Volume 4, Issue 3 pp. 531-535
Article
Free Access

Human aldolase B serum levels: A marker of liver injury

Masahiro Asaka

Masahiro Asaka

Third Department of Internal Medicine, Hokkaido University School of Medicine, Sapporo, Japan, 060 and Gastroenterology Section, Department of Medicine, Baylor College of Medicine, Houston Texas 77030

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Tamotsu Miyazaki

Tamotsu Miyazaki

Third Department of Internal Medicine, Hokkaido University School of Medicine, Sapporo, Japan, 060 and Gastroenterology Section, Department of Medicine, Baylor College of Medicine, Houston Texas 77030

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F. Blaine Hollinger

F. Blaine Hollinger

Third Department of Internal Medicine, Hokkaido University School of Medicine, Sapporo, Japan, 060 and Gastroenterology Section, Department of Medicine, Baylor College of Medicine, Houston Texas 77030

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Elliot Alpert

Corresponding Author

Elliot Alpert

Third Department of Internal Medicine, Hokkaido University School of Medicine, Sapporo, Japan, 060 and Gastroenterology Section, Department of Medicine, Baylor College of Medicine, Houston Texas 77030

Elliot Alpert, M.D., Gastroenterology Section 533 D, Department of Medicine, Baylor College of Medicine, Houston, Texas 77030.===Search for more papers by this author
First published: May‐June 1984
Citations: 20

Abstract

A solid-phase, noncompetitive radioimmunoassay has been developed for aldolase B in human serum and tissues. Aldolase B was purified from human liver, and specific antisera to purified aldolase B were obtained from chickens. Specific antihuman aldolase B IgG was purified by affinity chromatography. Disposable polypropylene plates were coated with affinity purified specific IgG antibody and used for radioimmunoassay with 125I-specific IgG antibody to aldolase B. The nonspecific binding was minimized by saturating the binding sites of the plates with 2% ovalbumin in 0.1% Tween 20. This radioimmunoassay is specific for the aldolase B subunit, with no cross-reactivity with human aldolase A or aldolase C subunits. Aldolase B is predominantly found in normal liver. Relatively high aldolase B levels are also observed in kidney. Serum levels of aldolase B in 21 normal subjects ranged from 21 to 39 ng per ml, with a mean of 28.7 ± 8.6 (2 S.D.) ng per ml. Forty of 42 (95%) patients with acute and chronic hepatitis without cirrhosis had serum aldolase B levels greater than 40 ng per ml. Serum aldolase B levels correlated well with total serum aldolase enzyme activities (r = 0.967) and SGPT (r = 0.951) in patients with liver diseases. In cancer patients, serum aldolase B was slightly elevated in 15 of 26 (58%) patients with cancer metastatic to the liver or primary liver cell carcinoma, whereas no elevation of serum aldolase B was observed in 16 cancer patients without liver metastasis. Measurements of aldolase B serum levels by radioimmunoassay appear to be a useful measure of liver cell necrosis from benign or malignant liver diseases.

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