医学
地塞米松
骨重建
N-末端末端肽
皮质类固醇
骨质疏松症
骨吸收
呼吸窘迫
内科学
糖皮质激素
吸收
妊娠期
内分泌学
怀孕
外科
骨钙素
碱性磷酸酶
酶
化学
生物
生物化学
遗传学
作者
Onome Ogueh,Gautam Khastgir,John Studd,J. Jones,Jamshid Alaghband‐Zadeh,Mark R. Johnson
标识
DOI:10.1111/j.1471-0528.1998.tb10157.x
摘要
Objective To assess the risk of maternal osteoporosis associated with antenatal corticosterioid administration for neonatal respiratory distress syndrome prophylaxis. Design Prospective longitudinal study. Setting Maternity unit of Chelsea and Westminster Hospital, London. Population Fourteen pregnant women who received dexamethasone therapy for fetal lung maturation in anticipation of delivery before 34 completed weeks of gestation. Methods Blood samples were collected before dexamethasone administration, 24 hours and 48 hours after the course of dexamethasone, and within 24 hours of delivery. Serum levels of carboxy terminal pro‐peptide of type I pro‐collagen (PICP) were measured to monitor the rate of bone formation, and serum levels of cross‐linked carboxy terminal telopeptide (ICTP) were measured as a marker of bone resorption. Main outcome measures Changes in the markers of bone turnover following dexamethasone administration. Results Serum PICP levels dropped 24 hours after dexamethasone therapy ( P = 0.001 ), but partially recovered by 48 hours ( P = 0.014 ) to reach higher than pre‐therapy levels at delivery ( P = 0.044 ). Although there were no corresponding changes in the serum levels of ICTP after 24 and 48 hours of therapy, levels increased from pretherapy to delivery ( P = 0.006 ). Conclusion Antenatal corticosteroid therapy leads to a transient suppression of, followed by an increase in, bone formation without any significant alteration in the pattern of bone resorption expected during pregnancy.
科研通智能强力驱动
Strongly Powered by AbleSci AI