| Abstract|| |
Background/Aim: To determine the frequency of celiac disease (CD)-predisposing human leukocyte antigen (HLA)-DQ genotypes in the Saudi population, where the prevalence of CD is 1.5% as recently reported in a mass screening study.
Patients and Methods: In a cross-sectional population-based study, a total of 192 randomly selected healthy school children (97 females, mean age 10.5 ± 2.2 years, all negative for tissue transglutaminase-IgA) were typed for D QA1 and D QB1 genes by polymerase chain reaction sequence–specific oligonucleotide probes.
Results: Of the 192 children, 52.7% carried the high-risk CD-associated HLA-DQ molecules: homozygous DQ2.5 ( 2.6%), DQ2.5/DQ2.2 ( 4.7%), heterozygous DQ2.5 ( 28.15%), homozygous DQ8 ( 4.2%), DQ8/DQ2.2 ( 3.6%), and double dose DQ2.2 ( 9.4%). Low-risk CD-associated HLA-DQ molecules (single dose DQ2.2 and heterozygous DQ8) constituted 3.6% and 9.4%, respectively. Among the very low–risk groups, individuals lacking alleles that contribute to DQ2/DQ8 variants (33.5%), 13.5% carried only one of the alleles of the high-risk HLA-DQ2.5 heterodimer called “half-heterodimer” (HLA-DQA1*05 in 12% and HLA-DQB1* 02 in 1.5%), and 20.8% lacked all the susceptible alleles (DQX.x). Gender distribution was not significantly different among the CD-risk groups.
Conclusion: We report one of the highest frequencies of CD-predisposing HLA-DQ genotypes among healthy general populations (52.7%) worldwide, which might partly explain the high prevalence of CD in the Saudi community.
Keywords: Celiac disease, genetic susceptibility, HLA typing, HLA-DQ2.5, HLA-DQ8, Saudi Arabia
|How to cite this article:|
Al-Hussaini A, Alharthi H, Osman A, Eltayeb-Elsheikh N, Chentoufi A. Genetic susceptibility for celiac disease is highly prevalent in the Saudi population. Saudi J Gastroenterol 2018;24:268-73
|How to cite this URL:|
Al-Hussaini A, Alharthi H, Osman A, Eltayeb-Elsheikh N, Chentoufi A. Genetic susceptibility for celiac disease is highly prevalent in the Saudi population. Saudi J Gastroenterol [serial online] 2018 [cited 2018 Sep 24];24:268-73. Available from: http://www.saudijgastro.com/text.asp?2018/24/5/268/235582
| Introduction|| |
Celiac Disease (CD) is an autoimmune enteropathy characterized by chronic inflammation of the small intestinal mucosa triggered by gluten uptake that occurs in genetically susceptible individuals. CD is a worldwide health problem, and its prevalence varies among different populations; this diversity is apparently determined by genetic and environmental factors. Human leukocyte antigen (HLA)-DQ2.5 protein (encoded by HLA-DQA1*05 and DQB1*02 alleles) and HLA-DQ8 protein (encoded by HLA-DQA1*03 and DQB1*03:02 alleles) are recognized predisposing factors for CD. The genes encoding for HLA-DQ molecules are found in a region known as class II on chromosome 6, known as -DQ. HLA-DQA1 and HLA-DQB1 genes encode for α- and β-heterodimers, respectively. These are cell surface receptors located on antigen presenting cells, and they form a cleft that binds gliadin peptides [Figure 1]. Following deamidation by tissue transglutaminase 2 (TTG2) and presentation to T-helper cells, T-helper cells are activated, causing secretion of inflammatory cytokines that result in villous atrophy. The preferential binding of HLA-DQ molecules to gluten peptides is a key step in the pathogenesis of CD; hence, the development of CD in individuals who are HLA-DQ2 and -DQ8 negative is extremely rare.
