). Methylation differences within HLA-DQB1 and HLADPB were observed. The polymorphic nature of the HLA region prohibited validation of the sites within HLADQB1, while the methylation difference at HLADPB was the result of an underlying genetic variant. The rs9276 variant (within HLADPB) disrupts the cg14373797 site causing a loss in methylation. Site-specific methylation changes due to underlying genetic variation was observed in the Fernandez-Jimenez study , and has also been reported in inflammatory bowel disease . Fernandez-Jimenez et al. suggested that the 13 CD associated SNPs which correlated with the methylation level of a single CpG site in the gene body of MMEL1 were methylation quantitative trait loci (mQTL).
Methylation differences at three CpG sites upstream of the SLC17A3 gene were also observed in CD individuals compared to non-affected healthy controls in the pilot cohort. SLC17A3 forms part of the extended HLA region and encodes a voltage-driven transporter protein that is involved in the urate elimination. Elevated uric acid levels are markers of oxidative stress and inflammation, where uric acid, an antioxidant is produced in response to inflammation and oxidative stress . Individuals with CD have elevated uric acid serum levels when compared to healthy controls which may reflect the inflammation and oxidative stress that is characteristic of CD even when following a GFD . Interestingly, the direction of methylation differences between the pilot and validation cohort were in opposite directions. Hypermethylation in CD individuals compared to healthy controls in the pilot cohort, while hypomethylation in CD individuals in the secondary cohort, at all three sites was seen. The location of the sites would suggest that alterations in methylation could affect chromatin interactions and/or transcription factor binding and influence the expression of SLC17A3 or downstream genes. Loss of function mutations in SLC17A3 have been shown to result in hyperuricemia  therefore, hypermethylation at these regions may result in elevated blood uric acid levels, which is consistent with elevated levels of uric acid levels seen in individuals with CD . Further testing in another cohort could help to elucidate whether methylation differences at these sites are present and the direction of the methylation difference. Following confirmation of the direction of methylation change, transcriptome analysis would help to determine whether these methylation differences induce expression changes in SLC17A3 or surrounding genes.
The distribution pattern of methylation seen at cg12310025 site near SLC17A3 (Fig. 3b) is not representative of underlying DNA patterns. Instead the tri modal pattern may be a result of cell-type specific methylation differences, environmental exposures or age-related . Interestingly, the distribution pattern is similar for both individuals with CD and healthy controls indicating that the patterns observed could be a result of the proportion of methylated and unmethylated cells in a sample. Saliva samples contain a heterogeneous collection of cells and thus the proportion of cell types in an individual’s sample could result in the differing methylation patterns observed. In addition, differences in environmental exposures between our participants may have led to small to moderate differences in DNA methylation variation. DNA methylation has been shown to be correlated with chronological age resulting in bi and tri modal patterns of methylation, and 23% of variation in DNA methylation can be attributed to chronological age .
The opposing direction of methylation differences near SLC17A3 between our two cohorts highlights the importance of validating findings, as well as the limitations of using smaller sample sizes. The differing results observed indicates that the smaller pilot cohort was not reflective of the larger validation cohort, or vice versa. In the pilot cohort recruitment of CD and non-affected controls were similar, whereas the validation cohort had a higher proportion of CD (69%) compared to controls (31%). Furthermore, individuals with a family history of CD are at a ten times higher risk of developing CD. The exclusion criteria for non-affected controls in the pilot cohort included a family history of disease. Whereas in the validation cohort, 38.4% of non-affected controls reported a family history of CD. This may have impacted on the results and led to the discrepancies observed.
Limitations of the study include use of self-reported data which can be subject to recall bias. Self-reporting of CD status may have led to false-positive CD classification. However, the CD cohort was restricted to individuals who had been diagnosed via an intestinal biopsy by a gastrointestinal specialist. Endoscopy reports for a subset of CD participants, were also obtained to verify the diagnosis to minimise the chance of misclassification. While the healthy control individuals within the pilot cohort were negative for CD serology and associated symptoms at recruitment, they carry the HLADQ2 or HLADQ8 susceptibility haplotypes and may develop CD in later life. In the validation cohort, false negative CD classification for controls is also possible given the high prevalence of CD (1 in 70) in the general population and that individuals with CD can be asymptomatic. The disproportionate number of female participants in the validation cohort is another factor. While CD is more frequent in females to males (1.33 to 1) this does not account for the 75% of female participants in the validation cohort. Recruitment setting may account for this as most attendees at the Gluten Free Expos were female due to the events being marketed as food and cooking demonstrations. Recruitment in a more gender neutral setting could help to correct this imbalance. However, as no differences in age at diagnosis, presenting symptoms or response to treatment has been reported between males and females with CD , it is unlikely sex impacted the results.
