Barbour Sean J, Canney Mark, Coppo Rosanna, Zhang Hong, Liu Zhi-Hong, Suzuki Yusuke, Matsuzaki Keiichi, Katafuchi Ritsuko, Induruwage Dilshani, Er Lee, Reich Heather N, Feehally John, Barratt Jonathan, Cattran Daniel C
University of British Columbia, Division of Nephrology, Vancouver, Canada; BC Renal, Vancouver, Canada.
University of British Columbia, Division of Nephrology, Vancouver, Canada; BC Renal, Vancouver, Canada.
Kidney Int. 2020 Oct;98(4):1009-1019. doi: 10.1016/j.kint.2020.04.042. Epub 2020 May 25.
Immunosuppression in IgA nephropathy (IgAN) should be reserved for patients at high-risk of disease progression, which KDIGO guidelines determine based solely on proteinuria 1g or more/day. To investigate if treatment decisions can be more accurately accomplished using individualized risk from the International IgAN Prediction Tool, we simulated allocation of a hypothetical immunosuppression therapy in an international cohort of adults with IgAN. Two decision rules for treatment were applied based on proteinuria of 1g or more/day or predicted risk from the Prediction Tool above a threshold probability. An appropriate decision was defined as immunosuppression allocated to patients experiencing the primary outcome (50% decline in eGFR or ESKD) and withheld otherwise. The net benefit and net reduction in treatment are the proportion of patients appropriately allocated to receive or withhold immunosuppression, adjusted for the harm from inappropriate decisions, calculated for all threshold probabilities from 0-100%. Of 3299 patients followed for 5.1 years, 522 (15.8%) experienced the primary outcome. Treatment allocation based solely on proteinuria of 1g or more/day had a negative net benefit (was harmful) because immunosuppression was increasingly allocated to patients without progressive disease. Compared to using proteinuria, treatment allocation using the Prediction Tool had a larger net benefit up to 23.4% (95% confidence interval 21.5-25.2%) and a larger net reduction in treatment up to 35.1% (32.3-37.8%). Thus, allocation of immunosuppression to high-risk patients with IgAN can be substantially improved using the Prediction Tool compared to using proteinuria.
IgA肾病(IgAN)的免疫抑制治疗应仅用于疾病进展高危患者,KDIGO指南仅根据每日蛋白尿1g及以上来判定。为研究使用国际IgAN预测工具得出的个体化风险是否能更准确地做出治疗决策,我们在一个国际成人IgAN队列中模拟了一种假设的免疫抑制疗法的分配。基于每日蛋白尿1g及以上或预测工具得出的高于阈值概率的风险应用了两种治疗决策规则。恰当决策定义为将免疫抑制治疗分配给出现主要结局(估算肾小球滤过率[eGFR]下降50%或终末期肾病[ESKD])的患者,否则不予分配。净获益和治疗净减少率是恰当分配接受或不接受免疫抑制治疗的患者比例,针对不当决策造成的危害进行了调整,计算了0 - 100%的所有阈值概率。在3299例随访5.1年的患者中,522例(15.8%)出现了主要结局。仅基于每日蛋白尿1g及以上进行治疗分配的净获益为负(有害),因为免疫抑制治疗越来越多地分配给了无疾病进展的患者。与使用蛋白尿标准相比,使用预测工具进行治疗分配的净获益高达23.4%(95%置信区间21.5 - 25.2%),治疗净减少率高达35.1%(32.3 - 37.8%)。因此,与使用蛋白尿标准相比,使用预测工具可显著改善IgAN高危患者免疫抑制治疗的分配。