中华医学杂志
中華醫學雜誌
중화의학잡지
National Medical Journal of China
2013年
11期
827-831
,共5页
严健华%孙瓅贤%赵肖奕%廉慧%阮燕萍%朱燕林%张抒扬%方全%范中杰
嚴健華%孫瓅賢%趙肖奕%廉慧%阮燕萍%硃燕林%張抒颺%方全%範中傑
엄건화%손력현%조초혁%렴혜%원연평%주연림%장서양%방전%범중걸
动脉粥样硬化%患病率%危险因素%肾动脉狭窄
動脈粥樣硬化%患病率%危險因素%腎動脈狹窄
동맥죽양경화%환병솔%위험인소%신동맥협착
Atherosclerosis%Prevalence%Risk factor%Renal artery stenosis
目的 探讨冠脉造影患者中动脉粥样硬化性肾动脉狭窄(ARAS)的患病率及其危险因素.方法 1996年1月至2006年12月,北京协和医院心内科因疑诊和确诊冠心病(CAD),同时行冠状动脉造影(CAG)及肾动脉造影术(RAG)患者2506例,任1支或2支肾动脉狭窄≥50%诊断为ARAS.分析ARAS患病率,同时进行单因素及多因素Logistic回归,分析其危险因素.结果 2506例患者,男1479例,女1027例,平均年龄(62.7±11.4)岁,ARAS患者409例(16.3%),其中≥75%狭窄214例(8.5%);双侧肾动脉狭窄98例(3.9%),其中双侧狭窄≥75% 27例(1.1%);单侧左肾ARAS162例(6.5%),其中狭窄≥75% 84例(3.4%);单侧右肾ARAS 149例(5.9%),其中狭窄≥75%72例(2.9%).单因素分析筛选后,Logistic回归分析发现,年龄>65岁(P =0.025,OR=1.358)、女性(P <0.01,OR=1.678)、高血压(P<0.01,OR=1.650)、外周血管疾病(P<0.01,OR=14.678)、肾功能不全(P<0.01,OR=1.835)、冠状动脉3支病变(P<0.01,OR=1.746)及左主干病变(P<0.01,OR=3.416)是ARAS的独立危险因素.结论 年龄>65岁、女性、有高血压、外周动脉疾病,血清肌酐升高以及冠心病尤其是3支及左主干病变患者,应行肾动脉评估,尽早发现ARAS.
目的 探討冠脈造影患者中動脈粥樣硬化性腎動脈狹窄(ARAS)的患病率及其危險因素.方法 1996年1月至2006年12月,北京協和醫院心內科因疑診和確診冠心病(CAD),同時行冠狀動脈造影(CAG)及腎動脈造影術(RAG)患者2506例,任1支或2支腎動脈狹窄≥50%診斷為ARAS.分析ARAS患病率,同時進行單因素及多因素Logistic迴歸,分析其危險因素.結果 2506例患者,男1479例,女1027例,平均年齡(62.7±11.4)歲,ARAS患者409例(16.3%),其中≥75%狹窄214例(8.5%);雙側腎動脈狹窄98例(3.9%),其中雙側狹窄≥75% 27例(1.1%);單側左腎ARAS162例(6.5%),其中狹窄≥75% 84例(3.4%);單側右腎ARAS 149例(5.9%),其中狹窄≥75%72例(2.9%).單因素分析篩選後,Logistic迴歸分析髮現,年齡>65歲(P =0.025,OR=1.358)、女性(P <0.01,OR=1.678)、高血壓(P<0.01,OR=1.650)、外週血管疾病(P<0.01,OR=14.678)、腎功能不全(P<0.01,OR=1.835)、冠狀動脈3支病變(P<0.01,OR=1.746)及左主榦病變(P<0.01,OR=3.416)是ARAS的獨立危險因素.結論 年齡>65歲、女性、有高血壓、外週動脈疾病,血清肌酐升高以及冠心病尤其是3支及左主榦病變患者,應行腎動脈評估,儘早髮現ARAS.
목적 탐토관맥조영환자중동맥죽양경화성신동맥협착(ARAS)적환병솔급기위험인소.방법 1996년1월지2006년12월,북경협화의원심내과인의진화학진관심병(CAD),동시행관상동맥조영(CAG)급신동맥조영술(RAG)환자2506례,임1지혹2지신동맥협착≥50%진단위ARAS.분석ARAS환병솔,동시진행단인소급다인소Logistic회귀,분석기위험인소.결과 2506례환자,남1479례,녀1027례,평균년령(62.7±11.4)세,ARAS환자409례(16.3%),기중≥75%협착214례(8.5%);쌍측신동맥협착98례(3.9%),기중쌍측협착≥75% 27례(1.1%);단측좌신ARAS162례(6.5%),기중협착≥75% 84례(3.4%);단측우신ARAS 149례(5.9%),기중협착≥75%72례(2.9%).단인소분석사선후,Logistic회귀분석발현,년령>65세(P =0.025,OR=1.358)、녀성(P <0.01,OR=1.678)、고혈압(P<0.01,OR=1.650)、외주혈관질병(P<0.01,OR=14.678)、신공능불전(P<0.01,OR=1.835)、관상동맥3지병변(P<0.01,OR=1.746)급좌주간병변(P<0.01,OR=3.416)시ARAS적독립위험인소.결론 년령>65세、녀성、유고혈압、외주동맥질병,혈청기항승고이급관심병우기시3지급좌주간병변환자,응행신동맥평고,진조발현ARAS.
Objective To explore the prevalence and risk factors of atherosclerotic renal artery stenosis (ARAS) in patients undergoing coronary angiography.Methods A total of 2506 patients with suspected and known coronary heart disease (CAD) at our hospital underwent simultaneous coronary and renal angiography.Renal artery stenosis was defined as at least one of renal artery stenosis ≥ 50% narrowing of luminal diameter.The prevalence of ARAS was summarized from the results of angiography.And single-and multi-variable logistic regression analysis was used to assess the relationship between clinical characteristics and ARAS.Results Among them,there were 1479 males and 1027 females with a mean age of 62.7 ±11.4 years.ARAS was detected in 409 patients (16.3%),including 214 (8.5%) with significant stenosis (≥75%) ; Bilateral ARAS was detected in 98 patients (3.9%),including 27 (1.1%) with significant stenosis (≥75%).Left and right ARAS were detected in 162 patients (6.5%) and 148 patients (5.9%)respectively,including 84 patients (3.4%) with significant stenosis (≥75%) in left ARAS and 72 patients (2.9%) in right ARAS.Univariate analysis indicated that age,females,diabetes,hypertension,stroke,peripheral artery disease,coronary heart disease,renal insufficiency,dyslipidemia and hyperuricemia were the predictor for ARAS(P < 0.05 or 0.01).Multivariate regression analysis demonstrated that age ≥65 years (P =0.025,OR =1.358),females (P < 0.01,OR =1.678),hypertension (P < 0.01,OR =1.650),peripheral artery disease (P < 0.01,OR =14.678),renal insufficiency (P < 0.01,OR =1.835),coronary heart disease including 3-vessel (P < 0.01,OR =1.746) and left main coronary (P < 0.01,OR =3.416)disease were independent risk factors for ARAS.Conclusion Renal angiography should be routinely performed in female patients aged ≥ 65 years with hypertension,peripheral artery disease,elevated creatinine and coronary heart disease,especially for 3-vessel and left main coronary disease to identify ARAS in time.