AJCN Tufts Nutrition Symposium, Boston & Online Sept 2009
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
QUICK SEARCH:   [advanced]


     

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Purchase Article
Right arrow View Shopping Cart
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Rahman, M. M
Right arrow Articles by Alvarez, J. O
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Rahman, M. M
Right arrow Articles by Alvarez, J. O
Agricola
Right arrow Articles by Rahman, M. M
Right arrow Articles by Alvarez, J. O
American Journal of Clinical Nutrition, Vol. 75, No. 1, 92-98, January 2002
© 2002 American Society for Clinical Nutrition

Original Research Communication

Synergistic effect of zinc and vitamin A on the biochemical indexes of vitamin A nutrition in children1,2,3

Mohammad M Rahman, Mohammad A Wahed, George J Fuchs, Abdullah H Baqui and Jose O Alvarez

1 From the International Centre for Diarrhoeal Disease Research, Dhaka, Bangladesh; the Department of Epidemiology & International Health, the School of Public Health, the University of Alabama at Birmingham; and the Division of Infectious Diseases and Geographic Medicine, Stanford University School of Medicine, Stanford, CA.

2 Supported by the Thrasher Research Fund.

3 Address reprint requests to MM Rahman, Data Management and Statistics, Public Health Department, County of Santa Clara, 3003 Moorpark Avenue, San Jose, CA 95128. E-mail: mujib_99{at}yahoo.com.


   ABSTRACT
TOP
 ABSTRACT
INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Background: Zinc deficiency limits the bioavailability of vitamin A. Because zinc and vitamin A deficiency often coexist in malnourished children, simultaneous zinc and vitamin A supplementation may improve the vitamin A deficiency in these children.

Objective: A randomized, double-blind, placebo-controlled intervention trial was conducted to evaluate whether combining zinc and vitamin A supplementation would improve the biochemical indexes of vitamin A nutriture.

Design: Children aged 12–35 mo were randomly assigned to 1 of 4 intervention groups: 20 mg Zn/d for 14 d (Z group), 60000 retinol equivalents (200000 IU) vitamin A on day 14 (A group), zinc plus vitamin A (ZA group), or placebo syrup and placebo capsule (placebo group). Venous blood was drawn at enrollment and on day 21.

Results: Mean serum retinol concentrations were not significantly different between the A and ZA groups. Among vitamin A–deficient children, the proportion of children who remained vitamin A deficient (serum retinol <0.7 µmol/L) after supplementation was 40.6% in the Z group, 37.5% in the A group, and 47.0% in the placebo group; only 13.3% in the ZA group remained vitamin A deficient (P < 0.05 compared with the placebo group). The proportion of children whose retinol binding protein concentrations remained low was significantly lower in the ZA group than in the other groups (P < 0.05).

Conclusion: Combined zinc and vitamin A supplementation improves vitamin A nutriture in vitamin A–deficient children.

Key Words: Zinc • vitamin A • malnutrition • supplementation • retinol binding protein • retinol • children


   INTRODUCTION
TOP
 ABSTRACT
 INTRODUCTION
SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
The results of several experimental and clinical studies suggest an interaction between zinc and vitamin A (1–3). Zinc deficiency is accompanied by a reduction in circulating retinol concentrations in animals (4–10), and vitamin A supplementation alone fails to revert this vitamin A deficiency. After the animals are given either zinc supplements or zinc-containing diets, however, their serum retinol concentrations improve, suggesting that the low serum retinol concentrations are related to zinc deficiency (4,5,7,10). The association of zinc deficiency and vitamin A metabolism is further supported by the simultaneous reduction in retinol and retinol binding protein (RBP) in zinc-deficient rats (11), which suggests that the low plasma retinol concentrations in zinc deficiency might be caused by an impaired ability of the deficient animals to mobilize hepatic retinol. Another study (12) showed that zinc deficiency reduces hepatic cellular RBP (cRBP), which is essential for the intracellular transport of vitamin A in addition to its well-established role in intercellular transport.

