间歇性禁食治疗慢性斑块型银屑病的疗效:一项IIb期临床试验

IF 1.9 Q3 DERMATOLOGY
Indian Dermatology Online Journal Pub Date : 2025-04-17 eCollection Date: 2025-05-01 DOI:10.4103/idoj.idoj_635_24
Shekhar Neema, Biju Vausdevan, Pratibha Misra, Senkadhir Vendhan, M K Sibin, Seema Patrikar
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引用次数: 0

摘要

背景:饮食措施已被用作牛皮癣治疗的辅助疗法。间歇性禁食(IF)是一种饮食模式,其中能量在固定时间内不被消耗,导致代谢从肝脏来源的葡萄糖转换为脂肪来源的酮。关于IF治疗牛皮癣的有效性的数据是有限的。目的和目的:本研究的目的是评估干扰素对慢性斑块型银屑病患者的疗效。研究的主要结果是28周时银屑病严重程度的变化,通过银屑病面积和严重程度指数(PASI)来测量。次要结局指标是各组动脉粥样硬化代谢参数和生物标志物的变化。患者和方法:本研究设计为随机平行组试验。临床参数,银屑病严重程度,空腹和餐后血糖,血脂,高敏c反应蛋白(hsCRP),血管内皮生长因子(VEGF),白细胞介素6 (IL-6),在基线,16周和28周采用标准方法测量。患者随机接受0.3 mg/Kg/周剂量的甲氨蝶呤治疗,伴有或不伴有间歇性禁食。结果:120例患者随机分为两组,每组60例:1组(甲氨蝶呤)和2组(甲氨蝶呤+间歇性禁食)。1组患者平均年龄为45.5(±12.9)岁,平均病程为5.06(±5.5)岁,PASI为17.1(±6.7)岁,皮肤生活质量指数(DLQI)为12.33(±5)岁。2组患者平均年龄为42.9(±14.6)年,平均病程为6.91(±6.2)年,PASI为16(±4.3)年,DLQI为11.9(±4.3)年。两组患者基线参数差异无统计学意义。在两组中,PASI、DLQI、VEGF和hsCRP从基线到16周和28周均有统计学差异。第16周,1组44例(73.3%)患者达到PASI50, 2组47例(78.3%)患者达到PASI50 (P = 0.8)。第28周,1组16例(36%)、2组27例(54.4%)患者维持PASI50 (P = 0.054)。第2组在16周和28周时体重和腰围的减少有统计学意义。与1组相比,2组在28周时VEGF、IL6和hsCRP均有统计学意义的降低。局限性:小样本量和随访缺失是本研究的主要局限性。结论:采用16:8方案进行间歇性禁食是治疗重度慢性斑块型银屑病的一种安全有效的辅助治疗方法。它有助于维持缓解并导致代谢参数和血管炎症标志物的改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of Intermittent Fasting in the Management of Chronic Plaque Psoriasis: A Phase IIb Clinical Trial.

Background: Dietary measures have been used as an adjunctive therapy in the management of psoriasis. Intermittent fasting (IF) is an eating pattern in which energy is not consumed for a fixed duration, resulting in metabolic switch from liver-derived glucose to adipose-derived ketones. The data regarding effectiveness of IF in psoriasis are limited.

Aim and objectives: The aim of this study was to assess efficacy of IF in patients with chronic plaque psoriasis. The primary outcome of the study was change in psoriasis severity as measured by psoriasis area and severity index (PASI) at 28 weeks. The secondary outcome measures were change in metabolic parameters and biomarkers for atherosclerosis in each group.

Patients and methods: The study was designed as a randomized parallel group trial. Clinical parameters, psoriasis severity, fasting and postprandial blood sugar, lipid profile, high sensitivity C-reactive protein (hsCRP), vascular endothelial growth factor (VEGF), and interleukin 6 (IL-6), were measured using standard methods at baseline, 16 weeks, and 28 weeks. Patients were randomized to receive methotrexate in the dose of 0.3 mg/Kg/week with or without intermittent fasting.

Results: A total of 120 patients were randomized in two groups of 60 each: group 1 (methotrexate) and group 2 (methotrexate and intermittent fasting). The mean age, mean duration of disease, PASI, and dermatology life quality index (DLQI) in group 1 were 45.5 (±12.9) years, 5.06 (±5.5) years, 17.1 (±6.7), and 12.33 (±5), respectively. The mean age, mean duration of disease, PASI, and DLQI in group 2 were and 42.9 (±14.6) years, 6.91 (±6.2) years, 16 (±4.3), and 11.9 (±4.3), respectively. There was no statistically significant difference in baseline parameters in two groups. In both the groups, there was a statistically significant difference in PASI, DLQI, VEGF, and hsCRP from baseline to 16 and 28 weeks. At week 16, 44 (73.3%) patients in group 1 and 47 (78.3%) in group 2 achieved PASI50 (P = 0.8). At week 28, 16 (36%) in group 1 and 27 (54.4%) patients in group 2 maintained PASI50 (P = 0.054). There was a statistically significant weight and waist circumference reduction at 16 weeks and 28 weeks in group 2. There was a statistically significant reduction in VEGF, IL6, and hsCRP at 28 weeks in group 2 as compared to group 1.

Limitations: The small sample size and loss to follow-up are major limitations of the study.

Conclusion: Intermittent fasting using 16: 8 protocol is easy to perform and a safe and effective adjuvant for managing severe chronic plaque psoriasis. It helps in maintaining remission and results in improvement in metabolic parameters and markers of vascular inflammation.

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来源期刊
CiteScore
2.00
自引率
11.80%
发文量
201
审稿时长
49 weeks
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