Impaired fasting glucose: How low should it go?

被引:97
作者
Shaw, JE
Dowse, GK
Zimmet, PZ
Chitson, P
Hodge, AM
Tuomilehto, J
de Courten, M
Alberti, KGMM
机构
[1] Int Diabet Inst, Melbourne, Vic, Australia
[2] Minist Hlth, Port Louis, Mauritius
[3] Natl Publ Hlth Inst, Dept Epidemiol & Hlth Promot, Helsinki, Finland
[4] Newcastle Univ, Human Diabet & Metab Res Ctr, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
关键词
D O I
10.2337/diacare.23.1.34
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE- Impaired fasting glucose (IFG) has been recently introduced as a stage of abnormal carbohydrate metabolism, but the evidence on which its glucose limits (fasting plasma glucose [FPG] 6.1-6.9 mmol/l) are based is not strong. The aim of this study was to determine if 6.1 mmol/l represents a clear cutoff in terms of the risk of future diabetes and in terms of elevated cardiovascular risk factor levels, and to examine the use of other lower limits of IFG. RESEARCH DESIGN AND METHODS- A population-based survey of the island of Mauritius was undertaken in 1987, with a follow-up survey 5 years later. On both occasions, an oral glucose tolerance test was performed and cardiovascular risk factors were measured. RESULTS- Data were available from 4,721 nondiabetic people at baseline, and from 3,542 at follow-up. At baseline, blood pressure, lipids, and obesity increased in a linear fashion with increasing FPG, with no evidence of a threshold effect. The risk of developing hypertension at follow-up was greater for those people with baseline FPG greater than or equal to 6.1 mmol/l (P < 0.001), The risk of developing diabetes at follow-up increased with increasing baseline FPG, but there was little evidence of a threshold near 6.1 mmol/l. CONCLUSIONS- Cardiovascular risk and risk of future diabetes increase continually with increasing FPG, and there is no threshold value on which to base a definition of IFG. If a lower limit of similar to 5.8 mmol/l is used, the category defines a group more similar to the group with impaired glucose tolerance, with regard to total prevalence and the risk of subsequent diabetes.
引用
收藏
页码:34 / 39
页数:6
相关论文
共 19 条
[1]  
Alberti KGMM, 1998, DIABETIC MED, V15, P539, DOI 10.1002/(SICI)1096-9136(199807)15:7<539::AID-DIA668>3.0.CO
[2]  
2-S
[3]   High blood glucose concentration is a risk factor for mortality in middle-aged nondiabetic men -: 20-year follow-up in the Whitehall Study, the Paris Prospective Study, and the Helsinki Policemen Study [J].
Balkau, B ;
Shipley, M ;
Jarrett, RJ ;
Pyörälä, K ;
Pyörälä, M ;
Forhan, A ;
Eschwège, E .
DIABETES CARE, 1998, 21 (03) :360-367
[4]  
Balkau B, 1997, DIABETES METAB, V23, P428
[5]   RELATIONSHIPS BETWEEN FASTING PLASMA GLUCOSE LEVELS AND INSULIN-SECRETION DURING INTRAVENOUS GLUCOSE-TOLERANCE TESTS [J].
BRUNZELL, JD ;
ROBERTSON, RP ;
LERNER, RL ;
HAZZARD, WR ;
ENSINCK, JW ;
BIERMAN, EL ;
PORTE, D .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1976, 42 (02) :222-229
[6]  
Chalmers J, 1999, J HYPERTENS, V17, P151
[7]   RISK-FACTORS FOR NIDDM IN WHITE-POPULATION - PARIS PROSPECTIVE-STUDY [J].
CHARLES, MA ;
FONTBONNE, A ;
THIBULT, N ;
WARNET, JM ;
ROSSELIN, GE ;
ESCHWEGE, E .
DIABETES, 1991, 40 (07) :796-799
[8]  
Charles MA, 1996, LANCET, V348, P1657, DOI 10.1016/S0140-6736(05)65719-4
[9]   Progression to type 2 diabetes among high-risk groups in Kin-Chen, Kinmen - Exploring the natural history of type 2 diabetes [J].
Chou, PS ;
Li, CL ;
Wu, GS ;
Tsai, ST .
DIABETES CARE, 1998, 21 (07) :1183-1187
[10]   The relationship between glucose and incident cardiovascular events [J].
Coutinho, M ;
Gerstein, HC ;
Wang, Y ;
Yusuf, S .
DIABETES CARE, 1999, 22 (02) :233-240