|Figure 1: Class II HLA-DQ: The genes encoding for HLA molecules are found in the major histocompatibility (MHC) complex on the short arm of chromosome 6 (6p21.3). HLA molecules involved in celiac disease are encoded in a region known as class II by genes known as -DQ. HLA-DQA1 gene encodes the α chain (α1 and α2), while DQB1 encodes the β chain (β1 and β2) of HLA-DQ protein. Both chains are associated as heterodimers on the surface of antigen-presenting cells and form a cleft that binds antigens and presents them to T-cells|
Click here to view
A variable distribution of CD-predisposing DQ alleles and environmental factors among different populations and ethnicities could explain the variable prevalence of CD that has been reported in different parts of the world. In the United States and Europe, where the prevalence of CD ranges between 0.5 and 2%, 25–30% of individuals carry HLA-DQ2 and DQ8 susceptibility heterodimers, whereas the low prevalence of HLA predisposing DQ2/DQ8 molecules in Far-East Asian countries could explain, in addition to the low wheat consumption, the anecdotal reports of CD in these countries.
We recently conducted a mass screening study in Saudi Arabia and estimated the prevalence rate of CD at 1.5% among 7930 school aged-children. Therefore, we propose that the high prevalence of CD among the pediatric Saudi population could be due to the common presence of CD-predisposing HLA-haplotypes-DQ2 and -DQ8. We conducted this cross-sectional study to define the frequency of DQ2 and DQ8 that have conferred high susceptibility to the development of CD in the Saudi population.
| Patients and Methods|| |
Study design and setting
The study was a cross-sectional, population-based study to determine the frequency of CD predisposing HLA-DQ genotypes among Saudi students of both sexes (6–15 years of age), attending primary and intermediate schools in Riyadh, between 2014 and 2016.
Study population and recruitment of participants
The details of the methodology of the CD mass screening study (including study population, recruitment of the students, inclusion and exclusion criteria, etc.), from which the study population for the present study was selected, have been described elsewhere. In brief, a total of 104 schools (61 Primary schools and 43 intermediate schools) were randomly selected using a probability proportionate sampling procedure. Parents of 7930 students (Mean age 11.22 ± 2.62 years, females 63%) have signed the informed consent forms and accepted participation in the mass screening study. The 5-milliliter blood specimens collected from each student were centrifuged at 2000 RPM for 10 minutes, and plasma was separated and stored at -20°C until analysis. Out of the 7930 serum specimens, we randomly selected 195 specimens for HLA typing. The inclusion criterion was TTG-IgA negative specimen. We excluded TTG positive specimens as our interest was principally to ascertain the frequency of HLA-DQ genotypes among non-Celiacs.
DNA was isolated from the whole blood using the Magna Pure compact instrument (Roche Diagnostics, Mannheim, Germany) and the MagNa Pure Nucleic Acid Isolation Kit (Roche Diagnostics, Mannheim, Germany) according to the manufacturer's instructions. HLA-Typing for celiac disease susceptibility genes was performed for the 195 randomly selected specimens using Sequence Specific Oligonucleotide (SSO) method. In summary, the SSO method is a DNA-based tissue typing technique using polymerase chain reaction to amplify the target DNA. The amplified product was hybridized with DQA1-specific and DQB1-specific nucleotide probes bound to fluorescently labeled beads that identified alleles encoded in the DNA sample. The process was carried out using Luminex technology in the Lab Type Kit (One lambda®, Canoga Park, USA). Reactivity patterns were interpreted with HLA Fusion software (One lambda®, Canoga Park, USA) to identify the alleles present. Further details of the procedure are available at http://www.onelambda.com.
