Objective: To review the clinical assessment of iron deficiency and ex
cess. Conclusions: Two key iron-related proteins in the human body are
ferritin, which is the iron storage protein, and the transferrin rece
ptor, which controls the entry of iron-bearing transferrin to cells. I
ntact ferritin and truncated transferrin-receptor molecules are presen
t in serum in direct quantitative proportion to their total tissue con
tent. Ferritin and transferrin-receptor production are precisely and r
eciprocally regulated at a posttranscriptional level. This is achieved
by an iron-responsive element-binding protein that interacts with iro
n-responsive elements in the mRNA of each, but with contrary effects.
Increases in serum ferritin reflect increased storage iron and in; cre
ases in serum transferrin receptor reflect cellular iron deficits. The
combined use of these two measurements allows accurate definition of
the entire range of body iron status. This is valid even in situations
where assessment of iron status has been notoriously problematic, inc
luding periods of rapid growth, in pregnancy, in conditions associated
with inflammation, and in trained athletes.