Claudia Stefanutti

ORCID: 0000-0003-3448-2426
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About
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Research Areas
  • Lipoproteins and Cardiovascular Health
  • Diabetes, Cardiovascular Risks, and Lipoproteins
  • Cancer, Lipids, and Metabolism
  • Lipid metabolism and disorders
  • Systemic Lupus Erythematosus Research
  • Atherosclerosis and Cardiovascular Diseases
  • Pharmaceutical Economics and Policy
  • Pancreatitis Pathology and Treatment
  • Blood Coagulation and Thrombosis Mechanisms
  • Microbial Metabolism and Applications
  • Cardiovascular Function and Risk Factors
  • Health Systems, Economic Evaluations, Quality of Life
  • Liver Disease Diagnosis and Treatment
  • Platelet Disorders and Treatments
  • Complement system in diseases
  • Antiplatelet Therapy and Cardiovascular Diseases
  • Erythrocyte Function and Pathophysiology
  • Cell Adhesion Molecules Research
  • Blood groups and transfusion
  • Renal Diseases and Glomerulopathies
  • Blood Pressure and Hypertension Studies
  • Cholesterol and Lipid Metabolism
  • Pregnancy and preeclampsia studies
  • Diabetes and associated disorders
  • Cardiovascular Disease and Adiposity

Policlinico Umberto I
2016-2025

Sapienza University of Rome
2015-2024

Medical University of Vienna
2023

Amgen (United States)
2022

Regeneron (United States)
2016-2021

University of Nis
2020

University of Belgrade
2020

Medical University of Lodz
2020

Primary Health Care
2020

New York Proton Center
2018

Katherine Wilemon Jasmine Patel Carlos A. Aguilar‐Salinas Catherine D. Ahmed Mutaz Al-Khnifsawi and 84 more Wael Almahmeed Rodrigo Alonso Khalid Al‐Rasadi Lina Badimón Luz Mery Bernal Martin P. Bogsrud Lynne T. Braun Liam R. Brunham Alberico L. Catapano Kristýna Cillíková Pablo Corral Regina Cuevas Joep C. Defesche Olivier Descamps Sarah D. de Ferranti Jean-Luc Eiselé Gerardo Elikir Emanuela Folco Tomáš Freiberger Francesco Fuggetta Isabel Gaspar Ákos G. Gesztes Urh Grošelj Ian Hamilton‐Craig Gabriele Hanauer-Mader Mariko Harada‐Shiba G. E. Hastings G. Kees Hovingh Maria Cristina de Oliveira Izar Allison Jamison Gunnar N. Karlsson Meral Kayıkçıoğlu Sue Koob Masahiro Koseki Stacey Lane Marcos M. Lima-Martínez Greizy López Tânia Leme da Rocha Martinez David Marais Letrillart Marion Pedro Mata Inese Maurina Diana Maxwell Roopa Mehta George A. Mensah André R. Miserez Dermot Neely Stephen J. Nicholls Atsushi Nohara Børge G. Nordestgaard Leiv Ose Athanasios Pallidis Jing Pang Jules Payne Amy L. Peterson Monica P. Popescu Raman Puri Kausik K. Ray Ashraf Reda Tiziana Sampietro Raúl D. Santos Inge Schalkers Laura Schreier Michael D. Shapiro Eric J.G. Sijbrands Daniel Soffer Claudia Stefanutti Mario Stoll Rody G. Sy Marta Lucía Tamayo Myra Tilney Lâle Tokgözoğlu Brian Tomlinson Antonio J. Vallejo‐Vaz Alejandra Vázquez-Cárdenas Patrícia Vieira de Luca David S Wald Gerald F. Watts Nanette K. Wenger M. Allison Wolf David A. Wood Aram Zegerius Thomas A. Gaziano Samuel S. Gidding

<h3>Importance</h3> Familial hypercholesterolemia (FH) is an underdiagnosed and undertreated genetic disorder that leads to premature morbidity mortality due atherosclerotic cardiovascular disease. affects 1 in 200 250 people around the world of every race ethnicity. The lack general awareness FH among public medical community has resulted only 10% population being diagnosed adequately treated. World Health Organization recognized as a health priority 1998 during consultation meeting Geneva,...

