continuous glucose monitor sensors and transmitters Search Results


90
Meiqi Trading Co continuous glucose monitor (cgm) device
(A) Flow diagram of study design and participating patients. (B) Changes of daily insulin dose. Data of the same subject at different follow‐up time points are connected by gray lines. False discovery rate (represented as q ‐value) was calculated using repeated‐measures one‐way analysis of variance corrected by Benjamini and Hochberg method for multiple comparisons, n = 14. (C) Postprandial glucose excursions expressed as percentage of baseline during steamed bun meal test (SBMT). All data are represented as mean ± SEM, * q < 0.05 by mixed‐effects model for repeated measures corrected by Benjamini and Hochberg method, n = 9–12. (D–H) Changes of glycemic variability (GV) indices at 1 week (T1W) calculated using continuous glucose monitor <t>(CGM)</t> data: (D) MAGE, (E) SDBG, (F) BG > 11.1 mmol/L, (G) LAGE, and (H) MBG. † p < .05 by paired t test (two‐tailed), n = 14. (I–J) Changes of GV indices at T1W, 1 month (T1M), and 3 months (T3M) calculated using self‐monitoring of blood glucose data: (I) TIR and (J) hypoglycemic episodes. $ q < 0.05 as stated in (B); # q < 0.05 by repeated‐measures Friedman test corrected by Benjamini and Hochberg method, n = 14. (K) Representative CGM 24‐h glucose profiles demonstrating improved glycemic stability in two patients <t>by</t> <t>WMT.</t> Values of some GV indices were the same for different participants. Thus, both points and connecting lines overlapped with each other, exhibiting fewer than 14 points. LAGE, largest amplitude of glycemic excursions; MAGE, mean amplitude of glycemic excursion; MBG, mean blood glucose; SDBG, SD of blood glucose; TIR, time in range; WMT, washed microbiota transplantation.
Continuous Glucose Monitor (Cgm) Device, supplied by Meiqi Trading Co, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/continuous+glucose+monitor+sensors+and+transmitters/continuous+glucose+monitor++cgm++device/pmc10859319-55-9-14
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continuous glucose monitor (cgm) device - by Bioz Stars, 2026-09
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90
Senseonics continuous blood glucose monitoring system
(A) Flow diagram of study design and participating patients. (B) Changes of daily insulin dose. Data of the same subject at different follow‐up time points are connected by gray lines. False discovery rate (represented as q ‐value) was calculated using repeated‐measures one‐way analysis of variance corrected by Benjamini and Hochberg method for multiple comparisons, n = 14. (C) Postprandial glucose excursions expressed as percentage of baseline during steamed bun meal test (SBMT). All data are represented as mean ± SEM, * q < 0.05 by mixed‐effects model for repeated measures corrected by Benjamini and Hochberg method, n = 9–12. (D–H) Changes of glycemic variability (GV) indices at 1 week (T1W) calculated using continuous glucose monitor <t>(CGM)</t> data: (D) MAGE, (E) SDBG, (F) BG > 11.1 mmol/L, (G) LAGE, and (H) MBG. † p < .05 by paired t test (two‐tailed), n = 14. (I–J) Changes of GV indices at T1W, 1 month (T1M), and 3 months (T3M) calculated using self‐monitoring of blood glucose data: (I) TIR and (J) hypoglycemic episodes. $ q < 0.05 as stated in (B); # q < 0.05 by repeated‐measures Friedman test corrected by Benjamini and Hochberg method, n = 14. (K) Representative CGM 24‐h glucose profiles demonstrating improved glycemic stability in two patients <t>by</t> <t>WMT.</t> Values of some GV indices were the same for different participants. Thus, both points and connecting lines overlapped with each other, exhibiting fewer than 14 points. LAGE, largest amplitude of glycemic excursions; MAGE, mean amplitude of glycemic excursion; MBG, mean blood glucose; SDBG, SD of blood glucose; TIR, time in range; WMT, washed microbiota transplantation.
Continuous Blood Glucose Monitoring System, supplied by Senseonics, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/continuous+glucose+monitor+sensors+and+transmitters/continuous+glucose+monitoring+system/us09568362-17-10-2
Average 90 stars, based on 1 article reviews
