Fariña-Hernández Arminda, González-Rinne Ana, Hernández-Bustabad Alberto, Guerra-Rodríguez Rita María, Saiz-Udaeta Ana Paola, Alonso-Titos Juana, Marrero Domingo, Rivero-González Antonio, Santana-Quintana Cristo Adonay, Ruíz-Esteban Pedro, Hernández Domingo
Nephrology Department, Hospital Universitario de Canarias, Instituto de Tecnologías Biomédicas, Universidad La Laguna, Santa Cruz de Tenerife, Spain.
Gastroenterology Department, Hospital Universitario de Canarias, Santa Cruz de Tenerife, Spain.
Nephron. 2024 Dec 23:1-11. doi: 10.1159/000543276.
Kidney transplantation (KT) is the treatment of choice for chronic kidney disease patients, but there is a continued loss of grafts in the long-term (50% at 10 years) due to either patient death or chronic allograft dysfunction. Metabolic syndrome (MS) is very prevalent after KT (30-40%) and its components contribute to the appearance of nonalcoholic fatty liver disease/metabolic dysfunction-associated fatty liver disease (NAFLD/MAFLD) and nonalcoholic steatohepatitis (NASH), which represent the hepatic component of MS. Furthermore, about 20-40% of KT recipients present early graft inflammation, including subclinical inflammation. Thus, the relationship between NAFLD-MAFLD/NASH and graft inflammation may be bidirectional, though no definite link between NAFLD-NASH and graft inflammation is currently known. Additionally, MS-related risk factors are associated with modern immunosuppressants and a negative synergistic effect on graft and patient survival seems plausible. Indeed, proinflammatory cytokines and adipokines released by adipose tissue can generate a low-grade inflammatory state and endothelial dysfunction, both involved in the appearance of CVD, and these disorders are associated with worsening liver lesions and subclinical and clinical atheromatosis. In this review, we discuss the recent clinical evidence regarding the prevalence and risk factors of MS and NAFLD/MAFLD following KT. Additionally, we propose the potential linking mechanism between NAFLD/MAFLD-NASH and post-KT graft inflammation, as well as alternative therapies for NAFLD after KT. Prevention of long-term life-threatening complications in this particular population rests upon better understanding and management of these severe clinical complications.
肾移植(KT)是慢性肾病患者的首选治疗方法,但由于患者死亡或慢性移植物功能障碍,长期来看移植物仍会持续丢失(10年时为50%)。代谢综合征(MS)在肾移植后非常普遍(30%-40%),其组成部分会导致非酒精性脂肪性肝病/代谢功能障碍相关脂肪性肝病(NAFLD/MAFLD)和非酒精性脂肪性肝炎(NASH)的出现,这些代表了MS的肝脏组成部分。此外,约20%-40%的肾移植受者会出现早期移植物炎症,包括亚临床炎症。因此,NAFLD-MAFLD/NASH与移植物炎症之间的关系可能是双向的,尽管目前尚不清楚NAFLD-NASH与移植物炎症之间的确切联系。此外,MS相关危险因素与现代免疫抑制剂有关,对移植物和患者生存产生负面协同效应似乎是合理的。事实上,脂肪组织释放的促炎细胞因子和脂肪因子可产生低度炎症状态和内皮功能障碍,二者均与心血管疾病的出现有关,且这些疾病与肝脏病变恶化以及亚临床和临床动脉粥样硬化相关。在本综述中,我们讨论了关于肾移植后MS和NAFLD/MAFLD的患病率及危险因素的最新临床证据。此外,我们提出了NAFLD/MAFLD-NASH与肾移植后移植物炎症之间的潜在联系机制,以及肾移植后NAFLD的替代治疗方法。预防这一特定人群的长期危及生命的并发症取决于对这些严重临床并发症的更好理解和管理。