ACHLORHYDRIA has been recognized as an associated feature of iron deficiency anaemia for many years (Faber, 1909; Witts, 1930). There has, however, been little agreement as to the part playcd by gastric acid in the absorption of iron from the intestinal tract. Early workers produced evidence that iron absorption was greater in the presence of normal gastric acidity than in cases of achlorhydria (Minot and Heath, 1932; Heilnieyer and Plotner, 1936;Barer and Fowler, 1937). Others found that this was not the case (Moore, Arrowsmith, Welch and Minnich, 1939; Grace, Doig and Wale 1954; Pirzio-Biroli, Bothwell and Finch, 1958).More recently Goldberg, Lochhcad and Dagg (1963) and Cook, Brown and Valberg (1964) have shown that in some circumstances iron is better absorbed by subjects with normal gastric acid than in those with a histamine fast achlorhydria.In the present investigation quantitative studies of both iron absorption and of gastric acid production have been made in patients with iron deficiency anaemia and additional observations have bccn made in normal subjects. The relationship betwccn iron absorption and gaatric secretory capacity is cxamincd.
METHODSHaenloglobin levels and mean corpuscular haemoglobin concentrations (MCHC) were mcasured by standard methods (Dacie and Lewis, 1963). Serum iron concentration was dctermincd by the method of Ramsay (1957). The secretion of gastric acid was measured by the continuous histamine infusion technique of Lawrie, Smith and Forrest (1964) which measures secretory rate after the maximum output has been obtained. Iron absorption was measured with a tracer dose of radioactive FeCI, which was given halfway through a standard test meal similar to that used by Pirzio-Biroli et al. (1958). Thc meal was eaten after an overnight fast. It consisted of tomato juice 2 fluid oz., bread 2 oz., butter + oz., chicken breast I oz., tinned pcaches 5 oz., and pcach juicc I fluid 02. The total iron content was io mg. In the first 17 tests iopc. of 59Fc was used as the tracer dose and faeces were collectcd for 8 days.Great care was taken throughout to ensure a complete faecal collection. The radioactivity of the faeces was measured in a ring of eight G26 Pb Geiger tubes and absorption was calculated from the difference between the amount of 59Fe ingested and the amount excreted. In the remaining nineteen tests the double isotope technique as adapted by Pirzio-Biroli et al. (1958) was used. As the oral dose, 1 2 . 3~~. of 55Fe was used, and after the meal was completed an intravenous dose of 0.7 pc. 59Fe as ferric citrate was given. The amounts of 55Fe and 59Fe in the red cells 14 days later were measured by liquid scintillation counting in a Packard Tricarb 3214 spectrometer aftcr chemical extraction (Eakins and Brown, 1966). Absorption of the oral iron was calculated from the formula:
Activity of "FeActivity of 9Fe in in blood sample intravenous dose ctivity of 59Fe Activity of 55Fe in in blood sample oral dosc 728 "/o "Fc absorbed = A X x IOO.