Riley Hospital for Children at Indiana University Health, Indianapolis, and University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania.
University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania.
Arthritis Care Res (Hoboken). 2018 Dec;70(12):1806-1813. doi: 10.1002/acr.23547. Epub 2018 Nov 8.
To investigate clinical manifestations of juvenile systemic sclerosis (SSc; scleroderma), including disease characteristics and patient quality of life, using the multinational Childhood Arthritis and Rheumatology Research Alliance (CARRA) Legacy Registry.
Patients with juvenile SSc were prospectively enrolled between 2010 and 2013. The diagnosis of juvenile SSc was determined by the enrolling pediatric rheumatologist, with the requirement for disease onset prior to age 18 years. Collected data included demographics, disease characteristics, medication exposure, and quality of life metrics.
In total, 64 patients with juvenile SSc were enrolled a median of 3.6 years after disease onset, which occurred at a median age of 10.3 years. The most common organ manifestations were dermatologic and vascular, followed by musculoskeletal, gastrointestinal, and pulmonary; in 38% of patients, ≥4 organ systems were affected. Patients with juvenile SSc had significantly more disability at enrollment compared with CARRA Legacy Registry patients with juvenile idiopathic arthritis, dermatomyositis, or systemic lupus erythematosus. Although physician-reported measures correlated most closely with arthritis, dermatologic manifestations, and pulmonary manifestations, poor patient-reported measures were associated with gastrointestinal involvement. During >50 person-years of follow-up, most organ manifestations remained stable, and no mortality or development of new solid organ involvement after enrollment was reported.
In the first multicenter prospective cohort of patients with juvenile SSc in North America, the disease burden was high: multiorgan manifestations were common, and functional disability was greater than that observed in patients with other childhood-onset rheumatic diseases. Gastrointestinal involvement had the greatest impact on quality of life.
通过多国儿童关节炎和风湿病研究联盟(CARRA)传统登记处,调查青少年全身性硬皮病(SSc;硬皮病)的临床表现,包括疾病特征和患者生活质量。
2010 年至 2013 年期间,前瞻性招募了青少年 SSc 患者。青少年 SSc 的诊断由参与的儿科风湿病学家确定,要求疾病在 18 岁之前发作。收集的数据包括人口统计学资料、疾病特征、药物暴露情况和生活质量指标。
共纳入 64 例青少年 SSc 患者,中位发病后 3.6 年(发病中位年龄为 10.3 岁)入组。最常见的器官表现为皮肤血管,其次是肌肉骨骼、胃肠道和肺部;38%的患者有≥4 个器官系统受累。与 CARRA 传统登记处的青少年特发性关节炎、皮肌炎或系统性红斑狼疮患者相比,青少年 SSc 患者在入组时残疾程度显著更高。尽管医生报告的测量结果与关节炎、皮肤表现和肺部表现相关性最强,但较差的患者报告测量结果与胃肠道受累有关。在超过 50 人年的随访期间,大多数器官表现保持稳定,且入组后无死亡或新发实体器官受累。
在北美首例青少年 SSc 的多中心前瞻性队列研究中,疾病负担较高:多器官表现常见,功能残疾比其他儿童发病的风湿病更为严重。胃肠道受累对生活质量的影响最大。