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Volume 15, Number 1—January 2009

Dispatch

Microsporidiosis and Malnutrition in Children with Persistent Diarrhea, Uganda

Siobhan M. MorComments to Author , James K. Tumwine, Elena N. Naumova, Grace Ndeezi, and Saul Tzipori
Author affiliations: Tufts Cummings School of Veterinary Medicine, North Grafton, Massachusetts, USA (S.M. Mor, S. Tzipori); Tufts University School of Medicine, Boston, Massachusetts, USA (S.M. Mor, E.N. Naumova); Makerere University Medical School, Kampala, Uganda (J.K. Tumwine, G. Ndeezi)

Suggested citation for this article

Abstract

We show that the microsporidian fungus Enterocytozoon bieneusi is associated with lower rates of weight gain in children in Uganda with persistent diarrhea. This relationship remained after controlling for HIV and concurrent cryptosporidiosis. Children with microsporidiosis were predicted to weigh 1.3 kg less than children without microsporidiosis at 5 years of age.

Enterocytozoon bieneusi is an important cause of persistent diarrhea, intestinal malabsorption, and wasting in HIV-positive adults. Mucosal damage associated with microsporidiosis is more extensive than that related to other opportunistic intestinal infections (1,2) and leads to substantial malabsorption of carbohydrates, fat, and essential nutrients (25). Although microsporidiosis is common in children <5 years of age, particularly those who live in developing countries (6,7) or who are HIV positive (6,8,9), the effects of infection on nutritional health of these vulnerable populations are not well documented. We reexamined anthropometric data of children in Uganda with persistent diarrhea (6) and used regression analysis to determine whether there is an association between microsporidiosis and reduced growth rates.

The Study

A total of 243 children <60 months of age with persistent diarrhea (>14 days) were enrolled at Mulago Hospital in Kampala, Uganda, from November 2002 through May 2003. After informed consent was obtained, demographic, anthropometric, and clinical information was collected from each child. E. bieneusi spores were detected in stool specimens by using a nested PCR with E. bieneusi–specific primers (7). Cryptosporidium oocysts were detected by using immunofluorescence microscopy, with confirmation and genotyping subsequently determined by PCR–restriction fragment length polymorphism analysis (10). HIV status was determined by using established methods, and children positive for HIV were referred to the Mulago Hospital Pediatric Infectious Disease Clinic for further care. The study population and results of primary analysis are described in more detail elsewhere (6).

Figure 1

Thumbnail of Nutritional status of children in Uganda with microsporidiosis with or without HIV or concurrent cryptosporidiosis. The infection status and number of children in each infection category are shown. Outliers are indicated with dots (1.5–3 interquartile ranges [IQRs]) or the asterisk (&gt;3 IQR). The dashed horizontal line indicates conventional cut-off for malnutrition (z-score &lt;2), horizontal lines in each column indicate the median score, and error bars indicate the highest and

Figure 1. Nutritional status of children in Uganda with microsporidiosis with or without HIV or concurrent cryptosporidiosis. The infection status and number of children in each infection category are shown. Outliers are indicated...

A complete set of anthropometric measures (age, weight, height, weight-for-age z-score, height-for-age z-score, and weight-for-height z-score) was available for 224 children. Wasting was twice as likely in children with microsporidiosis than in children without the infection (Table 1). Microsporidiosis was strongly associated with HIV and concurrent cryptosporidiosis. These infections likely compound the poor nutritional status of children with microsporidiosis, although this assessment is limited by sample size (Figure 1).

Linear regression models were used to describe weight and height gain in study children. Weight and height were treated as continuous dependent variables. When regressed on age, the slopes of the curves represent the rate of weight and height gain, respectively. All variables were transformed to the natural logarithmic scale.

For initial data exploration, several simple models were applied with children stratified according to HIV and Cryptosporidium spp. status. Within each strata, slope parameters were compared by using t tests to identify differences in growth rates between E. bieneusi–positive and –negative children. Growth rates were reduced in children with microsporidiosis across all HIV and Cryptosporidium strata (Table 2). In HIV-positive children, the rate of weight gain was lower in children with microsporidiosis than in those without microsporidiosis (model 1a vs. model 1b), and some evidence showed that this was also true for HIV-negative children (model 1c vs. model 1d). In children concurrently infected with Cryptosporidium spp., rates of weight (model 1e vs. model 1f) and height gain (model 2e vs. model 2f) were lower in children with microsporidiosis.

Figure 2

Thumbnail of Weight-for-age growth curves of study children (as modeled by multiple linear regression) and reference populations in Uganda (11). Curves represent the median weight-for-age, averaged between boys and girls and controlling for concurrent Cryptosporidium spp. infection. The difference, 95% confidence interval, and significance of the interaction term between Enterocytozoon bieneusi and age reflect the difference in growth rates of children with and without microsporidiosis in ln(kg)

Figure 2. Weight-for-age growth curves of study children (as modeled by multiple linear regression) and reference populations in Uganda (11). Curves represent the median weight-for-age, averaged between boys and girls and...

