C. Milionis, Ioannis Ilias, Anastasia Lekkou, E. Venaki, E. Koukkou
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引用次数: 0
摘要
妊娠糖尿病通常在妊娠晚期的第二或第三季度被诊断出来。它是准妈妈最常见的代谢性疾病之一,对母体和后代的健康都可能造成严重的短期和长期并发症。C 肽从胰腺 beta 细胞分泌到血液循环中,与胰岛素的分泌量相等。与胰岛素相比,C 肽的肝清除率几乎可以忽略不计,因此它的半衰期较长,是估测β细胞功能的有效生物标志物。由于激素和新陈代谢平衡的生理变化,妊娠会诱发胰岛素抵抗。胰岛β细胞补偿不足会导致高血糖。妊娠 24-28 周的标准口服葡萄糖耐量试验可确定诊断。前瞻性研究积累的证据表明,妊娠早期的 C 肽水平与随后罹患妊娠糖尿病的风险之间存在联系。妊娠初期 C 肽水平和代糖指数的升高可促使采取适当的二级预防策略。
Future clinical prospects of C-peptide testing in the early diagnosis of gestational diabetes
Gestational diabetes is typically diagnosed in the late second or third trimester of pregnancy. It is one of the most common metabolic disorders among expectant mothers, with potential serious short- and long-term complications for both maternal and offspring health. C-peptide is secreted from pancreatic beta-cells into circulation in equimolar amounts with insulin. It is a useful biomarker to estimate the beta-cell function because it undergoes negligible hepatic clearance and consequently it has a longer half-life compared to insulin. Pregnancy induces increased insulin resistance due to physiological changes in hormonal and metabolic homeostasis. Inadequate compensation by islet beta-cells results in hyperglycemia. The standard oral glucose tolerance test at 24-28 wk of gestation sets the diagnosis. Accumulated evidence from prospective studies indicates a link between early pregnancy C-peptide levels and the risk of subsequent gestational diabetes. Elevated C-peptide levels and surrogate glycemic indices at the beginning of pregnancy could prompt appropriate strategies for secondary prevention.