Department of Dermatology, University of Texas Southwestern Medical Center, Dallas.
University of Pittsburgh Scleroderma Center, Pittsburgh, Pennsylvania.
JAMA Dermatol. 2021 Apr 1;157(4):1-8. doi: 10.1001/jamadermatol.2020.5809.
Numerous classification systems for morphea subtypes exist, but none have been systematically evaluated for their ability to categorize patients with morphea into demographically and clinically coherent groups. Although some subtypes, such as linear morphea, are present across all the classification schemes, others list unique subtypes. This creates confusion among investigators and practitioners and impairs accurate categorization of patients for study and clinical evaluation.
To evaluate how frequently the commonly used morphea classification systems categorize patients with morphea into clinically relevant subtypes using cross-sectional analysis of 2 large patient cohorts.
DESIGN, SETTING, AND PARTICIPANTS: This cross-sectional study comprised 944 adults and children from 2 prospective cohorts-the Morphea in Adults and Children at the University of Texas Southwestern Medical Center (Dallas, Texas), which enrolled participants from July 20, 2007, to September 21, 2018, and the National Registry for Childhood-Onset Scleroderma at the University of Pittsburgh (Pittsburgh, Pennsylvania), which enrolled participants from October 23, 2002, to November 13, 2018.
Patient demographic characteristics, morphea subtype, quality-of-life measures, disease activity, and damage as measured by Localized Scleroderma Cutaneous Assessment Tool scores during initial visits.
A total of 944 participants (444 patients with adult-onset morphea and 500 patients with pediatric-onset morphea; 741 female participants [78%]; median age at onset, 16 years [interquartile range, 8-44 years]) were included in this study. Most participants were White (723 [77%]) and had the linear (474 [50%]) or generalized subtype of morphea (244 [26%]). With the use of the previously published Padua criteria, most patients were classified to have linear morphea (474 [50%]), followed by generalized morphea (244 [26%]), plaque morphea (141 [15%]), mixed morphea (38 [4%]), and pansclerotic morphea (3 [0.3%]). Overall, the Padua criteria successfully classified 900 patients (95%) in comparison with the Peterson criteria (533 [56%]) and the European Dermatology Forum classification (487 [52%]).
In this cross-sectional study of morphea subtype classification systems, the Padua criteria performed best in classifying patients into subgroups with cohesive demographic and clinical features, supporting its widespread use. However, they have ambiguities that might lead to misclassification, particularly in terms of generalized and pansclerotic morphea and descriptors such as morphea profunda. Consensus-based approaches are needed to address these ambiguities and develop a unified classification scheme.
存在许多硬皮病亚型的分类系统,但没有一个系统能够系统地评估它们将硬皮病患者分类为具有人口统计学和临床一致性的亚组的能力。虽然有些亚型,如线状硬皮病,存在于所有分类方案中,但其他方案则列出了独特的亚型。这给研究人员和临床医生造成了混乱,并影响了对患者进行准确分类以进行研究和临床评估。
通过对 2 个大型患者队列的横断面分析,评估常用硬皮病分类系统将硬皮病患者分类为临床相关亚型的频率。
设计、地点和参与者:这是一项横断面研究,纳入了来自 2 个前瞻性队列的 944 名成年人和儿童——德克萨斯州西南医学中心的成人和儿童硬皮病(达拉斯,德克萨斯州),该队列于 2007 年 7 月 20 日至 2018 年 9 月 21 日入组患者;匹兹堡大学儿童发病硬皮病国家登记处(宾夕法尼亚州匹兹堡),该队列于 2002 年 10 月 23 日至 2018 年 11 月 13 日入组患者。
患者的人口统计学特征、硬皮病亚型、生活质量指标、疾病活动度和通过局部硬皮病皮肤评估工具评分在初次就诊时的损害。
共有 944 名参与者(444 名成人发病硬皮病患者和 500 名儿童发病硬皮病患者;741 名女性参与者[78%];发病年龄中位数为 16 岁[四分位距,8-44 岁])纳入本研究。大多数参与者为白人(723 名[77%]),且患有线状(474 名[50%])或全身性(244 名[26%])硬皮病亚型。使用先前发表的帕多瓦标准,大多数患者被归类为线状硬皮病(474 名[50%]),其次是全身性硬皮病(244 名[26%])、斑块状硬皮病(141 名[15%])、混合性硬皮病(38 名[4%])和全身性硬皮病(3 名[0.3%])。总体而言,与彼得森标准(533 名[56%])和欧洲皮肤病学论坛分类(487 名[52%])相比,帕多瓦标准成功地对 900 名患者(95%)进行了分类。
在这项硬皮病亚型分类系统的横断面研究中,帕多瓦标准在将患者分类为具有凝聚力的人口统计学和临床特征的亚组方面表现最佳,支持其广泛应用。然而,它们存在模糊性,可能导致分类错误,特别是在广义和全身性硬皮病以及深部硬皮病等描述符方面。需要采用基于共识的方法来解决这些模糊性问题,并制定统一的分类方案。