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单剂量合成人促胰液素治疗自闭症和广泛性发育障碍无效。

Lack of benefit of a single dose of synthetic human secretin in the treatment of autism and pervasive developmental disorder.

作者信息

Sandler A D, Sutton K A, DeWeese J, Girardi M A, Sheppard V, Bodfish J W

机构信息

Olson Huff Center for Child Development, Thoms Rehabilitation Hospital, Asheville, NC 28803, USA.

出版信息

N Engl J Med. 1999 Dec 9;341(24):1801-6. doi: 10.1056/NEJM199912093412404.

Abstract

BACKGROUND

Secretin is a peptide hormone that stimulates pancreatic secretion. After recent publicity about a child with autism whose condition markedly improved after a single dose of secretin, thousands of children with autistic disorders may have received secretin injections.

METHODS

We conducted a double-blind, placebo-controlled trial of a single intravenous dose of synthetic human secretin in 60 children (age, 3 to 14 years) with autism or pervasive developmental disorder. The children were randomly assigned to treatment with an intravenous infusion of synthetic human secretin (0.4 microg per kilogram of body weight) or saline placebo. We used standardized behavioral measures of the primary and secondary features of autism, including the Autism Behavior Checklist, to assess the degree of impairment at base line and over the course of a four-week period after treatment.

RESULTS

Of the 60 children, 4 could not be evaluated - 2 received secretin outside the study, and 2 did not return for follow-up. Thus, 56 children (28 in each group) completed the study. As compared with placebo, secretin treatment was not associated with significant improvements in any of the outcome measures. Among the children in the secretin group, the mean total score on the Autism Behavior Checklist at base line was 59.0 (range of possible values, 0 to 158, with a larger value corresponding to greater impairment), and among those in the placebo group it was 63.2. The mean decreases in scores over the four-week period were 8.9 in the secretin group and 17.8 in the placebo group (mean difference, -8.9; 95 percent confidence interval, -19.4 to 1.6; P=0.11). None of the children had treatment-limiting adverse effects. After they were told the results, 69 percent of the parents of the children in this study said they remained interested in secretin as a treatment for their children.

CONCLUSIONS

A single dose of synthetic human secretin is not an effective treatment for autism or pervasive developmental disorder.

摘要

背景

促胰液素是一种刺激胰腺分泌的肽类激素。最近有报道称,一名自闭症患儿在注射一剂促胰液素后病情显著改善,此后数千名自闭症谱系障碍患儿可能接受了促胰液素注射。

方法

我们对60名年龄在3至14岁之间的自闭症或广泛性发育障碍儿童进行了一项双盲、安慰剂对照试验,给予单次静脉注射合成人促胰液素。这些儿童被随机分配接受静脉输注合成人促胰液素(0.4微克/千克体重)或生理盐水安慰剂治疗。我们使用标准化的行为测量方法评估自闭症的主要和次要特征,包括自闭症行为量表,以评估基线时以及治疗后四周内的损害程度。

结果

60名儿童中,4名无法进行评估——2名在研究外接受了促胰液素治疗,2名未返回进行随访。因此,56名儿童(每组28名)完成了研究。与安慰剂相比,促胰液素治疗在任何一项结局指标上均未显示出显著改善。促胰液素组儿童在自闭症行为量表上的基线平均总分是59.0(可能值范围为0至158,值越大表明损害越严重),安慰剂组为63.2。在四周期间,促胰液素组的平均得分下降了8.9,安慰剂组下降了17.8(平均差异为-8.9;95%置信区间为-19.4至1.6;P = 0.11)。没有儿童出现限制治疗的不良反应。在得知结果后,本研究中69%的儿童家长表示他们仍然对促胰液素作为其孩子的治疗方法感兴趣。

结论

单次注射合成人促胰液素对自闭症或广泛性发育障碍并非有效治疗方法。

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