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本文引用的文献

1
Systematic Review and Meta-analysis: Partial External Biliary Diversion in Progressive Familial Intrahepatic Cholestasis.系统评价与荟萃分析:进行性家族性肝内胆汁淤积症中的部分外引流术
J Pediatr Gastroenterol Nutr. 2020 Aug;71(2):176-183. doi: 10.1097/MPG.0000000000002789.
2
PAR2 Mediates Itch via TRPV3 Signaling in Keratinocytes.PAR2 通过角质形成细胞中的 TRPV3 信号转导介导瘙痒。
J Invest Dermatol. 2020 Aug;140(8):1524-1532. doi: 10.1016/j.jid.2020.01.012. Epub 2020 Jan 29.
3
Pruritus in patients with chronic liver disease and serum autotaxin levels in patients with primary biliary cholangitis.慢性肝病患者的瘙痒症与原发性胆汁性胆管炎患者的血清自分泌酶水平。
BMC Gastroenterol. 2019 Oct 24;19(1):169. doi: 10.1186/s12876-019-1092-z.
4
MRGPRX4 is a bile acid receptor for human cholestatic itch.MRGPRX4 是一种人类胆汁淤积性瘙痒的胆汁酸受体。
Elife. 2019 Sep 10;8:e48431. doi: 10.7554/eLife.48431.
5
Pleotropic Roles of Autotaxin in the Nervous System Present Opportunities for the Development of Novel Therapeutics for Neurological Diseases.自分泌运动因子在神经系统中的多效性作用为开发治疗神经系统疾病的新型疗法提供了机会。
Mol Neurobiol. 2020 Jan;57(1):372-392. doi: 10.1007/s12035-019-01719-1. Epub 2019 Jul 30.
6
MRGPRX4 is a G protein-coupled receptor activated by bile acids that may contribute to cholestatic pruritus.MRGPRX4 是一种 G 蛋白偶联受体,可被胆汁酸激活,可能与胆汁淤积性瘙痒有关。
Proc Natl Acad Sci U S A. 2019 May 21;116(21):10525-10530. doi: 10.1073/pnas.1903316116. Epub 2019 May 8.
7
Cholestatic pruritus: Emerging mechanisms and therapeutics.胆汁淤积性瘙痒:新出现的发病机制和治疗方法。
J Am Acad Dermatol. 2019 Dec;81(6):1371-1378. doi: 10.1016/j.jaad.2019.04.035. Epub 2019 Apr 19.
8
A Randomized, Controlled, Phase 2 Study of Maralixibat in the Treatment of Itching Associated With Primary Biliary Cholangitis.马利昔巴特治疗原发性胆汁性胆管炎相关瘙痒的随机、对照、2期研究
Hepatol Commun. 2019 Feb 1;3(3):365-381. doi: 10.1002/hep4.1305. eCollection 2019 Mar.
9
Autotaxin, bile acid profile and effect of ileal bile acid transporter inhibition in primary biliary cholangitis patients with pruritus.原发性胆汁性胆管炎瘙痒患者的自分泌酶、胆汁酸谱和回肠胆汁酸转运体抑制作用。
Liver Int. 2019 May;39(5):967-975. doi: 10.1111/liv.14069. Epub 2019 Feb 25.
10
Identification of a bilirubin receptor that may mediate a component of cholestatic itch.鉴定一种可能介导胆汁淤积性瘙痒的胆红素受体。
Elife. 2019 Jan 21;8:e44116. doi: 10.7554/eLife.44116.

胆汁淤积相关性瘙痒及其致痒原

Cholestasis-Associated Pruritus and Its Pruritogens.

作者信息

Langedijk Jacqueline A G M, Beuers Ulrich H, Oude Elferink Ronald P J

机构信息

Amsterdam University Medical Centers, Tytgat Institute for Liver and Intestinal Research, Research Institute Amsterdam Gastroenterology, Endocrinology and Metabolism (AGEM), University of Amsterdam, Amsterdam, Netherlands.

出版信息

Front Med (Lausanne). 2021 Mar 9;8:639674. doi: 10.3389/fmed.2021.639674. eCollection 2021.

DOI:10.3389/fmed.2021.639674
PMID:33791327
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8006388/
Abstract

Pruritus is a debilitating symptom of various cholestatic disorders, including primary biliary cholangitis (PBC), primary sclerosing cholangitis (PSC) and inherited progressive familial intrahepatic cholestasis (PFIC). The molecular mechanisms leading to cholestasis-associated pruritus are still unresolved and the involved pruritogens are indecisive. As a consequence of pruritus, patients suffer from sleep deprivation, loss of daytime concentration, auto-mutilation and sometimes even suicidal ideations. Current guideline-approved therapy of cholestasis-associated pruritus includes stepwise administration of several medications, which may alleviate complaints in some, but not all affected patients. Therefore, also experimental therapeutic approaches are required to improve patients' quality of life. This article reviews the current state of research on pruritogens and their receptors, and shortly discusses the most recent experimental therapies.

摘要

瘙痒是多种胆汁淤积性疾病的一种使人衰弱的症状,包括原发性胆汁性胆管炎(PBC)、原发性硬化性胆管炎(PSC)和遗传性进行性家族性肝内胆汁淤积症(PFIC)。导致胆汁淤积相关性瘙痒的分子机制仍未明确,且相关的致痒原也尚无定论。瘙痒会导致患者睡眠不足、白天注意力不集中、自残行为,有时甚至会产生自杀念头。目前指南批准的胆汁淤积相关性瘙痒治疗方法包括逐步使用多种药物,这可能会缓解部分但并非所有受影响患者的症状。因此,也需要实验性治疗方法来提高患者的生活质量。本文综述了致痒原及其受体的研究现状,并简要讨论了最新的实验性治疗方法。