<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(2)</volume><submitter>Green D</submitter><pubmed_abstract>&lt;h4>Rationale &amp; objective&lt;/h4>Trials failed to show that angioplasty and stenting of atherosclerotic renovascular disease (ARVD) conferred benefit when used as first-line therapy. However, some patients might benefit from kidney revascularization depending on their clinical phenotype and severity of renal artery stenosis (RAS). We investigated this hypothesis further.&lt;h4>Study design&lt;/h4>Data from the Angioplasty and Stenting for Renal Artery Lesions (ASTRAL) randomized trial and Salford ARVD observational study were included in a single analysis.&lt;h4>Setting &amp; participants&lt;/h4>Patients were grouped based on RAS severity (≥70%) and whether unilateral or bilateral, with the bilateral group including RAS in a single functioning kidney. High-risk clinical phenotypes included advanced chronic kidney disease (CKD) (estimated glomerular filtration rate &lt; 30 mL/min/1.73 m&lt;sup>2&lt;/sup>), rapid CKD progression (creatinine increase >100 μmol/l or >20% per year), refractory systolic hypertension (≥150 mm Hg on ≥3 agents), and heart failure (chronic or decompensated).&lt;h4>Exposures&lt;/h4>Medical therapy alone versus medial therapy and kidney revascularization.&lt;h4>Outcome&lt;/h4>Composite of end stage CKD, cardiovascular events, or all-cause mortality.&lt;h4>Analytical approach&lt;/h4>Cox proportional hazard model adjusted for age, self-reported gender, and estimated glomerular filtration rate. Analysis of all patients and selected subgroups.&lt;h4>Results&lt;/h4>In total, 1,644 patients (806 ASTRAL and 838 Salford). Median (IQR) age 72 (66-77) years. For bilateral severe RAS (≥70%) the HR for the composite outcome for revascularization compared with medical therapy was 0.70 (0.50-0.99), &lt;i>P&lt;/i> = 0.048. The clinical phenotype where benefit appeared to be greatest in the presence of bilateral severe disease was people with rapidly progressive kidney disease with a HR of 0.39 (0.22-0.71]). In the absence of bilateral severe RAS, there was no benefit to revascularization for any clinical phenotype.&lt;h4>Limitations&lt;/h4>The analyses included observational data.&lt;h4>Conclusions&lt;/h4>The presence of bilateral severe RAS may be the best predictor of benefit for kidney revascularization.</pubmed_abstract><journal>Kidney medicine</journal><pagination>101213</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12856476</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Patient Selection for Revascularization of Atherosclerotic Renal Artery Stenosis: Comparing the Importance of Stenosis Severity and Clinical Phenotype.</pubmed_title><pmcid>PMC12856476</pmcid><pubmed_authors>O'Keeffe H</pubmed_authors><pubmed_authors>Green D</pubmed_authors><pubmed_authors>Cleland JGF</pubmed_authors><pubmed_authors>Chrysochou C</pubmed_authors><pubmed_authors>Chinnadurai R</pubmed_authors><pubmed_authors>Lake E</pubmed_authors><pubmed_authors>Kalra PA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Patient Selection for Revascularization of Atherosclerotic Renal Artery Stenosis: Comparing the Importance of Stenosis Severity and Clinical Phenotype.</name><description>&lt;h4>Rationale &amp; objective&lt;/h4>Trials failed to show that angioplasty and stenting of atherosclerotic renovascular disease (ARVD) conferred benefit when used as first-line therapy. However, some patients might benefit from kidney revascularization depending on their clinical phenotype and severity of renal artery stenosis (RAS). We investigated this hypothesis further.&lt;h4>Study design&lt;/h4>Data from the Angioplasty and Stenting for Renal Artery Lesions (ASTRAL) randomized trial and Salford ARVD observational study were included in a single analysis.&lt;h4>Setting &amp; participants&lt;/h4>Patients were grouped based on RAS severity (≥70%) and whether unilateral or bilateral, with the bilateral group including RAS in a single functioning kidney. High-risk clinical phenotypes included advanced chronic kidney disease (CKD) (estimated glomerular filtration rate &lt; 30 mL/min/1.73 m&lt;sup>2&lt;/sup>), rapid CKD progression (creatinine increase >100 μmol/l or >20% per year), refractory systolic hypertension (≥150 mm Hg on ≥3 agents), and heart failure (chronic or decompensated).&lt;h4>Exposures&lt;/h4>Medical therapy alone versus medial therapy and kidney revascularization.&lt;h4>Outcome&lt;/h4>Composite of end stage CKD, cardiovascular events, or all-cause mortality.&lt;h4>Analytical approach&lt;/h4>Cox proportional hazard model adjusted for age, self-reported gender, and estimated glomerular filtration rate. Analysis of all patients and selected subgroups.&lt;h4>Results&lt;/h4>In total, 1,644 patients (806 ASTRAL and 838 Salford). Median (IQR) age 72 (66-77) years. For bilateral severe RAS (≥70%) the HR for the composite outcome for revascularization compared with medical therapy was 0.70 (0.50-0.99), &lt;i>P&lt;/i> = 0.048. The clinical phenotype where benefit appeared to be greatest in the presence of bilateral severe disease was people with rapidly progressive kidney disease with a HR of 0.39 (0.22-0.71]). In the absence of bilateral severe RAS, there was no benefit to revascularization for any clinical phenotype.&lt;h4>Limitations&lt;/h4>The analyses included observational data.&lt;h4>Conclusions&lt;/h4>The presence of bilateral severe RAS may be the best predictor of benefit for kidney revascularization.</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Feb</publication><modification>2026-06-20T03:21:08.895Z</modification><creation>2026-06-20T03:09:48.997Z</creation></dates><accession>S-EPMC12856476</accession><cross_references><pubmed>41623301</pubmed><doi>10.1016/j.xkme.2025.101213</doi></cross_references></HashMap>