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
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