Hair regrowth following TNF-α blockade in coexisting psoriasis vulgaris and alopecia areata

2013 ◽  
Vol 23 (4) ◽  
pp. 537-537 ◽  
Author(s):  
Sachiko Ono ◽  
Yoshiki Miyachi ◽  
Akiko Arakawa
2018 ◽  
Vol 59 (4) ◽  
pp. e318-e319
Author(s):  
Pablo Fernandez-Gonzalez ◽  
David Saceda-Corralo ◽  
Cristina Pindado-Ortega ◽  
Diego Buendia-Castaño ◽  
Montserrat Fernández-Guarino ◽  
...  

2018 ◽  
Vol 154 (10) ◽  
pp. 1145 ◽  
Author(s):  
Solam Lee ◽  
Beom Jun Kim ◽  
Young Bin Lee ◽  
Won-Soo Lee

2011 ◽  
Vol 21 (5) ◽  
pp. 779-780
Author(s):  
Kazutoshi Murao ◽  
Yasutoshi Hida ◽  
Mayumi Minato ◽  
Yoshiaki Kubo ◽  
Seiji Arase

2009 ◽  
Vol 34 (3) ◽  
pp. 413-413 ◽  
Author(s):  
L. D. El-Dars ◽  
S. Kamath ◽  
R. Logan

2011 ◽  
Vol 27 (2) ◽  
pp. 431-436 ◽  
Author(s):  
Tongyu Cao Wikramanayake ◽  
Rosa Rodriguez ◽  
Sonal Choudhary ◽  
Lucia M. Mauro ◽  
Keyvan Nouri ◽  
...  

2019 ◽  
Vol 77 (2) ◽  
pp. 139-142
Author(s):  
Ana Sofia Borges ◽  
Ana Brasileiro ◽  
Rita Ramos Pinheiro ◽  
André Lencastre

Introduction: Topical immunotherapy with diphenylcyclopropenone is a treatment option for patients with refractory or extensive alopecia areata. The aim of this study was to evaluate the clinical efficacy and tolerability of diphenylcyclopropenone therapy, in patients with alopecia areata, and identify possible prognostic factors that predict response to treatment. Methods: We conducted a retrospective study that included all patients diagnosed with alopecia areata and treated with diphenylcyclopropenone at our Department. Results: Twenty one patients were included for analysis (15 females and 6 males). Overall, nine patients (42.9%) had some hair regrowth with diphenylcyclopropenone therapy. Of these, five (55.6%) achieved pigmented terminal hair regrowth but with persistent patches of alopecia. Only one patient achieved > 90% of hair regrowth. Older age at onset, broader extent of alopecia at baseline and presence of nail dystrophy were all negative prognostic factors (p < 0.05). Atopy and thyroid dysfunction were not statistically significant as predictors of poor treatment outcome. Adverse effects were documented in 15 patients, most of them were mild and did not lead to treatment interruption. Conclusion: Diphenylcyclopropenone therapy is a viable treatment option in patients with extensive alopecia areata, although the response is partial in the majority of the cases. Limitations of this study include its retrospective nature and the limited number of patients.


PLoS ONE ◽  
2020 ◽  
Vol 15 (12) ◽  
pp. e0240221
Author(s):  
Talal Abd El-Raheem ◽  
Rania H. Mahmoud ◽  
Enas M. Hefzy ◽  
Mohamed Masoud ◽  
Reham Ismail ◽  
...  

Purpose & methods Several single-nucleotide polymorphisms (SNPs) in the promoter region of the TNF-α gene can cause variations in the gene regulatory sites and act as risk factors for some autoimmune disorders as alopecia areata (AA) and vitiligo. This study aimed to detect the serum TNF-α (sTNF) level (by ELISA) and the rs1800629 (by real-time PCR) among AA and vitiligo Egyptian patients and to determine their relation with disease duration and severity. In silico analysis of this SNP to study the molecular regulation of the mutant genotypes was also done. Results In AA patients, no risk was associated with the mutant genotypes vs. the normal genotype, or with A allele vs. G allele. The risk of vitiligo was significantly higher with the G/A and A/A genotypes compared with HCs (p = 0.011). Similarly, a significantly increased risk was noted in patients with A allele vs. G allele (p<0.0001). In AA and vitiligo patients, a significant increase in sTNF-α levels was noted in the mutant G/A genotypes vs. the normal G/G genotype (p<0.0001) and in the A allele vs the G allele (p<0.0001). According to the in silico analysis, this SNP could mainly affect the SP1 transcription factor binding site with subsequent effect on TNF-α expression. Conclusion According to results of the laboratory and the in silico study, the mutant TNF-α (308) genotypes were risk factors that conferred susceptibility to vitiligo among Egyptian patients but had no effect on the susceptibility to AA.


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