Efficacy of Clinical and Pathogenetic Treatment of Patients with Alopecia Areata Associated with Metabolic Syndrome

I. Horda
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Abstract

Alopecia areata (HA) is an autoimmune inflammatory disease of hair follicles (HF) with a nonscarring pattern of hair loss on a scalp and/or other areas of skin. The objective: to assess the efficacy of the developed complex pathogenetically justified method of treatment of patients with AA associated with MS using drugs for the correction of dyslipidaemia and insulin resistance. Materials and methods. 59 patients with alopecia areata of moderate severity associated with metabolic syndrome underwent complex pathogenetic treatment with correction of lipid and carbohydrate indicators. In the course of the study, patients were divided into 4 groups: 1A (n=16) – patients with AA, burdened with MS (3 components), who underwent basic therapy of AA and treatment of metabolic disorders with rosuvastatin at a dose of 10 mg per day; 1B (n=14) – patients with AA with MS (3 components), who were prescribed basic therapy and correction of metabolic disorders through diet; 1C (n=14) – patients with AA with MS (4–5 components), who received basic therapy, as well as rosuvastatin 10 mg per day and thioctacid 600 mg per day; 1D (n=15) – patients with AA, burdened with MS (4–5 components), who received basic therapy and followed a diet. Results. As a result of the study, the following predicted patterns were revealed: - the level of blood glucose in patients of group 1A after 6 months of treatment decreased by 5%, in patients of group ǀB – by 2%; in group 1A, the acceleration of the improvement dynamics of the HOMA index and triglycerides was determined, in contrast to group ǀB; the level of total cholesterol in group 1A compared to group ǀB was statistically significantly lower (p<0.05%); - statistically significant differences (p<0.05%) were found regarding the improvement of blood glucose and LDL levels after 6 months of treatment in patients of groups 1C and 1D in favour of group 1C, taking into account the improvement of these indicators in both groups during the study period; - compared to patients of group 1D, patients of group 1C after 6 months of treatment showed a statistically significant improvement in all the studied indicators that determine the severity of MS; - after 6 months of treatment of patients with AA, statistically more cases of recovery were found in group 1C compared to group 1A (p=0.041); after 12 months in group 1C, the frequency of cases of clinical recovery was statistically significantly higher (p=0.069) compared to group 1D (p=0.035) and group 1B (p=0.017); - the number of cases of a diagnosed positive effect (clinical recovery and partial effect), which began to manifest itself after 6 months and intensified after 12 months, prevailed in group 1A in contrast to group 1B, in which, on the contrary, an increase in the number of cases with no effect or deterioration was recorded; - the number of cases of a positive effect in group 1C after 6 months of dermatosis treatment statistically significantly exceeded the number of such cases in group 1D, and after 12 months of treatment this trend remained; - the calculation of the average annual growth rate of patients who were diagnosed with a positive effect during the study period in groups 1A and 1C revealed a higher growth rate compared to groups 1B and 1D: in group 1A it was on average 2.62% in contrast to group 1B, where it was half as much – 1.29%; in group 1C it was 2.21%, which was twice as high as that of the group 1D (1.12%). Conclusions. A pathogenetically substantiated method of treating patients with AA associated with MS, which consists of the complex use of drugs for the correction of dyslipidaemia and insulin resistance and basic therapy of AA has been developed. A positive effect was obtained on the implemented complex treatment.
对伴有代谢综合征的脱发患者进行临床和病因治疗的疗效
斑秃(Alopecia areata,HA)是一种自身免疫性毛囊炎(HF)疾病,在头皮和/或其他皮肤部位出现非瘢痕性脱发。 目的:评估使用纠正血脂异常和胰岛素抵抗的药物治疗伴有多发性硬化症的 AA 患者的复合病理合理治疗方法的疗效。 材料和方法。59 名中度脱发伴代谢综合征患者接受了纠正血脂和碳水化合物指标的复合病理学治疗。在研究过程中,患者被分为 4 组:1A组(n=16)--伴有MS(3种成分)的AA患者,接受AA基础治疗,并用罗伐他汀治疗代谢紊乱,剂量为每天10毫克;1B组(n=14)--伴有MS(3种成分)的AA患者,接受基础治疗,并通过饮食纠正代谢紊乱;1C(n=14)--患有多发性硬化症(4-5种)的AA患者,接受基础治疗,同时每天服用10毫克罗伐他汀和600毫克硫辛酸;1D(n=15)--患有多发性硬化症(4-5种)的AA患者,接受基础治疗,同时注意饮食。 研究结果研究结果显示了以下预测模式:-治疗6个月后,1A组患者的血糖水平降低了5%,ǀB组患者的血糖水平降低了2%;与ǀB组相比,1A组患者的HOMA指数和甘油三酯的改善速度加快;与ǀB组相比,1A组患者的总胆固醇水平在统计学上显著降低(p<0.05%);-在改善血糖方面发现了显著的统计学差异(p<0.0.05%); - 考虑到两组患者在研究期间的血糖和低密度脂蛋白水平的改善情况,发现1C组和1D组患者在治疗6个月后的血糖和低密度脂蛋白水平的改善情况有利于1C组; - 与1D组患者相比,1C组患者在治疗6个月后,在确定多发性硬化症严重程度的所有研究指标方面均有统计学意义上的显著改善; - 与1A组相比,AA患者在治疗6个月后,1C组的康复病例在统计学上多于1A组(P=0.041);12 个月后,与 1D 组(p=0.035)和 1B 组(p=0.1A 组与 1B 组相比,诊断出积极效果(临床康复和部分效果)的病例数更多,这种效果在 6 个月后开始显现,并在 12 个月后加强,而 1B 组则相反,无效果或病情恶化的病例数有所增加;- 在皮肤病治疗 6 个月后,1C 组疗效显著的病例数在统计学上明显超过 1D 组,而在治疗 12 个月后,这一趋势依然存在; - 在研究期间,计算 1A 组和 1C 组被诊断为疗效显著的病人的年平均增长率,结果显示,与 1B 组和 1D 组相比,年平均增长率更高:1A 组的平均增长率为 2.62%,而 1B 组仅为其一半 - 1.29%;1C 组为 2.21%,是 1D 组(1.12%)的两倍。 结论治疗多发性硬化症伴 AA 患者的病理证实方法已经开发出来,该方法由纠正血脂异常和胰岛素抵抗的药物以及 AA 的基础治疗组成。实施综合治疗取得了积极效果。
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