Morita Akimichi, Muramatsu Shinnosuke, Kubo Ryoji, Ikumi Kyoko, Sagawa Yoko, Saito Chiyo, Torii Kan, Nishida Emi
a Department of Geriatric and Environmental Dermatology , Nagoya City University Graduate School of Medical Sciences , Nagoya , Japan.
J Dermatolog Treat. 2018 Aug;29(5):496-500. doi: 10.1080/09546634.2017.1398394. Epub 2018 Jan 10.
Topical active vitamin D3 application alone or in combination with topical steroid application is widely used to treat psoriasis. In Japan, combined calcipotriol hydrate/betamethasone dipropionate ointment has been used for patients with psoriasis vulgaris since September 2014. Current evidence regarding the incidence of hypercalcemia due to the use of this combination product, however, is insufficient. We evaluated the incidence of hypercalcemia following combined calcipotriol hydrate/betamethasone dipropionate ointment in patients with severe psoriasis vulgaris.
Japanese patients (n = 22) with extensive plaque psoriasis (body surface area: 20-30%) applied the combined calcipotriol hydrate/betamethasone dipropionate ointment once daily for 8 weeks, and their serum Ca concentrations were measured periodically.
The mean serum Ca concentration changed only marginally, from 9.04 ± 0.34 mg/dL before treatment to 9.08 ± 0.39 mg/dL after 8 weeks of treatment. None of the patients had an elevated serum Ca concentration throughout the study. No cases of hypercalcemia were reported as an adverse event. No correlation was detected between the amount of the combined calcipotriol hydrate/betamethasone dipropionate ointment applied and changes in the serum Ca concentration.
The incidence of hypercalcemia due to topical application of a combined calcipotriol hydrate/betamethasone dipropionate ointment is low in Japanese patients with severe psoriasis vulgaris.
局部应用活性维生素D3单独或与局部应用类固醇联合使用广泛用于治疗银屑病。在日本,自2014年9月以来,卡泊三醇水合物/倍他米松二丙酸酯联合软膏已用于寻常型银屑病患者。然而,关于使用这种联合产品导致高钙血症发生率的现有证据不足。我们评估了卡泊三醇水合物/倍他米松二丙酸酯联合软膏治疗重度寻常型银屑病患者后高钙血症的发生率。
22例日本广泛性斑块状银屑病患者(体表面积:20 - 30%)每天使用一次卡泊三醇水合物/倍他米松二丙酸酯联合软膏,持续8周,并定期测量其血清钙浓度。
血清钙平均浓度仅略有变化,从治疗前的9.04±0.34mg/dL变为治疗8周后的9.08±0.39mg/dL。在整个研究过程中,没有患者的血清钙浓度升高。没有高钙血症病例报告为不良事件。所应用的卡泊三醇水合物/倍他米松二丙酸酯联合软膏的量与血清钙浓度变化之间未检测到相关性。
在日本重度寻常型银屑病患者中,局部应用卡泊三醇水合物/倍他米松二丙酸酯联合软膏导致高钙血症的发生率较低。