continuous blood glucose monitoring system - by Bioz Stars, 2026-09
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90
MiniMed Inc minilinktm real-time transmitter continuous glucose monitoring system (rt-cgms)
(A) Flow diagram of study design and participating patients. (B) Changes of daily insulin dose. Data of the same subject at different follow‐up time points are connected by gray lines. False discovery rate (represented as q ‐value) was calculated using repeated‐measures one‐way analysis of variance corrected by Benjamini and Hochberg method for multiple comparisons, n = 14. (C) Postprandial glucose excursions expressed as percentage of baseline during steamed bun meal test (SBMT). All data are represented as mean ± SEM, * q < 0.05 by mixed‐effects model for repeated measures corrected by Benjamini and Hochberg method, n = 9–12. (D–H) Changes of glycemic variability (GV) indices at 1 week (T1W) calculated using continuous glucose monitor <t>(CGM)</t> data: (D) MAGE, (E) SDBG, (F) BG > 11.1 mmol/L, (G) LAGE, and (H) MBG. † p < .05 by paired t test (two‐tailed), n = 14. (I–J) Changes of GV indices at T1W, 1 month (T1M), and 3 months (T3M) calculated using self‐monitoring of blood glucose data: (I) TIR and (J) hypoglycemic episodes. $ q < 0.05 as stated in (B); # q < 0.05 by repeated‐measures Friedman test corrected by Benjamini and Hochberg method, n = 14. (K) Representative CGM 24‐h glucose profiles demonstrating improved glycemic stability in two patients <t>by</t> <t>WMT.</t> Values of some GV indices were the same for different participants. Thus, both points and connecting lines overlapped with each other, exhibiting fewer than 14 points. LAGE, largest amplitude of glycemic excursions; MAGE, mean amplitude of glycemic excursion; MBG, mean blood glucose; SDBG, SD of blood glucose; TIR, time in range; WMT, washed microbiota transplantation.
Minilinktm Real Time Transmitter Continuous Glucose Monitoring System (Rt Cgms), supplied by MiniMed Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/continuous+glucose+monitor+sensors+and+transmitters/minilinktm+real+time+transmitter+continuous+glucose+monitoring+system++rt+cgms+/pmc05898706__pone__0194759__s004-127-69-61
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minilinktm real-time transmitter continuous glucose monitoring system (rt-cgms) - by Bioz Stars, 2026-09
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MiniMed Inc continuous glucose monitoring system sensor
(A) Flow diagram of study design and participating patients. (B) Changes of daily insulin dose. Data of the same subject at different follow‐up time points are connected by gray lines. False discovery rate (represented as q ‐value) was calculated using repeated‐measures one‐way analysis of variance corrected by Benjamini and Hochberg method for multiple comparisons, n = 14. (C) Postprandial glucose excursions expressed as percentage of baseline during steamed bun meal test (SBMT). All data are represented as mean ± SEM, * q < 0.05 by mixed‐effects model for repeated measures corrected by Benjamini and Hochberg method, n = 9–12. (D–H) Changes of glycemic variability (GV) indices at 1 week (T1W) calculated using continuous glucose monitor <t>(CGM)</t> data: (D) MAGE, (E) SDBG, (F) BG > 11.1 mmol/L, (G) LAGE, and (H) MBG. † p < .05 by paired t test (two‐tailed), n = 14. (I–J) Changes of GV indices at T1W, 1 month (T1M), and 3 months (T3M) calculated using self‐monitoring of blood glucose data: (I) TIR and (J) hypoglycemic episodes. $ q < 0.05 as stated in (B); # q < 0.05 by repeated‐measures Friedman test corrected by Benjamini and Hochberg method, n = 14. (K) Representative CGM 24‐h glucose profiles demonstrating improved glycemic stability in two patients <t>by</t> <t>WMT.</t> Values of some GV indices were the same for different participants. Thus, both points and connecting lines overlapped with each other, exhibiting fewer than 14 points. LAGE, largest amplitude of glycemic excursions; MAGE, mean amplitude of glycemic excursion; MBG, mean blood glucose; SDBG, SD of blood glucose; TIR, time in range; WMT, washed microbiota transplantation.
