Chemotactic cytokine receptor 5 (CCR5) gene promoter polymorphism (59029A/G) is associated with diabetic nephropathy in Japanese patients with type 2 diabetes: A 10-year longitudinal study

被引:23
作者
Mokubo, Atsuko
Tanaka, Yasushi
Nakajima, Kunihiro
Watada, Hirotaka
Hirose, Takahisa
Kawasumi, Masahiko
Sakai, Ken
Kanazawa, Akio
Maeda, Shiro
Hosokawa, Kazuhiro
Atsumi, Yoshihito
Matsuoka, Kenpei
Kawamori, Ryuzo
机构
[1] Juntendo Univ, Sch Med, Dept Med Metab & Endocrinol, Bunkyo Ku, Tokyo 1138421, Japan
[2] Tokyo Saiseikai Cent Hosp, Dept Internal Med, Minato Ku, Tokyo 1080073, Japan
[3] RIKEN, Inst Phys & Chem Res, Lab Diabet Nephropathy, SNP Res Ctr,Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan
关键词
CCR5; chemotactic cytokine; polymorphism; diabetes; nephropathy;
D O I
10.1016/j.diabres.2005.12.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We previously showed that polymorphisms of the promoter area of chemokine receptor 5 (CCR5) gene (59029G/A) and its agonist, regulated upon activation, normal T-cell expressed and secreted (RANTES) gene (-28C/G) were new candidates for susceptibility to diabetic nephropathy. The aim of this study was to confirm the effect of these polymorphisms on the development and progression of diabetic nephropathy. We performed a 10-year retrospective study of 191 Japanese type 2 diabetic patients with normoalbuminuria at baseline. The subjects were classified into two groups: (1) those with persistent normoalbuminuria (group N) and (2) those with progression from normoalbuminuria to microalbuminuria or overt proteinuria (group P). Then, their association with CCR5 59029G/A and RANTES -28C/G polymorphisms was assessed. The frequency of the RANTES -28G(+) genotype did nor differ between the two groups, but the CCR5 59029A(+) genotype had a significantly higher frequency in group P than in group N (83% versus 71%, p = 0.04). By discriminant analysis, only the CCR5 59029A(+) genotype showed an independent positive correlation with the onset or progression of nephropathy (p = 0.03, odds ratio = 2.41, 95% CI = 1.09-5.33). Therefore, the CCR5 59029A(+) genotype seems to be related the etiology of diabetic nephropathy in Japanese type 2 diabetics. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
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页码:89 / 94
页数:6
相关论文
共 23 条
[1]  
Abdi R, 2002, J AM SOC NEPHROL, V13, DOI 10.1681/ASN.V133754
[2]  
Al Sharif F, 1999, EUR J IMMUNOGENET, V26, P373
[3]  
American Diabetes Association, 2003, DIABETES CARE S1, V26, pS94
[4]   Macrophages in mouse type 2 diabetic nephropathy: Correlation with diabetic state and progressive renal injury [J].
Chow, F ;
Ozols, E ;
Nikolic-Paterson, DJ ;
Atkins, RC ;
Tesch, GH .
KIDNEY INTERNATIONAL, 2004, 65 (01) :116-128
[5]   THE ROLE OF MACROPHAGES IN DIABETIC GLOMERULOSCLEROSIS [J].
FURUTA, T ;
SAITO, T ;
OOTAKA, T ;
SOMA, J ;
OBARA, K ;
ABE, K ;
YOSHINAGA, K .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1993, 21 (05) :480-485
[6]   Multifactorial intervention and cardiovascular disease in patients with type 2 diabetes [J].
Gaede, P ;
Vedel, P ;
Larsen, N ;
Jensen, GVH ;
Parving, H ;
Pedersen, O .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (05) :383-393
[7]   Met-RANTES reduces vascular and tubular damage during acute renal transplant rejection:: blocking monocyte arrest and recruitment [J].
Gröne, HJ ;
Weber, C ;
Weber, KSC ;
Gröne, EF ;
Rabelink, T ;
Klier, CM ;
Wells, TNC ;
Proudfoot, AE ;
Schlöndorff, D ;
Nelson, PJ .
FASEB JOURNAL, 1999, 13 (11) :1371-1383
[8]   POSSIBLE ROLE OF TUMOR-NECROSIS-FACTOR AND INTERLEUKIN-1 IN THE DEVELOPMENT OF DIABETIC NEPHROPATHY [J].
HASEGAWA, G ;
NAKANO, K ;
SAWADA, M ;
UNO, K ;
SHIBAYAMA, Y ;
IENAGA, K ;
KONDO, M .
KIDNEY INTERNATIONAL, 1991, 40 (06) :1007-1012
[9]   PREVALENCE OF CAROTID ATHEROSCLEROSIS IN DIABETIC-PATIENTS - ULTRASOUND HIGH-RESOLUTION B-MODE IMAGING ON CAROTID ARTERIES [J].
KAWAMORI, R ;
YAMASAKI, Y ;
MATSUSHIMA, H ;
NISHIZAWA, H ;
NAO, K ;
HOUGAKU, H ;
MAEDA, H ;
HANDA, N ;
MATSUMOTO, M ;
KAMADA, T .
DIABETES CARE, 1992, 15 (10) :1290-1294
[10]   Polymorphism in RANTES chemokine promoter affects HIV-1 disease progression [J].
Liu, HL ;
Chao, D ;
Nakayama, EE ;
Taguchi, H ;
Goto, M ;
Xin, XM ;
Takamatsu, J ;
Saito, H ;
Ishikawa, Y ;
Akaza, T ;
Juji, T ;
Takebe, Y ;
Ohishi, T ;
Fukutake, K ;
Maruyama, Y ;
Yashiki, SJ ;
Sonoda, S ;
Nakamura, T ;
Nagai, Y ;
Iwamoto, A ;
Shioda, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (08) :4581-4585