Polymorphisms of the aldose reductase gene and susceptibility to diabetic microvascular complications

被引:56
作者
Demaine, AG [1 ]
机构
[1] Peninsula Med Sch, Mol Med Res Grp, Plymouth PL6 8BX, Devon, England
关键词
diabetic nephropathy; retinopathy; neuropathy; diabetes; aldose reductase; polyol pathway; genetics; OSMOTIC RESPONSE ELEMENT; DINUCLEOTIDE REPEAT POLYMORPHISM; LIPID-PEROXIDATION PRODUCT; STAGE RENAL-DISEASE; RISK-FACTORS; SEQUENCE DETERMINATION; JAPANESE PATIENTS; OXIDATIVE STRESS; BINDING PROTEIN; KETO REDUCTASES;
D O I
10.2174/0929867033457359
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Diabetes is a major cause of mortality and morbidity due to the long term microvascular complications of this disease. There is now convincing evidence to show that genetic factors together with elevated blood glucose play an important role in the susceptibility to diabetic nephropathy as well as retinopathy. The polyol pathway is thought to play an important role in the pathogenesis of diabetic microvascular complications. Aldose reductase is the first and rate-limiting enzyme of the polyol pathway. Polymorphisms in the promoter region as well as elsewhere in the gene have been associated with susceptibility to nephropathy, retinopathy as well as diabetic neuropathy. These associations have been replicated in patients with either type 1 or type 2 diabetes mellitus as well as across ethnic groups. These polymorphisms in the promoter region are also associated with expression of the gene. Although clinical trials using inhibitors of aldose reductase to treat diabetic microvascular complications have largely been unsuccessful, the identification of the susceptibility genes may help in the design of future drug regimens.
引用
收藏
页码:1389 / 1398
页数:10
相关论文
共 126 条
  • [51] PURIFICATION AND PROPERTIES OF 6 ALDO-KETO REDUCTASES FROM RAT ADRENAL-GLAND
    INAZU, N
    NAGASHIMA, Y
    SATOH, T
    FUJII, T
    [J]. JOURNAL OF BIOCHEMISTRY, 1994, 115 (05) : 991 - 999
  • [52] An aldose reductase inhibitor prevents glucose-induced increase in transforming growth factor-β and protein kinase C activity in cultured human mesangial cells
    Ishii, H
    Tada, H
    Isogai, S
    [J]. DIABETOLOGIA, 1998, 41 (03) : 362 - 364
  • [53] The level of erythrocyte aldose reductase: A risk factor for diabetic neuropathy?
    Ito, T
    Nishimura, C
    Takahashi, Y
    Saito, T
    Omori, Y
    [J]. DIABETES RESEARCH AND CLINICAL PRACTICE, 1997, 36 (03) : 161 - 167
  • [54] Osmotic response element is required for the induction of aldose reductase by tumor necrosis factor-α
    Iwata, T
    Sato, S
    Jimenez, J
    McGowan, M
    Moroni, M
    Dey, A
    Ibaraki, N
    Reddy, VN
    Carper, D
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (12) : 7993 - 8001
  • [55] JAGT DLV, 1995, BBA-PROTEIN STRUCT M, V1249, P117
  • [56] RISK-FACTORS FOR PROGRESSION OF BACKGROUND RETINOPATHY IN LONG-STANDING IDDM
    JANKA, HU
    WARRAM, JH
    RAND, LI
    KROLEWSKI, AS
    [J]. DIABETES, 1989, 38 (04) : 460 - 464
  • [57] JONES SA, 1995, J AM SOC NEPHROL, V5, P1483
  • [58] KalterLeibovici O, 1997, DIABETIC MED, V14, P858, DOI 10.1002/(SICI)1096-9136(199710)14:10<858::AID-DIA471>3.0.CO
  • [59] 2-V
  • [60] An aldose reductase intragenic polymorphism associated with diabetic retinopathy
    Kao, YL
    Donaghue, K
    Chan, A
    Knight, J
    Silink, M
    [J]. DIABETES RESEARCH AND CLINICAL PRACTICE, 1999, 46 (02) : 155 - 160