Hostname: page-component-78c5997874-fbnjt Total loading time: 0 Render date: 2024-11-16T12:57:24.410Z Has data issue: false hasContentIssue false

Contributions of ascariasis to poor nutritional status in children from Chiriqui Province, Republic of Panama

Published online by Cambridge University Press:  06 April 2009

D. L. Taren
Affiliation:
College of Public Health, University of South Florida
M. C. Nesheim
Affiliation:
Division of Nutritional Sciences, Cornell University
D. W. T. Crompton*
Affiliation:
Department of Zoology, University of Glasgow
Celia V. Holland
Affiliation:
Department of Zoology, Trinity College, Dublin
Irma Barbeau
Affiliation:
Division of Nutritional Sciences, Cornell University
Gloria Rivera
Affiliation:
Sistema Integrado de Salud, David, Republic of Panama
Diva Sanjur
Affiliation:
Division of Nutritional Sciences, Cornell University
Jean Tiffany
Affiliation:
Division of Nutritional Sciences, Cornell University
Katherine Tucker
Affiliation:
Division of Nutritional Sciences, Cornell University
*
*Reprint requests: D. W. T. Crompton. Department of Zoology. University of Glasgow, Glasgow G12 8QQ.

Summary

Relationships between ascariasis and lactose digestion and between ascariasis and food transit time from mouth to caecum were investigated in young children from Chiriqui Province, Republic of Panama. The breath hydrogen method was used in both studies. Ascaris-infected children showed a significantly poorer degree of lactose digestion following a test oral load than uninfected children. Recovery of the capacity of the children to digest lactose was still not fully complete for at least 3 weeks following anthelmintic treatment. On average, the mouth-to-caecum transit time was similar in infected and uninfected children, but among the Ascaris-infected children the transit time tended to be shorter in relation to the intensity of infection. Evidence from a cross-sectional survey indicated that ascariasis was significantly associated with reduced plasma vitamin A and carotenoid concentrations. This relationship remained after controlling for a range of socio-economic variables. Ascaris-infected children were frequently found to have lower haematocrits and blood haemoglobin concentrations than uninfected children, but these relationships could not be attributed to ascariasis alone.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1987

