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1.
J Cosmet Dermatol ; 23(5): 1905-1911, 2024 May.
Artículo en Inglés | MEDLINE | ID: mdl-38299446

RESUMEN

BACKGROUND: Psoriasis is an autoimmune disease which has an effect on the joints and skin. Tumor Necrosis Factor-Like Weak Inducer of Apoptosis (TWEAK) is a multi-functional cytokine which regulates the cellular processes and has been related to a variation of conditions. OBJECTIVES: To measure the level of serum TWEAK in psoriatic diseased persons and its relationship to the PASI score pre- and post-therapy with narrowband ultraviolet B phototherapy (NB-UVB) and methotrexate (MTX). METHODS: This randomized controlled trial was conducted on 40 patients and 20 healthy persons as controls. Patient Group was randomly subdivided to two groups. The 1st group consisted of 20 patients who received NB-UVB treatment. The 2nd group included 20 MTX-treated candidates. Blood samples were drawn from patients in order to detect serum TWEAK levels using ELISA. The research was registered on Clinical Trials Registration: RCT approval numbers: NCT0481191. RESULTS: The mean PASI score percent improvement after 12 weeks of treatment was higher in the MTX group (90%) than NB-UVB group (60%). The serum TWEAK level at baseline was 60.47 ± 12.6 pg/mL in NB-UVB group and 54.69 ± 21.7 pg/mL in MTX group which reduced to 24.93 ± 17.6 pg/mL and 32.13 ± 23.6 pg/mL, respectively (p < 0.001), after 12 weeks of treatment. There was a positive correlation between the serum levels of TWEAK and severity of PASI score (r = 0.399, p = 0.014). CONCLUSION: TWEAK grades in psoriasis are substantially higher than in controls. TWEAK levels were dramatically reduced during NB-UVB and MTX treatment. TWEAK may have a potential sign for psoriasis diagnosis and prognosis.


Asunto(s)
Citocina TWEAK , Metotrexato , Psoriasis , Terapia Ultravioleta , Humanos , Psoriasis/sangre , Psoriasis/radioterapia , Psoriasis/terapia , Psoriasis/tratamiento farmacológico , Psoriasis/diagnóstico , Citocina TWEAK/sangre , Metotrexato/administración & dosificación , Metotrexato/uso terapéutico , Terapia Ultravioleta/métodos , Femenino , Masculino , Adulto , Persona de Mediana Edad , Terapia Combinada , Fármacos Dermatológicos/uso terapéutico , Fármacos Dermatológicos/administración & dosificación , Índice de Severidad de la Enfermedad , Resultado del Tratamiento , Adulto Joven
2.
Arch Dermatol Res ; 311(8): 629-636, 2019 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-31236672

RESUMEN

Alopecia areata is a chronic relapsing autoimmune inflammatory hair disorder with no novel therapy. The objectives of this study are to compare the efficacy of topical calcipotriol vs narrow band ultraviolet B phototherapy (NB-UVB) in the treatment of alopecia areata and its correlation with serum vitamin D3 levels. A randomized-controlled trial has been conducted on 60 patients with scalp alopecia areata randomized into four groups; topical calcipotriol, NB-UVB, both and placebo. All patients were evaluated by assessment of severity of alopecia areata by severity of alopecia tool (SALT) score at baseline and 3 months after treatment and vitamin D3 levels at baseline and after 3 months. SALT score and vitamin D3 levels were significantly improved in all groups except placebo after treatment with (P = 0.026, P = 0.005, P = 0.004, P = 0.140) and (P = 0.028, P = 0.011, P = 0.003, P = 0.725), respectively. Combined therapy showed non-significant improvement in SALT score (P = 0.530, P = 0.643), respectively, and significant improvement in serum vitamin D3 levels than each line alone with (P = 0.021, P = 0.044), respectively. Both topical calcipotriol and NB-UVB are effective therapies in the treatment of AA and associated with improvement of SALT score and vitamin D3 levels.


Asunto(s)
Alopecia Areata/terapia , Calcitriol/análogos & derivados , Fármacos Dermatológicos/administración & dosificación , Terapia Ultravioleta/métodos , Administración Tópica , Adolescente , Adulto , Alopecia Areata/sangre , Alopecia Areata/diagnóstico , Calcitriol/administración & dosificación , Colecalciferol/sangre , Terapia Combinada/métodos , Femenino , Humanos , Masculino , Índice de Severidad de la Enfermedad , Resultado del Tratamiento , Adulto Joven
3.
Dermatitis ; 24(6): 296-301, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-24201460

RESUMEN

BACKGROUND: Atopic dermatitis (AD) is a chronic inflammatory skin disorder with an immunologic basis. It may have negative medical and social impacts on a patient and his family. OBJECTIVES: To assess serum level of vitamin D among children with AD and determine its association with AD severity using the AD Scoring System Index. STUDY DESIGN: A case-control study. PATIENTS AND METHODS: Twenty-nine patients with AD in the age group between 2 and 12 years were enrolled in the study. The severity of the disease was determined by the AD scoring system. Thirty controls were recruited. Serum levels of 25-hydroxyvitamin D3 [25(OH)D3] were tested using commercial automated chemiluminescent microparticle immunoassay. RESULTS: The mean value of vitamin D in children with AD was much lower than normal value, and there was a significant difference in the mean values of vitamin D between children with AD (5.4±1.9 ng/mL) and the controls (28.9±2.4 ng/mL). Serum 25(OH)D levels were found to be significantly higher in mild AD (14.6±3.5 ng/mL) compared with moderate (5.5±3.1 ng/mL) or severe AD (0.3±0.1 ng/mL); P<0.001. CONCLUSION: Patients with AD have lower serum vitamin D levels than normal. Vitamin D deficiency might be related to the severity of AD.


Asunto(s)
Dermatitis Atópica/sangre , Índice de Severidad de la Enfermedad , Deficiencia de Vitamina D/diagnóstico , Vitamina D/análogos & derivados , Estudios de Casos y Controles , Niño , Preescolar , Dermatitis Atópica/prevención & control , Suplementos Dietéticos , Femenino , Humanos , Lactante , Masculino , Valores de Referencia , Medición de Riesgo , Vitamina D/sangre , Deficiencia de Vitamina D/sangre
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