Yin Xiao-juan, Luo Fen-ping, Li Ai-hua, An Yu-lin, Feng Zhi-chun
Department of Pediatrics, Bayi Children's Hospital, General Hospital of Beijing Military Command, Beijing 100700, China.
Zhonghua Er Ke Za Zhi. 2008 Jan;46(1):9-12.
To investigate possible relationship between expression of surfactant protein B (SP-B) gene product and neonatal respiratory distress syndrome (NRDS) in Han ethnic group.
Unrelated 20 cases with NRDS of Han ethnic group were selected as NRDS group while unrelated 20 diseases cases of Han ethnic group with diseases were selected as control group. The cases in the control group had congenital heart disease or bronchopulmonary dysplasia or persistent pulmonary hypertension. Blood sample was taken from every case. Lung tissues were taken from the patients who died half an hour after death in the two groups. Expression of SP-B in lung tissue was determined with immunohistochemical tecnique. Genetic deficiency variant of SP-B intron IV was screened with polymerase chain reaction (PCR).
Two cases at gestational age 26 weeks and one case at gestational age 34 weeks and two cases at gestational age 42 weeks of NRDS groups had lower level expression of SP-B in lung tissue than those at the same age of NRDS. Expression of SP-B in lung tissue of control group increased with gestational age, but no such phenomenon was found in NRDS group. Further, two cases at gestational age 42 weeks of NRDS group had genetic deficiency variant of SP-B intron IV with gene analysis of five cases who had lower expression of SP-B. Clinical data suggest that patients at 42 weeks of gestational age had severe illness.
Decrease of SP-B expression may participate in occurrence of NRDS, genetic deficiency variant of SP-B intron IV exists in the NRDS cases of Han ethnic group of China.
探讨汉族新生儿呼吸窘迫综合征(NRDS)与表面活性蛋白B(SP-B)基因产物表达的可能关系。
选取20例汉族无关NRDS患儿作为NRDS组,另选取20例汉族无关疾病患儿作为对照组,对照组患儿患有先天性心脏病、支气管肺发育不良或持续性肺动脉高压。采集每组患儿的血样。从两组死亡半小时后的患儿身上获取肺组织。采用免疫组化技术检测肺组织中SP-B的表达。用聚合酶链反应(PCR)筛查SP-B内含子IV的基因缺陷变异。
NRDS组中,2例孕26周患儿、1例孕34周患儿和2例孕42周患儿肺组织中SP-B的表达水平低于同孕周的NRDS患儿。对照组肺组织中SP-B的表达随孕周增加而升高,但NRDS组未发现此现象。此外,对5例SP-B表达较低的患儿进行基因分析,发现NRDS组中2例孕42周患儿存在SP-B内含子IV的基因缺陷变异。临床资料显示,孕42周的患儿病情严重。
SP-B表达降低可能参与NRDS的发生,中国汉族NRDS病例存在SP-B内含子IV的基因缺陷变异。