The primary objective of this mentored career development award in patient-oriented research is for the candidate, Dr. Wynnis Tom, to acquire the skills and expertise to become an independent investigator leading clinical and genetic studies on pediatric inflammatory skin diseases, particularly psoriasis. Under the direction of Drs. Jane Burns and Kelly Frazer, the candidate has constructed a focused training program that includes intensive coursework and research training. The didactic component will include formal coursework on human genetics and genomics, clinical and translational research, biostatistics, and ethics, along with weekly seminars, regular face-to-face mentor meetings and participation in weekly laboratory meetings. In addition, this career development program will benefit from the oversight of a carefully selected Advisory Committee of senior research scientists with expertise in genetic analysis of complex human diseases, recruitment and study of large pediatric and parent cohorts, and clinical and translational research. The research for this proposal consists of a comparative study of gene expression profiles in children and adults with psoriasis and a prospective cohort study that will investigate single nucleotide polymorphisms (SNPs) in candidate susceptibility genes as prognostic markers for pediatric psoriasis patients. The three specific aims are: 1) To compare expression in lesional and unaffected or normal skin obtained from healthy children, children with psoriasis, adults with childhood-onset psoriasis, and adults with adult-onset psoriasis;2) To analyze SNPs in 14 genes previously associated with adult psoriasis and SNPs in 14 genes in the calcineurin/NFAT pathway in pediatric psoriasis subjects and their biological parents;and 3) To stratify genetic analysis by subject response to therapy and disease severity. The proposed studies will reveal how molecular pathways and genetic influences may be similar or different in pediatric psoriasis patients as compared to adults. Results may identify additional targets for drug development and predictors of disease course and response to pharmacotherapy in young patients suffering from psoriasis.
The proposed research will study psoriasis in children to look for how skin disease comes about and genes that affect the likelihood to have disease. This information may help to better direct the care of affected children.
|Becker, Lauren; Tom, Wynnis L; Eshagh, Karin et al. (2014) Excess adiposity preceding pediatric psoriasis. JAMA Dermatol 150:573-4|
|Eichenfield, Lawrence F; Tom, Wynnis L; Berger, Timothy G et al. (2014) Guidelines of care for the management of atopic dermatitis: section 2. Management and treatment of atopic dermatitis with topical therapies. J Am Acad Dermatol 71:116-32|
|Eichenfield, Lawrence F; Tom, Wynnis L; Chamlin, Sarah L et al. (2014) Guidelines of care for the management of atopic dermatitis: section 1. Diagnosis and assessment of atopic dermatitis. J Am Acad Dermatol 70:338-51|
|Sidbury, Robert; Davis, Dawn M; Cohen, David E et al. (2014) Guidelines of care for the management of atopic dermatitis: section 3. Management and treatment with phototherapy and systemic agents. J Am Acad Dermatol 71:327-49|
|Munden, A; Butschek, R; Tom, W L et al. (2014) Prospective study of infantile haemangiomas: incidence, clinical characteristics and association with placental anomalies. Br J Dermatol 170:907-13|
|Mercy, Katherine; Kwasny, Mary; Cordoro, Kelly M et al. (2013) Clinical manifestations of pediatric psoriasis: results of a multicenter study in the United States. Pediatr Dermatol 30:424-8|
|Paller, Amy S; Mercy, Katherine; Kwasny, Mary J et al. (2013) Association of pediatric psoriasis severity with excess and central adiposity: an international cross-sectional study. JAMA Dermatol 149:166-76|
|Caufield, Maura; Tom, Wynnis L (2013) Oral azathioprine for recalcitrant pediatric atopic dermatitis: clinical response and thiopurine monitoring. J Am Acad Dermatol 68:29-35|