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American Journal of Clinical Nutrition, Vol. 80, No. 3, 787-788, August 2004
© 2004 American Society for Clinical Nutrition


LETTERS TO THE EDITOR

Iron and zinc interactions

Frank T Wieringa and Marjoleine A Dijkhuizen

Department of Internal Medicine
University Medical Center Nijmegen
PO Box 9101
6500 HB Nijmegen
Netherlands
E-mail: wieringa{at}tiscali.nl

Clive E West

Division of Human Nutrition
Wageningen University
PO Box 8129
6700 EV Wageningen
Netherlands
E-mail: clive.west{at}wur.nl

Dear Sir:

In a letter to the Editor in the December issue of the Journal, Sreedhar (1) raises the question whether iron supplementation has a negative effect on zinc concentrations, because the data from various studies seem to be conflicting. Although Lind et al (2) already pointed out several reasons that could explain the differences between the studies, we think that there is a more important reason for such differences.

Note that the results of the study by Lind et al (3) and of our study (4) were similar. Both studies reported a significant effect of interaction between iron and zinc supplementation on hemoglobin concentrations (P = 0.021 and P = 0.06, respectively) but not on zinc concentrations (P value not reported and P = 0.13, respectively). The main difference between the studies is that iron supplementation had a modest negative effect on the prevalence of low zinc concentrations in the study by Lind et al, whereas iron supplementation appeared to have a slight positive effect in our study.

Whereas Lind et al attribute this difference to differences in initial zinc status, we believe that the most important reason for this difference is that we controlled for the effect of the acute phase response by excluding infants with a C-reactive protein concentration > 10 mg/L in the analysis of the prevalence of deficiency and by controlling for the acute phase response in the analysis of covariance. The acute phase response strongly influences the concentrations of many indicators of micronutrient status, including ferritin and zinc concentrations (5). In the study by Lind et al, it is conceivable that the morbidity in the iron group was higher than in the placebo group, which led to lower zinc concentrations in the iron group. Iron supplementation is known to affect morbidity (6, 7).

Rather than the results, it is the interpretation of the outcomes that differs between the reports because of the importance given to outcomes by the 2 sets of authors. For example, Lind et al report that the prevalence of iron deficiency anemia was reduced to 2% and 3% after supplementation with iron and iron combined with zinc, respectively: these prevalence values are similar to those reported by us (3% and 8%, respectively). Our conclusion is that supplementation with iron and zinc combined is as effective in reducing iron deficiency anemia as is supplementation with iron alone. Thus, combined supplementation should be recommended in populations with a high risk of both iron and zinc deficiency. However, Lind et al concluded that combined iron and zinc supplementation is not optimal, because the increase in hemoglobin concentrations in the combined supplementation group was not significant. From a physiologic point of view, this is completely correct. However, note that in the study by Lind et al, the prevalence of low serum zinc after supplementation was 9% higher in the iron-only group and 24% lower in the iron plus zinc group than in the placebo group. To us, this provides clear evidence of the benefit of combined supplementation with iron and zinc.

The discussion between Sreedhar and Lind et al again shows the need for defining what is meant by interactions, because several different definitions are currently used. One definition is based on statistical arguments, with an interaction being significant when the combined effect of 2 interventions on an outcome variable does not equal the additive effect of the 2 interventions alone. To take a hypothetical example, iron and zinc interact according to this definition when combined supplementation reduces the prevalence of anemia by 30%, while the single supplements reduce anemia prevalence by 40% and 15%, respectively. If the reduction of anemia prevalence had been 55% after combined supplementation, there is no interaction in the statistical sense. However, interactions can also be physiologically defined. This means that 2 nutrients are surmised to play a role in the same metabolic pathway. Using the same example, a 55% reduction in anemia prevalence by the combined supplement would signify an interaction in the physiologic sense, because both nutrients contribute to the effect.

However, with Bob Dylan in mind, it is clear that "all definitions can't be right all of the time." On the basis of the first definition, how should the occurrence of an effect of interaction between iron and zinc on ferritin concentrations in the absence of an effect on hemoglobin concentrations be interpreted? It would be very unsatisfactory if only the outcome measured would determine whether an interaction between 2 nutrients exists. In contrast, in the example of iron and zinc, a physiologic interaction is surmised, but we are not sure. Iron and zinc may contribute to higher hemoglobin concentrations via 2 completely separate pathways.

It is not surprising that this situation leads to confusion in discussions and interpretation of results. The term interaction needs to be clearly defined, not only whether it is used in the statistical or physiologic sense but also whether the interaction is antagonistic, synergistic, or additive in nature.

REFERENCES

  1. Sreedhar B. Conflicting evidence of iron and zinc interactions in humans: does iron affect zinc absorption? Am J Clin Nutr 2003;78:1226(letter).[Free Full Text]
  2. Lind T, Persson L-Å, Lönnerdal B. Reply to B Sreedhar. Am J Clin Nutr 2003;78:1226–7(letter).
  3. Lind T, Lonnerdal B, Stenlund H, et al. A community-based randomized controlled trial of iron and zinc supplementation in Indonesian infants: interactions between iron and zinc. Am J Clin Nutr 2003;77:883–90.[Abstract/Free Full Text]
  4. Dijkhuizen MA, Wieringa FT, West CE, Martuti S, Muhilal. Effects of iron and zinc supplementation in Indonesian infants on micronutrient status and growth. J Nutr 2001;131:2860–5.[Abstract/Free Full Text]
  5. Wieringa FT, Dijkhuizen MA, West CE, Northrop-Clewes CA, Muhilal. Estimation of the effect of the acute phase response on indicators of micronutrient status in Indonesian infants. J Nutr 2002;132:3061–6.[Abstract/Free Full Text]
  6. Dewey KG, Domellof M, Cohen RJ, Landa Rivera L, Hernell O, Lonnerdal B. Iron supplementation affects growth and morbidity of breast-fed infants: results of a randomized trial in Sweden and Honduras. J Nutr 2002;132:3249–55.[Abstract/Free Full Text]
  7. Oppenheimer SJ. Iron and its relation to immunity and infectious disease. J Nutr 2001;131:616S–33S.[Abstract/Free Full Text]



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F. T. Wieringa, J. Berger, M. A. Dijkhuizen, A. Hidayat, N. X. Ninh, B. Utomo, E. Wasantwisut, P. Winichagoon, and for the SEAMTIZI (South-East Asia Multi-country Tr
Combined Iron and Zinc Supplementation in Infants Improved Iron and Zinc Status, but Interactions Reduced Efficacy in a Multicountry Trial in Southeast Asia
J. Nutr., February 1, 2007; 137(2): 466 - 471.
[Abstract] [Full Text] [PDF]


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