Table 1.
Authors, year | Reference | Type of sensor | Subjects | Lower lag found during high insulin effect? |
---|---|---|---|---|
Sternberg et al., 1996 | [3] | Microdialysis | Type 1 diabetes— humans | Yes, but only in ~50% of subjects |
Thome-Duret et al., 1996 | [4] | Wilson-Reach sensor(GOX, non-mediated) | Type 1 diabetes—rats | Yes |
Wilhelm et al., 2006 | [21] | MiniMed (GOX, non-mediated) | Type 1 diabetes— humans | * |
Schmidke et al., 1998 | [7] | Heller sensor (GOX, osmium-mediated) | Non-diabetic rats | No |
Aussedat et al., 2000 | [5] | Wilson-Reach | Non-diabetic rats | Yes |
Rebrin et al., 1999 | [8] | MiniMed | Non-diabetic dogs | No |
Kulcu et al., 2003 | [6] | Cygnus, GOX, transdermal | Type 1 and Type 2 diabetes— humans | Yes |
Boyne et al., 2003 | [2] | MiniMed | Type 1 diabetes— humans | No |
Kamath et al., 2009 | [12] | Dexcom Seven+ (GOX, non-mediated) | Type 1diabetes— humans | Apparently yes, although not directly stated |
Compared with the rising glucose phase, during rapid decline after oral glucose and insulin administration, there was less of a lag of the sensor (vs. capillary blood as a reference), but there was also consistent calibration error (the sensor substantially underestimated blood glucose at high glucose levels), so this finding is difficult to interpret.
GOX, glucose oxidase.