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Diabetes, Vol 44, Issue 5 489-494, Copyright © 1995 by American Diabetes Association
Lack of relationship between an insertion/deletion polymorphism in the angiotensin I-converting enzyme gene and diabetic nephropathy and proliferative retinopathy in IDDM patients
L Tarnow, F Cambien, P Rossing, FS Nielsen, BV Hansen, L Lecerf, O Poirier, S Danilov and HH Parving
Steno Diabetes Center, Gentofte, Denmark.
Genotypic abnormalities of the renin-angiotensin system have been suggested
as a risk factor for the development of diabetic nephropathy and
proliferative retinopathy. We studied the relationship between an
insertion(I)/deletion (D) polymorphism in the angiotensin-converting enzyme
(ACE) gene in insulin-dependent diabetes mellitus (IDDM) patients with
diabetic nephropathy (121 men and 77 women, age 40.9 +/- 10 years, diabetes
duration 27 +/- 8 years) and in IDDM patients with normoalbuminuria (118
men and 74 women, age 42.7 +/- 10 years, diabetes duration 26 +/- 8 years).
A total of 155 patients (40%) had proliferative retinopathy, and 67
patients (17%) had no diabetic retinopathy. There was no difference in
genotype distribution between IDDM patients with diabetic nephropathy and
those with normalbuminuria: 63 (32%)/95 (48%)/40 (20%) vs. 67 (35%)/77
(41%)/46 (24%) had DD/ID/II genotypes, respectively. Patients with
nephropathy had higher plasma ACE levels (609 [151-1,504] micrograms/l)
compared with patients with normoalbuminuria (428 [55-1,630] micrograms/l)
(P < 0.001). Multiple linear regression analysis revealed that the
plasma ACE level in patients with nephropathy is partially determined by
ACE/ID polymorphism, mean arterial blood pressure, and glomerular
filtration rate (r2 = 0.30, P < 0.001). There was no difference in
genotype distribution between IDDM patients with proliferative retinopathy
and those without diabetic retinopathy: 52 (34%)/74 (48%)/29 (19%) vs. 26
(39%)/25 (37%)/16 (24%) had DD/ID/II genotypes, respectively. There was
also no difference in plasma ACE concentration detected among patients with
no, simplex, or proliferative retinopathy.(ABSTRACT TRUNCATED AT 250 WORDS)

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Copyright © 1995 by the American Diabetes Association.
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