Association of polymorphism in genes encoding κB inhibitors (IκB) with susceptibility to and phenotype of Graves' disease: a case-control study
© Kurylowicz et al; licensee BioMed Central Ltd. 2009
Received: 02 June 2009
Accepted: 03 November 2009
Published: 03 November 2009
Genes related to the nuclear factor-κB (NF-κB), a key transcription factor involved in regulation of immune responses, are interesting candidates for association studies in autoimmune disorders. The aim of this study was to investigate an association of polymorphisms in two genes encoding NF-κB inhibitors: IKBL (encoding inhibitor of κB-like) and NFKBIA (encoding κB inhibitor α), withsusceptibility to and phenotype of Graves' disease (GD).
A population-based, case-control association study comprising 481 patients with GD and 455 healthy controls was performed. We analyzed 3 single nucleotide polymorphisms (SNPs) in IKBL [promoter region -62T/A substitution (rs2071592), intron 1 C/T substitution (rs2071591) and exon 4 T/C substitution (rs3130062)] and 3 SNPs in NFKBIA [G/A substitution in 3' untranslated region (rs696) and two promoter region polymorphisms -297C/T (rs2233409) and -826C/T (rs2233406)] by the PCR-restriction fragment length polymorphism (RFLP) method.
The two SNPs in IKBL (rs2071592 and rs2071591) were in a strong linkage disequilibrium (D' = 0.835) and the AT haplotype was associated with susceptibility to GD (p < 10-4, OR = 1.61 [95%CI:1.21-2.14]). Moreover subgroup analysis revealed a gen-gen interaction between the investigated IKBL haplotype and HLA-DRB1*03 allele (p < 10-4). The investigated NFKBIA SNPs were not associated with susceptibility to GD. However, when correlated with phenotype, the -297T (rs2233409) and -826T (rs2233406) alleles were associated with the development of clinically evident ophthalmophaty (p = 0.004, pc = 0.07, OR = 1.65 [95%CI: 1.18-2.38] and p = 0.002, pc = 0.036, OR = 1.67 [95%CI: 1.20-2.36], respectively).
Our results suggest that SNPs in genes encoding NF-κB inhibitors may contribute to the development and clinical phenotype of GD.
The nuclear factor-κB (NF-κB) is an ubiquitous transcription factor of particular importance in normal inflammatory and immune responses and there is a growing amount of evidence that its deregulated activation may play a key role during development of common inflammatory and autoimmune diseases .
In mammals the NF-κB family consists of two types of proteins: the first group includes p105 and p100 that after proteolysis generate short active molecules (p50 and p52, respectively); whereas the second group includes p65, c-Rel and RelB proteins, that posses transcriptional activations domains. Both groups are characterized by the presence of a Rel homology domain which contains a nuclear localization sequence (NLS) and is involved in DNA binding. In non-stimulated cells the NF-κB proteins form homo- or heterodimers that are sequestered in cytoplasm via interaction with κB inhibitors (IκB). The IκB family comprises several members, including IκBα, IκBβ, IκBε and other related proteins (such as inhibitor of κB-like - IκBL or Bcl-3) that interact with NLS in the NF-κB proteins and in this way prevent their nuclear translocation. Numerous activating signals can trigger transduction pathways leading to dissociation of NF-κB from IκBs. The first step of this process involves activation of IκB kinases (IKK). IKK phosphorylate serine residuals in the N-terminal part of the IκB proteins that creates a binding site for subunits of the ubiquitin ligase complex and results in rapid polyubiquitination of IκB followed by its proteasomal degradation. Dissociation of IκB exposes the NLS in NF-κB proteins leading to their nuclear translocation and binding to promoters of target genes .
