Literature DB >> 34016266

Precision Medicine Approaches to Vascular Disease: JACC Focus Seminar 2/5.

Clint L Miller1, Amy R Kontorovich2, Ke Hao3, Lijiang Ma4, Conrad Iyegbe3, Johan L M Björkegren5, Jason C Kovacic6.   

Abstract

In this second of a 5-part Focus Seminar series, we focus on precision medicine in the context of vascular disease. The most common vascular disease worldwide is atherosclerosis, which is the primary cause of coronary artery disease, peripheral vascular disease, and a large proportion of strokes and other disorders. Atherosclerosis is a complex genetic disease that likely involves many hundreds to thousands of single nucleotide polymorphisms, each with a relatively modest effect for causing disease. Conversely, although less prevalent, there are many vascular disorders that typically involve only a single genetic change, but these changes can often have a profound effect that is sufficient to cause disease. These are termed "Mendelian vascular diseases," which include Marfan and Loeys-Dietz syndromes. Given the very different genetic basis of atherosclerosis versus Mendelian vascular diseases, this article was divided into 2 parts to cover the most promising precision medicine approaches for these disease types.
Copyright © 2021 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  cardiovascular; genetics; polygenic risk score; precision medicine; vascular

Mesh:

Year:  2021        PMID: 34016266      PMCID: PMC8916012          DOI: 10.1016/j.jacc.2021.04.001

Source DB:  PubMed          Journal:  J Am Coll Cardiol        ISSN: 0735-1097            Impact factor:   24.094


  112 in total

Review 1.  Understanding coronary artery disease using twin studies.

Authors:  Massimo Mangino; Tim Spector
Journal:  Heart       Date:  2012-11-10       Impact factor: 5.994

2.  Beta-blocker therapy does not alter the rate of aortic root dilation in pediatric patients with Marfan syndrome.

Authors:  Elif Seda Selamet Tierney; Brian Feingold; Beth F Printz; Sang C Park; Dionne Graham; Charles S Kleinman; C Becket Mahnke; Donna M Timchak; William H Neches; Welton M Gersony
Journal:  J Pediatr       Date:  2007-01       Impact factor: 4.406

3.  Aneurysm syndromes caused by mutations in the TGF-beta receptor.

Authors:  Bart L Loeys; Ulrike Schwarze; Tammy Holm; Bert L Callewaert; George H Thomas; Hariyadarshi Pannu; Julie F De Backer; Gretchen L Oswald; Sofie Symoens; Sylvie Manouvrier; Amy E Roberts; Francesca Faravelli; M Alba Greco; Reed E Pyeritz; Dianna M Milewicz; Paul J Coucke; Duke E Cameron; Alan C Braverman; Peter H Byers; Anne M De Paepe; Harry C Dietz
Journal:  N Engl J Med       Date:  2006-08-24       Impact factor: 91.245

4.  Cascade Screening for Familial Hypercholesterolemia and the Use of Genetic Testing.

Authors:  Joshua W Knowles; Daniel J Rader; Muin J Khoury
Journal:  JAMA       Date:  2017-07-25       Impact factor: 56.272

5.  The importance of mutation detection in Marfan syndrome and Marfan-related disorders: report of 193 FBN1 mutations.

Authors:  Paolo Comeglio; Philip Johnson; Gavin Arno; Glen Brice; Alison Evans; José Aragon-Martin; Filipe Pereira da Silva; Anatoli Kiotsekoglou; Anne Child
Journal:  Hum Mutat       Date:  2007-09       Impact factor: 4.878

6.  Integrative analysis of loss-of-function variants in clinical and genomic data reveals novel genes associated with cardiovascular traits.

Authors:  Benjamin S Glicksberg; Letizia Amadori; Nicholas K Akers; Katyayani Sukhavasi; Oscar Franzén; Li Li; Gillian M Belbin; Kristin L Ayers; Khader Shameer; Marcus A Badgeley; Kipp W Johnson; Ben Readhead; Bruce J Darrow; Eimear E Kenny; Christer Betsholtz; Raili Ermel; Josefin Skogsberg; Arno Ruusalepp; Eric E Schadt; Joel T Dudley; Hongxia Ren; Jason C Kovacic; Chiara Giannarelli; Shuyu D Li; Johan L M Björkegren; Rong Chen
Journal:  BMC Med Genomics       Date:  2019-07-25       Impact factor: 3.063

7.  Partitioning the heritability of coronary artery disease highlights the importance of immune-mediated processes and epigenetic sites associated with transcriptional activity.

Authors:  Majid Nikpay; Alexandre F R Stewart; Ruth McPherson
Journal:  Cardiovasc Res       Date:  2017-07-01       Impact factor: 10.787

8.  Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease.

