Evidence map›Paper›PMID 29466530›Full record

Observational studyJAMA cardiology2018

Cardiac Abnormalities in Patients With Hutchinson-Gilford Progeria Syndrome.

Ashwin Prakash, Leslie B Gordon, Monica E Kleinman, Ellen B Gurary, Joseph Massaro, Ralph D'Agostino, Mark W Kieran, Marie Gerhard-Herman, Leslie Smoot

Open access · bronzeAbstract readObservational Study
In one paragraph

Observational study in JAMA cardiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
4.2field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

61 citing papers in PubMed, 100 citations in OpenAlex.

  1. METTL14-Mediated mAging cell · 2026
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  6. AΙ-Driven Drug Repurposing: Applications and Challenges.Medicines (Basel, Switzerland) · 2025
    Review
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  16. What Causes Premature Coronary Artery Disease?Current atherosclerosis reports · 2024
    Review
  17. Article
  18. Article
  19. Article
  20. Article

1 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 6 institutions in 1 country.

Ashwin PrakashDepartment of Cardiology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.
Leslie B GordonDepartment of Anesthesiology, Preoperative and Pain Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.
Monica E KleinmanDepartment of Anesthesiology, Preoperative and Pain Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.
Ellen B GuraryDepartment of Mathematics and Statistics, Boston University, Harvard Clinical Research Institute, Boston, Massachusetts.
Joseph MassaroDepartment of Mathematics and Statistics, Boston University, Harvard Clinical Research Institute, Boston, Massachusetts.
Ralph D'AgostinoDepartment of Mathematics and Statistics, Boston University, Harvard Clinical Research Institute, Boston, Massachusetts.
Mark W KieranDivision of Hematology/Oncology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.
Marie Gerhard-HermanDepartment of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Leslie SmootDepartment of Cardiology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.
Boston Children's Hospital · USBoston University · USBaim Institute for Clinical Research · USBrigham and Women's Hospital · USHarvard University · USHasbro Children's Hospital · US

Funding

Harvard Clinical and Translational Science CenterUL1TR001102 · NCATS · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2013 to 2017
$106.2M
Phase II Trial of Lonafarnib, Pravastatin and Zoledronic Acid in ProgeriaRC2HL101631 · NHLBI · DANA-FARBER CANCER INST · PI KIERAN, MARK WILLIAM · 2009 to 2010
$3.3M
NCATS NIH HHS UL1 TR001102NHLBI NIH HHS RC2 HL101631
6 · The paper itself

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.

Indexed as

AdolescentBlood PressureChildChild, PreschoolCross-Sectional StudiesEchocardiographyElectrocardiographyFemaleHeartHeart MurmursHumansMaleMyocardiumProgeriaProspective StudiesPulse Wave Analysis

Identifiers

PMID29466530
PMCPMC5875332
OpenAlexW2792203963

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.