Research Article | Open Access
Nahide Onsun, Serpil Pirmit, Dilek Ozkaya, Şirin Çelik, Aylin Rezvani, F. Pelin Cengiz, Cigdem Kekik, "The HLA-Cw12 Allele Is an Important Susceptibility Allele for Psoriasis and Is Associated with Resistant Psoriasis in the Turkish Population", The Scientific World Journal, vol. 2019, Article ID 7848314, 5 pages, 2019. https://doi.org/10.1155/2019/7848314
The HLA-Cw12 Allele Is an Important Susceptibility Allele for Psoriasis and Is Associated with Resistant Psoriasis in the Turkish Population
Background. Psoriasis is a multifactorial immune-mediated inflammatory disease triggered by both genetic and environmental factors. The strong association between psoriasis and HLA-C06 allele has been demonstrated in various races. The HLA-C12 allele is closely related to the HLA-C06 family of alleles and shares identical sequences. To the best of our knowledge, there is no information about the relationship between HLA-C12 and psoriasis in the Turkish population. The present study aims to determine this relationship. Methods. This case control study involved 150 patients with plaque-type psoriasis and 145 age- and gender-matched healthy individuals. Severity of psoriasis was measured using the PASI scores of all patients and joint involvement was investigated with CASPAR criteria. HLA-C alleles were determined with a Tepnel-Lifecodes system. Results. HLA-C06, HLA-C12, and HLA-C04 alleles were most commonly observed in psoriasis patients. HLA-C06 and HLA-C12 were significantly more frequent in the psoriasis group. HLA-C06 was 4.11 times more common in psoriasis patients. An increase in PASI (Psoriasis Area Severity Index) scores was compatible with HLA-C12 positivity. A need for systemic treatment was highly noticeable in patients with the HLA-C12 allele. Conclusions. HLA-C12 was found as the second most frequent allele with psoriasis in Turkish population and was associated with severe psoriasis. Our study is limited as we could not investigate other potentially related alleles other than HLA-C alleles and risk factors increasing severity of psoriasis.
Psoriasis is a chronic inflammatory disease characterized by T-cell-mediated hyperproliferation of keratinocytes. Both environmental and genetic factors are involved in the aetiology of psoriasis . The HLA-C locus on chromosome 6p21.33 is accepted as a susceptibility locus for psoriasis. The association between psoriasis and the HLA-C06 allele has been demonstrated in various genetic studies [2–5]. Early-onset psoriasis is more likely to be familial and associated with HLA-C06, according to the results of population studies .
The HLA-C12 family of alleles is closely related to HLA-C06 alleles, sharing identical sequences in their alpha-2 domains, peptide binding pockets A, D, E, and all 3 introns . HLA-C12 has also been found to be a risk factor for psoriatic arthritis . Large epidemiological studies are lacking in Turkey. In a study done with limited number of patients the prevalence was found as 1.3% . Since there are limited numbers of studies that have been made in Turkey for genetic susceptibility factors in patients with psoriasis, we aimed to investigate frequency of HLA-C alleles in the Turkish population.
2. Patients and Methods
The study was approved by the Local Ethics Committee of Bezmialem Vakıf University, and written informed consent was obtained from all subjects. One hundred fifty patients (85 men and 65 women) with plaque-type psoriasis were recruited consecutively from the outpatient psoriasis clinic of our dermatology department. The control group consisted of 145 healthy donors who admitted to the Research Centre of Istanbul University (DETAM) for transplantation. The HLA identifications of the patient and control groups were performed in the Medical Biology Department of Istanbul University.
3. Genotyping for HLC Alleles
DNA from patient and control groups were isolated from peripheral blood collected into tubes with EDTA by using the “Precipitation with Sodium Chloride Salts” method. DNA samples which would be characterized were prepared for amplification with HLA-C kits (Tepnel Lifecodes). For each HLA characterization, a mix of mastermix, distilled water, and Taq polymerase enzyme was prepared and was completed with DNA. After this procedure, amplification was performed in a cycler (Perkin Elmer). Following the amplification process, 5 ml of samples was coated on plates (Costar). Then, samples were heated at 55°C for 7 minutes in a sonicator (Ultrasonic Cleaner) and were left to wait for 15 seconds followed by an addition of 15 ml of vortexed beads coming from the HLA-C kits. Then, samples were reloaded into the cycler device for the hybridization process. Towards the end of the cycle, 170 μL of a dilution+Streptavidin mix was added onto the samples and samples were loaded into a Luminex device (Lifematch fluoroanalyzer device, Tepnel Lifecodes). Assessments of samples were conducted automatically by the system.
