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BioMed Research International
Volume 2013 (2013), Article ID 721604, 6 pages
The Role of PTPN22 C1858T Gene Polymorphism in Diabetes Mellitus Type 1: First Evaluation in Greek Children and Adolescents
14th Department of Pediatrics, Faculty of Medicine, Aristotle University of Thessaloniki, Papageorgiou General Hospital, Ring Road Nea Efkarpia, 56403 Thessaloniki, Greece
21st Department of Pharmacology, Faculty of Medicine, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece
3Department of Hematology, Papageorgiou General Hospital, Ring Road Nea Efkarpia, 56403 Thessaloniki, Greece
Received 3 April 2013; Revised 27 May 2013; Accepted 20 June 2013
Academic Editor: Timothy B. Niewold
Copyright © 2013 Styliani Giza et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Type 1 diabetes mellitus (T1DM) is an autoimmune multifactorial disease. Protein tyrosine phosphatase nonreceptor type 22 (PTPN22) gene encodes lymphoid-specific tyrosine phosphatase (Lyp), an inhibitor of T cell activation. PTPN22 C1858T polymorphism was associated with T1DM in populations of Caucasian origin. The aim of this study was the investigation for the first time of the association of PTPN22 C1858T polymorphism with T1DM in Greek population. We studied 130 children and adolescents with T1DM and 135 healthy individuals of Greek origin. The polymorphism was genotyped using polymerase chain reaction with restriction fragment length polymorphism. C1858T and T1858T genotypes as well as 1858T allele were found more frequently in patients (10.8% and 5.8%, resp.) than in healthy individuals (5.9% and 3.0%, resp.) but at non statistically significant level. There was no statistically significant association found with gender, age at diagnosis, severity of onset, history of Hashimoto thyroiditis or family history of T1DM. Increased frequency of 1858T allele in patients than in controls, implying a probable association, agrees with results of similar studies on other populations. The inability to find a statistically significant difference is probably due to the decreased frequency of minor allele in Greek population, indicating the need for a larger sample.
Type 1 diabetes mellitus (T1DM) is characterized by autoimmune destruction of insulin-producing beta cells of pancreatic islets by CD4+ cytotoxic T lymphocytes with the contribution of CD8+ helper T lymphocytes, which leads to permanent impairment of glucose metabolism. It is considered a multifactorial disease, requiring the interaction of genetic and environmental factors in triggering autoimmunity . Although the exact pathogenesis of T1DM is unknown, several gene loci involved in disease outbreak have been identified. Among these, genes of human leukocyte antigen (HLA) class II, insulin (INS), cytotoxic T lymphocyte antigen-4 (CTLA-4), and protein tyrosine phosphatase non-receptor type 22 (PTPN22) play a key role .
PTPN22 gene is located on chromosome 1p13.3-p13.1 and encodes the lymphoid-specific tyrosine phosphatase (Lyp), an important inhibitor of the activation and proliferation of T lymphocytes. Downregulation is achieved through interaction of Lyp with the C-terminal Src tyrosine kinase (Csk), which suppresses T cell receptor (TCR) signaling . A single nucleotide polymorphism (SNP) at position 1858 (rs 2476601) of the encoding sequence of PTPN22 gene, consisting of the substitution of cytosine by thymine, results in mutation of arginine to tryptophan at codon 620 of Lyp. The mutation disturbs the Lyp-Csk interaction, leading to uncontrolled TCR signaling and inappropriate prolonged activation of T lymphocytes, which induces and maintains autoimmunity. Although Lyp is a known inhibitor of TCR signaling, the regulatory mechanism still remains under investigation. Therefore, the study of PTPN22 C1858T polymorphism is of enormous clinical and therapeutic interest, as Lyp could be the target of intervention against triggered autoimmunity. Nowadays, research focuses on factors which inhibit cellular function and more specifically dephosphorylation of TCR activation-dependent kinases induced by Lyp .
