Literature DB >> 29466530

Cardiac Abnormalities in Patients With Hutchinson-Gilford Progeria Syndrome.

Ashwin Prakash1,2, Leslie B Gordon3,4, Monica E Kleinman3,5, Ellen B Gurary6, Joseph Massaro6, Ralph D'Agostino6, Mark W Kieran7, Marie Gerhard-Herman8, Leslie Smoot1,2.   

Abstract

Importance: Hutchinson-Gilford progeria syndrome (HGPS) is an ultrarare disorder associated with premature death due to cardiovascular events during the second decade of life. However, because of its rarity (107 identified living patients), the natural history of cardiac disease remains uncharacterized. Therefore, meaningful cardiac end points for clinical trials have been difficult to establish. Objective: To examine the course of appearance of cardiac abnormalities in patients with HGPS to identify meaningful cardiac end points for use in future clinical trials. Design, Setting, and Participants: In this prospective, cross-sectional, observational study, 27 consecutive patients with clinically and genetically confirmed classic HGPS were evaluated at a single center for 1 visit from July 1, 2014, through February 29, 2016, before initiation of treatment. Exposure: Classic HGPS. Main Outcomes and Measures: Echocardiography was used to assess ventricular and valve function using standard techniques. Diastolic left ventricular (LV) function was assessed using tissue Doppler imaging. Previously published normative data were used to adjust findings to age and body size.
Results: This study included 27 patients (median age, 5.6 years; age range, 2-17 years; 15 [56%] male). Among echocardiographic indicators, LV diastolic dysfunction, defined as a tissue Doppler septal or lateral early velocity z score less than -2, was the most prevalent abnormality, seen in 16 patients (59%). Diastolic dysfunction was seen in all age groups, and its prevalence increased with age, mirroring findings seen during normal aging. Indicators of LV diastolic function were more abnormal in older patients. The z scores for lateral and septal early velocities were lower (r = -0.77, P < .001; and r = -0.66, P < .001, respectively), whereas those for the ratio of early mitral inflow velocity to early diastolic tissue Doppler myocardial velocity were higher (r = 0.80, P < .001; and r = 0.72, P < .001, respectively) in older patients. Other echocardiographic findings, including LV hypertrophy, LV systolic dysfunction, and valve disease, were less prevalent in the first decade and were seen more frequently in the second decade. Conclusions and Relevance: In this largest-to-date cohort of patients with HGPS, LV diastolic dysfunction was the most prevalent echocardiographic abnormality and its prevalence increased with aging. Echocardiographic indicators of LV diastolic function may be useful end points in future clinical trials in this patient population.

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Year:  2018        PMID: 29466530      PMCID: PMC5875332          DOI: 10.1001/jamacardio.2017.5235

Source DB:  PubMed          Journal:  JAMA Cardiol            Impact factor:   14.676


  31 in total

1.  Lamin a truncation in Hutchinson-Gilford progeria.

Authors:  Annachiara De Sandre-Giovannoli; Rafaëlle Bernard; Pierre Cau; Claire Navarro; Jeanne Amiel; Irène Boccaccio; Stanislas Lyonnet; Colin L Stewart; Arnold Munnich; Martine Le Merrer; Nicolas Lévy
Journal:  Science       Date:  2003-04-17       Impact factor: 47.728

2.  The fourth report on the diagnosis, evaluation, and treatment of high blood pressure in children and adolescents.

Authors: 
Journal:  Pediatrics       Date:  2004-08       Impact factor: 7.124

3.  The time relations of the blood-pressure changes after excision of the adrenal glands, with some observations on blood volume changes.

Authors:  H C Bazett
Journal:  J Physiol       Date:  1920-02-20       Impact factor: 5.182

4.  Tissue Doppler-derived diastolic myocardial velocities are abnormal in pediatric cardiac transplant recipients in the absence of endomyocardial rejection.

Authors:  Sebastian Strigl; Rose Hardy; Julie S Glickstein; Daphne T Hsu; Linda J Addonizio; Jacqueline M Lamour; Ashwin Prakash
Journal:  Pediatr Cardiol       Date:  2008-01-05       Impact factor: 1.655

5.  Cardiac electrical defects in progeroid mice and Hutchinson-Gilford progeria syndrome patients with nuclear lamina alterations.

Authors:  José Rivera-Torres; Conrado J Calvo; Anna Llach; Gabriela Guzmán-Martínez; Ricardo Caballero; Cristina González-Gómez; Luis J Jiménez-Borreguero; Juan A Guadix; Fernando G Osorio; Carlos López-Otín; Adela Herraiz-Martínez; Nuria Cabello; Alex Vallmitjana; Raul Benítez; Leslie B Gordon; José Jalife; José M Pérez-Pomares; Juan Tamargo; Eva Delpón; Leif Hove-Madsen; David Filgueiras-Rama; Vicente Andrés
Journal:  Proc Natl Acad Sci U S A       Date:  2016-10-31       Impact factor: 11.205

6.  Cardiovascular abnormalities in progeria. Case report and review of the literature.

Authors:  P B Baker; N Baba; C P Boesel
Journal:  Arch Pathol Lab Med       Date:  1981-07       Impact factor: 5.534

7.  Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome.

Authors:  Maria Eriksson; W Ted Brown; Leslie B Gordon; Michael W Glynn; Joel Singer; Laura Scott; Michael R Erdos; Christiane M Robbins; Tracy Y Moses; Peter Berglund; Amalia Dutra; Evgenia Pak; Sandra Durkin; Antonei B Csoka; Michael Boehnke; Thomas W Glover; Francis S Collins
Journal:  Nature       Date:  2003-04-25       Impact factor: 49.962

8.  Geometric method for measuring body surface area: a height-weight formula validated in infants, children, and adults.

