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Dietary fibre linked to decreased inflammation in overweight minority youth
Author(s) -
Miller S. J.,
Batra A. K.,
Shearrer G. E,
House B. T.,
Cook L. T.,
Pont S. J.,
Goran M. I.,
Davis J. N.
Publication year - 2016
Publication title -
pediatric obesity
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.226
H-Index - 69
eISSN - 2047-6310
pISSN - 2047-6302
DOI - 10.1111/ijpo.12017
Subject(s) - medicine , overweight , body mass index , anthropometry , inflammation , confounding , obesity , analysis of covariance , endocrinology , physiology , machine learning , computer science
Summary Objective The objective of this study was to examine the relationship between diet and inflammation, and adiposity in minority youth. Design and Methods The study was designed as a cross‐sectional analysis of 142 overweight (≥85th body mass index percentile) H ispanic and A frican– A merican adolescents (14–18 years) with the following measures: anthropometrics, adiposity via magnetic resonance imaging, dietary intake via 24‐h dietary recalls, and inflammation markers from fasting blood draws utilizing a multiplex panel. Partial correlations were estimated and analysis of covariance ( ancova ) models fit to examine the relationship among dietary variables, inflammation markers and adiposity measures with the following a priori covariates: T anner stage, ethnicity, sex, total energy intake, total body fat and total lean mass. Results Inference based on ancova models showed that the highest tertile of fibre intake (mean intake of 21.3 ± 6.1 g d −1 ) vs. the lowest tertile of fibre intake (mean intake of 7.4 ± 1.8 g d −1 ) was associated with 36% lower plasminogen activator inhibitor‐1 ( P = 0.02) and 43% lower resistin ( P = 0.02), independent of covariates. Similar results were seen for insoluble fibre. No other dietary variables included in this study were associated with inflammation markers. Conclusions These results suggest that increases in dietary fibre could play an important role in lowering inflammation and therefore metabolic disease risk in high‐risk minority youth.
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