Division of Gastroenterology and Hepatology, Department of Medicine, McGill University Health Centre, Montreal, QC, Canada.
Division of Gastroenterology and Hepatology, Department of Medicine, University Health Network and University of Toronto, Toronto, ON, Canada.
Can J Gastroenterol Hepatol. 2017;2017:4381864. doi: 10.1155/2017/4381864. Epub 2017 Mar 19.
. Serum fibrosis biomarkers have shown good accuracy in the liver transplant (LT) population. We employed a simple serum biomarker to elucidate incidence and predictors of advanced fibrosis after LT over a long follow-up period. . We included 440 consecutive patients who underwent LT between 1991 and 2013. Advanced liver fibrosis was defined as FIB-4 > 3.25 beyond 12 months after LT. . Over 2030.5 person-years (PY) of follow-up, 189 (43%) developed FIB-4 > 3.25, accounting for an incidence of 9.3/100 PY (95% confidence interval [CI], 8.1-10.7). Advanced fibrosis was predicted by chronic HCV infection (adjusted hazard ratio (aHR) = 3.96, 95% CI 2.92-5.36, < 0.001), hypoalbuminemia (aHR = 2.31, 95% CI 1.72-3.09; < 0.001), and hyponatremia (aHR = 1.48, 95% CI 1.09-2.01; = 0.01). LT recipients with more than 1 predictor had a higher incidence of advanced fibrosis, the highest being when all 3 predictors coexisted (log-rank: < 0.001). . Chronic HCV infection, hypoalbuminemia, and hyponatremia predict progression to advanced liver fibrosis following LT. Patients with these risk factors should be serially monitored using noninvasive fibrosis biomarkers and prioritized for interventions.
血清纤维化生物标志物在肝移植(LT)人群中显示出良好的准确性。我们采用一种简单的血清生物标志物,在较长的随访期间阐明 LT 后发生晚期纤维化的发生率和预测因素。
我们纳入了 1991 年至 2013 年间接受 LT 的 440 例连续患者。晚期肝纤维化定义为 LT 后 12 个月以上 FIB-4 > 3.25。
在超过 2030.5 人年(PY)的随访中,189 例(43%)发生了 FIB-4 > 3.25,发病率为 9.3/100 PY(95%置信区间[CI],8.1-10.7)。慢性 HCV 感染(调整后的危险比[aHR] = 3.96,95%CI 2.92-5.36, < 0.001)、低白蛋白血症(aHR = 2.31,95%CI 1.72-3.09; < 0.001)和低钠血症(aHR = 1.48,95%CI 1.09-2.01; = 0.01)预测晚期纤维化。具有多个预测因素的 LT 受者发生晚期纤维化的发生率更高,当所有 3 个预测因素共存时发生率最高(对数秩检验: < 0.001)。
慢性 HCV 感染、低白蛋白血症和低钠血症预测 LT 后进展为晚期肝纤维化。具有这些危险因素的患者应使用非侵入性纤维化生物标志物进行连续监测,并优先进行干预。