Micronutrients and Infection: Interactions and Implications with Enteric and Other Infections and Future Priorities

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1 S134 Micronutrients and Infection: Interactions and Implications with Enteric and Other Infections and Future Priorities Richard L. Guerrant, 1 Aldo A. M. Lima, 2 and Frances Davidson 3 1 Division of Geographic and International Medicine, University of Virginia School of Medicine, Charlottesville; 2 Clinical Research Unit, Federal University of Ceará, Fortaleza, Ceará, Brazil; 3 US Agency for International Development, Washington, DC Symposium presentations have focused on the elegant molecular science and the biologic mechanisms by which micronutrients play critical roles in cellular and humoral immune responses, cellular signaling and function, and even in the evolution of microbial virulence. The concluding session examined the practical issues of how best to evaluate the nutritionally atrisk host, especially in the areas of greatest need an analytical model of nutrient-immune interactions, implications of nutritional modulation of the immune response for disease, and the implications for international research and child health. This overview illustrated how malnutrition may be a major consequence of early childhood diarrhea and enteric infections, as enteric infections may critically impair intestinal absorptive function with potential longterm consequences for growth and development. The potentially huge, largely undefined DALY (disability-adjusted life years) impact of early childhood diarrheal illnesses demonstrates the importance of quantifying the long-term functional impact of largely preventable nutritional and infectious diseases, especially in children in developing areas. The complexity of the effects of key micronutrients (i.e., vitamins, trace minerals, essential amino acids, and polyunsaturated fatty acids) on host cellular and molecular immunomodulatory responses to infectious agents is matched only by their often overlooked importance in determining health, functionality, and disease. The development of new tools in molecular genetics now enables us to link the basic sciences of immunology and nutrient biochemistry to clinically important infectious diseases and field epidemiology and thus opens new opportunities to bring an understanding of molecular nutritional science to those in greatest need. Individual and national and international decisions to invest in measures to improve health are based on the availability and cost of effective interventions and on the value or health gained by the intervention. The health burden of diseases and injuries is increasingly quantified by the disability-adjusted life year (DALY) calculations that take into account both years of life lost and years lost to disability. The DALY burden of nutrition-related infectious diseases and their interactions, which are now beginning to be quantified, painfully demonstrate the magnitude of our unfinished agenda [1, 2]. Informed consent was obtained from parents and guardians of the children studied. This study was approved by human investigation committees at the Federal University of Ceará, Johns Hopkins University School of Medicine, and the University of Virginia. Grant support: NIH (AI and AI-26512). Reprints or correspondence: Dr. Richard L. Guerrant, Division of Geographic and International Medicine, University of Virginia School of Medicine, Box , Charlottesville, VA The Journal of Infectious Diseases 2000;182(Suppl 1):S by the Infectious Diseases Society of America. All rights reserved /2000/18203S-0020$02.00 Nutrition-infection interactions have potentially huge implications not just for traditionally defined overt recognized disease (e.g., diarrhea defined as liquid from one end of a long gastrointestinal canal) but also for subclinical problems (e.g., disrupted intestinal absorptive function from asymptomatic enteric infections or micronutrient deficiencies). Either of these overt or covert infectious or nutritional conditions may produce long-term additive or even synergistic effects on physical and cognitive function and thus on full health and productivity. These effects are illustrated by recent studies of intestinal helminths and by ourselves and others of long-term sequelae of early childhood diarrhea. Long-Term DALY Impact of Intestinal Helminths in School-Age Children An elegant series of placebo-controlled studies in Kenya and Jamaica revealed that school-age children treated with albendazole literally grew better and had improved physical activity, fitness, and school attendance plus improved cognitive function by several measures 9 weeks to 4 months later [3 13]. These studies enabled Bundy and Chan [14] to recalculate the DALY burden attributable to intestinal helminths and to effectively more than double their global DALYs from 18 to 39 million, a measure that more than doubles the cost-effectiveness calculations for interventions that avert these helminth DALYs and hence the huge importance for defining and applying effective interventions.