Authors:  Nathan O Stitziel; Kathleen E Stirrups; Nicholas G D Masca; Jeanette Erdmann; Paola G Ferrario; Inke R König; Peter E Weeke; Thomas R Webb; Paul L Auer; Ursula M Schick; Yingchang Lu; He Zhang; Marie-Pierre Dube; Anuj Goel; Martin Farrall; Gina M Peloso; Hong-Hee Won; Ron Do; Erik van Iperen; Stavroula Kanoni; Jochen Kruppa; Anubha Mahajan; Robert A Scott; Christina Willenberg; Peter S Braund; Julian C van Capelleveen; Alex S F Doney; Louise A Donnelly; Rosanna Asselta; Piera A Merlini; Stefano Duga; Nicola Marziliano; Josh C Denny; Christian M Shaffer; Nour Eddine El-Mokhtari; Andre Franke; Omri Gottesman; Stefanie Heilmann; Christian Hengstenberg; Per Hoffman; Oddgeir L Holmen; Kristian Hveem; Jan-Håkan Jansson; Karl-Heinz Jöckel; Thorsten Kessler; Jennifer Kriebel; Karl L Laugwitz; Eirini Marouli; Nicola Martinelli; Mark I McCarthy; Natalie R Van Zuydam; Christa Meisinger; Tõnu Esko; Evelin Mihailov; Stefan A Escher; Maris Alver; Susanne Moebus; Andrew D Morris; Martina Müller-Nurasyid; Majid Nikpay; Oliviero Olivieri; Louis-Philippe Lemieux Perreault; Alaa AlQarawi; Neil R Robertson; Karen O Akinsanya; Dermot F Reilly; Thomas F Vogt; Wu Yin; Folkert W Asselbergs; Charles Kooperberg; Rebecca D Jackson; Eli Stahl; Konstantin Strauch; Tibor V Varga; Melanie Waldenberger; Lingyao Zeng; Aldi T Kraja; Chunyu Liu; George B Ehret; Christopher Newton-Cheh; Daniel I Chasman; Rajiv Chowdhury; Marco Ferrario; Ian Ford; J Wouter Jukema; Frank Kee; Kari Kuulasmaa; Børge G Nordestgaard; Markus Perola; Danish Saleheen; Naveed Sattar; Praveen Surendran; David Tregouet; Robin Young; Joanna M M Howson; Adam S Butterworth; John Danesh; Diego Ardissino; Erwin P Bottinger; Raimund Erbel; Paul W Franks; Domenico Girelli; Alistair S Hall; G Kees Hovingh; Adnan Kastrati; Wolfgang Lieb; Thomas Meitinger; William E Kraus; Svati H Shah; Ruth McPherson; Marju Orho-Melander; Olle Melander; Andres Metspalu; Colin N A Palmer; Annette Peters; Daniel Rader; Muredach P Reilly; Ruth J F Loos; Alex P Reiner; Dan M Roden; Jean-Claude Tardif; John R Thompson; Nicholas J Wareham; Hugh Watkins; Cristen J Willer; Sekkar Kathiresan; Panos Deloukas; Nilesh J Samani; Heribert Schunkert
Journal:  N Engl J Med       Date:  2016-03-02       Impact factor: 91.245

9.  Genomic prediction of coronary heart disease.

Authors:  Gad Abraham; Aki S Havulinna; Oneil G Bhalala; Sean G Byars; Alysha M De Livera; Laxman Yetukuri; Emmi Tikkanen; Markus Perola; Heribert Schunkert; Eric J Sijbrands; Aarno Palotie; Nilesh J Samani; Veikko Salomaa; Samuli Ripatti; Michael Inouye
Journal:  Eur Heart J       Date:  2016-09-21       Impact factor: 29.983

10.  Improved cardiovascular risk prediction using targeted plasma proteomics in primary prevention.

Authors:  Renate M Hoogeveen; João P Belo Pereira; Nick S Nurmohamed; Veronica Zampoleri; Michiel J Bom; Andrea Baragetti; S Matthijs Boekholdt; Paul Knaapen; Kay-Tee Khaw; Nicholas J Wareham; Albert K Groen; Alberico L Catapano; Wolfgang Koenig; Evgeni Levin; Erik S G Stroes
Journal:  Eur Heart J       Date:  2020-11-01       Impact factor: 29.983

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  2 in total

1.  PBAT/gelatin hybrid nanofibers based on post-double network bond processing as a promising vascular substitute.

Authors:  Jiakun Nie; Changjie Jin; Yonghang Liu; Juan Du; Sihao Chen; Yujia Zheng; Binbin Lou
Journal:  RSC Adv       Date:  2022-08-09       Impact factor: 4.036

Review 2.  Inflammatory and Prothrombotic Biomarkers, DNA Polymorphisms, MicroRNAs and Personalized Medicine for Patients with Peripheral Arterial Disease.

Authors:  Pavel Poredoš; Mišo Šabovič; Mojca Božič Mijovski; Jovana Nikolajević; Pier Luigi Antignani; Kosmas I Paraskevas; Dimitri P Mikhailidis; Aleš Blinc
Journal:  Int J Mol Sci       Date:  2022-10-10       Impact factor: 6.208

  2 in total

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