Elsabaawy Maha, Afify Sameh, El-Azab Gasser, Gomaa Asmaa, Omar Nabil, Hashim Mohamed, Elsabaawy Dalia, Elshazly Helmy
Department of Hepatology and Gastroenterology, National Liver Institute, Menoufia University, Shebeen Elkoom, Egypt.
Department of Clinical Pharmacy, National Liver Institute, Menoufia University, Shebeen Elkoom, Egypt.
Clin Exp Hepatol. 2021 Sep;7(3):286-292. doi: 10.5114/ceh.2021.109412. Epub 2021 Oct 11.
Post-liver transplantation (LTx) bone diseases have been poorly investigated. The frequency of bone diseases (osteopenia and osteoporosis) after LTx is unknown.
To define prevalence and risk factors of bone disorders following LTx.
This prospective study was conducted on 100 consecutive adult patients who underwent living donor liver transplantation (LDLT) at the National Liver Institute (NLI) and survived longer than a year. Bone mineral density (BMD) was evaluated by dual-energy X-ray absorption (DEXA), as well as other pre- and postoperative risk factors.
The frequencies of osteopenia and osteoporosis were found to be 14% and 8% among post-LTx patients. Seven recipients of the osteoporotic group were males, with mean age, and body mass index (BMI) before and after LTx 49.5 ±7.4 years, 24.1 ±4.7 kg/m and 22.8 ±1.5 kg/m, respectively. A significant association between hepatitis C virus (HCV)-related cirrhosis, liver disease severity according to Child-Turcotte-Pugh (CTP) score, and alcoholism with decreased post-LTx BMD was substantiated ( < 0.05, 0.006). Post-LTx development of diabetes mellitus (DM), weight gain, use of corticosteroids and basiliximab all significantly affected decreased post-LTx BMD ( < 0.05). However, binary regression revealed that post-LTx occurrence of DM ( = 0.012, odds ratio [OR] = 0.099), the severity of liver disease ( = 0.023, OR = 0.217), and HCV ( = 0.011, OR = 0.173) are the main independent predictors of metabolic bone disease (MBD) occurrence one year after LTx.
Post-LTx bone disorders are not infrequent complications and should be more considered in those with HCV-related severe liver disease or developed DM after LTx.
肝移植术后骨病的研究较少。肝移植后骨病(骨质减少和骨质疏松)的发生率尚不清楚。
确定肝移植后骨病的患病率和危险因素。
本前瞻性研究对100例在国家肝脏研究所接受活体肝移植(LDLT)且存活超过一年的连续成年患者进行。通过双能X线吸收法(DEXA)评估骨密度(BMD)以及其他术前和术后危险因素。
肝移植术后患者中骨质减少和骨质疏松的发生率分别为14%和8%。骨质疏松组的7名受者为男性,肝移植前后的平均年龄、体重指数(BMI)分别为49.5±7.4岁、24.1±4.7kg/m²和22.8±1.5kg/m²。丙型肝炎病毒(HCV)相关肝硬化、根据Child-Turcotte-Pugh(CTP)评分的肝病严重程度以及酗酒与肝移植后BMD降低之间存在显著关联(P<0.05,P = 0.006)。肝移植后糖尿病(DM)的发生、体重增加、使用皮质类固醇和巴利昔单抗均显著影响肝移植后BMD降低(P<0.05)。然而,二元回归显示肝移植后DM的发生(P = 0.012,比值比[OR]=0.099)、肝病严重程度(P = 0.023,OR = 0.217)和HCV(P = 0.011,OR = 0.173)是肝移植后一年代谢性骨病(MBD)发生的主要独立预测因素。
肝移植后骨病是常见并发症,对于HCV相关严重肝病患者或肝移植后发生DM的患者应更多考虑。