2 JID 2000;182 (Suppl 1) Micronutrients and Infection S135 Potential Long-Term Burden of Early Childhood Diarrhea Table 1. Summary of long-term functional and growth impairment (at age 6 9 years) seen with early childhood diarrhea and parasitic infections. Early childhood risk at age 0 2 years Functional impairment at age 6 9 years Diarrheal illnesses Impaired growth.036 a Diarrheal illnesses Impaired fitness.034 b Diarrheal illnesses Cognitive impairment McCarthy Scales Draw-A-Design.012 c Backward WISC-III Digit Span.049 WISC-III Scaled Coding Test.031 Cryptosporidium infection Impaired fitness.017 Helminthic infection Impaired growth.004 d NOTE. Data are from [15]. a Independent of helminths, prior nutritional status, maternal education, or household income. b Independent of nutritional status, hematocrit, helminths, respiratoryillnesses, Giardia infection, maternal education, or household income. c Independent of hematocrit, early childhood parasites, maternal education, or household income. d Early childhood helminthic infections were also associated with impaired growth, independent of diarrhea, prior nutritional status, maternal education, or household income. Although a single or brief treatment is less definitively available for childhood diarrhea than it is for intestinal helminths, long-term cohort studies may provide clues about potential lasting consequences of repeated diarrheal illnesses in early childhood. In a prospective cohort of children whom we have followed at least twice weekly from birth as a part of a National Institutes of Health (international collaboration in infectious diseases research project) over the last 9 years, some children are now reaching ages 6 9 years and offer unique opportunities for review of the long-term impact of early childhood illnesses. Table 1 summarizes findings from our initial pilot studies in these cohort children, following their growth (by quarterly anthropometric measurements), their physical fitness and activity (evaluated by the Harvard step test and Kaulins and Willis actometers, respectively), and their cognitive function (by use of the McCarthy Scales Draw-A-Design and Wechsler Intelligence Scale for Children [WISC-III Scaled Coding and Digit Span tests]; Psychological Corp., San Antonio, TX]) [15]. As noted, diarrheal illness burdens in the first 2 years of life (early childhood diarrhea) appear to have profound and lasting effects on impaired growth, impaired physical fitness, and impaired cognitive function at age 6 9 years [15]. Furthermore, these effects on fitness are independent of nutritional status, helminths, respiratory illnesses, hematocrit, activity scores, maternal education, and household income, and on cognitive function (by McCarthy Draw-A-Design test) are independent of hematocrit and early childhood parasitic infections [15]. We have now confirmed and substantially extended our earlier findings in more children and with other tests that show substantial correlations of early childhood diarrhea with prolonged impairments of growth and cognitive function [16]. In fact, these effects are observed even under the best of circumstances: We recently documented the considerable improvements in this community in reduced diarrhea rates and mortality and in improved nutritional status, improvements not seen in nearby communities where surveillance did not take place (Moore SR, Lima AM, Guerrant RL, unpublished data). The magnitude and potential importance of the effect on fitness is illustrated by the 4% 8% reductions in Harvard step test scores seen with the average-to-maximal diarrheal burdens in children in northeast Brazil [15]. These results were roughly equivalent to those in Zimbabwe sugar cane cutters, who had a 4.3% improvement in Harvard step test scores when treated for schistosomiasis and experienced a corresponding 16.6% increase in work productivity [17]. Early childhood cryptosporidial infections per se are associated with significantly reduced physical fitness at age 6 9 years [15]. Finally, early childhood helminthic infections are also associated with prolonged impairment of growth. These findings extend the findings of previous studies to a much longer impact from much earlier helminthic infections [15, 16]. Thus, the potential long-term impairment in fitness and cognitive function, in addition to growth retardation from early childhood illnesses and diarrheal and other enteric and parasitic infections, may have profound human, economic, and total societal costs that long-term studies have only begun to quantify. Clearly, such documentation and appreciation of long-term effects