Therefore the coordinated degradation and resynthesis of the IκB proteins regulates NF-κB activity and any change in this delicate balance can interfere with normal NF-κB functions . Given the important role of the NF-κB transduction pathway in immune responses, NF-κB related genes are interesting candidates for susceptibility genes in autoimmune disorders. In our previous study we found that a promoter polymorphism (-94ins/del ATTG) in the gene encoding p105/p50, may be associated with susceptibility to and/or phenotype of Graves' disease (GD) . Polymorphism within genes encoding IκB proteins were found to be associated with development of other autoimmune conditions including: multiple sclerosis, rheumatoid arthritis, type 1 diabetes mellitus, systemic lupus erythematosus and Crohn's disease in different populations [5–12].
In the present study first, we analyzed an association of selected, potentially functional, polymorphisms in two genes encoding κB inhibitors: IKBL encoding IκBL and NFKBIA encoding IκBα with susceptibility to GD in Polish Caucasians. The analyzed IKBL and NFKBIA single nucleotide polymorphisms (SNPs) were selected based on previous associations studies in other autoimmune diseases. Next, we searched for a correlation with clinical phenotype of GD (gender, age of disease onset, presence of ophthalmophaty and family history of autoimmune thyroid diseases - AITD). Finally, we analyzed gene-gene interactions between IκB alleles and other established GD susceptibility markers (HLA-DRB1*03, CTLA-4 49A/G and PTPN22 1858C/T).
Subjects and methods
Clinical characteristics of patients with Graves' disease (GD).
Age of onset of GD (yr)*
38.79 ± 14.6
Disease duration (yr)*
4.72 ± 6.26
(NOSPECS class III and higher)
Family history of AITD
Therapy for hyperthyroidism:
The control group comprised 455 ethnically matched healthy subjects (119 male, 336 female, mean age 30.47 ( ± 10.07 years)) who had no family history of autoimmune diseases. The research program was approved by the Local Ethical Committees, and written informed consent was obtained from all of the participants.
Genomic DNA was extracted from peripheral blood mononuclear cells by the salting-out method . Genotyping of the selected polymorphisms in the IKBL and NFKBIA genes was performed by PCR amplification followed by digestion with a proper restriction enzyme (restriction fragment length polymorphism method - RFLP) [see Additional files 1]. The obtained restriction fragments were visualized on a 3% agarose gel. In the IKBL gene three polymorphisms were analyzed: a T/A substitution in position -62 of the promoter (rs2071592), a C/T substitution in intron 1 (rs2071591) and a T/C substitution in exon 4 (rs3130062), whereas in the NFKBIA gene: a G/A substitution in 3' untranslated region (3'UTR, rs696) and two promoter polymorphisms: a C/T substitution in position -297 (rs2233409) and C/T substitution in position -826 (rs2233406) were studied.
Genotype frequencies were compared between groups by chi-square (χ2) test on 2 × 2 or 3 × 2 contingency tables using Statistica software package (StatSoft Inc., Tulsa, OK) and p values less than 0.05 were considered significant. Additionally Bonferoni's correction for multiple testing was applied and a corrected p value (pc) is also presented. Odds ratios (OR) with 95% confidence intervals were calculated by the method of Woolf . Linkage disequilibrium (LD) was analyzed using the pairwise LD measure D' and haplotype blocks were constructed from population genotype data with the use of Haploview software , using the default algorithm for generating haplotype blocks based on methods established by Gabriel et al. . A D' value of 1 indicates complete LD between the two markers, D' value greater than 0.8 - strong LD, 0.2-0.8 - incomplete LD, whereas a D' less than 0.2 - negligible LD . Power analysis was performed using the DSS software available online http://www.dssresearch.com.