HLA-DQ genotype notation
The type and configuration of the DQA1 and DQB1 alleles determined the DQ molecule that formed as shown in [Table 1]. Individuals with HLA-DQ2 encoding genotypes [DQ2.5 (homozygous), DQ2.5 (heterozygous), DQ2.5/DQ2.2, DQ2.2] were denoted as DQ2 positive, while carriers of HLA-DQ8 encoding genotypes [DQ8 (homozygous), DQ8 (heterozygous), DQ8/DQ2.2]were denoted as DQ8 positive. We followed the WHO nomenclature  in which HLA is followed by a hyphen followed by the gene (e.g. DQA1, DQB1, etc.), an asterisk (separator), allele group (field 1), colon (field separator), and protein (field 2). Disease risks for each HLA genotype are based on the published data from Europe,,, as shown in [Table 2]. The genotyping procedure at King Fahad Medical City laboratory is continuously monitored for quality assurance by the College of American Pathologists.
|Table 1: Types of celiac disease risk heterodimers that result from the variable configuration of the DQA1 and DQB1 alleles|
Click here to view
This study was approved by the Institutional Review Board of King Fahad Medical City (number 11-066) and Ministry of Education in Saudi Arabia. All study participants, or their legal guardians, provided informed written consent prior to study enrollment.
Descriptive statistics (SPSS for Windows, version 21.0; SPSS Inc, Chicago, IL) were used to calculate the frequencies of the most common HLA types. Pearson's chi-squared test was used to test any association between gender and HLA-DQ molecules. A P value < 0.05 was considered statistically significant.
| Results|| |
Out of 195 randomly selected serum specimens, 3 specimens were excluded because they tested positive for TTG-IgA, and CD was confirmed on duodenal biopsies. The remaining 192 serum specimens (97 females; mean age 10.5 ± 2.2 years) tested negative for TTG-IgA and underwent HLA typing. The frequency of each HLA-DQ genotype is presented in [Table 3]. Of the 192 healthy children, 52.7% carried the CD-associated HLA-DQ molecules, DQ2 or DQ8 variants, making them highly susceptible to develop CD. The HLA-DQ2 positive group (DQ2.5 homo- or heterozygous, DQ2.5/DQ2.2, DQ2.2 homo- or heterozygous) constituted 48.5%, whereas the DQ8 positive group (DQ8 homo- or heterozygous, DQ8/DQ2.2) constituted 17.2% of the total cohort. Among individuals lacking alleles that contribute to DQ2/DQ8 variants (33.5%), 13.5% carried only one of the alleles of the risk HLA-DQ2 heterodimer called “half-heterodimer” (HLA-DQA1*05 in 12% and HLA-DQB1* 02 in 1.5%), and 20.8% lacked all the susceptible alleles (DQX.x).
|Table 3: Frequency of HLA-DQ genotypes among 192 healthy students and the associated risk to develop celiac disease|
Click here to view
The frequency of consanguinity in our study cohort was 41%, and the family history of CD was 2.6%. The consanguinity rate was similar in the 4 CD-risk groups. In addition, gender distribution was not significantly different among the 4 CD-risk groups, but there was a tendency for extremely high-risk HLA molecules to predominate among males (P = 0.08).
| Discussion|| |
Our data indicate that more than half of the Saudi pediatric population (52.7%) carries CD-predisposing HLA-DQ genotypes that confer high risk to develop CD, which might partly explain the recently reported high prevalence of CD in the Saudi community (1.5%). To the best of our knowledge, we report one of the highest frequencies of CD-predisposing HLA-DQ genotypes among healthy general populations worldwide. Frequencies of HLA DQ2 and DQ8 among other populations ranged between 0 and 28% and between 1 and 9%, respectively. It is generally assumed that the prevalence of CD risk alleles in Europe is between 25% and 30%. However, in Sweden, where the prevalence of CD was 2.13%, the frequency of CD-predisposing HLA-DQ genotypes was 53%. In addition to the strong genetic susceptibility, we believe that the high frequency of CD among the pediatric Saudi population could be because of the high intake of cereals (as most of the staple foods in Saudi community contain wheat, rye, or barley). The consumption of gluten-containing cereals in the Saudi population is very high according to the Food and Agriculture Organization data. The yearly cereal intake per person between 2009 and 2014 was 151 kg in Saudi Arabia, compared to 107 kg/person/year in North America and 137 kg/person/year in Europe.
