原发性胆汁性胆管炎的治疗成功与肠道微生物群:安全的高速公路?

IF 1.9 Q3 GASTROENTEROLOGY & HEPATOLOGY Minerva gastroenterology Pub Date : 2024-01-19 DOI:10.23736/S2724-5985.23.03590-8
Ludovico Abenavoli, Giuseppe Gm Scarlata, Emidio Scarpellini, Anna C Procopio, Francesca R Ponziani, Luigi Boccuto, Nenad Cetkovic, Francesco Luzza
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摘要

原发性胆汁性胆管炎(PBC)是一种慢性、胆汁淤积性自身免疫性疾病,其特点是胆管受到破坏。PBC 主要影响 40 至 60 岁的女性。抗线粒体抗体(AMA)的存在是 PBC 的一个血清学特征。这种高度特异性的抗体存在于约 95% 的该病患者体内。位于线粒体内膜的酶家族被称为 2-氧代酸脱氢酶复合物,是 AMA 的靶标。熊去氧胆酸(UDCA)是一种合成胆汁酸,能够保护胆管细胞免受胆汁酸蓄积引起的胆汁淤积性损伤,其作用机制尚未明确。UDCA 是 PBC 患者的金标准疗法,推荐剂量为 13-15 毫克/千克/天。然而,并非每位患者都能对治疗产生反应。另一方面,肠道微生物群通过尚不明确的生化途径在 PBC 的发病中起着关键作用。人们对其在药物治疗后作为潜在生物标志物的作用知之甚少。事实上,很少有研究分析 UDCA 治疗前后肠道微生物群组成的变化。因此,本综述对有关 PBC 患者治疗前后肠道微生物群组成变化的研究进行了审查。
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Therapeutic success in primary biliary cholangitis and gut microbiota: a safe highway?

Primary biliary cholangitis (PBC) is a chronic, cholestatic, autoimmune disease, characterized by destruction of bile ducts. PBC predominantly affects women between 40 and 60 years of age. The presence of antimitochondrial antibodies (AMA) is a serological feature of PBC. These highly specific antibodies are found in about 95% of patients with the disease. The family of enzymes located in the inner membrane of the mitochondria, called the 2-oxo-acid dehydrogenase complex represents the target of the AMA. Ursodeoxycholic acid (UDCA) is a synthetic bile acid capable of protecting cholangiocytes from cholestatic damage caused by the accumulation of bile acids with a mechanism of action not yet well clarified. UDCA represents the gold standard therapy for PBC patients with recommended dose of 13-15 mg/kg/day. However, not every patient responds to therapy. On the other hand, the gut microbiota plays a key role in the onset of PBC through still unclear biochemical pathways. Less is known about its role as a potential biomarker after drug treatment. Actually, few studies analyzed the changes in gut microbiota composition before and after UDCA treatment. For this reason, this review represents an examination of the studies carried out on changes in gut microbiota composition in patients affected by PBC before and after treatment.

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