Continuous Glucose Monitoring System Sensor, supplied by MiniMed Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/continuous+glucose+monitor+sensors+and+transmitters/glucose+sensor/pmc02769647-113-27-26
Average 90 stars, based on 1 article reviews
continuous glucose monitoring system sensor - by Bioz Stars, 2026-09
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MiniMed Inc continuous glucose monitoring system (cgms)
(A) Flow diagram of study design and participating patients. (B) Changes of daily insulin dose. Data of the same subject at different follow‐up time points are connected by gray lines. False discovery rate (represented as q ‐value) was calculated using repeated‐measures one‐way analysis of variance corrected by Benjamini and Hochberg method for multiple comparisons, n = 14. (C) Postprandial glucose excursions expressed as percentage of baseline during steamed bun meal test (SBMT). All data are represented as mean ± SEM, * q < 0.05 by mixed‐effects model for repeated measures corrected by Benjamini and Hochberg method, n = 9–12. (D–H) Changes of glycemic variability (GV) indices at 1 week (T1W) calculated using continuous glucose monitor <t>(CGM)</t> data: (D) MAGE, (E) SDBG, (F) BG > 11.1 mmol/L, (G) LAGE, and (H) MBG. † p < .05 by paired t test (two‐tailed), n = 14. (I–J) Changes of GV indices at T1W, 1 month (T1M), and 3 months (T3M) calculated using self‐monitoring of blood glucose data: (I) TIR and (J) hypoglycemic episodes. $ q < 0.05 as stated in (B); # q < 0.05 by repeated‐measures Friedman test corrected by Benjamini and Hochberg method, n = 14. (K) Representative CGM 24‐h glucose profiles demonstrating improved glycemic stability in two patients <t>by</t> <t>WMT.</t> Values of some GV indices were the same for different participants. Thus, both points and connecting lines overlapped with each other, exhibiting fewer than 14 points. LAGE, largest amplitude of glycemic excursions; MAGE, mean amplitude of glycemic excursion; MBG, mean blood glucose; SDBG, SD of blood glucose; TIR, time in range; WMT, washed microbiota transplantation.
Continuous Glucose Monitoring System (Cgms), supplied by MiniMed Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/continuous+glucose+monitor+sensors+and+transmitters/continuous+glucose+monitoring+system++cgms/pmc02901039-110-10-19
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MiniMed Inc guardian® real-time cgms
(A) Flow diagram of study design and participating patients. (B) Changes of daily insulin dose. Data of the same subject at different follow‐up time points are connected by gray lines. False discovery rate (represented as q ‐value) was calculated using repeated‐measures one‐way analysis of variance corrected by Benjamini and Hochberg method for multiple comparisons, n = 14. (C) Postprandial glucose excursions expressed as percentage of baseline during steamed bun meal test (SBMT). All data are represented as mean ± SEM, * q < 0.05 by mixed‐effects model for repeated measures corrected by Benjamini and Hochberg method, n = 9–12. (D–H) Changes of glycemic variability (GV) indices at 1 week (T1W) calculated using continuous glucose monitor <t>(CGM)</t> data: (D) MAGE, (E) SDBG, (F) BG > 11.1 mmol/L, (G) LAGE, and (H) MBG. † p < .05 by paired t test (two‐tailed), n = 14. (I–J) Changes of GV indices at T1W, 1 month (T1M), and 3 months (T3M) calculated using self‐monitoring of blood glucose data: (I) TIR and (J) hypoglycemic episodes. $ q < 0.05 as stated in (B); # q < 0.05 by repeated‐measures Friedman test corrected by Benjamini and Hochberg method, n = 14. (K) Representative CGM 24‐h glucose profiles demonstrating improved glycemic stability in two patients <t>by</t> <t>WMT.</t> Values of some GV indices were the same for different participants. Thus, both points and connecting lines overlapped with each other, exhibiting fewer than 14 points. LAGE, largest amplitude of glycemic excursions; MAGE, mean amplitude of glycemic excursion; MBG, mean blood glucose; SDBG, SD of blood glucose; TIR, time in range; WMT, washed microbiota transplantation.
Guardian® Real Time Cgms, supplied by MiniMed Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/continuous+glucose+monitor+sensors+and+transmitters/guardian++real+time+glucose+monitor/pmc04756700-132-11-18