of early childhood illnesses and infections (likely augmented by micronutrient deficiencies as noted below) will determine the huge potential cost saved (in dollars per DALY averted) by interventions that ameliorate these outcomes. Malnutrition as a Major Manifestation of Enteric Infections (with or without Diarrhea): The Vicious Cycles with Enteric Infections and Micronutrient Deficiencies The relationships between early childhood diarrheal illnesses, specific enteric infections, and intestinal helminthic infections and potentially long-term effects on growth, physical fitness, and cognitive impairment are summarized in figure 1 [15, 18, 19]. In addition to the short- and long-term impact of diarrheal illnesses (especially of persistent diarrhea) on impaired growth [20 23], specific enteric infections are increasingly recognized as predisposing to significant growth impairment. Several studies of cryptosporidiosis, enteroaggregative Escherichia coli infections, and Giardia infections (even without overt diarrhea) show they have substantial effects on growth [18, 19, 23, 24]. Thus, malnutrition might appropriately be considered largely as an emerging infectious disease. In addition, many true infectious diseases are largely the consequences of the effects of nutritional or micronutrient diseases [2]. Furthermore, the effects of malnutrition on both the P

3 S136 Guerrant et al. JID 2000;182 (Suppl 1) Figure 1. The vicious cycle of effects of enteric infections with or without overt diarrhea or persistent diarrhea (PD) on nutritional status and on physical and cognitive development [15, 18, 19]. incidence and duration of diarrheal illnesses have been well documented in studies in Brazil and elsewhere [20, 21, 25 28]. Although catch up growth may occur in settings in which repeated diarrheal and other illnesses do not occur with frequency [29], repeated diarrheal illnesses during the early development years substantially impair or ablate this critical catch-up growth [21, 22, 30]. The involvement of other childhood infections (e.g., measles, pneumonia, and malaria) plus the nutrient demand by enteric parasites through catabolism, malabsorption, and increased losses further compound this vicious cycle [31]. Micronutrient Roles The critical role of micronutrient malabsorption in the effects of diarrhea and enteric infections on growth and physical and cognitive development and the potential for micronutrients (including zinc, vitamin A, and perhaps others) in the effects of malnutrition on diarrheal illnesses largely remains to be fully defined. Several studies suggest that zinc and vitamin A may have key roles in determining the duration, frequency, and severity of diarrheal illnesses. Placebo-controlled supplementation trials of specific micronutrients have evaluated their importance in diarrheal diseases in developing areas. Zinc supplementation may reduce diarrhea duration, barrier disruption, and growth faltering in children with diarrhea [32 37]. Similarly, vitamin A deficiency is associated with impaired intestinal barrier function per se [38], and vitamin A may improve outcomes in children with acute or persistent diarrheal illnesses [37, 39 41]. The remarkable potential of micronutrient deficiency to not only impair host physiology and immunology but also to lead to permanently enhanced microbial virulence was shown in an elegant series of studies by Beck and colleagues [42 44]. They demonstrated enhanced coxsackievirus B-3 or A-19 virulence in selenium deficiency in Keshan s disease in China and in epidemic optic and peripheral neuropathy in Cuba, respectively [42 44]. This ability for host micronutrient deficiency to induce permanent mutations to greatly enhanced virulence in the microbial pathogen adds yet another dimension to the disturbing ways that micronutrient deficiencies and infectious diseases of poverty pose new and potentially widespread threats. Add to this the likely, but again poorly quantified, impact of malabsorption of key antimicrobial drugs (e.g., antiretrovirals and antituberculous drugs) on the emergence of drug resistance in impoverished areas of greatest need, and the potentially global magnitude of these threats can begin to be appreciated. Despite their complexity, these vicious cycles of infection and malnutrition must be critically reexamined and dissected via the new techniques offered by molecular evolution and physiology, so that they can be interrupted to the greatest extent possible. We need to understand the interactions of specific micronutrient deficiencies with diarrheal and other infectious diseases and specific infections