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. 2015 Aug 27;62(6):1731–1741. doi: 10.1002/hep.27932

Table 2.

Characteristics and Hepatic Copper Content of Patients With Various Liver Diseases

Etiology No. of Patients Gender (M/F) Mean Age (Years) Hepatic Copper Level of Patients (μg/g dry wt)
Mean 0– 50– 100– 150– 250+
WD 178 104/74 19.7 ± 11.0 770.6 ± 393.2 0 0 1 9 168
Heterozygote 24 20/4 19.5 ± 8.0 110.7 ± 51.8 1 12 7 3 1
PBC and PSC 48 13/35 44.5 ± 13.1 318.2 ± 299.7 6 7 5 7 23
Viral hepatitis 198 181/17 33.4 ± 10.3 50.1 ± 35.3 126 53 14 5 0
AIH 50 22/28 38.0.2 ± 15.6 82.1 ± 66.0 19 20 6 3 2
NASH 40 35/5 33.5 ± 13.3 40.4 ± 28.1 31 8 1 0 0
GS and DS 28 24/4 22.5 ± 8.0 37.3 ± 19.7 23 5 0 0 0
Hemochromatosis 9 9/0 31.8 ± 10.1 55.4 ± 77.3 7 1 0 0 1
IPH 10 8/2 41.4 ± 14.0 59.8 ± 29.0 4 5 1 0 0
Other diseases 32 26/6 33.8 ± 18.0 50.2 ± 39.5 20 9 1 2 0
Origin unknown 74 50/24 31.0 ± 18.9 165.0 ± 320.6 36 17 6 5 10
Total 691 492/199 29.8 ± 14.2 272.8 ± 388.3 273 137 42 33 206

Viral hepatitis, hepatitis B (180), other viral hepatitis (18); GS (26) and DS (2); other diseases, including neurologic diseases other than WD (8), hemolytic jaundice (5), polymyositis (5), venous occlusive disease (4), Budd‐Chiari syndrome (3), alcoholic hepatitis (3), lymphoma (1), glycogen storage disease (1), congenital hepatic fibrosis (1), and schistosomiasis Japonica (1). Origin unknown refers to other diseases origin unknown.

Abbreviations: M, male; F, female; GS, Gilbert syndrome; DS, Dubin‐Johnson syndrome.