Data on the interaction between zinc and vitamin A in humans are more limited and the results of such studies are inconclusive. Most studies of the interaction have been conducted in individuals with severe disease conditions, such as cystic fibrosis (13) and cirrhosis of the liver (14–18). Some studies showed an association between low zinc status and reduced retinol concentrations (19–21) and others did not (22–24). Studies in preterm infants (25) and in children with severe protein-energy malnutrition (26) showed improvement in serum RBP and retinol with zinc supplementation. In contrast, a population-based study in Thailand failed to show an effect of zinc supplementation on retinol or RBP concentrations in children (27).

In developing countries where protein-energy malnutrition is highly prevalent, children usually have multiple micronutrient deficiencies, particularly of zinc (28,29) and vitamin A (30). Reports from Bangladesh showed that >60% of children remain vitamin A deficient despite supplementation with large doses of vitamin A (31–33). Simultaneous zinc and vitamin A deficiency may be one of the explanations for the failure of vitamin A supplementation in these children. In this report, we study the effect of simultaneous zinc and vitamin A supplementation on vitamin A and RBP status in deficient children.


   SUBJECTS AND METHODS
TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
RESULTS
 DISCUSSION
 REFERENCES
 
Study population and sample
This study was conducted in urban slums in the older part of Dhaka City, the capital of Bangladesh. These slums were clusters of households with very high housing density and overall poor facilities (lacking an adequate water source, garbage removal, paved streets, street lighting, and gas supply). Most of the households (>90%) were constructed of poor, nondurable materials, and 82% had only one small room. One-third of the households had access to supplies of cooking gas, but these were usually shared. About two-thirds of the households had electricity and almost all households had access to safe drinking water through either pipes or tube wells. Most of the latrines (92%) were shared among multiple households and were often unhygienic (34). The infant mortality rate in the slums was {approx}138 per 1000 live births (35).

Children aged 12–35 mo of either sex who had not received any vitamin A supplementation within the past 4 mo were included in the study. However, children with severe malnutrition (weight-for-age <60% of the National Center for Health Statistics median), with signs or symptoms of vitamin A or zinc deficiency, or with any systemic illness such as diarrhea, respiratory infection, fever, or any other illness that warranted medical intervention at the time of enrollment were excluded. Informed consent was obtained from the parents for their children to participate in the study. The study was approved by the Ethical Review Committee of the International Centre for Diarrhoeal Disease Research, Bangladesh, and the Committee of Human Research, The University of Alabama at Birmingham.

Study design, randomization, and supplementation
This was a randomized, double-blind, placebo-controlled intervention trial. Children were randomly assigned to receive either zinc (Z group), vitamin A (A group), zinc plus vitamin A (ZA group), or placebo. The Z group received 5 mL (1 tsp) zinc syrup containing 20 mg elemental Zn/d for 14 d and a placebo capsule on day 14. The A group received 5 mL placebo syrup/d for 14 d and a 60000–retinol equivalents (RE) (200000 IU; 60-mg) vitamin A capsule on day 14. The ZA group received 5 mL (1 tsp) zinc syrup containing 20 mg elemental Zn/d for 14 d and a 60000-RE vitamin A capsule on day 14. The placebo group received 5 mL placebo syrup/d for 14 d and a placebo capsule on day 14.

A local pharmaceutical company (ACME Laboratories Ltd, Dhaka, Bangladesh) prepared the study syrups (zinc and placebo), which were supplied in identical 50-mL bottles. Each 50 mL placebo syrup contained 25 g sucrose, 5 g sorbitol, 50 mg methyl hydroxy benzoate, 15 mg propyl hydroxy benzoate, 5 mg lemon yellow color, 0.1 mL orange flavor, and 50 mL water. The zinc syrup contained all of the above plus 555.77 mg Zn as zinc sulfate (equivalent to 200 mg elemental Zn).

F Hoffmann-La Roche Ltd (Basel, Switzerland) manufactured and supplied the vitamin A and placebo capsules. The vitamin A capsules contained 60 mg (60000 RE) vitamin A as retinyl palmitate and 26.8 mg {alpha}-tocopherol equivalents ({alpha}-TE), or 40 IU, vitamin E (as all-rac-{alpha}-tocopherol), with soybean oil as an excipient. The placebo capsule contained 26.8 mg {alpha}-TE (as all-rac-{alpha}-tocopherol), with soybean oil as an excipient. The vitamin A and placebo capsules looked identical.

