Effects of Omeprazole on Iron Absorption: Preliminary Study/Omeprazol'un Demir Absorpsiyonundaki Etkileri: Ön Çalisma

Headnote

Abstract:

Objective: Increasing numbers of pediatric and adult patients are being treated with proton pump inhibitors (PPIs). PPIs are known to inhibit gastric acid secretion. Nonheme iron requires gastric acid for conversion to the ferrous form for absorption. Ninety percent of dietary and 100% of oral iron therapy is in the nonheme form. To the best of our knowledge, the effect of PPIs on iron absorption has not been studied in humans. Our study assessed the relationship between omeprazole therapy and iron absorption in healthy subjects.

Materials and Methods: We recruited 9 healthy volunteers between June 2010 and March 2011. Subjects with chronic illness, anemia, or use of PPI therapy were excluded. Serum iron concentrations were measured 1, 2, and 3 h after the ingestion of iron (control group). The measurements were repeated on a subsequent visit after 4 daily oral administrations of omeprazole at a dose of 40 mg (treatment group).

Results: One female and 8 male volunteers were enrolled in the study with a mean age of 33 years. There was no statistical difference detected between baseline, 1-h, 2-h, and 3-h iron levels between control and treatment groups.

Conclusion: Administration of omeprazole for a short duration does not affect absorption of orally administered iron in healthy individuals.

Key Words: Iron, Omeprazole, PPI, Proton pump inhibitors, Anemia

Özet:

Amaç: Giderek artan say?da pediatrik ve yeti?kin hastalar proton pompa inhibitörleri (PPI) ile tedavi edilmektedir. PPI'lar?n mide asidini inhibe ettikleri bilinmektedir. Heme'e ba?l? olmayan demir ferroz ?ekline geçerek absorb edilebilmesi için mide asidi gerektirir. Diyetteki demirin yüzde doksan? ve tedavide kullan?lan demirin yüzde yüzü heme'e ba?l? olmayan durumdad?r. Bilgimize göre PPI'lar?n demir absobsiyonunda nas?l etki etti?i insanlarda ara?t?r?lmam?st?r. Ara?t?rmam?z omeprazol tedavisi ile demir absorbsiyonu aras?ndaki ili?kiyi sa?l?kl? ki?ilerde incelemi?tir.

Gereç ve Yöntemler: Haziran 2010 ile Mart 2011 aras?nda 9 sa?l?kl? gönüllüyü çal??mamiz için davet ettik. Kronik hastal??? veya anemisi olan ki?ilerle PPI tedavisinde olan ki?ileri d??lad?k. Serum demir konsantrasyonunu demir al?m?ndan 1, 2, ve 3 saat sonra ölçtük (kontrol grubu). Bu ölçümleri bir sonraki ziyarette 4 günlük oral 40 mg dozunda omeprazol tedavisinden sonra tekrarlad?k (tedavi grubu).

Bulgular: Ortalama ya?lar? 33 y?l olan 8 erkek ve 1 kad?n gönüllü çal??mam?za kat?ld?. Kontrol grubu ile tedavi grubu aras?nda bazal, 1 saat, 2 saat, ve 3 saat sonraki demir konsantrasyonlar? aras?nda istatistiksel anlaml? bir fark görülmedi.

Sonuç: Sa?l?kl? ki?ilerde k?sa bir zaman sürecince verilen omeprazol oral olarak al?nan demirin absorbsiyonunu etkilemez.

Anahtar Sözcükler: Demir, Omeprazol, PPI, Proton pompa inhibitörleri, Anemi

Introduction

Gastric acid plays an important role in the absorption of iron. Dietary iron can be divided into 2 types with respect to absorption: the heme type, derived from animal blood and muscle, which is well absorbed and comprises about 10%- 30% of the normal Western diet, and the more common nonheme type, derived from plants (fruits, vegetables, grains, nuts), which requires an acidic gastric environment for absorption [1,2]. Although the heme component is absorbed independent of gastric pH, the nonheme part requires an acidic pH for absorption [3].

At physiologic pH and in the presence of oxygen, iron exists predominantly in the highly insoluble ferric Fe(III) form and therefore is poorly bioavailable [4]. Ingested ferrous ions are readily oxidized to ferric ions by dissolved oxygen [5]. Stomach acid is important in releasing iron from ligands in food and in solubilizing ferric iron by converting it to ferrous form [6].

