Maternal and fetal serum levels of caspase-cleaved fragments of cytokeratin-18 in intrahepatic cholestasis of pregnancy

被引:7
作者
Ersoy, Ali Ozgur [1 ]
Kirbas, Ayse [1 ]
Ozler, Sibel [1 ]
Ersoy, Ebru [1 ]
Ozgu-Erdinc, A. Seval [1 ]
Ergin, Merve [2 ]
Erkaya, Salim [1 ]
Uygur, Dilek [1 ]
Danisman, Nuri [1 ]
机构
[1] Zekai Tahir Burak Womens Hlth Care Training & Res, Dept Perinatol, TR-06230 Ankara, Turkey
[2] Ataturk Educ & Res Hosp, Dept Biochem, Ankara, Turkey
关键词
Apoptosis; bile acid; intrahepatic cholestasis; M30; neonatal outcome; pregnancy; BILIARY-CIRRHOSIS; BILE-SALTS; APOPTOSIS; LIVER; EXPRESSION; MARKER; INJURY; ACID; MITOCHONDRIA; HEPATOCYTES;
D O I
10.3109/14767058.2015.1011116
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: We aimed to investigate the relationship between intrahepatic cholestasis of pregnancy (ICP) and caspase-cleaved fragments of cytokeratin-18, also referred to as M30, a marker of apoptosis.Methods: In this case-control study, maternal and umbilical cord blood venous samples were obtained from 21 pregnant women with ICP and 22 healthy pregnant women as a control group. M30 levels were compared among the groups.Results: Maternal serum M30 levels were significantly higher in the severe ICP group than in the control (p<0.001) and mild ICP groups (p=0.006). The values were comparable between the mild ICP and the control groups. The umbilical cord serum M30 levels were also significantly greater in the severe ICP group than in the control group (p=0.001).Conclusions: Changes in M30 levels, as an apoptosis marker, may shed light on the pathogenesis of ICP. Explaining the mechanisms of bile acid (BA)-induced hepatocyte injury may contribute further therapeutic strategies for the treatment of human cholestatic diseases.
引用
收藏
页码:562 / 566
页数:5
相关论文
共 28 条
  • [1] [Anonymous], 2015, PLOS MED, DOI DOI 10.1016/J.AJ0G.2014.07.026.25046809
  • [2] Soluble intracellular adhesion molecule, M30 and M65 as serum markers of disease activity and prognosis in cholestatic liver diseases
    Denk, Gerald
    Omary, Ahmed-Jawid
    Reiter, Florian Paul
    Hohenester, Simon
    Wimmer, Ralf
    Holdenrieder, Stefan
    Rust, Christian
    [J]. HEPATOLOGY RESEARCH, 2014, 44 (13) : 1286 - 1298
  • [3] Toxic bile salts induce rodent hepatocyte apoptosis via direct activation of Fas
    Faubion, WA
    Guicciardi, ME
    Miyoshi, H
    Bronk, SF
    Roberts, PJ
    Svingen, PA
    Kaufmann, SH
    Gores, GJ
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (01) : 137 - 145
  • [4] Apoptotic pathways in primary biliary cirrhosis and autoimmune hepatitis
    Fox, CK
    Furtwaengler, A
    Nepomuceno, RR
    Martinez, OM
    Krams, SM
    [J]. LIVER, 2001, 21 (04): : 272 - 279
  • [5] URSODEOXYCHOLATE REDUCES HEPATOTOXICITY OF BILE-SALTS IN PRIMARY HUMAN HEPATOCYTES
    GALLE, PR
    THEILMANN, L
    RAEDSCH, R
    OTTO, G
    STIEHL, A
    [J]. HEPATOLOGY, 1990, 12 (03) : 486 - 491
  • [6] Bile acids increase response and expression of human myometrial oxytocin receptor
    Germain, AM
    Kato, S
    Carvajal, JA
    Valenzuela, GJ
    Valdes, GL
    Glasinovic, JC
    [J]. AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2003, 189 (02) : 577 - 582
  • [7] Intrahepatic cholestasis of pregnancy:: Relationships between bile acid levels and fetal complication rates
    Glantz, A
    Marschall, HW
    Mattsson, LÅ
    [J]. HEPATOLOGY, 2004, 40 (02) : 467 - 474
  • [8] Detection of the M30 neoepitope as a new tool to quantify liver apoptosis - Timing and patterns of positivity on frozen and paraffin-embedded sections
    Grassi, A
    Susca, M
    Ferri, S
    Gabusi, E
    D'Errico, A
    Farina, G
    Maccariello, S
    Zauli, D
    Bianchi, FB
    Ballardini, G
    [J]. AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2004, 121 (02) : 211 - 219
  • [9] Apoptosis: a mechanism of acute and chronic liver injury
    Guicciardi, ME
    Gores, GJ
    [J]. GUT, 2005, 54 (07) : 1024 - 1033
  • [10] Pregnancy outcome with intrahepatic cholestasis
    Heinonen, S
    Kirkinen, P
    [J]. OBSTETRICS AND GYNECOLOGY, 1999, 94 (02) : 189 - 193