For the first time, Bottini et al.  reported that 1858T allele was observed more frequently in patients with T1DM compared to healthy individuals from North America and Sardinia. Since then, studies have investigated the association of PTPN22 C1858T polymorphism with T1DM in various populations. The 1858T allele has been reported to be associated with T1DM in populations from Italy [6, 7], Germany [8, 9], Denmark , North America [11, 12], United Kingdom [13, 14], Spain  Ukraine , Estonia , Netherlands , Finland , France , Croatia , Norway , Poland , Russia , Colombia , Czech Republic and Azerbaijan , and Brazil  but not from India . This allele has been associated with other autoimmune diseases such as systemic lupus erythematosus (SLE) , rheumatoid arthritis (RA) , juvenile idiopathic arthritis , multiple sclerosis , autoimmune thyroid diseases , psoriasis , and Addison disease  but not with inflammatory bowel disease .
In Greece, two studies have been conducted in populations from Crete. The minor allele was not associated with psoriasis in the first study , while it was associated with SLE but not with RA in the second one . Given the fact that the frequency of minor allele varies between populations and that ongoing studies are important to confirm previous associations, the aim of this study was to assess the role of PTPN22 C1858T polymorphism in children and adolescents of Greek origin with T1DM.
2. Materials and Methods
This is a case-control study in a population of Greek origin. We studied 130 children and adolescents (73 males, 57 females) with T1DM (average age at entry to the study years, range 0.83–19.21) and 135 healthy subjects (72 male, 63 females) without a family history of T1DM. In order to minimize genetic heterogeneity, we included unrelated individuals with a history of at least three generations of Greek origin. Patients are followed up at the Pediatric Diabetes Outpatient Unit, 4th Department of Pediatrics, Faculty of Medicine, Aristotle University of Thessaloniki, Papageorgiou General Hospital. All patients were diagnosed with T1DM before the age of 15 years and were insulin dependent. Parameters included in the statistical analysis were gender, age at the entry to the study, age at diagnosis, severity of onset (presence or absence of ketoacidosis), personal history of Hashimoto thyroiditis (HT), and family history of T1DM of at least one first-degree relative. Control group consisted of children and adolescents older than 10 years, staff of Papageorgiou General Hospital, and students of the Medical Faculty of Aristotle University of Thessaloniki. Before entering the study, an informed consent was obtained by adult participants and parents or guardians of individuals younger than 18 years. The research protocol was declared at the service of ClinicalTrials.gov and approved by the Ethics Committee of Faculty of Medicine of Aristotle University of Thessaloniki. The study was conducted according to the criteria of the Declaration of Helsinki.
The method includes four stages: (a) genomic isolation of deoxyribonucleic acid (DNA), (b) polymerase chain reaction (PCR), (c) incubation of PCR products with restriction enzymes, and (d) electrophoresis. Whole blood was collected in a sterile vial containing anticoagulant ethylenediaminetetraacetic acid (EDTA). DNA was isolated using the QIAamp DNA Blood Mini Kit (QIAGEN Inc., CA, USA) according to the instructions of the manufacturer and was stored at −20°C. The piece of PTPN22 gene including polymorphism at position 1858 was amplified with specifically designed primers, PTPN22 forward 5-ACTGATAATGTTGCTTCAACGG-3 and PTPN22 reverse 5-TCACCAGCTTCCTCAACCAC-3. PCR products were incubated with the restriction enzyme RsaI (Fermentas, Germany) at 37°C overnight. The enzyme cuts C allele into two fragments of 172 base pairs (bp) and 46 bp, while T allele remains intact (218 bp). Electrophoresis of the products of digestion in 2.3% agarose gel followed.
Data were analyzed using the IBM program SPSS Statistics 19. Expected and observed frequencies of genotypes and alleles in patients and controls were compared in and tables, respectively, according to the Hardy-Weinberg equilibrium. The differences in frequencies of genotypes and alleles between patients and controls and between patient subgroups based on qualitative variables were analyzed by or Fisher exact test. Normal distribution of quantitative variables was examined using the Kolmogorov-Smirnov test. Normally distributed mean age at diagnosis was analyzed according to genotype analysis using analysis of variance (ANOVA). The level of statistical significance was defined at .
