Genetic susceptibility to end-stage renal disease

被引:45
作者
Schelling, JR
Zarif, L
Sehgal, A
Iyengar, S
Sedor, JR
机构
[1] Case Western Reserve Univ, Sch Med, Dept Epidemiol & Biostat, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Sch Med, Dept Med, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Sch Med, Dept Physiol & Biophys, Cleveland, OH 44106 USA
关键词
D O I
10.1097/00041552-199907000-00011
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
New methods have been developed to uncover the genotypes that result in complex diseases. End-stage renal disease is a complex disease, without a simple correspondence between genotype and phenotype. Both population-based and family-based epidemiological studies and analysis of model organisms suggest that the pathogenesis of end-stage renal disease may have a genetic component. A number of studies have analyzed candidate nephropathy genes with little success, but recently several well-designed studies of multiplex families with diabetic nephropathy have identified candidate nephropathy susceptibility loci. To date, kidney disease-oriented research has focused on effector mechanisms responsible for the initiation and progression of chronic renal disease. However, because end-stage renal disease is a complex disease, interruption of a single effector pathway is unlikely to result in significant therapeutic benefit. Further understanding of the pathogenesis of kidney disease and the development of new kidney disease therapies will require continued application of genetic and genomic tools to kidney disease research. Curr Opin Nephrol Hypertens 8:465-472. (C) 1999 Lippincott Williams & Wilkins.
引用
收藏
页码:465 / 472
页数:8
相关论文
共 72 条
[1]   Genes within and flanking the major histocompatibility region are risk factors for diabetes, insulin resistance, hypertension, and microalbuminuria in African-American women [J].
Acton, RT ;
Bell, DSH ;
Collins, J ;
Giger, JN ;
Go, RCP ;
Harrison, R ;
McDonald, R ;
Rivers, C ;
Roseman, JM ;
Taylor, HA ;
Vanichanan, C .
TRANSPLANTATION PROCEEDINGS, 1997, 29 (08) :3710-3712
[2]   Evaluation of risk factors for the development of nephropathy in patients with IDDM: Insertion/deletion angiotensin converting enzyme gene polymorphism, hypertension and metabolic control [J].
Barnas, U ;
Schmidt, A ;
Illievich, A ;
Kiener, HP ;
Rabensteiner, D ;
Kaider, A ;
Prager, R ;
Abrahamian, H ;
Irsigler, K ;
Mayer, G .
DIABETOLOGIA, 1997, 40 (03) :327-331
[3]  
Benigni A, 1996, SEMIN NEPHROL, V16, P151
[4]   Kidney disease in the first-degree relatives of African-Americans with hypertensive end-stage renal disease [J].
Bergman, S ;
Key, BO ;
Kirk, KA ;
Warnock, DG ;
Rostand, SG .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1996, 27 (03) :341-346
[5]   IS DIABETIC NEPHROPATHY AN INHERITED COMPLICATION [J].
BORCHJOHNSEN, K ;
NORGAARD, K ;
HOMMEL, E ;
MATHIESEN, ER ;
JENSEN, JS ;
DECKERT, T ;
PARVING, HH .
KIDNEY INTERNATIONAL, 1992, 41 (04) :719-722
[6]   Linkage of genetic markers on human chromosomes 20 and 12 to NIDDM in Caucasian sib pairs with a history of diabetic nephropathy [J].
Bowden, DW ;
Sale, M ;
Howard, TD ;
Qadri, A ;
Spray, BJ ;
Rothschild, CB ;
Akots, G ;
Rich, SS ;
Freedman, BI .
DIABETES, 1997, 46 (05) :882-886
[7]   Risk of end-stage renal disease in diabetes mellitus - A prospective cohort study of men screened for MRFIT [J].
Brancati, FL ;
Whelton, PK ;
Randall, BL ;
Neaton, JD ;
Stamler, J ;
Klag, MJ .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1997, 278 (23) :2069-2074
[8]   Renal disease susceptibility and hypertension are under independent genetic control in the fawn-hooded rat [J].
Brown, DM ;
Provoost, AP ;
Daly, MJ ;
Lander, ES ;
Jacob, HJ .
NATURE GENETICS, 1996, 12 (01) :44-51
[9]   RACE, SOCIOECONOMIC-STATUS, AND THE DEVELOPMENT OF END-STAGE RENAL-DISEASE [J].
BYRNE, C ;
NEDELMAN, J ;
LUKE, RG .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1994, 23 (01) :16-22
[10]  
Chen JW, 1997, DIABETIC MED, V14, P143, DOI 10.1002/(SICI)1096-9136(199702)14:2<143::AID-DIA316>3.0.CO