Oh Gia J, Waldo Anne, Paez-Cruz Francisco, Gipson Patrick E, Pesenson Anne, Selewski David T, Kamil Elaine S, Massengill Susan F, Lafayette Richard A, Modes Meg, Adler Sharon G, Desmond Hailey, Eikstadt Richard, Attalla Samara, Modi Zubin J, Troost Jonathan P, Gipson Debbie S
Division of Nephrology, Department of Pediatrics, Stanford University School of Medicine, Stanford, California, USA.
Division of Nephrology, Department of Pediatrics and Communicable Diseases, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Kidney Int Rep. 2019 Sep 9;4(11):1608-1616. doi: 10.1016/j.ekir.2019.08.019. eCollection 2019 Nov.
The goal of this study was to assess the occurrence of steroid-associated adverse events (SAAE) in patients with primary proteinuric kidney disease.
The Kidney Research Network Registry consists of children and adults with primary proteinuric kidney disease. SAAEs of interest were hypertension, hyperglycemia and diabetes, overweight and obesity, short stature, ophthalmologic complications, bone disorders, infections, and psychosis. Events were identified using codes, blood pressures, growth parameters, laboratory values, and medications. Poisson generalized estimating equations tested the association between steroid onset and dose on SAAE risk.
A total of 884 participants were included in the analysis; 534 (60%) were treated with steroids. Of these, 62% had at least one SAAE. The frequency of any SAAE after initiation of steroids was 293 per 1000 person-years. The most common SAAEs were hypertension (173.7 per 1000 person-years), diabetes (78.7 per 1000 person-years), obesity (66.8 per 1000 person-years), and infections (46.1 per 1000 person-years). After adjustment for demographics, duration of kidney disease, estimated glomerular filtration rate (eGFR), proteinuria, and other therapies, steroid exposure was associated with a 40% increase in risk of any SAAE (Relative risk [RR]: 1.4; 95% confidence interval [CI]: 1.3-1.6). A 1-mg/kg per day increase in steroid dose was associated with a 2.5-fold increase in risk of any SAAE.
Most patients with primary proteinuric kidney disease treated with steroids experienced at least one SAAE. Steroid therapy increased risk of hypertension, diabetes, weight gain, short stature, fractures, and infections after adjusting for disease-related factors. This study highlights the importance of surveillance and management of SAAE and provides rationale for the development of steroid minimization protocols.
本研究的目的是评估原发性蛋白尿性肾病患者中类固醇相关不良事件(SAAE)的发生率。
肾脏研究网络登记处纳入了患有原发性蛋白尿性肾病的儿童和成人。感兴趣的SAAE包括高血压、高血糖和糖尿病、超重和肥胖、身材矮小、眼科并发症、骨病、感染和精神病。通过编码、血压、生长参数、实验室值和用药情况来识别这些事件。泊松广义估计方程检验了类固醇起始剂量与SAAE风险之间的关联。
共有884名参与者纳入分析;534名(60%)接受了类固醇治疗。其中,62%至少发生了一次SAAE。类固醇起始治疗后任何SAAE的发生频率为每1000人年293例。最常见的SAAE是高血压(每1000人年173.7例)、糖尿病(每1000人年78.7例)、肥胖(每1000人年66.8例)和感染(每1000人年46.1例)。在对人口统计学、肾病病程、估计肾小球滤过率(eGFR)、蛋白尿和其他治疗进行调整后,类固醇暴露与任何SAAE风险增加40%相关(相对风险[RR]:1.4;95%置信区间[CI]:1.3 - 1.6)。类固醇剂量每天每千克增加1毫克与任何SAAE风险增加2.5倍相关。
大多数接受类固醇治疗的原发性蛋白尿性肾病患者至少经历了一次SAAE。在调整疾病相关因素后,类固醇治疗增加了高血压、糖尿病、体重增加、身材矮小、骨折和感染的风险。本研究强调了SAAE监测和管理的重要性,并为制定类固醇最小化方案提供了理论依据。