Genetics of kidney disease

被引:11
作者
Bowden, DW
机构
[1] Wake Forest Univ, Bowman Gray Sch Med, Ctr Human Genom, Winston Salem, NC 27157 USA
[2] Wake Forest Univ, Bowman Gray Sch Med, Dept Biochem, Winston Salem, NC 27157 USA
[3] Wake Forest Univ, Bowman Gray Sch Med, Dept Internal Med, Winston Salem, NC 27157 USA
关键词
inherited kidney disease; heritable renal disease; genome screening; familial genetic evaluation; candidate genes;
D O I
10.1046/j.1523-1755.63.s83.3.x
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 [临床医学]; 100201 [内科学];
摘要
Multiple lines of evidence suggest that susceptibility to develop end-stage renal disease (ESRD) has a significant genetic component. These studies include familial aggregation studies, comparisons of incidence rates between different racial or ethnic populations, and segregation analysis. Multiple approaches have been employed in an effort to identify genes that contribute to this genetic susceptibility. Many studies have now been carried out assessing the contribution of specific "candidate genes," that is, genes with functions consistent with involvement in renal pathogenesis. Independent evaluations of specific candidate genes have frequently provided contradictory results. This may be due, in part, to the modest contribution to genetic susceptibility that these genes impart. In contrast to the focused analysis of candidate genes, the genome scan approach employs a comprehensive evaluation of inheritance throughout the genome. The great potential advantage of the genome scan is the ability to identify chromosomal regions harboring novel, previously unrecognized, genes that contribute to renal disease. Results from whole genome scans of family collections are now beginning to appear and give the promise that multiple comprehensive genetic evaluations of end-stage renal disease will soon be available for evaluation.
引用
收藏
页码:8 / 12
页数:5
相关论文
共 18 条
[1]
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
[2]
Familial clustering of diabetic nephropathy in Brazilian type 2 diabetic patients [J].
Canani, LH ;
Gerchman, F ;
Gross, JL .
DIABETES, 1999, 48 (04) :909-913
[3]
Diabet Control Complications Trial Res Grp, 1997, DIABETES, V46, P1829
[4]
Is diabetic nephropathy inherited? Studies of glomerular structure in type 1 diabetic sibling pairs [J].
Fioretto, P ;
Steffes, MW ;
Barbosa, J ;
Rich, SS ;
Miller, ME ;
Mauer, M .
DIABETES, 1999, 48 (04) :865-869
[5]
Segregation analysis of urinary albumin excretion in families with type 2 diabetes [J].
Fogarty, DG ;
Hanna, LS ;
Wantman, M ;
Warram, JH ;
Krolewski, AS ;
Rich, SS .
DIABETES, 2000, 49 (06) :1057-1063
[6]
THE FAMILIAL RISK OF END-STAGE RENAL-DISEASE IN AFRICAN-AMERICANS [J].
FREEDMAN, BI ;
SPRAY, BJ ;
TUTTLE, AB ;
BUCKALEW, VM .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1993, 21 (04) :387-393
[7]
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
[8]
Sib-pair linkage analysis for susceptibility genes for microvascular complications among Pima Indians with type 2 diabetes [J].
Imperatore, G ;
Hanson, RL ;
Pettitt, DJ ;
Kobes, S ;
Bennett, PH ;
Knowler, WC .
DIABETES, 1998, 47 (05) :821-830
[9]
Segregation analysis of diabetic nephropathy in Pima Indians [J].
Imperatore, G ;
Knowler, WC ;
Pettitt, DJ ;
Kobes, S ;
Bennett, PH ;
Hanson, RL .
DIABETES, 2000, 49 (06) :1049-1056
[10]
Lei HH, 1998, J AM SOC NEPHROL, V9, P1270