Abstract 4364127: Fatty Liver, Big Heart Risk: Prevalent Cardiovascular Risk among Young Children with Subclinical and Clinical Hepatic Steatosis

A Ana Ramirez Tovar C Cristian Sanchez Torres (Emory University, Decatur, Georgia, United States) S Scott Gillespie L Liliana Aguayo (Emory University, Atlanta, Georgia, United States) H Helaina Huneault (Emory University, Atlanta, Georgia, United States) C Claudia Yaranga (Emory University, Atlanta, Georgia, United States) K Karla DeSantos (Emory University, Atlanta, Georgia, United States) C Christina Carapia-chaparro (Emory University, Atlanta, Georgia, United States) B Brittany James (Emory University, Atlanta, Georgia, United States) G Geetika Khanna (Children's Healthcare of Atlanta, Atlanta, Georgia, United States) J Jack Knight-Scott (Children's Healthcare of Atlanta, Atlanta, Georgia, United States) A Adina Alazraki (Children's Healthcare of Atlanta, Atlanta, Georgia, United States) S Shasha Bai M Miriam Vos (EMORY UNIVERSITY, Atlanta, Georgia, United States) J Jean Welsh (EMORY UNIVESITY, Atlanta, Georgia, United States)

Abstract

Background: Hepatic steatosis is closely linked to cardiometabolic risk factors (CMRF) in adults; however, less is known in childhood. In particular, data is lacking in younger children because of the challenges in the accurate measurement of liver fat. We investigated hepatic steatosis (HS) and cardiometabolic risks in pre-pubertal Hispanic/Latino children. Methods: This was a prospective cohort study including 130 Hispanic/Latino children aged 6–9 years old (NCT05292352). Eight binary cardiometabolic risk factors (CMRFs) were combined into one risk CMRFs score (range 0–8): waist-to-height ratio (WHR) ≥0.5, triglycerides ≥100 mg/dL, total cholesterol (TC) ≥170 mg/dL, HDL <45 mg/dL, LDL >110 mg/dL, fasting glucose ≥100 mg/dL, HbA1c ≥ 5.7% and insulin >15 μU/mL. High-risk was classified as ≥3 CMRFs. HS was measured via MRI-proton density fat fraction (MRI-PDFF) and was defined as low (<3%), subclinical (3-5%), and clinical (≥5%). Prevalences of individual CMRFs and high-risk classification were compared across HS categories using Fisher’s exact tests. Statistical analysis was performed using R v.4.3.2. Results: Mean (SD) age was 8.0 (1.1), 42.3% female, 56.2% had a BMI >95 th percentile. The most prevalent CMRFs were increased WHR (73.1%), elevated TC (33.1%), and low HDL (32.3%). Prevalence of several individual CMRFs rose with increasing HS (p-trend < 0.0003 for all). Among those with HS <3%, 3-<5%, and ≥5% respectively, prevalences were, 1) High triglycerides: 6.7%, 25.0%, and 54.3%, 2) Low HDL: 15%, 29.2%, 56.5%; 3) High WHR: 48.3%, 87.5%, and 97.8%, and 4) High insulin: 1.7%, 16.7%, 26.1%. There was no significant trend between elevated HS and prevalence of high LDL, TC, HbA1C, or fasting glucose. The prevalence of high-risk conditions (≥3 CMRFs) increased from 16.7% among those with low HS to 37.5% and 54.3% among those with subclinical and clinical HS, respectively. None of the patients had more than 6 CMRFs. Conclusion: Over one-third of children of Hispanic/Latino school-age with subclinical steatosis of 3 - <5 % had ≥3 CMRFs. These findings support re-evaluating current pediatric guidelines, which recommend screening beginning at age 10 and intervention only for HS ≥5%.

Article Details

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (15)

A

Ana Ramirez Tovar

C

Cristian Sanchez Torres

Emory University, Decatur, Georgia, United States

S

Scott Gillespie

L

Liliana Aguayo

Emory University, Atlanta, Georgia, United States

H

Helaina Huneault

Emory University, Atlanta, Georgia, United States

C

Claudia Yaranga

Emory University, Atlanta, Georgia, United States

K

Karla DeSantos

Emory University, Atlanta, Georgia, United States

C

Christina Carapia-chaparro

Emory University, Atlanta, Georgia, United States

B

Brittany James

Emory University, Atlanta, Georgia, United States

G

Geetika Khanna

Children's Healthcare of Atlanta, Atlanta, Georgia, United States

J

Jack Knight-Scott

Children's Healthcare of Atlanta, Atlanta, Georgia, United States

A

Adina Alazraki

Children's Healthcare of Atlanta, Atlanta, Georgia, United States

S

Shasha Bai

M

Miriam Vos

EMORY UNIVERSITY, Atlanta, Georgia, United States

J

Jean Welsh

EMORY UNIVESITY, Atlanta, Georgia, United States