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Dive into the research topics where Asmaa Mansour is active.

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Featured researches published by Asmaa Mansour.


Canadian Journal of Cardiology | 2013

Acute responses to intermittent and continuous exercise in heart failure patients.

Eve Normandin; Anil Nigam; Philippe Meyer; Martin Juneau; Thibaut Guiraud; Laurent Bosquet; Asmaa Mansour; Mathieu Gayda

BACKGROUND The purpose of this study was to compare cardiopulmonary responses, exercise adherence, tolerance, and safety of optimized high-intensity interval exercise (HIIE) compared with moderate-intensity continuous exercise (MICE) in patients with heart failure and reduced ejection fraction (HFREF). METHODS Twenty patients with HFREF (aged 61 ± 9.9 years) were randomly assigned to HIIE corresponding to 2 × 8 minutes of 30-second intervals at 100% of peak power output and 30-second passive recovery intervals and to a 22-minute MICE corresponding to 60% of peak power output. Gas exchange, electrocardiogram, and blood pressure were measured continuously. Cardiac troponin T (cTnT), C-reactive protein (CRP), and brain natriuretic peptide (BNP) were measured before, 20 minutes after, and 24 hours after HIIE and MICE. RESULTS Cardiopulmonary responses did not differ between MICE and HIIE. Higher exercise adherence and efficiency were observed on HIIE with a similar perceived exertion and time spent above 90% of peak oxygen consumption compared with MICE. Neither HIIE nor MICE caused any significant arrhythmias or increased CRP, BNP, or cTnT. CONCLUSIONS Compared with MICE, HIIE demonstrated a higher exercise adherence and was well tolerated in patients with HFREF, while still providing a high-level physiological stimulus and leaving indices of inflammation (CRP), myocardial dysfunction (BNP), and myocardial necrosis (cTnT) unaffected.


Transplant International | 2014

Long-term evolution, secular trends, and risk factors of renal dysfunction following cardiac transplantation.

K. Lachance; Michel White; Michel Carrier; Asmaa Mansour; Normand Racine; M. Liszkowski; Anique Ducharme; Simon de Denus

Recent reports suggest that individuals who underwent heart transplantation in the last decade have improved post‐transplant kidney function. The objectives of this retrospective study were to describe the incidence and to identify fixed and time‐dependent predictors of renal dysfunction in cardiac recipients transplanted over a 25‐year period (1983–2008). To illustrate temporal trends, patients (n = 306) were divided into five groups based on year of transplantation. The primary endpoint was the estimated glomerular filtration rate (eGFR) at year 1. Secondary endpoints were time to moderate (eGFR <60 ml/min/1.73 m2) and severe renal dysfunction (eGFR <30 ml/min/1.73 m2). Risk factor analyses relied on multivariable regression models. Kidney function was mildly impaired before transplant (median eGFR=61.0 ml/min/1.73 m2), improved at discharge (eGFR=72.3 ml/min/1.73 m2; P < 0.001), decreased considerably in the first year (eGFR = 54.7 ml/min/1.73 m2; P < 0.001), and deteriorated less rapidly thereafter. At year 1, 2004–2008 recipients exhibited a higher eGFR compared with all other patients (P < 0.001). Factors independently associated with eGFR at year 1 and with moderate and severe renal dysfunction included age, gender, pretransplant eGFR, blood pressure, glycemia, and use of prednisone (P < 0.05). In summary, kidney function worsens constantly up to two decades after cardiac transplantation, with the greatest decline occurring in the first year. Corticosteroid minimization and treatment of modifiable risk factors (hypertension, diabetes) may minimize renal deterioration.


