Timing of changes in interstitial and venous blood glucose measured with a continuous subcutaneous glucose sensor

被引:279
作者
Boyne, MS
Silver, DM
Kaplan, J
Saudek, CD
机构
[1] Johns Hopkins Univ, Sch Med, Div Endocrinol & Metab, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, Appl Phys Lab, Baltimore, MD 21287 USA
关键词
D O I
10.2337/diabetes.52.11.2790
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The objective of this study was to use a subcutaneous continuous glucose sensor to determine time differences in the dynamics of blood glucose and interstitial glucose. A total of 14 patients with type 1 diabetes each had two sensors (Medtronic/MiniMed CGMS) placed subcutaneously in the abdomen, acquiring data every 5 min. Blood glucose was sampled every 5 min for 8 It, and two liquid meals were given. A smoothing algorithm was applied to the blood glucose and interstitial glucose curves. The first derivatives of the glucose traces defined and quantified the timing of rises, peaks, falls, and nadirs. Altogether, 24 datasets were used for the analysis of time differences between interstitial and blood glucose and between sensors in each patient. Time differences between blood and interstitial glucose ranged from 4 to 10 min, with the interstitial glucose lagging behind blood glucose in 81% of cases (95% CIs 72.5 and 89.5%). The mean (+/-SD) difference between the two sensors in each patient was 6.7 +/- 5.1 min, representing random variation in sensor response. In conclusion, there is a time lag of interstitial glucose behind blood glucose, regardless of whether glycemia is rising or falling, but intersensor variability is considerable in this sensor system. Comparisons of interstitial and blood glucose kinetics must take statistical account of variability between sensors.
引用
收藏
页码:2790 / 2794
页数:5
相关论文
共 19 条
[1]  
FISCHER U, 1995, HORM METAB RES, V27, pA53
[2]   Problems associated with subcutaneously implanted glucose sensors [J].
Gerritsen, M .
DIABETES CARE, 2000, 23 (02) :143-145
[3]   Performance of subcutaneously implanted glucose sensors for continuous monitoring [J].
Gerritsen, M ;
Jansen, JA ;
Lutterman, JA .
NETHERLANDS JOURNAL OF MEDICINE, 1999, 54 (04) :167-179
[4]  
Gerritsen M, 2001, J BIOMED MATER RES, V54, P69, DOI 10.1002/1097-4636(200101)54:1<69::AID-JBM8>3.0.CO
[5]  
2-Q
[6]   CHARACTERIZATION BY MICRODIALYSIS OF INTERCELLULAR GLUCOSE LEVEL IN SUBCUTANEOUS TISSUE IN HUMANS [J].
JANSSON, PA ;
FOWELIN, J ;
SMITH, U ;
LONNROTH, P .
AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 255 (02) :E218-E220
[7]   INVITRO INSULIN RESISTANCE OF HUMAN ADIPOCYTES ISOLATED FROM SUBJECTS WITH NONINSULIN-DEPENDENT DIABETES-MELLITUS [J].
KASHIWAGI, A ;
VERSO, MA ;
ANDREWS, J ;
VASQUEZ, B ;
REAVEN, G ;
FOLEY, JE .
JOURNAL OF CLINICAL INVESTIGATION, 1983, 72 (04) :1246-1254
[8]  
Mastrototaro J, 1999, J PEDIATR ENDOCR MET, V12, P751
[9]   Spurious reporting of nocturnal hypoglycemia by CGMS in patients with tightly controlled type I diabetes [J].
McGowan, K ;
Thomas, W ;
Moran, A .
DIABETES CARE, 2002, 25 (09) :1499-1503
[10]   KEY METABOLITE KINETICS IN HUMAN SKELETAL-MUSCLE DURING ISCHEMIA AND REPERFUSION - MEASUREMENT BY MICRODIALYSIS [J].
MULLER, M ;
SCHMID, R ;
NIESZPAURLOS, M ;
FASSOLT, A ;
LONNROTH, P ;
FASCHING, P ;
EICHLER, HG .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1995, 25 (08) :601-607