RELATIONSHIPS AMONG SERUM IRON STATUS MARKERS, CHEMICAL AND HISTOCHEMICAL LIVER IRON CONTENT IN 117 PATIENTS WITH ALCOHOLIC AND NONALCOHOLIC HEPATIC-DISEASE
N. Milman et al., RELATIONSHIPS AMONG SERUM IRON STATUS MARKERS, CHEMICAL AND HISTOCHEMICAL LIVER IRON CONTENT IN 117 PATIENTS WITH ALCOHOLIC AND NONALCOHOLIC HEPATIC-DISEASE, Hepato-gastroenterology, 41(1), 1994, pp. 20-24
Histochemical and chemical liver iron and iron status markers (serum (
S-) ferritin, transferrin saturation) were determined in 109 patients
with various types of liver disease (71 alcoholic, 38 non-alcoholic di
sease) and 8 normal subjects. In the series as a whole there was a sig
nificant correlation between histochemical hepatocyte iron and chemica
l iron (rho = 0.48, p = 0.0001). Of the iron status markers, only S-fe
rritin showed clinically significant correlations with histochemical l
iver iron (rho = 0.54, p = 0.0001) and chemical liver iron (r = 0.45,
p = 0.0001) (log vs. log values. The highest correlation was found bet
ween S-ferritin and the product of chemical iron x ASAT (r = 0.61, p =
0.0001) (log vs. log values). None of the normal livers had stainable
hepatocyte iron; median chemical iron content was 15 mu mol/g dry wei
ght (range 8-25). The entire group of alcoholics had a median liver ir
on content of 21 mu mol/g; all patients had a hepatic iron index (hepa
tic iron/age) of under 1.4. In alcoholic liver disease, median chemica
l liver iron content was 15 mu mol/g (range 3-36) in 35 subjects with
grade 0 hepatocyte iron; 24 mu mol/g (range 6-90) in 25 subjects with
grade 1 + 2 hepatocyte iron; 30 mu mol/g (range 14-74) in 11 subjects
with grade 3 + 4 hepatocyte iron. Among subjects with alcoholic liver
disease and normal liver iron (< 26 mu mol/g), 39 % had stainable hepa
tocyte iron vs. 70 % in subjects with increased liver iron (greater th
an or equal to 26 mu mol/g). The corresponding figures in subjects wit
h non-alcoholic liver disease were 13 % and 20 %. This difference was
statistically significant (chi square = 20.9, p = 0.0001) and suggests
a redistribution of hepatocyte iron from ferritin to hemosiderin in a
lcoholic liver disease. Although chemical liver iron measurement remai
ns the method of reference, histochemical liver iron assessment appear
s to be of great value in the routine examination.