Alan L. Buchman
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Alan L. Buchman has a total of 83 co-authors. Here are the top co-authors by number of shared publications:
Antwan Atia
Department of Internal Medicine, East Tennessee State University, Johnson City, Tennessee, USA
3 shared publicationsChul Ahn
3 shared publicationsSharon Polensky
Northwestern University
3 shared publicationsAnita Wallin
Divisions of Gastroenterology
2 shared publicationsChul W. Ahn
Department of Clinical Sciences, The University of Texas Southwestern Medical School, Dallas, Texas
2 shared publicationsDonald J. Jenden
2 shared publications
Latest Publications
- 2 November 2011
- Published by Springer Nature
- p. 643-653
Nutrition in Inflammatory Bowel Disease
- 4 March 2011
- Published by Wiley in Journal of Parenteral and Enteral Nutrition
- Vol. 35 (2) , 229-240
Macronutrient Absorption Characteristics in Humans With Short Bowel Syndrome and Jejunocolonic Anastomosis: Starch Is the Most Important Carbohydrate Substrate, Although Pectin Supplementation May Modestly Enhance Short Chain Fatty Acid Production and Fluid Absorption
Background: Diet may play an important role in the management of patients with short bowel syndrome who have colon in continuity. However, macronutrient absorption has not been well characterized, and the most appropriate dietary constituents have not been well defined. Objective: To define carbohydrate absorption characteristics in patients with short bowel syndrome and determine the potential role of pectin as a dietary substrate. Methods: The authors studied the effect of a custom pectin‐based supplement in 6 subjects (3 male/3 female) aged 29–67 years with jejunocolonic anastomosis, 4 of whom required long‐term parental nutrition. Small intestinal absorption capacity, macronutrient and fluid balance, gastrointestinal transit time, and energy consumption were measured. Results: Data showed that 53% nitrogen, 50% fat, and 32% total energy were malabsorbed. In contrast, the majority (92%) of total carbohydrate was utilized. Fecal short‐chain fatty acids (SCFAs) were increased, an indication of increased fermentation. Although only 4% of starch was recovered in stool, it is indicative of considerable starch malabsorption, thus providing the main carbohydrate substrate, for colonic bacterial fermentation. In contrast, nonstarch polysaccharide was a relatively minor fermentation substrate with only 49% utilized. Eighty percent of the pectin was fermented. Supplementation was associated with increased total SCFAs, acetate, and propionate excretion. There was a trend observed toward greater fluid absorption (−5.9% ± 54.4% to 26.9% ± 25.2%) following pectin supplementation. Nonsignificant increases in gastric emptying time and orocolonic transit time were observed. Conclusion: Despite malabsorption, starch is the primary carbohydrate substrate for colonic bacterial fermentation in patients with short bowel syndrome, although soluble fiber intake also enhances colonic SCFA production.
- 4 March 2011
- Published by Wiley in Journal of Parenteral and Enteral Nutrition
- Vol. 35 (2) , 229-240
Macronutrient Absorption Characteristics in Humans With Short Bowel Syndrome and Jejunocolonic Anastomosis: Starch Is the Most Important Carbohydrate Substrate, Although Pectin Supplementation May Modestly Enhance Short Chain Fatty Acid Production and Fluid Absorption
Background: Diet may play an important role in the management of patients with short bowel syndrome who have colon in continuity. However, macronutrient absorption has not been well characterized, and the most appropriate dietary constituents have not been well defined. Objective: To define carbohydrate absorption characteristics in patients with short bowel syndrome and determine the potential role of pectin as a dietary substrate. Methods: The authors studied the effect of a custom pectin‐based supplement in 6 subjects (3 male/3 female) aged 29–67 years with jejunocolonic anastomosis, 4 of whom required long‐term parental nutrition. Small intestinal absorption capacity, macronutrient and fluid balance, gastrointestinal transit time, and energy consumption were measured. Results: Data showed that 53% nitrogen, 50% fat, and 32% total energy were malabsorbed. In contrast, the majority (92%) of total carbohydrate was utilized. Fecal short‐chain fatty acids (SCFAs) were increased, an indication of increased fermentation. Although only 4% of starch was recovered in stool, it is indicative of considerable starch malabsorption, thus providing the main carbohydrate substrate, for colonic bacterial fermentation. In contrast, nonstarch polysaccharide was a relatively minor fermentation substrate with only 49% utilized. Eighty percent of the pectin was fermented. Supplementation was associated with increased total SCFAs, acetate, and propionate excretion. There was a trend observed toward greater fluid absorption (−5.9% ± 54.4% to 26.9% ± 25.2%) following pectin supplementation. Nonsignificant increases in gastric emptying time and orocolonic transit time were observed. Conclusion: Despite malabsorption, starch is the primary carbohydrate substrate for colonic bacterial fermentation in patients with short bowel syndrome, although soluble fiber intake also enhances colonic SCFA production.