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MiniMed Inc ipro continuous glucose monitoring systems
(A) Flow diagram of study design and participating patients. (B) Changes of daily insulin dose. Data of the same subject at different follow‐up time points are connected by gray lines. False discovery rate (represented as q ‐value) was calculated using repeated‐measures one‐way analysis of variance corrected by Benjamini and Hochberg method for multiple comparisons, n = 14. (C) Postprandial glucose excursions expressed as percentage of baseline during steamed bun meal test (SBMT). All data are represented as mean ± SEM, * q < 0.05 by mixed‐effects model for repeated measures corrected by Benjamini and Hochberg method, n = 9–12. (D–H) Changes of glycemic variability (GV) indices at 1 week (T1W) calculated using continuous glucose monitor <t>(CGM)</t> data: (D) MAGE, (E) SDBG, (F) BG > 11.1 mmol/L, (G) LAGE, and (H) MBG. † p < .05 by paired t test (two‐tailed), n = 14. (I–J) Changes of GV indices at T1W, 1 month (T1M), and 3 months (T3M) calculated using self‐monitoring of blood glucose data: (I) TIR and (J) hypoglycemic episodes. $ q < 0.05 as stated in (B); # q < 0.05 by repeated‐measures Friedman test corrected by Benjamini and Hochberg method, n = 14. (K) Representative CGM 24‐h glucose profiles demonstrating improved glycemic stability in two patients <t>by</t> <t>WMT.</t> Values of some GV indices were the same for different participants. Thus, both points and connecting lines overlapped with each other, exhibiting fewer than 14 points. LAGE, largest amplitude of glycemic excursions; MAGE, mean amplitude of glycemic excursion; MBG, mean blood glucose; SDBG, SD of blood glucose; TIR, time in range; WMT, washed microbiota transplantation.
Ipro Continuous Glucose Monitoring Systems, supplied by MiniMed Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/continuous+glucose+monitor+sensors+and+transmitters/ipro+continuous+glucose+monitor+system/pmc05898706__pone__0194759__s004-814-49-58
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ipro continuous glucose monitoring systems - by Bioz Stars, 2026-09
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Human Kinetics Inc continuous glucose monitoring
(A) Flow diagram of study design and participating patients. (B) Changes of daily insulin dose. Data of the same subject at different follow‐up time points are connected by gray lines. False discovery rate (represented as q ‐value) was calculated using repeated‐measures one‐way analysis of variance corrected by Benjamini and Hochberg method for multiple comparisons, n = 14. (C) Postprandial glucose excursions expressed as percentage of baseline during steamed bun meal test (SBMT). All data are represented as mean ± SEM, * q < 0.05 by mixed‐effects model for repeated measures corrected by Benjamini and Hochberg method, n = 9–12. (D–H) Changes of glycemic variability (GV) indices at 1 week (T1W) calculated using continuous glucose monitor <t>(CGM)</t> data: (D) MAGE, (E) SDBG, (F) BG > 11.1 mmol/L, (G) LAGE, and (H) MBG. † p < .05 by paired t test (two‐tailed), n = 14. (I–J) Changes of GV indices at T1W, 1 month (T1M), and 3 months (T3M) calculated using self‐monitoring of blood glucose data: (I) TIR and (J) hypoglycemic episodes. $ q < 0.05 as stated in (B); # q < 0.05 by repeated‐measures Friedman test corrected by Benjamini and Hochberg method, n = 14. (K) Representative CGM 24‐h glucose profiles demonstrating improved glycemic stability in two patients <t>by</t> <t>WMT.</t> Values of some GV indices were the same for different participants. Thus, both points and connecting lines overlapped with each other, exhibiting fewer than 14 points. LAGE, largest amplitude of glycemic excursions; MAGE, mean amplitude of glycemic excursion; MBG, mean blood glucose; SDBG, SD of blood glucose; TIR, time in range; WMT, washed microbiota transplantation.
Continuous Glucose Monitoring, supplied by Human Kinetics Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/continuous+glucose+monitor+sensors+and+transmitters/continuous+glucose+monitoring/pm28422556-19-4-62
