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Estimating
the Prevalence of
Soy Protein Allergy
Steve L. Taylor, Ph.D.
Food allergies are becoming an increasingly important issue. True soybean allergy
involves the generation of allergen-specific IgE antibodies in certain individuals
upon exposure to soy protein. Soybeans contain several allergenic proteins. IgE-mediated
soybean allergy can be a serious condition because of low threshold doses for
the offending protein(s) and the possibility of severe reactions in some soy-allergic
individuals.
Soybeans are considered by worldwide regulatory authorities as one of the most
commonly allergenic foods. Soybean allergy is most common among infants and young
children because of exposure to soybean-based infant formula.1, 2 Many
infants outgrow soybean allergy, so the prevalence is lower in adults.3
Despite widespread acceptance of the notion that soybeans are a commonly allergenic
food, solid scientific information on the prevalence of soybean allergy in the
overall population does not exist. However, in my opinion, the prevalence of
soybean allergy can be estimated by extrapolation from existing information.
A rigorous estimate of the prevalence of soybean allergy would need to involve
several critical features: 1) a study of the general population; 2) clinical
demonstration of adverse reactions to soybean preferably by double-blind, placebo-controlled
food challenges (DBPCFC); 3) and clinical documentation of an IgE-mediated mechanism
for the adverse reaction. The literature relevant to the prevalence of soybean
allergy was screened, and no clinical studies were found that met these rigorous
criteria. Thus, the prevalence of soybean allergy must be estimated from a critical
examination of existing studies.
Only one study actually attempted to determine the prevalence of soybean allergy
directly in the general adult population. Bjornsson et al. indicated a 2 percent
prevalence of soy allergy among 1,397 unselected Swedish adults of ages 20-44
years.4 However, the diagnosis was based only on serum screening for soy-specific
IgE and is thus undoubtedly an over-estimate because no oral challenges were
done to confirm that adverse reactions to soy actually occurred in these individuals.
It is well known that individuals can have food-specific IgE in their serum without
clinical reactivity to oral challenge to that food, especially in the case of
legumes, like soybean.5 In other studies, fewer than 10 percent of patients with
positive soy-specific IgE levels reacted adversely on blinded oral challenge
6, 7; however these two studies cannot be used to estimate overall prevalence
of soybean allergy because they were confined to food-allergic subpopulations.
If we assumed that 10 percent of the Swedish subjects with soy-specific IgE would
have been challenge-positive, then the prevalence of soybean allergy is estimated
at about 0.2 percent in adults.
Clinical experience would suggest that the prevalence of soy allergy should be
higher among infants and young children than among adults. Yet, the prevalence
of soybean allergy among unselected Australian children was estimated at only
0.1 – 0.28 percent based upon a unique extrapolation strategy developed
initially by Hill et al.8 They determined the prevalence of milk allergy among
a cohort of high-risk infants (those born to families with allergies). Then,
they corrected this estimate to the general Australian population by estimating
the percentage of infants who would be considered high-risk (19.3 percent). Their
estimate of the prevalence of milk allergy among Australian infants was 2 percent,
which is in agreement with earlier studies of the prevalence of milk allergy
in other countries based on challenge trials of the general infant population.9,
10 The prevalence of soy allergy can be estimated from the prevalence of milk
allergy based upon data on the subsequent development of soy allergy in milk-allergic
infants who were switched to soy formula. Various investigations estimate that
5-14 percent of milk-allergic infants develop soy allergy.1, 10, 11, 12 Thus,
the prevalence of soybean allergy is estimated as 2 percent x 5-14 percent, or
0.1-0.28 percent.
Information from the infant formula industry could be used to confirm these estimates
because milk-allergic infants are often switched first to soybean-based infant
formula. A study by Cordle2 can be used to confirm the estimate of Hill et al.8
because it provides information on a large number of milk-allergic infants switched
to soybean formula. Cordle indicated that 26 out of 247 cows’ milk-allergic
infants (10.5 percent) were unable to tolerate soy-based infant formula. If 10.5
percent of cows’
milk-allergic infants have soy allergy, then an estimated prevalence
of soy allergy in the infant population would be 0.21 percent
(2.0 percent x 10.5 percent).
