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Pernille Poulsen a Department of Endocrinology and Internal
Medicine, Odense University Hospital, DK-5000 C Odense, Denmark, b Department of Endocrinology,
Hvidovre Hospital, DK-2650 Hvidovre, Denmark
Correspondence to: P Poulsen
p.poulsen{at}winsloew.ou.dk
Objective:
To study the influence of zygosity on the metabolic variables involved in the pathophysiology of type 2 diabetes.
Design:
Population based cross sectional study.
Setting:
Odense University Hospital, Denmark.
Participants:
125 monozygotic twin pairs and 178 dizygotic twin pairs of the same sex born between 1921 and 1940.
Main outcome measures:
Clinical characteristics of
monozygotic and dizygotic twins with or without a family history of
type 2 diabetes.
Results:
Absolute prevalences of type 2 diabetes and impaired glucose tolerance according to the World Health Organisation criteria were similar in both the monozygotic and the dizygotic twins
as were measurements of height, weight, body mass index, waist to hip
ratio, and fasting plasma glucose and insulin concentrations. During
the oral glucose tolerance test, monozygotic twins had a higher
incremental plasma insulin area under the curve than dizygotic twins
(10.05 (SD 0.68) v 9.89 (0.72) pmol/l×minutes, P<0.01)
indicating insulin resistance. In twins with normal glucose tolerance
and without first degree relatives or co-twins with type 2 diabetes or
impaired glucose tolerance, both the glucose and insulin areas under
the curve were higher among monozygotic twins (glucose 214.4 (88.3)
v 189.8 (78.4) mmol/l×minutes, P<0.05; insulin 20 040
(14 865-32 554) v 17 625 (12 330-23 640)
pmol/l×minutes, P=0.08).
Conclusion:
Zygosity influences both plasma glucose
and plasma insulin concentrations during an oral glucose tolerance test. This supports an intrauterine influence on glucose homeostasis and perhaps on insulin resistance in humans.
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