Average 90 stars, based on 1 article reviews
continuous glucose monitoring - by Bioz Stars, 2026-09
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Dexcom Inc g6 continuous glucose monitoring cgm
(A) Flow diagram of study design and participating patients. (B) Changes of daily insulin dose. Data of the same subject at different follow‐up time points are connected by gray lines. False discovery rate (represented as q ‐value) was calculated using repeated‐measures one‐way analysis of variance corrected by Benjamini and Hochberg method for multiple comparisons, n = 14. (C) Postprandial glucose excursions expressed as percentage of baseline during steamed bun meal test (SBMT). All data are represented as mean ± SEM, * q < 0.05 by mixed‐effects model for repeated measures corrected by Benjamini and Hochberg method, n = 9–12. (D–H) Changes of glycemic variability (GV) indices at 1 week (T1W) calculated using continuous glucose monitor <t>(CGM)</t> data: (D) MAGE, (E) SDBG, (F) BG > 11.1 mmol/L, (G) LAGE, and (H) MBG. † p < .05 by paired t test (two‐tailed), n = 14. (I–J) Changes of GV indices at T1W, 1 month (T1M), and 3 months (T3M) calculated using self‐monitoring of blood glucose data: (I) TIR and (J) hypoglycemic episodes. $ q < 0.05 as stated in (B); # q < 0.05 by repeated‐measures Friedman test corrected by Benjamini and Hochberg method, n = 14. (K) Representative CGM 24‐h glucose profiles demonstrating improved glycemic stability in two patients <t>by</t> <t>WMT.</t> Values of some GV indices were the same for different participants. Thus, both points and connecting lines overlapped with each other, exhibiting fewer than 14 points. LAGE, largest amplitude of glycemic excursions; MAGE, mean amplitude of glycemic excursion; MBG, mean blood glucose; SDBG, SD of blood glucose; TIR, time in range; WMT, washed microbiota transplantation.
G6 Continuous Glucose Monitoring Cgm, supplied by Dexcom Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/continuous+glucose+monitor+sensors+and+transmitters/cgm+dexcom+g6/10__1089_slash_dia__2022__2525__abstracts-2847-23-22
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g6 continuous glucose monitoring cgm - by Bioz Stars, 2026-09
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Dexcom Inc continuous glucose monitors
(A) Flow diagram of study design and participating patients. (B) Changes of daily insulin dose. Data of the same subject at different follow‐up time points are connected by gray lines. False discovery rate (represented as q ‐value) was calculated using repeated‐measures one‐way analysis of variance corrected by Benjamini and Hochberg method for multiple comparisons, n = 14. (C) Postprandial glucose excursions expressed as percentage of baseline during steamed bun meal test (SBMT). All data are represented as mean ± SEM, * q < 0.05 by mixed‐effects model for repeated measures corrected by Benjamini and Hochberg method, n = 9–12. (D–H) Changes of glycemic variability (GV) indices at 1 week (T1W) calculated using continuous glucose monitor <t>(CGM)</t> data: (D) MAGE, (E) SDBG, (F) BG > 11.1 mmol/L, (G) LAGE, and (H) MBG. † p < .05 by paired t test (two‐tailed), n = 14. (I–J) Changes of GV indices at T1W, 1 month (T1M), and 3 months (T3M) calculated using self‐monitoring of blood glucose data: (I) TIR and (J) hypoglycemic episodes. $ q < 0.05 as stated in (B); # q < 0.05 by repeated‐measures Friedman test corrected by Benjamini and Hochberg method, n = 14. (K) Representative CGM 24‐h glucose profiles demonstrating improved glycemic stability in two patients <t>by</t> <t>WMT.</t> Values of some GV indices were the same for different participants. Thus, both points and connecting lines overlapped with each other, exhibiting fewer than 14 points. LAGE, largest amplitude of glycemic excursions; MAGE, mean amplitude of glycemic excursion; MBG, mean blood glucose; SDBG, SD of blood glucose; TIR, time in range; WMT, washed microbiota transplantation.
Continuous Glucose Monitors, supplied by Dexcom Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/continuous+glucose+monitor+sensors+and+transmitters/continuous+glucose+monitors/pm41894403-23-13-17