Adjusted growth rate estimates were obtained by fitting a multiple linear regression model that controlled for the effect of sex, HIV status, and concurrent cryptosporidiosis. The independent variable of interest was an interaction term between E. bieneusi and age, which reflected the difference in the growth rates of children with and without microsporidiosis. Interaction terms between E. bieneusi, Cryptosporidium spp., HIV, and age were also explored but were excluded from the final model because they did not improve model fit. When we simultaneously adjusted for sex, HIV status, and concurrent cryptosporidiosis, rate of weight gain remained significantly lower in children with microsporidiosis (p = 0.014). However, rate of height gain was not significantly different between children with and without microsporidiosis (p = 0.151). Predicted weight-for-age growth curves are shown in Figure 2, which also displays reference curves for healthy Ugandan children (11). The growth trajectory of children with microsporidiosis was such that by age 5, these children were predicted to weigh ≈1.3 kg less than children without microsporidiosis. This finding exceeded the predicted difference in weight in children with and without HIV (0.74 kg) at the same age.

Conclusions

Given consistent reports of severe wasting and malnutrition in HIV-positive adults with microsporidiosis, it is conceivable that E. bieneusi infection early in life may result in malnutrition. Two cross-sectional studies attempted to correlate microsporidiosis with poor anthropometric status but did not find a significant association (7,12). However, the dichotomous method used for these assessments is sensitive to the choice of cut-off values. Although children who fall >2 SDs below the reference growth curves are conventionally categorized as malnourished, this cut-off does not denote a biologically meaningful distinction between healthy and malnourished children.

Using regression analysis, we present evidence that microsporidiosis is associated with growth faltering in children in Uganda. In this approach, anthropometric data were treated as continuous variables, thus avoiding arbitrary categorization of children into malnourished and normally nourished groups. Lack of evidence for an independent effect of microsporidiosis on linear growth might be explained by the fact that these children were currently infected with E. bieneusi, and longer intervals are needed to document decelerating linear growth. In contrast, weight-for-age reflects chronic and acute nutritional states. Because all study participants had a history of persistent diarrhea and stool was generally collected on the day of hospitalization, nosocomial acquisition of microsporidiosis was unlikely.

There are several limitations to this analysis. The causal role of E. bieneusi in childhood malnutrition cannot be inferred because of the retrospective and cross-sectional study design. Although intestinal infection in children may impair absorption of nutrients (as documented in adults), malnourished children may also have immune defects that predispose them to E. bieneusi infection. Because the PCR was specific for E. bieneusi, we cannot rule out that some children were infected with other microsporidian species. However, E. bieneusi is the more common of 2 species known to cause intestinal microsporidiosis (13,14). In previous studies at Mulago Hospital, 16.8% of children with acute diarrhea and 16.8% of children without diarrhea had microsporidiosis (7). Because all children in the current study had persistent diarrhea, direct comparison between groups was possible without the need to control for diarrhea status. However, we cannot comment on the effect of acute or subclinical infection on nutritional health. Residual confounding may exist through sociodemographic factors not accounted for in the analysis. Sociodemographic data were limited to the accessibility of safe drinking water and type of sanitary facility in the household, neither of which were associated with microsporidiosis (data not shown). Finally, use of cross-sectional data is a major limitation because measurements obtained at a single point in time do not capture individual growth trends. Such data make it difficult to assess the effect of a particular episode of illness on growth attainment (15). To this extent, longitudinal anthropometric assessment is the only means of detecting growth faltering that results from E. bieneusi infection in childhood.

Although our results suggest an association between reduced weight gain and microsporidiosis, further studies are required to determine the role of E. bieneusi in childhood malnutrition. Longitudinal studies enabling comparison of preinfection and postinfection weights in individual children are needed to establish the direction of causation. It will be particularly useful to identify whether the period of reduced weight gain is followed by catch-up growth. Because microsporidiosis is highly prevalent in children in developing countries, the finding that the infection has a lasting effect on growth would highlight the importance of nutritional rehabilitation and provide impetus to develop therapeutics suitable for use in young children.

Dr Mor is a veterinarian and doctoral candidate at the Cummings School of Veterinary Medicine at Tufts University. She is also an instructor at the School of Medicine at the same university. Her research interests include the clinical epidemiology of E. bieneusi, Cryptosporidium spp., other tropical infections, and zoonotic diseases of global health importance.

Acknowledgments

We thank the members of the Initiative for the Forecasting and Modeling of Infectious Diseases at Tufts University and anonymous reviewers for providing constructive comments on the manuscript.

