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1.
J Perinatol ; 30(9): 610-5, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20182437

ABSTRACT

OBJECTIVE: High-mobility group box-1 (HMGB1) is a potent inflammatory mediator and contributes to acute lung injury in adults. The role of HMGB1 in neonatal lung injury and the development of bronchopulmonary dysplasia (BPD) is unknown. We studied the association between HMGB1 levels in tracheal aspirates (TAs) and adverse outcomes (BPD/death) in ventilated premature infants (VPIs) and modulation of HMGB1 levels with dexamethasone (Dex) use. STUDY DESIGN: Infants born before 32 weeks gestation and requiring mechanical ventilation were enrolled. Serial TA samples were collected on days 1, 3, 5 and 7 and HMGB1 levels were measured. HMGB1 levels in TA samples were compared between infants with no BPD and infants who developed BPD or died. HMGB1 TA levels were also compared before and after using Dex. RESULT: In all, 24 infants (gestational age 26.4+/-1.9 weeks, birth weight 859+/-200 g) had no BPD, 60 infants (gestational age 25.4+/-1.8 weeks, birth weight 749+/-156 g) developed BPD or died before 36 weeks postmenstrual age. Mean HMGB1 level in first week of life was significantly lower in infants with no BPD (27.3+/-16.5 ng mg(-1)) compared with those who developed BPD or died (45.1+/-30.9 ng mg(-1), P=0.004). In total, 29 VPIs received Dex. There was no significant change in HMGB1 levels with steroid therapy (before 47.0+/-43.9, after 60.1.5+/-58.8, P=0.3). CONCLUSION: Our data suggest that higher HMGB1 levels in TA are associated with the development of BPD or death in VPI. Dex use had no effect on HMGB1 levels.


Subject(s)
Bronchopulmonary Dysplasia/metabolism , Homeodomain Proteins/metabolism , Sputum/metabolism , Bronchopulmonary Dysplasia/drug therapy , Bronchopulmonary Dysplasia/mortality , Dexamethasone/therapeutic use , Female , Humans , Infant, Extremely Low Birth Weight , Infant, Newborn , Infant, Premature , Male , Respiration, Artificial/adverse effects , Steroids/therapeutic use , Trachea
2.
J Matern Fetal Neonatal Med ; 13(4): 230-6, 2003 Apr.
Article in English | MEDLINE | ID: mdl-12854922

ABSTRACT

OBJECTIVES: To determine the risk factors for birth weight discordance in twins. METHODS: We used the United States (1995-97) Matched Multiple Birth File (n = 294 568) to assess the association between birth weight discordance and maternal sociodemographic, pregnancy and infant characteristics. RESULTS: Eighty-four per cent of the twins were 0-19% discordant, 11.1% were 20-29% discordant, 3.4% were 30-39% discordant, and 1.8% were > or = 2 40% discordant. The risk factors for birth weight discordance for same-sex twins were eclampsia (odds ratio (OR) 1.39,95% confidence interval (CI) 1.20, 1.61), pre-eclampsia (OR 1.31, 95% CI 1.24, 1.38), pre-existing hypertension (OR 1.32, 95% CI 1.12, 1.56), diabetes (OR 1.13, 95% CI 1.04, 1.24) and certain congenital anomalies. For opposite-sex twins, the risk factors for birth weight discordance were pre-eclampsia (OR 1.17, 95% CI 1.09, 1.27), pre-existing hypertension (OR 1.59,95% CI 1.32, 1.91), and certain congenital anomalies. Also, smoking and increased maternal age were associated with birth weight discordance in both same-sex and opposite-sex twins. CONCLUSIONS: Maternal hypertensive disorders, smoking and delayed childbearing were associated with intrapair birth weight discordance. The mechanisms of these associations deserve further investigation.


Subject(s)
Birth Weight , Diseases in Twins/epidemiology , Adolescent , Adult , Congenital Abnormalities , Eclampsia/complications , Female , Gestational Age , Humans , Hypertension/complications , Male , Maternal Age , Odds Ratio , Pre-Eclampsia/complications , Pregnancy , Pregnancy Complications , Pregnancy in Adolescence , Pregnancy in Diabetics/complications , Pregnancy, High-Risk , Risk Factors , Sex Factors , Smoking
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