Development of an adverse outcome pathway for intrahepatic cholestasis of pregnancy

被引:0
作者
Waspe, Jennifer [1 ]
Beronius, Anna [2 ]
机构
[1] Sheffield Teaching Hosp, Glossop Rd,Broomhall, Sheffield S10 2JF, S Yorkshire, England
[2] Karolinska Inst, Inst Environm Med, Solna, Sweden
来源
CURRENT RESEARCH IN TOXICOLOGY | 2022年 / 3卷
关键词
Cholestasis; Adverse outcome pathway; Reproductive medicine; Pregnancy; FARNESOID-X-RECEPTOR; SALT EXPORT PUMP; BILE-ACIDS; PROGESTERONE METABOLITES; CHOLIC-ACID; OXYTOCIN; FXR; MECHANISMS;
D O I
10.1016/j.crtox.2022.100065
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Adverse Outcome Pathways (AOPs) are a research synthesis tool, used primarily by toxicologists for numerous applications including: hypothesis generation, data integration, biomarker determination, and identification of gaps in current knowledge. The AOP model provides a means for evaluating critical interactions between stressors and biological systems which result in adversity, meaning there is significant potential value in using this model in clinical research. However, AOPs have so far not been applied in this context, which may be attributable to the fact that the method is not yet streamlined with established practices in evidence-based medicine, such as systematic review.Here, we present one approach to developing a clinically focused AOP for intrahepatic cholestasis of pregnancy; aiming to enhance understanding of the mechanistic link between this common, gestational liver disease and its association with preterm birth.Mechanistic aspects of the disease pathogenesis, and use of AOPs to broaden inclusion and improve integration of in vitro and in vivo data in clinical research are discussed.We also demonstrate for the first time how central components of systematic review can be integrated into the development of an AOP.
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页数:7
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[11]   A Clinical Approach to Intrahepatic Cholestasis of Pregnancy [J].
Diken, Zaid ;
Usta, Ihab M. ;
Nassar, Anwar H. .
AMERICAN JOURNAL OF PERINATOLOGY, 2014, 31 (01) :1-8
[12]   New Insights on Intrahepatic Cholestasis of Pregnancy [J].
Floreani, Annarosa ;
Gervasi, Maria Teresa .
CLINICS IN LIVER DISEASE, 2016, 20 (01) :177-+
[13]   Bile acids and their nuclear receptor FXR: Relevance for hepatobiliary and gastrointestinal disease [J].
Gadaleta, Raffaella M. ;
van Mil, Saskia W. C. ;
Oldenburg, Bas ;
Siersema, Peter D. ;
Klomp, Leo W. J. ;
van Erpecum, Karel J. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2010, 1801 (07) :683-692
[14]   Intrahepatic cholestasis of pregnancy [J].
Geenes, Victoria ;
Williamson, Catherine .
WORLD JOURNAL OF GASTROENTEROLOGY, 2009, 15 (17) :2049-2066
[15]   Bile acids increase response and expression of human myometrial oxytocin receptor [J].
Germain, AM ;
Kato, S ;
Carvajal, JA ;
Valenzuela, GJ ;
Valdes, GL ;
Glasinovic, JC .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2003, 189 (02) :577-582
[16]   The Oxytocin Receptor System: Structure, function, and regulation [J].
Gimpl, G ;
Fahrenholz, F .
PHYSIOLOGICAL REVIEWS, 2001, 81 (02) :629-683
[17]   Principles for modulation of the nuclear receptor superfamily [J].
Gronemeyer, H ;
Gustafsson, JÅ ;
Laudet, V .
NATURE REVIEWS DRUG DISCOVERY, 2004, 3 (11) :950-964
[18]   MAXIMAL RESPONSE TO OXYTOCIN OF THE ISOLATED MYOMETRIUM FROM PREGNANT PATIENTS WITH INTRAHEPATIC CHOLESTASIS [J].
ISRAEL, EJ ;
GUZMAN, ML ;
CAMPOS, GA .
ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA, 1986, 65 (06) :581-582
[19]  
Kota Sunil K, 2013, Indian J Endocrinol Metab, V17, P50, DOI 10.4103/2230-8210.107841
[20]   Farnesoid x receptor in human metabolism and disease: the interplay between gene polymorphisms, clinical phenotypes and disease susceptibility [J].
Koutsounas, Ioannis ;
Theocharis, Stamatios ;
Delladetsima, Ioanna ;
Patsouris, Efstratios ;
Giaginis, Constantinos .
EXPERT OPINION ON DRUG METABOLISM & TOXICOLOGY, 2015, 11 (04) :523-532