Cazzagon Nora, Gonzalez-Sanchez Ester, El-Mourabit Haquima, Wendum Dominique, Rainteau Dominique, Humbert Lydie, Corpechot Christophe, Chazouillères Olivier, Arrivé Lionel, Housset Chantal, Lemoinne Sara
Sorbonne Université, INSERM, Centre de Recherche Saint-Antoine (CRSA), Paris, France.
Department of Surgery, Oncology and Gastroenterology, University of Padova, Padova, Italy.
JHEP Rep. 2022 Dec 17;5(4):100649. doi: 10.1016/j.jhepr.2022.100649. eCollection 2023 Apr.
BACKGROUND & AIMS: Gallbladder enlargement is common in patients with primary sclerosing cholangitis (PSC). The gallbladder may confer hepatoprotection against bile acid overload, through the sequestration and cholecystohepatic shunt of bile acids. The aim of this study was to assess the potential impact of the gallbladder on disease features and bile acid homeostasis in PSC.
Patients with PSC from a single tertiary center who underwent liver MRI with three-dimensional cholangiography and concomitant analyses of serum bile acids were included. Gallbladder volume was measured by MRI and a cut-off of 50 ml was used to define gallbladder enlargement. Bile acid profiles and PSC severity, as assessed by blood tests and MRI features, were compared among patients according to gallbladder size (enlarged . normal-sized) or presence (removed conserved). The impact of cholecystectomy was also assessed in the knockout mouse model of PSC.
Sixty-one patients with PSC, all treated with ursodeoxycholic acid (UDCA), were included. The gallbladder was enlarged in 30 patients, whereas 11 patients had been previously cholecystectomized. Patients with enlarged gallbladders had significantly lower alkaline phosphatase, a lower tauro- glycoconjugate ratio and a higher UDCA . total bile acid ratio compared to those with normal-sized gallbladders. In addition, gallbladder volume negatively correlated with the hydrophobicity index of bile acids. Cholecystectomized patients displayed significantly higher aspartate aminotransferase and more severe bile duct strictures and dilatations compared to those with conserved gallbladder. In the knockout mice, cholecystectomy caused an increase in hepatic bile acid content and in circulating secondary bile acids, and an aggravation in cholangitis, inflammation and liver fibrosis.
Altogether, our findings indicate that the gallbladder fulfills protective functions in PSC.
In patients with primary sclerosing cholangitis (PSC), gallbladder status impacts on bile acid homeostasis and disease features. We found evidence of lessened bile acid toxicity in patients with PSC and enlarged gallbladders and of increased disease severity in those who were previously cholecystectomized. In the knockout mouse model of PSC, cholecystectomy causes an aggravation of cholangitis and liver fibrosis. Overall, our results suggest that the gallbladder plays a protective role in PSC.
胆囊增大在原发性硬化性胆管炎(PSC)患者中很常见。胆囊可能通过胆汁酸的螯合和胆囊肝分流,对胆汁酸过载起到肝脏保护作用。本研究的目的是评估胆囊对PSC疾病特征和胆汁酸稳态的潜在影响。
纳入来自单一三级中心的PSC患者,这些患者接受了肝脏磁共振成像(MRI)及三维胆管造影,并同时分析了血清胆汁酸。通过MRI测量胆囊体积,以50ml为界值定义胆囊增大。根据胆囊大小(增大.正常大小)或是否存在(切除.保留),比较患者的胆汁酸谱以及通过血液检查和MRI特征评估的PSC严重程度。还在PSC基因敲除小鼠模型中评估了胆囊切除术的影响。
纳入61例均接受熊去氧胆酸(UDCA)治疗的PSC患者。30例患者胆囊增大,11例患者先前已行胆囊切除术。与胆囊正常大小的患者相比,胆囊增大的患者碱性磷酸酶显著降低,牛磺糖缀合物比例较低,UDCA.总胆汁酸比例较高。此外,胆囊体积与胆汁酸的疏水性指数呈负相关。与胆囊保留的患者相比,胆囊切除术后的患者天冬氨酸转氨酶显著升高,胆管狭窄和扩张更严重。在基因敲除小鼠中,胆囊切除术导致肝脏胆汁酸含量和循环中次级胆汁酸增加,胆管炎、炎症和肝纤维化加重。
总之,我们的研究结果表明胆囊在PSC中发挥保护作用。
在原发性硬化性胆管炎(PSC)患者中,胆囊状态影响胆汁酸稳态和疾病特征。我们发现有证据表明,PSC患者胆囊增大时胆汁酸毒性降低,而先前接受胆囊切除术的患者疾病严重程度增加。在PSC基因敲除小鼠模型中,胆囊切除术会加重胆管炎和肝纤维化。总体而言,我们的结果表明胆囊在PSC中起保护作用。