In this study the distribution of genotypes in patients and controls did not differ significantly from the expected Hardy-Weinberg equilibrium ( and , resp.). The 1858T allele was detected more frequently in patients (5.8%) compared to controls (3.0%) but at nonstatistically significant level (, odds ratio, (OR) 2.00, and confidence interval (CI) 0.83–4.81). The T1858T genotype showed a reduced incidence in patients (0.8%) and was not detected in controls. The C1858T genotype was significantly more frequent in patients (10.0%) compared to controls (5.9%), but a statistically significant difference was not found. Because of the low frequency of 1858T allele, the C1858T and T1858T genotypes were grouped for statistical analysis. The C1858T and T1858T genotypes were detected more frequently in patients (10.9%) than in healthy subjects (5.9%) but not in a statistically significant level (Table 1).
There was a trend towards higher frequency of C1858T and T1858T genotypes in males. The frequency of C1858T and T1858T genotypes was 12.3% in males versus 6.9% in females in the patient group, while 8.8% versus 4.8%, respectively, in the control group (Table 2). However, the distribution of C1858T and T1858T genotypes carrying the predisposing allele did not differ significantly between males and females in the patient group as well as compared with the control group (Table 3).
The mean age at diagnosis was years (range 0.57–14.59). Statistical analysis after grouping patients according to age at diagnosis found that the PTPN22 C1858T polymorphism had the same effect in patients with early onset (age at diagnosis ≤10 years) as well as to those with late onset (age at diagnosis >10 years) of T1DM. The mean age at diagnosis was similar in patients with C1858T and T1858T genotypes as well as in those with C1858C genotype (7.68 and 7.31, years resp., ). Furthermore, there was a tendency for the 1858T pubertal carriers to be more susceptible to T1DM than prepubertal ().
Investigating the possible association of the PTPN22 C1858T polymorphism with more severe clinical manifestation at diagnosis, assessed by the presence or absence of ketoacidosis, patients with C1858T and T1858T genotypes were diagnosed with ketoacidosis more often (11.5% versus 7.7%) but not in a statistically significant higher rate.
Moreover, we investigated the role of PTPN22 C1858T polymorphism in autoimmunity. Among C1858T and T1858T genotype carriers, HT presented with marginally increased incidence (14.8% T1DM + HT versus 9.7% T1DM only). We did not find statistically significant association of PTPN22 C1858T polymorphism with a positive family history of T1DM. The distribution of PTPN22 C1858T polymorphism in patients according to the analyzed parameters is shown in Table 3.
In this case-control study, the role of PTPN22 C1858T polymorphism was investigated for the first time in children and adolescents of Greek origin with T1DM. The first report of the association of PTPN22 C1858T polymorphism with T1DM by Bottini et al.  was confirmed by several association studies [5–26]. This finding was reinforced by recently published meta-analyses which suggest that PTPN22 C1858T polymorphism may contribute to the predisposition of the T1DM especially in populations of Europe and America. However, the investigators conclude that there is still need for more studies to support these findings [39–44]. In the present study population, although increased 1858T allele frequency was confirmed in patients with T1DM, the result was not statistically significant. However, OR of 1858T versus 1858C allele in patients compared to controls was similar to that of other studies .
