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Long-term evaluation of a micronutrient-fortified biscuit used for addressing micronutrient deficiencies in primary school children

Published online by Cambridge University Press:  02 January 2007

ME van Stuijvenberg*
Affiliation:
Nutritional Intervention Research Unit, Medical Research Council, PO Box 19070, Tygerberg 7505, South Africa
MA Dhansay
Affiliation:
Nutritional Intervention Research Unit, Medical Research Council, PO Box 19070, Tygerberg 7505, South Africa
CM Smuts
Affiliation:
Nutritional Intervention Research Unit, Medical Research Council, PO Box 19070, Tygerberg 7505, South Africa
CJ Lombard
Affiliation:
Biostatistics Unit, Medical Research Council, PO Box 19070, Tygerberg 7505, South Africa
VB Jogessar
Affiliation:
Department of Haematology, Faculty of Medicine, University of Natal, PO Box 17039, Congella 4013, South Africa
AJS Benadé
Affiliation:
Nutritional Intervention Research Unit, Medical Research Council, PO Box 19070, Tygerberg 7505, South Africa
*
*Corresponding author: Email [email protected]
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Abstract

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Objective:

To evaluate the long-term effect on micronutrient status of a β-carotene-, iron- and iodine-fortified biscuit given to primary school children as school feeding.

Design:

Children receiving the fortified biscuit were followed in a longitudinal study for 2.5 years (n=108); in addition, cross-sectional data from three subsequent surveys conducted in the same school are reported.

Setting:

A rural community in KwaZulu-Natal, South Africa.

Subjects:

Children aged 6–11 years attending the primary school where the biscuit was distributed.

Results:

There was a significant improvement in serum retinol, serum ferritin, haemoglobin, transferrin saturation and urinary iodine during the first 12 months of the biscuit intervention. However, when the school reopened after the summer holidays, all variables, except urinary iodine, returned to pre-intervention levels. Serum retinol increased again during the next 9 months, but was significantly lower in a subsequent cross-sectional survey carried out directly after the summer holidays; this pattern was repeated in two further cross-sectional surveys. Haemoglobin gradually deteriorated at each subsequent assessment, as did serum ferritin (apart from a slight increase at the 42-month assessment at the end of the school year).

Conclusions:

This study has shown that fortification of a biscuit with β-carotene at a level of 50% of the Recommended Dietary Allowance (RDA) was enough to maintain serum retinol concentrations from day to day, but not enough to sustain levels during the long school holiday break. Other long-term solutions, such as local food production programmes combined with nutrition education, should also be examined. The choice of the iron compound used as fortificant in the biscuit needs further investigation.