The children were randomly assigned by a person not involved in the study who used permuted blocks of random numbers. Sets of 2 bottles and 1 capsule for each child were serially numbered according to the randomization list and corresponding to the study serial numbers.

Sample size
A total of 800 children were randomly assigned; blood samples were collected from the first 411 children enrolled in the study after informed consent was obtained. This sample size was adequate to see an effect of combined zinc and vitamin A on the biochemical indexes of vitamin A status. The larger sample (n = 800) was needed to evaluate the effect of zinc and vitamin A supplementation on morbidity and is reported elsewhere (36). centeracteristics of the 411 children from whom blood samples were collected were similar to those of the remaining children.

Supplementation procedure
At enrollment, a health assistant fed the child 5 mL (1 tsp) syrup from the numbered bottle that corresponded to the randomization list and showed the child' mother how to administer the medicines at home. The mother was given one bottle containing 50 mL (10 tsp) syrup and was instructed to feed her child one spoonful of syrup each morning after breakfast. Also, the mother was instructed to save the bottle after the syrup was finished and to request a replacement if the bottle was broken or lost. After 7 d, the health assistant visited the child at home and calculated the amount of syrup given by subtracting the amount left over from 50 mL. Each mother was asked whether she had encountered any problems when feeding the syrup (eg, whether the child liked the syrup or vomited) and was then given another 50-mL bottle of syrup. On day 14, the health assistant again visited the child at home and measured the amount of intake and recorded her finding. Mothers were asked about any problems encountered while feeding the syrup. Then the health assistant fed the child a vitamin A or placebo capsule.

Collection of blood samples
Venous blood (3 mL) was obtained at enrollment and again on day 21 and after 3 mo. For blood drawing, the children were brought to the International Centre for Diarrhoeal Disease Research, Bangladesh, hospital. The blood samples were kept for 0.5 h to allow the blood to clot and were then transferred to the nutritional biochemistry laboratory located in the same building. In the laboratory, the serum was separated and stored at -70°C. The serum samples were later analyzed for retinol, RBP, C-reactive protein, and zinc.

Biochemical analysis
Serum retinol was measured by HPLC (Millipore Corp, Bedford, MA) (37). RBP was measured by radioimmunodiffusion with a commercially available kit from Boehring Diagnostics (La Jolla, CA) (38). C-reactive protein was measured by the immune turbidimetry method (38). Zinc was measured by atomic absorption spectrophotometry (Shimadzu AA 65015; Shimadzu, Nakagyoku, Japan) (39).

Anthropometric measurement
Weight was measured by using a balance with a precision of 10 g (Seca, Hamburg, Germany). Length was measured with a locally constructed length board with a precision of 0.1 cm.

Data analysis
Data were entered into a personal computer with use of SPSS for WINDOWS (version 8.0; SPSS Inc, Chicago). Anthropometric calculations (weight-for-age, weight-for-height, and height-for-age z scores) were made with the National Center for Health Statistics package (version 3.0; Centers for Disease Control and Prevention, Atlanta). Data were cleaned by visual and logical checks and were analyzed by using the SPSS program. Initially, descriptive statistics were analyzed. The proportion of children in each group who were vitamin A deficient after supplementation was compared by using the chi-square test. An analysis of covariance with the day 1 value as the covariate was done on postsupplementation changes in serum zinc, retinol, and RBP concentrations. Bonferroni corrections were done to adjust for multiple comparisons. Statistical significance was accepted at a probability level of 0.05.


   RESULTS
TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
DISCUSSION
 REFERENCES
 
Of the 411 children supplemented, 103 were in the Z group, 104 were in the A group, 103 were in the ZA group, and 101 were in the placebo group. The number of children available for the second blood drawing on day 21 was 84, 85, 86, and 84 from the 4 groups, respectively (total n = 339). Of the 72 children who dropped out, 40 were excluded from the study because they had received an additional vitamin A capsule through the national Expanded Program on Immunization clinic; parents of the other 32 children who dropped out withdrew their consent for blood drawing. Baseline centeracteristics of these 72 children did not differ significantly from those of the 339 children who completed the study. The baseline centeracteristics of the children in the 4 groups were also not significantly different (Table 1Go). Forty-four percent of the children were <2 y of age. All children received breast milk at least for some time, and 70% of them were still receiving breast milk at the time of enrollment. Most of children were underweight (weight for age < -2.0 z scores) or stunted (height-for-age < -2.0 z scores). Ninety-two percent of the children had received a vitamin A capsule before their enrollment in the study. The median (range) time gap between enrollment and prior vitamin A supplementation was 5 (4–12) mo; in most instances it was between 4 and 6 mo. Ninety percent of the mothers reported that their children took the syrup without any problem, 6% of the mothers forced their children to feed because they usually do not want to take any type of medicine, and 4% of the children vomited once or twice during the 14 d.