The analysis of correlation between wheat consumption, HLA-DQ2 and DQ8 frequency, and CD prevalence showed a significant correlation between the combination of both risk factors and the incidence of CD worldwide. In Africa, there is a gradient in CD prevalence from North to South; the prevalence of CD among Northern populations (such as Saharawi, Libya, Tunisia, and Egypt) shows a high frequency of HLA-DQ2 ( 23-39%) and high level of wheat consumption, which is much higher (0.8–5.6%) than the CD prevalence in the southern populations (such as Papua New Guinea, Burkina Faso, Rwanda, Tanzania, and Cameroon) where the frequency of HLA-DQ2 is low (0–15%) and where the staple diet is low in wheat.,,,, A review of medical literature for the mass screening studies performed in Asia, including our study, indicates a gradient in CD prevalence. The highest rates were reported from the west of the continent (Saudi Arabia 1.5–2% and Iran 0.8–1%),, intermediate rates from India (0.4%), and only anecdotal reports of CD from the Far East., This observation is corroborated by a gradient distribution of HLA-DQ molecules (Saudi Arabia 52.7% (present study), Iran 58%, North India 31.9%, and less than 10% in Japan and China)., Likewise, the level of wheat consumption in West Asian countries is very high compared to the low wheat consumption in Far-Eastern countries. No CD prevalence studies were conducted in Japan or China; however, the low frequency of HLA-DQ molecules in these countries predicts low prevalence rates for CD.,
The importance of HLA-DQ genotyping in clinical practice emerges from two important pieces of information. First, the absence of HLA-DQ2 and DQ8 molecules is significant for its high negative predictive value, as it strongly argues against the diagnosis of CD.,, Second, HLA-DQ molecular typing allows for the definition of a CD risk gradient associated with each particular HLA-DQ status., In this regard, it is useful to consider HLA-DQ genotype gradient risk as a first step in selecting individuals who must undergo serologic follow-up; this “2-step CD-screening approach” is especially important in high-risk groups (such as family members of a celiac case, individuals with an autoimmune disease such as type 1 diabetes, and certain conditions associated with CD, e.g., Down and Turner syndromes). Such a strategy should assist in the early diagnosis of CD in at-risk individuals who often have unclear symptoms. An early diagnosis means early intervention with a gluten-free diet, which may prevent the development of significant comorbidities., Some researchers took this “2-step approach” further and proposed using the HLA-DQ molecular test as a first step in mass screening of the general population for CD.,,, Based on our study, more than half of the Saudi population is genetically susceptible to develop CD, and consequently, the 2-step approach would be much less cost-effective than a one-step approach (i.e., screening with TTG-IgA). The cost effectiveness of the 2-step approach is dependent on the frequency of the HLA risk alleles in the studied population. The lower the prevalence of HLA risk alleles, the larger the percentage of the population that could be excluded from further testing of TTG-IgA. Based on the current knowledge and the need for cost-effectiveness, it is clear that any future screening program should be tailored to the characteristics of the specific target population.
The majority of HLA-DQ risk gradient studies in CD originated from Europe and the United States,,,,, and the detailed information of HLA-DQ risk gradient on CD patient cohorts from diverse ethnic groups is lacking. These studies confirmed that DQ2.5 haplotype homozygosity, DQ2.5/DQ8, and DQ2.5/DQ2.2 conferred the highest risk for CD and were associated with the earliest onset and most severe phenotype. The prevalence of HLA-DQ2 and -DQ8 in the general population varies geographically. Our data, similar to the data from the Middle East and South America, show a higher frequency of HLA-DQ8 ( 17-20%) among the general population compared to 1–9% among Caucasians. In addition, the prevalence of “high-risk” CD predisposing genotypes is higher in the Saudi population compared to the European population. These differences suggest that variable combinations of HLA-DQ risk alleles in Saudi CD patients might confer different risk gradients for some HLA-DQ molecules compared to Caucasian CD patients. Therefore, studies that explore the HLA-DQ genotypes of Saudi CD patients and compare them to the HLA-DQ data among the controls reported here are needed to enable clinicians in Saudi Arabia to categorize HLA-DQ molecules into risk groups. This information will help local physicians in genetic counseling of CD families to determine more precise CD occurrence risks and appropriate plans for serologic follow-ups.
