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Diabetes, Vol 46, Issue 2 287-291, Copyright © 1997 by American Diabetes Association
Polymorphism in the 5'-end of the aldose reductase gene is strongly associated with the development of diabetic nephropathy in type I diabetes
AE Heesom, ML Hibberd, A Millward and AG Demaine
Department of Medicine, Plymouth Postgraduate Medical School, University of Plymouth, U.K.
Recent studies suggest that the gene encoding aldose reductase (ALR2), the
enzyme that converts glucose to sorbitol, may confer susceptibility to
microvascular disease. DNA from 275 British Caucasian patients with type I
diabetes and 102 normal healthy control patients were typed for a (CA)n
dinucleotide repeat polymorphic marker in the 5'-region of the ALR2 gene
using polymorase chain reaction (PCR). A highly significant decrease in the
frequency of the Z+2 allele was found in patients with nephropathy
(nephropathy group) compared with those with no complications after a
20-year duration of diabetes (uncomplicated group) (12.7 vs. 38.2%,
respectively, chi2 = 18.6, P < 0.00001); this was accompanied by an
increase in the Z-2 allele in the nephropathy group (32.0 vs. 12.7% in the
uncomplicated group). The nephropathy group also had a significant decrease
in the Z/Z+2 genotype compared with the uncomplicated patients (10.7 vs.
44.7%, chi2 = 16.0, P < 0.0001) and an increased frequency of the Z/Z-2
genotype. There was no significant association with diabetic retinopathy.
These results demonstrate that the ALR2 gene may play a role in
susceptibility to diabetic nephropathy; individuals with the Z+2 allele are
more than seven times less likely to develop diabetic renal disease than
those without this marker. This marker may prove valuable in screening for
patients with diabetic nephropathy at diagnosis of diabetes.

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Copyright © 1997 by the American Diabetes Association.
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