Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Eur J Pediatr. 2021 May;180(5):1431-1441. doi: 10.1007/s00431-020-03910-2. Epub 2021 Jan 3.
Patients with childhood-onset systemic lupus erythematosus (cSLE) are at risk of becoming short adults. To evaluate the growth patterns and risk factors of short final height, a retrospective study was conducted in 97 patients (87 females, 90%) with cSLE who grew from the time of diagnosis and reached their final height. The primary outcome was the final height. Participants were divided into participants with short final height (final height standard deviation score (HSDS) < - 2, n = 22, 23%) and participants with normal final height (final HSDS ≥ - 2, n = 75, 77%). At diagnosis, the mean age was 11.3 ± 2.4 years and HSDS was - 0.5 ± 1.3. The participants reached the final height of 1.51 ± 0.08 m (final HSDS - 1.3 ± 0.1) at mean age of 16.2 ± 2.3 years. The HSDS of participants with short final height steadily declined throughout the course of SLE (p = 0.02), and were significantly lower than participants with normal final height at any time point (p < 0.001). In participants with normal final height, HSDS significantly declined from baseline until 2 years after diagnosis (p = 0.01), and then became stable thereafter. The independent risk factors for short final height were the male sex, short stature at diagnosis, low body weight at final height, and cumulative corticosteroid dose.Conclusion: A substantial number of the participants with cSLE became short adults. Adequate nutrition and corticosteroid minimization should be emphasized in patients at high risk for short final height. What is known? • Growth failure is common in SLE due to many risk factors including chronic inflammation, malnutrition, and long-term use of corticosteroids. • In comparison to growth failure, final height is a better indicator of growth as the prevalence of growth failure is variable depending on definitions, patient age and pubertal status. What is new? • Nearly one fourth of children with SLE have short final height. • The independent risk factors for short final height were the male sex, short stature at diagnosis, low body weight at final height, and cumulative corticosteroid dose.
患者患有儿童期起病的系统性红斑狼疮 (cSLE),有成为矮个子成人的风险。为了评估矮小终身高的生长模式和危险因素,对 97 例从诊断时开始生长并达到终身高的 cSLE 患儿(87 名女性,90%)进行了回顾性研究。主要结局为终身高。将参与者分为终身高矮小者(终身高标准差评分(HSDS)< - 2,n = 22,23%)和终身高正常者(终 HSDS ≥ - 2,n = 75,77%)。诊断时,平均年龄为 11.3 ± 2.4 岁,HSDS 为 - 0.5 ± 1.3。参与者在平均年龄 16.2 ± 2.3 岁时达到 1.51 ± 0.08 m 的终身高(终 HSDS - 1.3 ± 0.1)。终身高矮小者的 HSDS 在 SLE 病程中持续下降(p = 0.02),且在任何时间点均显著低于终身高正常者(p < 0.001)。在终身高正常者中,HSDS 自基线开始直至诊断后 2 年显著下降(p = 0.01),此后保持稳定。终身高矮小的独立危险因素为男性、诊断时身材矮小、终身高时体重低和累积皮质类固醇剂量。结论:相当一部分 cSLE 患儿成为矮个子成人。应重视终身高矮小风险较高的患者的充足营养和皮质类固醇最小化。已知? • 由于多种危险因素,包括慢性炎症、营养不良和长期使用皮质类固醇,SLE 患儿常发生生长障碍。 • 与生长障碍相比,终身高是更好的生长指标,因为生长障碍的患病率因定义、患者年龄和青春期状态而异。新内容? • 近四分之一的 SLE 患儿终身高矮小。 • 终身高矮小的独立危险因素为男性、诊断时身材矮小、终身高时体重低和累积皮质类固醇剂量。