Incidence of Type 2 diabetes in England and its association with baseline impaired fasting glucose: The Ely study 1990-2000

Aim  To determine the incidence of Type 2 diabetes and to examine the effect of different cut‐points for impaired fasting glucose (IFG) on diabetes incidence. Methods  Population‐based longitudinal study (1990–2000) with clinical, anthropometric and biochemical measurements, including an oral glucos...

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Published inDiabetic medicine Vol. 24; no. 2; pp. 200 - 207
Main Authors Forouhi, N. G., Luan, J., Hennings, S., Wareham, N. J.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.02.2007
Blackwell
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Abstract Aim  To determine the incidence of Type 2 diabetes and to examine the effect of different cut‐points for impaired fasting glucose (IFG) on diabetes incidence. Methods  Population‐based longitudinal study (1990–2000) with clinical, anthropometric and biochemical measurements, including an oral glucose tolerance test (OGTT), in 1040 non‐diabetic adults aged 40–69 years at baseline. Baseline glucose status was defined as normoglycaemia < 5.6, IFG‐lower 5.6–6.0 and IFG‐original 6.1–6.9 mmol/l. The all‐IFG group included fasting glucose values of 5.6–6.9 mmol/l. Results  The 10‐year cumulative incidence of diabetes was 7.3 per 1000 person‐years. Diabetes incidence was 2.4 [95% confidence interval (CI) 1.2, 4.8], 6.2 (4.0, 9.8) and 17.5 (12.5, 24.5) per 1000 person‐years in those with normoglycaemia, IFG‐lower and IFG‐original, respectively. Compared with normoglycaemia, the age/sex‐adjusted risk [hazard ratio (HR) and 95% CI] for incident diabetes was greatest in the IFG‐original category (HR 6.9; 3.1, 15.2) and increased to a lesser degree in the IFG‐lower (HR 2.5; 1.1, 5.7) and all‐IFG categories (HR 4.1; 1.9, 8.7). When adjusted for confounding factors, the magnitude and direction of associations persisted, with HR 1.9, 4.4 and 2.9, for the categories IFG‐lower, IFG‐original and all‐IFG, respectively. Conclusions  Diabetes incidence is more strongly related to IFG defined as fasting glucose between 6.1 and 6.9 mmol/l than to the lower category of 5.6–6.0 mmol/l, or entire range of 5.6–6.9 mmol/l. Future studies should examine the association of IFG with cardiovascular outcomes, but for diabetes risk our study supports the use of the IFG cut‐point at 6.1 mmol/l.
AbstractList Abstract Aim  To determine the incidence of Type 2 diabetes and to examine the effect of different cut‐points for impaired fasting glucose (IFG) on diabetes incidence. Methods  Population‐based longitudinal study (1990–2000) with clinical, anthropometric and biochemical measurements, including an oral glucose tolerance test (OGTT), in 1040 non‐diabetic adults aged 40–69 years at baseline. Baseline glucose status was defined as normoglycaemia < 5.6, IFG‐lower 5.6–6.0 and IFG‐original 6.1–6.9 mmol/l. The all‐IFG group included fasting glucose values of 5.6–6.9 mmol/l. Results  The 10‐year cumulative incidence of diabetes was 7.3 per 1000 person‐years. Diabetes incidence was 2.4 [95% confidence interval (CI) 1.2, 4.8], 6.2 (4.0, 9.8) and 17.5 (12.5, 24.5) per 1000 person‐years in those with normoglycaemia, IFG‐lower and IFG‐original, respectively. Compared with normoglycaemia, the age/sex‐adjusted risk [hazard ratio (HR) and 95% CI] for incident diabetes was greatest in the IFG‐original category (HR 6.9; 3.1, 15.2) and increased to a lesser degree in the IFG‐lower (HR 2.5; 1.1, 5.7) and all‐IFG categories (HR 4.1; 1.9, 8.7). When adjusted for confounding factors, the magnitude and direction of associations persisted, with HR 1.9, 4.4 and 2.9, for the categories IFG‐lower, IFG‐original and all‐IFG, respectively. Conclusions  Diabetes incidence is more strongly related to IFG defined as fasting glucose between 6.1 and 6.9 mmol/l than to the lower category of 5.6–6.0 mmol/l, or entire range of 5.6–6.9 mmol/l. Future studies should examine the association of IFG with cardiovascular outcomes, but for diabetes risk our study supports the use of the IFG cut‐point at 6.1 mmol/l.
