Department of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.
Department of Pathology, National Taiwan University Hospital, Taipei, Taiwan.
J Pediatr. 2019 May;208:30-37.e1. doi: 10.1016/j.jpeds.2018.12.006. Epub 2019 Mar 8.
To assess the diagnostic and prognostic usefulness of the serum matrix metallopeptidase-7 (MMP-7) level for biliary atresia in infants with cholestasis after hepatoportoenterostomy.
We enrolled 100 infants with cholestasis (age, 43.56 ± 1.97 days; 62 males) with a direct bilirubin level of >1 mg/dL, of whom 36 (36%) were diagnosed with biliary atresisa. The MMP-7 levels in serum samples collected during the cholestasis workup and 6 months after hepatoportoenterostomy were assessed by enzyme-linked immunosorbent assay. We quantified liver fibrosis by Picro Sirius red staining of collagen in specimens from the 81 infants with cholestasis.
Infants with biliary atresisa had a significantly higher serum MMP-7 level than that of non-biliary atresisa infants with cholestasis of equivalent age (P < .0001). Receiver operating characteristic analysis showed that a serum MMP-7 level of >1.43 ng/mL was predictive of biliary atresisa in infants with cholestasis (diagnostic accuracy, 88%). There was a positive correlation between the serum MMP-7 level and the severity of liver fibrosis (P = .0002). Survival analysis showed that the frequency of liver transplantation was significantly higher in infants with biliary atresisa with a serum MMP-7 level of >10.30 ng/mL compared with a serum MMP-7 level of ≤10.30 ng/mL after hepatoportoenterostomy (hazard ratio, 4.22; P = .02).
The serum MMP-7 level, which reflects the severity of liver fibrosis and can be determined noninvasively, may facilitate the diagnosis of biliary atresisa among infants with cholestasis. Moreover, the serum MMP-7 level after hepatoportoenterostomy is associated with a need for liver transplantation in infants with biliary atresisa.
评估血清基质金属蛋白酶-7(MMP-7)水平对行肝门空肠吻合术后胆汁淤积婴儿胆道闭锁的诊断和预后价值。
我们纳入了 100 名胆汁淤积婴儿(年龄 43.56±1.97 天;男性 62 名),其直接胆红素水平>1mg/dL,其中 36 名(36%)被诊断为胆道闭锁。通过酶联免疫吸附试验评估了在胆汁淤积检查期间和肝门空肠吻合术后 6 个月采集的血清样本中的 MMP-7 水平。我们通过对 81 名胆汁淤积婴儿的胶原进行皮尔斯 Sirius 红染色来量化肝纤维化。
胆道闭锁婴儿的血清 MMP-7 水平明显高于同龄非胆道闭锁胆汁淤积婴儿(P<0.0001)。受试者工作特征分析显示,血清 MMP-7 水平>1.43ng/mL 可预测胆汁淤积婴儿的胆道闭锁(诊断准确性为 88%)。血清 MMP-7 水平与肝纤维化严重程度呈正相关(P=0.0002)。生存分析显示,与肝门空肠吻合术后 MMP-7 水平≤10.30ng/mL 的婴儿相比,血清 MMP-7 水平>10.30ng/mL 的胆道闭锁婴儿需要肝移植的频率显著更高(风险比 4.22;P=0.02)。
血清 MMP-7 水平反映了肝纤维化的严重程度,可以进行非侵入性检测,可能有助于诊断胆汁淤积婴儿的胆道闭锁。此外,肝门空肠吻合术后的血清 MMP-7 水平与胆道闭锁婴儿需要肝移植相关。