The studies conducted in different populations can indirectly reveal an interesting feature of PTPN22 C1858T polymorphism, the large geographical variation in the frequency of the 1858T allele. There is a tendency for increased frequency of the 1858T allele in healthy Caucasian populations in Europe (from southern to northern). More specifically, its frequency was found to be 2% in Italy, 6% in Spain, 12% in Sweden, and 15.5% in Finland. However, it seems to be almost absent in populations from Asia and Africa . In Greece, the 1858T allele frequency was found to be low (2.69–2.91%) in 3 independent groups of healthy individuals from Crete [37, 38]. A similar incidence (3.0%) was found in the control group of the study population. Therefore, the main comparison standard for the outcome of this study is more appropriate to be published studies involving populations of Southern Europe where the frequency of the 1858T allele in healthy individuals is relatively low [5–7, 14]. The low frequency of the 1858T allele in this study may be one of the causes of the lack of a statistically significant association between the PTPN22 C1858T polymorphism and T1DM, because it limits the power of the study. The low frequency of the minor allele supports the need of a larger sample. Furthermore, the purpose of this study becomes more obvious. As a result, published data on the role of the PTPN22 C1858T polymorphism in individuals of Greek origin with TD1M are required. Until today, preliminary unpublished data of association studies in two patient populations of Greek origin with T1DM did not confirm the well-documented association of PTPN22 C1858T polymorphism with T1DM  in complete agreement with this study. Our data are the first published, and, although they imply a probable association, they indicate the need for a larger sample. However, the lack of association between PTPN22 C1858T polymorphism and T1DM in children and adolescents of Greek origin retains its research value, taking into account the geographical variation in the frequency of the 1858T allele, the genetic diversity of individuals, and the multifactorial nature of T1DM. Moreover, for the interpretation of our results it should take into account the different genetic background of populations concerning HLA class II genes as well as the variable effect of known or unknown predisposing environmental factors.
Although T1DM is an autoimmune disease without gender differentiation in prevalence, we found a tendency towards higher frequency of C1858T and T1858T genotypes in males. The lack of statistically significant association of the PTPN22 C1858T polymorphism with gender agrees with the majority of studies [7, 12, 13, 18, 25, 27]. In regard to the relationship of PTPN22 C1858T polymorphism with T1DM, some studies have suggested a gender differentiation in prevalence in favour of females [8, 10, 15, 16] and only one in favour of males . While a few studies revealed a statistically significant association of the PTPN22 C1858T polymorphism with gender, a recently published meta-analysis suggests that males who carried the 1858T allele were more susceptible to T1DM than females . As a result, the interaction of the PTPN22 C1858T polymorphism with gender in TD1 M requires further investigation.
It has been reported that genetic factors may influence the age of diagnosis. In this context, it was examined whether predisposing 1858T allele is associated with the age at diagnosis of T1DM. The mean age at diagnosis in 1858T allele carriers was similar to those of the remaining patients, in agreement with the conclusions of other researchers [8, 12, 13, 21, 27]. The results in terms of the possible effect of PTPN22 C1858T polymorphism in age of diagnosis are controversial, as it was associated with lower age of diagnosis  in 2 studies and particularly in the group of female patients [10, 15].
Taking into account the fact that autoimmune diseases accumulate in individuals and families, we studied the possibility of association of PTPN22 C1858TT polymorphism with personal history of HT and family history of T1DM without positive results in the study population. Recently published meta-analysis suggests association of the PTPN22 C1858T polymorphism with HT . However, only 2 studies revealed a statistically significant association with the concordance of HT and T1DM [7, 9]. Therefore, further investigation is required—particularly in children and adolescent population—for the combined effect of the PTPN22 C1858T polymorphism and other factors in HT onset in patients with TD1 M. We investigated the contribution of the PTPN22 C1858T polymorphism to the aggregation of T1DM within families. The inability to find an increased frequency of the 1858T allele in patients with positive family history of T1DM is probably explained by the sample size.
In conclusion, the finding of increased frequency of the 1858T allele in patients with T1DM compared to healthy subjects agrees with the results of similar studies in other populations. The inability to detect statistically significant differences may be due to low frequency of the minor allele in Greek population. In order to make safe conclusions regarding the association of the PTPN22 C1858T polymorphism with T1DM in Greek population, a larger sample is needed because of the found rarity of the 1858T allele in Greeks.
Conflict of Interests
No conflict of interests has been declared by the authors.
The study was conducted with the financial support of the Northern Greece Diabetes Association.
- E. A. M. Gale, “The rise of childhood type 1 diabetes in the 20th century,” Diabetes, vol. 51, no. 12, pp. 3353–3361, 2002.
- S. S. Rich, P. Concannon, H. Erlich et al., “The type 1 diabetes genetics consortium,” Annals of the New York Academy of Sciences, vol. 1079, pp. 1–8, 2006.
