Early hypoglycemia is not an independent risk factor for 2-year cognitive impairment in small for gestational age preterm infants of less than 32 weeks.

IF 3 3区 医学 Q1 PEDIATRICS
Martina Palazzo, Alessio Correani, Margherita Bonanni, Enrica Ferretti, Rita D'Ascenzo, Chiara Biagetti, Ilaria Burattini, Paola Cogo, Virgilio Carnielli
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引用次数: 0

Abstract

The objective of this study is to evaluate whether early hypoglycemia is an independent risk factor for 2-year cognitive (COG) impairment in small for gestational age (SGA) preterm infants with gestational age (GA) < 32 weeks. We retrospectively reviewed data of 1364 preterm infants with a GA 24+0/7-31+6/7 weeks. Infants were classified based on blood glucose concentrations within the first 6 h of life (HOL) as < or ≥ 40 mg/dL (Glyc < 40[Birth-6HOL] and Glyc ≥ 40[Birth-6HOL], respectively) and subsequently by birth weight z-score as SGA or appropriate for gestational age (AGA). Propensity score matching analyses were conducted for each comparison. Multiple logistic regression was used to evaluate the association of Glyc < 40[Birth-6HOL] with 2-year COG impairment, defined as a Bayley-III score < 85, in SGA infants. Out of the 747 preterm infants who met the inclusion criteria, 173 (23.2%) were classified as Glyc < 40[Birth-6HOL], and 574 (76.8%) as Glyc ≥ 40[Birth-6HOL]. The proportion of SGA infants was significantly higher in Glyc < 40[Birth-6HOL] than in Glyc ≥ 40[Birth-6HOL] (25.4 vs 18.3%, p = 0.039). The incidence of 2-year COG impairment was significantly higher in SGA infants compared to matched AGA counterparts both in Glyc < 40[Birth-6HOL] (+ 20%, p = 0.040) and Glyc ≥ 40[Birth-6HOL] (+ 17%, p = 0.029). Neither in the entire cohort nor in the SGA infants, Glyc < 40[Birth-6HOL] was significantly associated with 2-year COG impairment (aOR: 1.077, p = 0.768; 0.993, p = 0.935; respectively) after the adjustment for GA, sex, Apgar score at 5 min < 7, SGA status, complications of prematurity, duration of mechanical ventilator support > 7 days, cumulative energy intakes from birth to 36 weeks, and maternal university level.

Conclusion:  Among SGA preterm infants with GA between 24+0/7 and 31+6/7 weeks/days, hypoglycemia within the first 6 HOL was not an independent risk factor for 2-year COG impairment.

What is known: • Hypoglycemia is associated with poor neurodevelopmental outcomes in preterm infants. • Small for gestational age (SGA) preterm infants are more prone to cognitive (COG) impairment compared to AGA counterparts.

What is new: • In a large cohort of preterm infants < 32 weeks, the incidence of hypoglycemia within the first 6 hours of life (HOL) was higher in SGA compared to AGA. • Hypoglycemia within the first 6 HOL was not an independent risk factor for 2-year COG impairment in SGA preterm infants.

早期低血糖并不是小于32周的小胎龄早产儿2岁认知障碍的独立危险因素。
本研究的目的是评估早期低血糖是否是胎龄(GA) +0/7-31+6/7周的小胎龄(SGA)早产儿2岁认知(COG)障碍的独立危险因素。根据婴儿出生后6小时内的血糖浓度(HOL)分别分类为[birth - 6hol]和血糖≥40[birth - 6hol],随后根据出生体重z分数(z-score)分类为SGA或适合胎龄(AGA)。对每次比较进行倾向评分匹配分析。采用多元logistic回归评估Glyc [Birth-6HOL]与2年COG损害的关系,定义为Bayley-III评分[Birth-6HOL],定义为Glyc≥40[Birth-6HOL]为574(76.8%)。Glyc [Birth-6HOL]组SGA婴儿比例显著高于Glyc≥40[Birth-6HOL]组(25.4% vs 18.3%, p = 0.039)。在Glyc [Birth-6HOL] (+ 20%, p = 0.040)和Glyc≥40[Birth-6HOL] (+ 17%, p = 0.029)中,SGA婴儿2年COG损伤的发生率均显著高于AGA配对婴儿。无论是在整个队列中还是在SGA婴儿中,Glyc [Birth-6HOL]都与2岁时的COG损伤显著相关(aOR: 1.077, p = 0.768;0.993, p = 0.935;分别)调整GA、性别、5 min 7 d时Apgar评分、出生至36周累积能量摄入量和母亲大学水平后。结论:在GA在24+0/7 ~ 31+6/7周/天的SGA早产儿中,前6周的低血糖并不是2年COG损伤的独立危险因素。•低血糖与早产儿神经发育不良有关。•小胎龄(SGA)早产儿比AGA早产儿更容易出现认知障碍(COG)。新发现:•在一组< 32周的早产儿中,SGA组出生后6小时内低血糖的发生率高于AGA组。•前6个月的低血糖并不是SGA早产儿2年COG损伤的独立危险因素。
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来源期刊
CiteScore
5.90
自引率
2.80%
发文量
367
审稿时长
3-6 weeks
期刊介绍: The European Journal of Pediatrics (EJPE) is a leading peer-reviewed medical journal which covers the entire field of pediatrics. The editors encourage authors to submit original articles, reviews, short communications, and correspondence on all relevant themes and topics. EJPE is particularly committed to the publication of articles on important new clinical research that will have an immediate impact on clinical pediatric practice. The editorial office very much welcomes ideas for publications, whether individual articles or article series, that fit this goal and is always willing to address inquiries from authors regarding potential submissions. Invited review articles on clinical pediatrics that provide comprehensive coverage of a subject of importance are also regularly commissioned. The short publication time reflects both the commitment of the editors and publishers and their passion for new developments in the field of pediatrics. EJPE is active on social media (@EurJPediatrics) and we invite you to participate. EJPE is the official journal of the European Academy of Paediatrics (EAP) and publishes guidelines and statements in cooperation with the EAP.
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