Department of Gastroenterology, Osaka City University Graduate School of Medicine, Osaka, Japan.
Department of Intestinal Inflammation Research, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan.
J Gastroenterol Hepatol. 2018 Mar;33(3):631-637. doi: 10.1111/jgh.13969.
Secondary loss of response to adalimumab (ADA-LOR) commonly occurs in patients with Crohn's disease (CD) treated with adalimumab (ADA). We evaluated the efficacy of concomitant elemental diet (ED) therapy to reduce ADA-LOR in adult CD patients.
Patients were divided into either an ED (≥900 kcal/day) or a non-ED group (<900 kcal/day). Cumulative non-ADA-LOR rates were compared between groups. The effects of ED intake to reduce ADA-LOR were also assessed in antitumor necrosis factor-alpha (TNF-α)-naïve and infliximab (IFX)-intolerant or refractory CD patients. Serum ADA and TNF-α levels were measured.
We enrolled 117 CD patients into the ED (n = 25) or non-ED (n = 92) groups. Although the cumulative non-ADA-LOR rate was higher in the ED group than in the non-ED group, ED intake was not an independent reducing factor for ADA-LOR (adjusted hazard ratio = 0.725; 95% confidence interval: 0.448-1.180; P = 0.196) in all patients. ED intake was significantly more effective in reducing ADA-LOR in IFX-intolerant or refractory patients than in anti-TNF-α-naïve patients in a dose-related manner (P for interaction <0.20). Serum ADA levels did not differ between the groups. Serum TNF-α levels were significantly lower in the ED group than in the non-ED group at week 28 (P = 0.044) and week 52 (P = 0.043).
Concomitant ED therapy reduced ADA-LOR in IFX-intolerant or refractory patients in a dose-related manner. Reductions in the TNF-α levels by concomitant ED intake may contribute to reduce ADA-LOR in CD patients.
接受阿达木单抗(ADA)治疗的克罗恩病(CD)患者常出现 ADA 应答丧失(ADA-LOR)。我们评估了同时应用要素饮食(ED)治疗以降低 CD 成年患者 ADA-LOR 的疗效。
患者分为 ED(≥900kcal/天)或非 ED 组(<900kcal/天)。比较两组累积无 ADA-LOR 率。还评估了 ED 摄入对 TNF-α 拮抗剂初治和不耐受或难治性 CD 患者降低 ADA-LOR 的作用。检测血清 ADA 和 TNF-α 水平。
我们纳入 117 例 CD 患者至 ED(n=25)或非 ED 组(n=92)。尽管 ED 组累积无 ADA-LOR 率高于非 ED 组,但 ED 摄入不是 ADA-LOR 的独立降低因素(调整后的危险比=0.725;95%置信区间:0.448-1.180;P=0.196)。ED 摄入与剂量相关,在 IFX 不耐受或难治性患者中降低 ADA-LOR 的效果明显优于 TNF-α 拮抗剂初治患者(交互作用 P 值<0.20)。两组间血清 ADA 水平无差异。ED 组在第 28 周(P=0.044)和第 52 周(P=0.043)时的血清 TNF-α 水平显著低于非 ED 组。
同时应用 ED 治疗可使 IFX 不耐受或难治性患者以剂量依赖方式降低 ADA-LOR。同时摄入 ED 降低 TNF-α 水平可能有助于降低 CD 患者的 ADA-LOR。