View this table:
[in this window]
[in a new window]
  		TABLE 1 . Baseline characteristics of the study children1
 
Baseline and postsupplementation serum zinc concentrations are shown in Table 2Go. Compared with the baseline values, serum zinc concentrations increased only in the Z and ZA groups, suggesting that the zinc supplementation was effective. The postsupplementation serum zinc concentration in the Z group was significantly higher than that in any other group (data not shown).


View this table:
[in this window]
[in a new window]
  		TABLE 2 . Baseline (day 1) serum zinc concentrations and changes in concentrations after supplementation (day 21 – day 1)1
 
The mean postsupplementation changes in serum retinol were not significantly different among the 4 groups (Table 3Go). However, there were trends in the A and ZA groups (P = 0.05 and 0.12, respectively). The mean changes in serum RBP were also not significantly different among the 4 groups (Table 3Go).


View this table:
[in this window]
[in a new window]
  		TABLE 3 . Baseline (day 1) serum retinol and serum retinol binding protein (RBP) concentrations and changes in concentrations after supplementation (day 21 - day 1)1
 
The proportion of children with low serum retinol concentrations (serum retinol < 0.7 µmol/L) after supplementation was significantly lower in the ZA and A groups than in the placebo group (Figure 1Go). The proportion of children with low RBP concentrations (<17.0 mg/L) was significantly lower in the ZA group than in the other 3 groups (Figure 1Go), indicating an improvement in RBP status with combined zinc and vitamin A supplementation.



View larger version (15K):
[in this window]
[in a new window]
  		FIGURE 1. . Improvements in vitamin A status with supplementation. Shown is the percentage of children with low serum retinol (<0.7 µmol/L) and low retinol binding protein (RBP; <17.0 mg/L) concentrations before ({square}) and after ({blacksquare}) supplementation. Z group, received 20 mg Zn/d for 14 d; A group, received 60000 retinol equivalents (200000 IU) vitamin A on day 14; ZA group, received both zinc and vitamin A. *,**Significantly different from placebo group (chi-square test with Bonferroni' correction): *P < 0.001, **P < 0.05. {dagger}Significantly different from all other groups, P < 0.01 (chi-square test with Bonferroni' correction).

 
The postsupplementation vitamin A status in a subgroup of children who were initially vitamin A deficient (serum retinol < 0.7 µmol/L) is shown in Figure 2Go. The proportion of vitamin A–deficient children after supplementation was significantly lower only in the ZA group. Although 37.5% of the children remained vitamin A deficient in the A group, only 13% remained vitamin A deficient in the ZA group.



View larger version (10K):
[in this window]
[in a new window]
  		FIGURE 2. . Percentage of initially vitamin A–deficient children ({square}; serum retinol concentration < 0.7 µmol/L) whose serum retinol concentrations returned to normal ({blacksquare}) after supplementation. Z group, received 20 mg Zn/d for 14 d; A group, received 60000 retinol equivalents (200000 IU) vitamin A on day 14; ZA group, received both zinc and vitamin A. *Significantly different from placebo group, P = 0.01, and significantly different from Z group, P = 0.04 (chi-square test with Bonferroni' correction).

 

   DISCUSSION
TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
REFERENCES
 
The results of the present study show that only combined zinc and vitamin A supplementation successfully reverted the deficiency in vitamin A–deficient children; supplementation with zinc or vitamin A alone did not. This finding indicates that there is a synergistic effect of zinc and vitamin A on vitamin A status. Although >90% of the children in the present study had received a vitamin A capsule as part of the National Vitamin A Week campaign 4–6 mo before enrollment, 38% of these children were still vitamin A deficient. After receiving another large dose of vitamin A during the study, a significant number of children in all groups except the ZA group remained vitamin A deficient. Thus, vitamin A status improved significantly in children who received both zinc and vitamin A, but not in those who received vitamin A alone.

This failure to improve vitamin A status in a significant number of children in the A group is consistent with our previous findings (31–33). In our earlier study, 61% of infants aged <6 mo remained vitamin A deficient despite receiving 3 doses of 15 mg (15000 RE, or 50000 IU) vitamin A at monthly intervals (32). We propose that these failures are related to a concomitant zinc deficiency in these vitamin A–deficient children.

Vitamin A binds to RBP within the cytoplasm of the hepatocyte, forming holo-RBP, which is secreted into the blood. Prealbumin, which is also synthesized in the liver, forms a trimolecular complex of retinol, RBP, and prealbumin circulating in the liver, apparently to prevent filtration and loss of vitamin A in the urine. Thus, zinc affects vitamin A status because it affects synthesis of the transport protein, which, in turn, transports retinol from the liver to the blood and other target tissues (40,41). Zinc also participates in the synthesis of cRBP, which is essential for the intracellular transport of retinol within liver hepatocytes. Hence, zinc is essential for both intra- and intercellular transport of vitamin A. In the present study, although the mean RBP concentrations on day 21 were not significantly different among groups, the proportion of children with low RBP was significantly lower in the ZA group than in the A group (Figure 1Go). This observation can likely be explained by the synergy between zinc and vitamin A, which resulted in the improved circulating retinol concentrations.

Other than its essential role in vitamin A transport, zinc aids in the absorption of vitamin A in the intestine (42,43). In adult male rats with experimentally induced zinc deficiency, retinol absorption is markedly reduced; in contrast, essential fatty acid deficiency exerts only a mild effect on the absorption of retinol (42). Compared with the essential fatty acids, dietary zinc has a more pronounced effect on phospholipids, which are necessary for the absorption of vitamin A (4243). Addition of essential fatty acids fails to counteract the adverse effect of zinc deficiency on vitamin A absorption (43). In zinc deficiency there is a defect in the biliary secretion of phosphoslipids into the gut lumen. It was postulated that, because of the lack of phospholipids, the enterocyte of zinc-deficient rats fails to form chylomicrons, the principal carriers of dietary lipids and lipid-soluble nutrients.

In contrast with our findings, Udomkesmalee et al (27) found no synergistic effect of zinc and vitamin A on the biochemical indexes of vitamin A nutriture in Thai children. The Thai study differed from ours in several ways: those children were much older (6–13 y) than the children in the present study; their total plasma protein and albumin concentrations were within normal ranges, suggesting better nutritional status; and they had normal results on relative-dose-response tests, indicating normal vitamin A stores. Hence, no improvement of serum retinol with simultaneous zinc and vitamin A supplementation was possible. In our study, serum retinol also did not increase in children with adequate vitamin A status. Only in children who were vitamin A deficient did serum retinol concentrations improve. Although circulating retinol and RBP did not improve in the Thai children, improved dark adaptation time was observed in the zinc group. Also, the proportion of abnormal conjunctival impression cytology results decreased in children who received both zinc and vitamin A (27). In another study (44), children who were supplemented with both zinc and vitamin A tended to show higher proliferative responsiveness of T lymphocytes to purified protein derivatives than did those treated with placebo (P = 0.08). All of these observations suggest the existence of an interaction between zinc and vitamin A in children.

In the present study, postsupplementation concentrations of RBP and retinol in the zinc-supplemented group were not significantly different from those in the placebo group. However, the change from baseline was significant in the zinc group, but not in the placebo group. Despite the increment in RBP, the increment in circulating retinol was not significant. The reason for this could be that the zinc status of our study children, although lower than that of the Thai children, was not very severely depleted ( ± SD serum zinc concentration: 11.2 ± 2.9 µmol/L). It is likely that the beneficial effect of zinc supplementation on serum retinol is observed only when zinc is limiting (ie, deficient to the extent that it may interfere with protein and enzyme synthesis). Above a certain threshold of serum zinc, vitamin A transport is not dependent on serum zinc concentrations; below that threshold, however, vitamin A release and transport from the liver are strongly influenced by serum zinc concentrations (45). An earlier Indian study that reported a significant improvement in RBP and retinol with short-term (5 d) zinc supplementation was conducted in severely malnourished children whose plasma zinc concentrations were very low (26). In a group of American preterm infants, those receiving intravenous zinc supplementation showed significant improvements in serum retinol concentrations (25). These findings suggest that zinc supplementation may be beneficial only in vitamin A–deficient subjects.

