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Citation

Kim, Daeeun; Justice, Anne E.; Chittoor, Geetha; Blanco, Estela; Burrows, Raquel A.; Graff, Mariaelisa; Howard, Annie Green; Wang, Yujie; Rohde, Rebecca R.; & Buchanan, Victoria L., et al. (2022). Genetic Determinants of Metabolic Biomarkers and Their Associations with Cardiometabolic Traits in Hispanic/Latino Adolescents. Pediatric Research, 92(2), 563-571. PMCID: PMC9005573

Abstract

BACKGROUND: Metabolic regulation plays a significant role in energy homeostasis, and adolescence is a crucial life stage for the development of cardiometabolic disease (CMD). This study aims to investigate the genetic determinants of metabolic biomarkers-adiponectin, leptin, ghrelin, and orexin-and their associations with CMD risk factors.
METHODS: We characterized the genetic determinants of the biomarkers among Hispanic/Latino adolescents of the Santiago Longitudinal Study (SLS) and identified the cumulative effects of genetic variants on adiponectin and leptin using biomarker polygenic risk scores (PRS). We further investigated the direct and indirect effect of the biomarker PRS on downstream body fat percent (BF%) and glycemic traits using structural equation modeling.
RESULTS: We identified putatively novel genetic variants associated with the metabolic biomarkers. A substantial amount of biomarker variance was explained by SLS-specific PRS, and the prediction was improved by including the putatively novel loci. Fasting blood insulin and insulin resistance were associated with PRS for adiponectin, leptin, and ghrelin, and BF% was associated with PRS for adiponectin and leptin. We found evidence of substantial mediation of these associations by the biomarker levels.
CONCLUSIONS: The genetic underpinnings of metabolic biomarkers can affect the early development of CMD, partly mediated by the biomarkers.
IMPACT: This study characterized the genetic underpinnings of four metabolic hormones and investigated their potential influence on adiposity and insulin biology among Hispanic/Latino adolescents. Fasting blood insulin and insulin resistance were associated with polygenic risk score (PRS) for adiponectin, leptin, and ghrelin, with evidence of some degree of mediation by the biomarker levels. Body fat percent (BF%) was also associated with PRS for adiponectin and leptin. This provides important insight on biological mechanisms underlying early metabolic dysfunction and reveals candidates for prevention efforts. Our findings also highlight the importance of ancestrally diverse populations to facilitate valid studies of the genetic architecture of metabolic biomarker levels.

URL

http://dx.doi.org/10.1038/s41390-021-01729-7

Reference Type

Journal Article

Year Published

2022

Journal Title

Pediatric Research

Author(s)

Kim, Daeeun
Justice, Anne E.
Chittoor, Geetha
Blanco, Estela
Burrows, Raquel A.
Graff, Mariaelisa
Howard, Annie Green
Wang, Yujie
Rohde, Rebecca R.
Buchanan, Victoria L.
Voruganti, V. Saroja
Almeida, Marcio
Peralta, Juan M.
Lehman, Donna M.
Curran, Joanne E.
Comuzzie, Anthony G.
Duggirala, Ravindranath
Blangero, John
Albala, Cecilia
Santos, José L.
Angel, Bárbara
Lozoff, Betsy
Gahagan, Sheila
North, Kari E.

Article Type

Regular

PMCID

PMC9005573

Data Set/Study

Santiago Longitudinal Study

Continent/Country

Chile

Race/Ethnicity

Hispanic Ancestry

ORCiD

Howard, AG - 0000-0003-0837-8166