P. Cacoub et al., PROTEIC PROFILE AND IRON-DEFICIENCY - SIG NIFICANCE OF ALBUMIN-TRANSFERRIN RATIOS, La Revue de medecine interne, 17(8), 1996, pp. 627-634
From a clinical standpoint the search for iron deficiency is based upo
n serum ferritin. However, serum ferritin values may be pathologic in
other numerous pathological conditions such as inflammation, liver dis
eases, malignant hematologic disorders, hemolysis, etc. Proteic profil
e combines the analyze of proteins variations: protein results are con
verted in percent of normal values referenced for the technique used.
It has been suggested that on the protein profile, an increase in seru
m transferrin level compared to a normal serum albumin level (DAT : di
fference albumin - transferrin), appears early in the course of iron d
eficiency. In order to know the value of a pathologic DAT greater than
or equal to 28% in the diagnosis of iron deficiency, we prospectively
studied 156 patients consecutively hospitalized in an internal medici
ne department. Iron deficiency was defined by a low serum ferritin lev
el. Diagnosis performance (sensitivity, specificity, positive and nega
tive predictive values) of different biologic markers of iron deficien
cy (serum iron, saturation of total iron-binding capacity, low mean er
ythrocyte volume) and DAT was compared to the performance of low serum
ferritin values. With the exception of low serum ferritin (which have
by definition a specificity and a positive predictive value of 100%),
pathologic DAT appeared as the best index of iron deficiency with the
highest sensitivity (67.4%), specificity (97.3%), positive predicitiv
e value (91.2%), negative predicitive value (87.7%) and diagnosis effi
cacy (sensitivity x specificity = 0.66). A pathologic DAT associated t
o a low serum ferritin level increased the diagnosis performance of bo
th tests to 0.72. Diagnosis efficacy of DAT was not changed (0.66) in
83 patients with a confounding factor for ser um ferritin analysis (in
flammation, liver diseases, malignant hematologic disorders, hemolysis
) when diagnosis efficacy of all other tests decreased. There was a ne
gative correlation between serum ferritin level and DAT level (r = -0.
55; P < 0.0001). In conclusion, an increase of ser urn transferrin of
more than 28% compared to serum albumin on a proteic profile gives a s
ignificant benefit for the diagnosis of iron deficiency. This benefit
increases when data of both DAT and serum ferritin are associated.