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1.
Br J Dermatol ; 169(2): 406-11, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23495851

ABSTRACT

BACKGROUND: Genetic predisposition to psoriasis, an inflammatory skin disease affecting 0·2-4% of the world population, is well established. Thus far, 41 psoriasis susceptibility loci reach genome-wide significance (P ≤ 5 × 10(-8) ). Identification of genetic susceptibility loci in diverse populations will help understand the underlying biology of psoriasis susceptibility. OBJECTIVES: The primary objective of this study was to examine psoriasis susceptibility associations previously reported in Chinese and caucasian populations in a Pakistani cohort. METHODS: Blood samples and phenotype data were collected from psoriasis cases and controls in Islamabad, Pakistan. DNA was isolated and genotypes of selected susceptibility markers were determined. The data were analysed using χ(2) tests or logistic regression for psoriasis association. RESULTS: HLA-Cw6 showed the strongest association [odds ratio (OR) 2·43, P = 2·3 × 10(-12) ]. HLA-Cw1 showed marginally significant association (OR 1·66, P = 0·049), suggesting that the HLA-Cw1-B46 risk haplotype may be present in the Pakistani population. Three other loci (IL4/IL13, NOS2, TRAF3IP2) showed nominally significant association (P < 0·05). CONCLUSIONS: HLA-Cw6 is strongly associated with psoriasis susceptibility in the Pakistani population, as has been found in every other population studied. In addition, HLA-Cw1 showed marginal association, reflecting the relative geographical proximity and thus likely genetic relatedness to other populations in which the HLA-Cw1-B46 haplotype is known to be associated. A larger cohort and a denser marker set will be required for further analysis of psoriasis associations in the South Asian population.


Subject(s)
Genetic Loci/genetics , Psoriasis/genetics , Adaptor Proteins, Signal Transducing , Adult , Age of Onset , Female , Genetic Predisposition to Disease/genetics , Genome-Wide Association Study , Genotype , HLA-C Antigens/genetics , Haplotypes , Humans , Interleukin-13/genetics , Male , Nitric Oxide Synthase Type II/genetics , Pakistan/ethnology , Polymorphism, Single Nucleotide , Tumor Necrosis Factor Receptor-Associated Peptides and Proteins/genetics
2.
Br J Dermatol ; 135(1): 86-8, 1996 Jul.
Article in English | MEDLINE | ID: mdl-8776365

ABSTRACT

We report a randomized, double-blind study, comparing the relative efficacy and tolerability of oral terbinafine, given for 1, 2 or 4 weeks, in tinea capitis. Of 161 evaluable patients, 53 were treated with terbinafine for 1 week, 51 for 2 weeks and 57 for 4 weeks. Isolated pathogens included Trichophyton violaceum (71.5%), T. tonsurans (14.9%), T. verrucosum (4.3%), Microsporum audouinii (4.3%), M. canis (2.5%), T. schoenleinii (1.9%) and T. mentagrophytes (0.6%). The final evaluation, at 12 weeks, showed cure rates of 73.6, 80.4 and 85.9%, in the respective groups. The adverse effects noted, were not drug related. In our opinion, terbinafine given for 1, 2 or 4 weeks, is equally effective for most cases of tinea capitis.


Subject(s)
Antifungal Agents/administration & dosage , Naphthalenes/administration & dosage , Tinea Capitis/drug therapy , Adolescent , Antifungal Agents/therapeutic use , Child , Child, Preschool , Double-Blind Method , Drug Administration Schedule , Female , Follow-Up Studies , Fungi/isolation & purification , Humans , Male , Naphthalenes/therapeutic use , Terbinafine , Tinea Capitis/microbiology , Treatment Outcome
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