Genetic epidemiology of chronic kidney disease

被引:4
|
作者
Estrella, Michelle M. [3 ]
Sperati, Chistopher J. [3 ]
Kao, Wen H. L. [4 ]
Parekh, Rulan S. [1 ,2 ,4 ]
机构
[1] Hosp Sick Children, Sick Kids Res Inst, Univ Hlth Network, Toronto, ON M5G 1X8, Canada
[2] Univ Toronto, Toronto, ON, Canada
[3] Johns Hopkins Sch Med, Dept Med, Baltimore, MD USA
[4] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Epidemiol, Toronto, ON, Canada
来源
关键词
chronic kidney disease; genetic; genome-wide association study; MYH9; UMOD; GLOMERULAR-FILTRATION-RATE; URINARY ALBUMIN EXCRETION; STAGE RENAL-DISEASE; WIDE LINKAGE SCAN; AFRICAN-AMERICANS; SERUM CREATININE; HYPERTENSIVE FAMILIES; DIABETIC-NEPHROPATHY; SUSCEPTIBILITY GENES; BLOOD-PRESSURE;
D O I
10.1097/MNH.0b013e328338185f
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
Purpose of review To provide a brief review of methods used in genetic epidemiology studies, an update of recent significant findings in genome-wide studies of kidney disease, and a discussion of the clinical implications of these findings. Recent findings Recent developments in genetic epidemiology methodologies, specifically the use of genome-wide panels of single nucleotide polymporphisms (SNPs) for association analyses, have yielded exciting insights into the underlying pathogenesis of chronic kidney disease and its progression. The two most notable and promising genetic discoveries are those of MYH9 and UMOD, both of which have been replicated in separate populations. Summary Genomic studies have the potential to yield exciting new areas of biological research, potential targets for treatment, and ultimately markers of disease risk. This review addresses recent genetic studies and their implications in chronic kidney disease care.
引用
收藏
页码:283 / 291
页数:9
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