- S. Cohen, H. Dadi, E. Shaoul, N. Sharfe, and C. M. Roifman, “Cloning and characterization of a lymphoid-specific, inducible human protein tyrosine phosphatase, Lyp,” Blood, vol. 93, no. 6, pp. 2013–2024, 1999.
- X. Yu, J. P. Sun, Y. He et al., “Structure, inhibitor, and regulatory mechanism of Lyp, a lymphoid-specific tyrosine phosphatase implicated in autoimmune diseases,” Proceedings of the National Academy of Sciences of the United States of America, vol. 104, no. 50, pp. 19767–19772, 2007.
- N. Bottini, L. Musumeci, A. Alonso et al., “A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes,” Nature Genetics, vol. 36, no. 4, pp. 337–338, 2004.
- A. Petrone, C. Suraci, M. Capizzi et al., “The protein tyrosine phosphatase nonreceptor 22 (PTPN22) Is associated with high GAD antibody titer in latent autoimmune diabetes in adults: non insulin requiring autoimmune diabetes (NIRAD) study 3,” Diabetes Care, vol. 31, no. 3, pp. 534–538, 2008.
- P. Saccucci, E. Del Duca, N. Rapini et al., “Association between PTPN22 C1858T and type 1 diabetes: a replication in continental Italy,” Tissue Antigens, vol. 71, no. 3, pp. 234–237, 2008.
- H. Kahles, E. Ramos-Lopez, B. Lange, O. Zwermann, M. Reincke, and K. Badenhoop, “Sex-specific association of PTPN22 1858T with type 1 diabetes but not with Hashimoto's thyroiditis or Addison's disease in the German population,” European Journal of Endocrinology, vol. 153, no. 6, pp. 895–899, 2005.
- G. Dultz, N. Matheis, M. Dittmar, B. Röhrig, K. Bender, and G. J. Kahaly, “The protein tyrosine phosphatase non-receptor type 22 C1858T polymorphism is a joint susceptibility locus for immunthyroiditis and autoimmune diabetes,” Thyroid, vol. 19, no. 2, pp. 143–148, 2009.
- C. Nielsen, D. Hansen, S. Husby, and S. T. Lillevang, “Sex-specific association of the human PTPN22 1858T-allele with type 1 diabetes,” International Journal of Immunogenetics, vol. 34, no. 6, pp. 469–473, 2007.
- W. Zheng and J. X. She, “Genetic association between a lymphoid tyrosine phosphatase (PTPN22) and type 1 diabetes,” Diabetes, vol. 54, no. 3, pp. 906–908, 2005.
- A. K. Steck, S. Y. Liu, K. McFann et al., “Association of the PTPN22/LYP gene with type 1 diabetes,” Pediatric Diabetes, vol. 7, no. 5, pp. 274–278, 2006.
- D. Smyth, J. D. Cooper, J. E. Collins et al., “Replication of an association between the lymphoid tyrosine phosphatase locus (LYP/PTPN22) with type 1 diabetes, and evidence for its role as a general autoimmunity locus,” Diabetes, vol. 53, no. 11, pp. 3020–3023, 2004.
- D. J. Smyth, J. D. Cooper, J. M. M. Howson et al., “PTPN22 Trp620 explains the association of chromosome 1p13 with type 1 diabetes and shows a statistical interaction with HLA class II genotypes,” Diabetes, vol. 57, no. 6, pp. 1730–1737, 2008.
- J. L. Santiago, A. Martínez, H. de la Calle et al., “Susceptibility to type 1 diabetes conferred by the PTPN22 C1858T polymorphism in the Spanish population,” BMC Medical Genetics, vol. 8, article 54, 2007.
- M. Fedetz, F. Matesanz, A. Caro-Maldonado et al., “The 1858T PTPN22 gene variant contributes to a genetic risk of type 1 diabetes in a Ukrainian population,” Tissue Antigens, vol. 67, no. 5, pp. 430–433, 2006.
- K. Douroudis, E. Prans, K. Haller et al., “Protein tyrosine phosphatase non-receptor type 22 gene variants at position 1858 are associated with type 1 and type 2 diabetes in Estonian population,” Tissue Antigens, vol. 72, no. 5, pp. 425–430, 2008.