Type
Research Article
Copyright
Copyright © CABI Publishing 2001

References

1Ramalingaswami, V. Challenges and opportunities – one vitamin, two minerals. World Health Forum 1992; 13: 222–31.Google ScholarPubMed
2Van Stuijvenberg, ME, Kvalsvig, JD, Faber, M, Kruger, M, Kenoyer, DG, Benadé, AJS. Effect of iron-, iodine-, and β-carotene-fortified biscuits on the micronutrient status of primary school children: a randomized controlled trial. Am. J. Clin. Nutr. 1999; 69: 497503. [erratum in Am. J. Clin. Nutr. 1999; 69: 1294].CrossRefGoogle ScholarPubMed
3National Research Council. Recommended Dietary Allowances, 10th ed. Washington, DC: National Academy Press, 1989.Google Scholar
4Catignani, GL, Bieri, JG. Simultaneous determination of retinol and α-tocopherol in serum or plasma by liquid chromatography. Clin. Chem. 1983; 29: 708–12.CrossRefGoogle ScholarPubMed
5Dunn, JT, Crutchfield, HE, Gutekunst, R, Dunn, AD. Methods for Measuring Iodine in Urine. The Hague: International Council for Control of Iodine Deficiency Disorders, 1993; 160.Google ScholarPubMed
6Tichelaar, HY, Smuts, CM, Kvalsvig, JD, Van Stuijvenberg, ME, Laubscher, R, Faber, M, Benadé, AJS. Randomised study of cognitive effects of ω3 fatty acid supplementation in undernourished rural school children. S. Afr. J. Clin. Nutr. 2000; 13: 100 [abstract].Google Scholar
7World Health Organization (WHO). Indicators for Assessing Vitamin A Deficiency and Their Application in Monitoring and Evaluating Intervention Programmes. Geneva: World Health Organization, 1996.Google Scholar
8WHO/UNICEF/ICCIDD. Indicators for Assessing Iodine Deficiency Disorders and Their Control Through Salt Iodization. Geneva: World Health Organization, 1994.Google Scholar
9Faber, M, Smuts, CM, Benadé, AJS. Dietary intake of primary school children in relation to food production in a rural area in KwaZulu-Natal, South Africa. Int. J. Food Sci. Nutr. 1999; 50: 5764.CrossRefGoogle Scholar
10Thatcher, AJ, Lee, CM, Erdman, JW. Tissue stores of β-carotene are not conserved for later use as a source of vitamin A during compromised vitamin A status in Mongolian gerbils. J. Nutr. 1998; 128: 1179–85.CrossRefGoogle Scholar
11Siegenberg, D, Baynes, RD, Bothwell, TH, Macfarlane, BJ, Lamparelli, RD, Car, NG, MacPhail, P, Schmidt, U, Tal, A, Mayat, F. Ascorbic acid prevents the dose-dependent inhibitory effects of polyphenols and phytates on nonheme-iron absorption. Am. J. Clin. Nutr. 1991; 53: 537–41.CrossRefGoogle ScholarPubMed
12Derman, D, Sayer, M, Lynch, SR, Charlton, RW, Bothwell, TH. Iron absorption from a cereal-based meal containing cane sugar fortified with ascorbic acid. Br. J. Nutr. 1977; 38: 261–9.CrossRefGoogle ScholarPubMed
13Pineda, O, Ashmead, HD, Perez, JM, Lemus, CP. Effectiveness of iron amino acid chelate on the treatment of iron deficiency anemia in adolescents. J. Appl. Nutr. 1994; 46: 213.Google Scholar
14Name, JJ. Food fortification with amino acid chelated minerals. Seminar on Food Fortification for Better LivingCairo, Egypt16 September 1995.Google Scholar
15Iost, C, Name, JJ, Jeppsen, RB, Ashmead, HD. Repleting hemoglobin in iron deficiency anemia in young children through liquid milk fortification with bioavailable iron amino acid chelate. J. Am. Coll. Nutr. 1998; 17: 187–94.CrossRefGoogle ScholarPubMed
16Albion Laboratories, Inc. Ferrochel Technical Monograph. UT, USA: Albion Laboratories, Inc., 1995; 16.Google Scholar
17Gordeuk, V, Mukiibi, J, Hasstedt, SJ, et al. Iron overload in Africa. Interaction between a gene and dietary iron content. N. Engl. J. Med. 1992; 326: 95100.CrossRefGoogle ScholarPubMed
18Witte, DL. Can serum ferritin be effectively interpreted in the presence of the acute-phase response? Clin. Chem. 1991; 37: 484–5.CrossRefGoogle ScholarPubMed
19Hulthén, L, Lindstedt, G, Lundberg, P-A, Hallberg, L. Effect of a mild infection on serum ferritin concentration – clinical and epidemiological implications. Eur. J. Clin. Nutr. 1998; 52: 376–9.CrossRefGoogle ScholarPubMed
20Jooste, PL, Weight, MJ, Lombard, CJ. Short-term effectiveness of mandatory iodization of table salt, at an elevated iodine concentration, on the iodine and goiter status of schoolchildren with endemic goiter. Am. J. Clin. Nutr. 2000; 71: 7580.CrossRefGoogle ScholarPubMed