Journal article
Cytochrome P450 (CYP2D6) Genotype is Associated with Elevated Systolic Blood Pressure in Preterm Infants after Discharge from the Neonatal Intensive Care Unit
The Journal of pediatrics, Vol.159(1), pp.104-109
07/2011
DOI: 10.1016/j.jpeds.2011.01.002
PMCID: PMC3115515
PMID: 21353244
Abstract
To determine genetic and clinical risk factors associated with elevated systolic blood pressure (ESBP) in preterm infants after discharge from the neonatal intensive care unit (NICU).
A convenience cohort of infants born at <32 weeks gestational age was followed after NICU discharge. We retrospectively identified a subgroup of subjects with ESBP (systolic blood pressure [SBP] >90th percentile for term infants). Genetic testing identified alleles associated with ESBP. Multivariate logistic regression analysis was performed for the outcome ESBP, with clinical characteristics and genotype as independent variables.
Predictors of ESBP were cytochrome P450, family 2, subfamily D, polypeptide 6 (CYP2D6) (rs28360521) CC genotype (OR, 2.92; 95% CI, 1.48-5.79), adjusted for outpatient oxygen therapy (OR, 4.53; 95% CI, 2.23-8.81) and history of urinary tract infection (OR, 4.68; 95% CI, 1.47-14.86). Maximum SBP was modeled by multivariate linear regression analysis: maximum SBP = 84.8 mm Hg + 6.8 mm Hg if cytochrome P450, family 2, subfamily D, polypeptide 6 (CYP2D6) CC genotype + 6.8 mm Hg if discharged on supplemental oxygen + 4.4 mm Hg if received inpatient glucocorticoids (P = .0002).
ESBP is common in preterm infants with residual lung disease after discharge from the NICU. This study defines clinical factors associated with ESBP, identifies a candidate gene for further testing, and supports the recommendation to monitor blood pressure before age 3 years, as is suggested for term infants.
Details
- Title: Subtitle
- Cytochrome P450 (CYP2D6) Genotype is Associated with Elevated Systolic Blood Pressure in Preterm Infants after Discharge from the Neonatal Intensive Care Unit
- Creators
- John M Dagle - Department of Pediatrics, University of Iowa, Iowa City, IATyler J Fisher - Carver College of Medicine, University of Iowa, Iowa City, IASusan E Haynes - Department of Pediatrics, University of Iowa, Iowa City, IASusan K Berends - Department of Pediatrics, University of Iowa, Iowa City, IAPatrick D Brophy - Department of Pediatrics, University of Iowa, Iowa City, IAFrank H Morriss - Department of Pediatrics, University of Iowa, Iowa City, IAJeffrey C Murray - Department of Pediatrics, University of Iowa, Iowa City, IA
- Resource Type
- Journal article
- Publication Details
- The Journal of pediatrics, Vol.159(1), pp.104-109
- DOI
- 10.1016/j.jpeds.2011.01.002
- PMID
- 21353244
- PMCID
- PMC3115515
- NLM abbreviation
- J Pediatr
- ISSN
- 0022-3476
- eISSN
- 1097-6833
- Publisher
- Elsevier Inc
- Grant note
- R01 HD052953, R01 HD57192, P30 ES05605, and K08 DK064333 / National Institutes of Health FY2006-575 and FY2008-260 / March of Dimes
- Language
- English
- Date published
- 07/2011
- Academic Unit
- Anatomy and Cell Biology; Stead Family Department of Pediatrics; Epidemiology; Pediatric Dentistry; Craniofacial Anomalies Research Center; Biochemistry and Molecular Biology; Dental Research; Neonatology
- Record Identifier
- 9984025262702771
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