Time trends regarding the etiology of renal artery stenosis: 18 years' experience from the China Center for Cardiovascular Disease

被引:26
作者
Xiong, Hong-liang [1 ,2 ]
Peng, Meng [3 ]
Jiang, Xiong-jing [1 ,2 ]
Che, Wu-qiang [1 ,2 ]
Dong, Hui [1 ,2 ]
Chen, Yang [1 ,2 ]
Zou, Yu-bao [1 ,2 ]
Gao, Run-lin [1 ,2 ]
Liu, Li-sheng [1 ,2 ]
机构
[1] Chinese Acad Med Sci, Fuwai Hosp, Dept Cardiol, Natl Ctr Cardiovasc Dis, Beijing, Peoples R China
[2] Peking Union Med Coll, 167 Beilishi Rd, Beijing 100037, Peoples R China
[3] Zhengzhou Univ, Dept Cardiol, Affiliated Hosp 1, Zhengzhou, Henan, Peoples R China
关键词
distribution; etiology; renal artery stenosis; trend; RHEUMATOLOGY; 1990; CRITERIA; FIBROMUSCULAR DYSPLASIA; TAKAYASUS-ARTERITIS; RISK-FACTORS; MANAGEMENT; DIAGNOSIS; CLASSIFICATION; HYPERTENSION; ASSOCIATION; COMMON;
D O I
10.1111/jch.13356
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
The time trends regarding the etiology of renal artery stenosis (RAS) are changing, but few investigations have focused on these issues. This study aimed to analyze the time trends regarding the etiology of RAS in a large patient sample from the China Center for Cardiovascular Disease. Consecutive inpatients with RAS from January 1999 to December 2016 were enrolled in this study. The etiologic diagnosis of RAS was based on established criteria. We retrospectively analyzed the time trends regarding the etiology of RAS during an 18-year period. A total of 2905 patients with RAS were enrolled. There were 2393 (82.4%) patients with atherosclerosis (AS), 345 (11.9%) with Takayasu arteritis (TA), 126 (4.3%) with fibromuscular dysplasia (FMD), and 41 (1.4%) with other causes. Among all patients (n = 2905), patients aged <= 40 years (n = 450), patients aged >40years (n = 2455), female patients (n = 1097), male patients (n = 1808), female patients aged >40years (n = 808), and male patients aged >40years (n = 1647), there were a gradual increase in the proportion of atherosclerotic RAS (P < 0.05), a gradual decrease in the proportion of RAS caused by TA (P < 0.05), and almost no change in the proportion of RAS caused by FMD during the 18-year period (P > 0.05). The data show that the primary causes of RAS are AS, TA, and FMD. The proportion of RAS caused by AS and TA gradually increased and decreased, respectively, over time, and the proportion of RAS caused by FMD showed no significant change.
引用
收藏
页码:1302 / 1309
页数:8
相关论文
共 35 条
  • [1] Standards of Medical Care in Diabetes-2014
    不详
    [J]. DIABETES CARE, 2014, 37 : S14 - S80
  • [2] THE EFFECT OF AGE ON PREVALENCE OF SECONDARY FORMS OF HYPERTENSION IN 4429 CONSECUTIVELY REFERRED PATIENTS
    ANDERSON, GH
    BLAKEMAN, N
    STREETEN, DHP
    [J]. JOURNAL OF HYPERTENSION, 1994, 12 (05) : 609 - 615
  • [3] AREND WP, 1990, ARTHRITIS RHEUM, V33, P1129
  • [4] Bicakcigil M, 2009, CLIN EXP RHEUMATOL, V27, pS59
  • [5] Bokhari M.R., 2018, RENAL ARTERY STENOSI
  • [6] Spontaneous dissection of the celiac artery
    Chaillou, P
    Moussu, P
    Noel, SF
    Sagan, C
    Pistorius, MA
    Langlard, JM
    Patra, P
    [J]. ANNALS OF VASCULAR SURGERY, 1997, 11 (04) : 413 - 415
  • [7] Takayasu's Arteritis and Its Role in Causing Renal Artery Stenosis
    Chaudhry, Muhammad A.
    Latif, Faisal
    [J]. AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 2013, 346 (04) : 314 - 318
  • [8] Treatment of hypertension in patients with renal artery stenosis due to fibromuscular dysplasia of the renal arteries
    Chrysant, Steven G.
    Chrysant, George S.
    [J]. CARDIOVASCULAR DIAGNOSIS AND THERAPY, 2014, 4 (01) : 36 - 43
  • [9] Epidemiology and Natural History of Atherosclerotic Renovascular Disease
    Chrysochou, Constantina
    Kalra, Philip A.
    [J]. PROGRESS IN CARDIOVASCULAR DISEASES, 2009, 52 (03) : 184 - 195
  • [10] Difference between renal and splenic resistive index as a novel criterion in Doppler evaluation of renal artery stenosis
    Grupp, Clemens
    Koziolek, Michael J.
    Wallbach, Manuel
    Hoxhold, Kerstin
    Mueller, Gerhard A.
    Bramlage, Carsten
    [J]. JOURNAL OF CLINICAL HYPERTENSION, 2018, 20 (03) : 582 - 588