It has been speculated that inhibition of gastric acid secretion may lead to reduction in iron and vitamin B12 absorption [7]. The development of iron malabsorption has been shown in a variety of hypo- or achlorhydric conditions. Heath and Patek observed that among patients with iron- deficiency anemia, the rate of the hemoglobin response to iron therapy was lower in those who had achlorhydria than in those without [8]. Goldberg et al., using radiolabeled iron, showed that patients with achlorhydria have diminished absorption of iron [9]. These data clearly demonstrate the importance of gastric acid secretion in iron absorption.

Increasing numbers of pediatric and adult patients are being treated with proton pump inhibitors (PPIs), often for several months. There is a limited amount of research specifically looking at the effects of PPIs and absorption of orally administered iron. Our study is the first such human study to assess this relationship in healthy subjects.

Materials and Methods

The protocol was approved by the institutional review board and written informed consent was obtained from all subjects. Subjects were recruited from a pool of healthy volunteers, 18 to 50 years old, who responded to our advertisement. Those with low ferritin levels <10 ng/mL for females, <20 ng/mL for males) or anemia (hemoglobin <115 g/L for females, <130 g/L for males), pregnant, or with malabsorption disorders, major gastrointestinal surgery, malignancy or any chronic conditions involving the gastrointestinal system, renal disease, or hematological, cardiac, or pulmonary conditions were excluded during the screening visit. Menstruating females came to their study visits 10-13 days after their last day of menstrual bleeding in order to synchronize menstrual cycles at the time of testing. All subjects were asked to continue their regular diet as we intended this study to be applicable to real-life situations.

At the second visit, baseline serum iron level and total iron-binding capacity were obtained after a minimum of 8 h of fasting. Ferrous sulfate (650 mg; 130 mg of elemental iron) was then administered orally as a tablet preparation, followed by determination of serum iron concentration 1, 2, and 3 h after the ingestion of iron. Male subjects returned 1 week and female subjects returned 1 month later for their last visit. Subjects were instructed to take omeprazole (40 mg) daily 30 min before breakfast for 4 days prior to their third visit (post-PPI), when after a minimum of 8 h of fasting, subjects were given 40 mg of omeprazole. During this visit, 650 mg of ferrous sulfate was administered orally. Serum iron concentration was measured before and 1, 2, and 3 h after the ingestion of iron. Baseline and post-omeprazole serum iron level determination was done around the same time of the day at each visit.

Statistical Analysis

Sample calculations were made using PASS (Power Analysis and Sample Size 2002, Number Crunch Statistical Systems, Kaysville, UT, USA). A sample size of 10 achieves 80% power to detect a difference of -50 (decrease by 50 µg/dL) between the baseline mean of 100 µg/dL and day 7 mean of 50 µg/dL with an estimated standard deviation of 50 µg/dL and with a significance level (alpha) of 0.05 using a 2-sided paired t-test.

Each subject served as her/his own control. Thus, serum iron concentrations were compared for the control vs. treatment conditions using the t-test for paired samples. Tests of significance were 2-sided and evaluated at the p<0.05 level. Data analyses were conducted using SPSS (Version 19, IBM SPSS Statistics, Somers, NY, USA).

Results

We recruited 9 healthy volunteers, 8 males and 1 female, who completed the study between June 2010 and March 2011. Mean age at the time of study was 33. A single blood sample in 2 subjects was hemolyzed and therefore excluded from the analysis.

Serum iron levels measured before taking omeprazole (control) and after 5 days of omeprazole therapy (treatment) were compared (Figure 1). When serum iron concentrations at different time points were compared between the control and treatment groups, there was no statistical difference (Table 1).

Discussion

After oral administration of PPI, the onset of the antisecretory effect of omeprazole occurs within 1 h, with the maximum effect occurring within 2 h [10]. The inhibitory effect of omeprazole on acid secretion increases with repeated once-daily dosing, reaching a plateau after 4 days. Bastani et al. showed a significant rise in serum iron concentration of 164±32% µg/dL above baseline 2 h after oral ingestion, plateauing afterwards [11]. These studies suggested that a 5-day course of PPI treatment would be sufficient length of treatment and 3 h of serum iron-level monitoring would be sufficient to detect serum changes in iron levels following the ingestion of iron preparation.