with or without overt symptoms in order to evaluate their short- and long-term functional consequences. Only with a concerted effort aimed at correcting host deficiencies as well as acquisition of infections from the environment can these increasingly recognized vicious cycles be effectively interrupted. The economic and biologic imperatives to address these micronutrient and infectious diseases of poverty only await the will to direct appropriate resources to their recognition and solution. Sound basic and field data thus become critical to defining these global threats in order to direct our societal priorities. Commitments for Effective Changes An indication of the potential huge relevance of micronutrient deficiencies to development is that the US Agency for International Development (USAID) has identified micronutrient deficiencies as a priority. The USAID is firmly committed to the implementation of programs based on the best scientific evidence. We have identified micronutrient deficiencies as one way to make some inroads into the large and overwhelming problem of malnutrition in low-income countries and its role in disease and mortality particularly in women and children. As a development agency we are concerned with the translation of scientific findings into programs and policies that will benefit vulnerable populations. To this end we need assistance from the participants at this important workshop and appreciate the opportunity to participate here and thank the conveners. There is a clear need for good quality research in order to improve policies and programs in all sectors. It is sometimes thought that lack of funding is the main constraint to truly useful research. However, the problem is more complex. Not all researchers aim to have an impact on policy and program decisions or select research questions and conduct studies with

4 JID 2000;182 (Suppl 1) Micronutrients and Infection S137 program and policy relevance. Even when the research is relevant, it is often ignored by decision-makers. Indeed, many research findings do not reach the population they are intended to benefit. Research informs policies and programs most effectively when there is a genuine collaboration that links researchers, policy makers, and those most affected by the issues under consideration. This is a departure from the notion that the proper audience for most research is other researchers. If the resulting research products are to be useful to health system managers and policy makers, their information needs must be factored into the research from the start. Research that clearly defines the dimensions of a problem and identifies its underlying causes can be a catalyst for change, even if the researchers themselves do not recommend a specific course of action. The credibility of the research process also affects the chances for application of research findings. This includes the perceived accuracy and objectivity and appropriateness of the research design and methods. Integral to this is the need for well-developed research hypotheses and clearly defined study cohorts. An important screen for this in lowincome countries is the extent to which the research design includes the collaboration of in-country investigators, in order to build indigenous research capability and ensure the dissemination of research results. Barriers to the practical application of research results need to be identified at the outset of the research. Review of past experience would aid researchers to ensure that their programs do not duplicate previous failures. One solution might be the formal establishment of an international collaborative effort to promote evidence-based scientific investigation for public policy application. Clearly, the identification of barriers is of critical concern to international agencies concerned with improving the health and well being of vulnerable populations. When this is done collaboratively, better decisions can be made about the allocation of funds and evaluation of the relevance of study findings. In summary, the complex interactions between micronutrient deficiencies and infectious diseases have potentially huge longterm developmental and societal impacts. These effects range from individual long-term functional impairment to effects on microbial virulence or (through drug malabsorption) antimicrobial resistance. Only with a joining of new molecular understanding with careful field epidemiology can we appreciate the magnitude of these challenges or the optimal approach to their solutions. Priority Directions Priorities that we have identified to maximize the effects of research on public policy are as follows: 1. Link basic bench molecular mechanistic studies with field work in endemic areas of greatest relevance. 