Transplant International | 2018

Pregnancy after heart transplantation: a well-thought-out decision? The Quebec provincial experience - a multi-centre cohort study

Olina Dagher; Nassiba Alami Laroussi; Michel Carrier; Renzo Cecere; Eric Charbonneau; Simon de Denus; Nadia Giannetti; Line Leduc; Bernard Cantin; Asmaa Mansour; Nancy Poirier; Marie-Josée Raboisson; Michel White; Anique Ducharme

Despite reports of successful pregnancies in heart transplant (HTx) recipients, many centers recommend their patients against maternity. We reviewed our provincial experience of pregnancy in HTx recipients by performing charts review of all known gestations following HTx in the province of Quebec (Canada), stratified between planned and unplanned pregnancies. Long‐term survival was compared to HTx recipient women of childbearing age who did not become pregnant. Eighteen pregnancies, 56% unplanned, occurred in eight patients, 10.1 (2.6–27.0) years after HTx. Immunosuppression was CNI‐based, with a mean dose increase of 48.3% (tacrolimus) and 26.5% (cyclosporine), without rejection. Cardiometabolic complications were high compared to the general Canadian population, including preeclampsia (15.4% vs. 5.5%), hypertension (38.5% vs. 4.6%), and diabetes (15.4% vs. 5.6%). Mean gestational age was 35.1 (23.4–39.6) weeks (72.2% live births; 53.8% prematurity). Mean birthweight was 2418 (660–3612) g. Serum creatinine increased during pregnancy, becoming significant after delivery (P = 0.0239), and returning to preconception level in all but three patients within a year. After 4.6 (1.2–17.2) years of follow‐up, two rejection episodes occurred in one patient. Long‐term mortality was similar to overall HTx women (Kaplan–Meier; P = 0.8071). Pregnancy in HTx carries high cardiometabolic complications and decreased kidney function, but is feasible with acceptable outcomes and no impact on mothers survival.


Clinical Transplantation | 2018

Cardiopulmonary, biomarkers, and vascular responses to acute hypoxia following cardiac transplantation

Maria Sanz-de la Garza; Nadia Iannino; Vincent Finnerty; Asmaa Mansour; Lucie Blondeau; Mathieu Gayda; Diana Chaar; Martin G. Sirois; Normand Racine; Simon de Denus; François Harel; Michel White

Previous studies have suggested good adaptation of cardiac transplant (CTx) recipients to exposure to a high altitude. No studies have investigated the cardiopulmonary and biomarker responses to acute hypoxic challenges following CTx. Thirty‐six CTx recipients and 17 age‐matched healthy controls (HC) were recruited. Sixteen (16) patients (42%) had cardiac allograft vasculopathy (CAV). Cardiopulmonary responses to maximal and submaximal exercise at 21% O2, 20‐minutes hypoxia (11.5% O2), and following a 10‐minute exposure to 11.5% O2 using 30% of peak power output were completed. Vascular endothelial growth factor (VEGF), interleukin‐6 (IL‐6), suppression of tumorigenicity 2 (ST2) were measured at baseline and at peak stress. Endothelial peripheral function was assessed using near‐infrared spectroscopy. Compared with HC, CTx presented a lesser O2 desaturation both at rest (−19.4 ± 6.8 [CTx] vs −24.2 ± 6.0% O2 [HC], P < 0.05) and following exercise (−23.2 ± 4.9 [CTx] vs −26.2 ± 4.7% O2 [HC], P < 0.05). CTx patients exhibited a significant decrease in peak oxygen uptake. IL‐6 and VEGF levels were significantly higher in CTx recipients in basal conditions but did not change in response to acute stress. CTx patients exhibit a favorable ventilatory and overall response to hypoxic stress. These data provide further insights on the good adaptability of CTx to exposure to high altitude.


