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1.
Arch Dermatol Res ; 310(5): 425-430, 2018 Jul.
Article in English | MEDLINE | ID: mdl-29605863

ABSTRACT

Recently, multiple culprits-in addition to melanocytes-have been implicated in the pathogenesis of vitiligo. Among those factors are fibroblasts. However, their exact role has not been clearly elucidated. The aim of the study was to evaluate the possible role played by fibroblasts in vitiligo via studying the expression Tenascin C and DKK1 in acral versus non-acral vitiligo lesions. This case-control study included 19 non-segmental vitiligo patients and ten controls. All patients were subjected to thorough clinical evaluation. Both Tenascin C and DKK1 were measured in lesional and peri-lesional skin of acral and non-acral lesions using ELISA technique. The measured levels of Tenascin C and DKK1 were significantly higher in the vitiligo group when compared to controls in all assessed sites (P < 0.05). Tenascin C was found to be significantly higher in lesional areas compared to peri-lesional ones only in the acral sites. DKK1 was significantly higher in lesional areas in all assessed sites (P < 0.05). The current work suggests a malfunction of fibroblasts in vitiligo, through demonstrating significant up-regulation of two melanogenesis inhibitory products (Tenascin C and DKK1) in patients compared to controls. Larger scale studies are warranted to detect the possible implications of such findings on vitiligo treatment.


Subject(s)
Fibroblasts/metabolism , Intercellular Signaling Peptides and Proteins/metabolism , Melanocytes/pathology , Skin/metabolism , Tenascin/metabolism , Vitiligo/metabolism , Adult , Case-Control Studies , Female , Fibroblasts/pathology , Humans , Hypopigmentation , Intercellular Signaling Peptides and Proteins/genetics , Male , Middle Aged , Skin/pathology , Tenascin/genetics , Vitiligo/pathology , Young Adult
2.
J Cosmet Dermatol ; 16(2): 258-264, 2017 Jun.
Article in English | MEDLINE | ID: mdl-28382785

ABSTRACT

BACKGROUND: The escalating urge for a youthful-looking skin instigates continuous innovations with minimally invasive procedures. Readymade growth factors and autologous platelet-rich plasma (PRP) represent such therapeutic interventions. OBJECTIVE: Compare the efficacy and safety of PRP to readymade growth factors in skin rejuvenation. PATIENTS AND METHODS: Twenty adult females with Fitzpatrick skin types III-IV and Glogau photoaging types II and III were enrolled in this study. They underwent a split face therapy where each side was randomly assigned to treatment by either readymade growth factors (area A) or autologous PRP (area B). All patients received six sessions at 2-weeks interval. Evaluation was carried out using Global Aesthetic Improvement Scale (GAIS) and optical coherence tomography (OCT). Patients were followed up for 6 months. RESULTS: Both procedures yielded significant improvement regarding both GAIS (skin turgor and overall vitality) and OCT (epidermal and dermal thickness) assessment. Significant negative correlation was detected between patients' age, sun exposure, and GAIS. Burning sensation was significantly higher in area A. Patient satisfaction was significantly higher in area B. Improvement was more sustained in area B on follow-up. CONCLUSION: Platelet-rich plasma is effective and safe for skin rejuvenation, comparable to readymade growth factors with noticeable higher longevity.


Subject(s)
Cosmetic Techniques , Intercellular Signaling Peptides and Proteins , Platelet-Rich Plasma , Rejuvenation , Skin , Adult , Female , Humans , Middle Aged , Prospective Studies
3.
Acta Dermatovenerol Croat ; 23(3): 165-70, 2015.
Article in English | MEDLINE | ID: mdl-26476899

ABSTRACT

Psoriasis is a chronic inflammatory dermatosis that has a substantial impact on the quality of life. Goeckerman's technique (GT) has been implemented for the treatment of psoriasis with high clearance rates and long periods of remission. The objective of this article was to evaluate the efficacy and safety of modified GT (crude coal tar 2.5% plus UVA) as an alternative therapeutic modality for psoriatic patients with skin types III-V. Twenty two patients with moderate, severe, and erythrodermic psoriasis were included in this study. All patients received modified GT (crude coal tar 2.5% plus UVA) six days per week for a period of 3 months. Assessment of the rate of reduction of psoriasis area severity index (PASI) was performed, as well as photographic documentation of each patient at baseline and after completion of therapy. There was a significant reduction in PASI scores after therapy in all patients (P=0.001). The rate of PASI reduction after therapy was >50% in 63.6% of patients; 27.3% of patients achieved >75% reduction and 9.1% of patients achieved 26-50% reduction. No serious side effects were reported in any of the patients. Modified GT is a safe and effective therapeutic option for patients with moderate and severe psoriasis.


Subject(s)
Coal Tar/therapeutic use , Keratolytic Agents/therapeutic use , Psoriasis/drug therapy , Psoriasis/radiotherapy , Ultraviolet Rays , Ultraviolet Therapy/methods , Adolescent , Adult , Chronic Disease , Combined Modality Therapy , Female , Humans , Male , Middle Aged , Prospective Studies , Quality of Life , Severity of Illness Index , Treatment Outcome
4.
Arch Dermatol Res ; 307(4): 299-307, 2015 May.
Article in English | MEDLINE | ID: mdl-25450635

ABSTRACT

T helper (Th)1 insufficiency was recently found to be related to the pathogenesis of pemphigus vulgaris (PV). Decreased Th1 response was particularly noticed in the early stages of PV. Therefore, administration of interferon alpha in the early stages of aggressive PV may lead to rapid control of the acute stage of the disease. Our aim was to evaluate the role of interferon alpha in the treatment of PV. 30 patients with acute severe PV (>60 % affection) and 30 age and sex-matched healthy subjects were included in this RCT. Patients were randomly divided into two groups (A and B). Group B patients received interferon retard (one subcutaneous injection/week for 4 weeks) in addition to our protocol for the treatment of PV (systemic pulse corticosteroids/cyclophosphamide in combination with sulphasalazine and pentoxifylline) that was administered to all the included patients. IFN-γ and IL-4 were estimated by ELISA before treatment, after 4 weeks and at the end of the study duration (12 weeks). Clinical assessment was done by PAAS on a biweekly basis. All PV patients showed significantly (P < 0.001) elevated levels of IL-4 and significantly (P < 0.001) depressed mean concentration of IFN-γ as compared with healthy controls. Twelve weeks after therapy both groups showed significant improvement in their mean PAAS being more evident and more rapid in group B. IFN-γ was elevated significantly and IL-4 was dropped significantly in group B patients in comparison to group A (P < 0.001). As a conclusion, interferon therapy in severe PV could achieve a more prompt and better clinical response.


Subject(s)
Immunologic Factors/therapeutic use , Interferon-alpha/therapeutic use , Pemphigus/drug therapy , Pemphigus/immunology , Th1 Cells/immunology , Th2 Cells/immunology , Adult , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Cyclophosphamide/therapeutic use , Drug Therapy, Combination , Enzyme-Linked Immunosorbent Assay , Female , Glucocorticoids/therapeutic use , Humans , Immunosuppressive Agents/therapeutic use , Interferon alpha-2 , Interferon-gamma/blood , Interleukin-4/blood , Male , Middle Aged , Pentoxifylline/therapeutic use , Phosphodiesterase Inhibitors/therapeutic use , Recombinant Proteins/therapeutic use , Sulfasalazine/therapeutic use
5.
PLoS One ; 9(6): e99286, 2014.
Article in English | MEDLINE | ID: mdl-24915010

ABSTRACT

Vitiligo is the most common depigmentation disorder of the skin. Oxidative stress is implicated as one of the probable events involved in vitiligo pathogenesis possibly contributing to melanocyte destruction. Evidence indicates that certain genes including those involved in oxidative stress and melanin synthesis are crucial for development of vitiligo. This study evaluates the oxidative stress status, the role of catalase (CAT) and catechol-O-Methyltransferase (COMT) gene polymorphisms in the etiology of generalized vitiligo in Egyptians. Total antioxidant capacity (TAC) and malondialdehyde (MDA) levels as well as CAT exon 9 T/C and COMT 158 G/A polymorphisms were determined in 89 patients and 90 age and sex-matched controls. Our results showed significantly lower TAC along with higher MDA levels in vitiligo patients compared with controls. Meanwhile, genotype and allele distributions of CAT and COMT polymorphisms in cases were not significantly different from those of controls. Moreover, we found no association between both polymorphisms and vitiligo susceptibility. In conclusion, the enhanced oxidative stress with the lack of association between CAT and COMT polymorphisms and susceptibility to vitiligo in our patients suggest that mutations in other genes related to the oxidative pathway might contribute to the etiology of generalized vitiligo in Egyptian population.


Subject(s)
Catalase/genetics , Catechol O-Methyltransferase/genetics , Genetic Predisposition to Disease , Oxidative Stress/genetics , Polymorphism, Single Nucleotide/genetics , Vitiligo/enzymology , Vitiligo/genetics , Adult , Antioxidants/metabolism , Biomarkers/metabolism , Case-Control Studies , Demography , Egypt , Exons/genetics , Female , Gene Frequency/genetics , Humans , Male , Malondialdehyde/metabolism , Risk Factors
6.
J Immunol Res ; 2014: 380405, 2014.
Article in English | MEDLINE | ID: mdl-25759827

ABSTRACT

BACKGROUND: Tumor necrosis factor-alpha (TNF-α) is an important proinflammatory cytokine which plays an important role in the immunopathogenesis of Behcet's disease (BD). B cell activating factor (BAFF) and its homolog A proliferation inducing ligand (APRIL) are members of the tumor necrosis factor family. BAFF binds to 3 receptors, B cell activating factor receptor (BAFF-R), transmembrane activator and calcium modulator ligand interactor (TACI), and B cell maturation antigen (BCMA) that are expressed by B cells. OBJECTIVE: Estimation of the serum levels of TNF-α, APRIL, BAFF, and BCMA in patients with BD in an effort to evaluate their degree of involvement in the pathogenesis and development of BD. PATIENTS AND METHODS: This study included 30 male patients fulfilling the international study group criteria for the diagnosis of BD. Twenty age-matched healthy male volunteers served as control. Serum samples were used for quantification of TNF-α, APRIL, BCMA, BAFF, and hsCRP using ELISA techniques. RESULTS: The mean serum levels of TNF-α, APRIL, BCMA, and BAFF were more elevated in cases than in controls in a statistically significant manner (P < 0.001). Positive correlation was observed between hs-CRP and BDCAF (Behcet's disease current activity forum) index (r 0.68, P < 0.001). None of the TNF family members tested was affected by a positive pathergy test. CONCLUSIONS: Patients have significantly higher levels of TNF family members' (TNF-α, BAFF, APRIL, and BCMA) compared to controls which might contribute to the pathogenesis of BD.


Subject(s)
B-Lymphocytes/immunology , Behcet Syndrome/diagnosis , Biomarkers/blood , Adolescent , Adult , B-Cell Activating Factor/blood , Behcet Syndrome/immunology , C-Reactive Protein/metabolism , Diphenylamine/analogs & derivatives , Diphenylamine/blood , Humans , Male , Middle Aged , Transmembrane Activator and CAML Interactor Protein/blood , Tumor Necrosis Factor Ligand Superfamily Member 13/blood , Tumor Necrosis Factor-alpha/blood , Young Adult
8.
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
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