诉诸司法。

B. Dimond
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引用次数: 237

摘要

背景:一组小肠结肠炎儿童暴露于含麻疹疫苗(MCV)和自闭症样发育退化之间的时间相关性已经被报道。在这些儿童的回肠活检中检测到麻疹病毒(MV),其患病率高于发育正常的儿科对照。本研究检验了MCV暴露对肠道病理的剂量反应效应假设,作为因果关系的证据。方法/主要发现:将早期发育正常和自闭症样发育退化的儿童分为两组:再次暴露的儿童(n=23),他们接种了不止一剂含麻疹疫苗(MCV),和一次暴露的儿童(n=23),他们只接种了一剂含麻疹疫苗。各组按性别、年龄和第一次接触内窥镜的时间进行匹配。比较包括:继发性(20)胃肠道(GI)和相关身体症状以及内镜和组织学疾病的观察者盲法评分。再次暴露儿童的20项身体症状得分明显高于一次暴露儿童,包括尿失禁、存在严重回肠淋巴样增生、上皮损伤的活检次数和急性炎症的儿童数量。急性炎症的标志物包括受影响的儿童数量和受影响的活检比例结论/意义:数据确定了对症状的再挑战效应和对肠道病理的生物梯度效应,将MCV暴露与自闭症样发育退化和小肠结肠炎联系起来。
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Access to justice.
Background: A temporal association between exposure to measles-containing vaccine (MCV) and autistic-like developmental regression in a sub-set of children with enterocolitis has been reported. Measles virus (MV) was detected in ileal biopsies from these children at higher prevalence than in developmentally normal paediatric controls. This study tested the hypothesis of a dose-response effect of MCV exposure on intestinal pathology, as evidence of a causal association. Methodology/Principle Findings: Children with normal early development and autistic-like developmental regression were divided into two groups: reexposed children (n=23), who had received more than one dose of a measlescontaining vaccine (MCV), and once-exposed children (n=23), who had received only one dose of MCV. The groups were matched for sex, age, and time-elapsed from first exposure to endoscopy. Comparisons included: secondary (2o) gastrointestinal (GI) and related physical symptoms and observer-blinded scores of endoscopic and histological disease. Re-exposed children scored significantly higher than once-exposed for 2o physical symptoms including incontinence, presence of severe ileal lymphoid hyperplasia, number of biopsies with epithelial damage and number of children with acute inflammation. Markers of acute inflammation included number of children affected and proportion of biopsies affected Conclusion/Significance: The data identify a re-challenge effect on symptoms and a biological gradient effect on intestinal pathology, which links MCV exposure to autistic-like developmental regression and enterocolitis.
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