Authors:  G B Haycock; G J Schwartz; D H Wisotsky
Journal:  J Pediatr       Date:  1978-07       Impact factor: 4.406

9.  Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome.

Authors:  Robert D Goldman; Dale K Shumaker; Michael R Erdos; Maria Eriksson; Anne E Goldman; Leslie B Gordon; Yosef Gruenbaum; Satya Khuon; Melissa Mendez; Renée Varga; Francis S Collins
Journal:  Proc Natl Acad Sci U S A       Date:  2004-06-07       Impact factor: 11.205

10.  Phenotype and course of Hutchinson-Gilford progeria syndrome.

Authors:  Melissa A Merideth; Leslie B Gordon; Sarah Clauss; Vandana Sachdev; Ann C M Smith; Monique B Perry; Carmen C Brewer; Christopher Zalewski; H Jeffrey Kim; Beth Solomon; Brian P Brooks; Lynn H Gerber; Maria L Turner; Demetrio L Domingo; Thomas C Hart; Jennifer Graf; James C Reynolds; Andrea Gropman; Jack A Yanovski; Marie Gerhard-Herman; Francis S Collins; Elizabeth G Nabel; Richard O Cannon; William A Gahl; Wendy J Introne
Journal:  N Engl J Med       Date:  2008-02-07       Impact factor: 91.245

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  20 in total

Review 1.  Genomic instability and innate immune responses to self-DNA in progeria.

Authors:  Susana Gonzalo; Nuria Coll-Bonfill
Journal:  Geroscience       Date:  2019-07-06       Impact factor: 7.713

2.  Extraskeletal Calcifications in Hutchinson-Gilford Progeria Syndrome.

Authors:  C M Gordon; R H Cleveland; K Baltrusaitis; J Massaro; R B D'Agostino; M G Liang; B Snyder; M Walters; X Li; D T Braddock; M E Kleinman; M W Kieran; L B Gordon
Journal:  Bone       Date:  2019-05-08       Impact factor: 4.398

3.  Metabolomic profiling suggests systemic signatures of premature aging induced by Hutchinson-Gilford progeria syndrome.

Authors:  Gustavo Monnerat; Geisa Paulino Caprini Evaristo; Joseph Albert Medeiros Evaristo; Caleb Guedes Miranda Dos Santos; Gabriel Carneiro; Leonardo Maciel; Vânia Oliveira Carvalho; Fábio César Sousa Nogueira; Gilberto Barbosa Domont; Antonio Carlos Campos de Carvalho
Journal:  Metabolomics       Date:  2019-06-28       Impact factor: 4.290

4.  Telomerase therapy reverses vascular senescence and extends lifespan in progeria mice.

Authors:  Anahita Mojiri; Brandon K Walther; Chongming Jiang; Gianfranco Matrone; Rhonda Holgate; Qiu Xu; Elisa Morales; Guangyu Wang; Jianhua Gu; Rongfu Wang; John P Cooke
Journal:  Eur Heart J       Date:  2021-11-07       Impact factor: 35.855

5.  Phosphorylated Lamin A/C in the Nuclear Interior Binds Active Enhancers Associated with Abnormal Transcription in Progeria.

Authors:  Kohta Ikegami; Stefano Secchia; Omar Almakki; Jason D Lieb; Ivan P Moskowitz
Journal:  Dev Cell       Date:  2020-03-23       Impact factor: 12.270

6.  Paradoxical aortic stiffening and subsequent cardiac dysfunction in Hutchinson-Gilford progeria syndrome.

Authors:  S-I Murtada; Y Kawamura; A W Caulk; H Ahmadzadeh; N Mikush; K Zimmerman; D Kavanagh; D Weiss; M Latorre; Z W Zhuang; G S Shadel; D T Braddock; J D Humphrey
Journal:  J R Soc Interface       Date:  2020-05-27       Impact factor: 4.118

7.  Endothelial progerin expression causes cardiovascular pathology through an impaired mechanoresponse.

Authors:  Selma Osmanagic-Myers; Attila Kiss; Christina Manakanatas; Ouafa Hamza; Franziska Sedlmayer; Petra L Szabo; Irmgard Fischer; Petra Fichtinger; Bruno K Podesser; Maria Eriksson; Roland Foisner
Journal:  J Clin Invest       Date:  2018-12-18       Impact factor: 14.808

8.  Progerin accelerates atherosclerosis by inducing endoplasmic reticulum stress in vascular smooth muscle cells.

Authors:  Magda R Hamczyk; Ricardo Villa-Bellosta; Víctor Quesada; Pilar Gonzalo; Sandra Vidak; Rosa M Nevado; María J Andrés-Manzano; Tom Misteli; Carlos López-Otín; Vicente Andrés
Journal:  EMBO Mol Med       Date:  2019-04       Impact factor: 12.137

Review 9.  Molecular and Cellular Mechanisms Driving Cardiovascular Disease in Hutchinson-Gilford Progeria Syndrome: Lessons Learned from Animal Models.

Authors:  Ignacio Benedicto; Beatriz Dorado; Vicente Andrés
Journal:  Cells       Date:  2021-05-11       Impact factor: 6.600

Review 10.  Targeting senescent cells to attenuate cardiovascular disease progression.

Authors:  Ping Song; Qiang Zhao; Ming-Hui Zou
Journal:  Ageing Res Rev       Date:  2020-04-13       Impact factor: 10.895

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