- A. Zhernakova, P. Eerligh, C. Wijmenga, P. Barrera, B. O. Roep, and B. P. C. Koeleman, “Differential association of the PTPN22 coding variant with autoimmune diseases in a Dutch population,” Genes and Immunity, vol. 6, no. 6, pp. 459–461, 2005.
- R. Hermann, K. Lipponen, M. Kiviniemi et al., “Lymphoid tyrosine phosphatase (LYP/PTPN22) Arg620Trp variant regulates insulin autoimmunity and progression to type 1 diabetes,” Diabetologia, vol. 49, no. 6, pp. 1198–1208, 2006.
- C. Chelala, S. Duchatelet, M. L. Joffret et al., “PTPN22 R620W functional variant in type 1 diabetes and autoimmunity related traits,” Diabetes, vol. 56, no. 2, pp. 522–526, 2007.
- M. Korolija, I. P. Renar, M. Hadžija et al., “Association of PTPN22 C1858T and CTLA-4 A49G polymorphisms with type 1 diabetes in Croatians,” Diabetes Research and Clinical Practice, vol. 86, no. 3, pp. e54–e57, 2009.
- L. C. Stene, K. S. Rønningen, M. Bjørnvold, D. E. Undlien, and G. Joner, “An inverse association between history of childhood eczema and subsequent risk of type 1 diabetes that is not likely to be explained by HLA-DQ, PTPN22, or CTLA4 polymorphisms,” Pediatric Diabetes, vol. 11, no. 6, pp. 386–393, 2010.
- M. Fichna, M. Zurawek, D. Januszkiewicz-Lewandowska, P. Fichna, and J. Nowak, “PTPN22, PDCD1 and CYP27B1 polymorphisms and susceptibility to type 1 diabetes in Polish patients,” International Journal of Immunogenetics, vol. 37, no. 5, pp. 367–372, 2010.
- D. Zhebrun, Y. Kudryashova, A. Babenko et al., “Association of PTPN22 1858T/T genotype with type 1 diabetes, Graves' disease but not with rheumatoid arthritis in Russian population,” Aging, vol. 3, no. 4, pp. 368–373, 2011.
- L. M. Gomez, J. M. Anaya, C. I. Gonzalez et al., “PTPN22 C1858T polymorphism in Colombian patients with autoimmune diseases,” Genes & Immunity, vol. 6, no. 7, pp. 628–631, 2005.
- O. Cinek, O. Hradsky, G. Ahmedov et al., “No independent role of the -1123 G > C and + 2740 A > G variants in the association of PTPN22 with type 1 diabetes and juvenile idiopathic arthritis in two Caucasian populations,” Diabetes Research and Clinical Practice, vol. 76, no. 2, pp. 297–303, 2007.
- P. C. Chagastelles, M. Romitti, M. R. Trein, E. Bandinelli, B. Tschiedel, and N. B. Nardi, “Association between the 1858T allele of the protein tyrosine phosphatase nonreceptor type 22 and type 1 diabetes in a Brazilian population,” Tissue Antigens, vol. 76, no. 2, pp. 144–148, 2010.
- V. Baniasadi and S. N. Das, “No evidence for association of PTPN22 R620W functional variant C1858T with type 1 diabetes in Asian Indians,” Journal of Cellular and Molecular Medicine, vol. 12, no. 3, pp. 1061–1062, 2008.
- W. W. Lea and Y. H. Lee, “The association between the PTPN22 C1858T polymorphism and systemic lupus erythematosus: a meta-analysis update,” Lupus, vol. 20, no. 1, pp. 51–57, 2011.
- M. C. Totaro, B. Tolusso, V. Napolioni et al., “PTPN22 1858C>T polymorphism distribution in europe and association with rheumatoid arthritis: case-control study and meta-analysis,” PLoS ONE, vol. 6, no. 9, Article ID e24292, 2011.
