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波兰孕妇孕中期羊水内必需元素和有毒元素浓度与胎儿染色体异常之间的关联

Association between the Concentrations of Essential and Toxic Elements in Mid-Trimester Amniotic Fluid and Fetal Chromosomal Abnormalities in Pregnant Polish Women.

作者信息

Suliburska Joanna, Pankiewicz Jakub, Sajnóg Adam, Paczkowska Magdalena, Nowakowska Beata, Bakinowska Ewa, Barałkiewicz Danuta, Kocyłowski Rafał

机构信息

Department of Human Nutrition and Dietetics, Poznan University of Life Sciences, Wojska Polskiego St. 31, 60-624 Poznan, Poland.

PreMediCare New Med Medical Center, ul. Drużbickiego 13, 61-693 Poznan, Poland.

出版信息

Diagnostics (Basel). 2022 Apr 13;12(4):979. doi: 10.3390/diagnostics12040979.

Abstract

The present study aimed to investigate the relationship between the concentrations of essential and toxic elements present in the amniotic fluid (AF) and fetal chromosomal abnormalities in pregnant women. A total of 156 pregnant white Polish women aged between 20 and 43 years and screened to detect high risk for chromosomal defects in the first trimester were included in the study. AF samples were collected from these women during routine diagnostic and treatment procedures at mid-gestation (15-22 weeks of their pregnancies). The concentrations of various minerals in the AF were determined by inductively coupled plasma mass spectrometry. Genomic hybridization and cytogenetic karyotyping were performed to detect chromosomal aberrations in the fetuses. The genetic analysis revealed chromosomal aberrations in 19 fetuses (over 12% of all the evaluated women). The major abnormalities identified were trisomy 21 (N = 11), trisomy 18 (N = 2), and triploidy (N = 2). Fetuses with chromosomal abnormalities more frequently showed lower manganese concentration in the AF in the second trimester as compared to those with normal karyotype. A coincidence was observed between high iron levels in the AF and a higher risk of chromosomal abnormalities in the fetuses.

摘要

本研究旨在探讨羊水(AF)中必需元素和有毒元素的浓度与孕妇胎儿染色体异常之间的关系。共有156名年龄在20至43岁之间的波兰白人孕妇参与了该研究,她们在孕早期经过筛查被判定为染色体缺陷高危人群。在孕中期(怀孕15至22周)的常规诊断和治疗过程中,采集了这些孕妇的羊水样本。采用电感耦合等离子体质谱法测定羊水中各种矿物质的浓度。进行基因组杂交和细胞遗传学核型分析以检测胎儿的染色体畸变。遗传分析显示,19名胎儿存在染色体畸变(占所有评估孕妇的12%以上)。鉴定出的主要异常为21三体(N = 11)、18三体(N = 2)和三倍体(N = 2)。与核型正常的胎儿相比,染色体异常的胎儿在孕中期羊水中锰浓度更低。观察到羊水中高铁水平与胎儿染色体异常风险较高之间存在关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b339/9026427/629464dc1dde/diagnostics-12-00979-g001.jpg

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