Tolvaptan safety in autosomal-dominant polycystic kidney disease; a focus on idiosyncratic drug-induced liver injury liabilities

被引:0
|
作者
Hammond, Sean [1 ,2 ]
Meng, Xiaoli [1 ]
Barber, Jane [2 ]
Mosedale, Merrie [3 ]
Chadwick, Amy [1 ]
Watkins, Paul B. [3 ]
Naisbitt, Dean J. [1 ]
机构
[1] Univ Liverpool, Ctr Drug Safety Sci, Dept Pharmacol & Therapeut, Liverpool L69 3GE, England
[2] ApconiX, Alderley Edge SK10 4TG, England
[3] UNC Eshelman Sch Pharm, Div Pharmacotherapy & Expt Therapeut, Chapel Hill, NC 27599 USA
关键词
hypersensitivity; drug induced liver injury; tolvaptan; T-cell; idiosyncratic; ADPKD; NONPEPTIDE AVP ANTAGONIST; T-CELLS; HEART-FAILURE; IN-VITRO; ORAL TOLVAPTAN; PHARMACOKINETICS; PHARMACODYNAMICS; VASOPRESSIN; METABOLITES; IDENTIFICATION;
D O I
10.1093/toxsci/kfae142
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Tolvaptan is a vasopressin V2 receptor antagonist which has proven to be an effective and mostly well-tolerated agent for the treatment of autosomal-dominant polycystic kidney disease. However, its administration is associated with rare but serious idiosyncratic liver injury, which has warranted a black box warning on the drug labels and frequent monitoring of liver blood tests in the clinic. This review outlines mechanistic investigations that have been conducted to date and constructs a working narrative as an explanation for the idiosyncratic drug-induced liver injury (IDILI) events that have occurred thus far. Potential risk factors which may contribute to individual susceptibility to DILI reactions are addressed, and key areas for future investigative/clinical development are highlighted.
引用
收藏
页码:11 / 27
页数:17
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