4.6 Article

Cardiac Abnormalities in Patients With Hutchinson-Gilford Progeria Syndrome

期刊

JAMA CARDIOLOGY
卷 3, 期 4, 页码 326-334

出版社

AMER MEDICAL ASSOC
DOI: 10.1001/jamacardio.2017.5235

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资金

  1. Progeria Research Foundation [PRFCLIN2007-02, PRFCLIN2009-03]
  2. National Heart, Lung, and Blood Institute [1RC2HL101631-0]
  3. Harvard Clinical and Translational Science Center (National Center for Research Resources) [UL1 TR001102]
  4. Harvard Clinical and Translational Science Center (National Center for Advancing Translational Sciences, National Institutes of Health Award) [UL1 TR001102]

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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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