1243-P: NMR-Derived Biomarkers Identify Cardiometabolic Disease Risk in Youth
| Autor: | Maureen Sampson, Alfredo Villalobos-Perez, Lilian Mabundo, Stephanie T. Chung, Abby G. Meyers, James D. Otvos, Amber B. Courville, Samantha Matta, Sheela N. Magge, Celeste K. Cravalho |
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| Rok vydání: | 2020 |
| Předmět: |
medicine.medical_specialty
endocrine system diseases business.industry Endocrinology Diabetes and Metabolism nutritional and metabolic diseases Disease Type 2 diabetes medicine.disease Obesity Blood pressure Insulin resistance Endocrinology Internal medicine Internal Medicine medicine Prediabetes Hemoglobin business Lipoprotein |
| Zdroj: | Diabetes. 69 |
| ISSN: | 1939-327X 0012-1797 |
| DOI: | 10.2337/db20-1243-p |
| Popis: | Youth with obesity have increased risk for cardiometabolic (CM) disease but identifying those at highest risk remains a challenge. 4 potential biomarkers are “byproducts” of clinical NMR LipoProfile® lipid testing: LPIR (Lipoprotein Insulin Resistance Index), GlycA (inflammation marker), BCAA (total branched-chain amino acids), and glycine. All are strongly related to insulin resistance (IR) and type 2 diabetes (T2D) in adults (glycine inversely), but their clinical utility in youth is unclear. We compared fasting levels of these biomarkers in 184 youth (42 lean normal glucose tolerant (NGT), 88 obese NGT and 54 obese with abnormal glucose tolerance (AGT; 20 with T2D and 34 with prediabetes) and determined their relationships with HOMA-IR (homeostatic model of IR) and hemoglobin A1c (HbA1c). Compared to lean and obese NGT, AGT youth had higher systolic blood pressure and HbA1c (Table). All 4 biomarkers were higher in youth with obesity vs. lean, while only LPIR was higher in AGT youth vs. obese NGT (Table). While all 4 were correlated with HOMA-IR, LPIR had the strongest correlation (LPIR: r=0.6; GlycA: r=0.4, glycine: r=-0.4, BCAA: r=0.2, all P Disclosure S.T. Chung: None. S. Matta: None. A. Meyers: None. C.K. Cravalho: None. A. Villalobos-Perez: None. L. Mabundo: None. A.B. Courville: None. M.L. Sampson: None. J.D. Otvos: Employee; Self; LabCorp. S.N. Magge: None. Funding National Institutes of Health (to S.T.C., L.M., A.B.C.) |
| Databáze: | OpenAIRE |
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