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. 2023 Dec 7;7(12):e0320.
doi: 10.1097/HC9.0000000000000320. eCollection 2023 Dec 1.

Nutrition assessment and MASH severity in children using the Healthy Eating Index

Collaborators, Affiliations

Nutrition assessment and MASH severity in children using the Healthy Eating Index

Ajay Kumar Jain et al. Hepatol Commun. .

Abstract

Background: Pediatric metabolic-associated fatty liver disease (MAFLD) is a global health problem, with lifestyle modification as its major therapeutic strategy. Rigorous characterization of dietary content on MAFLD in children is lacking. We hypothesized an objectively measured healthier diet would positively modulate MAFLD.

Methods: Diet was assessed using the Nutrition Data System for Research in children enrolled from 10 tertiary clinical centers to determine the Healthy Eating Index (HEI, 0-100) and individual food components.

Results: In all, 119 children were included (13.3 ± 2.7 y), 80 (67%) male, 67 (18%) White, and 90 (76%) Hispanic, with an average body mass index Z-score of 2.2 ± 0.5. Diet was classified as low HEI < 47.94 (n = 39), mid HEI ≥ 47.94 and < 58.89 (n = 41), or high HEI ≥ 58.89 (n=39). Children with high HEI (healthier diet) had lower body weight (p = 0.005) and more favorable lipids. Mean serum triglycerides for low, mid, and high HEI were 163, 148, and 120 mg/dL, respectively; p = 0.04 mid versus high, p = 0.01 low versus high. Mean HDL was 38, 41 and 43 mg/dL; p = 0.02 low vs high. Less severe steatosis was noted with added sugar ≤ 10% of calories (p = 0.03). Higher lobular inflammation is associated with a higher percentage of calories from fat (OR (95% CI) = 0.95 (0.91-1.00), p = 0.04).

Conclusions: In children with MAFLD, high HEI is associated with lower body weight and more favorable lipids, while added sugar and fat intake has individual histologic features. Differential consumption of major dietary components may modify both metabolic risk factors and histologic liver injury, highlighting the importance of objective diet assessments in children with MAFLD.

Trial registration: ClinicalTrials.gov NCT01529268.

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Conflict of interest statement

Ajay Jain is a consultant for Mirum and Camp 4. Philip Rosenthal has research support from Abbvie, Albireo, Arrowhead, Gilead, Merck, Mirum, Takeda, and Travere. Philip Rosenthal is a consultant for Albireo, Audentes, BioMarin, Dicerna, Encoded, Gilead, MedinCell, Mirum, RNAV8, Takeda, Taysha, Travere. Jean Molleston reports Abbie, Albireo, Gilead, Shire, and the CF Foundation. Karen Murray reports to Albireo, Gilead, ICN Board of Directors. Brent Tetri reports to Akero, Arrowhead, Boehringer Ingelheim, BMS, Clinical Care Options, Durect, GSK, Glympse, Hepion, High Tide, HistoIndex, Labcorp, LG Chem, Madrigal, Merck, Sagimet, Senseion, Target RWE, and 89Bio; Stock options: HepGene, and HeptaBio; Institutional research grants: BMS, HighTide, Intercept, Inventiva, and Madrigal. Stavra Xanthakos reports to Target NASH. The remaining authors have no conflicts to report.

Figures

FIGURE 1
FIGURE 1
Shown here is the CONSORT diagram. Abbreviation: CBDR, Cysteamine bitartrate delayed-release.

References

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