Genetic basis of preterm birth

被引:16
|
作者
Nesin, Mirjana [1 ]
机构
[1] Boston Univ, Med Ctr, Sch Med, Dept Pediat,Div Neonatol, Boston, MA 02118 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2007年 / 12卷
关键词
genetic predisposition; preterm birth; genetic polymorphism; single nucleotide polymorphism; polymorphism of innate immunity genes; genomics; proteonomics; review;
D O I
10.2741/2052
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
Epidemiologic data show that women who deliver prematurely often have a personal and/ or family history of preterm birth ( PTB) and that racial and ethnic differences influence the incidence of PTB. This may indicate genetic predisposition to PTB. However, since races and ethnic groups tend to share environmental factors ( exposure to toxins, living conditions, diet, smoking), epidemiologic data may just confirm environmental influences on PTB. Alternatively, PTB may represent a consequence of gene-environment interactions. Infection and inflammation correlate with increased risk for preterm premature rupture of amniotic membranes ( PPROM) and PTB. Immunomodulatory molecules and their receptors regulate these processes and many of them are products of polymorphic genes. Single nucleotide polymorphisms ( SNPs) of a gene may lead to a differential expression of its product. So far, SNPs for several genes have been implicated in PTB. If it is confirmed that polymorphism( s) in particular gene( s) correlates with PTB, it may become possible to develop targeted diagnostic and therapeutic approaches tailored towards unique genetic characteristics of a mother/ fetus pair.
引用
收藏
页码:115 / 124
页数:10
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