Perhaps the largest factor that may have contributed to the difference in results between the Fernandez-Jimenez  and our study was the different tissues used, duodenal mucosal tissue vs saliva. Saliva, like intestinal mucosa contains a mixture of different cell types, including epithelial and immune cells. To account for cell heterogeneity, surrogate variable analysis was used to identify and adjust for this variation within samples, however given the cell type specific methylation profiles seen in duodenal tissue, it is possible that the differences in the mixture of cell populations in whole saliva compared with the epithelial and immune duodenal fractions, may have also contributed to the lack of large methylation differences between CD and health controls.
Another factor that may have contributed to the absence of any large DNA methylation differences, was that all our CD individuals had been diagnosed at least 2 years prior, were on a strict gluten free diet, and reported being symptom free. Our rationale for using CD individuals without active disease was to identify DNA methylation markers that were unique to CD regardless of disease state. We had hypothesised that any DNA methylation changes that occurred in the development of CD would be permanently maintained given that a CD diagnosis is lifelong. The presence of a CD epigenetic signature in both active and GFD-treated CD individuals in the Fernandez study supported this approach . However, a previous study by the same group showed methylation differences in the promoter of NFκB was less pronounced in GFD-treated CD and controls, compared to methylation differences between individuals with active CD and controls . Epigenetic profiles can change over time and during disease progression . It is possible that the use of longer term GFD-treated individuals and saliva instead of duodenal tissues could explain the absence of large methylation differences. Longitudinal studies comparing DNA methylation profiles at diagnosis and then following treatment on a GFD with healthy controls could help to differentiate DNA methylation changes that are disease state specific.
In this study probes targeting non-CpG sites were removed prior to analyses. In humans non-CpG methylation was traditionally thought to be limited to embryonic stem cells, however recent evidence has shown that it accounts for 35% of total DNA methylation in the adult brain, and is functionally active with methylation and demethylation of these sites linked to transcriptional regulation of genes with promoters characterized by a low-density of CpG sites . Further investigation into methylation levels at non-CpG sites is warranted to determine whether non-CpG methylation has a role in CD.
Our study identified a differentially methylated region near the SLC17A3 gene that may be associated with CD, however that remains to be validated. Further work in individuals newly diagnosed with CD, as well as in intestinal and saliva samples of individuals with CD is needed to determine whether unique DNA methylation patterns are associated with CD and to conform to previously published studies.
Availability of data and materials
The dataset(s) supporting the conclusions of this article is (are) available in the NCBI’s Gene Expression Ombnibus repository , and are accessible through GEO Series accession number GSE119078.
Differentially methylated probe
Differentially methylated region
False discovery rate
Illumina Infinium HumanMethylation450 BeadChip
minor allele frequency
Green PH, Lebwohl B, Greywoode R. Celiac disease. J Allergy Clin Immunol. 2015;135(5):1099–106 quiz 1107.
Lebwohl B, Sanders DS, Green PHR: Coeliac disease. Lancet. 2017.
Anderson RP. Coeliac disease is on the rise. Med J Aust. 2011;194(6):278–9.
Gujral N, Freeman HJ, Thomson AB. Celiac disease: prevalence, diagnosis, pathogenesis and treatment. World J Gastroenterol. 2012;18(42):6036–59.
Kneepkens CM, von Blomberg BM. Clinical practice : coeliac disease. Eur J Pediatr. 2012;171(7):1011–21.
Sollid LM, Thorsby E. HLA susceptibility genes in celiac disease: genetic mapping and role in pathogenesis. Gastroenterology. 1993;105(3):910–22.
Anderson RP, Henry MJ, Taylor R, Duncan EL, Danoy P, Costa MJ, Addison K, Tye-Din JA, Kotowicz MA, Knight RE, et al. A novel serogenetic approach determines the community prevalence of celiac disease and informs improved diagnostic pathways. BMC Med. 2013;11:188.