Average 86 stars, based on 1 article reviews
continuous glucose monitors - by Bioz Stars, 2026-09
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Dexcom Inc g6 subcutaneous continuous glucose monitoring
(A) Flow diagram of study design and participating patients. (B) Changes of daily insulin dose. Data of the same subject at different follow‐up time points are connected by gray lines. False discovery rate (represented as q ‐value) was calculated using repeated‐measures one‐way analysis of variance corrected by Benjamini and Hochberg method for multiple comparisons, n = 14. (C) Postprandial glucose excursions expressed as percentage of baseline during steamed bun meal test (SBMT). All data are represented as mean ± SEM, * q < 0.05 by mixed‐effects model for repeated measures corrected by Benjamini and Hochberg method, n = 9–12. (D–H) Changes of glycemic variability (GV) indices at 1 week (T1W) calculated using continuous glucose monitor <t>(CGM)</t> data: (D) MAGE, (E) SDBG, (F) BG > 11.1 mmol/L, (G) LAGE, and (H) MBG. † p < .05 by paired t test (two‐tailed), n = 14. (I–J) Changes of GV indices at T1W, 1 month (T1M), and 3 months (T3M) calculated using self‐monitoring of blood glucose data: (I) TIR and (J) hypoglycemic episodes. $ q < 0.05 as stated in (B); # q < 0.05 by repeated‐measures Friedman test corrected by Benjamini and Hochberg method, n = 14. (K) Representative CGM 24‐h glucose profiles demonstrating improved glycemic stability in two patients <t>by</t> <t>WMT.</t> Values of some GV indices were the same for different participants. Thus, both points and connecting lines overlapped with each other, exhibiting fewer than 14 points. LAGE, largest amplitude of glycemic excursions; MAGE, mean amplitude of glycemic excursion; MBG, mean blood glucose; SDBG, SD of blood glucose; TIR, time in range; WMT, washed microbiota transplantation.
G6 Subcutaneous Continuous Glucose Monitoring, supplied by Dexcom Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/continuous+glucose+monitor+sensors+and+transmitters/continuous+infusion+insulin+pumps+sets+subcutaneous/pmc12622854-6-6-11
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Dexcom Inc continuous glucose monitor cgm
(A) Flow diagram of study design and participating patients. (B) Changes of daily insulin dose. Data of the same subject at different follow‐up time points are connected by gray lines. False discovery rate (represented as q ‐value) was calculated using repeated‐measures one‐way analysis of variance corrected by Benjamini and Hochberg method for multiple comparisons, n = 14. (C) Postprandial glucose excursions expressed as percentage of baseline during steamed bun meal test (SBMT). All data are represented as mean ± SEM, * q < 0.05 by mixed‐effects model for repeated measures corrected by Benjamini and Hochberg method, n = 9–12. (D–H) Changes of glycemic variability (GV) indices at 1 week (T1W) calculated using continuous glucose monitor <t>(CGM)</t> data: (D) MAGE, (E) SDBG, (F) BG > 11.1 mmol/L, (G) LAGE, and (H) MBG. † p < .05 by paired t test (two‐tailed), n = 14. (I–J) Changes of GV indices at T1W, 1 month (T1M), and 3 months (T3M) calculated using self‐monitoring of blood glucose data: (I) TIR and (J) hypoglycemic episodes. $ q < 0.05 as stated in (B); # q < 0.05 by repeated‐measures Friedman test corrected by Benjamini and Hochberg method, n = 14. (K) Representative CGM 24‐h glucose profiles demonstrating improved glycemic stability in two patients <t>by</t> <t>WMT.</t> Values of some GV indices were the same for different participants. Thus, both points and connecting lines overlapped with each other, exhibiting fewer than 14 points. LAGE, largest amplitude of glycemic excursions; MAGE, mean amplitude of glycemic excursion; MBG, mean blood glucose; SDBG, SD of blood glucose; TIR, time in range; WMT, washed microbiota transplantation.
Continuous Glucose Monitor Cgm, supplied by Dexcom Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/continuous+glucose+monitor+sensors+and+transmitters/blood+glucose+monitor/arxiv__2507__19609-47-1-6
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Image Search Results


