King Faisal Specialist Hospital and Research Centre, Environmental Health Program (MBC#03), P.O. Box: 3354, Riyadh, 11211, Saudi Arabia.
Center for Autism Research, King Faisal Specialist Hospital and Research Centre, P.O. Box: 3354, Riyadh, 11211, Saudi Arabia.
Sci Rep. 2023 Apr 28;13(1):6969. doi: 10.1038/s41598-023-33715-w.
This prospective study assessed the exposure to phthalates of preterm neonates who received total parenteral nutrition (TPN) during their stay in the neonatal intensive care unit (NICU) and the risk of neurodevelopment delays at the age of 2 months. Our study recruited 33 preterm neonates who required TPN upon NICU admission. Urine samples for analyzing phthalate metabolites were obtained at admission and then daily until the last day of receiving TPN. Phthalates in the daily TPN received by the preterm neonates were analyzed. The neurodevelopment of the neonates was assessed using the Ages and Stages Questionnaire Edition 3 (ASQ-3). Diethyl phthalate and butyl benzyl phthalate were found in all TPN samples, while 27% and 83% contained dibutyl phthalate and di-(2-ethylhexyl) phthalate (DEHP), respectively. Yet, the daily dose of each phthalate that our preterm neonates received from TPN was much lower than the recommended tolerable limit. Urinary levels of monobenzyl phthalate and four metabolites of DEHP [i.e., mono-(2-ethylhexyl) phthalate (MEHP), mono-(2-ethyl-5-hydroxyhexyl) phthalate, mono-(2-ethyl-5-oxohexyl) phthalate (MEOHP), and mono-(2-ethyl-5-carboxypentyl) phthalate (MECPP)] and the sum of four DEHP metabolites (∑DEHP) increased significantly in preterm neonates before discharge. However, these levels were not correlated with their phthalate parent compounds in TPN, suggesting other sources of exposure in the NICU. At 2 months, we found that urinary levels of mono-iso-butyl phthalate (MiBP), MECPP, MEHP, and ∑DEHP were inversely related to fine motor skills. After adjusting for head circumference, the inverse relationships remained significant, suggesting direct effects from phthalates. Given the extreme vulnerability of our population, it is critical to minimize exposure to phthalates during their NICU stay.
这项前瞻性研究评估了在新生儿重症监护病房(NICU)接受全肠外营养(TPN)的早产儿接触邻苯二甲酸酯的情况,以及他们在 2 个月大时神经发育延迟的风险。我们的研究招募了 33 名在 NICU 入院时需要 TPN 的早产儿。在入院时和随后每天采集尿液样本,以分析邻苯二甲酸酯代谢物,直至接受 TPN 的最后一天。分析了早产儿每日接受的 TPN 中的邻苯二甲酸酯。使用 Ages and Stages Questionnaire Edition 3(ASQ-3)评估新生儿的神经发育。所有 TPN 样本中均发现了邻苯二甲酸二乙酯和丁基苄基邻苯二甲酸酯,而 27%和 83%的样本分别含有邻苯二甲酸二丁酯和邻苯二甲酸二(2-乙基己基)酯(DEHP)。然而,我们的早产儿从 TPN 中接受的每种邻苯二甲酸的日剂量都远低于推荐的可耐受限度。在早产儿出院前,单苄基邻苯二甲酸酯和 DEHP 的四种代谢物[即单(2-乙基己基)邻苯二甲酸酯(MEHP)、单(2-乙基-5-羟基己基)邻苯二甲酸酯、单(2-乙基-5-氧代己基)邻苯二甲酸酯(MEOHP)和单(2-乙基-5-羧基戊基)邻苯二甲酸酯(MECPP)]以及四种 DEHP 代谢物的总和(∑DEHP)的尿液水平显著升高。然而,这些水平与 TPN 中的邻苯二甲酸母体化合物无关,表明在 NICU 中有其他暴露源。在 2 个月时,我们发现尿液中单异丁基邻苯二甲酸酯(MiBP)、MECPP、MEHP 和∑DEHP 水平与精细运动技能呈负相关。在调整头围后,这种负相关仍然显著,表明邻苯二甲酸有直接影响。鉴于我们人群的极端脆弱性,在 NICU 期间尽量减少接触邻苯二甲酸至关重要。