10.1001/jamacardio.2019.5173 article EN JAMA Cardiology 2020-01-02

Evolocumab, a fully human monoclonal antibody directed against proprotein convertase subtilisin–kexin type 9, is widely used in adult patients to lower low-density lipoprotein (LDL) cholesterol levels. Its effects pediatric with heterozygous familial hypercholesterolemia are not known.

10.1056/nejmoa2019910 article EN New England Journal of Medicine 2020-08-29

Abstract Background and Aims Homozygous familial hypercholesterolaemia (HoFH) is a rare genetic disorder characterized by severely elevated LDL cholesterol (LDL-C) premature atherosclerotic cardiovascular disease. In the pivotal Phase 3 HoFH trial (NCT03399786), evinacumab significantly decreased LDL-C in patients with HoFH. This study assesses long-term safety efficacy of adult adolescent Methods this open-label, single-arm, (NCT03409744), aged ≥12 years who were evinacumab-naïve or had...

10.1093/eurheartj/ehae325 article EN cc-by-nc European Heart Journal 2024-06-10

Proteins play a crucial role in metabolism, maintaining fluid and acid-base balance antibody synthesis. Dietary proteins are important nutrients classified into: 1) animal (meat, fish, poultry, eggs dairy), and, 2) plant (legumes, nuts soy). modification is one of the most lifestyle changes that has been shown to significantly decrease risk cardiovascular (CV) disease (CVD) by attenuating related factors. The CVD burden reduced optimum diet through replacement unprocessed meat with low...

10.1016/j.clnu.2020.05.017 article EN cc-by-nc-nd Clinical Nutrition 2020-05-27

Abstract Extremely high plasma triglyceride (TG) concentration is a recognized risk factor for acute pancreatitis (AP). In order to evaluate the therapeutic efficacy of plasma‐exchange plasmapheresis in treating patients with severe hypertriglyceridemia (sHTG), 17 who had not responded conventional medical therapy (fat‐free diet plus pharmaceutical interventions) were referred exchange (TPE) multicenter frame case series study. Two hundred seventeen TPE sessions performed, and ongoing five...

10.1111/j.1525-1594.2009.00810.x article EN Artificial Organs 2009-07-22

Hypercholesterolaemia is amongst the most common conditions encountered in medical profession.It remains one of key modifiable cardiovascular risk factors and there have been recent advances stratification methods treatment options available.In this review, we provide a background into hypercholesterolaemia for non-specialists consider merits different assessment tools available.We also detailed considerations as to: i) when to start treatment, ii) what targets aim iii) role low density...

10.5114/aoms.2018.72238 article EN cc-by-nc-sa Archives of Medical Science 2018-01-01

Mutations in the genes for low-density lipoprotein receptor (LDLR), apolipoprotein B, and proprotein convertase subtilisin/kexin type 9 have been reported to cause heterozygous homozygous familial hypercholesterolemia (FH).The objective is examine influence of double heterozygous, compound or mutations underlying FH on efficacy alirocumab.Patients from 6 alirocumab trials with elevated cholesterol (LDL-C) diagnosis were sequenced LDLR, 9, LDLR adaptor protein 1 (LDLRAP1), signal-transducing...

10.1016/j.jacl.2017.12.008 article EN cc-by-nc-nd Journal of clinical lipidology 2017-12-28

Abstract Aims Children with heterozygous familial hypercholesterolaemia (HeFH) show greater carotid intima-media thickness (cIMT). Evolocumab, a proprotein convertase subtilisin/kexin type 9 inhibitor monoclonal antibody, substantially reduced LDL cholesterol (LDL-C) in children HeFH. We investigated evolocumab’s effect on cIMT progression. Methods and results HAUSER-RCT was randomized, placebo-controlled trial. One hundred fifty-seven paediatric patients FH (age: 10–17 years) LDL-C &amp;gt;...

10.1093/eurjpc/zwae369 article EN cc-by European Journal of Preventive Cardiology 2024-11-12
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