In this randomized controlled trial we carefully adjusted for confounding factors, including age, sex, initial nutritional status, and concentrations of C-reactive protein, serum zinc, and retinol. We observed that vitamin A alone failed to correct vitamin A deficiency in a large proportion of the children, whereas combined zinc and vitamin A supplementation effectively corrected the vitamin A deficiency, suggesting the existence of a synergistic effect of zinc and vitamin A. These findings support combined zinc and vitamin A supplementation in undernourished children, in children with suspected zinc deficiency, and, more generally, in children from very poor communities where both undernutrition and low zinc concentrations may be prevalent.


   ACKNOWLEDGMENTS
 
We sincerely thank Sten H Vermund, Charles Stephensen, Grace Marquis, Nalini Sathiakumar, and Karan Singh for reviewing the article and Grace Marquis for extensively editing the article.


   REFERENCES
TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 

  1. Smith JC Jr. The vitamin A-zinc connection: a review. Ann N Y Acad Sci 1980;355:62–75.[Medline]
  2. Solomons NW, Russell RM. The interaction of vitamin A and zinc: implications for human nutrition. Am J Clin Nutr 1980;33:2031–40.[Free Full Text]
  3. Christian P, West KP Jr. Interactions between zinc and vitamin A: an update. Am J Clin Nutr 1998;8(suppl):435S–41S.
  4. Stevenson JW, Earle IP. Studies on parakeratosis in swine. J Anim Sci 1956;15:1036–45.[Abstract/Free Full Text]
  5. Smith JC Jr, McDaniel EG, Fan FF, Halsted JA. Zinc: a trace element essential in vitamin A metabolism. Science 1973;181:954–5.[Abstract/Free Full Text]
  6. Smith JC Jr, Brown ED, McDaniel EG, Chan W. Alterations in vitamin A metabolism during zinc deficiency and food and growth restriction. J Nutr 1976;106:569–74.
  7. Brown ED, Chan W, Smith JC Jr. Vitamin A metabolism during the repletion of zinc deficient rats. J Nutr 1976;106:563–8.
  8. Carney SM, Underwood BA, Loerch JD. Effects of zinc and vitamin A deficient diets on the hepatic mobilization and urinary excretion of vitamin A in rats. J Nutr 1976;106:1773–81.
  9. Duncan JR, Hurley LS. An interaction between zinc and vitamin A in pregnant and fetal rats. J Nutr 1978;108:1431–8.
  10. Ette SI, Basu TK, Dickerson JW. Short-term effect of zinc sulphate on plasma and hepatic concentrations of vitamins A and E in normal weanling rats. Nutr Metab 1979;23:11–6.[Medline]
  11. Smith JE, Brown ED, Smith JC Jr. The effect of zinc deficiency on the metabolism of retinol-binding protein in the rat. J Lab Clin Med 1974;84:692–7.[Medline]
  12. Mobarhan S, Greenberg B, Mehta R, Friedman H, Barch D. Zinc deficiency reduces hepatic cellular retinol-binding protein in rats. Int J Vitam Nutr Res 1992;62:148–54.[Medline]
  13. Jacob RA, Sandstead HH, Solomons NW, Rieger C, Rothberg R. Zinc status and vitamin A transport in cystic fibrosis. Am J Clin Nutr 1978;31:638–44.[Abstract/Free Full Text]
  14. Patek AJ Jr, Haig C. The occurrence of abnormal dark adaptation and its relation to vitamin A metabolism in patients with cirrhosis of the liver. J Clin Invest 1939;18:609–16.
  15. Vallee BL, Hoch FL. Zinc in horse liver alcohol dehydrogenase. J Biol Chem 1957;225:185–95.[Free Full Text]
  16. Halsted JA, Hackley B, Rudzki C, Smith JC Jr. Plasma zinc concentration in liver diseases. Comparison with normal controls and certain other chronic diseases. Gastroenterology 1968;54:1098–105.[Medline]
  17. Russell RM, Morrison SA, Smith FR, Oaks EV, Carney EA. Vitamin-A reversal of abnormal dark adaptation in cirrhosis. Study of effects on the plasma retinol transport system. Ann Intern Med 1978;88:622–6.
  18. Morrison SA, Russell RM, Carney EA, Oaks EV. Zinc deficiency: a cause of abnormal dark adaptation in cirrhotics. Am J Clin Nutr 1978;31:276–81.[Abstract/Free Full Text]
  19. Kozlowski BW, Taylor ML, Baer MT, Blyler EM, Trahms C. Anticonvulsant medication use and circulating levels of total thyroxine, retinol binding protein, and vitamin A in children with delayed cognitive development. Am J Clin Nutr 1987;46:360–8.[Abstract/Free Full Text]
  20. Coutsoudis A, Coovadia HM, Broughton M, Salisbury RT, Elson I. Micronutrient utilisation during measles treated with vitamin A or placebo. Int J Vitam Nutr Res 1991;61:199–204.[Medline]
  21. Ahmed F, Barua S, Mohiduzzaman M, et al. Interactions between growth and nutrient status in school-age children of urban Bangladesh. Am J Clin Nutr 1993;58:334–8.[Abstract/Free Full Text]
  22. Chase HP, Hambidge KM, Barnett SE, Houts-Jacobs MJ, Lenz K, Gillespie J. Low vitamin A and zinc concentrations in Mexican-American migrant children with growth retardation. Am J Clin Nutr 1980;33:2346–9.[Abstract/Free Full Text]
