SPINA-GBeta
SPINA-GBeta is a calculated biomarker for pancreatic beta cell function.[1][a] It represents the maximum amount of insulin that beta cells can produce per time-unit (e.g. in one second). How to determine GBetaThe index is derived from a mathematical model of insulin-glucose homeostasis.[2] For diagnostic purposes, it is calculated from fasting insulin and glucose concentrations with: .[1] [I](∞): Fasting Insulin plasma concentration (μU/mL) Clinical significanceValiditySPINA-GBeta significantly correlates with the M value in glucose clamp studies and (better than HOMA-Beta) with the two-hour value in oral glucose tolerance testing (OGTT), glucose rise in OGTT, subscapular skinfold, truncal fat content and the HbA1c fraction.[1] It has the additional advantage that it circumvents the HOMA-blind zone, which renders the calculation of HOMA-Beta impossible if the fasting glucose concentration is 3.5 mmol/L (63 mg/dL) or below.[3] Unlike HOMA-Beta, SPINA-Beta can be sensibly calculated in the whole range of measurements.[1] ReliabilityIn repeated measurements, SPINA-GBeta had higher retest reliability than HOMA-Beta, a measurement for beta cell function from the homeostasis model assessment.[1][4] Clinical utilityIn the FAST study, an observational case-control sequencing study including 300 persons from Germany, SPINA-GBeta differed more clearly between subjects with and without diabetes than the corresponding HOMA-Beta index.[4] Scientific implications and other usesTogether with the reconstructed insulin receptor gain (SPINA-GR), SPINA-GBeta provides the foundation for the definition of a fasting based disposition index of insulin-glucose homeostasis (SPINA-DI).[4] In combination with SPINA-GR and whole-exome sequencing, calculating SPINA-GBeta helped to identify a new form of monogenetic diabetes (MODY) that is characterised by primary insulin resistance and results from a missense variant of the type 2 ryanodine receptor (RyR2) gene (p.N2291D).[5] Pathophysiological implicationsIn several populations, SPINA-GBeta correlated with the area under the glucose curve and 2-hour concentrations of glucose, insulin and proinsulin in oral glucose tolerance testing, concentrations of free fatty acids, ghrelin and adiponectin, and the HbA1c fraction.[4] Predictive aspectsIn a longitudinal evaluation of the NHANES study, a large sample of the general US population, over 10 years, reduced SPINA-GBeta significantly predicted all-cause mortality[6]. See alsoNotes
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