TY - JOUR
T1 - Needle-free injection of basal insulin improves fasting glucose variability as assessed by continuous glucose monitoring in T2DM
T2 - a prospective randomized multicenter open-label crossover study
AU - Sun, Fei
AU - Gao, Bin
AU - Yang, Aili
AU - Ren, Lijun
AU - Xing, Ying
AU - Ma, Kaiyan
AU - Tian, Li
AU - Li, Simin
AU - Heng, Chunni
AU - Liu, Hao
AU - Zhou, Jie
AU - Ji, Qiuhe
N1 - Publisher Copyright:
© 2022 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2022
Y1 - 2022
N2 - Background: Fasting glucose variability (FGV) extensively promotes the onset and development of diabetic complications. This study aimed to evaluate the FGV in type 2 diabetes mellitus (T2DM) patients administered basal insulin using a needle-free insulin injector (NFII). Research design and methods: This was a prospective randomized multicenter open-label crossover study. We randomly assigned 48 T2DM patients to receive basal insulin by NFII or conventional insulin pen (CIP) for 7–14 days and were then crossed over after washout. We conducted continuous glucose monitoring to investigate the FGV, our primary outcome was a composite parameter of the FGV with a fasting blood glucose target between 4.4 and 6.1 mmol/L. Results: The coefficient of variation for sensor glucose at 6 a.m. with CIP was 11.67 (8.70,14.81)% vs. 9.48 (6.48,12.24)% with NFII (p = 0.003), and the coefficient of variation for mean sensor glucose at 5–6 a.m. with CIP was 12.70 (9.17,16.56)% vs. 9.23 (7.01,11.98)% with NFII (p < 0.001). The overall basal insulin dosage with CIP injection was 18.00 (16.00, 20.00) IU vs. 16.00 (12.00, 19.00) IU during NFII (p < 0.003). Conclusion: Compared with CIP, the use of the NFII to inject basal insulin improved FGV in T2DM. Clinical trial registration: https://www.chictr.org.cnIdentifier is ChiCTR2000034674.
AB - Background: Fasting glucose variability (FGV) extensively promotes the onset and development of diabetic complications. This study aimed to evaluate the FGV in type 2 diabetes mellitus (T2DM) patients administered basal insulin using a needle-free insulin injector (NFII). Research design and methods: This was a prospective randomized multicenter open-label crossover study. We randomly assigned 48 T2DM patients to receive basal insulin by NFII or conventional insulin pen (CIP) for 7–14 days and were then crossed over after washout. We conducted continuous glucose monitoring to investigate the FGV, our primary outcome was a composite parameter of the FGV with a fasting blood glucose target between 4.4 and 6.1 mmol/L. Results: The coefficient of variation for sensor glucose at 6 a.m. with CIP was 11.67 (8.70,14.81)% vs. 9.48 (6.48,12.24)% with NFII (p = 0.003), and the coefficient of variation for mean sensor glucose at 5–6 a.m. with CIP was 12.70 (9.17,16.56)% vs. 9.23 (7.01,11.98)% with NFII (p < 0.001). The overall basal insulin dosage with CIP injection was 18.00 (16.00, 20.00) IU vs. 16.00 (12.00, 19.00) IU during NFII (p < 0.003). Conclusion: Compared with CIP, the use of the NFII to inject basal insulin improved FGV in T2DM. Clinical trial registration: https://www.chictr.org.cnIdentifier is ChiCTR2000034674.
KW - basal insulin
KW - continuous glucose monitoring
KW - fasting glucose variability
KW - needle-free insulin injection
KW - type 2 diabetes mellitus
UR - https://www.scopus.com/pages/publications/85142258737
U2 - 10.1080/17425247.2022.2147504
DO - 10.1080/17425247.2022.2147504
M3 - 文章
C2 - 36378018
AN - SCOPUS:85142258737
SN - 1742-5247
VL - 19
SP - 1725
EP - 1734
JO - Expert Opinion on Drug Delivery
JF - Expert Opinion on Drug Delivery
IS - 12
ER -