The genotyping system identified 13 alleles in the HLA-C loci: HLA-C01, HLA-C02, HLA-C03, HLA-C04, HLA-C05, HLA-C06, HLA-C07, HLA-C08, HLA-C12, HLA-C14, HLA-C15, HLA-C16, and HLA-C17. The frequency of each HLA-C allele was evaluated, and the most frequent alleles were determined in both groups.
Severity of psoriasis was measured with the Psoriasis Area and Severity Index (PASI) by two experienced dermatologists, and the mean was taken. The severity of psoriasis was regarded as mild in patients with a PASI score between 1 and 5; moderate in those with a PASI score between 5 and 10; and severe in those with a PASI score of 10 or higher.
All patients with joint symptoms were examined by an experienced rheumatologist. Psoriatic arthritis diagnosis was made according to the CASPAR criteria.
4. Statistical Analysis
Categorical variables were summarized as counts and percentages; continuous variables were summarized as means, standard deviations, medians, and minimum and maximum values.
Categorical variables were compared using chi square or Fisher’s exact tests, where appropriate. Continuous variables were compared with the Student t-test or Mann-Whitney U, depending on the distribution pattern of the data. The estimation of the effects of several parameters on the presence of specific HLA-C alleles was evaluated with univariate logistic regression models. Results were summarized by using odds ratios, 95% confidence intervals of odds ratios, and p values. Odds ratios for psoriatic arthritis and PASI > 10 were calculated by SPSS.
The overall significance level of the analyses was set to 0.05. Licensed SPSS version 21.0 was used for analysis.
HLA-C allele frequencies of psoriasis patients and those of the control group are shown in Figure 1. HLA-C06 (n=83, 55.7%), HLA-C12 (n=53, 35%), and HLA-C04 (n=48, 32%) were the most commonly identified alleles in the psoriasis group. The most frequent alleles in the control group were HLA-C04 (n=54, 37.2%) and HLA-C07 (n=54, 37.2%). There were significant differences between the psoriasis and control groups (Figure 1). HLA-C01, HLA-C06, and HLA-C12 alleles were significantly frequent in psoriasis patients compared to controls (8.1 % vs 2.1%; 55.7 % vs 23.4 %; 36.9 % vs 17.9; P= 0.02; P= < 0.001; P= < 0.001). HLA-C07 and HLA-C15 were more frequent in control group rather than psoriasis group (37.2 % vs 16.8 %; 14.5 % vs 4%; P= < 0.001; P= 0.002). There were no statistical significant differences related to other alleles between psoriasis and patient groups.
The strong association between psoriasis and HLA-C06 allele was confirmed in the Turkish population. HLA-C06 positivity was present in 55.7 % of patient group. HLA-C06 increases the risk of psoriasis by 4.11 times, whilst carrying the HLA-C12 allele increases the risk by 2.68 times. An association between HLA-C06 and early onset of psoriasis was also observed (Table 1). Furthermore, there was a significant association between HLA-C12 and the Psoriasis Area Severity Index (PASI). The mean PASI score of the 53 patients with HLA-C12-positive was 12.8, while the mean PASI score of HLA-C12-negative patients was 8.39 (Tables 2, 3, and 4 and Figure 2). The difference was statistically significant (P= 0.011).
Almost all psoriasis patients carrying the HLA-C12 allele had PASI scores over 10 and they were resistant to topical and conventional systemic treatments and phototherapy (Table 5). It seems that HLA-C12 increases severity of psoriasis in the Turkish population (Table 6).
The human lymphocyte antigen (HLA) that is located on chromosome 6p21.3 has been associated with both susceptibility and resistance to the development of autoimmune diseases. Studies in different races showed that HLA-C06 is strongly associated with susceptibility for psoriasis [2–5]. Although the HLA-C06 allele is widely accepted as a susceptibility gene for psoriasis, the relationship between HLA-C06 and psoriasis is not definite, as seen with HLA-B27 and ankylosing spondylitis, and other genes may contribute in the development of psoriasis.
Helms and associates observed that HLA-C alleles have intronic differences and that one difference distinguishes HLA-C06:02 and HLA-C12 alleles from all others . According to Helms, HLA-C06 and HLA-C12 differ by five amino acid replacements. HLA-C12 alleles are also associated with HLA-B group alleles that are related to psoriasis (HLA-B38:01 and HLA-B39:01) in Caucasians .
Helms observed in the study that, although HLA-C06:02 was found in the majority of overtransmitted haplotype harboured by HLA-C12:03, HLA-C12 was also associated with HLA-B alleles that play a role in psoriasis (HLA-B38:01 and HLA-B901). Mabuchi et al. suggested that HLA-C12:02 and HLA-C06:02 are allied alleles sharing identical sequences . Mabuchi also found that HLA-C06 was associated with early-onset psoriasis and that late-onset of psoriasis was significantly associated with HLA-C12. In contrast, a Brazilian study group found an association between HLA-C12 and early onset of psoriasis . Recently, Liao and associates stated that HLA-B27 and HLA-C12 were associated with psoriatic arthritis in the Chinese population .
