A new antiglycolytic agent

被引:14
作者
le Roux, CW [1 ]
Wilkinson, SD [1 ]
Pavitt, DV [1 ]
Muller, BR [1 ]
Alaghband-Zadeh, J [1 ]
机构
[1] Charing Cross Hosp, Dept Chem Pathol, London W6 8RF, England
关键词
D O I
10.1258/000456304322664681
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background Glycolysis is not completely or predictably inhibited by the glucose preservative currently in use, with glucose values falling by as much as 0.5 mmol/L during a 2-4-h period after sample collection. Immediate centrifugation of all samples is also impractical and therefore misdiagnosis of disease can occur, especially if more emphasis is being placed on fasting glucose for the diagnosis of diabetes. Methods Glycolysis at room temperature was evaluated over time using glyceraldehyde alone as well as in conjunction with standard antiglycolytic agents. Results Glyceraldehyde alone does not inhibit glycolysis completely. The combination of 11 mmol/L glyceraldehyde, 119 mmol/L sodium fluoride and 21.7 mmol/L potassium oxalate gave the best antiglycolytic results, The glucose values measured in samples stored at room temperature for 48 h was no different from those measured in samples centrifuged immediately after venepuncture and this is clinically superior to conventionally used sodium fluoride and potassium oxalate. Conclusion Plasma glucose concentrations obtained from blood collected into tubes containing glyceraldehyde, sodium fluoride and potassium oxalate will more closely reflect those of the patient at venepuncture.
引用
收藏
页码:43 / 46
页数:4
相关论文
共 9 条
[1]  
[Anonymous], DEF DIAGN CLASS DIAB
[2]  
ASTLES R, 1994, CLIN CHEM, V40, P1327
[3]  
CHAN AYW, 1989, CLIN CHEM, V35, P315
[4]   EFFECT OF DELAY IN SEPARATING PLASMA FOR GLUCOSE MEASUREMENT UPON THE INTERPRETATION OF ORAL GLUCOSE-TOLERANCE TESTS [J].
CHAN, AYW ;
COCKRAM, CS ;
SWAMINATHAN, R .
ANNALS OF CLINICAL BIOCHEMISTRY, 1990, 27 :73-74
[5]  
DEPASQUA A, 1984, LANCET, V2, P1165
[6]  
KAPLAN LA, 1980, CLIN CHEM, V26, P175
[7]   New diagnostic criteria for diabetes mellitus: are we any further forward? [J].
Lamb, EJ ;
Day, AP .
ANNALS OF CLINICAL BIOCHEMISTRY, 2000, 37 :588-592
[8]  
Landt M, 2000, CLIN CHEM, V46, P1144
[9]  
MEITES S, 1979, CLIN CHEM, V25, P531