Sibley Colin P, Turner Mark A, Cetin Irene, Ayuk Paul, Boyd C A Richard, D'Souza Stephen W, Glazier Jocelyn D, Greenwood Susan L, Jansson Thomas, Powell Theresa
Division of Human Development, Acadamic Unit of Child Health, The Medical School, University of Manchester, St. Mary's Hospital, Manchester M13 OJH, UK.
Pediatr Res. 2005 Nov;58(5):827-32. doi: 10.1203/01.PDR.0000181381.82856.23. Epub 2005 Sep 23.
The placenta is essential to nutrition before birth. Recent work has shown that a range of clearly defined alterations can be found in the placentas of infants with intrauterine growth restriction (IUGR). In the mouse, a placental specific knockout of a single imprinted gene, encoding IGF-2, results in one pattern of alterations in placenta structure and function which leads to IUGR. We speculate that the alterations in the human placenta can also be grouped into patterns, or phenotypes, that are associated with specific patterns of fetal growth. Identifying the placental phenotypes of different fetal growth patterns will improve the ability of clinicians to recognize high-risk patients, of laboratory scientists to disentangle the complexities of IUGR, and of public health teams to target interventions aimed at ameliorating the long-term adverse effects of inadequate intrauterine growth.
胎盘对于出生前的营养供应至关重要。最近的研究表明,在患有宫内生长受限(IUGR)的婴儿胎盘中可以发现一系列明确的改变。在小鼠中,单个印记基因(编码IGF-2)的胎盘特异性敲除会导致胎盘结构和功能的一种改变模式,进而导致宫内生长受限。我们推测,人类胎盘的改变也可以分为与特定胎儿生长模式相关的模式或表型。识别不同胎儿生长模式的胎盘表型将提高临床医生识别高危患者的能力、实验室科学家理清宫内生长受限复杂性的能力,以及公共卫生团队针对旨在改善宫内生长不足长期不良影响的干预措施的针对性。