Genetics of perinatal brain injury in the preterm infant

被引:39
作者
Baier, RJ [1 ]
机构
[1] Univ Manitoba, Dept Pediat & Child Hlth, Hlth Sci Ctr, Winnipeg, MB R3E 0L8, Canada
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2006年 / 11卷
关键词
prematurity; brain injury; intraventricular hemorrhage; periventricular leukomalacia; genetics; cytokine; review;
D O I
10.2741/1890
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Due to developmental immaturity of the central nervous system, effects of an adverse intrauterine environment and need for intensive care postnatally, preterm infants are at high risk of sustaining brain injury in the perinatal period. Infants who suffer brain injury in the perinatal period are at risk for long-term neurodevelopmental sequelae. Clinical and experimental data supports a significant role for inflammatory mediators in the pathophysiology of perinatal brain injury. Abnormalities in coagulation proteins in the sick preterm newborn may accentuate the risk for intraventricular hemorrhage. Polymorphisms in TNF alpha, IL-1 beta, IL-4, IL-6 and IL-10 as well as mutations in coagulation proteins have been investigated as potential candidate genes to modify risk and or severity of perinatal brain injury. Preliminary evidence suggests a role for cytokine genes as risk modifiers for IVH and PVL.
引用
收藏
页码:1371 / 1387
页数:17
相关论文
共 201 条
[51]   Glutamate receptor-mediated oligodendrocyte toxicity in periventricular leukomalacia: A protective role for topiramate [J].
Follett, PL ;
Deng, WB ;
Dai, WM ;
Talos, DM ;
Massillon, LJ ;
Rosenberg, PA ;
Volpe, JJ ;
Jensen, FE .
JOURNAL OF NEUROSCIENCE, 2004, 24 (18) :4412-4420
[52]   Expression of a dominant negative mutant of interleukin-1 beta converting enzyme in transgenic mice prevents neuronal cell death induced by trophic factor withdrawal and ischemic brain injury [J].
Friedlander, RM ;
Gagliardini, V ;
Hara, H ;
Fink, KB ;
Li, WW ;
MacDonald, G ;
Fishman, MC ;
Greenberg, AH ;
Moskowitz, MA ;
Yuan, JY .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (05) :933-940
[53]   Interleukin-10 reverses acute detrimental effects of endotoxin-induced inflammation on perinatal cerebral hypoxia-ischemia [J].
Froen, JF ;
Munkeby, BH ;
Stray-Pedersen, B ;
Saugstad, OD .
BRAIN RESEARCH, 2002, 942 (1-2) :87-94
[54]   Acute excitotoxic injury induces expression of monocyte chemoattractant protein-1 and its receptor, CCR2, in neonatal rat brain [J].
Galasso, JM ;
Miller, MJ ;
Cowell, RM ;
Harrison, JK ;
Warren, JS ;
Silverstein, FS .
EXPERIMENTAL NEUROLOGY, 2000, 165 (02) :295-305
[55]   Inhibition of TNF-α can attenuate or exacerbate excitotoxic injury in neonatal rat brain [J].
Galasso, JM ;
Wang, PY ;
Martin, D ;
Silverstein, FS .
NEUROREPORT, 2000, 11 (02) :231-235
[56]   Monocyte chemoattractant protein-1 is a mediator of acute excitotoxic injury in neonatal rat brain [J].
Galasso, JM ;
Liu, Y ;
Szaflarski, J ;
Warren, JS ;
Silverstein, FS .
NEUROSCIENCE, 2000, 101 (03) :737-744
[57]  
GARCIA JH, 1995, AM J PATHOL, V147, P1477
[58]   Ischemic and excitotoxic brain injury is enhanced in mice lacking the p55 tumor necrosis factor receptor [J].
Gary, DS ;
Bruce-Keller, AJ ;
Kindy, MS ;
Mattson, MP .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1998, 18 (12) :1283-1287
[59]  
GILLES FH, 1971, BIOL NEONATE, V18, P426
[60]   BRIEF CLINICAL AND LABORATORY OBSERVATIONS [J].
GODDARDFINEGOLD, J ;
ARMSTRONG, D ;
ZELLER, RS .
JOURNAL OF PEDIATRICS, 1982, 100 (05) :796-799