2. Define the role of specific enteric and other infections, with or without overt symptoms (e.g., diarrhea) in contributing to micronutrient deficiencies. 3. Determine the mechanisms of the effects of micronutrient deficiencies on increased susceptibility to infection and when and how they can be reversed. 4. Identify the effects of age on susceptibility to effects of micronutrient deficiencies and on their reversibility by replacement therapy. 5. Quantify, when possible, both short- and potential longterm functional and developmental consequences in humans of micronutrient deficiencies and of micronutrient deficiency infection interactions. 6. Define potential effects of micronutrient deficiencies on microbial genetics that lead to (potentially irreversible) enhanced virulence or resistance. References 1. Murray CJL, Lopez AD. The global burden of disease: a comprehensive assessment of mortality and disability from diseases, injuries, and risk factors in 1900 and projected to Cambridge, MA: Harvard University Press, Guerrant RL, Blackwood BL. Threats to global health and survival: the growing crises of tropical infectious diseases our unfinished agenda [Review]. Clin Infect Dis 1999;28: Adams EJ, Stephenson LS, Latham MC, Kinoti SN. Physical activity and growth of Kenyan school children with hookworm, Trichuris trichiura and Ascaris lumbricoides infections are improved after treatment with albendazole. J Nutr 1994;124: Nokes C, Bundy DA. Compliance and absenteeism in school children: implications for helminth control. Trans R Soc Trop Med Hyg 1993;87: Nokes C, Bundy DA. Trichuris trichiura infection and mental development in children [letter; comment]. Lancet 1992;339: Nokes C, Grantham-McGregor SM, Sawyer AW, Cooper ES, Bundy DA. Parasitic helminth infection and cognitive function in school children. Proc R Soc Lond B Biol Sci 1992;247: Nokes C, Grantham-McGregor SM, Sawyer AW, Cooper ES, Robinson BA, Bundy DA. Moderate to heavy infections of Trichuris trichiura affect cognitive function in Jamaican school children. Parasitology 1992;104: Stephenson LS. Helminth parasites, a major factor in malnutrition. World Health Forum 1994;15: Stephenson LS, Latham MC, Adams EJ, Kinoti SN, Pertet A. Physical fitness, growth and appetite of Kenyan school boys with hookworm, Trichuris trichiura and Ascaris lumbricoides infections are improved four months after a single dose of albendazole. J Nutr 1993;123: Stephenson LS, Latham MC, Kurz KM, Kinoti SN. Single dose metrifonate or praziquantel treatment in Kenyan children. II. Effects on growth in relation to Schistosoma haematobium and hookworm egg counts. Am J Trop Med Hyg 1989;41: Stephenson LS, Latham MC, Kurz KM, Kinoti SN, Brigham H. Treatment with a single dose of albendazole improves growth of Kenyan school children with hookworm, Trichuris trichiura, and Ascaris lumbricoides infections. Am J Trop Med Hyg 1989;41: Hadju V, Stephenson LS, Abadi K, Mohammed HO, Bowman DD, Parker RS. Improvements in appetite and growth in helminth-infectedschoolboys

5 S138 Guerrant et al. JID 2000;182 (Suppl 1) three and seven weeks after a single dose of pyrantel pamoate. Parasitology 1996;113: Callender JE, Grantham-McGregor S, Walker S, Cooper ES. Trichuris infection and mental development in children [letter; comments]. Lancet 1992;339: Chan MS. The global burden of intestinal nematode infections fifty years on [review]. Parasitol Today 1997;13: Guerrant DI, Moore SR, Lima AAM, Patrick PD, Schorling JB, Guerrant RL. Association of early childhood diarrhea and cryptosporidiosis with impaired physical fitness and cognitive function four seven years later in a poor urban community in northeast Brazil. Am J Trop Med Hyg 1999;61: Moore SR, Lima AAM, Schorling JB, Conaway M, Guerrant RL. Early childhood diarrhea and helminthiases associated with long-term stunting [abstract 568]. Am J Trop Med Hyg 1999;61: Ndamba J, Makaza N, Munjoma M, Gomo E, Kaondera KC. The physical fitness and work performance of agricultural workers infected with Schistosoma mansoni in Zimbabwe. Ann Trop Med Parasitol 1993;87: Checkley W, Gilman RH, Epstein LD, et al. Asymptomatic and symptomatic cryptosporidiosis: their acute effect on weight gain in Peruvian children. Am J Epidemiol 1997;145: Steiner TS, Lima AAM, Nataro JP, Guerrant RL. Enteroaggregative Escherichia coli produce intestinal inflammation and growth impairment and cause interleukin-8 release from intestinal epithelial cells. J Infect Dis 1998;177: Black RE, Brown