Sultanik P, Kramer L, Soudan D, Bouam S, Meritet J-F, Vallet-Pichard A, Fontaine H, Bousquet L, Boueyre E, Corouge M, Sogni P, Pol S, Mallet V
Université Paris Descartes, Paris, France.
Assistance Publique - Hôpitaux de Paris (AP-HP), Groupe Hospitalier Cochin Port Royal, Paris, France.
Aliment Pharmacol Ther. 2016 Sep;44(5):505-13. doi: 10.1111/apt.13722. Epub 2016 Jul 12.
There is a relationship between liver stiffness measurement (LSM) and outcome of HCV patients.
To evaluate the performance of LSM to predict outcome of HCV patients at risk of liver-related complication.
We established a retrospective longitudinal cohort of 341 HCV patients with unequivocal cirrhosis. All underwent LSM and were followed from September 2006 to July 2015. Outcome measure was a composite end-point of end-stage liver disease (ESLD) and/or hepatocellular carcinoma (HCC). Cox models and areas under receiver operating characteristic (AUROC) curves were used to evaluate independent risk factors of outcome.
Overall, LSM was below the 12.5 kPa threshold in 129 (37.8%) patients, including three-fourth and one-third of patients with or without a sustained virological response respectively. Liver disease progressed in 136 (39.9%) patients after a median observational period of 23.5 months. Older age, male gender, alcohol use disorders, metabolic syndrome and LSM were independent risk factors of liver disease progression. Age, alcohol use disorders and LSM were independently associated with ESLD. Age, gender and metabolic syndrome, but not LSM, were associated with HCC. The AUROC curves for disease progression, ESLD and HCC were 0.67, 0.70 and 0.58 respectively. Patients with a liver stiffness >12.5 kPa were at the highest risk of liver disease progression; below 12.5 kPa, liver stiffness was not discriminant.
Liver stiffness measurement is not a surrogate of disease progression of HCV patients with cirrhosis. HCV patients with cirrhosis should undergo the recommended follow-up, regardless of liver stiffness measurement.
肝脏硬度测量(LSM)与丙型肝炎病毒(HCV)患者的预后之间存在关联。
评估LSM预测有肝脏相关并发症风险的HCV患者预后的性能。
我们建立了一个回顾性纵向队列,纳入341例明确诊断为肝硬化的HCV患者。所有患者均接受了LSM检查,并于2006年9月至2015年7月进行随访。结局指标为终末期肝病(ESLD)和/或肝细胞癌(HCC)的复合终点。采用Cox模型和受试者操作特征曲线下面积(AUROC)评估预后的独立危险因素。
总体而言,129例(37.8%)患者的LSM低于12.5 kPa阈值,其中分别有四分之三和三分之一的患者获得或未获得持续病毒学应答。在中位观察期23.5个月后,136例(39.9%)患者的肝病进展。年龄较大、男性、酒精使用障碍、代谢综合征和LSM是肝病进展的独立危险因素。年龄、酒精使用障碍和LSM与ESLD独立相关。年龄、性别和代谢综合征与HCC相关,但LSM与HCC无关。疾病进展、ESLD和HCC的AUROC曲线分别为0.67、0.70和0.58。肝脏硬度>12.5 kPa的患者肝病进展风险最高;低于12.5 kPa时,肝脏硬度无鉴别意义。
肝脏硬度测量不是肝硬化HCV患者疾病进展的替代指标。肝硬化的HCV患者应接受推荐的随访,无论肝脏硬度测量结果如何。