Although 52.7% of the Saudi population carries high-risk HLA-DQ molecules, only 1.5% develop CD. This underscores the role of additional genetic or environmental factors. CD is a multigenetic disorder, which means that the expression of these HLA-DQ2 or HLA-DQ8 molecules is necessary but not sufficient to cause disease. Genome-wide association studies have identified a large number of non-HLA genes associated with CD, such as those coding for cytokines, chemokines and their receptors, cell adhesion molecules, and T- and B-cell activators.,,,, The high consanguineous marriage rate in the Saudi community (40–60%), and the clustering of CD cases in certain families are important reasons to conduct genome-wide association studies in Saudi Arabia. These studies would enhance the identification of new non-HLA genetic loci, which could shed light on new genes and genetic pathways involved in disease pathogenesis, and the possibility of a monogenic-form of CD could be explored.
Data on the differences in the association between HLA-DQ molecules in male and female subjects from the general population are scarce in the literature. Our mass screening study in Saudi Arabia, like many others, confirmed CD to be more prevalent in females than in males (F:M = 2-4:1), but data from our present study showed no difference between females and males in the frequency of high-risk HLA-DQ molecules. These data are in agreement with a large Italian study. This observation suggests that the HLA genes, perse, probably have no role on the CD sex bias. The causes of the CD sex bias are not yet clear, and other genetic (non-HLA) or non-genetic factors, such as exposures to environmental agents, endogenous hormones, sexual dimorphism of the immune response, X inactivation, genes on X or Y chromosomes, and epigenetic modifications, have been considered as potential causes of the sex discrepancy.,,
| Conclusion|| |
The high genetic susceptibility of the Saudi population could partly explain the recently reported high prevalence of CD in the Saudi community. Based on this finding, HLA-DQ typing should not be used as a screening test to exclude CD. As the CD-risk gradient associated with HLA-DQ molecules among Caucasians cannot be extrapolated and applied completely to Arabs, it remains to be determined how different HLA-DQ molecules modify the risk of developing CD in the Saudi population. Our data offers a first step toward defining the genetic structure of HLA-DQ molecules in different regions of Saudi Arabia. More research is needed to define the role of non-HLA genetic and environmental factors.
The authors extend their appreciations to King Abdulaziz City for Science and Technology for funding this work through a research grant Number: A-T-32-48.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Husby S, Koletzko S, Korponay-Szabó IR, Mearin ML, Phillips A, Shamir R, et al
. European Society for Pediatric Gastroenterology, Hepatology, and Nutrition guidelines for the diagnosis of coeliac disease. J Pediatr Gastroenterol Nutr 2012;54:136–60.
Kupfer SS, Jabri B. Pathophysiology of celiac disease. Gastrointest Endosc Clin N
Karell K, Louka AS, Moodie SJ, Ascher H, Clot F, Greco L, et al
. HLA types in celiac disease patients not carrying the DQA1*05-DQB1*02 (DQ2) heterodimer: Results from the European Genetics Cluster on Celiac Disease. Hum Immunol. 2003;64:469–77.
Sollid LM, Lie BA. Celiac disease genetics: Current concepts and practical applications. Clin Gastroenterol Hepatol 2005;3:843–51.
Govind K, Makharia. Celiac disease screening in Southern and East Asia. Dig Dis 2015;33:167–74.
Al-Hussaini A, Troncone R, Khormi M, AlTuraiki M, Alkhamis W, Alrajhi M, et al
. Mass screening for celiac disease among school-aged children: Toward exploring celiac iceberg in Saudi Arabia. J Pediatr Gastroenterol Nutr 2017;65:646–51.
