24 research outputs found
Accuracy of Continuous Glucose Monitoring Measurements in Normo-Glycemic Individuals
<div><p>Background</p><p>The validity of continuous glucose monitoring (CGM) is well established in diabetic patients. CGM is also increasingly used for research purposes in normo-glycemic individuals, but the CGM validity in such individuals is unknown. We studied the accuracy of CGM measurements in normo-glycemic individuals by comparing CGM-derived versus venous blood-derived glucose levels and measures of glycemia and glycemic variability.</p><p>Methods</p><p>In 34 healthy participants (mean age 65.7 years), glucose was simultaneously measured every 10 minutes, via both an Enlite<sup>®</sup> CGM sensor, and in venous blood sampled over a 24-hour period. Validity of CGM-derived individual glucose measurements, calculated measures of glycemia over daytime (09:00h-23:00h) and nighttime (23:00h-09:00h), and calculated measures of glycemic variability (e.g. 24h standard deviation [SD]) were assessed by Pearson correlation coefficients, mean absolute relative difference (MARD) and paired t-tests.</p><p>Results</p><p>The median correlation coefficient between CGM and venous glucose measurements per participant was 0.68 (interquartile range: 0.40–0.78), and the MARD was 17.6% (SD = 17%). Compared with venous sampling, the calculated measure of glycemia during daytime was 0.22 mmol/L higher when derived from CGM, but no difference was observed during nighttime. Most measures of glycemic variability were lower with CGM than with venous blood sampling (e.g., 24h SD: 1.07 with CGM and 1.26 with venous blood; p-value = 0.004).</p><p>Conclusion</p><p>In normo-glycemic individuals, CGM-derived glucose measurements had good agreement with venous glucose levels. However, the measure of glycemia was higher during the day and most measures of glycemic variability were lower when derived from CGM.</p></div
Per-person Pearson correlations coefficients between venous- and continuous glucose monitoring (CGM)- derived glucose levels.
<p>Bar chart showing the distribution of the Pearson correlations between paired CGM and venous glucose measurements determined for each of the 34 participants. Dashed line represents the median per-person Pearson correlation.</p
Venous- and continuous glucose monitoring (CGM)- derived glucose during 24h period.
<p>Data presented as the mean (SE) glucose level every 10 minutes. In red, the continuous glucose monitoring measurement data. In blue, the venous blood glucose measurement data.</p
Bland-Altman plots of individual glucose measurements.
<p>Each dot represents one paired (CGM and venous) glucose measurement (N = 4,523 data points derived from 34 participants). The bias of the measurements (represented as the solid lines) and the ± 1.96 SD (dotted lines) are presented for the measurements obtained (A) over 24 hours, (B) during the day (09.00h–23.00h), and (C) during the night (23.00h–09.00h).</p
Characteristics of the study population.
<p>Data represent mean with standard deviation unless stated otherwise.</p><p>Characteristics of the study population.</p
Table_6_High Adiposity Is Associated With Higher Nocturnal and Diurnal Glycaemia, but Not With Glycemic Variability in Older Individuals Without Diabetes.docx
Background<p>It is well known that adiposity is a risk factor for insulin resistance and type 2 diabetes mellitus. In the present study, we aimed to investigate the associations of measures of adiposity with indices of glycemia and of glycemic variability over a 72-h period in non-diabetic older adults.</p>Methods<p>This cross-sectional study was conducted in non-diabetic individuals from the Active and Healthy Aging Study (N = 228), Switchbox (N = 116), and the Growing Old Together Study (N = 94). Body mass index (BMI) and waist circumference were measured, and indices of glycemia and glycemic variability were derived from continuous glucose monitoring (CGM) using the Mini-Med<sup>®</sup> CGM system. Associations between adiposity and CGM were studied separately for the three cohorts, and derived estimates were subsequently meta-analyzed.</p>Results<p>After meta-analyzing the results from the separate cohorts, individuals with a higher BMI had higher levels of glycemia. Individuals with BMI between 30 and 35 kg/m<sup>2</sup> had 0.28 mmol/L [95% confidence interval (CI): 0.12–0.44] higher 72 h-mean glucose concentration, 0.26 mmol/L (0.10–0.42) higher diurnal glucose (6:00 a.m. to 0:00 a.m.), and 0.39 mmol/L (0.19; 0.59) higher nocturnal glucose (3:00 a.m. to 6:00 a.m.) than participants with a normal weight (BMI 18.5–25 kg/m<sup>2</sup>). However, no associations were observed between higher BMI and glycemic variability. Results for glycemia and glycemic variability were similarly observed for a high waist circumference.</p>Conclusion<p>High adiposity associates with constant higher mean glucose levels over the day in non-diabetic older adults.</p