This study was supported by grant R21A1068474 from the National Institutes for Allergy and Infectious Diseases (S.M.M and S.T.) and by the University of Sydney Traveling Scholarship Fund (S.M.M.).

References

  1. Schmidt W, Schneider T, Heise W, Schulzke JD, Weinke T, Ignatius R, Mucosal abnormalities in microsporidiosis. AIDS. 1997;11:158994. DOIPubMed
  2. Kotler DP, Francisco A, Clayton F, Scholes JV, Orenstein JM. Small intestinal injury and parasitic diseases in AIDS. Ann Intern Med. 1990;113:4449.PubMed
  3. Molina JM, Sarfati C, Beauvais B, Lemann M, Lesourd A, Ferchal F, Intestinal microsporidiosis in human immunodeficiency virus-infected patients with chronic unexplained diarrhea: prevalence and clinical and biologic features. J Infect Dis. 1993;167:21721.PubMed
  4. Lambl BB, Federman M, Pleskow D, Wanke CA. Malabsorption and wasting in AIDS patients with microsporidia and pathogen-negative diarrhea. AIDS. 1996;10:73944. DOIPubMed
  5. Asmuth DM, DeGirolami PC, Federman M, Ezratty CR, Pleskow DK, Desai G, Clinical features of microsporidiosis in patients with AIDS. Clin Infect Dis. 1994;18:81925.PubMed
  6. Tumwine JK, Kekitiinwa A, Bakeera-Kitaka S, Ndeezi G, Downing R, Feng X, Cryptosporidiosis and microsporidiosis in Ugandan children with persistent diarrhea with and without concurrent infection with the human immunodeficiency virus. Am J Trop Med Hyg. 2005;73:9215.PubMed
  7. Tumwine JK, Kekitiinwa A, Nabukeera N, Akiyoshi DE, Buckholt MA, Tzipori S. Enterocytozoon bieneusi among children with diarrhea attending Mulago Hospital in Uganda. Am J Trop Med Hyg. 2002;67:299303.PubMed
  8. Leelayoova S, Vithayasai N, Watanaveeradej V, Chotpitayasunondh T, Therapong V, Naaglor T, Intestinal microsporidiosis in HIV-infected children with acute and chronic diarrhea. Southeast Asian J Trop Med Public Health. 2001;32:337.PubMed
  9. Wanachiwanawin D, Chokephaibulkit K, Lertlaituan P, Ongrotchanakun J, Chinabut P, Thakerngpol K. Intestinal microsporidiosis in HIV-infected children with diarrhea. Southeast Asian J Trop Med Public Health. 2002;33:2415.PubMed
  10. Tumwine JK, Kekitiinwa A, Nabukeera N, Akiyoshi DE, Rich SM, Widmer G, Cryptosporidium parvum in children with diarrhea in Mulago Hospital, Kampala, Uganda. Am J Trop Med Hyg. 2003;68:7105.PubMed
  11. Cortinovis I, Vella V, Ndiku N, Milani S. Weight, height and arm circumference of children under 5 in the district of Mbarara, south-west Uganda. Ann Hum Biol. 1997;24:55768. DOIPubMed
  12. Leelayoova S, Subrungruang I, Rangsin R, Chavalitshewinkoon-Petmitr P, Worapong J, Naaglor T, Transmission of Enterocytozoon bieneusi genotype a in a Thai orphanage. Am J Trop Med Hyg. 2005;73:1047.PubMed
  13. Samie A, Obi CL, Tzipori S, Weiss LM, Guerrant RL. Microsporidiosis in South Africa: PCR detection in stool samples of HIV-positive and HIV-negative individuals and school children in Vhembe district, Limpopo Province. Trans R Soc Trop Med Hyg. 2007;101:54754. DOIPubMed
  14. Espern A, Morio F, Miegeville M, Illa H, Abdoulaye M, Meyssonnier V, Molecular study of microsporidiosis due to Enterocytozoon bieneusi and Encephalitozoon intestinalis among human immunodeficiency virus–infected patients from two geographical areas: Niamey, Niger, and Hanoi, Vietnam. J Clin Microbiol. 2007;45:29993002. DOIPubMed
  15. McMurray C. Cross-sectional anthropometry: what can it tell us about the health of young children? Health Transit Rev. 1996;6:14768.PubMed

Figures

Tables

Suggested citation for this article: Mor SM, Tumwine JK, Naumova EN, Ndeezi G, Tzipori S. Microsporidiosis and malnutrition in children with persistent diarrhea, Uganda. Emerg Infect Dis [serial on the Internet]. 2009 Jan [date cited]. Available from http://wwwnc.cdc.gov/eid/article/15/1/07-1536.htm

DOI: 10.3201/eid1501.071536

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Table of Contents – Volume 15, Number 1—January 2009

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