Wilkins-Haug L, Roberts D J, Morton C C
Department of Obstetrics and Gynecology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA.
Am J Obstet Gynecol. 1995 Jan;172(1 Pt 1):44-50. doi: 10.1016/0002-9378(95)90082-9.
Our purpose was to determine the frequency of confined placental mosaicism in newborns with unexplained intrauterine growth retardation compared with infants with appropriate in utero growth.
Amnion, chorion, and villi from 12 growth-retarded infants and 24 appropriately grown, matched controls were karyotyped. Fluorescence in situ hybridization with chromosome-specific probes was then used to confirm the karyotypic abnormality at additional uncultured placental sites.
Karyotype analysis revealed placental mosaicism involving either aneuploidy or polyploidy in three of 12 (25%) cases versus two of 24 (8.3%) controls. Fluorescence in situ hybridization confirmed the karyotypic abnormalities in the placentas from growth-retarded infants only.
Confined placental mosaicism was identified three times more frequently from placentas of growth-retarded infants compared with those of newborns with appropriate growth. Molecular studies of the placentas suggested a wider distribution of cells with abnormal karyotypes in cases compared with controls and support a biologic influence of placental mosaicism on fetal growth.
我们的目的是确定与子宫内生长正常的婴儿相比,原因不明的子宫内生长迟缓新生儿中局限性胎盘嵌合体的发生率。
对12例生长迟缓婴儿和24例生长正常的匹配对照的羊膜、绒毛膜和绒毛进行核型分析。然后使用染色体特异性探针进行荧光原位杂交,以确认在其他未培养的胎盘部位的核型异常。
核型分析显示,12例病例中有3例(25%)存在涉及非整倍体或多倍体的胎盘嵌合体,而24例对照中有2例(8.3%)。荧光原位杂交仅在生长迟缓婴儿的胎盘中证实了核型异常。
与生长正常的新生儿相比,生长迟缓婴儿的胎盘中局限性胎盘嵌合体的发生率高出三倍。对胎盘的分子研究表明,与对照组相比,病例中核型异常的细胞分布更广泛,支持胎盘嵌合体对胎儿生长的生物学影响。