Of course, this type of approach to estimating the prevalence
of soybean allergy has a significant potential flaw. It assumes
that only infants with cows’ milk allergy will develop
soy allergy in infancy. But in all likelihood, at least for young
infants (those less than 2 years of age, the age group typically
exposed to infant formula), that is probably true for the vast
majority of cases.
Many infants with soybean allergy will outgrow their soybean
allergy within a few years. Thus, using the prevalence of soy
allergy in infants to estimate the prevalence in the overall
population would require a significant adjustment for this development
of oral tolerance. In studies on a limited number of soy-allergic
infants, 50-100 percent of the infants became tolerant of soybeans
within 2-3 years.3, 13 It is thought that the development of
oral tolerance to soybean follows the same pattern as for milk
and egg, where much larger numbers of infants have been followed.
In an evaluation of several studies, Eggleston estimated that
70 percent of children who developed food allergies at ages less
than 3 years would outgrow the allergy within a few years.14
Most of these infants were sensitive to milk and egg, although
some were allergic to soy or wheat. In a preceding paragraph,
the estimated range of soybean allergy in infants was 0.1-0.28
percent. If we assume that 70 percent of these infants will outgrow
their soybean allergy, the estimated prevalence in the overall
population would be 0.02-0.056 percent. Of course, this assumes
that all sensitization to soybeans is initiated in infancy. While
this is not true, the majority of soy allergy likely does emanate
from sensitization during infancy.
Since most soy allergy is outgrown, the prevalence of soybean
allergy should be higher among infants than among adults. The
only study of the prevalence of soybean allergy among adults
is the estimate of 0.2 percent for Swedish adults – higher
than predicted based on this logic.
Despite the continuing uncertainties, the prevalence of soybean
allergy in the general population is probably not higher than
0.2 percent and could be as low as 0.1 percent (290-580,000 individuals)
among the U.S. population. This likely prevalence for soybean
allergy contrasts with prevalence estimates of 1.9 percent for
crustacean allergy, 0.6 percent for peanut allergy, 0.5 percent
for tree nut allergy, and 0.4 percent for fish allergy.15, 16
Editor’s Note: This work is a contribution
from the University of Nebraska Cooperative Extension Division,
Lincoln, Nebraska, Journal Series No. _____.
ABOUT THE AUTHOR
Steve Taylor, Ph.D. is a professor in the Department of Food Science and Technology
at the University of Nebraska, and is co-director of the Food Allergy Research
and Resource Program. He received his doctorate in biochemistry from the University
of California
– Davis.
REFERENCES
1) Zeiger RS, Sampson HA, Bock SA, et al. J. Pediatr. 1999; 134:614-622.
2) Cordle CT. J. Nutr. 2004; 134:1213S-1219S.
3) Sampson HA, Scanlon SM. J. Pediatr. 1989;115:23-27.
4) Bjornsson E, Janson C, Plaschke P, et al. Ann. Allergy Asthma Immunol. 1996;
77:327-332.
5) Bernhisel-Broadbent J, Sampson HA. J. Allergy Clin. Immunol. 1989; 83:435-440.
6) Giampietro PG, Ragno V, Daniele S, et al. Ann. Allergy 1992; 69:143-146.
7) Magnolfi CF, Zani G, Lacava L, et al. Ann. Allergy Asthma Immunol. 1996; 77:197-
201.
8) Hill DJ, Hosking CS, Zhie CY, et al. Environ. Toxicol. Pharmacol. 1997;4:101-110.
9) Jakobsson I, Lindberg T. Acta Paediatr. Scand. 1979; 68:853-859.
10) Host A, Halken S. Allergy 1990; 45:587-596.
11) Cantani A, Ferrara M, Rango V, Businco L. Riv. Eur. Sci. Med.
Farmacol.1990;12:311-318.
12) Klemola T, Vanto T, Juntunen-Backman K, et al. J. Pediatr. 2002; 140:219-224.
13) Bock SA. J. Allergy Clin. Immunol. 1982; 69:173-177.
14) Eggleston PA. Ann. Allergy 1987; 59(5 Pt. 2):179-182.
15) Sicherer SH, Munoz-Furlong A, Burks AW, Sampson HA. J. Allergy
Clin. Immunol. 1999; 103:559-562.
16) Sicherer SH, Munoz-Furlong A., Sampson HA. J. Allergy Clin. Immunol.
2004; 114:159-165.
Reprinted from The Soy Connection newsletter, published by the United Soy Bean
Board.
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