Patrick A Stone1, Haley Schlarb2, John E Campbell3, David Williams3, Stephanie N Thompson2, Molly John4, James R Campbell3, Ali F AbuRahma3. 1. Division of Vascular and Endovascular Surgery, West Virginia University, Charleston, WVa. Electronic address: pstone0627@yahoo.com. 2. Department of Health, Education and Research, Charleston Area Medical Center, Charleston, WVa. 3. Division of Vascular and Endovascular Surgery, West Virginia University, Charleston, WVa. 4. Division of Internal Medicine, West Virginia University, Charleston, WVa.
Abstract
BACKGROUND: High-sensitivity C-reactive protein (hsCRP) and brain natriuretic peptide (BNP) have been shown to be independent predictors of adverse cardiovascular outcomes and increased risk of secondary interventions or limb loss in patients with peripheral arterial disease (PAD). To assist clinicians in decision-making about treatment approaches and predicting postprocedure mortality and morbidity, we retrospectively examined patients with preprocedure hsCRP and BNP levels who underwent elective angioplasty or stent placement for lower extremity PAD. METHODS: The study period was from January 1, 2007, to December 31, 2012, and patients were included who had angioplasty or stenting for PAD. Minimal required follow-up for study inclusion was at least one postoperative ankle-brachial index, contrast angiography, or duplex imaging of the treated limb. Events of interest included major adverse limb events (MALE), defined as target vessel revascularization, amputation, or disease progression by 1 year, and major adverse cardiovascular events (MACE; stroke, myocardial infarction, or death) by 2 years. Elevated/abnormal values for our biomarkers of interest were established by the upper limits of our institution's clinical laboratory reference range (hsCRP, >0.80 mg/dL; BNP, >100 pg/mL). RESULTS: A total of 159 limbs in 118 patients were included in analysis (42% men; median age [range], 64 [42-87] years). All limbs were symptomatic (Rutherford classification: 1-6). Iliac artery revascularization without other adjunct lower extremity intervention was performed in 60% of the limbs. High hsCRP levels (>0.80 mg/dL) were present in 32 patients (27%) and high BNP values (>100 pg/mL) in 24 patients (20%). Kaplan-Meier analysis with log-rank comparison demonstrated that elevated hsCRP levels were associated with MALE but only in limbs receiving interventions distal to the iliac arteries (P = .005). High BNP levels did not affect MALE rates (P = .821). Conversely, both elevated BNP levels (hazard ratio, 5.6; 95% confidence interval [CI], 2.0-5.8; P = .001) and hsCRP levels (hazard ratio, 2.9; 95% CI, 1.1-7.6; P = .034) predicted MACE at 2 years in the presence of confounders in Cox proportional hazards multivariate analysis. Patients with high preintervention values of hsCRP and BNP were 10.6 times (95% CI, 2.6-42.9; P = .001) more likely to experience MACE than were patients with normal hsCRP and BNP values. CONCLUSIONS: After lower extremity endovascular interventions, elevated preprocedural hsCRP levels are associated with MALE (femoral-popliteal interventions), and elevated levels of hsCRP and BNP are associated with late cardiovascular events.
BACKGROUND: High-sensitivity C-reactive protein (hsCRP) and brain natriuretic peptide (BNP) have been shown to be independent predictors of adverse cardiovascular outcomes and increased risk of secondary interventions or limb loss in patients with peripheral arterial disease (PAD). To assist clinicians in decision-making about treatment approaches and predicting postprocedure mortality and morbidity, we retrospectively examined patients with preprocedure hsCRP and BNP levels who underwent elective angioplasty or stent placement for lower extremity PAD. METHODS: The study period was from January 1, 2007, to December 31, 2012, and patients were included who had angioplasty or stenting for PAD. Minimal required follow-up for study inclusion was at least one postoperative ankle-brachial index, contrast angiography, or duplex imaging of the treated limb. Events of interest included major adverse limb events (MALE), defined as target vessel revascularization, amputation, or disease progression by 1 year, and major adverse cardiovascular events (MACE; stroke, myocardial infarction, or death) by 2 years. Elevated/abnormal values for our biomarkers of interest were established by the upper limits of our institution's clinical laboratory reference range (hsCRP, >0.80 mg/dL; BNP, >100 pg/mL). RESULTS: A total of 159 limbs in 118 patients were included in analysis (42% men; median age [range], 64 [42-87] years). All limbs were symptomatic (Rutherford classification: 1-6). Iliac artery revascularization without other adjunct lower extremity intervention was performed in 60% of the limbs. High hsCRP levels (>0.80 mg/dL) were present in 32 patients (27%) and high BNP values (>100 pg/mL) in 24 patients (20%). Kaplan-Meier analysis with log-rank comparison demonstrated that elevated hsCRP levels were associated with MALE but only in limbs receiving interventions distal to the iliac arteries (P = .005). High BNP levels did not affect MALE rates (P = .821). Conversely, both elevated BNP levels (hazard ratio, 5.6; 95% confidence interval [CI], 2.0-5.8; P = .001) and hsCRP levels (hazard ratio, 2.9; 95% CI, 1.1-7.6; P = .034) predicted MACE at 2 years in the presence of confounders in Cox proportional hazards multivariate analysis. Patients with high preintervention values of hsCRP and BNP were 10.6 times (95% CI, 2.6-42.9; P = .001) more likely to experience MACE than were patients with normal hsCRP and BNP values. CONCLUSIONS: After lower extremity endovascular interventions, elevated preprocedural hsCRP levels are associated with MALE (femoral-popliteal interventions), and elevated levels of hsCRP and BNP are associated with late cardiovascular events.
Authors: Gavin J Bryce; Christopher J Payne; Simon C Gibson; Dominique S Byrne; Christian Delles; John McClure; David B Kingsmore Journal: J Vasc Surg Date: 2012-10-09 Impact factor: 4.268
Authors: A Buffon; G Liuzzo; L M Biasucci; P Pasqualetti; V Ramazzotti; A G Rebuzzi; F Crea; A Maseri Journal: J Am Coll Cardiol Date: 1999-11-01 Impact factor: 24.094
Authors: Tryfon Vainas; Frank R M Stassen; Rick de Graaf; Eric L L Twiss; Selma B Herngreen; Rob J Th J Welten; Luc H J M van den Akker; Marja P van Dieijen-Visser; Cathrien A Bruggeman; Peter J E H M Kitslaar Journal: J Vasc Surg Date: 2005-08 Impact factor: 4.268
Authors: Thomas Mueller; Benjamin Dieplinger; Werner Poelz; Georg Endler; Oswald F Wagner; Meinhard Haltmayer Journal: Clin Chem Date: 2008-11-06 Impact factor: 8.327
Authors: Silvia Bleda; Joaquin De Haro; Francisco Acin; Cesar Varela; Leticia Esparza; Ignacio López de Maturana Journal: Ann Vasc Surg Date: 2013-02-10 Impact factor: 1.466
Authors: Michael Sobel; Mayumi Yagi; Katherine Moreno; Ted R Kohler; Gale L Tang; Errol S Wijelath; Julieann Marshall; Richard D Kenagy Journal: Eur J Vasc Endovasc Surg Date: 2018-10-19 Impact factor: 7.069
Authors: Zoltan Ruzsa; Rafał Januszek; Viktor Óriás; Michał Chyrchel; Joanna Wojtasik-Bakalarz; Jerzy Bartuś; Saleh Arif; Paweł Kleczyński; Tomasz Tokarek; Andras Nyerges; Agata Stanek; Dariusz Dudek; Stanisław Bartuś Journal: Ann Transl Med Date: 2020-03