Suppr超能文献

羊水中端粒缩短:异常胎儿发育的早期生物标志物?

Reduced telomere length in amniocytes: an early biomarker of abnormal fetal development?

机构信息

Cytogénétique Médicale, CHU Clermont-Ferrand, CHU Estaing, F-63000 Clermont-Ferrand, France.

INSERM U1240 Imagerie Moléculaire et Stratégies Théranostiques, Université Clermont Auvergne, Clermont-Ferrand, France.

出版信息

Hum Mol Genet. 2022 Aug 23;31(16):2669-2677. doi: 10.1093/hmg/ddac054.

Abstract

Telomeres protect chromosome ends and control cell division and senescence. During organogenesis, telomeres need to be long enough to ensure the cell proliferation necessary at this stage of development. Previous studies have shown that telomere shortening is associated with growth retardation and congenital malformations. However, these studies were performed in newborns or postnatally, and data on telomere length (TL) during the prenatal period are still very limited. We measured TL using quantitative PCR in amniotic fluid (AF) and chorionic villi (CV) samples from 69 control fetuses with normal ultrasound (52 AF and 17 CV) and 213 fetuses (165 AF and 48 CV) with intrauterine growth retardation (IUGR) or congenital malformations diagnosed by ultrasound. The samples were collected by amniocentesis at the gestational age (GA) of 25.0 ± 5.4 weeks and by CV biopsy at 18.1 ± 6.3 weeks. In neither sample type was TL influenced by GA or fetal sex. In AF, a comparison of abnormal versus normal fetuses showed a significant telomere shortening in cases of IUGR (reduction of 34%, P < 10-6), single (29%, P < 10-6) and multiple (44%, P < 10-6) malformations. Similar TL shortening was also observed in CV from abnormal fetuses but to a lesser extent (25%, P = 0.0002; 18%, P = 0.016; 20%, P = 0.004, respectively). Telomere shortening was more pronounced in cases of multiple congenital anomalies than in fetuses with a single malformation, suggesting a correlation between TL and the severity of fetal phenotype. Thus, TL measurement in fetal samples during pregnancy could provide a novel predictive marker of pathological development.

摘要

端粒保护染色体末端并控制细胞分裂和衰老。在器官发生过程中,端粒需要足够长以确保在发育的这个阶段所需的细胞增殖。先前的研究表明,端粒缩短与生长迟缓及先天性畸形有关。然而,这些研究是在新生儿或出生后进行的,关于产前阶段端粒长度(TL)的数据仍然非常有限。我们使用定量 PCR 测量了 69 例超声正常的胎儿(52 例羊水样本和 17 例绒毛膜样本)和 213 例胎儿(165 例羊水样本和 48 例绒毛膜样本)的 TL,这些胎儿患有宫内生长受限(IUGR)或超声诊断的先天性畸形。这些样本是通过在妊娠龄 25.0±5.4 周时进行羊膜穿刺术和在 18.1±6.3 周时进行绒毛膜活检收集的。在这两种样本类型中,TL 均不受胎龄或胎儿性别影响。在羊水样本中,异常胎儿与正常胎儿的比较显示 IUGR 病例中端粒显著缩短(减少 34%,P<10-6),单发性(29%,P<10-6)和多发性(44%,P<10-6)畸形也是如此。异常胎儿的绒毛膜样本也观察到类似的 TL 缩短,但程度较轻(25%,P=0.0002;18%,P=0.016;20%,P=0.004)。多发性先天性异常病例中的端粒缩短比单一畸形胎儿更为明显,表明 TL 与胎儿表型严重程度之间存在相关性。因此,在妊娠期间对胎儿样本进行 TL 测量可能为病理性发育提供一种新的预测标志物。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验