Minasyan Mari, Suchy Wiktoria, Fedak Andrzej, Gamrat-Żmuda Aleksandra, Hubalewska-Dydejczyk Alicja, Valassi Elena, Gilis-Januszewska Aleksandra
Chair and Department of Endocrinology, Jagiellonian University Medical College, Kraków, Poland.
Students' Scientific Circle of Department of Endocrinology, Jagiellonian University Medical College, Kraków, Poland.
Front Endocrinol (Lausanne). 2025 Oct 24;16:1660316. doi: 10.3389/fendo.2025.1660316. eCollection 2025.
Cushing syndrome (CS) and mild autonomous cortisol secretion syndrome (MACS) are states of endogenous hypercortisolemia, associated with multiple metabolic complications. The data on the impact of cortisol on the liver are inconsistent at times. From one perspective, some studies proved hepatotoxic cortisol action. Elevated liver enzymes and liver steatosis are common findings in patients with newly diagnosed CS and MACS (liver steatosis prevalence: 20%-66% and 25%-57%, respectively). Normocortisolemic subjects with liver steatosis/metabolic-associated steatohepatitis seem to have higher cortisol concentration than the healthy population. In contrast, other studies suggest that the liver impairment prevalence in hypercortisolemic patients with so many metabolic comorbidities would be expected to be much higher than it is reported. They postulate anti-inflammatory cortisol action as a preventive factor for liver disease progression in subjects with CS and MACS. The data on the hepatic safety profile of hypercortisolemia pharmacotherapy seems to be conflicting at times. Antihypercortisolemic medical therapy can potentially cause liver impairment; therefore, implementing the treatment of hypercortisolemia is often challenging in patients with liver dysfunction. We present two CS cases with baseline liver impairment, which improved on the treatment with steroidogenesis inhibitors. The case reports are followed by literature review regarding liver dysfunction in endogenous hypercortisolemia, impact of hypothalamic-pituitary-adrenal axis on the liver, and liver safety profile of medical treatment used in endogenous hypercortisolemia.
库欣综合征(CS)和轻度自主性皮质醇分泌综合征(MACS)是内源性皮质醇增多症的状态,与多种代谢并发症相关。关于皮质醇对肝脏影响的数据有时并不一致。从一个角度来看,一些研究证明了皮质醇具有肝毒性作用。在新诊断的CS和MACS患者中,肝酶升高和肝脂肪变性是常见表现(肝脂肪变性患病率分别为20% - 66%和25% - 57%)。患有肝脂肪变性/代谢相关脂肪性肝炎的皮质醇正常受试者的皮质醇浓度似乎高于健康人群。相比之下,其他研究表明,患有多种代谢合并症的皮质醇增多症患者的肝脏损害患病率预计会比报告的要高得多。他们推测皮质醇的抗炎作用是CS和MACS患者肝脏疾病进展的预防因素。关于皮质醇增多症药物治疗的肝脏安全性概况的数据有时似乎相互矛盾。抗皮质醇增多症药物治疗可能会导致肝脏损害;因此,对于肝功能不全的患者,实施皮质醇增多症的治疗往往具有挑战性。我们报告了两例基线时有肝脏损害的CS病例,在使用类固醇生成抑制剂治疗后病情有所改善。病例报告之后是关于内源性皮质醇增多症中肝功能障碍、下丘脑 - 垂体 - 肾上腺轴对肝脏的影响以及内源性皮质醇增多症所用药物治疗的肝脏安全性概况的文献综述。