The Shwachman Award of the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition 2002: acceptance. Dietary management of the malnourished child with chronic diarrhea: both nurture and nature.

I am honored to receive the 2002 Shwachman Award. In 1961, I had the pleasure of sharing lunch with Harry Shwachman when, representing the New England Pediatric Society, he awarded me a prize for the best paper written by an intern that year. My interest in studying the problems of infants with malnutrition and chronic diarrhea began at Yale–New Haven Hospital that same year with a patient named Stevie who had what was then called “intestinal decomposition” in Germany and “intractable diarrhea of infancy” in America, a condition with an extraordinarily high mortality and with no obvious cause. My clinical mentor at that time, Dr. Nelson Ordway, suggested we use a modular casein formula in this malnourished infant whose chronic diarrhea seemed to occur only when he was fed. We tested a series of modular formulas with different carbohydrate sources, including one made with ripe bananas purchased by my wife Veda. Stevie recovered on a formula whose carbohydrate source was starch oligomer. While I was Chief Resident in Pediatrics at Yale, Dr. Russell Blattner contacted me about joining his Pediatric faculty at Baylor. I told Dr. Blattner that I wanted to work in the subspecialty discipline of pediatric nutrition and gastroenterology. Dr. Blattner was unsure of the need for this subspecialty, but offered to establish this service if, while serving as House Staff Director at Texas Children’s Hospital, I could demonstrate any value in this discipline! Arriving in 1964, I discovered many babies like Stevie on the Baylor-affiliated infant wards and we began to study their problems in detail (1–23). These babies had a syndrome of diet driven chronic diarrhea that Bill Klish, my first GI Fellow, named Acquired Monosaccharide Intolerance (AMI), because of the glucose found in the stool (2). The house staff called the disorder “Slick-Gut Syndrome” because of the partial villous atrophy seen on small bowel biopsy (10,11). The modular refeeding method (1) resulted in some success, but there were many failures. A major advance in AMI management occurred in 1969, when total parenteral nutrition (TPN) was implemented. The combination of modular formulas and TPN resulted in recovery of most AMI cases and a nearly 50% reduction in mortality on the infant wards. This convinced Dr. Blattner of our clinical relevance as subspecialists and he permitted us in 1970 to establish the Pediatric Nutrition and Gastroenterology Service at Baylor, a service presently headed by Dr. Bill Klish. From 1965– 70, I carried out studies of malnutrition in Jamaica with Dr. John Waterlow, who became my nutrition mentor, and Dr. George Alleyne, my clinical collaborator (13). My fellows and I studied malnourished infants with Drs. Fernando Viteri and Jorge Alvarado in Guatemala (14,15), Dr. Adalberto Parra in Mexico (16,17) and Dr. Francisco Carrazza in Brazil (18–20). From each of these clinical collaborations, we became more skilled in diagnosis and management of malnutrition and chronic diarrhea. From 1978 to 1993, I was director of the U.S. Department of Agriculture Children’s Nutrition Research Center at Baylor and Texas Children’s Hospital (CNRC). After this administrative responsibility, I enjoyed sabbatical training in molecular biology in Switzerland with Dr. Erwin Sterchi, my molecular mentor. We have now sequenced the maltase-glucoamylase cDNA and gene (21)(unpublished). As before, it was another patient, Kevin, whose problem stimulated our research interest. Kevin was a child with genetic glucoamylase deficiency and it was he who opened the molecular era of my clinical career in 1998 (22, 23). I thus turned from the clinical study of infants with acquired carbohydrate intolerance to those with genetic carbohydrate intolerance—a transition from diseases of nurture to diseases of nature. I want to recognize the support and collaboration provided by my wife, Veda Nichols RN, MPH, during my career and the abiding encouragement from all my family. I thank Drs. John Udall, William Klish and Fernando Viteri for the nomination; Dr. Klish for his kind introduction; the Shwachman Committee; and the members of NASPGHAN for this singular honor. Journal of Pediatric Gastroenterology and Nutrition 36:168–169 © February 2003 Lippincott Williams & Wilkins, Inc., Philadelphia

[1]  D. Swallow,et al.  Congenital Maltase-Glucoamylase Deficiency Associated With Lactase and Sucrase Deficiencies , 2002, Journal of pediatric gastroenterology and nutrition.

