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屏气发作儿童中乳糜泻的发生率。

Frequency of coeliac disease in children with breath-holding spells.

作者信息

Işikay Sedat, Hızlı Şamil

机构信息

Department of Pediatric Neurology, Gaziantep Children's Hospital, Gaziantep, Turkey.

出版信息

J Paediatr Child Health. 2014 Nov;50(11):916-9. doi: 10.1111/jpc.12639. Epub 2014 Jun 13.

DOI:10.1111/jpc.12639
PMID:24923596
Abstract

AIM

Iron deficiency anaemia (IDA), which is reported very commonly among patients with breath holding spells (BHS), is the most common presentation of coeliac disease (CD). In that aspect, IDA may be a common pathway linking these two diseases. The aim of this study was to evaluate the frequency of CD in patients with BHS.

METHODS

We studied 348 children with BHS, and 470 age- and sex-matched controls with no known disease. Serological screening for CD was performed in all patients by searching for serum tissue transglutaminase immunoglobulin A.

RESULTS

The first group consisted of 348 children with BHS (231 males, 117 females; mean age 2.23 ± 1.84 years), and the second group consisted of 470 healthy children (284 males, 186 females; mean age 2.11 ± 1.98 years). A total of 300 (86.2%) patients had cyanotic type of BHS only, 27 (7.8%) had pallid type of BHS only and 21 (6%) had mixed type of BHS. The prevalence of IDA was statistically significantly higher in BHS patients compared with controls. Tissue transglutaminase immunoglobulin A was not detected as positive in any patients in either group; therefore, endoscopic and histopathological examinations were not performed.

CONCLUSIONS

Our report is the first to describe the frequency of tissue transglutaminase immunoglobulin A positivity in patients with BHS. There was no evidence of a relationship between CD and BHS, but IDA seems to be an important risk factor in the development of BHS. Therefore, serological screening for CD in patients with BHS does not seem to be necessary.

摘要

目的

缺铁性贫血(IDA)在屏气发作(BHS)患者中报道极为常见,是乳糜泻(CD)最常见的表现形式。从这方面来看,IDA可能是连接这两种疾病的共同途径。本研究的目的是评估BHS患者中CD的发生率。

方法

我们研究了348例BHS患儿以及470例年龄和性别匹配、无已知疾病的对照儿童。通过检测血清组织转谷氨酰胺酶免疫球蛋白A对所有患者进行CD的血清学筛查。

结果

第一组由348例BHS患儿组成(男231例,女117例;平均年龄2.23±1.84岁),第二组由470例健康儿童组成(男284例,女186例;平均年龄2.11±1.98岁)。共有300例(86.2%)患者仅为青紫型BHS,27例(7.8%)仅为苍白型BHS,21例(6%)为混合型BHS。与对照组相比,BHS患者中IDA的患病率在统计学上显著更高。两组中均未检测到任何患者的组织转谷氨酰胺酶免疫球蛋白A呈阳性;因此,未进行内镜和组织病理学检查。

结论

我们的报告首次描述了BHS患者中组织转谷氨酰胺酶免疫球蛋白A阳性的发生率。没有证据表明CD与BHS之间存在关联,但IDA似乎是BHS发生的一个重要危险因素。因此,对BHS患者进行CD的血清学筛查似乎没有必要。

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引用本文的文献

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2
Breath-holding spells in infants.婴儿屏气发作
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