- 1 January 2011
- Published by Elsevier in Journal of Gastrointestinal Surgery
- Vol. 15 (1) , 97-100
Mesenteric Vascular Thromboembolism in Inflammatory Bowel Disease: A Single Center Experience
- 1 January 2011
- Published by Elsevier in Journal of Gastrointestinal Surgery
- Vol. 15 (1) , 97-100
Mesenteric Vascular Thromboembolism in Inflammatory Bowel Disease: A Single Center Experience
- 1 June 2010
- Published by Oxford University Press (OUP) in Inflammatory Bowel Diseases
- Vol. 16 (6) , 962-973
Teduglutide, a novel mucosally active analog of glucagon-like peptide-2 (GLP-2) for the treatment of moderate to severe Crohnʼs disease
Teduglutide, an analog of glucagon-like peptide-2 (GLP-2), is associated with trophic effects on gut mucosa. Its role in the treatment of active Crohn's disease (CD) was assessed in a pilot, randomized, placebo-controlled, double-blinded, dose-ranging study. Subjects with moderate-to-severe CD were randomized 1:1:1:1 to placebo or 1 of 3 doses of teduglutide (0.05, 0.10, or 0.20 mg/kg daily) delivered as a daily subcutaneous injection for 8 weeks. The primary outcome measure was the percentage of subjects in each group that responded to treatment, defined as a decrease in Crohn's Disease Activity Index (CDAI) score to 100 points. At week 8 there was an optional 12-week open-label period of treatment with teduglutide 0.10 mg/kg/d. One hundred subjects were enrolled and 71 completed the study. The mean baseline CDAI score was 290.8 +/- 57.6 and was similar across groups. There were numerically higher response and remission rates in all teduglutide-treated groups as compared with placebo, although the percentage of subjects who achieved a clinical response or remission was more substantial, and seen as early as week 2 of treatment in the highest dose (0.2 mg/kg/d) group (44% response and 32% remission versus 32% response and 20% remission in the placebo group). Of subjects who had not achieved remission during the 8-week placebo-controlled phase in the higher-dose group, 50% achieved remission during the more prolonged, open-label treatment phase. Plasma citrulline was similar across groups at baseline, but increased substantially over time in all teduglutide groups when compared with placebo at week 8. Adverse events were not different between placebo and active treatment groups. Teduglutide is a novel and potentially effective therapy for inducing remission and mucosal healing in patients with active moderate-to-severe CD. Further clinical investigation of this growth factor is warranted.
