TY - JOUR
T1 - Correlation of Vitamin E, uric acid and diet composition with histologic features of pediatric nonalcoholic fatty liver disease
AU - the NASH CRN Research Group
AU - Vos, Miriam B.
AU - Colvin, Ryan
AU - Belt, Patricia
AU - Molleston, Jean P.
AU - Murray, Karen F.
AU - Rosenthal, Philip
AU - Schwimmer, Jeffrey
AU - Tonascia, James
AU - Unalp, Aynur
AU - Lavine, Joel E.
AU - Abrams, Stephanie
AU - Arceo, Diana
AU - Espinosa, Denise
AU - Fairly, Leanel Angeli
AU - Hawkins, Carol
AU - Liu, Yao Chang
AU - Stager, Margaret
AU - McCullough, Arthur
AU - Dasarathy, Srinivasan
AU - Sargent, Ruth
AU - Coffey, Melissa
AU - Young, Melissa
AU - Mohan, Parvathi
AU - Nair, Kavita
AU - Abdelmalek, Manal
AU - Diehl, Anna Mae
AU - Gottfried, Marcia
AU - Guy, Cynthia
AU - Killenberg, Paul
AU - Kwan, Samantha
AU - Pan, Yi Ping
AU - Piercy, Dawn
AU - Smith, Melissa
AU - Bhimalli, Prajakta
AU - Chalasani, Naga
AU - Cummings, Oscar W.
AU - Lee, Lydia
AU - Ragozzino, Linda
AU - Vuppalanchi, Raj
AU - Byam, Elizabeth
AU - Klipsch, Ann
AU - Subbarao, Girish
AU - Pfeifer, Kimberly
AU - Scheimann, Ann
AU - Torbenson, Michael
AU - Barlow, Sarah
AU - Derdoy, Jose
AU - Hoffmann, Joyce
AU - King, Debra
AU - Aouizerat, Bradley
N1 - Funding Information:
Grant Support: The NASH CRN is supported by the National Institute of Diabetes and Digestive Diseases (NIDDK) grants U01DK061732 (Case Western Reserve University), U01DK061713 (Duke University Medical Center), U01DK061737 (Indiana University), U01DK061718 (St. Louis University), U01DK061734 (University of California, San Diego), U01DK061738 (University of California, San Francisco), U01DK061728 (University of Washington), U01DK061731 (Virginia Commonwealth University), and U01DK061730 (Johns Hopkins University) and the National Institute of Child Health and Human Development (NICHD). Other grant support includes the following: National Institutes of Health General Clinical Research Centers or Clinical and Translational Science Awards: UL1RR024989, M01RR000750, RR02413101, M01RR000827, UL1RR02501401, M01RR000065, M01RR00188, M01RR020359. Vos is supported by NIH (NIDDK) K23DK080953 and the Children's Digestive Health and Nutrition Foundation/Nestle Nutrition Award.
PY - 2012/1/1
Y1 - 2012/1/1
N2 - Objectives - Nonalcoholic fatty liver disease (NAFLD) is the most common chronic liver disease in children in the United States. Although changes in diet are often recommended to improve NAFLD, little is known regarding diet influence on histologic features of the disease. Methods - This was a prospective, cross-sectional registry based study. Children (n=149) enrolled in the multi-center NASH Clinical Research Network had demographic, anthropometric, clinical, laboratory and histology data obtained, including the Block Brief Food Questionnaire. Subjects were grouped by presence or absence of steatohepatitis and grades of histologic features according to NASH-CRN criteria. Results - No significant differences were found between children with steatosis compared to steatohepatitis for fraction of calories from fat, carbohydrates, and protein. Sugar sweetened beverage consumption was low and did not correlate with histologic features, although uric acid, a surrogate marker for fructose intake, was significantly increased in those with definite NASH (p=. 008). For all groups, Vitamin E consumption was insufficient compared to the recommended daily allowance. Median consumption of Vitamin E was lower in children with higher grade of steatosis (8.4 vs 6.1 vs 6.9 for grade I, II and III respectively, p = .05). Those consuming less Vitamin C had increased ballooning degeneration (p = 0.05). Conclusions - Children with NAFLD have a diet that is insufficient in Vitamin E and this may contribute to the pathophysiology of NAFLD. In children with NAFLD, reported sugar sweetened beverage consumption is low; however uric acid, which may reflect total fructose consumption, was significantly associated with NASH and should be further evaluated.
AB - Objectives - Nonalcoholic fatty liver disease (NAFLD) is the most common chronic liver disease in children in the United States. Although changes in diet are often recommended to improve NAFLD, little is known regarding diet influence on histologic features of the disease. Methods - This was a prospective, cross-sectional registry based study. Children (n=149) enrolled in the multi-center NASH Clinical Research Network had demographic, anthropometric, clinical, laboratory and histology data obtained, including the Block Brief Food Questionnaire. Subjects were grouped by presence or absence of steatohepatitis and grades of histologic features according to NASH-CRN criteria. Results - No significant differences were found between children with steatosis compared to steatohepatitis for fraction of calories from fat, carbohydrates, and protein. Sugar sweetened beverage consumption was low and did not correlate with histologic features, although uric acid, a surrogate marker for fructose intake, was significantly increased in those with definite NASH (p=. 008). For all groups, Vitamin E consumption was insufficient compared to the recommended daily allowance. Median consumption of Vitamin E was lower in children with higher grade of steatosis (8.4 vs 6.1 vs 6.9 for grade I, II and III respectively, p = .05). Those consuming less Vitamin C had increased ballooning degeneration (p = 0.05). Conclusions - Children with NAFLD have a diet that is insufficient in Vitamin E and this may contribute to the pathophysiology of NAFLD. In children with NAFLD, reported sugar sweetened beverage consumption is low; however uric acid, which may reflect total fructose consumption, was significantly associated with NASH and should be further evaluated.
KW - nonalcoholic steatohepatitis
KW - nutrition
KW - sugar-sweetened beverages
KW - vitamin C
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U2 - 10.1097/MPG.0b013e318229da1a
DO - 10.1097/MPG.0b013e318229da1a
M3 - Article
C2 - 22197855
AN - SCOPUS:84855346047
SN - 0277-2116
VL - 54
SP - 90
EP - 96
JO - Journal of Pediatric Gastroenterology and Nutrition
JF - Journal of Pediatric Gastroenterology and Nutrition
IS - 1
ER -