Postnatal infection is associated with widespread abnormalities of brain development in premature newborns

被引:135
作者
Chau, Vann [1 ]
Brant, Rollin [2 ]
Poskitt, Kenneth J. [1 ,3 ]
Tam, Emily W. Y. [4 ]
Synnes, Anne [1 ]
Miller, Steven P. [1 ,4 ]
机构
[1] Univ British Columbia, Dept Pediat, Vancouver, BC V6T 1W5, Canada
[2] Univ British Columbia, Dept Stat, Vancouver, BC V6T 1W5, Canada
[3] Univ British Columbia, Dept Radiol, Vancouver, BC V6T 1W5, Canada
[4] Univ Calif San Francisco, Dept Neurol, San Francisco, CA USA
关键词
WHITE-MATTER INJURY; PRETERM INFANTS; BIRTH; LIPOPOLYSACCHARIDE; LESIONS; SEPSIS; MODEL;
D O I
10.1038/pr.2011.40
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
INTRODUCTION: Infection is a risk factor for adverse neurodevelopmental outcome in preterm newborns. Our objective was to characterize the association of postnatal infection with adverse microstructural and metabolic brain development in premature newborns. RESULTS: In 34/117 newborns studied, clinical signs were accompanied by positive cultures whereas 17 had clinical signs of sepsis alone. White matter injury (WMI) was identified in 34 newborns. In multivariate regression models, infected newborns had brain imaging measures indicative of delayed brain development: lower N-acetylaspartate/choline, elevated average diffusivity (D-AV), and decreased white matter fractional anisotropy. These widespread brain abnormalities were found in both newborns with positive-culture infection and in those with clinical infection. DISCUSSION: These findings suggest that postnatal infection, even without a positive culture, is an important risk factor for widespread abnormalities in brain development. These abnormalities extend beyond brain injuries apparent with conventional magnetic resonance injury (MRI). METHODS: 117 preterm newborns (24-32 wk gestation) were studied prospectively at a median of 32.0 and 40.3 wk ostmenstrual age with MRI (WMI, hemorrhage), magnetic resonance (MR) spectroscopy (metabolism), and diffusion tensor imaging (microstructure). Newborns were categorized as having "no infection," "clinical infection," or "positive-culture infection." We compared brain injuries as well as metabolic and microstructural development across these infection groups.
引用
收藏
页码:274 / 279
页数:6
相关论文
共 29 条
[21]   INCIDENCE AND EVOLUTION OF SUBEPENDYMAL AND INTRA-VENTRICULAR HEMORRHAGE - STUDY OF INFANTS WITH BIRTH WEIGHTS LESS THAN 1,500 GM [J].
PAPILE, LA ;
BURSTEIN, J ;
BURSTEIN, R ;
KOFFLER, H .
JOURNAL OF PEDIATRICS, 1978, 92 (04) :529-534
[22]   Presumed and definite bacteremia in extremely low gestational age newborns [J].
Patel, Sonal ;
Dammann, Olaf ;
Martin, Camilia R. ;
Allred, Elizabeth N. ;
Leviton, Alan .
ACTA PAEDIATRICA, 2011, 100 (01) :36-41
[23]   Does placental inflammation relate to brain lesions and volume in preterm infants? [J].
Reiman, Milla ;
Kujari, Harry ;
Maunu, Jonna ;
Parkkola, Riitta ;
Rikalainen, Hellevi ;
Lapinleimu, Helena ;
Lehtonen, Liisa ;
Haataja, Leena .
JOURNAL OF PEDIATRICS, 2008, 152 (05) :642-647
[24]   Adverse neurodevelopment in preterm infants with postnatal sepsis or necrotizing enterocolitis is mediated by white matter abnormalities on magnetic resonance imaging at term [J].
Shah, Divyen K. ;
Doyle, Lex W. ;
Anderson, Peter J. ;
Bear, Merilyn ;
Daley, Andrew J. ;
Hunt, Rod W. ;
Inder, Terrif E. .
JOURNAL OF PEDIATRICS, 2008, 153 (02) :170-175
[25]   Fluctuating pressure-passivity is common in the cerebral circulation of sick premature infants [J].
Soul, Janet S. ;
Hammer, Peter E. ;
Tsuji, Miles ;
Saul, J. Philip ;
Bassan, Haim ;
Limperopoulos, Catherine ;
Disalvo, Donald N. ;
Moore, Marianne ;
Akins, Patricia ;
Ringer, Steven ;
Volpe, Joseph J. ;
Trachtenberg, Felicia ;
Du Plessis, Adre J. .
PEDIATRIC RESEARCH, 2007, 61 (04) :467-473
[26]   Neurodevelopmental and growth impairment among extremely low-birth-weight infants with neonatal infection [J].
Stoll, BJ ;
Hansen, NI ;
Adams-Chapman, I ;
Fanaroff, AA ;
Hintz, SR ;
Vohr, B ;
Higgins, RD .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2004, 292 (19) :2357-2365
[27]   Late-onset sepsis in very low birth weight neonates: The experience of the NICHD Neonatal Research Network [J].
Stoll, BJ ;
Hansen, N ;
Fanaroff, AA ;
Wright, LL ;
Carlo, WA ;
Ehrenkranz, RA ;
Lemons, JA ;
Donovan, EF ;
Stark, AR ;
Tyson, JE ;
Oh, W ;
Bauer, CR ;
Korones, SB ;
Shankaran, S ;
Laptook, AR ;
Stevenson, DK ;
Papile, LA ;
Poole, WK .
PEDIATRICS, 2002, 110 (02) :285-291
[28]   Brain injury in premature infants: a complex amalgam of destructive and developmental disturbances [J].
Volpe, Joseph J. .
LANCET NEUROLOGY, 2009, 8 (01) :110-124
[29]   Variability in cerebral oxygen delivery is reduced in premature neonates exposed to chorioamnionitis [J].
Yanowitz, TD ;
Potter, DM ;
Bowen, A ;
Baker, RW ;
Roberts, JM .
PEDIATRIC RESEARCH, 2006, 59 (02) :299-304