To determine the incidence of Type 2 diabetes and to examine the effect of different cut-points for impaired fasting glucose (IFG) on diabetes incidence. Population-based longitudinal study (1990-2000) with clinical, anthropometric and biochemical measurements, including an oral glucose tolerance test (OGTT), in 1040 non-diabetic adults aged 40-69 years at baseline. Baseline glucose status was defined as normoglycaemia < 5.6, IFG-lower 5.6-6.0 and IFG-original 6.1-6.9 mmol/l. The all-IFG group included fasting glucose values of 5.6-6.9 mmol/l. The 10-year cumulative incidence of diabetes was 7.3 per 1000 person-years. Diabetes incidence was 2.4 [95% confidence interval (CI) 1.2, 4.8], 6.2 (4.0, 9.8) and 17.5 (12.5, 24.5) per 1000 person-years in those with normoglycaemia, IFG-lower and IFG-original, respectively. Compared with normoglycaemia, the age/sex-adjusted risk [hazard ratio (HR) and 95% CI] for incident diabetes was greatest in the IFG-original category (HR 6.9; 3.1, 15.2) and increased to a lesser degree in the IFG-lower (HR 2.5; 1.1, 5.7) and all-IFG categories (HR 4.1; 1.9, 8.7). When adjusted for confounding factors, the magnitude and direction of associations persisted, with HR 1.9, 4.4 and 2.9, for the categories IFG-lower, IFG-original and all-IFG, respectively. Diabetes incidence is more strongly related to IFG defined as fasting glucose between 6.1 and 6.9 mmol/l than to the lower category of 5.6-6.0 mmol/l, or entire range of 5.6-6.9 mmol/l. Future studies should examine the association of IFG with cardiovascular outcomes, but for diabetes risk our study supports the use of the IFG cut-point at 6.1 mmol/l.
AIMTo determine the incidence of Type 2 diabetes and to examine the effect of different cut-points for impaired fasting glucose (IFG) on diabetes incidence.METHODSPopulation-based longitudinal study (1990-2000) with clinical, anthropometric and biochemical measurements, including an oral glucose tolerance test (OGTT), in 1040 non-diabetic adults aged 40-69 years at baseline. Baseline glucose status was defined as normoglycaemia < 5.6, IFG-lower 5.6-6.0 and IFG-original 6.1-6.9 mmol/l. The all-IFG group included fasting glucose values of 5.6-6.9 mmol/l.RESULTSThe 10-year cumulative incidence of diabetes was 7.3 per 1000 person-years. Diabetes incidence was 2.4 [95% confidence interval (CI) 1.2, 4.8], 6.2 (4.0, 9.8) and 17.5 (12.5, 24.5) per 1000 person-years in those with normoglycaemia, IFG-lower and IFG-original, respectively. Compared with normoglycaemia, the age/sex-adjusted risk [hazard ratio (HR) and 95% CI] for incident diabetes was greatest in the IFG-original category (HR 6.9; 3.1, 15.2) and increased to a lesser degree in the IFG-lower (HR 2.5; 1.1, 5.7) and all-IFG categories (HR 4.1; 1.9, 8.7). When adjusted for confounding factors, the magnitude and direction of associations persisted, with HR 1.9, 4.4 and 2.9, for the categories IFG-lower, IFG-original and all-IFG, respectively.CONCLUSIONSDiabetes incidence is more strongly related to IFG defined as fasting glucose between 6.1 and 6.9 mmol/l than to the lower category of 5.6-6.0 mmol/l, or entire range of 5.6-6.9 mmol/l. Future studies should examine the association of IFG with cardiovascular outcomes, but for diabetes risk our study supports the use of the IFG cut-point at 6.1 mmol/l.
