High risk of cardiovascular mortality in individuals with impaired fasting glucose is explained by conversion to diabetes - The Hoorn Study

被引:93
作者
Rijkelijkhuizen, Josina M.
Bouter, Lex M.
Nijpels, Giel
Stehouwer, Coen D. A.
Heine, Robert J.
Dekker, Jacqueline M.
机构
[1] Vrije Univ Amsterdam, Ctr Med, EMGO Inst, NL-1081 BT Amsterdam, Netherlands
[2] Vrije Univ Amsterdam, Med Ctr, Dept Gen Practice, NL-1081 HV Amsterdam, Netherlands
[3] Vrije Univ Amsterdam, Med Ctr, Dept Endocrinol, NL-1081 HV Amsterdam, Netherlands
[4] Univ Limburg, Acad Hosp Maastricht, Dept Internal Med, Maastricht, Netherlands
关键词
D O I
10.2337/dc06-1238
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE - To optimize identification of future diabetic patients, the American Diabetes Association (ADA) introduced criteria for impaired fasting glucose (IFG) in 1997 (IFG 6.1 mmol/l [IFG6.1]) and lowered the threshold from 6.1 to 5.6 mmol/l (IFG5.6) in 2003. Our aim was to assess the consequences of lowering the IFG cutoff on the risk of cardiovascular disease (CVD) mortality and to evaluate whether this risk is explained by a conversion to type 2 diabetes within 6.4 years. RESEARCH DESIGN AND METHODS - in a population-based cohort, the Hoom Study, plasma glucose was determined in 1989 and 1996 (n = 1,428). Subjects were classified in 1989 according to 1997 and 2003 ADA criteria. Subjects with IFG in 1989 were further classified according to diabetes status in 1996. Hazard ratios for CVD mortality (n = 81) in the period 1996-2005 were adjusted for age and sex. RESULTS - Subjects with IFG6. 1, but not IFG5.6, had a significantly higher CVD mortality risk than normal fasting glucose (NFG) subjects. Subjects who converted from IFG to diabetes (IFG6.1: 42%; IFG5.6: 21%) had a more than twofold risk of CVD mortality (IFG6.1: 2.47 [1.17-5.19]; IFG5.6: 2.14 [1.12-4.10]) than subjects with NFG. IFG subjects who did not develop diabetes did not have significantly higher CVD mortality risks (IFG6.1: 1.50 [0.72-3.15]; IFG5.6: 1.15 [0.69-1.93]). CONCLUSIONS - The lower cutoff for IFG (ADA 2003 criteria) results in a category of IFG that no longer represents a high-risk state of CVD. Furthermore, only subjects who convert from IFG to diabetes have a high risk of CVD mortality.
引用
收藏
页码:332 / 336
页数:5
相关论文
共 26 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]  
[Anonymous], 1999, Diabetologia, V42, P647
[4]   Is there glycemic threshold for mortality risk? [J].
Balkau, B ;
Bertrais, S ;
Ducimetiere, P ;
Eschwege, E .
DIABETES CARE, 1999, 22 (05) :696-699
[5]   Creating a pandemic of prediabetes:: the proposed new diagnostic criteria for impaired fasting glycaemia [J].
Borch-Johnsen, K ;
Colagiuri, S ;
Balkau, B ;
Glümer, C ;
Carstensen, B ;
Ramachandran, A ;
Dong, Y ;
Gao, W .
DIABETOLOGIA, 2004, 47 (08) :1396-1402
[6]   Lowering the criterion for impaired fasting glucose will not provide clinical benefit [J].
Davidson, MB ;
Landsman, PB ;
Alexander, CM .
DIABETES CARE, 2003, 26 (12) :3329-3330
[7]   Relation of impaired fasting and postload glucose with incident type 2 diabetes in a Dutch population - The Hoorn study [J].
de Vegt, F ;
Dekker, JM ;
Jager, A ;
Hienkens, E ;
Kostense, PJ ;
Stehouwer, CDA ;
Nijpels, G ;
Bouter, LM ;
Heine, RJ .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 285 (16) :2109-2113
[8]   Hyperglycaemia is associated with all-cause and cardiovascular mortality in the Hoorn population:: the Hoorn Study [J].
de Vegt, F ;
Dekker, JM ;
Ruhé, HG ;
Stehouwer, CDA ;
Nijpels, G ;
Bouter, LM ;
Heine, RJ .
DIABETOLOGIA, 1999, 42 (08) :926-931
[9]   Counterpoint: Impaired fasting glucose: The case against the new American Diabetes Association guidelines [J].
Dekker, JM ;
Balkau, B .
DIABETES CARE, 2006, 29 (05) :1173-1175
[10]   HYPERTRIGLYCERIDEMIA AS A RISK FACTOR OF CORONARY HEART-DISEASE MORTALITY IN SUBJECTS WITH IMPAIRED GLUCOSE-TOLERANCE OR DIABETES - RESULTS FROM THE 11-YEAR FOLLOW-UP OF THE PARIS PROSPECTIVE-STUDY [J].
FONTBONNE, A ;
ESCHWEGE, E ;
CAMBIEN, F ;
RICHARD, JL ;
DUCIMETIERE, P ;
THIBULT, N ;
WARNET, JM ;
CLAUDE, JR ;
ROSSELIN, GE .
DIABETOLOGIA, 1989, 32 (05) :300-304