医学
胆道闭锁
干血斑
胆汁淤积
胃肠病学
置信区间
内科学
基质金属蛋白酶9
基质金属蛋白酶
肝移植
移植
遗传学
生物
作者
Chee‐Seng Lee,Yen‐Hsuan Ni,Huey‐Ling Chen,Jia–Feng Wu,Hong‐Yuan Hsu,Yin‐Hsiu Chien,Ni‐Chung Lee,Wuh‐Liang Hwu,Ting‐An Yen,Huey‐Huey Chua,Yu‐Ju Chen,Yu‐Lin Wang,Mei‐Hwei Chang
标识
DOI:10.1097/mpg.0000000000003701
摘要
Objectives: Timely diagnosis is a critical challenge and is associated with improved survival of biliary atresia (BA) patients. We aimed to measure matrix metalloproteinase-7 (MMP-7) levels in BA patients within 3 days of birth using the dried blood spot (DBS) method and evaluate its potential as a screening tool. Methods: The study enrolled 132 patients, including 25 patients diagnosed with BA and 107 non-BA patients with other congenital or perinatal conditions from the National Taiwan University Children Hospital. The stored DBS samples collected from 48 to 72 hours of life were retrieved from newborn screening centers. MMP-7 on the DBS was quantified using a sensitive sandwich enzyme-linked immunosorbent assay (ELISA). Results: The MMP-7 levels of BA patients on the DBS were significantly higher than those of non-BA patients (19.2 ± 10.4 vs 5.6 ± 2.7 ng/mL, P value < 0.0001). MMP-7 levels in non-BA patients, including 5 patients with hepatobiliary structural anomaly, 9 patients with intrahepatic cholestasis, and 93 patients with other perinatal diseases, were 11.6 ± 4.2 ng/mL, 6.9 ± 3.0 ng/mL, and 5.2 ± 2.1 ng/mL, respectively. The DBS MMP-7 level showed good accuracy for identifying BA, with an area under the curve of 93.7% [95% confidence interval (CI): 87.7%–99.7%]. The MMP-7 cutoff at 8.0 ng/mL showed a sensitivity of 92.0% (95% CI: 75.0%–98.6%) and specificity of 92.5% (95% CI: 85.9%–96.1%) for detecting BA from other congenital or perinatal diseases. Conclusions: MMP-7 DBS analysis can be used to distinguish BA from other conditions as early as 3 days of age.
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