KH, Becker S. Malnutrition is a determining factor in diarrheal duration but not incidence among young children in a longitudinal study in rural Bangladesh. Am J Clin Nutr 1984;39: Schorling JB, Guerrant RL. Diarrhea and catch-up growth. Lancet 1990; 335: Guerrant RL, Schorling JB, McAuliffe JF, de Souza MA. Diarrhea as a cause and effect of malnutrition: diarrhea prevents catch-up growth and malnutrition increases diarrhea frequency and duration. Am J Trop Med Hyg 1992;47: Guerrant RL, Lima AAM, Guerrant DI, Moore SR, Patrick PD, Schorling JB. Early childhood diarrhea correlates with impaired physical fitness and cognitive function; early Cryptosporidium infections correlate with impaired fitness, and early helminthic infections with growth shortfalls 4 7 years later in a poor urban community in Northeast Brazil [abstract]. Presented at the National Institute of Allergy and Infectious Diseases International Centers for Tropical Disease Research, 8th annual meeting, Bethesda, Maryland, Checkley W, Gilman RH, Epstein LD, et al. The adverse effects of Cryptosporidium parvum infection on the growth of children [abstract]. Presented at the National Institute of Allergy and Infectious Diseases (NIAID) 5th annual meeting of the NIAID International Centers for Tropical Research, Bethesda, Maryland, Tompkins AM, Dunn DT, Hayes RJ. Nutritional status and risk of morbidity among young Gambian children allowing for social and environmental factors. Trans R Soc Trop Med Hyg 1989;83: Schorling JB, McAuliffe JF, de Souza MA, Guerrant RL. Malnutrition is associated with increased diarrhoea incidence and duration among children in an urban Brazilian slum. Int J Epidemiol 1990;19: Moore SR, Schorling JB, Lima AAM, Guerrant RL. Secular trends in the epidemiology of diarrhea and malnutrition in an urban Brazilian shantytown, [abstract]. Presented at the NIH Tropical Medicine Research Center meeting, Natal, Brazil, Tompkins A. Nutritional status and severity of diarrhoea among preschool children in rural Nigeria. Lancet 1981;1: Briend A, Hasan KZ, Aziz KMA, Hoque BA. Are diarrhoea control programmes likely to reduce childhood malnutrition? Observations fromrural Bangladesh. Lancet 1989;2: Mata L. Diarrheal disease as a cause of malnutrition. Am J Trop Med Hyg 1992;47: Keusch GT. Nutrition-infection interactions. In: Guerrant RL, Walker DH, Weller PF, eds. Tropical infectious diseases: principles, pathogens and practice. Philadelphia: Churchill Livingstone, 1999: Bhan MK, Bhandari N. The role of zinc and vitamin A in persistent diarrhea among infants and young children [review]. J Pediatr Gastroenterol Nutr 1998;26: Ruel MT, Rivera JA, Santizo MC, Lonnerdal B, Brown KH. Impact of zinc supplementation on morbidity from diarrhea and respiratory infections among rural Guatemalan children. Pediatrics 1997;99: Roy SK, Tompkins AM, Akramuzzaman SM, et al. Randomised controlled trial of zinc supplementation in malnourished Bangladeshi children with acute diarrhoea. Arch Dis Child 1997;77: Roy SK, Behrens RH, Haider R, et al. Impact of zinc supplementation on intestinal permeability in Bangladeshi children with acute diarrhoea and persistent diarrheoea syndrome. J Pediatr Gastroenterol Nutr 1992;15: Sazawal S, Black RE, Bhan MK, et al. Zinc supplementation reduces the incidence of persistent diarrhea and dysentery among low socioeconomic children in India. J Nutr 1996;126: Beisel WR, Black RE, West KP Jr, Sommer A. Micronutrients in Infection. In: Guerrant RL, Walker DH, Weller PF, eds. Tropical infectious diseases: principles, pathogens, and practice. Philadelphia: Churchill Livingstone, 1999: Quadro L, Gamble MV, Vogel S, et al. Retinol and retinol-binding protein: gut integrity and the immune response. J Infect Dis 2000;182(suppl 1): Hossain S, Biswas R, Kabir I, et al. Single dose vitamin A treatment in acute shigellosis in Bangladesh children: randomised double blind controlled trial. BMJ 1998;316: Walser BL, Lima AM, Guerrant RL. Effects of high-dose oral vitamin A on diarrheal episodes among children with persistent diarrhea in a Northeast Brazilian community. Am J Trop Med Hyg 1996;54: Sommer A. Vitamin A deficiency, child health, and survival. Nutrition 1997;13: Beck MA, Kolbeck PC, Rohr LH, Shi Q, Morris VC, Levander OA. Benign human enterovirus becomes virulent in selenium-deficient mice. J Med Virol 1994;43: Beck MA, Esworthy RS, Ho YS, Chu FF. Glutathione peroxidase protects mice from viral-induced myocarditis. FASEB J 1998;12: Beck MA. Influence of antioxidant nutrients on viral infection. J Infect Dis 2000;182(suppl 1):93 6.

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