Genotyping results, linkage disequilibrium analysis and construction of haplotypes
Distribution of IKBL and NFKBIA genotypes in patients with Graves' disease (GD) and in healthy controls
GD (%)N = 481
Controls (%)N = 455
p/pc value OR (95%CI)
p = 0.001*
pc = 0.018
OR = 1.54 (1.20-1.99)
p = 0.001*
pc = 0.018
OR = 1.52(1.18-1.98)
The frequency of the allele -62A in IKBL was greater in GD compared to controls (39.0% vs. 30.4%, p = 0.0001, pc = 0.0018; OR = 1.46 [95% CI:1.20-1.77]). A significant association was also observed for genotypes (p = 0.001, pc = 0.018): genotypes possessing the A allele (AA homozygotes and AT heterozygotes) were found more frequently in GD patients (62.0% vs. 50.3%, p = 0.001, pc = 0.018) producing OR of 1.54 [95% CI:1.20-1.99] suggesting a dominant model of inheritance (statistical power - SP = 95.1%). For the intronic C/T substitution, an association of the T allele with GD was found (36.1% vs. 30.4%, p = 0.01, pc = 0.18; OR = 1.29 [95% CI:1.06-1.56]) and consistently, genotypes possessing this allele (TT homozygotes and CT heterozygotes) were more frequent in GD patients (61.3% vs. 51.0%, p = 0.001, pc = 0.018; OR = 1.52 [95% CI:1.18-1.98], SP = 88.9%). The T/C SNP in exon 4 of the IKBL was not associated with GD.
Frequencies of IKBL haplotypes in patients with Graves' disease (GD) and in healthy controls.
N = 481(%)
N = 455 (%)
promoter -62 T/A
intron 1 C/T
None of the three SNPs analyzed in the NFKBIA gene was found to be associated with GD (Table 2).
Correlation with the clinical phenotype of GD
Distribution of IKBL and NFKBIA genotypes was compared in subgroups of GD patients stratified by clinical parameters, including gender, age of GD onset, presence of clinically evident ophthalmopathy, family history of autoimmune thyroid diseases and smoking habits.
Distribution of IKBL and NFKBIA genotypes in subgroups of patients with Graves' disease stratified by clinical activity of thyroid associated ophtalmopathy assessed according to the OSPECS classification.
p/pc value OR (95%CI)
NOSPECS ≥ III (%)
N = 170
NOSPECS ≤ II (%)
N = 289
p = 0.01*
pc = 0.18
OR = 1.65 (1.10-2.48)
p = 0.01*
pc = 0.18
OR = 1.67 (1.12-2.48)
Frequencies of NFKBIA promoter haplotypes in subgroups of patients with Graves' disease stratified by clinical activity of thyroid associated ophtalmopathy assessed according to the NOSPECS classification.
NOSPECS ≥ III
NOSPECS ≤ II
N = 170 (%)
N = 289 (%)
No other associations between the studied IKBL and NFKBIA polymorphisms and the clinical phenotype of GD were observed (data not shown).
Interaction studies with known susceptibility loci
Finally we analyzed the distribution of IKBL and NFKBIA alleles in subgroups of GD patients stratified by genetic markers: HLA DRB1*03, CTLA4 49G and PTPN 22 1858T alleles [see Additional file 2]. The frequency of the IKBL -62A allele was significantly greater in HLA DRB1*03 carriers compared to the rest of GD subjects (57.9% vs. 25.7%, p < 10-4, pc < 10-4, OR = 14.32 [95%CI: 7.02-29.22], SP = 100%). For the IKBL exon 4 T/C SNP, the T allele was more frequent in HLA DRB1*03 carriers (96.1% vs. 89.9%, p = 0.047, pc = 0.846; OR = 2.73 [95%CI: 0.98-7.60], SP = 52.2%). Moreover, we observed a higher frequency of the IKBL -62A allele in CTLA4 49G positive patients (65.4% vs. 53.7%, p = 0.02, pc = 0.36; OR = 1.62 [95%CI: 1.09-2.44], SP = 65.7%).
The present study investigated a role of selected polymorphisms within genes encoding IκB: IKBL (encoding IκBL) and NFKBIA (encoding IκBα) in development of Grave's disease (GD) in the Polish population.
