Kjærgaard Maria, Thiele Maja, Jansen Christian, Stæhr Madsen Bjørn, Görtzen Jan, Strassburg Christian, Trebicka Jonel, Krag Aleksander
Department and Gastroenterology and Hepatology, Odense University Hospital, Odense, Denmark.
Odense Patient data Explorative Network (OPEN), Odense, Denmark.
PLoS One. 2017 Apr 4;12(4):e0173992. doi: 10.1371/journal.pone.0173992. eCollection 2017.
Food intake increases liver stiffness, but it is believed that liver stiffness returns to baseline two hours after a meal. The aim of this study was to investigate the impact of different sized meals on liver stiffness. Liver and spleen stiffness was measured with transient elastography (TE) and real-time 2-dimensional shear wave elastography (2D-SWE). Patients ingested a 625 kcal and a 1250 kcal liquid meal on two consecutive days. We measured liver and spleen elasticity, Controlled attenuation parameter (CAP) and portal flow at baseline and after 20, 40, 60, 120 and 180 minutes. Sixty patients participated, 83% with alcoholic liver disease. Twenty-eight patients had METAVIR fibrosis score F0-3 and 32 patients had cirrhosis. Liver stiffness, spleen stiffness and CAP increased after both meals for all stages of fibrosis. False positive 2D-SWE liver stiffness measurements caused 36% and 52% of patients with F0-3 fibrosis to be misclassified with higher stages of fibrosis after the moderate and high caloric meal. Likewise, 10% and 13% of compensated cirrhosis patients were misclassified with clinically significant portal hypertension after the two meals. We observed similar misclassification rates with TE. After three hours, liver stiffness remained elevated more than 20% from baseline in up to 50% of patients.
Liver stiffness, spleen stiffness and CAP increase after a meal across all stages of fibrosis and across elastography techniques. Up to half of patients may be misclassified with higher stages of fibrosis, if they are assessed after less than three hours fasting period.
食物摄入会增加肝脏硬度,但一般认为餐后两小时肝脏硬度会恢复至基线水平。本研究旨在调查不同食量对肝脏硬度的影响。采用瞬时弹性成像(TE)和实时二维剪切波弹性成像(2D-SWE)测量肝脏和脾脏硬度。患者连续两天分别摄入625千卡和1250千卡的流食。我们在基线以及进食后20、40、60、120和180分钟测量肝脏和脾脏弹性、控制衰减参数(CAP)以及门静脉血流。60名患者参与研究,其中83%患有酒精性肝病。28名患者的METAVIR纤维化评分F0 - 3,32名患者患有肝硬化。在所有纤维化阶段,两餐进食后肝脏硬度、脾脏硬度和CAP均升高。在摄入中等热量和高热量餐后,F0 - 3纤维化患者中分别有36%和52%因2D-SWE肝脏硬度测量出现假阳性而被误分类为更高纤维化阶段。同样,两餐进食后,分别有10%和13%的代偿期肝硬化患者被误分类为具有临床意义的门静脉高压。使用TE我们观察到了类似的误分类率。三小时后,高达50%的患者肝脏硬度仍比基线水平升高超过20%。
在所有纤维化阶段以及不同弹性成像技术中,餐后肝脏硬度、脾脏硬度和CAP均会升高。如果在禁食期少于三小时后进行评估,高达一半的患者可能会被误分类为更高的纤维化阶段。