Zeng Guixiang, Lian Jingjing, Shen Jiajia, Shi Yuan
Chongqing Key Laboratory of Pediatrics, Ministry of Education Key Laboratory of Child Development and Disorders, Department of Neonatology, National Clinical Research Center for Child Health and Disorders, Children's Hospital of Chongqing Medical University, Chongqing, China.
Department of Neonatology, Nanning Maternity and Child Health Hospital, Nanning, China.
Front Pediatr. 2025 Aug 4;13:1611877. doi: 10.3389/fped.2025.1611877. eCollection 2025.
Intrauterine growth restriction (IUGR) significantly affects neonatal development, but its pathogenesis is not fully understood. Klotho protein is involved in aging-related diseases, and its role in fetal growth is unclear. This study aims to explore Klotho's role in IUGR.
A case-control study was conducted at Nanning Maternal and Child Health Care Hospital from July 2023 to June 2024. Fifty-two neonates (gestational age ≥34 weeks and <42 weeks) were divided into the appropriate for gestational age (AGA) group ( = 30) and the IUGR group ( = 22). Venous and umbilical cord blood were collected to measure Klotho, growth hormone (GH), and insulin-like growth factor 1 (IGF-1). Placental tissues were examined for histopathology and immunohistochemistry.
The IUGR group showed placental morphological changes, including increased syncytial knots and inflammation. Klotho expression in placental tissue was significantly reduced ( < 0.0001), while IGF-1 levels increased ( < 0.001) and GH levels decreased ( < 0.001). Soluble α-Klotho levels were lower in maternal venous blood ( < 0.0001) and umbilical cord blood ( < 0.01). GH and IGF-1 levels in maternal venous blood and umbilical cord blood were altered in IUGR cases.
Reduced Klotho expression in IUGR cases, along with changes in GH and IGF-1, suggests disruptions in metabolic processes affecting fetal growth and development. These findings suggest a potential involvement of Klotho in placental changes and fetal development, warranting further mechanistic studies.
宫内生长受限(IUGR)显著影响新生儿发育,但其发病机制尚未完全明确。klotho蛋白与衰老相关疾病有关,其在胎儿生长中的作用尚不清楚。本研究旨在探讨klotho在IUGR中的作用。
于2023年7月至2024年6月在南宁市妇幼保健院进行病例对照研究。52例新生儿(胎龄≥34周且<42周)分为适于胎龄(AGA)组(n = 30)和IUGR组(n = 22)。采集静脉血和脐带血以检测klotho、生长激素(GH)和胰岛素样生长因子1(IGF-1)。对胎盘组织进行组织病理学和免疫组织化学检查。
IUGR组胎盘出现形态学改变,包括合体结节增多和炎症。胎盘组织中klotho表达显著降低(P < 0.0001),而IGF-1水平升高(P < 0.001),GH水平降低(P < 0.001)。母体静脉血(P < 0.0001)和脐带血(P < 0.01)中可溶性α-klotho水平较低。IUGR病例中母体静脉血和脐带血中的GH和IGF-1水平发生改变。
IUGR病例中klotho表达降低,同时伴有GH和IGF-1的变化,提示影响胎儿生长发育的代谢过程受到破坏。这些发现表明klotho可能参与胎盘变化和胎儿发育,值得进一步进行机制研究。