Treatment of Hailey-Hailey Disease With Low-Dose Naltrexone

被引:18
作者
Albers, Lauren N. [1 ]
Arbiser, Jack L. [1 ,2 ]
Feldman, Ron J. [1 ]
机构
[1] Emory Univ, Sch Med, Dept Dermatol, 1525 Clifton Rd,First Floor, Atlanta, GA 30322 USA
[2] Atlanta Vet Adm Med Ctr, Decatur, GA USA
关键词
D O I
10.1001/jamadermatol.2017.2446
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
IMPORTANCE Hailey-Hailey disease is a severe genetic blistering disease of intertriginous skin locations that can lead to poor quality of life and increased morbidities. Multiple therapies are available with inconsistent outcomes and potentially severe adverse effects. OBJECTIVE To determine whether low-dose naltrexone is an effective treatment for Hailey-Hailey disease. DESIGN, SETTING, AND PARTICIPANTS This study was a case series performed at a dermatology outpatient clinic of 3 patients with severe Hailey-Hailey disease recalcitrant to at least 4 therapies. INTERVENTIONS Low-dose naltrexone, 3 mg nightly, titrated to 4.5 mg nightly in 2 patients. MAIN OUTCOMES AND MEASURES Reduction in size of lesions as well as subjective improvement of symptoms. RESULTS All 3 patients noted significant healing of erosions and plaques starting from the peripheral aspect within 1 to 2 weeks of treatment, and clinical resolution of lesions within 2 months. Discontinuation of low-dose naltrexone resulted in flaring of symptoms, which cleared within 2 to 3 days on rechallenge with low-dose naltrexone. CONCLUSIONS AND RELEVANCE We present herein 3 cases of patients with severe Hailey-Hailey disease treated with low-dose naltrexone who achieved clinical resolution of symptoms. The success of these cases suggests low-dose naltrexone as a novel therapy for Hailey-Hailey disease. The possible mechanism may involve low-dose naltrexone influencing opioid or toll-like receptor signaling to improve calcium mobilization and improve keratinocyte differentiation and wound healing. Future studies are needed to clarify the mechanism and to define the role of low-dose naltrexone for treatment of Hailey-Hailey disease.
引用
收藏
页码:1018 / 1020
页数:3
相关论文
共 8 条
[1]   Management of familial benign chronic pemphigus [J].
Arora, Harleen ;
Bray, Fleta N. ;
Cervantes, Jessica ;
Aizpurua, Leyre A. Falto .
CLINICAL COSMETIC AND INVESTIGATIONAL DERMATOLOGY, 2016, 9 :281-290
[2]   Activation of the δ-opioid receptor promotes cutaneous wound healing by affecting keratinocyte intercellular adhesion and migration [J].
Bigliardi, P. L. ;
Neumann, C. ;
Teo, Y. L. ;
Pant, A. ;
Bigliardi-Qi, M. .
BRITISH JOURNAL OF PHARMACOLOGY, 2015, 172 (02) :501-514
[3]   Efficacy of magnesium chloride in the treatment of Hailey-Hailey disease: from serendipity to evidence of its effect on intracellular Ca2+ homeostasis [J].
Borghi, Alessandro ;
Rimessi, Alessandro ;
Minghetti, Sara ;
Corazza, Monica ;
Pinton, Paolo ;
Virgili, Annarosa .
INTERNATIONAL JOURNAL OF DERMATOLOGY, 2015, 54 (05) :543-548
[4]   Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease [J].
Hu, ZL ;
Bonifas, JM ;
Beech, J ;
Bench, G ;
Shigihara, T ;
Ogawa, H ;
Ikeda, S ;
Mauro, T ;
Epstein, EH .
NATURE GENETICS, 2000, 24 (01) :61-65
[5]  
Izquierdo D, 2016, MOL MED LETT, V1, P5
[6]   Low dose naltrexone for induction of remission in Crohn's disease [J].
Segal, Dan ;
MacDonald, John K. ;
Chande, Nilesh .
COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2014, (02)
[7]   Human keratinocytes express functional CD14 and toll-like receptor 4 [J].
Song, PI ;
Park, YM ;
Abraham, T ;
Harten, B ;
Zivony, A ;
Neparidze, N ;
Armstrong, CA ;
Ansel, JC .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2002, 119 (02) :424-432
[8]   The use of low-dose naltrexone (LDN) as a novel anti-inflammatory treatment for chronic pain [J].
Younger, Jarred ;
Parkitny, Luke ;
McLain, David .
CLINICAL RHEUMATOLOGY, 2014, 33 (04) :451-459