Department of Surgery, College of Medicine, The Pennsylvania State University, Hershey, Pennsylvania, USA.
Department of Public Health Sciences, College of Medicine, The Pennsylvania State University, Hershey, Pennsylvania, USA.
J Pain Symptom Manage. 2019 Sep;58(3):427-436. doi: 10.1016/j.jpainsymman.2019.05.013. Epub 2019 May 31.
The Ehlers-Danlos Syndromes (EDSs) are a set of rare heritable disorders of connective tissue, characterized by defects in the structure and synthesis of extracellular matrix elements that lead to a myriad of problems including joint hypermobility and skin abnormalities. Because EDS affects multiple organ systems, defining clear boundaries and recognizing overlapping clinical features shared by disease phenotypes is challenging.
The objective of this study was to seek evidence of phenotypic subgroups of patients with distinctive symptom profiles and describe these resulting subgroups.
Data were extracted from a repository assembled 2001-2013 by the National Institute on Aging Intramural Research Program. Agglomerative hierarchical clustering was used to form distinct subgroups of patients with respect to the domains of pain, physical and mental fatigue, daytime sleepiness, and nighttime sleep. Domains were selected based on literature review, clinician expertise, and guidance from patient advisors.
One hundred seventy-five patients met all inclusion criteria. Three subgroups were identified. The Pain Dominant subgroup (39 patients) had the highest mean pain values, but lowest mean values of other symptoms. The High Symptom Burden subgroup (71 patients) had high mean values in all domains. The Mental Fatigue subgroup (65 patients) had a high mean value for mental fatigue and daytime sleepiness, but a lower mean value for pain.
The subgroups aligned with clinical observation of the heterogeneous nature of EDS, with overlapping symptoms between subtypes and a wide divergence in degree of symptoms within subtypes. This exploratory study helps characterize the various phenotypes and comorbidities of patients with EDS.
埃勒斯-当洛斯综合征(EDS)是一组罕见的遗传性结缔组织疾病,其特征是细胞外基质成分的结构和合成缺陷,导致包括关节过度活动和皮肤异常在内的多种问题。由于 EDS 影响多个器官系统,因此定义明确的边界并识别疾病表型之间共享的重叠临床特征具有挑战性。
本研究的目的是寻找具有独特症状谱的患者表型亚组的证据,并描述这些亚组。
数据取自国家老龄化研究所 2001-2013 年内部研究计划建立的资料库。使用聚集层次聚类法根据疼痛、身体和精神疲劳、白天嗜睡和夜间睡眠等领域形成具有不同症状特征的患者亚组。根据文献综述、临床医生的专业知识以及患者顾问的指导选择领域。
175 名患者符合所有纳入标准。确定了三个亚组。疼痛主导亚组(39 名患者)疼痛平均值最高,但其他症状平均值最低。高症状负担亚组(71 名患者)所有领域的平均值均较高。精神疲劳亚组(65 名患者)精神疲劳和白天嗜睡的平均值较高,但疼痛平均值较低。
这些亚组与 EDS 的异质性临床观察一致,亚型之间存在重叠症状,而亚型内症状的严重程度存在广泛差异。这项探索性研究有助于描述 EDS 患者的各种表型和合并症。