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. Author manuscript; available in PMC: 2013 Aug 1.
Published in final edited form as: Diabet Med. 2012 Aug;29(8):1067–1073. doi: 10.1111/j.1464-5491.2011.03545.x

Table 1.

A summary of published reports that have compared the magnitude of sensor lag measured during rising glucose (or low insulin effect) to lag measured during falling glucose (or high insulin effect)

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.