OBJECTIVE: To evaluate the prevalence of incidental renal artery stenosis due to atherosclerosis and associated risk factors in patients with peripheral arterial disease (PAD). MATERIALS AND METHODS: To determine renal artery stenosis, aortofemoropopliteal digital substraction angiographies (DSA) of 629 consecutive patients with PAD were prospectively reviewed. Angiographies were performed as catheter angiography with automated pump injection. Of the patients, 540 were male (86%) and 89 female (14%) (mean age+/-S.D.: 61.5+/-11.1 years). Statistical analysis was performed to determine the association of significant renal artery stenosis (> or =60% diameter stenosis) with patient demographics (age, sex, reason for angiography and smoking status), medical history (diabetes mellitus, hypertension and coronary artery disease), laboratory values (blood creatinine, fasting glucose, triglycerides, LDL, HDL and total cholesterol) and distribution of PAD (aortoiliac, femoropopliteal and crural diseases and multisegment involvement). RESULTS: Renal artery disease was found in 33% (207 of 629) of all patients with peripheral arterial disease, and 9.6% of patients (n=60) had significant (> or =60%) renal artery stenosis. Only age and hypertension (blood pressure systolic >140 mmHg or diastolic >90 mmHg) were independent risk factors for significant renal artery stenosis on multivariate analysis. Mean age of patients with RAS was 66.5+/-8.9 years compared with 61+/-11.2 years for patients without RAS (p<0.001). Hypertension was found in 41% of the patients in control group and in 63% of the patients in RAS group (p=0.01). CONCLUSION: Incidental renal artery stenosis which can be mild or significant is a relatively common finding among patients with peripheral arterial disease. Advance age and hypertension are closely associated with significant renal artery stenosis.
OBJECTIVE: To evaluate the prevalence of incidental renal artery stenosis due to atherosclerosis and associated risk factors in patients with peripheral arterial disease (PAD). MATERIALS AND METHODS: To determine renal artery stenosis, aortofemoropopliteal digital substraction angiographies (DSA) of 629 consecutive patients with PAD were prospectively reviewed. Angiographies were performed as catheter angiography with automated pump injection. Of the patients, 540 were male (86%) and 89 female (14%) (mean age+/-S.D.: 61.5+/-11.1 years). Statistical analysis was performed to determine the association of significant renal artery stenosis (> or =60% diameter stenosis) with patient demographics (age, sex, reason for angiography and smoking status), medical history (diabetes mellitus, hypertension and coronary artery disease), laboratory values (blood creatinine, fasting glucose, triglycerides, LDL, HDL and total cholesterol) and distribution of PAD (aortoiliac, femoropopliteal and crural diseases and multisegment involvement). RESULTS:Renal artery disease was found in 33% (207 of 629) of all patients with peripheral arterial disease, and 9.6% of patients (n=60) had significant (> or =60%) renal artery stenosis. Only age and hypertension (blood pressure systolic >140 mmHg or diastolic >90 mmHg) were independent risk factors for significant renal artery stenosis on multivariate analysis. Mean age of patients with RAS was 66.5+/-8.9 years compared with 61+/-11.2 years for patients without RAS (p<0.001). Hypertension was found in 41% of the patients in control group and in 63% of the patients in RAS group (p=0.01). CONCLUSION: Incidental renal artery stenosis which can be mild or significant is a relatively common finding among patients with peripheral arterial disease. Advance age and hypertension are closely associated with significant renal artery stenosis.
Authors: Felix Streckenbach; Felix G Meinel; Felix Ammermann; Anke Busse; Andreas Neumann; Thomas Heller; Marc-André Weber; Ebba Beller Journal: BMC Med Imaging Date: 2021-06-02 Impact factor: 1.930
Authors: Mireille E Emans; Karien van der Putten; Birgitta K Velthuis; Jan J J de Vries; Maarten J Cramer; Yves G C J America; Hans L Hillege; Louis Meiss; Pieter A F M Doevendans; Branko Braam; Carlo A J M Gaillard Journal: BMC Cardiovasc Disord Date: 2012-09-18 Impact factor: 2.298