Blood Pressure-Related Genes and the Progression of IgA Nephropathy

被引:13
|
作者
Kim, Sun Moon [2 ]
Chin, Ho Jun [2 ,3 ]
Oh, Yun Kyu [1 ,2 ]
Kim, Yon Su [2 ,3 ]
Kim, Suhnggwon [2 ,3 ]
Lim, Chun Soo [1 ,2 ,3 ]
机构
[1] Seoul Natl Univ, Boramae Hosp, Dept Internal Med, Seoul 156707, South Korea
[2] Seoul Natl Univ, Dept Internal Med, Coll Med, Seoul 156707, South Korea
[3] Seoul Natl Univ, Kidney Res Inst, Coll Med, Med Res Ctr, Seoul 156707, South Korea
来源
NEPHRON CLINICAL PRACTICE | 2009年 / 113卷 / 04期
关键词
IgA nephropathy; Hypertension; Genetic polymorphism; Angiotensinogen; Gender; RENIN-ANGIOTENSIN SYSTEM; GENDER-SPECIFIC ASSOCIATION; RENAL-DISEASE; ESSENTIAL-HYPERTENSION; DIABETIC-NEPHROPATHY; CONVERTING ENZYME; JAPANESE PATIENTS; POLYMORPHISM; IMPACT; SYNTHASE;
D O I
10.1159/000235948
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
Background/Aims: Hypertension is one of the most significant prognostic factors of immunoglobulin A nephropathy (IgAN). We investigated the role of polymorphisms of hypertension-related genes in the clinical impact of IgAN. Methods: A total of 238 IgAN and 300 healthy cohorts were studied. The polymorphisms of angiotensinogen (AGT M235T), the angiotensin II type 1 receptor (A1166C), aldosterone synthase (C-344T), alpha-adducin (G460W) and endothelin-1 (K198N and 3A/4A) were determined. Results: The genotype distributions of the polymorphisms were similar between patients and controls. The individual genotypes taken alone were not associated with the development of hypertension or progression of renal dysfunction. Although AGT M235T was not associated with the development of hypertension in either sex, men with M235T TT were found to be at an increased risk of IgAN progression compared to those with the other genotypes (p = 0.019). In the Cox regression model with adjustment for clinical risk factors, including age at diagnosis, hypertension, serum creatinine and urinary protein excretion at renal biopsy, AGT M235T TT variant was an independent risk factor only for male patients (hazard ratio 5.848; p = 0.005). Conclusion: Our results suggest that the AGT M235T polymorphism is associated with the progression of IgAN in Korean male patients. Copyright (C) 2009 S. Karger AG, Basel
引用
收藏
页码:C301 / C308
页数:8
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