Department of Physical Medicine and Rehabilitation, Health Sciences University Ankara Training and Research Hospital, Ankara, Turkey.
Department of Dermatology, Health Sciences University Ankara Training and Research Hospital, Ankara, Turkey.
Sci Rep. 2020 Feb 10;10(1):2245. doi: 10.1038/s41598-020-59167-0.
Isotretinoin (ISO) is a drug which is used for the treatment of severe and refractory acne vulgaris (AV), over the last few decades. The drug has various musculoskeletal side effects. The aim of this study was to investigate relationship between serum 25 hydroxy (OH) vitamin D levels and the ISO-induced musculoskeletal side effects in patients with AV. We included 87 patients receiving ISO and had musculoskeletal symptoms as adverse effect (AE) group. Another 90 patients receiving ISO for AV and had any musculoskeletal complaints were recruited as control (C) group. Locomotor system examination of the patients was performed by the same clinician. Serum 25 OH vitamin D levels of the all participants were measured. Patients in the AE group were divided into three subgroups by serum 25 OH vitamin D levels. Patients with serum 25 OH vitamin D level lower than 10 ng/ml was classified as Group I, the ones between 10-20 ng/ml as Group II and those higher than 20 ng/ml were classified as Group III. AE and C groups were similar in terms of age and sex (p > 0.05). There was no statistically significant difference in the mean serum vitamin D levels between two groups (p = 0.17). Also, there was no significant difference in number of arthralgia (p = 0.30), myalgia (p = 0.29), low back pain (p = 0.10) and sacroiliitis (p = 0.17) between three subgroups in AE group. In addition, we found no statistically significant correlation between the serum vitamin D levels and age, cumulative dose of ISO, arthralgia, myalgia and sacroiliitis parameters in AE group (p > 0.05). Serum 25 OH vitamin D levels between the AE and C groups were similar. We also found that no significant difference in musculoskeletal adverse events between AE subgroups. Therefore, it can be concluded that vitamin D deficiency has no effect on the musculoskeletal adverse events in patients receiving ISO.
异维 A 酸(ISO)是一种用于治疗严重和难治性寻常痤疮(AV)的药物,在过去几十年中。该药物有各种肌肉骨骼的副作用。本研究的目的是探讨血清 25 羟(OH)维生素 D 水平与 AV 患者 ISO 诱导的肌肉骨骼副作用之间的关系。我们纳入了 87 名因不良反应(AE)而接受 ISO 治疗并出现肌肉骨骼症状的患者作为 AE 组。另招募了 90 名因 AV 接受 ISO 治疗且有任何肌肉骨骼投诉的患者作为对照组(C 组)。由同一位临床医生对患者进行运动系统检查。测量所有参与者的血清 25OH 维生素 D 水平。根据血清 25OH 维生素 D 水平将 AE 组患者分为三组。血清 25OH 维生素 D 水平低于 10ng/ml 的患者为 I 组,10-20ng/ml 之间的患者为 II 组,高于 20ng/ml 的患者为 III 组。AE 组和 C 组在年龄和性别方面无统计学差异(p>0.05)。两组间平均血清维生素 D 水平无统计学差异(p=0.17)。此外,AE 组三组间的关节痛(p=0.30)、肌痛(p=0.29)、腰痛(p=0.10)和骶髂关节炎(p=0.17)的发生率无显著差异。此外,我们还发现 AE 组中血清维生素 D 水平与年龄、ISO 累积剂量、关节痛、肌痛和骶髂关节炎参数之间无统计学相关性(p>0.05)。AE 组和 C 组之间的血清 25OH 维生素 D 水平相似。我们还发现 AE 亚组之间的肌肉骨骼不良事件无显著差异。因此,可以得出结论,维生素 D 缺乏对接受 ISO 治疗的患者的肌肉骨骼不良反应没有影响。