Decreased placental expression of hPGH, IGF-I and IGFBP-1 in pregnancies complicated by fetal growth restriction

被引:43
作者
Koutsaki, Maria [1 ]
Sifakis, Stavros [2 ]
Zaravinos, Apostolos [1 ]
Koutroulakis, Dimitrios [2 ]
Koukoura, Ourania [2 ]
Spandidos, Demetrios A. [1 ]
机构
[1] Univ Crete, Sch Med, Lab Clin Virol, Iraklion 71003, Crete, Greece
[2] Univ Hosp Crete, Dept Obstet & Gynecol, Iraklion, Crete, Greece
关键词
Fetal growth; Fetal growth restriction; Human Placental Growth Hormone; Insulin-like Growth Factor-I; IGF-binding Protein 1; IGF-binding Protein 3; FACTOR-BINDING PROTEIN-1; HUMAN CHORIONIC-GONADOTROPIN; RETARDED HUMAN FETUSES; INTRAUTERINE GROWTH; GENE-EXPRESSION; PRETERM DELIVERY; GESTATIONAL-AGE; AMNIOTIC-FLUID; FACTOR SYSTEM; FACTOR AXIS;
D O I
10.1016/j.ghir.2010.12.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Objective: The human Placental Growth Hormone (hPGH) and the Insulin-like Growth Factor (IGF) system are implicated in fetal development. This study aimed to evaluate the expression of hPGH. IGF-I, IGFBP-1 and IGFBP-3 genes in placentas from pregnancies complicated by fetal growth restriction (FGR). Design: The study group was comprised of term placentas from 47 FGR-complicated pregnancies of no recognizable cause. Thirty-seven placentas from normal pregnancies with appropriate for gestational age birth weight were used as controls. The expression status of the genes was evaluated by quantitative real-time PCR. Results: hPGH, IGF-I and IGFBP-1 exhibited significantly lower expression compared to the controls (p= 0.003, p = 0.049 and p= 0.001, respectively). Numerically, lower IGFBP-3 expression was also demonstrated in the FGR-affected group, without however reaching statistical significance (p = 0.129). Significant co-expression patterns were detected among the study genes in both the FGR and normal pregnancies. Conclusion: Decreased placental expression levels of hPGH, IGF-I and IGFBP-1 were demonstrated in pregnancies with FGR. Whether these alterations are a causative factor of FGR or accompany other pathogenetic mechanisms requires further investigation. (C) 2010 Growth Hormone Research Society. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:31 / 36
页数:6
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