One-Hour Plasma Glucose Identifies Insulin Resistance and β-Cell Dysfunction in Individuals With Normal Glucose Tolerance Cross-sectional data from the Relationship between Insulin Sensitivity and Cardiovascular Risk (RISC) study

被引:94
作者
Manco, Melania [1 ]
Panunzi, Simona [2 ]
Macfarlane, David P. [3 ]
Golay, Alain [4 ]
Melander, Olle [5 ]
Konrad, Thomas [6 ]
Petrie, John R. [7 ]
Mingrone, Geltrude [8 ]
机构
[1] Bambino Gesu Pediat Hosp, Ist Ricovero & Cura Carattere Sci, Rome, Italy
[2] CNR, Ist Analisi Sistemi & lnformat Antonio Ruberti, BioMatLab, Rome, Italy
[3] Univ Dundee, Biomed Res Inst, Dundee, Scotland
[4] Univ Hosp Geneva, Geneva, Switzerland
[5] Lund Univ, Univ Hosp, Dept Clin Sci, Malmo, Sweden
[6] Goethe Univ Frankfurt, Pediat Clin, Frankfurt, Germany
[7] Univ Glasgow, BHF Cardiovasc Res Ctr, Glasgow, Lanark, Scotland
[8] Catholic Univ, Sch Med, Rome, Italy
关键词
TESTS; INTERVENTION; PREDICTOR; MEAL;
D O I
10.2337/dc09-2261
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
OBJECTIVE- Some individuals with normal glucose tolerance (NGT) exhibit a 1-h excursion of plasma glucose during oral glucose tolerance testing as high as that of individuals with impaired glucose tolerance (IGT). The aim of this study was to characterize their metabolic phenotype. RESEARCH DESIGN AND METHODS- A total of 1,205 healthy volunteers (aged 29-61 years) underwent assessment of 1) oral glucose tolerance and 2) insulin sensitivity (standardized euglycemic-hyperinsulinemic clamp), as part of the Relationship between Insulin Sensitivity and Cardiovascular Risk (RISC) study. RESULTS- One-hour plasma glucose correlated better than 2-h plasma glucose with total insulin secretion (r = 0.43), beta-cell glucose sensitivity (r = -0.46), and beta-cell rate sensitivity (r = -0.18). Receiver operating characteristic analysis identified 8.95 mmol/l as the best cutoff value for prediction of IGT from 1-h plasma glucose (sensitivity 77% and specificity 80%). Participants with NGT with 1-h plasma glucose >8.95 mmol/l had larger waist circumference, higher BMI, lower insulin sensitivity, higher fasting glucose, and higher insulin secretion than their counterparts with 1-h plasma glucose <= 8.95 mmol/l (P < 0.001 for all comparisons). Moreover, they exhibited lower beta-cell glucose sensitivity (P < 0.001), beta-cell rate sensitivity (P < 0.001), and potentiation factor (P = 0.026). When compared with conventionally defined IGT, they were not different in waist circumference and BMI, hepatic insulin extraction, beta-cell glucose sensitivity, beta-cell rate sensitivity, and potentiation factor but did have greater insulin sensitivity along with reduced basal (P = 0.001) and total insulin secretion (P = 0.002). CONCLUSIONS- Higher values of 1-h plasma glucose may identify an intermediate condition between NGT and IGT characterized by greater insulin resistance, reduced beta-cell glucose sensitivity, and reduced beta-cell rate sensitivity.
引用
收藏
页码:2090 / 2097
页数:8
相关论文
共 22 条
[1]
Contributions of β-cell dysfunction and insulin resistance to the pathogenesis of impaired glucose tolerance and impaired fasting glucose [J].
Abdul-Ghani, MA ;
Tripathy, D ;
DeFronzo, RA .
DIABETES CARE, 2006, 29 (05) :1130-1139
[2]
One-hour plasma glucose concentration and the metabolic syndrome identify subjects at high risk for future type 2 diabetes [J].
Abdul-Ghani, Muhammad A. ;
Abdul-Ghani, Tamam ;
Ali, Nibal ;
DeFronzo, Ralph A. .
DIABETES CARE, 2008, 31 (08) :1650-1655
[3]
What is the best predictor of future type 2 diabetes? [J].
Abdul-Ghani, Muhammad A. ;
Williams, Ken ;
DeFronzo, Ralph A. ;
Stern, Michael .
DIABETES CARE, 2007, 30 (06) :1544-1548
[4]
Minimal Contribution of Fasting Hyperglycemia to the Incidence of Type 2 Diabetes in Subjects With Normal 2-h Plasma Glucose [J].
Abdul-Ghani, Muhammad A. ;
Stern, Michael P. ;
Lyssenko, Valeriya ;
Tuomi, Tiinamaija ;
Groop, Leif ;
DeFronz, Ralph A. .
DIABETES CARE, 2010, 33 (03) :557-561
[5]
Primary Defects in β-Cell Function Further Exacerbated by Worsening of Insulin Resistance Mark the Development of Impaired Glucose Tolerance in Obese Adolescents [J].
Cali, Anna M. G. ;
Man, Chiara Dalla ;
Cobelli, Claudio ;
Dziura, James ;
Seyal, Aisha ;
Shaw, Melissa ;
Allen, Karin ;
Chen, Shu ;
Caprio, Sonia .
DIABETES CARE, 2009, 32 (03) :456-461
[6]
Postprandial blood glucose is a stronger predictor of cardiovascular events than fasting blood glucose in type 2 diabetes mellitus, particularly in women: Lessons from the San Luigi Gonzaga Diabetes Study [J].
Cavalot, F ;
Petrelli, A ;
Traversa, M ;
Bonomo, K ;
Fiora, E ;
Conti, M ;
Anfossi, G ;
Costa, G ;
Trovati, M .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2006, 91 (03) :813-819
[7]
The relationship between glucose and incident cardiovascular events [J].
Coutinho, M ;
Gerstein, HC ;
Wang, Y ;
Yusuf, S .
DIABETES CARE, 1999, 22 (02) :233-240
[8]
β-cell function in subjects spanning the range from normal glucose tolerance to overt diabetes:: A new analysis [J].
Ferrannini, E ;
Gastaldelli, A ;
Miyazaki, Y ;
Matsuda, M ;
Mari, A ;
DeFronzo, RA .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2005, 90 (01) :493-500
[9]
Insulin resistance and hypersecretion in obesity [J].
Ferrannini, E ;
Natali, A ;
Bell, P ;
CavalloPerin, P ;
Lalic, N ;
Mingrone, G .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (05) :1166-1173
[10]
Beta-cell dysfunction and glucose intolerance: results from the San Antonio metabolism (SAM) study [J].
Gastaldelli, A ;
Ferrannini, E ;
Miyazaki, Y ;
Matsuda, M ;
DeFronzo, RA .
DIABETOLOGIA, 2004, 47 (01) :31-39