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Diabetes, Vol 43, Issue 1 40-46, Copyright © 1994 by American Diabetes Association
Abnormal insulin secretion, not insulin resistance, is the genetic or primary defect of MODY in the RW pedigree
WH Herman, SS Fajans, FJ Ortiz, MJ Smith, J Sturis, GI Bell, KS Polonsky and JB Halter
Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor 48109-0354.
Maturity-onset diabetes of the young (MODY) is a form of
non-insulin-dependent diabetes mellitus (NIDDM) associated with
autosomal-dominant inheritance. In the RW pedigree, MODY is associated with
polymorphic DNA markers on chromosome 20q. To determine the early
abnormalities of insulin action and insulin secretion in MODY, we studied
nondiabetic members of the RW pedigree with and without the gene marker.
Six nondiabetic marker-negative and 5 nondiabetic marker-positive members
of the RW pedigree were studied, as were 4 diabetic marker-positive family
members. Unrelated, young, healthy subjects served as comparison groups.
Insulin action and insulin secretion were assessed with a frequently
sampled intravenous glucose tolerance test. Insulin secretion was further
assessed during constant glucose infusion by deconvolution of plasma
C-peptide and by pulse analysis. The nondiabetic marker-positive group had
normal sensitivity to insulin and unimpaired acute insulin response to
intravenous glucose (AIRglu). However, the nondiabetic marker-positive
group had decreased mean plasma C-peptide concentration and reduced
absolute amplitude of insulin secretory oscillations during prolonged
glucose infusion. These responses to prolonged glucose infusion were
similar to those observed in the diabetic group. No alterations of insulin
secretion were observed in the nondiabetic marker-negative family members.
Deranged and deficient insulin secretion, and not insulin resistance,
appears to be the genetic or primary abnormality that characterizes
nondiabetic individuals who are predisposed to MODY in the RW
pedigree.(ABSTRACT TRUNCATED AT 250 WORDS)

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Copyright © 1994 by the American Diabetes Association.
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