Lee Dale, Baldassano Robert N, Otley Anthony R, Albenberg Lindsey, Griffiths Anne M, Compher Charlene, Chen Eric Z, Li Hongzhe, Gilroy Erin, Nessel Lisa, Grant Amy, Chehoud Christel, Bushman Frederic D, Wu Gary D, Lewis James D
*Department of Pediatrics, Division of Gastroenterology, Hepatology and Nutrition, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania; †Department of Pediatric, Division of Gastroenterology and Nutrition Seattle Children's Hospital, Seattle, Washington; and University of Washington; ‡Department of Pediatrics, IWK Health Centre, Halifax, NS, Canada; §Department of Pediatrics, Division of Gastroenterology, Hepatology and Nutrition, Hospital for Sick Children, University of Toronto, Toronto, ON, Canada; ||School of Nursing, University of Pennsylvania, Philadelphia, Pennsylvania; ¶Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; **Department of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; and ††Department of Medicine, Division of Gastroenterology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Inflamm Bowel Dis. 2015 Aug;21(8):1786-93. doi: 10.1097/MIB.0000000000000426.
Therapeutic targets in pediatric Crohn's disease include symptoms, quality of life (QOL), and mucosal healing. Although partial enteral nutrition (PEN), exclusive enteral nutritional (EEN), and anti-tumor necrosis factor alpha (anti-TNF) therapy all improve symptoms, the comparative effectiveness of these approaches to improve QOL and achieve mucosal healing has not been assessed prospectively.
In a prospective study of children initiating PEN, EEN, or anti-TNF therapy for Crohn's disease, we compared clinical outcomes using the Pediatric Crohn's Disease Activity Index (PCDAI), QOL (IMPACT score), and mucosal healing as estimated by fecal calprotectin (FCP). PCDAI, IMPACT, FCP, and diet (prompted 24-h recall) were measured at baseline and after 8 weeks of therapy.
We enrolled 90 children with active Crohn's disease (PCDAI, 33.7 ± 13.7; and FCP, 976 ± 754), of whom 52 were treated with anti-TNF, 22 with EEN, and 16 with PEN plus ad lib diet. Clinical response (PCDAI reduction ≥15 or final PCDAI ≤10) was achieved by 64% on PEN, 88% EEN, and 84% anti-TNF (test for trend P = 0.08). FCP ≤250 μg/g was achieved with PEN in 14%, EEN 45%, and anti-TNF 62% (test for trend P = 0.001). Improvement in overall QOL was not statistically significantly different between the 3 groups (P = 0.86). However, QOL improvement was the greatest with EEN in the body image (P = 0.03) domain and with anti-TNF in the emotional domain (P = 0.04).
Although PEN improved clinical symptoms, EEN and anti-TNF were more effective for decreasing mucosal inflammation and improving specific aspects of QOL.
儿童克罗恩病的治疗目标包括症状、生活质量(QOL)和黏膜愈合。尽管部分肠内营养(PEN)、全肠内营养(EEN)和抗肿瘤坏死因子α(抗TNF)治疗均能改善症状,但这些方法改善生活质量和实现黏膜愈合的相对有效性尚未进行前瞻性评估。
在一项针对开始接受PEN、EEN或抗TNF治疗的克罗恩病儿童的前瞻性研究中,我们使用儿童克罗恩病活动指数(PCDAI)、生活质量(IMPACT评分)以及通过粪便钙卫蛋白(FCP)评估的黏膜愈合情况来比较临床结局。在基线和治疗8周后测量PCDAI、IMPACT、FCP和饮食情况(通过24小时饮食回顾提示)。
我们纳入了90例活动期克罗恩病儿童(PCDAI为33.7±13.7;FCP为976±754),其中52例接受抗TNF治疗,22例接受EEN治疗,16例接受PEN加自由饮食治疗。接受PEN治疗的患者临床缓解率(PCDAI降低≥15或最终PCDAI≤10)为64%,接受EEN治疗的为88%,接受抗TNF治疗的为84%(趋势检验P=0.08)。接受PEN治疗的患者中14%实现FCP≤250μg/g,接受EEN治疗的为45%,接受抗TNF治疗的为62%(趋势检验P=0.001)。三组间总体生活质量改善情况无统计学显著差异(P=0.86)。然而,在身体形象方面(P=0.03),EEN改善生活质量的效果最佳;在情感方面(P=0.04),抗TNF改善生活质量的效果最佳。
尽管PEN改善了临床症状,但EEN和抗TNF在减轻黏膜炎症和改善生活质量的特定方面更有效。