Frequency and burden of gastrointestinal symptoms in familial dysautonomia.

Chethan Ramprasad, Lucy Norcliffe-Kaufmann, Jose-Alberto Palma, Joseph Levy, Yian Zhang, Christy L Spalink, Abraham Khan, Scott Smukalla, Horacio Kaufmann, Lea Ann Chen
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引用次数: 5

Abstract

Purpose: Familial dysautonomia (FD) is a rare hereditary sensory and autonomic neuropathy (HSAN-3) that is clinically characterized by impaired pain and temperature perception and abnormal autonomic function. Patients with FD have gastrointestinal dysmotility and report a range of gastrointestinal symptoms that have yet to be systematically evaluated. The aim of this study was to establish the frequency and severity of gastrointestinal symptoms in patients with FD.

Methods: The validated National Institutes of Health Patient-Reported Outcomes Measurement Information System (PROMIS) survey questionnaire, together with additional FD-specific questions, were distributed to 202 living patients with genetically confirmed FD who had been identified from the New York University FD Patient Registry or, when relevant, to their respective caretaker. As a comparison group, we used a general US adult population for whom PROMIS scores were available (N = 71,812).

Results: Of the 202 questionnaires distributed, 77 (38%) were returned, of which 53% were completed by the patient. Median age of the respondents was 25 years, and 44% were male. Gastrostomy tube was the sole nutrition route for 25% of the patients, while 53% were reliant on the gastrostomy tube only for liquid intake. The prevalence of gastrointestinal symptoms was significantly higher in each of the eight domains of PROMIS in patients with FD than in the controls. Gastrointestinal symptoms as measured by raw scores on the PROMIS scale were significantly less severe in the FD patient group than in the control population in all domains with the exception of the abdominal pain domain. The surveys completed by caregivers reported the same burden of symptoms as those completed only by patients.

Conclusion: Gastrointestinal symptoms affect nearly all patients with FD. Gastrointestinal symptoms are more prevalent in adult patients with FD than in the average US adult population but are less severe in the former.

家族性自主神经异常患者胃肠道症状的频率和负担。
目的:家族性自主神经异常(Familial dysautonomia, FD)是一种罕见的遗传性感觉和自主神经病变(HSAN-3),临床表现为疼痛和温度感知受损以及自主神经功能异常。FD患者有胃肠运动障碍,并报告了一系列胃肠道症状,这些症状尚未得到系统评估。本研究的目的是确定FD患者胃肠道症状的频率和严重程度。方法:将经过验证的美国国立卫生研究院患者报告结果测量信息系统(PROMIS)调查问卷和额外的FD特异性问题分发给202名遗传证实的FD患者,这些患者已从纽约大学FD患者登记处确定,或在相关时确定给各自的护理人员。作为对照组,我们使用了可获得PROMIS评分的普通美国成年人(N = 71,812)。结果:共发放问卷202份,回收问卷77份(38%),其中患者自行填写问卷53%。受访者的中位年龄为25岁,44%为男性。25%的患者仅通过胃造口管获取营养,53%的患者仅通过胃造口管获取液体。与对照组相比,FD患者在PROMIS的8个域中,胃肠道症状的发生率均显著升高。根据PROMIS量表的原始评分,FD患者组的胃肠道症状在除腹痛外的所有领域都明显轻于对照组。由护理人员完成的调查报告的症状负担与仅由患者完成的调查相同。结论:几乎所有FD患者都有胃肠道症状。胃肠症状在成年FD患者中比在美国平均成年人群中更为普遍,但前者较轻。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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