Elevated white blood cell count in subjects with impaired glucose tolerance

被引:77
作者
Ohshita, K
Yamane, K
Hanafusa, M
Mori, H
Mito, K
Okubo, M
Hara, H
Kohno, N
机构
[1] Hiroshima Univ, Grad Sch Biomed Sci, Programs Appl Biomed, Dept Mol & Internal Med,Div Clin Med Sci,Minami K, Hiroshima 7348551, Japan
[2] Nippon Telegraph & Tel W Corp, Chugoku Hlth Adm Ctr, Hiroshima, Japan
关键词
D O I
10.2337/diacare.27.2.491
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE - Impaired glucose tolerance (IGT) and impaired fasting glucose (IFG) differ in their risk of all-cause and cardiovascular mortality, but previous cross-sectional studies have suggested little difference in their levels of lipids or blood pressure. We compared the white blood cell (WBC) count between subjects with IFG and IGT. RESEARCH DESIGN AND METHODS - The subjects were 4,720 nondiabetic Japanese men aged 24-84 years. Based on the 75-g oral glucose tolerance test, the subjects were classified into the following four groups: normal fasting glucose/normal glucose tolerance (n = 3,753), isolated IFG (n = 290), isolated IGT (n = 476), and IFG/IGT (n = 201). We compared the WBC count among the four groups and investigated variables that showed a significant association with the WBC count. RESULTS - The isolated IGT group had a significantly higher WBC count than the isolated IFG group (6,530 vs. 6,210/mm(3), P < 0.05). By stepwise analyses, age, triglycerides, HDL cholesterol, fasting insulin, and 2-h postchallenge plasma glucose (PG) showed an independent association with the WBC count (adjusted R-2 = 0.057). In the analysis stratified by smoking status, the WBC count was independently associated with 2-h PG and triglycerides, irrespective of smoking status. CONCLUSIONS - Individuals with isolated IGT had a significantly higher WBC count than those with isolated IFG. The WBC count was associated with 2-h PG and various components of the metabolic syndrome.
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页码:491 / 496
页数:6
相关论文
共 35 条
[1]   Plasma glucose within the normal range is not associated with carotid atherosclerosis - Prospective results in subjects with normal glucose tolerance from the Bruneck Study [J].
Bonora, E ;
Kiechl, S ;
Willeit, J ;
Oberhollenzer, F ;
Egger, G ;
Bonadonna, R ;
Muggeo, M .
DIABETES CARE, 1999, 22 (08) :1339-1346
[2]   Glucose tolerance and cardiovascular mortality -: Comparison of fasting and 2-hour diagnostic criteria [J].
Borch-Johnsen, K ;
Neil, A ;
Balkau, B ;
Larsen, S ;
Nissinen, A ;
Pekkanen, J ;
Tuomilehto, J ;
Jousilahti, P ;
Lindstrom, J ;
Pyörälä, M ;
Pyörälä, K ;
Eschwege, E ;
Gallus, G ;
Garancini, MP ;
Bouter, LM ;
Dekker, JM ;
Heine, RJ ;
Nijpels, HG ;
Stehouwer, CDA ;
Feskens, EJM ;
Kromhout, D ;
Peltonen, M ;
Pajak, A ;
Eriksson, J ;
Qiao, Q .
ARCHIVES OF INTERNAL MEDICINE, 2001, 161 (03) :397-405
[3]   White blood cell count: An independent predictor of coronary heart disease mortality among a national cohort [J].
Brown, DW ;
Giles, WH ;
Croft, JB .
JOURNAL OF CLINICAL EPIDEMIOLOGY, 2001, 54 (03) :316-322
[4]   INSULIN IS A PROMINENT MODULATOR OF THE CYTOKINE-STIMULATED EXPRESSION OF ACUTE-PHASE PLASMA-PROTEIN GENES [J].
CAMPOS, SP ;
BAUMANN, H .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (04) :1789-1797
[5]  
CORRE F, 1971, LANCET, V2, P632
[6]   Association of impaired glucose homeostasis with preclinical carotid atherosclerosis in women: Impact of the new American Diabetes Association criteria [J].
De Michele, M ;
Panico, S ;
Celentano, E ;
Covetti, G ;
Intrieri, M ;
Zarrilli, F ;
Sacchetti, L ;
Tang, R ;
Bond, MG ;
Rubba, P .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2002, 51 (01) :52-56
[7]   GRANULOCYTE FUNCTION IN CORONARY-ARTERY DISEASE [J].
DESERVI, S ;
RICEVUTI, G ;
MAZZONE, A ;
GHIO, S ;
ZITO, A ;
RAFFAGHELLO, S ;
SPECCHIA, G .
AMERICAN JOURNAL OF CARDIOLOGY, 1991, 68 (07) :B64-B68
[8]   Elevated white blood cell count and carotid plaque thickness - The Northern Manhattan Stroke Study [J].
Elkind, MS ;
Cheng, JF ;
Boden-Albala, B ;
Paik, MC ;
Sacco, RL .
STROKE, 2001, 32 (04) :842-849
[9]   LEUKOCYTES AND THE RISK OF ISCHEMIC DISEASES [J].
ERNST, E ;
HAMMERSCHMIDT, DE ;
BAGGE, U ;
MATRAI, A ;
DORMANDY, JA .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1987, 257 (17) :2318-2324
[10]   Inflammatory cytokine concentrations are acutely increased by hyperglycemia in humans - Role of oxidative stress [J].
Esposito, K ;
Nappo, F ;
Marfella, R ;
Giugliano, G ;
Giugliano, F ;
Ciotola, M ;
Quagliaro, L ;
Ceriello, A ;
Giugliano, D .
CIRCULATION, 2002, 106 (16) :2067-2072