  23. Hunt IF, Murphy NJ, Cleaver AE, et al. Zinc supplementation during pregnancy in low-income teenagers of Mexican descent: effects on selected blood constituents and on progress and outcome of pregnancy. Am J Clin Nutr 1985;42:815–28.[Abstract/Free Full Text]
  24. Dorea JG, De Araujo MO. Zinc and vitamin A in liver of foetuses and infants. Acta Paediatr Scand 1988;77:85–8.[Medline]
  25. Hustead VA, Greger JL, Gutcher GR. Zinc supplementation and plasma concentration of vitamin A in preterm infants. Am J Clin Nutr 1988;47:1017–21.[Abstract/Free Full Text]
  26. Shingwekar AG, Mohanram M, Reddy V. Effect of zinc supplementation on plasma levels of vitamin A and retinol-binding protein in malnourished children. Clin Chim Acta 1979;93:97–100.[Medline]
  27. Udomkesmalee E, Dhanamitta S, Sirisinha S, et al. Effect of vitamin A and zinc supplementation on the nutriture of children in Northeast Thailand. Am J Clin Nutr 1992;56:50–7.[Abstract/Free Full Text]
  28. Kumar S, Rao KS. Plasma and erythrocyte zinc levels in protein-calorie malnutrition. Nutr Metab 1973;15:364–71.[Medline]
  29. Kutumbale AS, Chaparwal BC, Mehta S, Vijayvargiya R, Mathur PS. Zinc levels in serum and erythrocytes in protein calorie malnutrition. Indian Pediatr 1976;13:837–40.[Medline]
  30. Cohen N, Jalil MA, Rahman H, et al. Landholding, wealth and risk of blinding malnutrition in rural Bangladeshi households. Soc Sci Med 1985;21:1269–72.
  31. Rahman MM, Mahalanabis D, Wahed MA, Islam MA, Habte D. Administration of 25,000 IU vitamin A doses at routine immunisation in young infants. Eur J Clin Nutr 1995;49:439–45.[Medline]
  32. Rahman MM, Mahalanabis D, Alvarez JO, et al. Acute respiratory infections prevent improvement of vitamin A status in young infants supplemented with vitamin A. J Nutr 1996;126:628–33.
  33. Mahalanabis D, Rahman MM, Wahed MA, Islam MA, Habte D. Vitamin A megadose during early infancy on serum retinol concentration and acute side effects and residual effect on 6 month follow-up. Nutr Res 1997;17:649–59.
  34. Arifeen SE, Mahbub AQM, eds. A survey of slums in Dhaka metropolitan area—1991. Dhaka, Bangladesh: International Centre for Diarrhoeal Disease Research, Bangladesh (in association with the Centre for Urban Studies, Dhaka University, Dhaka, Bangladesh), 1993. [ICDDR,B working paper no. 39 (urban MCH-FP working paper no. 11).]
  35. Thwin AA, Islam MA, Baqui AH, Reinke WA, Black RE. Health and demographic profile of the urban population of Bangladesh: an analysis of selected indicators. Dhaka, Bangladesh: MCH-FP Extension Project (Urban), Health and Population Extension Division, International Centre for Diarrhoeal Disease Research, Bangladesh, 1996.
  36. Rahman MM, Vermund SH, Wahed MA, Fuchs GJ, Baqui AH, Alvarez JO. Simultaneous zinc and vitamin A supplementation in Bangladeshi children: randomized double blind controlled trial. BMJ 2001;323:314–8.[Abstract/Free Full Text]
  37. Bieri JG, Tolliver TJ, Catignani GL. Simultaneous determination of alpha-tocopherol and retinol in plasma or red cells by high pressure liquid chromatography. Am J Clin Nutr 1979;32:2143–9.[Abstract/Free Full Text]
  38. Mancini G, Carbonara AD, Heremans JF. Immunochemical quantitation of antigens by single radial immunodiffusion. Immunochemistry 1965;2:235–54.[Medline]
  39. Smith JC Jr, Butrimovitz GP, Purdy WC. Direct measurement of zinc in plasma by atomic absorption spectroscopy. Clin Chem 1979;25: 1487–91.[Free Full Text]
  40. Mejia LA. Vitamin A-nutrient interrelationships. In: Bauernfeind JC, ed. Nutrition basics and applied science—a series of monographs. New York: Academic Press, 1986:89–100.
  41. Terhune MW, Sandstead HH. Decreased RNA polymerase activity in mammalian zinc deficiency. Science 1972;177:68–9.[Abstract/Free Full Text]
  42. Ahn J, Koo SI. Effects of zinc and essential fatty acid deficiencies on the lymphatic absorption of vitamin A and secretion of phospholipids. J Nutr Biochem 1995;6:595–603.
  43. Ahn J, Koo SI. Intraduodenal phosphatidycholine infusion restores the lymphatic absorption of vitamin A and oleic acid in zinc-deficient rats. J Nutr Biochem 1995;6:604–12.
  44. Kramer TR, Udomkesmalee E, Dhanamitta S, et al. Lymphocyte responsiveness of children supplemented with vitamin A and zinc. Am J Clin Nutr 1993;58:566–70.[Abstract/Free Full Text]
  45. Baly DL, Golub MS, Gershwin ME, Hurley LS. Studies of marginal zinc deprivation in rhesus monkeys. III. Effects on vitamin A metabolism. Am J Clin Nutr 1984;40:199–207.[Abstract/Free Full Text]
Received for publication July 10, 2000. Accepted for publication March 2, 2001.




