The Latest Advances in Pharmacogenetics and Pharmacogenomics in the Treatment of Psoriasis

被引:0
作者
Ryan, Caitriona [2 ]
Menter, Alan [2 ]
Warren, Richard B. [1 ]
机构
[1] Univ Manchester, Manchester Acad Hlth Sci Ctr, Salford Royal NHS Fdn Trust, Dermatol Ctr, Salford M6 8HD, Lancs, England
[2] Baylor Res Inst, Dept Dermatol, Dallas, TX USA
关键词
VITAMIN-D-RECEPTOR; TUMOR-NECROSIS-FACTOR; INTERLEUKIN-12/23; MONOCLONAL-ANTIBODY; SINGLE-NUCLEOTIDE POLYMORPHISMS; FACTOR-ALPHA GENE; RHEUMATOID-ARTHRITIS; CYCLOSPORINE PHARMACOKINETICS; DOUBLE-BLIND; T-CELL; METHOTREXATE THERAPY;
D O I
10.1007/BF03256357
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Systemic and biologic treatments used for the treatment of moderate to severe psoriasis show significant variability in efficacy, are associated with varying degrees of toxicity and, in the case of biologic therapies, are expensive. There is a great need for non-invasive biomarkers to predict treatment outcomes from these therapies and individualize care for psoriasis patients. Identification of pharmacogenetic and pharmacogenomic markers of treatment, response may be useful in predicting clinical response to psoriasis therapies and would help in the development of individually tailored treatment. This would increase the cost effectiveness of treatment and reduce unnecessary exposure to treatment toxicity. This review details the current status of pharmacogenetic and pharmacogenomic markers in psoriasis and explores how these research tools may ultimately lead to safer, more directed treatments. Until now, pharmacogenetic studies in psoriasis have been underpowered to produce reliable results, and many have not recorded treatment response or toxicities prospectively in an objective and reproducible manner. Large-scale collaborations and use of patient registries for systemic and biologic treatments in well characterized patient populations that are uniformly treated and systemically evaluated could play a valuable role in advancing the field of pharmacogenetics and pharmacogenomics of psoriasis.
引用
收藏
页码:81 / 93
页数:13
相关论文
共 114 条
[31]  
Gross C, 1996, J BONE MINER RES, V11, P1850
[32]   Global Gene Expression Analysis Reveals Evidence for Decreased Lipid Biosynthesis and Increased Innate Immunity in Uninvolved Psoriatic Skin [J].
Gudjonsson, Johann E. ;
Ding, Jun ;
Li, Xing ;
Nair, Rajan P. ;
Tejasvi, Trilokraj ;
Qin, Zhaohui S. ;
Ghosh, Debashis ;
Aphale, Abhishek ;
Gumucio, Deborah L. ;
Voorhees, John J. ;
Abecasis, Goncalo R. ;
Elder, James T. .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2009, 129 (12) :2795-2804
[33]   Influence of-308 A/G polymorphism in the tumor necrosis factor α gene on etanercept treatment in rheumatoid arthritis [J].
Guis, Sandrine ;
Balandraud, Nathalie ;
Bouvenot, Julien ;
Auger, Isabelle ;
Toussirot, Eric ;
Wendling, Daniel ;
Mattei, Jean-Pierre ;
Nogueira, Leonor ;
Mugnier, Benedicte ;
Legeron, Pierre ;
Landt, Olfert ;
Serre, Guy ;
Roudier, Jean ;
Roudier, Chantal .
ARTHRITIS & RHEUMATISM-ARTHRITIS CARE & RESEARCH, 2007, 57 (08) :1426-1430
[34]   Long-term prognosis in patients with psoriasis [J].
Gulliver, W. .
BRITISH JOURNAL OF DERMATOLOGY, 2008, 159 :2-9
[35]  
Gulliver W, 2008, BRIT J DERMATOL, V159, P1392
[36]   A novel G/C single-nucleotide polymorphism in the double 28-bp repeat thymidylate synthase allele [J].
Gusella, M. ;
Bolzonella, C. ;
Crepaldi, G. ;
Ferrazzi, E. ;
Padrini, R. .
PHARMACOGENOMICS JOURNAL, 2006, 6 (06) :421-424
[37]   Identification of cellular pathways of "Type 1," Th17 T cells, and TNF- and inducible nitric oxide synthase-producing dendritic cells in autoimmune inflammation through pharmacogenomic study of cyclosporine a in psoriasis [J].
Haider, Asifa S. ;
Lowes, Michelle A. ;
Suarez-Farinas, Mayte ;
Zaba, Lisa C. ;
Cardinale, Irma ;
Khatcherian, Artemis ;
Novitskaya, Inna ;
Wittkowski, Knut M. ;
Krueger, James G. .
JOURNAL OF IMMUNOLOGY, 2008, 180 (03) :1913-1920
[38]   Novel insight into the agonistic mechanism of alefacept in vivo: Differentially expressed genes may serve as biomarkers of response in psoriasis patients [J].
Haider, Asifa S. ;
Lowes, Michelle A. ;
Gardner, Humphrey ;
Bandaru, Raj ;
Darabi, Kamruz ;
Chamian, Francesca ;
Kikuchi, Toyoko ;
Gilleaudeau, Patricia ;
Whalen, Mary S. ;
Cardinale, Irma ;
Novitskaya, Inna ;
Krueger, James G. .
JOURNAL OF IMMUNOLOGY, 2007, 178 (11) :7442-7449
[39]   Vitamin D receptor gene polymorphisms, particularly the novel A-1012G promoter polymorphism, are associated with vitamin D3 responsiveness and non-familial susceptibility in psoriasis [J].
Halsall, JA ;
Osborne, JE ;
Pringle, JH ;
Hutchinson, PE .
PHARMACOGENETICS AND GENOMICS, 2005, 15 (05) :349-355
[40]   A novel polymorphism in the 1A promoter region of the vitamin D receptor is associated with altered susceptibilty and prognosis in malignant melanoma [J].
Halsall, JA ;
Osborne, JE ;
Potter, L ;
Pringle, JH ;
Hutchinson, PE .
BRITISH JOURNAL OF CANCER, 2004, 91 (04) :765-770