Pinto-Sanchez MI, Verdu EF, Liu E, Bercik P, Green PH, Murray JA, Guandalini S, Moayyedi P. Gluten introduction to infant feeding and risk of celiac disease: systematic review and meta-analysis. J Pediatr. 2016;168:132–43 e133.
Marild K, Stephansson O, Montgomery S, Murray JA, Ludvigsson JF. Pregnancy outcome and risk of celiac disease in offspring: a nationwide case-control study. Gastroenterology. 2012;142(1):39–45 e33.
Lebwohl B, Spechler SJ, Wang TC, Green PH, Ludvigsson JF. Use of proton pump inhibitors and subsequent risk of celiac disease. Dig Liver Dis. 2014;46(1):36–40.
Marild K, Ye W, Lebwohl B, Green PH, Blaser MJ, Card T, Ludvigsson JF. Antibiotic exposure and the development of coeliac disease: a nationwide case-control study. BMC Gastroenterol. 2013;13:109.
Riddle MS, Murray JA, Porter CK. The incidence and risk of celiac disease in a healthy US adult population. Am J Gastroenterol. 2012;107(8):1248–55.
Liu L, Li Y, Tollefsbol TO. Gene-environment interactions and epigenetic basis of human diseases. Curr Issues Mol Biol. 2008;10(1–2):25–36.
Fernandez-Jimenez N, Garcia-Etxebarria K, Plaza-Izurieta L, Romero-Garmendia I, Jauregi-Miguel A, Legarda M, Ecsedi S, Castellanos-Rubio A, Cahais V, Cuenin C, et al. The methylome of the celiac intestinal epithelium harbours genotype-independent alterations in the HLA region. Sci Rep. 2019;9(1):1298.
Wei SH, Balch C, Paik HH, Kim YS, Baldwin RL, Liyanarachchi S, Li L, Wang Z, Wan JC, Davuluri RV, et al. Prognostic DNA methylation biomarkers in ovarian cancer. Clin Cancer Res. 2006;12(9):2788–94.
Toth K, Galamb O, Spisak S, Wichmann B, Sipos F, Valcz G, Leiszter K, Molnar B, Tulassay Z. The influence of methylated septin 9 gene on RNA and protein level in colorectal cancer. Pathol Oncol Res. 2011;17(3):503–9.
Hearn NL, Coleman AS, Ho V, Chiu CL, Lind JM. Comparing DNA methylation profiles in saliva and intestinal mucosa. BMC Genomics. 2019;20(1):163.
Chiu CL, Hearn NL, Lind JM. Development of a risk score for Extraintestinal manifestations of coeliac disease. Medicine (Baltimore). 2016;95(15):e3286.
Bienvenu F, Besson Duvanel C, Seignovert C, Rouzaire P, Lachaux A, Bienvenu J. Evaluation of a point-of-care test based on deamidated gliadin peptides for celiac disease screening in a large pediatric population. Eur J Gastroenterol Hepatol. 2012;24(12):1418–23.
World Health Organization. The SURF Report 2 - Surveillance of chronic disease: risk factors: country-level data and comparable estimates. 2005. p. 22.
Monsuur AJ, de Bakker PI, Zhernakova A, Pinto D, Verduijn W, Romanos J, Auricchio R, Lopez A, van Heel DA, Crusius JB, et al. Effective detection of human leukocyte antigen risk alleles in celiac disease using tag single nucleotide polymorphisms. PLoS One. 2008;3(5):e2270.
Pidsley R, YW CC, Volta M, Lunnon K, Mill J, Schalkwyk LC. A data-driven approach to preprocessing Illumina 450K methylation array data. BMC Genomics. 2013;14:293.
Aryee MJ, Jaffe AE, Corrada-Bravo H, Ladd-Acosta C, Feinberg AP, Hansen KD, Irizarry RA. Minfi: a flexible and comprehensive bioconductor package for the analysis of Infinium DNA methylation microarrays. Bioinformatics. 2014;30(10):1363–9.
Chen YA, Lemire M, Choufani S, Butcher DT, Grafodatskaya D, Zanke BW, Gallinger S, Hudson TJ, Weksberg R. Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarray. Epigenetics. 2013;8(2):203–9.
Leek JT, Johnson WE, Parker HS, Jaffe AE, Storey JD. The sva package for removing batch effects and other unwanted variation in high-throughput experiments. Bioinformatics. 2012;28(6):882–3.