Marsh SG and WHO Nomenclature Committee for Factors of the HLA System. Nomenclature for factors of the HLA system, update January 2012. Tissue Antigens 2012;79:393–97.
Megiorni F, Mora B, Bonamico M, Barbato M, Nenna R, Maiella G, et al
. HLA-DQ and risk gradient for celiac disease. Hum Immunol 2009;70:55–9.
Ruiz-Ortiz E, Montraveta M, Cabré E, Herrero-Mata MJ, Pujol-Borrell R, Palou E, et al
. HLA-DQ2/DQ8 and HLA-DQB1*02 homozygosity typing by real-time polymerase chain reaction for the assessment of celiac disease genetic risk: Evaluation of a Spanish celiac population. Tissue Antigens 2014;84:545–53.
Margaritte-Jeannin P, Babron MC, Bourgey M, Louka AS, Clot F, Percopo S, et al
. HLA-DQ relative risks for coeliac disease in European populations: A study of the European Genetics Cluster on Coeliac Disease. Tissue Antigens 2004;63:562–67.
Lionetti E, Catassi C. Co-localization of gluten consumption and HLA-DQ2 and -DQ8 genotypes, a clue to the history of celiac disease. Dig Liver Dis 2014;46:1057–63.
Sandstrom O, Rose'n A, Lagerqvist C, Carlsson A, Hernell O, Högberg L, et al
. Transglutaminase IgA antibodies in a celiac disease mass screening and the role of HLA-DQ genotyping and endomysial antibodies in sequential testing. J Pediatr Gastroenterol Nutr 2013;57:472–76.
Abadie V, Sollid LM, Barreiro LB, Jabri B. Integration of genetic and immunological insights into a model of celiac disease pathogenesis. Annu Rev Immunol 2011;29:493–525.
Accomando S, Cataldo F. The global village of celiac disease. Dig Liver Dis. 2004 Jul; 36(7):492-8.
Saberi-Firouzi M, Omrani GR, Nejabat M, Mehrabani D, Khademolhosseini F. Prevalence of celiac disease in Shiraz, southern Iran. Saudi J Gastroenterol 2008;14:135–8.
] [Full text]
Farahmand F, Mir-Nasseri MM, Shahraki T, Yourdkhani F, Ghotb S, Modaresi V, et al
. Prevalence of occult celiac disease in healthy Iranian school age children. Arch Iran Med 2012;15:342–5.
Sood A, Midha V, Sood N, Avasthi G, Sehgal A. Prevalence of CD among school children in Punjab, North India. J Gastroenterol Hepatol 2006;21:1622–5.
Yuan J, Gao J, Li X, Liu F, Wijmenga C, Chen H, et al
. The tip of the celiac iceberg in China: A systematic review and meta-analysis. PLOS One 2013;8:e81151.
Rostami-Nejad M, Romanos J, Rostami K, Ganji A, Ehsani-Ardakani MJ, Bakhshipour AR, et al
. Allele and haplotype frequencies for HLA-DQ in Iranian celiac disease patients. World J Gastroenterol 2014;20:6302–8.
Yachha SK. Celiac disease: India on the global map. J Gastroenterol Hepatol 2006;21:1511–3.
Pietzak MM, Schofield TC, McGinniss MJ, Nakamura RM. Stratifying risk for celiac disease in a large at-risk United States population by using HLA alleles. Clin Gastroenterol Hepatol 2009;7:966–71.
Al-Hussaini A, Sulaiman N, Al-Zahrani M, Alenizi A, El Haj I. Prevalence of Celiac Disease among Type 1 Diabetic Children. BMC Gastroenterol 2012;12:180.
Ventura A, Magazzu G, Greco L. Duration of exposure to gluten and risk for autoimmune disorders in patients with celiac disease. SIGEP Study Group for Autoimmune Disorders in Celiac Disease. Gastroenterology 1999;2:297–303.
