Plasma concentrations of Lp(a) lipoprotein and TGF-β1 are altered in preeclampsia

被引:0
|
作者
Djurovic, S
Schjetlein, R
Wisloff, F
Haugen, G
Husby, H
Berg, K
机构
[1] Univ Oslo, Inst Med Genet, N-0315 Oslo, Norway
[2] Dept Med Genet, Oslo, Norway
[3] Ulleval Univ Hosp, Hematol Res Lab, Oslo, Norway
[4] Univ Oslo, Natl Hosp, Dept Obstet & Gynecol, Oslo, Norway
[5] Ulleval Univ Hosp, Dept Obstet & Gynecol, Oslo, Norway
关键词
activation of TGF-beta(1); fetal growth retardation; Lp(a) lipoprotein; placenta; preeclampsia; severe preeclampsia; TGF-beta; TGF-beta(1);
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
This study was performed to investigate the possible association between preeclampsia and the plasma concentrations of Lp(a) lipoprotein and TGF-beta(1) in a large series of patients, Additionally, correlation between the concentrations of these molecules and the severity of preeclampsia or fetal growth retardation was evaluated. Following clinical examination and biochemical analyses, both electroimmunoassay and RIA technique were used for quantitative determinations of plasma Lp(a) lipoprotein. ELISA technique was used to measure the active form of TGF-beta(1) in plasma of pregnant normotensive and preeclamptic women. We examined 154 women with preeclampsia (preeclampsia group) and 76 healthy, pregnant normotensive women (control group). The preeclampsia group was further divided into the following subgroups: mild preeclampsia, severe preeclampsia and preeclampsia with fetal growth retardation. Plasma levels of Lp(a) lipoprotein were lower in the total preeclampsia group as well as in all preeclampsia subgroups (5.45+/-7.41, 5.58+/-8.02, 5.08+/-5.38, and 4.32+/-5.28 mg/dl in the total preeclampsia group, and in subgroups with mild preeclampsia, severe preeclampsia, and preeclampsia with fetal growth retardation, respectively) than in the control group (7.84+/-9.26 mg/dl) as determined by quantitative electroimmunoassay. Corresponding results were obtained with a radioimmunoassay (166.03+/-200.2 U/l in the total preeclampsia group vs. 229.18+/-257.7 U/l in controls). There was good correlation between the two methods used for Lp(a) lipoprotein measurement. The differences between controls and the total preeclampsia group as well as each preeclampsia subgroup were statistically significant by a non-parametric test (one-way Kruskal-Wallis test). Plasma concentrations of the active form of TGF-beta(1) were increased in all preeclampsia subgroups as well as in the total group (5.63+/-1.68 ng/ml) compared to controls (4.67+/-1.33 ng/ml). This increase in TGF-beta(1) was statistically highly significant. Plasma concentrations of Lp(a) lipoprotein and the active form of TGF-beta(1) did not differ significantly between the preeclampsia subgroups. The outcome of this study may suggest involvement of both parameters in the pathophysiology of preeclampsia and may substantiate the notion of a multifactorial etiology of the disease.
引用
收藏
页码:371 / 376
页数:6
相关论文
共 50 条
  • [1] Altered serum concentrations of TGF-β1 and Lp(a) lipoprotein and their correlation in patients with first acute myocardial infarction
    Djurovic, S
    Thelle, DS
    Ringstad, J
    Christensen, B
    Berg, K
    NUTRITION METABOLISM AND CARDIOVASCULAR DISEASES, 1999, 9 (05) : 250 - 254
  • [2] Changes of Plasma uPA and TGF-β1 in Patients with Preeclampsia
    Fan, Minghua
    Xu, Yongping
    Qiu, Jianqing
    2016 3RD INTERNATIONAL SYMPOSIUM ON ENGINEERING TECHNOLOGY, EDUCATION AND MANAGEMENT (ISETEM 2016), 2016, : 144 - 148
  • [3] Increased plasma concentrations of TGF-β1 after hormone replacement therapy
    Djurovic, S
    Os, I
    Hofstad, AE
    Abdelonoor, M
    Westheim, A
    Berg, K
    JOURNAL OF INTERNAL MEDICINE, 2000, 247 (02) : 279 - 285
  • [4] Increased blood plasma concentrations of TGF-β1 and TGF-β2 after treatment with intravenous immunoglobulins in childhood autoimmune diseases
    Rissmann, Anke
    Pieper, Stefanie
    Adams, Ines
    Brune, Thomas
    Wiemann, Dagobert
    Reinhold, Dirk
    PEDIATRIC ALLERGY AND IMMUNOLOGY, 2009, 20 (03) : 261 - 265
  • [5] Fetal concentrations of the growth factors TGF-α and TGF-β1 in relation to normal and restricted fetal growth at term
    Briana, Despina D.
    Liosi, Sofia
    Gourgiotis, Dimitrios
    Boutsikou, Maria
    Marmarinos, Antonios
    Baka, Stavroula
    Hassiakos, Dimitrios
    Malamitsi-Puchner, Ariadne
    CYTOKINE, 2012, 60 (01) : 157 - 161
  • [6] The elevated plasma lipoprotein(a) concentrations in preeclampsia do not precede the development of the disorder
    Bar, J
    Harell, D
    Bardin, R
    Pardo, J
    Chen, R
    Hod, M
    Sullivan, M
    THROMBOSIS RESEARCH, 2002, 105 (01) : 19 - 23
  • [7] Transforming growth factor-β1 (TGF-β1) in plasma is associated with preeclampsia risk in Peruvian women with systemic inflammation
    Muy-Rivera, M
    Sanchez, SE
    Vadachkoria, S
    Qiu, CF
    Bazul, V
    Williams, MA
    AMERICAN JOURNAL OF HYPERTENSION, 2004, 17 (04) : 334 - 338
  • [8] Associations of maternal oestradiol, cortisol, and TGF-β1 plasma concentrations with thyroid autoantibodies during pregnancy and postpartum
    Sakkas, Grigorios E.
    Paltoglou, George
    Linardi, Anastasia
    Gryparis, Alexandros
    Nteka, Eleni
    Chalarakis, Nikos
    Mantzou, Aimilia
    Vrachnis, Nikolaos
    Iliodromiti, Zoe
    Koukkou, Eftychia
    Deligeoroglou, Efthymios
    Sakkas, Grigorios E.
    Mastorakos, George
    CLINICAL ENDOCRINOLOGY, 2018, 89 (06) : 789 - 797
  • [9] Altered Cerebrospinal Fluid Concentrations of TGFβ1 in Patients with Drug-Resistant Epilepsy
    Yu, Weihua
    Zou, Yan
    Du, Yingshi
    Luo, Jing
    Zhang, Man
    Yang, Wenxiu
    Wang, Xuefeng
    Lu, Yang
    NEUROCHEMICAL RESEARCH, 2014, 39 (11) : 2211 - 2217
  • [10] Platelet aggregation and TGF-beta1 plasma levels in pregnant women with preeclampsia
    Serrao Peracoli, Maria Terezinha
    Ferreira Menegon, Fernanda Tereza
    Medeiros Borges, Vera Therezinha
    de Araujo Costa, Roberto Antonio
    Thomazini-Santos, Izolete Aparecida
    Peracoli, Jose Carlos
    JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2008, 79 (01) : 79 - 84