McGregor K, Bernatsky S, Colmegna I, Hudson M, Pastinen T, Labbe A, Greenwood CM. An evaluation of methods correcting for cell-type heterogeneity in DNA methylation studies. Genome Biol. 2016;17:84.
Smyth GK. Linear models and empirical bayes methods for assessing differential expression in microarray experiments. Stat Appl Genet Mol Biol. 2004;3:Article3.
Peters TJ, Buckley MJ, Statham AL, Pidsley R, Samaras K, R VL, Clark SJ, Molloy PL. De novo identification of differentially methylated regions in the human genome. Epigenetics Chromatin. 2015;8:6.
Yeung KR, Chiu CL, Pidsley R, Makris A, Hennessy A, Lind JM. DNA methylation profiles in preeclampsia and healthy control placentas. Am J Physiol Heart Circ Physiol. 2016;310(10):H1295–303.
Phipson B, Maksimovic J, Oshlack A. missMethyl: an R package for analyzing data from Illumina's HumanMethylation450 platform. Bioinformatics. 2016;32(2):286–8.
Ventham NT, Kennedy NA, Adams AT, Kalla R, Heath S, O'Leary KR, Drummond H, Consortium IB, Consortium IC, Wilson DC, et al. Integrative epigenome-wide analysis demonstrates that DNA methylation may mediate genetic risk in inflammatory bowel disease. Nat Commun. 2016;7:13507.
Ames BN, Cathcart R, Schwiers E, Hochstein P. Uric acid provides an antioxidant defense in humans against oxidant- and radical-caused aging and cancer: a hypothesis. Proc Natl Acad Sci U S A. 1981;78(11):6858–62.
Piatek-Guziewicz A, Ptak-Belowska A, Przybylska-Felus M, Pasko P, Zagrodzki P, Brzozowski T, Mach T, Zwolinska-Wcislo M. Intestinal parameters of oxidative imbalance in celiac adults with extraintestinal manifestations. World J Gastroenterol. 2017;23(44):7849–62.
Zheng M, Ma JW. Research progress in the genetics of hyperuricaemia and gout. Yi Chuan. 2016;38(4):300–13.
Breton CV, Marsit CJ, Faustman E, Nadeau K, Goodrich JM, Dolinoy DC, Herbstman J, Holland N, LaSalle JM, Schmidt R, et al. Small-magnitude effect sizes in epigenetic end points are important in Children's environmental health studies: the Children's environmental health and disease prevention research Center's epigenetics working group. Environ Health Perspect. 2017;125(4):511–26.
Johansson A, Enroth S, Gyllensten U. Continuous aging of the human DNA Methylome throughout the human lifespan. PLoS One. 2013;8(6):e67378.
Jansson-Knodell CL, King KS, Larson JJ, Van Dyke CT, Murray JA, Rubio-Tapia A. Gender-based differences in a population-based cohort with celiac disease: more alike than unalike. Dig Dis Sci. 2018;63(1):184–92.
Fernandez-Jimenez N, Castellanos-Rubio A, Plaza-Izurieta L, Irastorza I, Elcoroaristizabal X, Jauregi-Miguel A, Lopez-Euba T, Tutau C, de Pancorbo MM, Vitoria JC, et al. Coregulation and modulation of NFkappaB-related genes in celiac disease: uncovered aspects of gut mucosal inflammation. Hum Mol Genet. 2014;23(5):1298–310.
Martin-Subero JI, Esteller M. Profiling epigenetic alterations in disease. Adv Exp Med Biol. 2011;711:162–77.
Guo JU, Su Y, Shin JH, Shin J, Li H, Xie B, Zhong C, Hu S, Le T, Fan G, et al. Distribution, recognition and regulation of non-CpG methylation in the adult mammalian brain. Nat Neurosci. 2014;17(2):215–22.
Edgar R, Domrachev M, Lash AE. Gene expression omnibus: NCBI gene expression and hybridization array data repository. Nucleic Acids Res. 2002;30(1):207–10.
The authors would like to acknowledge the contribution of all individuals who participated in this study.
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This study was approved by the Western Sydney University Human Ethics Committee (H10513) and the Macquarie University Human Ethics Committee (5201700199). All individuals in this study provided written informed consent to participate.
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Hearn, N.L., Chiu, C.L. & Lind, J.M. Comparison of DNA methylation profiles from saliva in Coeliac disease and non-coeliac disease individuals. BMC Med Genomics 13, 16 (2020). https://doi.org/10.1186/s12920-020-0670-9