- Y. H. Lee, S. C. Bae, and G. G. Song, “The association between the functional PTPN22 1858 C/T and MIF -173 C/G polymorphisms and juvenile idiopathic arthritis: a meta-analysis,” Inflammation Research, vol. 61, no. 5, pp. 411–415, 2012.
- Y. H. Lee, S. J. Choi, J. D. Ji, and G. G. Song, “The association between the PTPN22 C1858T polymorphism and systemic sclerosis: a meta-analysis,” Molecular Biology Reports, vol. 39, no. 3, pp. 3103–3108, 2012.
- L. Luo, B. Cai, F. Liu, X. Hu, and L. Wang, “Association of Protein Tyrosine Phosphatase Nonreceptor 22 (PTPN22) C1858T gene polymorphism with susceptibility to autoimmune thyroid diseases: a meta-analysis,” Endocrine Journal, vol. 59, no. 5, pp. 439–445, 2012.
- Y. Li, W. Liao, M. Chang et al., “Further genetic evidence for three psoriasis-risk genes: ADAM33, CDKAL1, and PTPN22,” Journal of Investigative Dermatology, vol. 129, no. 3, pp. 629–634, 2009.
- M. Roycroft, M. Fichna, D. McDonald et al., “The tryptophan 620 allele of the lymphoid tyrosine phosphatase (PTPN22) gene predisposes to autoimmune Addison's disease,” Clinical Endocrinology, vol. 70, no. 3, pp. 358–362, 2009.
- A. Latiano, O. Palmieri, M. R. Valvano et al., “Evaluating the role of the genetic variations of PTPN22, NFkB1 and FcGRIIIA genes in inflammatory bowel disease: a meta-analysis,” Inflammatory Bowel Diseases, vol. 13, no. 10, pp. 1212–1219, 2007.
- M. I. Zervou, F. Castro-Giner, P. Sidiropoulos, D. T. Boumpas, A. D. Tosca, and S. Krueger-Krasagakis, “The protein tyrosine phosphatase, non-receptor type 22 R620W polymorphism does not confer susceptibility to psoriasis in the genetic homogeneous population of Crete,” Genetic Testing and Molecular Biomarkers, vol. 14, no. 1, pp. 107–111, 2010.
- E. Eliopoulos, M. I. Zervou, A. Andreou et al., “Association of the PTPN22 R620W polymorphism with increased risk for SLE in the genetically homogeneous population of Crete,” Lupus, vol. 20, no. 5, pp. 501–506, 2011.
- H. Peng, M. Zhou, W. D. Xu, et al., “Association of PTPN22 C1858T polymorphism and type 1 diabetes: a meta-analysis,” Immunological Investigations, vol. 41, no. 5, pp. 484–496, 2012.
- S. Tang, W. Peng, C. Wang, H. Tang, and Q. Zhang, “Association of the PTPN22 gene (+1858C/T, -1123G/C) polymorphisms with type 1 diabetes mellitus: a systematic review and meta-analysis,” Diabetes Research and Clinical Practice, vol. 97, no. 3, pp. 446–452, 2012.
- Y. H. Lee and G. G. Song, “Meta-analysis of the family-based association between the PTPN22 C1858T polymorphism and type 1 diabetes,” Molecular Biology Reports, vol. 40, no. 1, pp. 211–215, 2013.
- J. Zheng, S. Ibrahim, F. Petersen, and X. Yu, “Meta-analysis reveals an association of PTPN22 C1858T with autoimmune diseases, which depends on the localization of the affected tissue,” Genes & Immunity, vol. 13, no. 8, pp. 641–652, 2012.
- X. F. Wang, Z. X. Chen, Y. C. Shao, et al., “Population-based and family-based studies on the protein tyrosine phosphatase non-receptor 22 gene polymorphism and type 1 diabetes: a meta-analysis,” Gene, vol. 517, no. 2, pp. 191–196, 2013.
- C. Xuan, L. M. Lun, J. X. Zhao, et al., “PTPN22 gene polymorphism (C1858T) is associated with susceptibility to type 1 diabetes: a meta-analysis of 19, 495 cases and 25, 341 controls,” Annals of Human Genetics, vol. 77, no. 3, pp. 191–203, 2013.