Department of Cardiology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.
Department of Pediatrics, Harvard Medical School, Boston, Massachusetts.
JAMA Cardiol. 2018 Apr 1;3(4):326-334. doi: 10.1001/jamacardio.2017.5235.
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.
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.
Classic HGPS.
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.
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.
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.
哈钦森-吉尔福德早衰综合征(HGPS)是一种罕见的疾病,由于心血管事件,患者常在生命的第二个十年死亡。然而,由于其罕见性(107 名已确认的存活患者),心脏病的自然病史仍未得到描述。因此,对于临床试验来说,有意义的心脏终点很难确定。
检查 HGPS 患者心脏异常的出现过程,以确定用于未来临床试验的有意义的心脏终点。
设计、地点和参与者:在这项前瞻性、横断面、观察性研究中,2014 年 7 月 1 日至 2016 年 2 月 29 日,在一家中心对 27 例经临床和基因确诊的经典 HGPS 患者进行了 1 次就诊评估,这些患者在开始治疗前均接受了评估。
经典 HGPS。
使用标准技术通过超声心动图评估心室和瓣膜功能。使用组织多普勒成像评估左心室(LV)舒张功能。使用以前发表的正常数据将发现调整为年龄和体型。
本研究纳入了 27 例患者(中位年龄 5.6 岁;年龄范围 2-17 岁;15 例[56%]为男性)。在超声心动图指标中,LV 舒张功能障碍(定义为组织多普勒间隔或侧壁早期速度 z 评分小于-2)最为常见,16 例(59%)患者存在这种异常。舒张功能障碍见于所有年龄组,且随着年龄的增长而更为常见,与正常衰老过程中的发现一致。老年患者的 LV 舒张功能指标更为异常。侧壁和间隔早期速度的 z 评分较低(r=-0.77,P<.001;r=-0.66,P<.001),而早期二尖瓣流入速度与早期舒张组织多普勒心肌速度的比值较高(r=0.80,P<.001;r=0.72,P<.001)。在老年患者中,其他超声心动图表现,包括 LV 肥厚、LV 收缩功能障碍和瓣膜疾病,在第一个十年中更为少见,而在第二个十年中更为常见。
在这项迄今为止最大的 HGPS 患者队列中,LV 舒张功能障碍是最常见的超声心动图异常,且其患病率随年龄增长而增加。LV 舒张功能的超声心动图指标可能是该患者群体未来临床试验的有用终点。