Nuclear Magnetic Resonance Derived Biomarkers for Evaluating Cardiometabolic Risk in Youth and Young Adults Across the Spectrum of Glucose Tolerance
Autor: | Sheela N. Magge, Alfredo Villalobos-Perez, Abby G. Meyers, Maureen Sampson, Joshua M. Dawson, Celeste K. Cravalho, Samantha Matta, Vandhna R. Sharma, Stephanie T. Chung, James D. Otvos |
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Rok vydání: | 2021 |
Předmět: |
Blood Glucose
Male Magnetic Resonance Spectroscopy glucose tolerance Endocrinology Diabetes and Metabolism medicine.medical_treatment Type 2 diabetes 030204 cardiovascular system & hematology Endocrinology 0302 clinical medicine insulin resistance cardiometabolic risk Prediabetes Original Research youth Prognosis Cardiovascular Diseases Homeostatic model assessment Female Adult medicine.medical_specialty Adolescent Lipoproteins 030209 endocrinology & metabolism Diseases of the endocrine glands. Clinical endocrinology Young Adult 03 medical and health sciences Insulin resistance Thinness Diabetes mellitus Internal medicine medicine Humans Obesity GlycA business.industry Insulin nutritional and metabolic diseases RC648-665 medicine.disease NMR Diabetes Mellitus Type 2 lipoprotein insulin resistance index Case-Control Studies business Amino Acids Branched-Chain Biomarkers Dyslipidemia Follow-Up Studies |
Zdroj: | Frontiers in Endocrinology, Vol 12 (2021) Frontiers in Endocrinology |
ISSN: | 1664-2392 |
DOI: | 10.3389/fendo.2021.665292 |
Popis: | Youth with obesity have an increased risk for cardiometabolic disease, but identifying those at highest risk remains a challenge. Four biomarkers that might serve this purpose are “by products” 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 and type 2 diabetes (T2DM) in adults (glycine inversely) and are independent of biological and methodological variations in insulin assays. However, their clinical utility in youth is unclear. We compared fasting levels of these biomarkers in 186 youth (42 lean normal glucose tolerant (NGT), 88 obese NGT, 23 with prediabetes (PreDM), and 33 with T2DM. All four biomarkers were associated with obesity and glycemia in youth. LPIR and GlycA were highest in youth with PreDM and T2DM, whereas glycine was lowest in youth with T2DM. While all four were correlated with HOMA-IR (Homeostatic Model Assessment for Insulin Resistance), LPIR had the strongest correlation (LPIR: r = 0.6; GlycA: r = 0.4, glycine: r = −0.4, BCAA: r = 0.2, all P < 0.01). All four markers correlated with HbA1c (LPIR, GlycA, BCAA: r ≥ 0.3 and glycine: r = −0.3, all P < 0.001). In multi-variable regression models, LPIR, GlycA, and glycine were independently associated with HOMA-IR (Adjusted R2 = 0.473, P < 0.001) and LPIR, glycine, and BCAA were independently associated with HbA1c (Adjusted R2 = 0.33, P < 0.001). An LPIR index of >44 was associated with elevated blood pressure, BMI, and dyslipidemia. Plasma NMR-derived markers were related to adverse markers of cardiometabolic risk in youth. LPIR, either alone or in combination with GlycA, should be explored as a non-insulin dependent predictive tool for development of insulin resistance and diabetes in youth.Clinical Trial RegistrationClinicaltrials.gov, identifier NCT:02960659 |
Databáze: | OpenAIRE |
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