[2]  D. Swallow,et al.  Disaccharidase Activities in Dyspeptic Children: Biochemical and Molecular Investigations of Maltase-Glucoamylase Activity , 2002, Journal of pediatric gastroenterology and nutrition.

[3]  B. Nichols,et al.  Contribution of villous atrophy to reduced intestinal maltase in infants with malnutrition. , 2000, Journal of pediatric gastroenterology and nutrition.

[4]  B. Nichols,et al.  Human Small Intestinal Maltase-glucoamylase cDNA Cloning , 1998, The Journal of Biological Chemistry.

[5]  A. Pastorino,et al.  [Asthma - Clinical and epidemiological aspects of 237 outpatients in a specialized pediatric unit] , 1998, Jornal de pediatria.

[6]  B. Nichols,et al.  Effects of malnutrition on expression and activity of lactase in children. , 1997, Gastroenterology.

[7]  B. Nichols,et al.  Mosaic Expression of Brush‐Border Enzymes in Infants with Chronic Diarrhea and Malnutrition , 1992, Journal of Pediatric Gastroenterology and Nutrition - JPGN.

[8]  B. Nichols,et al.  Pathogenesis of Small‐Intestinal Mucosal Lesions in Chronic Diarrhea of Infancy: I. A Light Microscopic Study , 1990, Journal of Pediatric Gastroenterology and Nutrition - JPGN.

[9]  B. Nichols,et al.  Pathogenesis of Small‐Intestinal Mucosal Lesions in Chronic Diarrhea of Infancy: II. An Electron Microscopic Study , 1990, Journal of pediatric gastroenterology and nutrition.

[10]  B. Nichols,et al.  Dietary Origin of Retained H+ in Infants with Acquired Monosaccharide Intolerance , 1989, Journal of Pediatric Gastroenterology and Nutrition - JPGN.

[11]  R. Shulman,et al.  A carbon-13 breath test to characterize glucose absorption and utilization in children. , 1988, Journal of pediatric gastroenterology and nutrition.

[12]  R. Shulman,et al.  Absorption and Oxidation of Glucose Polymers of Different Lengths in Young Infants , 1986, Pediatric Research.

[13]  B. Nichols,et al.  Disaccharidase Activities, Jejunal Morphology, and Carbohydrate Tolerance in Children with Chronic Diarrhea , 1985, Journal of pediatric gastroenterology and nutrition.

[14]  P. Klein,et al.  [13C]Acetate Oxidation in Infants After Oral Versus Rectal Administration: A Kinetic Model , 1985, Journal of Pediatric Gastroenterology and Nutrition - JPGN.

[15]  C. S. Irving,et al.  Carbohydrate malabsorption in infants with diarrhea studied with the breath hydrogen test. , 1983, The Journal of pediatrics.

[16]  B. Nichols,et al.  Comparison of acquired monosaccharide intolerance and acute diarrheal syndrome. , 1982, Journal of Pediatric Gastroenterology and Nutrition - JPGN.

[17]  B. Nichols,et al.  The Effect of Intestinal Solute Load on Water Secretion in Infants with Acquired Monosaccharide Intolerance , 1980, Pediatric Research.

[18]  P. Whitington Intestinal surface area in infants with acquired monosaccharide intolerance. , 1978, Jornal de Pediatria.

[19]  B. Nichols,et al.  Modular Formula: an approach to management of infants with specific or complex food intolerances. , 1976, The Journal of pediatrics.

[20]  W. Klish,et al.  Energy metabolism and hormonal profile in children with edematous protein-calorie malnutrition. , 1975, The Journal of pediatrics.

[21]  F. Viteri,et al.  Therapeutic implications of electrolyte, water, and nitrogen losses during recovery from protein-calorie malnutrition. , 1974, The Journal of pediatrics.

[22]  B. Nichols,et al.  Changes in growth hormone, insulin, and thyroxine values, and in energy metabolism of marasmic infants. , 1973, The Journal of pediatrics.

[23]  F. Viteri,et al.  Clinical significance of muscle potassium depletion in protein-calorie malnutrition. , 1972, The Journal of pediatrics.

[24]  G. Alleyne,et al.  Relationship between muscle potassium and total body potassium in infants with malnutrition. , 1969, The Journal of pediatrics.