Kielar Danuta, Jones Andrew M, Wang Xia, Stirnadel-Farrant Heide, Katial Rohit K, Bansal Abhinav, Garg Manu, Sharma Chandrakant, Thakar Shubhankar, Ye Qin
BioPharmaceuticals Medical, AstraZeneca, Cambridge, UK.
Late-Stage Development, Respiratory & Immunology, BioPharmaceuticals R&D, AstraZeneca, Gaithersburg, MD, USA.
Int J Nephrol Renovasc Dis. 2023 Dec 21;16:269-280. doi: 10.2147/IJNRD.S431375. eCollection 2023.
Blood eosinophils can increase in response to infection, inflammation, and hypersensitivity reactions, yet their involvement in the progression of chronic kidney disease (CKD) is poorly understood. This study explores the relationship between blood eosinophils and CKD progression among patients in a real-world setting.
This retrospective study analyzed data obtained from the Optum de-identified electronic health records dataset in the United States. Patients diagnosed with CKD stage 3 or 4 (International Classification of Diseases diagnosis code or estimated glomerular filtration rate [eGFR] <60 mL/min) between January 2011 and March 2018 were included and followed until progression to the next CKD stage, death, or dropout. The primary objective of this study was to assess the relationship between blood eosinophil counts (bEOS) and CKD progression, adjusting for clinical and demographic features as well as known risk factors for CKD stages 3-4. The primary outcomes were CKD progression and all-cause mortality.
We found that high eosinophilic levels (bEOS ≥300 cells/µL) were associated with CKD progression from stage 3 to stages 4 or 5 (hazard ratio [HR] ranging from 1.30 to 1.50) and from stages 4 to 5 (HR ranging from 1.28 to 1.50). Among patients with CKD progression, those with blood eosinophils ≥300 cells/µL appeared to have a relatively lower eGFR, higher all-cause mortality, and reduced time to CKD progression and death than those with <300 cells/µL. Factors including sex, race, hypertension, anemia, and treatments for cardiovascular and hematopoietic drugs were associated with CKD progression.
Elevated eosinophils may increase the risk for CKD progression. Larger studies are needed to assess whether the risk of mortality is increased among patients with elevated eosinophils.
血液嗜酸性粒细胞可因感染、炎症和超敏反应而增加,但其在慢性肾脏病(CKD)进展中的作用尚不清楚。本研究在真实世界环境中探讨血液嗜酸性粒细胞与CKD进展之间的关系。
这项回顾性研究分析了从美国Optum去识别电子健康记录数据集中获得的数据。纳入2011年1月至2018年3月期间诊断为CKD 3期或4期(国际疾病分类诊断代码或估计肾小球滤过率[eGFR]<60 mL/分钟)的患者,并随访至进展到下一个CKD阶段、死亡或退出研究。本研究的主要目的是评估血液嗜酸性粒细胞计数(bEOS)与CKD进展之间的关系,并对临床和人口统计学特征以及CKD 3-4期的已知危险因素进行校正。主要结局为CKD进展和全因死亡率。
我们发现,高嗜酸性粒细胞水平(bEOS≥300个细胞/µL)与CKD从3期进展到4期或5期(风险比[HR]为1.30至1.50)以及从4期进展到5期(HR为1.28至1.50)相关。在CKD进展的患者中,血液嗜酸性粒细胞≥300个细胞/µL的患者似乎比<300个细胞/µL的患者具有相对较低的eGFR、较高的全因死亡率以及缩短的CKD进展和死亡时间。包括性别、种族、高血压、贫血以及心血管和造血药物治疗等因素与CKD进展相关。
嗜酸性粒细胞升高可能增加CKD进展的风险。需要开展更大规模的研究来评估嗜酸性粒细胞升高的患者死亡率是否增加。