Section of Dermatology, Department of Clinical Medicine and Surgery, Federico II University, Naples, Italy -
Section of Dermatology, Department of Clinical Medicine and Surgery, Federico II University, Naples, Italy.
G Ital Dermatol Venereol. 2020 Dec;155(6):749-753. doi: 10.23736/S0392-0488.18.06012-1. Epub 2018 Sep 20.
Over recent years, the link between obesity, metabolic syndrome and Hidradenitis suppurativa (HS) has been explored. It has been demonstrated that HS patients have a high prevalence of the metabolic syndrome and an increased frequency of insulin resistance. The objective of our study is to estimate the effectiveness of an oral supplementation based on myo-inositol (MI), folic acid and liposomal magnesium (Levigon, Sanitpharma; Milan, Italy) on the clinical and metabolic profile of patients affected by HS.
Twenty subjects with HS and an impaired glucose metabolism were enrolled. Group A: 10 subjects received for 6 months MI 2000 mg, liposomal magnesium and folic acid associated to topical antibiotic therapy (clindamycin gel 1%), systemic antibiotic therapy (clindamycin 300 mg b.i.d. and rifampicin 600 mg daily for 6 weeks) and a normocaloric diet group B: 10 subjects received topical and systemic antibiotic therapy associated to a normocaloric diet for 6 months.
After 6 months group A patients showed an average reduction of Sartorius Score from 38.3±7.75 to 27.3±13.53 (P value <0.04) while in the control group there was a reduction of the Sartorius from 38.4±7.88 to 31.1±8.02 (P value =0.55). Moreover in group A Homeostasis Model Assessment of Insulin Resistance (HOMA-IR) was significantly reduced from 2.43±0.35 to 2.1±0.31 (P<0.01) whereas in group B HOMA-IR did not significantly decrease (2.51±0.65 at T0 at 2.40±0.67 at T1).
Our study underlines the importance of the evaluation of metabolic profile in patients with HS. Moreover, it suggests that the supplementation of MI, folic acid and liposomal magnesium in HS can improve the efficacy of concomitant therapies and the metabolic profile.
近年来,肥胖症、代谢综合征和化脓性汗腺炎(HS)之间的联系已经得到了探索。已经证明,HS 患者代谢综合征的患病率较高,胰岛素抵抗的频率也增加。我们研究的目的是评估基于肌醇(MI)、叶酸和脂质体镁(Levigon,Sanitpharma;米兰,意大利)的口服补充剂对患有 HS 的患者的临床和代谢特征的有效性。
共纳入 20 例葡萄糖代谢受损的 HS 患者。A 组:10 例患者接受 MI 2000mg、脂质体镁和叶酸联合局部抗生素治疗(克林霉素凝胶 1%)、全身抗生素治疗(克林霉素 300mg bid 和利福平 600mg 每日一次,共 6 周)和正常热量饮食;B 组:10 例患者接受局部和全身抗生素治疗联合正常热量饮食,共 6 个月。
6 个月后,A 组患者的 Sartorius 评分从 38.3±7.75 平均降低至 27.3±13.53(P 值<0.04),而对照组从 38.4±7.88 降低至 31.1±8.02(P 值=0.55)。此外,A 组患者的稳态模型评估的胰岛素抵抗(HOMA-IR)从 2.43±0.35 显著降低至 2.1±0.31(P<0.01),而 B 组 HOMA-IR 没有显著降低(T0 时为 2.51±0.65,T1 时为 2.40±0.67)。
我们的研究强调了评估 HS 患者代谢特征的重要性。此外,它表明在 HS 中补充 MI、叶酸和脂质体镁可以提高联合治疗的疗效和代谢特征。