Non-invasive assessment of liver fibrosis in C282Y homozygous HFE hemochromatosis

被引:30
|
作者
Legros, Ludivine [1 ,2 ,3 ]
Bardou-Jacquet, Edouard [1 ,2 ,3 ,4 ]
Latournerie, Marianne [1 ,2 ]
Guillygomarc'h, Anne [1 ,2 ]
Turlin, Bruno [4 ,5 ]
Le Lan, Caroline [1 ,2 ]
Desille, Yoann [1 ,2 ]
Laine, Fabrice [6 ]
Moirand, Romain [1 ,2 ,3 ,4 ]
Brissot, Pierre [1 ,2 ,3 ,4 ]
Deugnier, Yves [1 ,2 ,4 ]
Guyader, Dominique [1 ,2 ,4 ]
机构
[1] CHU Rennes, Liver Dis Unit, F-35033 Rennes, France
[2] CHU Rennes, Natl Reference Ctr Rare Iron Overload Dis Genet O, F-35033 Rennes, France
[3] CHU Rennes, INSERM, UMR991, F-35033 Rennes, France
[4] Univ Rennes 1, CHU Rennes, Rennes, France
[5] CHU Rennes, Dept Pathol, F-35033 Rennes, France
[6] CHU Rennes, INSERM, Clin Invest Unit, CIC0203, F-35033 Rennes, France
关键词
liver fibrosis; transient elastography; serum ferritin; cirrhosis; hyaluronic acid; TRANSIENT ELASTOGRAPHY; GENETIC HEMOCHROMATOSIS; STIFFNESS MEASUREMENT; HEPATIC-FIBROSIS; DIAGNOSIS; CIRRHOSIS; BIOPSY; RELIABILITY; PREDICTION;
D O I
10.1111/liv.12762
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & AimsC282Y homozygotes with serum ferritin (SF) levels >1000g/L and/or increased serum transaminase levels are at risk of severe F3/F4 fibrosis. Current practical guidelines recommend liver biopsy in such individuals. This prospective observational cohort study aimed to evaluate non-invasive alternative means such as hyaluronic acid (HA) and transient elastography (TE) for the assessment of severe fibrosis in patients with SF >1000g/L or elevated transaminases. MethodsBetween September 2005 and April 2013, 77 patients diagnosed C282Y homozygotes underwent a liver biopsy because of SF >1000g/L and/or increased transaminases according to current guidelines, with concomitant TE. All of them had clinical and biological evaluation, including HA measurement in 52 cases. ResultsA total of 19.5% of patients had F3-F4 severe fibrosis. HA was higher in patients with severe fibrosis, but did not accurately predict severe fibrosis. TE was significantly higher in patients with severe fibrosis (17.2 vs. 4.9 kPa; P<0.05) and was able to accurately predict fibrosis stage in 47/61 (77%) patients with valid measurement using a lower threshold of 6.4 kPa and an upper threshold of 13.9 kPa. Efficient assessment of severe fibrosis was not possible in patients with intermediate TE values. ConclusionAn algorithm that successively employed SF and TE can accurately classify severe fibrosis in 61% of patients, restricting the need for liver biopsy to the 39% of patients with intermediate or unvalid TE values. This algorithm should be validated in independent cohorts before extended use.
引用
收藏
页码:1731 / 1738
页数:8
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