Jung Kyu Sik, Kim Beom Kyung, Kim Seung Up, Chon Young Eun, Chun Kyeong Hyeon, Kim Sung Bae, Lee Sang Hoon, Ahn Sung Soo, Park Jun Yong, Kim Do Young, Ahn Sang Hoon, Park Young Nyun, Han Kwang-Hyub
Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.
Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea; Institute of Gastroenterology, Yonsei University College of Medicine, Seoul, Korea; Liver Cirrhosis Clinical Research Center, Seoul, Korea.
PLoS One. 2014 Jun 5;9(6):e98689. doi: 10.1371/journal.pone.0098689. eCollection 2014.
BACKGROUND & AIMS: Controlled attenuation parameter (CAP) can measure hepatic steatosis. However, factors affecting its accuracy have not been described yet. This study investigated predictors of discordance between liver biopsy (LB) and CAP.
A total of 161 consecutive patients with chronic liver disease who underwent LB and CAP were enrolled prospectively. Histological steatosis was graded as S0 (<5%), S1 (5-33%), S2 (34-66%), and S3 (>66% of hepatocytes). Cutoff CAP values were calculated from our cohort (250, 301, and 325 dB/m for ≥ S1, ≥ S2, and S3). Discordance was defined as a discrepancy of at least two steatosis stages between LB and CAP.
The median age (102 males and 59 females) was 49 years. Repartition of histological steatosis was as follows; S0 26.1% (n = 42), S1 49.7% (n = 80), S2 20.5% (n = 33), and S3 3.7% (n = 6). In multivariate linear regression analysis, CAP value was independently associated with steatosis grade along with body mass index (BMI) and interquartile range/median of CAP value (IQR/MCAP) (all P<0.05). Discordance was identified in 13 (8.1%) patients. In multivariate analysis, histological S3 (odd ratio [OR], 9.573; 95% confidence interval [CI], 1.207-75.931; P = 0.033) and CAP value (OR, 1.020; 95% CI, 1.006-1.034; P = 0.006) were significantly associated with discordance, when adjusting for BMI, IQR/MCAP, and necroinflammation, reflected by histological activity or ALT level.
Patients with high grade steatosis or high CAP values have a higher risk of discordance between LB and CAP. Further studies are needed to improve the accuracy of CAP interpretation, especially in patients with higher CAP values.
受控衰减参数(CAP)可用于测量肝脂肪变性。然而,影响其准确性的因素尚未见报道。本研究调查了肝活检(LB)与CAP结果不一致的预测因素。
前瞻性纳入161例连续接受LB和CAP检查的慢性肝病患者。组织学脂肪变性分级为S0(<5%)、S1(5 - 33%)、S2(34 - 66%)和S3(>66%的肝细胞)。根据我们的队列计算出截断CAP值(≥S1为250 dB/m、≥S2为301 dB/m、≥S3为325 dB/m)。不一致定义为LB和CAP之间至少有两个脂肪变性阶段的差异。
患者中位年龄49岁(男性102例,女性59例)。组织学脂肪变性分布如下:S0为26.1%(n = 42),S1为49.7%(n = 80),S2为20.5%(n = 33),S3为3.7%(n = 6)。多因素线性回归分析显示,CAP值与脂肪变性分级、体重指数(BMI)以及CAP值的四分位间距/中位数(IQR/MCAP)独立相关(均P<0.05)。13例(8.1%)患者存在不一致情况。多因素分析显示,调整BMI、IQR/MCAP以及由组织学活性或丙氨酸氨基转移酶(ALT)水平反映的坏死性炎症后,组织学S3(比值比[OR],9.573;95%置信区间[CI],1.207 - 75.931;P = 0.033)和CAP值(OR,1.020;95% CI,1.006 - 1.034;P = 0.006)与不一致显著相关。
重度脂肪变性或CAP值高的患者,LB与CAP结果不一致的风险更高。需要进一步研究以提高CAP解读的准确性,尤其是在CAP值较高的患者中。