共 50 条
A randomized trial of diphenylcyclopropenone (DPCP) combined with anthralin versus DPCP alone for treating moderate to severe alopecia areata
被引:16
|作者:
Ghandi, Narges
[1
,2
]
Daneshmand, Romina
[1
]
Hatami, Parvaneh
[1
]
Abedini, Robabeh
[1
,2
]
Nasimi, Maryam
[1
,2
]
Aryanian, Zeinab
[1
,3
]
Vance, Terrence M.
[4
,5
]
机构:
[1] Univ Tehran Med Sci, Autoimmune Bullous Dis Res Ctr, Tehran 1199663911, Iran
[2] Univ Tehran Med Sci, Sch Med, Dept Dermatol, Razi Hosp, Tehran 1199663911, Iran
[3] Babol Univ Med Sci, Dept Dermatol, Babol 4717647745, Iran
[4] Brown Univ, Dept Dermatol, Warren Alpert Med Sch, Providence, RI 02912 USA
[5] Brown Univ, Dept Epidemiol, Sch Publ Hlth, Providence, RI 02912 USA
关键词:
Alopecia areata;
Diphenylcyclopropenone;
DPCP;
Anthralin;
Hair loss;
TOPICAL IMMUNOTHERAPY;
DIPHENCYPRONE;
COMBINATION;
EFFICACY;
D O I:
10.1016/j.intimp.2021.107971
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Background: Alopecia areata (AA) is a chronic autoimmune disorder. Finding the best treatment regimen for it remains a challenge. Currently, one of the best documented treatment modalities for AA is topical immunotherapy. Aim: To evaluate the safety and efficacy of combined DPCP and anthralin versus standard protocol (DPCP alone). Methods: A prospective randomized clinical trial was conducted on 50 patients with Alopecia areata who received DPCP alone (group D) or in combination with anthralin (group D/A). Percentage of hair regrowth after 6 months of treatment and the incidence of drug-related adverse effects were evaluated and compared between the two groups. Results: Complete hair regrowth was observed among three patients in each group (18.75% in Group D and 15.79% in Group D/A) after 6 months. Moreover, 25% and 31% of patients in group D and 21% and 47% of patients in group D/A had > 75% and > 50% hair regrowth respectively at the end of the study (P-value: 0.696). In addition, earlier age of onset, chronicity of lesions, nail involvement, facial hair loss and extensive lesions at baseline were associated with poor clinical outcome. Conclusion: DPCP and anthralin was as effective as DPCP alone and anthralin did not add to the effect of DPCP in treating AA.
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