Hamijoyo Laniyati, Sapartini Gartika, Rahmadi Andri R, Wachjudi Rachmat G, Dewi Sumartini, Ghrahani Reni, Praptama Suhendra, Rainy Nisa R, Usman Stefanie Y, Suryajaya Bernard S, Candrianita Sasfia, Sutedja Endang, Setiabudiawan Budi
Rheumatology Division, Faculty of Medicine, Department of Internal Medicine, 61809Universitas Padjadjaran/Hasan Sadikin General Hospital, Bandung, Indonesia.
Lupus Study Group, Immunology Study Center, Faculty of Medicine, 106075Universitas Padjadjaran, Bandung, Indonesia.
Lupus. 2022 May;31(6):759-764. doi: 10.1177/09612033221093482. Epub 2022 Apr 5.
The clinical presentation of childhood-onset systemic lupus erythematosus (SLE) is generally perceived to differ from that of adult-onset SLE.
We aimed to compare the demographic and clinical manifestation between childhood-onset vs. adult-onset SLE in a cohort of Indonesian patients at tertiary care centers.
This retrospective study included patients in the Hasan Sadikin Lupus Registry from 2008 until December 2017. The demographics, clinical presentations, and outcomes were compared between childhood-onset SLE (<18 years old) (Group 1) and adult-onset SLE (≥18 years old) (Group 2).
Eight hundred seventy patients were involved into this study. The proportion of childhood-onset SLE was 20% (174 patients). The mean age of group 1 versus group 2 was 13.56 ± 3.04 vs 30.41 ± 8.54 years. The following clinical manifestations at SLE diagnosis were significantly more common in childhood-onset than in adult-onset SLE patients: hematological disorder ( = 0.033) and arthritis ( = 0.006). While discoid rash ( = 0.036) and photosensitivity ( < 0.001) were significantly found higher in adult-onset SLE. Cyclophosphamide therapy was significantly more common to be used in childhood-onset (38.5% vs 21.0%, = <0.001). However, frequency of mortality on follow-up tended to be higher in childhood-onset group (11.5% vs 7.0%, = 0.208).
Arthritis and hematologic involvements at SLE diagnosis were more prominent in childhood-onset compared to adult-onset patients, and mortality in childhood-onset SLE during follow-up relatively higher. This data may suggest the need for more aggressive management approach to childhood-onset patients with SLE.
儿童期起病的系统性红斑狼疮(SLE)的临床表现通常被认为与成人期起病的SLE不同。
我们旨在比较印度尼西亚三级医疗中心队列中儿童期起病与成人期起病的SLE患者的人口统计学和临床表现。
这项回顾性研究纳入了2008年至2017年12月在哈桑·萨迪金狼疮登记处登记的患者。比较儿童期起病的SLE(<18岁)(第1组)和成人期起病的SLE(≥18岁)(第2组)的人口统计学、临床表现和结局。
870名患者参与了本研究。儿童期起病的SLE比例为20%(174例患者)。第1组与第2组的平均年龄分别为13.56±3.04岁和30.41±8.54岁。在SLE诊断时,以下临床表现儿童期起病的患者比成人期起病的患者更常见:血液系统疾病(P = 0.033)和关节炎(P = 0.006)。而成人期起病的SLE患者盘状红斑(P = 0.036)和光过敏(P < 0.001)的发生率明显更高。环磷酰胺治疗在儿童期起病的患者中使用更为常见(38.5%对21.0%,P = <0.001)。然而,随访期间儿童期起病组的死亡率倾向于更高(11.5%对7.0%,P = 0.208)。
与成人期起病的患者相比,儿童期起病的患者在SLE诊断时关节炎和血液系统受累更为突出,且儿童期起病的SLE患者随访期间的死亡率相对较高。这些数据可能表明需要对儿童期起病的SLE患者采取更积极的管理方法。