Advances in Understanding the Mechanism of Transitional Neonatal Hypoglycemia and Implications for Management

被引:15
作者
Stanescu, Diana L. [1 ]
Stanley, Charles A. [1 ]
机构
[1] Univ Penn, Childrens Hosp Philadelphia, Dept Pediat, Div Endocrinol,Perelman Sch Med, 34th St & Civ Ctr Blvd, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
Hyperinsulinism; Transitional hypoglycemia; High-risk newborn; KATP channel; Hypoxia inducible factor; Congenital hyperinsulinism; Pancreatic islets; ATP CHANNEL TRAFFICKING; PANCREATIC BETA-CELLS; HEALTHY TERM INFANTS; 1ST; 5; DAYS; ENDOCRINE-SOCIETY; GLUCOSE; BABIES; FETAL; ASSOCIATION; MATURATION;
D O I
10.1016/j.clp.2021.11.007
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Our lack of basic knowledge about the basic mechanisms of transitional hypoglycemia and other forms of hypoglycemia in newborns underlies the ongoing controversies over standards for managing these conditions. To address this deficiency, the authors evaluated regulation of insulin secretion in fetal, newborn, and adult rats. The results demonstrate that transitional hypoglycemia in normal neonates and persistent hypoglycemia in high-risk infants both reflect altered beta-cell insulin regulation. These findings provide a new foundation for improving detection and management and preventing hypoglycemic brain injury in normal neonates and, especially, in infants with persistent hypoglycemia and genetic forms of congenital hyperinsulinism.
引用
收藏
页码:55 / +
页数:19
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