Our study was done in healthy subjects to minimize factors other than PPIs that may influence iron absorption. We did not restrict the diet of the subjects to maintain real-life applicability. In rats that were on a normal diet, omeprazole did not alter iron absorption, in agreement with our results [12].

Previous human and animal studies suggested that omeprazole may inhibit iron absorption in iron-depleted states. Two adult patients with iron deficiency anemia from erosive gastritis had their anemia corrected only after discontinuation of omeprazole [13]. Omeprazole inhibits iron absorption in rats that were fed an iron-deficient diet [12]. Another study showed that treatment of patients with hereditary hemochromatosis with PPIs led to significant reduction in the volume of blood removed annually [14]. In that report, postprandial iron absorption studies in 14 subjects with hemochromatosis demonstrated decreased absorption of nonheme iron from a test meal by approximately 50% after 7 days of PPI therapy. These studies suggest that PPIs may inhibit iron absorption in iron-depleted as well as iron- overloaded individuals.

Although our sample size was small, it was calculated based on prior studies in which serum iron levels decreased by 50% after 7 days or more of PPI therapy in hemochromatosis patients and a case report by Sharma et al. [13,14]. Ad hoc sample size calculations using iron levels from the 3 h following treatment showed that we would have needed 117,268 subjects in each group for the observed difference to be statistically significant. This suggests that the small sample size is not likely to account for our observations.

Conclusions

Our study demonstrates that short duration of omeprazole use does not affect iron absorption in iron-replete healthy individuals who are on a normal diet. Since omeprazole's effect was shown in iron-depletion or iron-overload states, it is plausible that omeprazole may have an effect on iron absorption only in abnormal iron metabolic states. Although short-term omeprazole therapy does not appear to affect iron absorption, since PPIs are increasingly being used for longer durations, further studies are warranted to evaluate their effects on long-term use.

Competing Interests

There are no financial or nonfinancial competing interests to disclose by any of the authors.

References

References

1. Khatib MA, Rahim O, Kania R, Molloy P. Iron deficiency anemia: induced by long-term ingestion of omeprazole. Dig Dis Sci 2002;47:2596-2597.

2. Massey AC. Microcytic anemia. Differential diagnosis and management of iron deficiency anemia. Med Clin North Am 1992;76:549-566.

3. Johnson LR. Physiology of the Gastrointestinal Tract, 2th ed. New York, Raven Press, 1987.

4. McKie AT, Barrow D, Latunde-Dada GO, Rolfs A, Sager G, Mudaly E, Mudaly M, Richardson C, Barlow D, Bomford A, Peters TJ, Raja KB, Shirali S, Hediger MA, Farzaneh F, Simpson RJ. An iron-regulated ferric reductase associated with the absorption of dietary iron. Science 2001;291:1755- 1759.

5. Goto K, Tamura H, Nagayama M. Mechanism of oxygenation of ferrous ion in neutral solution. Inorg Chem 1970;9:963- 964.

6. Miret S, Simpson RJ, McKie AT. Physiology and molecular biology of dietary iron absorption. Annu Rev Nutr 2003;23:283-301.

7. Reynolds JC. The clinical importance of drug interactions with antiulcer therapy. J Clin Gastroenterol 1990;12(Suppl 2):54-63.

8. Heath CW, Patek AJ. The anemia of iron deficiency. Medicine 1937;16:267-350.

9. Goldberg A, Lochhead AC, Dagg JH. Histamine-fast achlorhydria and iron absorption. Lancet 1963;1:848-850.

10. Medical Economics. Physicians' Desk Reference 2002. Thomson PDR, Oradell, NJ, USA, 2001.

11. Bastani B, Islam S, Boroujerdi N. Iron absorption after single pharmacological oral iron loading test in patients on chronic peritoneal dialysis and in healthy volunteers. Perit Dial Int 2000;20:662-666.

12. Golubov J, Flanagan P, Adams P. Inhibition of iron absorption by omeprazole in rat model. Dig Dis Sci 1991;36:405-408.

13. Sharma VR, Brannon MA, Carloss EA. Effect of omeprazole on oral iron replacement in patients with iron deficiency anemia. South Med J 2004;97:887-889.

14. Hutchinson C, Geissler CA, Powell JJ, Bomford A. Proton pump inhibitors suppress absorption of dietary non-haem iron in hereditary haemochromatosis. Gut 2007;56:1291- 1295.