- 1 June 2010
- Published by Oxford University Press (OUP) in Inflammatory Bowel Diseases
- Vol. 16 (6) , 962-973
Teduglutide, a novel mucosally active analog of glucagon-like peptide-2 (GLP-2) for the treatment of moderate to severe Crohnʼs disease
Teduglutide, an analog of glucagon-like peptide-2 (GLP-2), is associated with trophic effects on gut mucosa. Its role in the treatment of active Crohn's disease (CD) was assessed in a pilot, randomized, placebo-controlled, double-blinded, dose-ranging study. Subjects with moderate-to-severe CD were randomized 1:1:1:1 to placebo or 1 of 3 doses of teduglutide (0.05, 0.10, or 0.20 mg/kg daily) delivered as a daily subcutaneous injection for 8 weeks. The primary outcome measure was the percentage of subjects in each group that responded to treatment, defined as a decrease in Crohn's Disease Activity Index (CDAI) score to 100 points. At week 8 there was an optional 12-week open-label period of treatment with teduglutide 0.10 mg/kg/d. One hundred subjects were enrolled and 71 completed the study. The mean baseline CDAI score was 290.8 +/- 57.6 and was similar across groups. There were numerically higher response and remission rates in all teduglutide-treated groups as compared with placebo, although the percentage of subjects who achieved a clinical response or remission was more substantial, and seen as early as week 2 of treatment in the highest dose (0.2 mg/kg/d) group (44% response and 32% remission versus 32% response and 20% remission in the placebo group). Of subjects who had not achieved remission during the 8-week placebo-controlled phase in the higher-dose group, 50% achieved remission during the more prolonged, open-label treatment phase. Plasma citrulline was similar across groups at baseline, but increased substantially over time in all teduglutide groups when compared with placebo at week 8. Adverse events were not different between placebo and active treatment groups. Teduglutide is a novel and potentially effective therapy for inducing remission and mucosal healing in patients with active moderate-to-severe CD. Further clinical investigation of this growth factor is warranted.
- 1 November 2009
- Published by Elsevier in Gastroenterology
- Vol. 137 (5) , S1-S6
Micronutrients in Parenteral Nutrition: Too Little or Too Much? The Past, Present, and Recommendations for the Future
- 1 November 2009
- Published by Elsevier in Gastroenterology
- Vol. 137 (5) , S1-S6
Micronutrients in Parenteral Nutrition: Too Little or Too Much? The Past, Present, and Recommendations for the Future
- 1 November 2009
- Published by Elsevier in Gastroenterology
- Vol. 137 (5) , S119-S128
The Addition of Choline to Parenteral Nutrition
- 1 November 2009
- Published by Elsevier in Gastroenterology
- Vol. 137 (5) , S119-S128
The Addition of Choline to Parenteral Nutrition
- 31 May 2009
- Published by Elsevier in Gastroenterology
- Vol. 136 (5) , A-140-140
899 Pectin Supplementation Increases Colonic Short Chain Fatty Acid Production(SCFA) in Patients with Short Bowel Syndrome(SBS)
- 31 May 2009
- Published by Elsevier in Gastroenterology
- Vol. 136 (5) , A-140-140
899 Pectin Supplementation Increases Colonic Short Chain Fatty Acid Production(SCFA) in Patients with Short Bowel Syndrome(SBS)
- 3 March 2009
- Published by Wolters Kluwer Health in American Journal of Gastroenterology
- Vol. 104 (3) , 543-545
Medical Device Development: Design, Engineering, Testing and Legal Issues Protection—Steps in the Process to Success
The American Journal of Gastroenterology is published by Nature Publishing Group (NPG) on behalf of the American College of Gastroenterology (ACG). Ranked the #1 clinical journal covering gastroenterology and hepatology*, The American Journal of Gastroenterology (AJG) provides practical and professional support for clinicians dealing with the gastroenterological disorders seen most often in patients. Published with practicing clinicians in mind, the journal aims to be easily accessible, organizing its content by topic, both online and in print. www.amjgastro.com, *2007 Journal Citation Report (Thomson Reuters, 2008)
- 3 March 2009
- Published by Wolters Kluwer Health in American Journal of Gastroenterology
- Vol. 104 (3) , 543-545
Medical Device Development: Design, Engineering, Testing and Legal Issues Protection—Steps in the Process to Success
The American Journal of Gastroenterology is published by Nature Publishing Group (NPG) on behalf of the American College of Gastroenterology (ACG). Ranked the #1 clinical journal covering gastroenterology and hepatology*, The American Journal of Gastroenterology (AJG) provides practical and professional support for clinicians dealing with the gastroenterological disorders seen most often in patients. Published with practicing clinicians in mind, the journal aims to be easily accessible, organizing its content by topic, both online and in print. www.amjgastro.com, *2007 Journal Citation Report (Thomson Reuters, 2008)