(A) Flow diagram of study design and participating patients. (B) Changes of daily insulin dose. Data of the same subject at different follow‐up time points are connected by gray lines. False discovery rate (represented as q ‐value) was calculated using repeated‐measures one‐way analysis of variance corrected by Benjamini and Hochberg method for multiple comparisons, n = 14. (C) Postprandial glucose excursions expressed as percentage of baseline during steamed bun meal test (SBMT). All data are represented as mean ± SEM, * q < 0.05 by mixed‐effects model for repeated measures corrected by Benjamini and Hochberg method, n = 9–12. (D–H) Changes of glycemic variability (GV) indices at 1 week (T1W) calculated using continuous glucose monitor (CGM) data: (D) MAGE, (E) SDBG, (F) BG > 11.1 mmol/L, (G) LAGE, and (H) MBG. † p < .05 by paired t test (two‐tailed), n = 14. (I–J) Changes of GV indices at T1W, 1 month (T1M), and 3 months (T3M) calculated using self‐monitoring of blood glucose data: (I) TIR and (J) hypoglycemic episodes. $ q < 0.05 as stated in (B); # q < 0.05 by repeated‐measures Friedman test corrected by Benjamini and Hochberg method, n = 14. (K) Representative CGM 24‐h glucose profiles demonstrating improved glycemic stability in two patients by WMT. Values of some GV indices were the same for different participants. Thus, both points and connecting lines overlapped with each other, exhibiting fewer than 14 points. LAGE, largest amplitude of glycemic excursions; MAGE, mean amplitude of glycemic excursion; MBG, mean blood glucose; SDBG, SD of blood glucose; TIR, time in range; WMT, washed microbiota transplantation.