This article has been cited by other articles:


Home page
 Postgrad. Med. J.Home page
A Shenkin
Micronutrients in health and disease.
Postgrad. Med. J., September 1, 2006; 82(971): 559 - 567.
[Abstract] [Full Text] [PDF]

Home page
 Am. J. Clin. Nutr.Home page
K. Alarcon, P. W Kolsteren, A. M Prada, A. M Chian, R. E Velarde, I. L Pecho, and T. F Hoeree
Effects of separate delivery of zinc or zinc and vitamin A on hemoglobin response, growth, and diarrhea in young Peruvian children receiving iron therapy for anemia
Am. J. Clinical Nutrition, November 1, 2004; 80(5): 1276 - 1282.
[Abstract] [Full Text] [PDF]

Home page
 Am. J. Clin. Nutr.Home page
M. M Rahman, F. Tofail, M. A Wahed, G. J Fuchs, A. H Baqui, and J. O Alvarez
Short-term supplementation with zinc and vitamin A has no significant effect on the growth of undernourished Bangladeshi children
Am. J. Clinical Nutrition, January 1, 2002; 75(1): 87 - 91.
[Abstract] [Full Text] [PDF]

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Purchase Article
Right arrow View Shopping Cart
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Rahman, M. M
Right arrow Articles by Alvarez, J. O
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Rahman, M. M
Right arrow Articles by Alvarez, J. O
Agricola
Right arrow Articles by Rahman, M. M
Right arrow Articles by Alvarez, J. O

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS