Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 6 de 6
Filtrer
Plus de filtres










Base de données
Gamme d'année
1.
Clin Exp Dermatol ; 46(3): 532-540, 2021 Apr.
Article de Anglais | MEDLINE | ID: mdl-33030217

RÉSUMÉ

BACKGROUND: Hidradenitis suppurativa (HS) is a chronic, relapsing and debilitating inflammatory disease associated with profound morbidity. AIM: In this multicentre study, we investigated the demographic and clinical features of HS, and determined risk factors of disease severity. METHODS: In total, 1221 patients diagnosed with HS from 29 centres were enrolled, and the medical records of each patient were reviewed. RESULTS: The mean age of disease onset was 26.2 ± 10.4 years, and almost 70% (n = 849) of patients were current or former smokers. Mean disease duration was 8.9 ± 8.4 years with a delay in diagnosis of 5.8 ± 3.91 years. Just over a fifth (21%; n = 256) of patients had a family history of HS. The axillary, genital and neck regions were more frequently affected in men than in women, and the inframammary region was more frequently affected in women than in men (P < 0.05 for all). Acne (40.8%), pilonidal sinus (23.6%) and diabetes mellitus (12.6%) were the most prevalent associated diseases. Of the various therapies used, antibiotics (76.4%) were most common followed by retinoids (41.7%), surgical interventions (32.0%) and biologic agents (15.4%). Logistic regression analysis revealed that the most important determinants of disease severity were male sex (OR = 2.21) and involvement of the genitals (OR = 3.39) and inguinal region (OR = 2.25). More severe disease was associated with comorbidity, longer disease duration, longer diagnosis delay and a higher number of smoking pack-years. CONCLUSIONS: Our nationwide cohort study found demographic and clinical variation in HS, which may help broaden the understanding of HS and factors associated with disease severity.


Sujet(s)
Hidrosadénite suppurée/diagnostic , Acné juvénile/complications , Adulte , Consommation d'alcool/effets indésirables , Études transversales , Complications du diabète , Femelle , Hidrosadénite suppurée/complications , Humains , Mâle , Obésité/complications , Sinus pilonidal/complications , Études rétrospectives , Facteurs de risque , Indice de gravité de la maladie , Fumer/effets indésirables
2.
Med Princ Pract ; 25(3): 247-53, 2016.
Article de Anglais | MEDLINE | ID: mdl-26683851

RÉSUMÉ

OBJECTIVES: The aim of this study was to investigate the elastic properties of the aorta and the myocardial performance index of the left ventricle (LV) in patients with lichen planus (LP). SUBJECTS AND METHODS: A total of 54 patients with LP and 50 controls were enrolled in the study. The 2 groups were well-matched regarding age, gender, body mass index, any smoking history, diabetes mellitus and systolic and diastolic blood pressure (SBP and DBP). The echocardiographic examination was performed on the study subjects and the controls. Aortic elasticity parameters and the myocardial performance index of the LV were calculated. The Student t test, the x03C7;2 test and multiple linear regression were used for the statistical analysis. RESULTS: Aortic strain (AS, 4.77 ± 1.81 vs. 8.95 ± 2.22; p < 0.001) and aortic distensibility (AD, 0.25 ± 0.009 vs. 0.42 ± 0.120; p < 0.001) were significantly lower, and aortic stiffness index ß (ASIß, 3.65 ± 1.03 vs. 2.70 ± 0.91; p < 0.001) was significantly higher in the LP group than in the controls. The myocardial performance index (Tei index) was significantly higher in the LP group than in the control group (p = 0.001). The duration of the LP was negatively correlated with AS (r = -0.364, p < 0.001) and AD (r = -0.279, p = 0.006), and positively correlated with the Tei index (r = 0.324, p = 0.001) and ASIß (r = 0.364, p < 0.001). After adjustment for relevant confounders (age, male gender, smoking, SBP, DBP, diabetes mellitus and low- and high-density lipoprotein cholesterol), LP and its duration were still associated with AS, AD and ASIß. CONCLUSION: In this study, AS and AD were lower and ASIß and myocardial performance index higher in LP patients than in controls.


Sujet(s)
Maladies de l'aorte/épidémiologie , Cardiomyopathies/épidémiologie , Lichen plan/épidémiologie , Rigidité vasculaire , Adulte , Maladies de l'aorte/imagerie diagnostique , Débit cardiaque , Cardiomyopathies/imagerie diagnostique , Échocardiographie , Femelle , Humains , Mâle , Adulte d'âge moyen
3.
Genet Mol Res ; 13(3): 4788-96, 2014 Jul 02.
Article de Anglais | MEDLINE | ID: mdl-25062414

RÉSUMÉ

Behçet's disease (BD) is a multisystemic inflammatory disease believed to be triggered by microbial or environmental factors on a genetic platform. Clinically, it may have an impact on many body systems, including the mucocutaneous, ocular, articular, vascular, and neurological systems. In this study, we aimed to determine the HLA-B51 subtypes and their correlations with the clinical findings of BD. Fifty-one patients with BD and 44 gender- and age-matched healthy subjects were included in this study. The HLA-B51 subtypes of all participants were determined, and the correlations of the clinical manifestations of the disease with the HLA-B51 subtypes were analyzed. HLA-B51 positivity was found to be significantly higher in the patient group (P < 0.001, RR = 15.20), which had significantly more frequent HLA-B5101, HLA-B5102(01), HLA-B5109, and HLA-B5122 subtypes than the healthy subjects (all P < 0.05). Furthermore, considering the correlation between the genetic makeup and clinical findings, the HLA-B5109 subtype was found to be less frequent in patients with papulopustular skin lesions (P = 0.042). The frequency of HLA-B5103 was significantly higher in patients with central nervous system involvement (P = 0.015). There may be a relationship between HLA-B5102(01), HLA-B5109, and HLA-B5122 in addition to HLA-B51 and HLA-B5101(01) in Turkish patients with BD. The HLA-B5109 subtype can be protective against papulopustular lesion development; however, the HLA-B5103 subtype may pose a risk for neuro-Behçet development in BD.


Sujet(s)
Maladie de Behçet/génétique , Études d'associations génétiques , Antigène HLA-B51/génétique , Système nerveux/anatomopathologie , Ulcère buccal/anatomopathologie , Peau/anatomopathologie , Adulte , Sujet âgé , Allèles , Maladie de Behçet/immunologie , Maladie de Behçet/anatomopathologie , Études cas-témoins , Femelle , Expression des gènes , Fréquence d'allèle , Génotype , Antigène HLA-B51/immunologie , Humains , Mâle , Adulte d'âge moyen , Système nerveux/immunologie , Ulcère buccal/immunologie , Phénotype , Peau/immunologie , Turquie
4.
Redox Rep ; 18(5): 200-4, 2013.
Article de Anglais | MEDLINE | ID: mdl-24020719

RÉSUMÉ

OBJECTIVES: Ultraviolet B is a potent oxidative stress (OS) inducer in the skin; however, there are no data about the systemic oxidative effect of narrow band ultraviolet B (NB-UVB) phototherapy. In this study, we aimed to investigate the change in the OS status of psoriatic patients who were treated by NB-UVB phototherapy and to determine the relationships between OS, psoriasis severity, and systemic inflammatory condition. METHODS: Twenty-four psoriatic patients were treated with a total of 30 sessions of NB-UVB irradiation. Psoriasis area and severity index (PASI), serum levels of high sensitive C-reactive protein (hsCRP), total antioxidant status (TAS), total oxidant status (TOS), the oxidative stress index (OSI), serum paraoxonase (PON), and arylesterase (ARE) activities before and after NB-UVB therapy were determined. RESULTS: PASI scores significantly decreased after NB-UVB therapy (P = 0.001). The pre- and post-treatment hsCRP and TAS levels were similar (P = 0.253 and 0.301, respectively). TOS and OSI values significantly increased after phototherapy (both P < 0.001). PON and ARE activities did not change after treatment (both P > 0.05). There was no correlation between PASI and hsCRP, TAS, TOS, OSI, PON, and ARE values (P > 0.05). CONCLUSION: A systemic OS may emerge in psoriatic patients treated by NB-UVB phototherapy.


Sujet(s)
Antioxydants/métabolisme , Aryldialkylphosphatase/métabolisme , Oxydants/métabolisme , Psoriasis/métabolisme , Psoriasis/thérapie , Traitement par ultraviolets/méthodes , Adolescent , Adulte , Femelle , Humains , Mâle , Adulte d'âge moyen , Études prospectives , Jeune adulte
5.
Clin Exp Dermatol ; 38(7): 701-6, 2013 Oct.
Article de Anglais | MEDLINE | ID: mdl-23601201

RÉSUMÉ

BACKGROUND: Vitiligo is an acquired depigmentation disorder, and oxidative stress is suggested to have a major role in its aetiopathogenesis. AIM: To assess whether oxidative stress has a greater role in generalized than in localized vitiligo. METHODS: We assessed 31 patients with active vitiligo (17 localized, 14 generalized) and 38 healthy controls. Serum total oxidant status (TOS), total antioxidant status (TAS) and oxidative stress index (OSI) were determined. RESULTS: Patients with vitiligo had significantly lower TAS and higher TOS and OSI values than controls. Both localized and generalized vitiligo were associated with lower TAS and higher TOS and OSI values, compared with controls, and all three did not differ with vitiligo type. CONCLUSIONS: A systemic oxidative stress exists in patients with vitiligo. These results indicate that the global antioxidant capacity of patients might have been exhausted through a defence mechanism against oxidative processes. The imbalance in TOS/TAS status may have an important role in the aetiopathogenesis of vitiligo, regardless of the clinical variant of the disease.


Sujet(s)
Antioxydants/métabolisme , Espèces réactives de l'oxygène/sang , Vitiligo/sang , Adulte , Études cas-témoins , Femelle , Humains , Mâle , Adulte d'âge moyen , Stress oxydatif/physiologie , Vitiligo/étiologie , Vitiligo/physiopathologie , Jeune adulte
6.
J Eur Acad Dermatol Venereol ; 20(8): 969-73, 2006 Sep.
Article de Anglais | MEDLINE | ID: mdl-16922947

RÉSUMÉ

BACKGROUND: Mastocytosis is a rare, heterogeneous group of disorder with abnormal increase of mast cells in one or more organ systems. OBJECTIVE: To evaluate the demographic and clinical features of cutaneous mastocytosis (CM). METHODS: Records of 55 patients with cutaneous mastocytosis were retrospectively analysed. RESULTS: Of the 22 females and 33 males, 80% had urticaria pigmentosa/maculopapular CM and 20% had mastocytoma. Of all cases, 81.8% had first lesions in childhood. The most common presentation was involvement of trunk together with extremities. Thirteen (23.6%) patients had history of bulla; Darier's sign was positive in 34 of 38 patients. Itching was the most common complaint, provocated by hot weather/bath. CONCLUSION: Clinical presentations of urticaria pigmentosa/maculopapular CM and mastocytoma are similar regarding gender, age of onset, age of diagnosis, and presence of Darier's sign and history of bulla. In contrast to mastocytoma, urticaria pigmentosa/maculopapular CM lesions were frequently located on trunk together with extremities.


Sujet(s)
Mastocytose cutanée/épidémiologie , Adolescent , Adulte , Âge de début , Enfant , Enfant d'âge préscolaire , Femelle , Humains , Nourrisson , Nouveau-né , Mâle , Mastocytose cutanée/classification , Mastocytose cutanée/physiopathologie , Adulte d'âge moyen , Études rétrospectives
SÉLECTION CITATIONS
DÉTAIL DE RECHERCHE
...