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Allen, A. H. V. & Ridley, D. S. (1970). Further observations on the formol–ether concentration technique for faecal parasites. Journal of Clinical Pathology 23, 343–52.CrossRefGoogle ScholarPubMed
Bhattacharyya, A. K. (1982). Xerophthalmia and ascariasis in chronic severe Kwashiorkor-Marasmus syndrome (KMS). Bulletin of the Calcutta School of Tropical Medicine 30, 6870.Google Scholar
Bhattacharyya, A. K., Debnath, B. & Dutta, P. (1980). Serum retinol in ascariasis. Bulletin of the Calcutta School of Tropical Medicine 28, 24–6.Google Scholar
Bond, J. H. & Levitt, M. D. (1972). Use of pulmonary hydrogen (H2) measurements to quantitate carbohydrate absorption. Journal of Clinical Investigation 51, 1219–25.CrossRefGoogle ScholarPubMed
Bond, J. H. & Levitt, M. D. (1975). Investigation of small bowel transit time in man utilizing pulmonary hydrogen (H2) measurements. Journal of Laboratory Clinical Medicine 85, 546–55.Google ScholarPubMed
Brown, K. H., Gilman, R. H., Khatun, M. & Ahmed, M. G. (1980). Absorption of macronutrients from a rice vegetable diet before and after treatment of ascariasis in children. American Journal of Clinical Nutrition 33, 1975–82.CrossRefGoogle ScholarPubMed
Carreba, E., Nesheim, M. C. & Crompton, D. W. T. (1984). Lactose maldigestion in Ascaris-infected preschool children. American Journal of Clinical Nutrition 39, 255–64.Google Scholar
Cerf, B. J., Rohde, J. E. & Soesanto, T. (1981). Ascaris and malnutrition in a Balinese village: a conditional relationship. Tropical and Geographical Medicine 33, 367–73.Google Scholar
Crofts, T. J. (1977). Bowel transit times and intestinal parasites in the Shipibo Indians of Peru. Tropical Doctor 7, 115–18.CrossRefGoogle ScholarPubMed
Crompton, D. W. T., Nesheim, M. C. & Pawlowski, Z. S. (1985). Ascariasis and its Public Health Significance. London and Basingstoke: Taylor & Francis Ltd.Google Scholar
Dallman, P. R. (1977). New approaches to screening for iron deficiency. Journal of Pediatrics 90, 678–81.CrossRefGoogle ScholarPubMed
Forsum, E., Nesheim, M. C. & Crompton, D. W. T. (1981). Nutritional aspects of Ascaris-infection in young protein-deficient pigs. Parasitology 83, 497512.CrossRefGoogle Scholar
Gupta, M. C. (1985). Ascariasis and malnutrition in children: studies in India and Guatemala. In Ascariasis and its Public Health Significance (ed. Crompton, D. W. T., Nesheim, M. C. and Pawlowski, Z. S.), pp. 203–11. London and Basingstoke: Taylor & Francis Ltd.Google Scholar
Gupta, M. C., Mithal, S., Arara, K. L. & Tandon, B. N. (1977). Effects of periodic deworming on nutritional status of Ascaris-infected pre-school children receiving supplementary food. Lancet 2, 108–10.CrossRefGoogle Scholar
Hall, A. (1982). Intestinal helminths of man: the interpretation of faecal egg counts. Parasitology 85, 605–13.CrossRefGoogle Scholar
Interdepartmental Committee For Nutrition And National Defense (1963). Manual for Nutrition Surveys, 2nd Edn, U.S. Government Printing Office, Washington, D.C.Google Scholar
International Anemia Consultative Group (1979). Iron deficiency in infancy and childhood. Report of the International Anemia Consultative Group. Washington D.C.; Nutrition Foundation.Google Scholar
International Vitamin A Consultative Group (1984). Biochemical methodologies for the assessment of vitamin A status. Report of the International Vitamin A Consultative Group. Washington D.C; Nutrition Foundation.Google Scholar
La Brooy, B. J., Male, P. I., Beavis, A. K. & Misiewicz, J. T. (1983). Assessment of the reproductivity of the lactulose H2 breath test as a measure of mouth to caecum transit time. Gut 24, 893–6.CrossRefGoogle Scholar
Lifshitz, F. (1980). Carbohydrate malabsorption. In Clinical Disorders in Pediatric Gastroenterology and Nutrition, (ed. Lifshitz, F.), pp. 229–40. New York and Basel: Marcel Dekker Inc.Google Scholar
Mahalanabis, D., Jalan, K. N., Maitra, T. K. & Agarwal, S. K. (1976). Vitamin A absorption in ascariasis. American Journal of Clinical Nutrition 9, 1372–5.CrossRefGoogle Scholar
Mahalanabis, D., Simpson, T. W., Chakroborty, M. L., Bhattacharjee, A. K. & Mukherjee, K. H. (1979). Malabsorption of water miscible vitamin A in children with giardiasis and ascariasis. American Journal of Clincal Nutrition 32, 313–18.CrossRefGoogle ScholarPubMed
Martin, J., Crompton, D. W. T., Carrera, E. & Nesheim, M. C. (1984). Mucosal surface lesions in young protein-deficient pigs infected with Ascaris suum (Nematoda). Parasitology 88, 333–40.CrossRefGoogle ScholarPubMed
National Center For Health Statistics (1976). NCHS Growth Charts 1976. Monthly Vital Statistics Report No.3, DHEW Publication 7601120, Vol.25.Google Scholar
Reddy, V., Vijayaraghavan, K. & Mathur, K. K. (1986). Effect of deworming and vitamin A administration on serum vitamin A levels in pre-school children. Journal of Tropical Pediatrics 32, 196–9.CrossRefGoogle Scholar
Schultz, M. C. (1982). Ascariasis: nutritional implications. Review of Infectious Diseases 4, 815–19.CrossRefGoogle ScholarPubMed
Sivakumar, B. & Reddy, V., (1975). Absorption of vitamin A in children with ascariasis. Journal of Tropical Medicine and Hygiene 78, 114–15.Google ScholarPubMed
Solomons, N. W. (1983). The use of H2 breath-analysis tests in gastrointestinal diagnosis. Current Concepts in Gastroenterology 8, 3040.Google Scholar
Statistical Analysis Systems (1982). SAS Users' Guide, (ed. Cary, N. C.). North Carolina: SAS Institute Inc.Google Scholar
Stephenson, L. S. (1978). Nutritional and economic implications of Ascaris infection in Kenya. Ph.D. dissertation, Cornell University.Google Scholar
Stephenson, L. S. (1984). Methods to evaluate nutritional and economic implications of Ascaris infection. Social Science and Medicine 19, 1061–5.CrossRefGoogle ScholarPubMed
Stephenson, L. S., Crompton, D. W. T., Latham, M. C., Schulpen, T. W. J., Nesheim, M. C. & Jansen, A. A. J. (1980 a). Relationship between Ascaris infection and growth of malnourished pre-school children in Kenya. American Journal of Clinical Nutrition 33, 1165–72.CrossRefGoogle ScholarPubMed
Stephenson, L. S., Pond, W. G., Nesheim, M. C., Krook, L. P. & Crompton, D. W. T. (1980 b). Ascaris suum: nutrient absorption, growth and intestinal pathology in young pigs experimentally infected with 15-day-old larvae. Experimental Parasitology 49, 1525.CrossRefGoogle ScholarPubMed
Tripathy, K., Duque, E., Bolanos, O., Lotero, H. & Mayoral, L. G. (1972). Malabsorption syndrome in ascariasis. American Journal of Clinical Nutrition 25, 1276–81.CrossRefGoogle ScholarPubMed
Underwood, B. A. (1984). Vitamin A. In Tropical and Geographical Medicine (ed. Warren, K. S. and Mahmoud, A. A. F.), pp. 1028–33. New York: McGraw-Hill Book Co.Google Scholar
Willett, W. C., Kilama, W. L. & Klhamia, C. M. (1979). Ascaris and growth rates: a randomized trial of treatment. American Journal of Public Health 69, 987–91.CrossRefGoogle Scholar
Young, F. W. & Young, R. C. (1968). The differentiation of family structure in rural Mexico. Journal of Marriage and the Family 30, 154–61.CrossRefGoogle Scholar
Zeller, R. A. & Carmines, E. G. (1982). SAS User's Guide, (ed. Cary, N. C.), North Carolina: SAS Institute Inc.Google Scholar