Summary
Summary: The point mutation at position 3243 of the tRNALeu(UUR) of the mitochondrial DNA is associated with mitochondrial encephalomyopathy, lactic
acidosis and strokes (MELAS) as well as with mitochondrial diabetes and deafness (MIDD).
A defect in insulin secretion has been found in most of these patients. However, there
have been controversial findings to which extent insulin resistance contributes to
pathogenesis. The aim of the present investigation was to study the insulin sensitivity
index (SI), insulin secretion (AIRGlucose) and glucose effectiveness (Sg) in patients with the 3243-mutation.
Material and Methods: 7 patients of a large pedigree (some of the members who were not investigated had
MELAS) and 3 siblings of another family in whom the 3243-mutation had been detected,
as well as 23 non-related, healthy control subjects underwent a modified intravenous
glucose tolerance test (Bergman's minimal model). In addition, a screening of islet
cell antibodies (ICA) was performed.
Results: All patients except for one with known diabetes mellitus revealed normal glucose
tolerance. There was no difference between patients and controls for SI, AIRGlucose or Sg. However, when looking at the individual results, there were 4 closely related
members of the large family with very poor insulin sensitivity. The other 2 patients
of this pedigree were more distantly related and extremely insulin sensitive. The
siblings of the other family revealed normal or even a very good insulin sensitivity.
In one patient, ICA were detected.
Conclusions: The 3243-mutation does not seem to be causative for insulin resistance in our patients.
Whether nuclear genes are involved and indirectly influence the expression of the
3243-mutation or, more likely, directly lead to impaired insulin sensitivity in some
of our patients cannot be answered by our data. It remains open whether there is a
difference in the pathogenesis of diabetes between patients with MIDD and those with
MELAS.
Key words:
MIDD - Insulin resistance - 3243-mutation - Islet cell antibodies
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Prof. Dr. H. Laube
Med. Klinik III und Poliklinik
Universität Giessen
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