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1.
Dermatol Ther ; 30(2)2017 Mar.
Article in English | MEDLINE | ID: mdl-27998025

ABSTRACT

New treatment modalities for vitiligo acting by changing certain cytokines and metalloproteinases are newly emerging. The aim of this work is to To assess the efficacy of trichloroacetic acid (TCA) chemical peel, dermapen, and fractional CO2 laser in treatment of stable non-segmental vitiligo and to detect their effects on IL-17 and MMP-9 levels. Thirty patients with stable vitiligo were recruited in a randomized controlled study. They were randomly categorized into three equal groups. Group 1: TCA peel, Group 2: dermapen machine, and Group 3: Fractional CO2 laser. Skin biopsies were taken from treated areas and from control areas for which MMP-9 and IL-17 tissue levels were measured using ELISA. The 30 vitiligo patients had low basal tissue MMP-9 levels and high baseline IL-17 tissue levels. As regards the three different used modalities, all of them caused rise in MMP-9 as well as IL-17 levels and almost their levels were much more elevated with repetition of the previously mentioned traumatic procedures. TCA 25% peel proved to be the most effective modality both clinically and laboratory and it can be used prior or with other conventional therapies in the treatment of vitiligo.


Subject(s)
Caustics/administration & dosage , Chemexfoliation , Cosmetic Techniques , Lasers, Gas/therapeutic use , Low-Level Light Therapy/instrumentation , Skin Pigmentation , Skin , Trichloroacetic Acid/administration & dosage , Vitiligo/therapy , Administration, Cutaneous , Adolescent , Adult , Biopsy , Caustics/adverse effects , Chemexfoliation/adverse effects , Cosmetic Techniques/adverse effects , Cosmetic Techniques/instrumentation , Egypt , Female , Humans , Interleukin-17/metabolism , Lasers, Gas/adverse effects , Low-Level Light Therapy/adverse effects , Male , Matrix Metalloproteinase 9/metabolism , Middle Aged , Miniaturization , Needles , Skin/drug effects , Skin/enzymology , Skin/immunology , Skin/radiation effects , Skin Pigmentation/drug effects , Skin Pigmentation/radiation effects , Time Factors , Treatment Outcome , Trichloroacetic Acid/adverse effects , Vitiligo/diagnosis , Vitiligo/enzymology , Vitiligo/immunology , Young Adult
2.
Dermatol Ther ; 29(6): 406-412, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27528547

ABSTRACT

Pathogenesis of vitiligo is believed to be multifactorial disease with a wide variety of therapeutic modalities. The aim of this work is to assess the efficacy of oral mini-pulse steroids (OMP) plus Nb-U.V.B in comparison to OMP alone and Nb-U.V.B alone in treating stable vitiligo. A prospective randomized controlled study including 45 patients categorized into three groups receiving therapy for 3 months; Group A received Nb-U.V.B plus OMP, Group B received OMP alone while Group C received Nb-U.V.B alone. Clinical assessment and PCR evaluation of bFGF, ICAM1, and ELISA for AMA were done. Patients receiving Nb-U.V.B plus OMP and using Nb-U.V.B alone gave statistically significant clinical response than those treated with OMP alone. Statistically significant rise of BFGF was noticed after treatment with Nb-U.V.B plus OMP and with Nb-U.V.B alone. Patients treated with OMP alone and with Nb-U.V.B alone showed statistically significant drop of ICAM-1 after therapy. NB-U.V.B plus OMP and Nb-U.V.B alone were found to be clinically superior over OMP alone in treating stable vitiligo patients, hence suggesting that adding OMP to Nb-U.V.B can maintain clinical and laboratory success for a longer period of time and with less relapse.


Subject(s)
Glucocorticoids/administration & dosage , Prednisone/administration & dosage , Skin Pigmentation/drug effects , Skin Pigmentation/radiation effects , Ultraviolet Therapy , Vitiligo/therapy , Administration, Oral , Adolescent , Adult , Aged , Autoantibodies/blood , Combined Modality Therapy , Egypt , Female , Fibroblast Growth Factor 2/genetics , Glucocorticoids/adverse effects , Humans , Intercellular Adhesion Molecule-1/genetics , Male , Middle Aged , Prednisone/adverse effects , Prospective Studies , Pulse Therapy, Drug , Time Factors , Treatment Outcome , Ultraviolet Therapy/adverse effects , Vitiligo/blood , Vitiligo/genetics , Vitiligo/physiopathology , Young Adult
3.
Int J Dermatol ; 55(12): 1329-1335, 2016 Dec.
Article in English | MEDLINE | ID: mdl-27420410

