PMID- 10023638 OWN - NLM STAT- MEDLINE DCOM- 19990223 LR - 20190815 IS - 1523-6838 (Electronic) IS - 0272-6386 (Linking) VI - 33 IP - 2 DP - 1999 Feb TI - Effect of ACE gene on diabetic nephropathy in NIDDM patients with insulin resistance. PG - 276-81 AB - We investigated the influence of the angiotensin-converting enzyme (ACE) gene on the onset and/or progression of diabetic nephropathy in 62 Japanese patients with non-insulin-dependent diabetes mellitus (NIDDM; type II diabetes). Because a number of factors are believed to be involved in the onset and/or progression of diabetic nephropathy, especially in patients with NIDDM, we selected the patients with well-matched risk factors, duration of disease, glycemic control, blood pressure, and others. All patients had normal renal function and none were receiving ACE inhibitors. Patients were divided into three groups according to albumin excretion rate (AER): group A, patients with an AER less than 15 microg/min (n = 29); group B, patients with an AER between 15 and 70 microg/min (n = 19); and group C, patients with an AER greater than 70 microg/min (n = 14). The glucose disposal rate was estimated using a euglycemic hyperinsulinemic clamp. We determined the mean glucose disposal rate in 132 patients with NIDDM (6.49 mg/kg/min). Patients with a glucose disposal rate less than the mean rate were considered to have a high degree of insulin resistance (n = 36). The presence of an insertion/deletion (I/D) polymorphism of the ACE gene was determined by the polymerase chain reaction method. Among patients with a high degree of insulin resistance, diabetic nephropathy was present in 2 of 11 patients with the II genotype of the ACE gene compared with 19 of 25 patients with the ID or DD genotype (P = 0.0024). The prevalence of diabetic nephropathy was greater in patients with both significant insulin resistance and the D allele (19 of 25) than in the remaining patients (14 of 37; odds ratio, 5.20). These results suggest that the ACE gene influences the onset and/or progression of diabetic nephropathy in patients with NIDDM with significant insulin resistance. FAU - Kuramoto, N AU - Kuramoto N AD - Department of Internal Medicine II, Chiba University School of Medicine, Japan. FAU - Iizuka, T AU - Iizuka T FAU - Ito, H AU - Ito H FAU - Yagui, K AU - Yagui K FAU - Omura, M AU - Omura M FAU - Nozaki, O AU - Nozaki O FAU - Nishikawa, T AU - Nishikawa T FAU - Tsuchida, H AU - Tsuchida H FAU - Makino, H AU - Makino H FAU - Saito, Y AU - Saito Y FAU - Kanatsuka, A AU - Kanatsuka A LA - eng PT - Journal Article PL - United States TA - Am J Kidney Dis JT - American journal of kidney diseases : the official journal of the National Kidney Foundation JID - 8110075 RN - EC 3.4.15.1 (Peptidyl-Dipeptidase A) SB - IM MH - Diabetes Mellitus, Type 2/blood/complications/*physiopathology MH - Diabetic Nephropathies/blood/etiology/*physiopathology MH - Female MH - Glucose Clamp Technique MH - Humans MH - *Insulin Resistance MH - Male MH - Middle Aged MH - Odds Ratio MH - Peptidyl-Dipeptidase A/*genetics MH - Polymorphism, Genetic EDAT- 1999/02/19 00:00 MHDA- 1999/02/19 00:01 CRDT- 1999/02/19 00:00 PHST- 1999/02/19 00:00 [pubmed] PHST- 1999/02/19 00:01 [medline] PHST- 1999/02/19 00:00 [entrez] AID - S0272-6386(99)70300-8 [pii] AID - 10.1016/s0272-6386(99)70300-8 [doi] PST - ppublish SO - Am J Kidney Dis. 1999 Feb;33(2):276-81. doi: 10.1016/s0272-6386(99)70300-8.