Journal: Journal of Diabetes

Article Title: Washed microbiota transplantation reduces glycemic variability in unstable diabetes

doi: 10.1111/1753-0407.13485

Figure Lengend Snippet: (A) Flow diagram of study design and participating patients. (B) Changes of daily insulin dose. Data of the same subject at different follow‐up time points are connected by gray lines. False discovery rate (represented as q ‐value) was calculated using repeated‐measures one‐way analysis of variance corrected by Benjamini and Hochberg method for multiple comparisons, n = 14. (C) Postprandial glucose excursions expressed as percentage of baseline during steamed bun meal test (SBMT). All data are represented as mean ± SEM, * q < 0.05 by mixed‐effects model for repeated measures corrected by Benjamini and Hochberg method, n = 9–12. (D–H) Changes of glycemic variability (GV) indices at 1 week (T1W) calculated using continuous glucose monitor (CGM) data: (D) MAGE, (E) SDBG, (F) BG > 11.1 mmol/L, (G) LAGE, and (H) MBG. † p < .05 by paired t test (two‐tailed), n = 14. (I–J) Changes of GV indices at T1W, 1 month (T1M), and 3 months (T3M) calculated using self‐monitoring of blood glucose data: (I) TIR and (J) hypoglycemic episodes. $ q < 0.05 as stated in (B); # q < 0.05 by repeated‐measures Friedman test corrected by Benjamini and Hochberg method, n = 14. (K) Representative CGM 24‐h glucose profiles demonstrating improved glycemic stability in two patients by WMT. Values of some GV indices were the same for different participants. Thus, both points and connecting lines overlapped with each other, exhibiting fewer than 14 points. LAGE, largest amplitude of glycemic excursions; MAGE, mean amplitude of glycemic excursion; MBG, mean blood glucose; SDBG, SD of blood glucose; TIR, time in range; WMT, washed microbiota transplantation.

Article Snippet: Three days before WMT, patients were implanted with a continuous glucose monitor (CGM) device (MeiQi Medical Instruments Co., Ltd., Huzhou, China).

Techniques: Two Tailed Test, Transplantation Assay

Washed microbiota transplantation (WMT) alters profiles of serum metabolites. (A) Heatmap showing changes of serum metabolites determined by non‐targeted metabolomics, n = 11–14. (B) Heatmap of Spearman's correlation coefficients between serum metabolites and glycemic variability (GV) indices. (C) The 8 positively correlated metabolites between fecal and serum compartments. Color range varies from light red (weaker correlation) to dark red (stronger correlation). Statistical methods were the same as stated in Figure . AUC, area under the curve; BG, blood glucose; CGM, continuous glucose monitor; CV, coefficient of variation; HbA1c, glycated hemoglobin; LAGE, largest amplitude of glycemic excursions; MBG, mean blood glucose; PPGE, postprandial glucose excursion; SBMT, steamed bun meal test; SMBG, self‐monitoring of blood glucose; TIR, time in range.

Journal: Journal of Diabetes

Article Title: Washed microbiota transplantation reduces glycemic variability in unstable diabetes

doi: 10.1111/1753-0407.13485

Figure Lengend Snippet: Washed microbiota transplantation (WMT) alters profiles of serum metabolites. (A) Heatmap showing changes of serum metabolites determined by non‐targeted metabolomics, n = 11–14. (B) Heatmap of Spearman's correlation coefficients between serum metabolites and glycemic variability (GV) indices. (C) The 8 positively correlated metabolites between fecal and serum compartments. Color range varies from light red (weaker correlation) to dark red (stronger correlation). Statistical methods were the same as stated in Figure . AUC, area under the curve; BG, blood glucose; CGM, continuous glucose monitor; CV, coefficient of variation; HbA1c, glycated hemoglobin; LAGE, largest amplitude of glycemic excursions; MBG, mean blood glucose; PPGE, postprandial glucose excursion; SBMT, steamed bun meal test; SMBG, self‐monitoring of blood glucose; TIR, time in range.

Article Snippet: Three days before WMT, patients were implanted with a continuous glucose monitor (CGM) device (MeiQi Medical Instruments Co., Ltd., Huzhou, China).

Techniques: Transplantation Assay