Neema Shekhar, Vausdevan Biju, Misra Pratibha, Vendhan Senkadhir, Sibin M K, Patrikar Seema
Department of Dermatology, Base Hospital, Lucknow, Uttar Pradesh, India.
Department of Dermatology, AFMC, Pune, Maharashtra, India.
Indian Dermatol Online J. 2025 Apr 17;16(3):389-396. doi: 10.4103/idoj.idoj_635_24. eCollection 2025 May-Jun.
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.
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.
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.
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 ( = 0.8). At week 28, 16 (36%) in group 1 and 27 (54.4%) patients in group 2 maintained PASI50 ( = 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.
The small sample size and loss to follow-up are major limitations of the study.
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.
饮食措施已被用作银屑病管理的辅助疗法。间歇性禁食(IF)是一种饮食模式,在固定时间段内不摄入能量,从而导致代谢从肝脏衍生的葡萄糖转变为脂肪衍生的酮。关于IF对银屑病有效性的数据有限。
本研究的目的是评估IF对慢性斑块状银屑病患者的疗效。该研究的主要结局是在28周时通过银屑病面积和严重程度指数(PASI)测量的银屑病严重程度变化。次要结局指标是每组代谢参数和动脉粥样硬化生物标志物的变化。
该研究设计为随机平行组试验。在基线、16周和28周时使用标准方法测量临床参数、银屑病严重程度、空腹和餐后血糖、血脂谱、高敏C反应蛋白(hsCRP)、血管内皮生长因子(VEGF)和白细胞介素6(IL-6)。患者被随机分为接受每周0.3mg/Kg剂量甲氨蝶呤治疗,其中一组同时进行间歇性禁食,另一组不进行。
总共120名患者被随机分为两组,每组60名:第1组(甲氨蝶呤)和第2组(甲氨蝶呤和间歇性禁食)。第1组的平均年龄、平均病程、PASI和皮肤病生活质量指数(DLQI)分别为45.5(±12.9)岁、5.06(±5.5)年、17.1(±6.7)和12.33(±5)。第2组的平均年龄、平均病程、PASI和DLQI分别为42.9(±14.6)岁、6.91(±6.2)年、16(±4.3)和11.9(±4.3)。两组的基线参数无统计学显著差异。在两组中,从基线到16周和28周,PASI、DLQI、VEGF和hsCRP均有统计学显著差异。在第16周时,第1组44名(73.3%)患者和第2组47名(78.3%)患者达到PASI50(P = 0.8)。在第28周时,第1组16名(36%)患者和第2组27名(54.4%)患者维持PASI50(P = 0.054)。第2组在第16周和28周时体重和腰围有统计学显著降低。与第1组相比,第2组在第28周时VEGF、IL-6和hsCRP有统计学显著降低。
样本量小和失访是该研究的主要局限性。
采用16:8方案的间歇性禁食易于实施,是治疗重度慢性斑块状银屑病的一种安全有效的辅助方法。它有助于维持缓解,并改善代谢参数和血管炎症标志物。