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| Name | Class |
|---|---|
| University of Valencia | OTHER |
| Carlos III Health Institute | OTHER_GOV |
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Premature infants are highly susceptible to oxidative stress because of the immaturity of their antioxidant defense system. The use of prenatal glucocorticosteroids administered to the mother improves respiratory function and overall outcome. The investigators hypothesize that prenatal glucocorticosteroids favor the expression and competence of the antioxidant defense system.
This is an observational study recruiting extremely low gestational age neonates (<28 weeks gestation) whose mothers received or not full scheduled prenatal glucocorticosteroids. Healthy term newly born infants acted as controls.
At birth cord blood were drawn for the following analytical determinations: reduced and oxidized glutathione; malondialdehyde; superoxide dismutase; catalase; glutathione peroxidase; glutathione reductase; glutathione s-transferase. In addition, first urine voided was collected for ortho-tyrosine/phenylalanine and 8-hydroxy-2-oxo-deoxyguanosine/2-deoxyguanosine determination. Analytical data and clinical outcomes are compared.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| PRENATAL CORTICOSTEROIDS | Extremely low gestational age neonates (<28 weeks gestation) whose mothers received full course of betamethasone before delivery. | ||
| NON PRENATAL CORTICOSTEROIDS | Extremely low gestational age neonates (<28 weeks gestation) whose mothers did not receive full course of betamethasone before delivery. |
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| Measure | Description | Time Frame |
|---|---|---|
| Evaluation of glutathione redox status in cord blood. | at birth |
| Measure | Description | Time Frame |
|---|---|---|
| Evaluation of antioxidant activity. | at birth |
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Inclusion Criteria:
Exclusion Criteria:
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Extremely low gestational age neonates < 28 weeks gestation whose mothers received or not antenatal glucocorticosteroids.
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| Name | Affiliation | Role |
|---|---|---|
| MAXIMO VENTO, PHD, MD | Valencian Agency of Health | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Division of Neonatology; University Hospital La Fe | Valencia | Valencia | 46009 | Spain |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 18270477 | Background | Arima M, Kumai T, Asoh K, Takeba Y, Murano K, Goto K, Tsuzuki Y, Mizuno M, Kojima T, Kobayashi S, Koitabashi Y. Effects of antenatal dexamethasone on antioxidant enzymes and nitric oxide synthase in the rat lung. J Pharmacol Sci. 2008 Feb;106(2):242-8. doi: 10.1254/jphs.fp0060844. Epub 2008 Feb 9. | |
| 18043518 | Background |
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| ID | Term |
|---|---|
| D047928 | Premature Birth |
| D004417 | Dyspnea |
| ID | Term |
|---|---|
| D007752 | Obstetric Labor, Premature |
| D007744 | Obstetric Labor Complications |
| D011248 | Pregnancy Complications |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
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| Chandrasekar I, Eis A, Konduri GG. Betamethasone attenuates oxidant stress in endothelial cells from fetal lambs with persistent pulmonary hypertension. Pediatr Res. 2008 Jan;63(1):67-72. doi: 10.1203/PDR.0b013e31815b43ee. |
| 15710178 | Background | Asikainen TM, White CW. Antioxidant defenses in the preterm lung: role for hypoxia-inducible factors in BPD? Toxicol Appl Pharmacol. 2005 Mar 1;203(2):177-88. doi: 10.1016/j.taap.2004.07.008. |
| 14713347 | Background | Asikainen TM, White CW. Pulmonary antioxidant defenses in the preterm newborn with respiratory distress and bronchopulmonary dysplasia in evolution: implications for antioxidant therapy. Antioxid Redox Signal. 2004 Feb;6(1):155-67. doi: 10.1089/152308604771978462. |
| D000091642 | Urogenital Diseases |
| D012120 | Respiration Disorders |
| D012140 | Respiratory Tract Diseases |
| D012818 | Signs and Symptoms, Respiratory |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |