Diagnostic Accuracy of Serum Matrix Metalloproteinase‐7 for Biliary Atresia

The diagnosis of biliary atresia (BA) remains a clinical challenge because affected infants have signs, symptoms, and serum liver biochemistry that are also seen in those with other causes of neonatal cholestasis (non‐BA). However, an early diagnosis and prompt surgical treatment are required to imp...

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Published inHepatology (Baltimore, Md.) Vol. 68; no. 6; pp. 2069 - 2077
Main Authors Yang, Li, Zhou, Ying, Xu, Pei‐pei, Mourya, Reena, Lei, Hai‐yan, Cao, Guo‐qing, Xiong, Xiao‐li, Xu, Hui, Duan, Xu‐fei, Wang, Na, Fei, Lin, Chang, Xiao‐pan, Zhang, Xi, Jiang, Meng, Bezerra, Jorge A., Tang, Shao‐tao
Format Journal Article
LanguageEnglish
Published United States Wolters Kluwer Health, Inc 01.12.2018
John Wiley and Sons Inc
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ISSN0270-9139
1527-3350
1527-3350
DOI10.1002/hep.30234

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Summary:The diagnosis of biliary atresia (BA) remains a clinical challenge because affected infants have signs, symptoms, and serum liver biochemistry that are also seen in those with other causes of neonatal cholestasis (non‐BA). However, an early diagnosis and prompt surgical treatment are required to improve clinical outcome. Recently, the relative abundance of serum matrix metalloproteinase‐7 (MMP‐7) was suggested to have discriminatory features for infants with BA. To test the hypothesis that elevated serum concentration of MMP‐7 is highly diagnostic for BA, we determined the normal serum concentration of MMP‐7 in healthy control infants, and then in 135 consecutive infants being evaluated for cholestasis. The median concentration for MMP‐7 was 2.86 ng/mL (interquartile range, IQR: 1.32‐5.32) in normal controls, 11.47 ng/mL (IQR: 8.54‐24.55) for non‐BA, and 121.1 ng/mL (IQR: 85.42‐224.4) for BA (P < 0.0001). The area under the curve of MMP‐7 for the diagnosis of BA was 0.9900 with a cutoff value of 52.85 ng/mL; the diagnostic sensitivity and specificity were 98.67% and 95.00%, respectively, with a negative predictive value of 98.28%. Conclusion: Serum MMP‐7 assay has high sensitivity and specificity to differentiate BA from other neonatal cholestasis, and may be a reliable biomarker for BA.
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Supported by the National Science foundation of China (NSFC‐30973137, NSFC‐81700501) and the National Institutes of Health (DK‐64008, DK‐83781, and DK‐78392) (to J.A.B.).
These authors contributed equally to this work.
ISSN:0270-9139
1527-3350
1527-3350
DOI:10.1002/hep.30234