Table_2_High Adiposity Is Associated With Higher Nocturnal and Diurnal Glycaemia, but Not With Glycemic Variability in Older Individuals Without Diabetes.docx
Background<p>It is well known that adiposity is a risk factor for insulin resistance and type 2 diabetes mellitus. In the present study, we aimed to investigate the associations of measures of adiposity with indices of glycemia and of glycemic variability over a 72-h period in non-diabetic older adults.</p>Methods<p>This cross-sectional study was conducted in non-diabetic individuals from the Active and Healthy Aging Study (N = 228), Switchbox (N = 116), and the Growing Old Together Study (N = 94). Body mass index (BMI) and waist circumference were measured, and indices of glycemia and glycemic variability were derived from continuous glucose monitoring (CGM) using the Mini-Med<sup>®</sup> CGM system. Associations between adiposity and CGM were studied separately for the three cohorts, and derived estimates were subsequently meta-analyzed.</p>Results<p>After meta-analyzing the results from the separate cohorts, individuals with a higher BMI had higher levels of glycemia. Individuals with BMI between 30 and 35 kg/m<sup>2</sup> had 0.28 mmol/L [95% confidence interval (CI): 0.12–0.44] higher 72 h-mean glucose concentration, 0.26 mmol/L (0.10–0.42) higher diurnal glucose (6:00 a.m. to 0:00 a.m.), and 0.39 mmol/L (0.19; 0.59) higher nocturnal glucose (3:00 a.m. to 6:00 a.m.) than participants with a normal weight (BMI 18.5–25 kg/m<sup>2</sup>). However, no associations were observed between higher BMI and glycemic variability. Results for glycemia and glycemic variability were similarly observed for a high waist circumference.</p>Conclusion<p>High adiposity associates with constant higher mean glucose levels over the day in non-diabetic older adults.</p
Fasting and Continuous Glucose Monitoring parameters over 72-hour period for carriers of the protective (CC) and risk (CT/TT) alleles of rs7903146 in <i>TCF7L2</i>.
<p>Fasting and Continuous Glucose Monitoring parameters over 72-hour period for carriers of the protective (CC) and risk (CT/TT) alleles of rs7903146 in <i>TCF7L2</i>.</p
Glucose rhythm over the three days, stratified per genotype group.
<p>Mean glucose rhythms during 72 hours for carriers of the protective alleles (black line) and the risk alleles (grey line) of rs7903146 in <i>TCF7L2</i>. The time span between the dotted black lines (3.00–6.00h) represents the nocturnal hours during which people are (on average) fast asleep.</p
Table_5_High Adiposity Is Associated With Higher Nocturnal and Diurnal Glycaemia, but Not With Glycemic Variability in Older Individuals Without Diabetes.docx
Background<p>It is well known that adiposity is a risk factor for insulin resistance and type 2 diabetes mellitus. In the present study, we aimed to investigate the associations of measures of adiposity with indices of glycemia and of glycemic variability over a 72-h period in non-diabetic older adults.</p>Methods<p>This cross-sectional study was conducted in non-diabetic individuals from the Active and Healthy Aging Study (N = 228), Switchbox (N = 116), and the Growing Old Together Study (N = 94). Body mass index (BMI) and waist circumference were measured, and indices of glycemia and glycemic variability were derived from continuous glucose monitoring (CGM) using the Mini-Med<sup>®</sup> CGM system. Associations between adiposity and CGM were studied separately for the three cohorts, and derived estimates were subsequently meta-analyzed.</p>Results<p>After meta-analyzing the results from the separate cohorts, individuals with a higher BMI had higher levels of glycemia. Individuals with BMI between 30 and 35 kg/m<sup>2</sup> had 0.28 mmol/L [95% confidence interval (CI): 0.12–0.44] higher 72 h-mean glucose concentration, 0.26 mmol/L (0.10–0.42) higher diurnal glucose (6:00 a.m. to 0:00 a.m.), and 0.39 mmol/L (0.19; 0.59) higher nocturnal glucose (3:00 a.m. to 6:00 a.m.) than participants with a normal weight (BMI 18.5–25 kg/m<sup>2</sup>). However, no associations were observed between higher BMI and glycemic variability. Results for glycemia and glycemic variability were similarly observed for a high waist circumference.</p>Conclusion<p>High adiposity associates with constant higher mean glucose levels over the day in non-diabetic older adults.</p