In our study, we observed that HLA-C06 is the most frequent allele in patients with psoriasis and was associated with early onset of psoriasis. HLA-C12 was the second most frequent allele and was associated with PASI scores higher than 10. Those patients carrying HLA-C12 were also resistant to phototherapy, topical medications, and conventional systemic treatment. It is well documented that obesity, smoking, and alcohol intake play a role in the severity of psoriasis. Unfortunately, we did not investigate those risk factors in patients with high PASI scores in our study group. Evaluation of psoriatic arthritis with CASPAR criteria was done by an experienced rheumatologist. We could not find significant association of arthritis neither with HLA-C06 nor with HLA-C12. A multicenter meta-analysis showed that genetic risk factors can differ in different populations. Thus, HLA-C12 may not be a genetic risk factor universally and can show differences depending on ethnic origin. Our results do not match with Japanese and Brazilian results because we could not observe any association between HLA-C12 and early or late onset of psoriasis. In contrast with a Chinese study, we did not observe any association between HLA-C12 and psoriatic arthritis. So, it seems that HLA-C12 may play role as a genetic susceptibility allele in psoriasis in some populations but associations may show differences. These differences may depend on ethnic origin.
In conclusion, we think that HLA-C12 is an important susceptibility allele in the Turkish population for psoriasis and may be associated with high PASI scores. Our study is limited because we could not investigate other related genes and risk factors for severe psoriasis.
The data used to support the findings of this study are available from the corresponding author upon request.
Conflicts of Interest
The authors declare that they have no conflicts of interest.
- C. E. Griffiths and J. N. Barker, “Pathogenesis and clinical features of psoriasis,” The Lancet, vol. 370, no. 9583, pp. 263–271, 2007.
- F. Capon, M. Munro, R. Trembath, and J. Barker, “Searching for the majör susceptibility gene,” Journal of Investigative Dermatology, vol. 118, pp. 745–751, 2002.
- W. Łuszczek, W. Kubicka, M. Cislo et al., “Strong association of HLA-Cw6 allele with juvenile psoriasis in Polish patients,” Immunology Letters, vol. 85, no. 1, pp. 59–64, 2003.
- X.-J. Zhang, P.-P. He, Z.-X. Wang et al., “Evidence for a major psoriasis susceptibility locus at 6p21(PSORS1) and a novel candidate region at 4q31 by genome-wide scan in Chinese hans,” Journal of Investigative Dermatology, vol. 119, no. 6, pp. 1361–1366, 2002.
- N. Kundakci, T. Oskay, U. Olmez et al., “Association of psoriasis vulgaris with HLA class I and class II antigens in the Turkish population, acording to the age of onset,” International Journal of Dermatology, vol. 41, no. 6, pp. 345–348, 2002.
- J. E. Guojónsson, A. Kárason, A. A. Antonsdóttir et al., “HLA-CW6 positive and HLA CW6 negative patients with psoriasis vulgaris have distinct clinical features,” Journal of Investigative Dermatology, vol. 122, pp. 1401–1405, 2002.
- C. Helms, N. L. Saccone, L. Cao et al., “Localization of PSORS1 to a haplotype block harboring HLA-C and distrinct from corneodesmosin and HCR,” Human Genetics, vol. 118, pp. 466–476, 2005.
- N. Kundakci, Ü. Türsen, M. O. A. Babiker, and E. Gürgey, “The evaluation of the sociodemographic and clinical features of Turkish psoriasis patients,” International Journal of Dermatology, vol. 41, no. 4, pp. 220–224, 2002.
- T. Mabuchi, T. Ota, Y. Manabe et al., “HLA⁎C-12.02 is susceptibility factor in late-onset type of psoriasis in Japanese,” The Journal of Dermatology, vol. 41, no. 8, pp. 697–704, 2014.
- A. C. Biral, R. F. Magalhaes, I. J. R. Wastowski et al., “Association of HLA,B,C genes and TNF microsatellite polymorphism with psoriasis vulgaris: a study o genetic risk in Brazilian patients,” European Journal of Rheumatology, vol. 16, pp. 523–529, 2006.
- H. T. Liao, K. C. Lin, Y. T. Chang et al., “Human Leuocyte Antigen and clinical and demographic characteristics in psoriatic arthritis and psoriasis in Chinese patients,” Journal of Rheumatology, vol. 35, pp. 891–895, 2008.
Copyright © 2019 Nahide Onsun 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.