ABSTRACT

BACKGROUND: Vitiligo is an autoimmune depigmentation disorder. Polymorphisms in the vitamin D receptor (VDR) have been found to be associated with vitiligo. OBJECTIVES: To evaluate the potential association between VDR gene polymorphisms (ApaI, TaqI, and FokI) and vitiligo susceptibility, and to detect if there is correlation between serum 25-hydroxyvitamin D [25(OH)D] levels and vitiligo and between VDR gene polymorphisms and 25(OH)D levels in vitiligo. MATERIALS AND METHODS: Seventy-five patients with vitiligo and 75 age and sex-matched controls were subjected to detailed history taking and dermatological examination to determine the extent and clinical type of vitiligo. A blood sample (5 ml) was retrieved to investigate VDR gene polymorphisms and serum 25(OH)D level. RESULTS: Our results showed that the serum level of vitamin D is statistically significantly lower in patients than controls. The frequency of the ApaI variant a allele, the variant genotype (aa), and the variant genotype (tt) were significantly higher among the vitiligo cases than among controls. Our study also showed that the serum 25(OH)D levels were not significantly different among the different ApaI, TaqI, and FokI genotypes. CONCLUSION: The present study showed that serum level of 25(OH)D is statistically significantly lower in patients than controls, so screening for vitamin D deficiency seems of value in patients with vitiligo for the possibility of vitamin D supplementation. We also report that VDR gene polymorphisms may be a risk for the development of vitiligo in an Egyptian population.


Subject(s)
Genetic Predisposition to Disease , Receptors, Calcitriol/genetics , Vitamin D/analogs & derivatives , Vitiligo/blood , Vitiligo/genetics , Adolescent , Adult , Aged , Case-Control Studies , Egypt , Gene Frequency , Genotype , Humans , Middle Aged , Polymorphism, Genetic , Vitamin D/blood , Young Adult
4.
J Dermatolog Treat ; 23(1): 4-10, 2012 Feb.
Article in English | MEDLINE | ID: mdl-20819024

ABSTRACT

BACKGROUND: The most serious side effects of systemic steroids include osteoporosis and suprarenal suppression. Many steroid regimens have been suggested to minimize these side effects; one of them is oral steroid pulse therapy. OBJECTIVE: To compare the side effects of a daily oral steroid regimen versus a weekly oral steroid pulse regimen on bone mineral density and suprarenal suppression. METHODS: Thirty patients with different skin diseases were divided into two groups: 15 for oral daily steroids (ODS) (group 1) and 15 for weekly oral pulse steroids (WOPS) (group 2). They were evaluated for bone mineral density (measured by DEXA) and suprarenal suppression (measured by serum cortisol level), morphological changes and blood sugar. Treatment was continued for 6 months to 3 years. RESULTS: Cushingoid features in group 1 were observed in 73%, yet they were not detectable in group 2. Disturbed blood sugar in group 1 was 33% and 0% in group 2. The serum cortisol level was lower in patients on ODS than those on WOPS. The effect of WOPS on bone mineral density was very limited in comparison with the ODS. CONCLUSION: Weekly oral steroid pulse therapy induces no significant bone loss and no suprarenal suppression and can be an alternative option in the treatment of chronic disorders requiring long-term oral steroid therapy.


Subject(s)
Adrenal Glands/drug effects , Blood Glucose/drug effects , Bone Density/drug effects , Glucocorticoids/administration & dosage , Prednisone/administration & dosage , Administration, Oral , Adult , Aged , Cushing Syndrome/chemically induced , Diabetes Mellitus/chemically induced , Drug Administration Schedule , Female , Glucocorticoids/adverse effects , Glucocorticoids/pharmacology , Humans , Hydrocortisone/blood , Hyperglycemia/chemically induced , Male , Middle Aged , Prednisone/adverse effects , Prednisone/pharmacology , Young Adult
5.
J Am Acad Dermatol ; 63(2): 259-65, 2010 Aug.
Article in English | MEDLINE | ID: mdl-20462666

ABSTRACT

BACKGROUND: Leukocytoclastic vasculitis (LCV) and necrolytic acral erythema (NAE) are skin disorders associated with hepatitis C virus (HCV) infection. However, they have not been found to occur simultaneously in the same patient. OBJECTIVE: We sought to analyze the role of serum HCV-RNA levels and HCV genotype in the pathogenesis of both LCV and NAE in an attempt to assess whether these two parameters play a role in mutual exclusivity of LCV and NAE in the same patient. METHODS: The study included 11 patients with LCV and 13 with NAE, all of whom were infected with HCV. All 24 patients were evaluated for the quantitative levels of HCV-RNA, using real-time polymerase chain reaction. HCV genotyping was performed on 10 patients in each group (N = 20). RESULTS: Patients with LCV had a higher prevalence of moderate and high levels of HCV-RNA viremia (P = .038) than those with NAE. However, there was no significant difference in HCV genotype between LCV and NAE groups (P = .211). LIMITATIONS: Small number of cases is a limitation. CONCLUSION: Viral load seems to play a role in determining the response of the skin to HCV infection. High levels of HCV viremia were found to be significantly associated with LCV but not with NAE. HCV viremia may play a role in the development of LCV in HCV-infected patients.


