Francisco Mary Pat, Wagner Mary H, Sherman James M, Theriaque Douglas, Bowser Ellen, Novak Donald A
Departments of Pediatrics, University of Florida, Gainesville, Florida 32610, USA.
J Pediatr Gastroenterol Nutr. 2002 Jul;35(1):79-83. doi: 10.1097/00005176-200207000-00017.
Inadequate treatment of pancreatic insufficiency in patients with cystic fibrosis (CF) causes malabsorption of nutrients with significant sequelae. The objective of this study was to measure the effect of acid suppressant therapy on fat absorption in patients with CF who received a pH-sensitive, enteric-coated microtablet enzyme product.
A double-blind, placebo-controlled crossover study of 12 children and 10 adults with pancreatic insufficient CF was performed. All subjects were receiving pancrelipase therapy (Pancrease MT10 and MT16; Ortho-McNeil, Springhouse, PA, U.S.A.) and for the study also received either placebo or ranitidine (Zantac; Glaxo-Wellcome, Research Triangle Park, NC U.S.A.) 5 mg/kg or 10 mg/kg daily. The adult subjects also received omeprazole therapy (Prilosec; AstraZeneca/Merck, Wilmington, DE, U.S.A.), 20 mg daily, as adjuvant therapy to pancreatic enzymes. Serial 3-day fat-balance studies were performed in the Clinical Research Center. The data were analyzed using individual paired t tests that compared each treatment with placebo and two repeated-measures, general linear model F tests.
The linear model for all subjects showed no overall adjuvant drug effect on fat absorption, P = 0.32. A second linear model F test analysis of adult subjects, comparing all four drug treatments (placebo, ranitidine 5 and 10 mg/kg daily and omeprazole), also showed no difference in fat absorption, P = 0.15. Paired t test subgroup analysis of the adults showed an improvement of 4.97% (P = 0.003) in mean fat absorption comparing low-dose ranitidine to placebo. All other t test analyses showed no significant change in fat absorption between placebo and acid suppressant treatment. There was marked intersubject and intrasubject variability in fat absorption.
No overall significant improvement in fat absorption could be demonstrated with adjuvant therapy. Fat absorption measured by 3-day fat-balance studies varied greatly even when comparing the same subject for placebo and baseline treatments, despite identical dietary fat and enzyme intakes. The large variability limited our ability to test for a difference in fat absorption and has significant implication for the use of this test, considered the gold standard, for determining enzyme dosage adequacy.
囊性纤维化(CF)患者胰腺功能不全治疗不充分会导致营养物质吸收不良并产生严重后果。本研究的目的是测定抑酸疗法对接受pH敏感型肠溶微片酶产品治疗的CF患者脂肪吸收的影响。
对12名儿童和10名胰腺功能不全的CF成年患者进行了一项双盲、安慰剂对照交叉研究。所有受试者均接受胰酶疗法(胰酶胶囊MT10和MT16;美国新泽西州春屋市奥多-麦克尼尔公司),且在研究中还每日接受安慰剂或雷尼替丁(善胃得;美国北卡罗来纳州三角研究园葛兰素威康公司)5mg/kg或10mg/kg的治疗。成年受试者还每日接受奥美拉唑疗法(洛赛克;美国特拉华州威尔明顿阿斯利康/默克公司)20mg作为胰酶的辅助治疗。在临床研究中心进行了连续3天的脂肪平衡研究。使用个体配对t检验对数据进行分析,该检验将每种治疗与安慰剂进行比较,并进行了两次重复测量的一般线性模型F检验。
所有受试者的线性模型显示,辅助药物对脂肪吸收无总体影响,P = 0.32。对成年受试者进行的第二次线性模型F检验分析,比较了所有四种药物治疗(安慰剂、每日5mg/kg和10mg/kg的雷尼替丁以及奥美拉唑),结果也显示脂肪吸收无差异,P = 0.15。对成年受试者的配对t检验亚组分析显示,与安慰剂相比,低剂量雷尼替丁使平均脂肪吸收提高了4.97%(P = 0.003)。所有其他t检验分析均显示,安慰剂与抑酸治疗之间的脂肪吸收无显著变化。脂肪吸收在受试者间和受试者内均存在显著差异。
辅助治疗未能证明脂肪吸收有总体显著改善。即使在比较同一受试者的安慰剂和基线治疗时,尽管饮食脂肪和酶摄入量相同,但通过3天脂肪平衡研究测得的脂肪吸收仍有很大差异。这种巨大的变异性限制了我们检测脂肪吸收差异的能力,并且对于使用这一被视为金标准的检测方法来确定酶剂量是否充足具有重要意义。