Use of HbA
1c
in Predicting Progression to
Diabetes in French Men and Women
Data from an Epidemiological Study on the Insulin Resistance Syndrome
(DESIR)
CELINE DROUMAGUET, MD, MSC
1
BEVERLEY BALKAU, PHD
1,2
DOMINIQUE SIMON, MD, PHD
1,2,3
EMILE CACES, MSC
4
JEAN TICHET, MD
4
MARIE ALINE CHARLES, MD
1,2
EVELINE ESCHWEGE, MD
1,2
THE DESIR STUDY GROUP*
OBJECTIVE — Early identification of subjects at high risk for diabetes is essential, and ran-
dom HbA
1c
(A1C) may be more practical than fasting plasma glucose (FPG). The predictive value
of A1C, in comparison to FPG, is evaluated for 6-year incident diabetes.
RESEARCH DESIGN AND METHODS — From the French cohort study Data from an
Epidemiological Study on the Insulin Resistance Syndrome (DESIR), 1,383 men and 1,437
women, aged 30 – 65 years, were volunteers for a routine health check-up. Incident diabetes was
defined by FPG 7.0 mmol/l or treatment by antidiabetic drugs. Multivariate logistic regression
models were used to predict diabetes at 6 years. Receiver operating characteristic curves com-
pared the predictive values of A1C and FPG.
RESULTS — At 6 years, 30 women (2.1%) and 60 men (4.3%) had developed diabetes.
Diabetes risk increased exponentially with A1C in both sexes (P 0.001). After stratifying on
FPG, A1C predicted diabetes only in subjects with impaired fasting glucose (IFG) (FPG 6.10
mmol/l): the odds ratio (95% CI) for a 1% increase in A1C was 7.20 (3.00 –17.00). In these
subjects, an A1C of 5.9% gave an optimal sensitivity of 64% and specificity of 77% to predict
diabetes.
CONCLUSIONS — A1C predicted diabetes, even though the diagnosis of diabetes was
based on FPG, but it was less sensitive and specific than FPG. It could be used as a test if fasting
blood sampling was not available or in association with FPG. In subjects with IFG, A1C is better
than glucose to evaluate diabetes risk, and it could be used to select subjects for intensive early
intervention.
Diabetes Care 29:1619 –1625, 2006
T
he prevalence of type 2 diabetes is
increasing worldwide, and it is pro-
jected that the number of adults
with diabetes will double between 2000
and 2030 (1). This means a large burden
for the health care system. Recent clinical
trials have demonstrated that lifestyle
(2– 4) or pharmaceutical (4 – 6) interven-
tions in individuals with impaired glucose
tolerance (IGT) can delay or prevent dia-
betes; thus high-risk subjects should be
identified for early intensive lifestyle
counseling or even pharmaceutical treat-
ment (7).
Fasting and 2-h plasma glucose after
an oral glucose tolerance test (OGTT) are
currently used to identify subjects at high
risk of diabetes (8): those with impaired
fasting glucose (IFG) and IGT. However,
the OGTT is not common in clinical prac-
tice, because it is time consuming, costly,
and less reproducible (9) than measure-
ment of fasting plasma glucose (FPG).
HbA
1c
(A1C), an indirect measure of
mean blood glucose over the previous
2–3 months, is correlated with FPG and
2-h plasma glucose (10 –12). A1C is more
reproducible than FPG (13) and within-
subject coefficients of variation are 1.7
and 5.7%, respectively (14). Moreover,
measurement of A1C does not require
that the subject is fasting. The use of A1C
could better integrate chronic hypergly-
cemia than FPG.
Few studies have investigated pre-
dicting diabetes using A1C and none in a
Caucasian population. Moreover, previ-
ous investigations were in populations at
high risk of diabetes. A study in Pima In-
dians (15) reported that A1C was an in-
dependent predictor for diabetes only in
individuals with IGT, not in subjects with
normal 2-h plasma glucose. The same re-
lation was found in a Chinese study (16).
To determine whether A1C predicted
incident diabetes after a 6-year follow-up
in a Caucasian population, we analyzed
data from the prospective French cohort
study: Data from an Epidemiological
Study on the Insulin Resistance Syn-
drome (DESIR).
RESEARCH DESIGN AND
METHODS — The 3,854 subjects
studied, aged 30 – 65 years, were in-
cluded in 1994–1996 in the DESIR
Study, a follow-up study on the develop-
ment of the insulin resistance syndrome.
They were volunteers for a routine health
check-up in seven Health Examination
Centers financed by the French Social Se-
curity in the center-west of France. All
participants gave informed consent, and
the study was approved by an ethics com-
mittee (Comite ´ Consultatif de Protection
●●●●●●●●●●●●●●●●●●●●●●●●●●●●●●●●●●●●●●●●●●●●●●●●●
From the
1
Institut National de la Sante ´ et de la Recherche Me ´ dicale U258, Villejuif, France; the
2
Faculte ´ de
Me ´decine, University of Paris-Sud, Villejuif, France; the
3
Service de Diabe ´tologie et Me ´tabolisme, Groupe
Hospitalier Pitie ´-Salpe ˆtrie ` re, Paris, France; and the
4
Institut inter-Re ´ gional pour la Sante ´ , La Riche, France.
Address correspondence and reprint requests to Beverley Balkau, INSERM U258-IFR69, 16 avenue Paul
Vaillant-Couturier, 94807 Villejuif cedex, France. E-mail: balkau@vjf.inserm.fr.
Received for publication 23 December 2005 and accepted in revised form 13 April 2006
*A complete list of DESIR Study Group members can be found in the APPENDIX.
Abbreviations: DESIR, Data from an Epidemiological Study on the Insulin Resistance Syndrome; FPG,
fasting plasma glucose; IFG, impaired fasting glucose; IGT, impaired glucose tolerance; OGTT, oral glucose
tolerance test; ROC, receiver operating characteristic.
A table elsewhere in this issue shows conventional and Syste `me International (SI) units and conversion
factors for many substances.
DOI: 10.2337/dc05-2525
© 2006 by the American Diabetes Association.
The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby
marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.
Cardiovascular and Metabolic Risk
O R I G I N A L A R T I C L E
DIABETES CARE, VOLUME 29, NUMBER 7, JULY 2006 1619
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