Subject(s)
Erythema/epidemiology , Erythema/virology , Hepacivirus/genetics , Hepatitis C, Chronic/epidemiology , Vasculitis, Leukocytoclastic, Cutaneous/epidemiology , Vasculitis, Leukocytoclastic, Cutaneous/virology , Adult , Erythema/pathology , Female , Genotype , Hepacivirus/growth & development , Humans , Male , Middle Aged , Necrosis , Prevalence , RNA, Viral/genetics , Reverse Transcriptase Polymerase Chain Reaction , Skin/pathology , Untranslated Regions/genetics , Vasculitis, Leukocytoclastic, Cutaneous/pathology , Viral Load , Viremia/epidemiology , Young Adult
6.
J Dermatol Sci ; 54(2): 76-87, 2009 May.
Article in English | MEDLINE | ID: mdl-19303745

ABSTRACT

OBJECTIVES: To build a critical appraisal of the available literature to evaluate the effectiveness of topical calcineurin inhibitors in treatment of atopic dermatitis (AD), in comparison to topical corticosteroids (TCs) and/or placebo. DESIGN: systematic review and meta-analysis. DATA SOURCES: electronic search of MEDLINE Pubmed along the last 10 years (1997-2006). STUDY SELECTION: randomized control trials of TCIs reporting efficacy outcomes, in comparison to TCs or vehicle (placebo) or both. DATA SYNTHESIS: of 210 articles, 19 studies were included, 10 for tacrolimus and 9 for pimecrolimus, involving 7378 patients of whom 2771 applied tacrolimus, 1783 applied pimecrolimus, and 2824 were controls. Both drugs were significantly more effective than a vehicle. However, two long-term trials comparing demonstrated the value of pimecrolimus in reduction of flares and steroid-sparing effect after 6 months. Compared to TCs, both 0.1% and 0.03% tacrolimus ointments were as effective as moderate potency TCs, and more effective than a combined steroid regimen. Tacrolimus was more effective than mild TCs. CONCLUSIONS: TCIs in AD are more effective than placebo. Although less effective than TCs, pimecrolimus has its value in long-term maintenance and as a steroid-sparing agent in AD, whenever used early enough, at first appearance of erythema and/or itching. In treatment of moderate to severe AD, topical tacrolimus is as effective as moderately potent TCs, and more effective than mild preparations. Chronic AD lesions of the face and flexures are the most justified indication for topical calcineurin inhibitors.


Subject(s)
Calcineurin Inhibitors , Dermatitis, Atopic/drug therapy , Enzyme Inhibitors/therapeutic use , Immunosuppressive Agents/therapeutic use , Tacrolimus/analogs & derivatives , Tacrolimus/therapeutic use , Adrenal Cortex Hormones/therapeutic use , Dermatitis, Atopic/immunology , Humans
7.
Photodermatol Photoimmunol Photomed ; 24(5): 256-9, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18811867

ABSTRACT

BACKGROUND: Psoriasis is a common and relapsing disease, which is both physically and psychologically disabling. Narrowband UVB (NB-UVB) is used in fair-skinned population in suberythemogenic doses with good results; however, in the darker skin population (skin types III, IV, V) erythemogenic doses have not been thoroughly investigated. AIM: A left-right bilateral comparative trial was carried out to compare the suberythemogenic dose of NB-UVB vs. erythemogenic dose in the treatment of dark-skinned psoriatic patients. PATIENTS AND METHODS: The study was conducted on 20 patients with chronic plaque psoriasis. The left side was treated with the dose causing minimal erythema [100% of minimal erythema dose (MED)] while the right side received 70% of this MED (suberythemogenic side). RESULTS: Our results revealed no statistically significant difference in PASI final and in the percentage of reduction of PASI score between both sides as well as the total number of sessions (P-value>0.05), while the total cumulative UVB dose on the suberythemogenic side was significantly lower (P-value<0.001). CONCLUSION: Our study recommends reducing the dose regimen of NB-UVB and consequently the cumulative UVB dose by using the suberythemogenic dosing schedule even in dark skin population.


Subject(s)
Psoriasis/therapy , Skin Pigmentation , Ultraviolet Rays , Ultraviolet Therapy , Adult , Aged , Chronic Disease , Female , Humans , Male , Middle Aged , Ultraviolet Therapy/methods
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