Interstitial measurements of glucose, glycerol and lactate in adolescents with decompensated type 1 diabetes

被引:0
作者
Petriczko, Elzbieta [1 ]
Horodnicka-Jozwa, Anita [1 ]
Grabowska-Wnuk, Wioletta [1 ,2 ]
Sienko, Magdalena [1 ]
Syrenicz, Anhelli [3 ]
Walczak, Mieczyslaw [1 ]
机构
[1] Pomeranian Med Univ, Dept Pediat Endocrinol Diabetol Metab Dis & Cardi, PL-71252 Szczecin, Poland
[2] Quinn Elizabeth Hosp, Dept Pediat, Kings Lynn, England
[3] Pomeranian Med Univ, Dept Endocrinol Metab & Internal Dis, PL-71252 Szczecin, Poland
关键词
microdialysis; diabetes type 1; adipose tissue; glucose; glycerol; lactate; insulin; SUBCUTANEOUS ADIPOSE-TISSUE; BLOOD-GLUCOSE; MICRODIALYSIS; INSULIN; LIPOLYSIS; HYPOGLYCEMIA; CHILDREN; SURGERY; SYSTEM; FLUID;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE: The study was undertaken to assess the interstitial, adipose tissue concentrations of glucose, lactate and glycerol in teenagers with diabetes type 1 who suffered from the disease for a minimum of 5 years, in whom it was impossible to reach a satisfactory level of metabolic control of the disease. METHODS: Using microdialysis technique interstitial concentrations of glucose lactate and glycerol was measured in adipose tissue during 24-48 hours. Nineteen teenagers with poorly controlled type 1 diabetes (HbA1c 8.9 +/- 2.85%) were compared with six adolescent control subjects. RESULTS: A statistically significant differences in concentration values of interstitial glucose between the investigated and control groups were found (10.4 vs. 4.26 mmol/l p=0.001). The values of interstitial concentrations of lactates did not significantly differ in the two groups (2.96 vs. 2.54 mmol/l NS). The average daily glycerol concentrations in the investigated group were statistically significantly lower than those in the control group (258.26 vs. 397.88 mu mol/l, p=0.019). No such difference was detected in average night concentrations of glycerol (157.78 vs. 361.4 mu mol/l, NS). CONCLUSIONS: Authors conclude that microdialysis is the only one minimal invasive method for investigating adipose tissue metabolism in vivo and provides a novel opportunity for glucose and lipids metabolism monitoring in adolescents with diabetes type 1. In our observations interstitial glycerol concentrations, measured in abdominal subcutaneous adipose tissue as an index of lipolysis, were not significantly influenced by hyperglycemia in diabetic adolescents.
引用
收藏
页码:559 / 567
页数:9
相关论文
共 30 条
  • [1] Ahlsson Fredrik, 2004, Pediatr Crit Care Med, V5, P89, DOI 10.1097/01.PCC.0000102396.02043.22
  • [2] Effect of fasting on young adults who have symptoms of hypoglycemia in the absence of frequent meals
    Alken, J.
    Petriczko, E.
    Marcus, C.
    [J]. EUROPEAN JOURNAL OF CLINICAL NUTRITION, 2008, 62 (06) : 721 - 726
  • [3] MICRODIALYSIS OF ADIPOSE-TISSUE
    ARNER, P
    BOLINDER, J
    [J]. JOURNAL OF INTERNAL MEDICINE, 1991, 230 (04) : 381 - 386
  • [4] ARNER P, 1997, MICROLINE, V3
  • [5] Glucose monitoring with long-term subcutaneous microdialysis in neonates
    Baumeister, FAM
    Rolinski, B
    Busch, R
    Emmrich, P
    [J]. PEDIATRICS, 2001, 108 (05) : 1187 - 1192
  • [6] Blaak EE, 1999, CLIN SCI, V97, P421, DOI [10.1042/CS19980334, 10.1042/cs0970421]
  • [7] LONG-TERM CONTINUOUS GLUCOSE MONITORING WITH MICRODIALYSIS IN AMBULATORY INSULIN-DEPENDENT DIABETIC-PATIENTS
    BOLINDER, J
    UNGERSTEDT, U
    ARNER, P
    [J]. LANCET, 1993, 342 (8879) : 1080 - 1085
  • [8] Self-monitoring of blood glucose in type I diabetic patients: Comparison with continuous microdialysis measurements of glucose in subcutaneous adipose tissue during ordinary life conditions
    Bolinder, J
    HagstromToft, E
    Ungerstedt, U
    Arner, P
    [J]. DIABETES CARE, 1997, 20 (01) : 64 - 70
  • [9] Microdialysis technique as a monitoring system for acute complications of diabetes
    Ciechanowska, Anna
    Ladyzynski, Piotr
    Wojcicki, Jan M.
    Sabalinska, Stanislawa
    Krzymien, Janusz
    Pulawska, Elzbieta
    Karnafel, Waldemar
    Foltynski, Piotr
    Kawiak, Jerzy
    [J]. ARTIFICIAL ORGANS, 2008, 32 (01) : 45 - 51
  • [10] EBLAD P, 1996, J CEREB BLOOD FLOW M, V16, P637