Intrahepatic Cholestasis of Pregnancy Clinical Trial
Official title:
to Investigate the Maternal Serum IL-17 Levels in Pregnant Women With Intrahepatic Cholestasis of Pregnancy
The aim of this study is to investigate maternal and fetal serum IL-17 levels in pregnant women with intrahepatic cholestasis of pregnancy and to find out if Th-17 cells have a role in progress of intrahepatic cholestasis of pregnancy.
Intrahepatic cholestasis of pregnancy (ICP) is the most prevalent pregnancy-specific liver
disease. It occurs mainly in the second or third trimester of pregnancy. It typically
resolves after delivery spontaneously but it is associated with an increased risk of adverse
fetal outcomes.
The cause of ICP is heterogeneous, pathophysiology is poorly understood and therapies have
been empiric. Genetic predispositions, environmental influences, dietary factors and
hormonal influences have been studied and cited in the literature.
Comparing with placebo, ursodeoxycholic acid (UDCA) has been shown improvement in treatment
of pruritus in previous studies. S-adenosylmethionine, guar gum, activated charcoal,
dexamethasone, cholestyramine, etc. are not effective in the treatment of symptoms.
CD4+ T cells are an essential regulators of immune responses and inflammatory diseases. They
are also called chief of orchestra cells of immune system. The balance between T
helper-(Th)1, Th-2 and Th-17 cells and their cytokinergic interaction are crucial for the
response of the organism. Th17 and its specific cytokine IL-17 are responsible for
pathogenesis of autoimmune diseases as autoimmune uveitis, experimental autoimmune
encephalomyelitis in animal models and potentially also in human autoimmune diseases such as
multiple sclerosis, Crohn's disease, rheumatoid arthritis, psoriasis, primary biliary
cirrhosis. Recently, IL-17 targeted therapies (secukinumab, ixekizumab and brodalumab) are
being studied in Phase III clinical trials to evaluate their overall efficacy and safety for
certain autoimmune diseases.
Th-17 levels have been investigated in normal and abnormal pregnancies and results were
incompatible with each other. Some researchers have said that the level of IL-17 increased
during pregnancy but the others not.
Low serum IL-17 is associated with premature birth. Up-regulation of the IL-17 is associated
with preeclampsia.
K. Harada et all. (2009) demonstrated that IL-17-positive cells are associated with the
chronic inflammation of bile ducts in primary biliary cirrhosis(PBC). Also, some authors
demonstrated that Th-17-related cytokines were increased significantly in patients with PBC.
Maho Ichikawa et all. presented a case of male newborn infant who showed progressive severe
cholestasis with selectively high Levels of Serum IL- 17.
Based on all this information, we decided to investigate maternal and fetal serum IL-17
levels of pregnants with ICP and the effects of UDCA therapy on it and find out if Th-17
cells have a role in progress of ICP.
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Observational Model: Case Control, Time Perspective: Prospective
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