Skip to main content
Log in

A Pharmacogenetic Study of Psoriasis Risk Variants in a Greek Population and Prediction of Responses to Anti-TNF-α and Anti-IL-12/23 Agents

  • Short Communication
  • Published:
Molecular Diagnosis & Therapy Aims and scope Submit manuscript

Abstract

Introduction

Psoriasis is a highly divergent disease with many disease phenotypes, but there are currently no established biomarkers to predict the therapeutic outcomes of systemic treatments. With the introduction of biologic therapies during the last decade and with new treatments constantly emerging, there is a great need to validate biomarkers that have been reported to be associated with treatment response, and to introduce new biomarkers of possible clinical value.

Methods

In the current study, we aimed to investigate the association of psoriasis-related polymorphisms that have previously been reported to effect the anti-tumor necrosis factor alpha (anti-TNF-α) therapies (etanercept, adalimumab, and infliximab) and anti-interleukin-12/23 (anti-IL-12/23) biologic therapy (ustekinumab) in a Greek cohort of psoriasis patients.

Results

Rs10484554 in the HLA-C gene showed an association with a good response to anti-TNF-α agents but not to ustekinumab, while rs151823 and rs26653 in the ERAP1 gene showed associations with a good response to anti-IL-12/23 therapy.

Conclusion

This study is the first in the field of pharmacogenetics in Greek psoriasis patients. Further, larger studies are required to validate our findings and replicate them in various populations.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

References

  1. Strange A, Capon F, Spencer CC, et al. A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. Nat Genet. 2010;42:985–90.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Yin X, Low HQ, Wang L, et al. Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility. Nat Commun. 2015;6:6916.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Sun LD, Cheng H, Wang ZX, et al. Association analyses identify six new psoriasis susceptibility loci in the Chinese population. Nat Genet. 2010;42:1005–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Julia A, Tortosa R, Hernanz JM, et al. Risk variants for psoriasis vulgaris in a large case–control collection and association with clinical subphenotypes. Hum Mol Genet. 2012;21:4549–57.

    Article  CAS  PubMed  Google Scholar 

  5. Masouri S, Stefanaki I, Kypreou KP, et al. Replication of risk variants for psoriasis in a Southern European case–control study: correlation with clinical subphenotypes. Br J Dermatol. 2015;173:552–4.

    Article  CAS  PubMed  Google Scholar 

  6. Vasilopoulos Y, Manolika M, Zafiriou E, et al. Pharmacogenetic analysis of TNF, TNFRSF1A, and TNFRSF1B gene polymorphisms and prediction of response to anti-TNF therapy in psoriasis patients in the Greek population. Mol Diagn Ther. 2012;16:29–34.

    Article  CAS  PubMed  Google Scholar 

  7. Tejasvi T, Stuart PE, Chandran V, et al. TNFAIP3 gene polymorphisms are associated with response to TNF blockade in psoriasis. J Invest Dermatol. 2012;132:593–600.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Gallo E, Cabaleiro T, Román M, et al. The relationship between tumour necrosis factor (TNF)-α promoter and IL12B/IL-23R genes polymorphisms and the efficacy of anti-TNF-α therapy in psoriasis: a case–control study. Br J Dermatol. 2013;169:819–29.

    Article  CAS  PubMed  Google Scholar 

  9. Prieto-Pérez R, Cabaleiro T, Daudén E, et al. Gene polymorphisms that can predict response to anti-TNF therapy in patients with psoriasis and related autoimmune diseases. Pharmacogenomics J. 2013;13:297–305.

    Article  PubMed  Google Scholar 

  10. Prieto-Pérez R, Cabaleiro T, Daudén E, et al. Genetics of psoriasis and pharmacogenetics of biological drugs. Autoimmune Dis. 2013;2013:613086.

    PubMed  PubMed Central  Google Scholar 

  11. Talamonti M, Botti E, Galluzzo M, et al. Pharmacogenetics of psoriasis: HLA-Cw6 but not LCE3B/3C deletion nor TNFAIP3 polymorphism predisposes to clinical response to interleukin 12/23 blocker ustekinumab. Br J Dermatol. 2013;169:458–63.

    Article  CAS  PubMed  Google Scholar 

  12. Lysell J, Padyukov L, Kockum I, et al. Genetic association with ERAP1 in psoriasis is confined to disease onset after puberty and not dependent on HLA-C*06. J Invest Dermatol. 2013;133:411–7.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Liu Y, Helms C, Liao W, et al. A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci. PLoS Genet. 2008;4:e1000041.

    Article  PubMed  PubMed Central  Google Scholar 

  14. Galluzzo M, Boca AN, Botti E et al. IL12B (p40) gene polymorphisms contribute to ustekinumab response prediction in psoriasis. Dermatology. 2016;232. doi:10.1159/000441719.

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Sofia Masouri.

Ethics declarations

Conflict of interest

The authors—Sofia Masouri, Irene Stefanaki, Giorgos Ntritsos, Katerina P. Kypreou, Eleni Drakaki, Evangelos Evangelou, Electra Nicolaidou, Alexandros John Stratigos, and Christina Antoniou—have no conflicts of interest that are directly relevant to the content of this study.

Funding

There was no funding for this study.

Ethical Approval and Informed Consent

The Scientific and Ethics Committee of Andreas Sygros Hospital (Athens, Greece) approved the research protocol for this study (ethics approval number 3049). All participants gave written informed consent for their participation in the study.

Additional information

S. Masouri and I. Stefanaki equally contributed to the study.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary material 1 (DOCX 12 kb)

Supplementary material 2 (DOCX 11 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Masouri, S., Stefanaki, I., Ntritsos, G. et al. A Pharmacogenetic Study of Psoriasis Risk Variants in a Greek Population and Prediction of Responses to Anti-TNF-α and Anti-IL-12/23 Agents. Mol Diagn Ther 20, 221–225 (2016). https://doi.org/10.1007/s40291-016-0198-z

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s40291-016-0198-z

Keywords

Navigation