Aim  To determine the incidence of Type 2 diabetes and to examine the effect of different cut‐points for impaired fasting glucose (IFG) on diabetes incidence. Methods  Population‐based longitudinal study (1990–2000) with clinical, anthropometric and biochemical measurements, including an oral glucose tolerance test (OGTT), in 1040 non‐diabetic adults aged 40–69 years at baseline. Baseline glucose status was defined as normoglycaemia < 5.6, IFG‐lower 5.6–6.0 and IFG‐original 6.1–6.9 mmol/l. The all‐IFG group included fasting glucose values of 5.6–6.9 mmol/l. Results  The 10‐year cumulative incidence of diabetes was 7.3 per 1000 person‐years. Diabetes incidence was 2.4 [95% confidence interval (CI) 1.2, 4.8], 6.2 (4.0, 9.8) and 17.5 (12.5, 24.5) per 1000 person‐years in those with normoglycaemia, IFG‐lower and IFG‐original, respectively. Compared with normoglycaemia, the age/sex‐adjusted risk [hazard ratio (HR) and 95% CI] for incident diabetes was greatest in the IFG‐original category (HR 6.9; 3.1, 15.2) and increased to a lesser degree in the IFG‐lower (HR 2.5; 1.1, 5.7) and all‐IFG categories (HR 4.1; 1.9, 8.7). When adjusted for confounding factors, the magnitude and direction of associations persisted, with HR 1.9, 4.4 and 2.9, for the categories IFG‐lower, IFG‐original and all‐IFG, respectively. Conclusions  Diabetes incidence is more strongly related to IFG defined as fasting glucose between 6.1 and 6.9 mmol/l than to the lower category of 5.6–6.0 mmol/l, or entire range of 5.6–6.9 mmol/l. Future studies should examine the association of IFG with cardiovascular outcomes, but for diabetes risk our study supports the use of the IFG cut‐point at 6.1 mmol/l.
Author Hennings, S.
Forouhi, N. G.
Wareham, N. J.
Luan, J.
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  surname: Forouhi
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  surname: Wareham
  fullname: Wareham, N. J.
  organization: Medical Research Council (MRC) Epidemiology Unit, Elsie Widdowson Laboratories, Cambridge, UK
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Issue 2
Keywords Endocrinopathy
Type 2 diabetes
impaired fasting glucose
1990-2000
Metabolic diseases
Fast
Epidemiology
diabetes
Glycemia
Incidence
Language English
License CC BY 4.0
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PublicationTitle Diabetic medicine
PublicationTitleAlternate Diabet Med
PublicationYear 2007
Publisher Blackwell Publishing Ltd
Blackwell
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De Vegt F, Dekker JM, Jager A, Hienkens E, Kostense PJ, Stehouwer CD et al. Relation of impaired fasting and postload glucose with incident type 2 diabetes in a Dutch population: The Hoorn Study. JAMA 2001; 285: 2109-2113.
Meigs JB, Muller DC, Nathan DM, Blake DR, Andres R. The natural history of progression from normal glucose tolerance to type 2 diabetes in the Baltimore Longitudinal Study of Aging. Diabetes 2003; 52: 1475-1484.
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Tirosh A, Shai I, Tekes-Manova D, Israeli E, Pereg D, Shochat T et al. Normal fasting plasma glucose levels and type 2 diabetes in young men. N Engl J Med 2005; 353: 1454-1462.
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Snippet Aim  To determine the incidence of Type 2 diabetes and to examine the effect of different cut‐points for impaired fasting glucose (IFG) on diabetes incidence....
To determine the incidence of Type 2 diabetes and to examine the effect of different cut-points for impaired fasting glucose (IFG) on diabetes incidence....
Abstract Aim  To determine the incidence of Type 2 diabetes and to examine the effect of different cut‐points for impaired fasting glucose (IFG) on diabetes...
AIMTo determine the incidence of Type 2 diabetes and to examine the effect of different cut-points for impaired fasting glucose (IFG) on diabetes...
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StartPage 200
SubjectTerms Adult
Aged
Biological and medical sciences
diabetes
Diabetes Mellitus, Type 2 - epidemiology
Diabetes. Impaired glucose tolerance
Endocrine pancreas. Apud cells (diseases)
Endocrinopathies
England - epidemiology
Etiopathogenesis. Screening. Investigations. Target tissue resistance
Female
Glucose Tolerance Test
Humans
Hypoglycemia - epidemiology
impaired fasting glucose
Incidence
Longitudinal Studies
Male
Medical sciences
Middle Aged
Prevalence
Risk Factors
Title Incidence of Type 2 diabetes in England and its association with baseline impaired fasting glucose: The Ely study 1990-2000
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