Cardiovascular risk factors after antenatal exposure to betamethasone: 30-year follow-up of a randornised controlled trial

被引:344
作者
Dalziel, SR
Walker, NK
Parag, V
Martell, C
Rea, HH
Rodgers, A
Harding, JE
机构
[1] Univ Auckland, Liggins Inst, Auckland 1, New Zealand
[2] Univ Auckland, Clin Trials Res Unit, Auckland 1, New Zealand
[3] Univ Auckland, Div Maori & Pacific Hlth, Auckland 1, New Zealand
[4] Univ Auckland, Dept Med, Auckland, New Zealand
关键词
D O I
10.1016/S0140-6736(05)66617-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Antenatal betamethasone treatment is widely used for the prevention of neonatal respiratory distress syndrome in preterm infants and substantially reduces neonatal mortality and morbidity. Fetal exposure to excess glucocorticoids has been proposed as one of the core mechanisms of the fetal origins of adult disease hypothesis. We assessed whether antenatal exposure to betamethasone for the prevention of neonatal respiratory distress syndrome affects cardiovascular risk factors at 30 years of age. Methods We followed up at age 30 years 534 individuals whose mothers participated in a double-blind, placebo-controlled, randomised trial of antenatal betamethasone for the prevention of neonatal respiratory distress syndrome. Mothers received two doses of betamethasone or placebo given by intramuscular injection 24 h apart. Follow-up assessments included anthropometry; measurement of blood pressure, blood lipids (after overnight fasting), and early morning cortisol levels; and a 75 g oral glucose tolerance test. Findings There were no differences between those exposed to betamethasone and to placebo in body size, blood lipids, blood pressure, plasma cortisol, prevalence of diabetes, or history of cardiovascular disease. After a 75 g oral glucose tolerance test, participants exposed to betamethasone had higher plasma insulin concentrations at 30 min (60.5 vs 52.0 mIU/L; ratio of geometric means 1.16 [95% CI 1.03 to 1.31], p=0.02) and lower glucose concentrations at 120 min (4.8 vs 5.1 mmol/L; difference -0.26 mmol/L [-0.53 to 0.001, p=0.05) than did those exposed to placebo. Interpretation Antenatal exposure to betamethasone might result in insulin resistance in adult offspring, but has no clinical effect on cardiovascular risk factors at 30 years of age. Thus, obstetricians should continue to use a single course of antenatal betamethasone for the prevention of neonatal respiratory distress syndrome.
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页码:1856 / 1862
页数:7
相关论文
共 31 条
[1]   Repeated doses of antenatal corticosteroids in animals: A systematic review [J].
Aghajafari, F ;
Murphy, K ;
Matthews, S ;
Ohlsson, A ;
Amankwah, K ;
Hannah, M .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2002, 186 (04) :843-849
[2]  
[Anonymous], 1994, NIH Consens Statement, V12, P1
[3]  
[Anonymous], 2003, Cochrane Database Syst Rev
[4]  
[Anonymous], 2002, World Health Report, 2002: Reducing risks, promoting healthy life
[5]  
Barker DJ., 1998, Mothers, babies, and health in later life, V2
[6]   GLUCOCORTICOID EXPOSURE INUTERO - NEW MODEL FOR ADULT HYPERTENSION [J].
BENEDIKTSSON, R ;
LINDSAY, RS ;
NOBLE, J ;
SECKL, JR ;
EDWARDS, CRW .
LANCET, 1993, 341 (8841) :339-341
[7]   Relation of serial changes in childhood body-mass index to impaired glucose tolerance in young adulthood [J].
Bhargava, SK ;
Sachdev, HS ;
Fall, CHD ;
Osmond, C ;
Lakshmy, R ;
Barker, DJP ;
Biswas, SKD ;
Ramji, S ;
Prabhakaran, D ;
Reddy, KS .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (09) :865-875
[8]  
Bland JM, 1996, BMJ-BRIT MED J, V312, P1153
[9]  
Crowley P, 2000, COCHRANE DB SYST REV, DOI DOI 10.1002/14651858.CD000065
[10]   The New Zealand Socioeconomic Index: developing and validating an occupationally-derived indicator of socio-economic status [J].
Davis, P ;
McLeod, K ;
Ransom, M ;
Ongley, P ;
Pearce, N ;
Howden-Chapman, P .
AUSTRALIAN AND NEW ZEALAND JOURNAL OF PUBLIC HEALTH, 1999, 23 (01) :27-33