The first observation made in this study is a possible association of the two SNPs in the promoter (-62 T/A) and in the first intron (C/T) of the IKBL with susceptibility to GD. The IKBL gene is located on the telomeric end of the central MHC (major histocompatibility complex) on chromosome 6. Since it was initially described by Allock et al. , the -62 T/A SNP was found to disrupt an E-box binding element in the IKBL promoter - a sequence that can also be found in promoter and enhancer regions of the wide-variety of B and T cell lineage specific genes. Moreover, independent functional studies reported an association of the -62A allele with a decrease of the IKBL promoter activity that can result in disinhibition of the NF-κB mediated inflammatory response [22, 23]. In our dataset we observed a higher frequency of the -62A allele in patients with GD compared to the healthy subjects. In Australians, this allele constituted a part of the diabetogenic haplotype [7, 23]. On contrary, in the Japanese population an association between the -62T allele and development of rheumatoid arthritis was reported . However, subsequent replication case-control and family-based studies failed to confirm this association in Caucasians, suggesting that genetic susceptibility linked to IKBL may vary in different ethnic groups [24, 25].
While possible consequences of the -62 T/A SNP are examined, the functional importance of the C/T substitution in the first IKBL intron remains unknown. In the present study we observed an association of the intron1 T allele with development of GD in Polish population. In the previous report the T allele was linked to the resistance to rheumatoid arthritis in Japanese  and to our knowledge, this SNP has not been studied in other autoimmune diseases. In general, intronic polymorphisms may act as markers linked to the functional, causative variants . In the studied population we observed a strong linkage disequilibrium between the promoter -62 T/A and intron 1 C/T SNPs, and therefore we suppose that the observed association may be secondary to the linkage with the -62A allele. Moreover, a preliminary interaction analysis with the established GD susceptibility markers revealed a possible interaction between the studied IKBL variants and a HLADRB1*03 alleles - known as probably the most significant genetic predisposing factor to GD in Caucasians. However genes located within the MHC complex are in a strong linkage disequilibrium and certain alleles may occur in combination at a greater frequency than would be predicted by random association. This phenomenon hinders the distinction between genes primarily involved in conferring susceptibility to a disease and markers for the effect of a nearby gene . Therefore, a further study involving HLA-DR genotyping of the Polish controls, as well as adequately powered replication studies in other Caucasian populations are required to determine the independent role of IKBL SNPs and HLADRB1*03 alleles in pathogenesis of Graves' disease. The possible interaction between IKBL SNPs and CTLA-4 49A/G polymorphism must be judged very cautiously (statistical power < 80% and pc > 0.05).
The second IκB gene analyzed in this study was NFKBIA. In previous reports two promoter polymorphisms within this gene (-826 C/T and -297 C/T substitutions) were associated with prevalence of rheumatoid arthritis and systemic lupus erythematosus in the Taiwanese population [9, 10]. In silico analysis revealed that the -297 C/T SNP is situated close to the sites of NF-κB binding in the NFKBIA promoter. In turn, the -826 C/T substitution disrupts a putative binding site of transcription factor GATA-2 [9, 10]. In our dataset, the comparison of genotype and allele frequencies of these SNPs revealed no differences between GD patients and healthy subjects. However, when correlated with phenotype, the -297T and -826T alleles (alone, as well as in a haplotype) were found to be associated with presence of clinically evident ophthalmophaty. Interestingly, these alleles have been previously associated with development of chronic inflammatory diseases in Caucasians . It is reported that pharmacological inhibition of the NF-κB pathway in patients with active ophthalmophaty results in the suppression of inflammation and in the decreased glycosaminoglycans production by orbital fibroblasts . Therefore it can be assumed that allelic differences in the NFKBIA promoter that affect IκBα expression may influence regulation of the inflammatory response in the orbit tissue. However the genotype-phenotype correlation should be treated as preliminary since the analysis was underpowered and pc > 0.05. Future replication studies are required to confirm our observation.
In conclusion, SNPs in genes encoding IκBL and IκBα may contribute to the development or clinical phenotype of GD. However, since it is not possible to conclude if these loci represent primary etiological variants, further replication and functional studies are required to evaluate a role of IκB polymorphisms in development of thyroid autoimmunity.
This work was supported by the Polish Ministry of Science and Higher Education Grant No. 2 PO5B 120 29.
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