American Heart Journal | 2018

A comparison of the effects of selective and non-selective mineralocorticoid antagonism on glucose homeostasis of heart failure patients with glucose intolerance or type II diabetes: A randomized controlled double-blind trial

Sandra Korol; Michel White; Eileen O’Meara; François Tournoux; Normand Racine; Anique Ducharme; Jean-Lucien Rouleau; Mark Liszkowski; Asmaa Mansour; Martin Jutras; Marie-Claude Guertin; Mathieu Bernier; Joel Lavoie; Grégoire Leclair; Paul-Eduard Neagoe; Diana Chaar; Martin G. Sirois; Simon de Denus

&NA; Mineralocorticoid receptor antagonists (MRAs) decrease morbidity and mortality in patients with heart failure (HF). However, spironolactone, a non‐selective MRA, has been shown to exert a harmful effect on glucose homeostasis. The objective of this multicenter, randomized, controlled, double‐blind trial was to compare the effects of spironolactone to those of the selective MRA eplerenone on glucose homeostasis among 62 HF patients with glucose intolerance or type II diabetes. Trial registration number: NCT01586442.


Journal of the American College of Cardiology | 2016

MOLECULAR IMAGING OF THE HUMAN PULMONARY VASCULAR ENDOTHELIUM IN PULMONARY HYPERTENSION: THE PULMOBIND SAFETY AND PROOF OF PRINCIPLE TRIAL

Jocelyn Dupuis; François Harel; David Langleben; Steve Provencher; Alain Fournier; Quang T. Nguyen; Vincent Finnerty; Myriam Létourneau; Xavier Levac; Asmaa Mansour; Gad Abikhzer; Jean Guimond

The adrenomedullin receptor is densely expressed in the pulmonary vascular endothelium. PulmoBind, an adrenomedullin receptor ligand, was developed for molecular diagnosis of pulmonary vascular disease. To evaluate the safety of PulmoBind SPECT imaging and its capacity to detect pulmonary vascular


Jacc-cardiovascular Interventions | 2011

Description and Assessment of a Common Reference Method for Fluoroscopic and Transesophageal Echocardiographic Localization and Guidance of Mitral Periprosthetic Transcatheter Leak Reduction

Haïfa Mahjoub; Stéphane Noble; Reda Ibrahim; Jeannot Potvin; Eileen O'Meara; Annie Dore; François Marcotte; Jacques Crépeau; Raoul Bonan; Asmaa Mansour; Denis Bouchard; Anique Ducharme; Arsène Basmadjian


European Journal of Nuclear Medicine and Molecular Imaging | 2017

Molecular imaging of the human pulmonary vascular endothelium in pulmonary hypertension: a phase II safety and proof of principle trial

François Harel; David Langleben; Steve Provencher; Alain Fournier; Vincent Finnerty; Quang T. Nguyen; Myriam Létourneau; Xavier Levac; Gad Abikhzer; Jean Guimond; Asmaa Mansour; Marie-Claude Guertin; Jocelyn Dupuis


Archive | 2012

Clinical Research Acute Responses to Intermittent and Continuous Exercise in Heart Failure Patients

Eve Normandin; Anil Nigam; Philippe Meyer; Thibaut Guiraud; Laurent Bosquet; Asmaa Mansour; Mathieu Gayda


Pharmacogenomics | 2018

A prospective study of the impact of AGTR1 A1166C on the effects of candesartan in patients with heart failure

Simon de Denus; Marie-Pierre Dubé; René Fouodjio; Thao Huynh; Marie-Hélène Leblanc; Serge Lepage; Richard Sheppard; Nadia Giannetti; Joel Lavoie; Asmaa Mansour; Sylvie Provost; Valérie Normand; Ian Mongrain; Mathieu Langlois; Eileen O'Meara; Anique Ducharme; Normand Racine; Marie-Claude Guertin; Jacques Turgeon; Michael Phillips; Jean-Lucien Rouleau; Jean-Claude Tardif; Michel White

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Michel White

Montreal Heart Institute

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Normand Racine

Montreal Heart Institute

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Eileen O'Meara

Montreal Heart Institute

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Joel Lavoie

Montreal Heart Institute

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S. de Denus

Université de Montréal

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Simon de Denus

Montreal Heart Institute

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