Liu E, Lee HS, Aronsson CA, Hagopian WA, Koletzko S, Rewers MJ, et al
. Risk of pediatric celiac disease according to HLA haplotype and country. N Engl J Med 2014;371:42–9.
Bjorck S, Lynch K, Brundin C, Agardh D. Repeated screening is necessary for detection of celiac disease but can be restricted to at genetic risk birth cohorts. J Pediatr Gastroenterol Nutr 2016;62:271–5.
Mearin ML, Ivarsson A, Dickey W. Coeliac disease: Is it time for mass screening? Best practice & research. Clin Gastroenterol 2005;19:441–52.
Francavilla R, Castellaneta S. Inverting the Diagnostic Pyramid in Celiac Disease: HLA Typing for Screening Suspects of Celiac Disease. J Pediatr Gastroenterol Nutr 2016;63:e20.
Stanković B1, Radlović N, Leković Z, Ristić D, Radlović V, Nikčević G, et al
. HLA genotyping in pediatric celiac disease patients. Bosn J Basic Med Sci 2014;14:171–6.
The Allele Frequency Net Database. 2012; 2012 Available at: www.allelefrequencies.net. [Last accessed on 2017 Dec 15].
El-Hazmi M, Al-Swailem AR, Warsy AS, al-Swailem AM, Sulaimani R, al-Meshari AA. Consanguinity among the Saudi Arabian population. J Med Genet 1995;32:623–6.
Dubois PC, Trynka G, Franke L, Hunt KA, Romanos J, Curtotti A, et al
. Multiple common variants for celiac disease influencing immune gene expression. Nat Genet 2010;42:295–302.
Einarsdottir E, Koskinen LL, de Kauwe AL, Dukes E, Mustalahti K, Balogh M, et al
. Genome-wide analysis of extended pedigrees confirms IL2-IL21 linkage and shows additional regions of interest potentially influencing coeliac disease risk. Tissue Antigens 2011;78:428–37.
Plaza-Izurieta L, Castellanos-Rubio A, Irastorza I, Fernández-Jimenez N, Gutierrez G; CEGEC, et al
. Revisiting genome wide association studies (GWAS) in coeliac disease: Replication study in Spanish population and expression analysis of candidate genes. J Med Genet 2011;48:493–6.
Garner CP, Murray JA, Ding YC, Tien Z, van Heel DA, Neuhausen SL. Replication of celiac disease UK genome-wide association study results in a US population. Hum Mol Genet 2009;18:4219–25.
Trynka G, Wijmenga C, van Heel DA. A genetic perspective on coeliac disease. Trends Mol Med 2010;16:537–50.
Al-Aama JY, Shaik NA, Banaganapalli B, Salama MA, Rashidi O, Sahly AN, et al
. Whole exome sequencing of a consanguineous family identifies the possible modifying effect of a globally rare AK5 allelic variant in celiac disease development among Saudi patients. PLOS One 2017;12:e0176664.
Megiorni F, Mora B, Bonamico M, Barbato M, Montuori M, Viola F, et al
. HLA-DQ and Susceptibility to Celiac Disease: Evidence for Gender Differences and Parent-of-Origin Effects. Am J Gastroenterol 2008;103:997–1003.
Julier C, Hyer RN, Davies J, Merlin F, Soularue P, Briant L, et al
. Insulin-IGF2 region on chromosome 11p encodes a gene implicated in HLA-DR4- dependent diabetes susceptibility. Nature 1991;354:155–9.
Lockshin MD. Sex differences in autoimmune disease. Lupus 2006;15:753–6.
Selmi C, Invernizzi P, Gershwin ME. The X chromosome and systemic sclerosis. Curr Opin Rheumatol 2006;18:601–5.
Dr. Abdulrahman Al-Hussaini
Division of Pediatric Gastroenterology, Children's Specialized Hospital, King Fahad Medical City, College of Medicine, Alfaisal University, Riyadh
Kingdom of Saudi Arabia
Source of Support: None, Conflict of Interest: None
[Table 1], [Table 2], [Table 3]