SPINA-GBeta | |
---|---|
Reference range | 0.64–3.73 pmol/s |
Calculator | https://doi.org/10.5281/zenodo.7479856 |
Purpose | Medical diagnosis, research |
Test of | Pancreatic beta cell function |
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).
The 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)
[G](∞): Fasting
blood glucose concentration (mg/dL)
Dβ:
EC50 for glucose at beta cells (7 mmol/L)
G3: Parameter for
pharmacokinetics (58,8 s/L)
SPINA-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]
In repeated measurements, SPINA-GBeta had higher retest reliability than HOMA-Beta, a measurement for beta cell function from the homeostasis model assessment. [1] [4]
In 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]
Together 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]
In 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]
SPINA-GBeta | |
---|---|
Reference range | 0.64–3.73 pmol/s |
Calculator | https://doi.org/10.5281/zenodo.7479856 |
Purpose | Medical diagnosis, research |
Test of | Pancreatic beta cell function |
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).
The 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)
[G](∞): Fasting
blood glucose concentration (mg/dL)
Dβ:
EC50 for glucose at beta cells (7 mmol/L)
G3: Parameter for
pharmacokinetics (58,8 s/L)
SPINA-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]
In repeated measurements, SPINA-GBeta had higher retest reliability than HOMA-Beta, a measurement for beta cell function from the homeostasis model assessment. [1] [4]
In 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]
Together 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]
In 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]