Co-inheritance of specific genotypes of HSPG and ApoE gene increases risk of type 2 diabetic nephropathy

被引:28
作者
Liu, LM [1 ]
Xiang, KS [1 ]
Zheng, TS [1 ]
Zhang, R [1 ]
Li, M [1 ]
Li, J [1 ]
机构
[1] Shanghai Jiaotong Univ Affiliated Sixth Peoples H, Shanghai Diabet Inst, Dept Endocrinol & Metab, Shanghai 200233, Peoples R China
关键词
HSPG gene; ApoE gene; polymorphism; co-inheritance; type 2 diabetes mellitus; diabetic nephropathy;
D O I
10.1023/A:1027364121738
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The objective of this paper is to investigate co-inheritance of specific HSPG and ApoE genotypes in the development of Chinese type 2 diabetic nephropathy. PCR-RFLP was used to detect HSPG and ApoE genotypes in 385 Chinese subjects including 298 patients with type 2 diabetes mellitus (T2DM) and 87 non-diabetic controls (Non-DM). The T2DM group was subdivided into patients with (TDN; n = 218) and without diabetic nephropathy (Non-DN; n = 80). The latter group was further subdivided into groups of patients with microalbuminuria nephropathy (DN-1; n = 129) and severe diabetic nephropathy (DN-2; n = 89). We then compared the relative frequencies of various HSPG and ApoE genotypes and alleles among the groups, searching for predictive trends. The T allele of the HSPG gene occurred more frequently in the DN-2 group than in the Non-DN or DN-1 groups, their Fisher's exact p was 1.05 x 10(-3) and 6.58 x 10(-6); odds ratios were 2.09 (95% CI 1.32 - 3.30) and 2.48 (95% CI 1.64 - 3.74), respectively. The E2 allele of the ApoE gene occurred more frequently in the T2DM than in the Non-DM group, the Fisher's exact p was 0.0087; odds ratio was 3.45 (95% CI 1.30 - 9.81). Genotype analysis showed that the TT or TG of HSPG gene were paired with the E2/2 or E2/3 of ApoE gene significantly more frequently in the TDN group than in the Non-DN group, with an odds ratio of 3.03 (95% CI 1.03 - 8.90). There was no significant differences in other combinations of genotypes in HSPG and ApoE genes between TDN and Non-DN group. These results suggest that the HSPG T allele is a risk factor for the development of severe diabetic nephropathy in type 2 diabetic patients, and that the ApoE E2 allele is a risk factor for the occurrence of type 2 diabetes mellitus in Chinese general population. In addition, we find that co-inheritance of T/E2 confers a higher risk of type 2 diabetes mellitus progression to diabetic nephropathy in Chinese.
引用
收藏
页码:353 / 358
页数:6
相关论文
共 14 条
[1]   APOLIPOPROTEIN-E SYNTHESIS IN HUMAN-KIDNEY, ADRENAL-GLAND, AND LIVER [J].
BLUE, ML ;
WILLIAMS, DL ;
ZUCKER, S ;
KHAN, SA ;
BLUM, CB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (01) :283-287
[2]   Genetic determinants of diabetic nephropathy [J].
Chowdhury, TA ;
Dyer, PH ;
Kumar, S ;
Barnett, AH ;
Bain, SC .
CLINICAL SCIENCE, 1999, 96 (03) :221-230
[3]   Apolipoprotein E genetic polymorphism, remnant lipoproteins, and nephropathy in type 2 diabetic patients [J].
Eto, M ;
Saito, M ;
Okada, M ;
Kume, Y ;
Kawasaki, F ;
Matsuda, M ;
Yoneda, M ;
Matsuki, M ;
Takigami, S ;
Kaku, K .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2002, 40 (02) :243-251
[4]   FAMILIAL PREDISPOSITION TO NEPHROPATHY IN AFRICAN-AMERICANS WITH NON-INSULIN-DEPENDENT DIABETES-MELLITUS [J].
FREEDMAN, BI ;
TUTTLE, AB ;
SPRAY, BJ .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1995, 25 (05) :710-713
[5]   Genetic variation of the heparan sulfate proteoglycan gene (Perlecan gene) - Association with urinary albumin excretion in IDDM patients [J].
Hansen, PM ;
Chowdhury, T ;
Deckert, T ;
Hellgren, A ;
Bain, SC ;
Pociot, F .
DIABETES, 1997, 46 (10) :1658-1659
[6]  
LINDAHL U, 1989, ANN NY ACAD SCI, V556, P36
[7]   LIPOPROTEIN RECEPTORS AND CHOLESTEROL HOMEOSTASIS [J].
MAHLEY, RW ;
INNERARITY, TL .
BIOCHIMICA ET BIOPHYSICA ACTA, 1983, 737 (02) :197-222
[8]  
MOORHEAD JF, 1982, LANCET, V2, P1309
[9]   FAMILIAL PREDISPOSITION TO RENAL-DISEASE IN 2 GENERATIONS OF PIMA-INDIANS WITH TYPE-2 (NON-INSULIN-DEPENDENT) DIABETES-MELLITUS [J].
PETTITT, DJ ;
SAAD, MF ;
BENNETT, PH ;
NELSON, RG ;
KNOWLER, WC .
DIABETOLOGIA, 1990, 33 (07) :438-443
[10]  
RICHARD P, 1994, CLIN CHEM, V40, P24