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首页> 外文期刊>European journal of pediatrics >Ascorbate acid concentration in airways lining fluid from infants who develop chronic lung disease of prematurity.
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Ascorbate acid concentration in airways lining fluid from infants who develop chronic lung disease of prematurity.

机译:患有早产儿慢性肺部疾病的婴儿的呼吸道衬里液中的抗坏血酸浓度较高。

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摘要

Chronic lung disease of prematurity (CLD) remains a common cause of morbidity and mortality in preterm infants. Oxygen toxicity remains a major risk factor for the development of CLD and as a consequence the antioxidant status of CLD babies is a major focus of interest. In the present study, we determined whether ascorbate, urate, and total glutathione concentrations were decreased in infants who developed CLD when compared to those who did not. From 34 preterm infants, 141 serial bronchoalveolar lavage fluid (BALF) and plasma samples were collected: 12 developed CLD (median gestation 26 weeks, range 23-28 weeks, median birth weight 780 g, range 630-1070 g), 16 developed and recovered from respiratory distress syndrome (RDS) (median gestation 31 weeks, range 26-39 weeks, median birth weight 1820 g, range 840-4160 g), and six were ventilated for non-respiratory reasons, (median gestation 35 weeks, range 32-38 weeks, median birth weight 2180 g, range 1100-2860 g). Following birth, the concentration of BALF ascorbate, urate and glutathione decreased over the 1st week in all three groups. Thereafter, BALF ascorbate increased in RDS and control infants during the 2nd week but this increase was delayed by 2 weeks in the CLD infants. No differences were noted between the RDS and CLD groups for urate and total glutathione in BALF or urate in plasma. BALF protein concentration was similar in all three groups except for a rise at day 7 in the CLD group but this did not reach statistical significance. Conclusion. A delayed increase in bronchoalveolar lavage fluid ascorbate concentration might be associated with an increased risk of developing chronic lung disease of prematurity.
机译:慢性早产儿肺部疾病(CLD)仍然是早产儿发病和死亡的常见原因。氧气毒性仍然是导致CLD发生的主要危险因素,因此,CLD婴儿的抗氧化剂状态成为人们关注的主要焦点。在本研究中,我们确定了患CLD的婴儿与未患CLD的婴儿相比,抗坏血酸,尿酸和总谷胱甘肽浓度是否降低。从34例早产儿中,收集了141份连续性支气管肺泡灌洗液(BALF)和血浆样本:12例发育中的CLD(中位妊娠26周,范围23-28周,中位出生体重780 g,范围630-1070 g),16例发育中和从呼吸窘迫综合征(RDS)中恢复(中位妊娠31周,范围26-39周,中位出生体重1820 g,范围840-4160 g),其中6位因非呼吸原因而通气(中位妊娠35周,范围32-38周,中位数出生体重2180克,范围1100-2860克)。出生后,所有三个组的第一周BALF抗坏血酸,尿酸和谷胱甘肽的浓度均下降。此后,RDS和对照组婴儿的BALF抗坏血酸在第二周增加,但CLD婴儿的这种增加被推迟了2周。在RDS和CLD组之间,BALF中的尿酸盐和总谷胱甘肽或血浆中的尿酸盐没有发现差异。除CLD组在第7天升高外,所有三个组的BALF蛋白浓度均相似,但这未达到统计学意义。结论。支气管肺泡灌洗液中抗坏血酸浓度的延迟增加可能与患早产儿慢性肺病的风险增加有关。

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