Yang Meng, Xie Jingyuan, Ouyang Yan, Zhang Xiaoyan, Shi Manman, Li Xiao, Wang Zhaohui, Shen Pingyan, Ren Hong, Zhang Wen, Wang Weiming, Chen Nan
Department of Nephrology, Institute of Nephrology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Oncotarget. 2017 Sep 7;8(43):73603-73612. doi: 10.18632/oncotarget.20701. eCollection 2017 Sep 26.
ABO blood group antigens have been reported to be associated with inflammation and infections which have been largely implicated in the onset and progression of immune-mediated diseases. This study aimed to evaluate the association between ABO blood group and progression of IgA nephropathy (IgAN). We retrospectively enrolled 919 biopsy-proven IgAN patients with a minimum follow-up of 1 year and eGFR≥15ml/min/1.73m at the time of renal biopsy. Patients in non-B antigen group (type O/A) had lower baseline eGFR, higher systolic blood pressure (SBP), uric acid, lactate dehydrogenase, high-sensitive C-reactive protein and tumor necrosis factor-α compared to patients in B antigen group(type B/AB). After a median follow-up of 57.46 months, 124(13.5%) patients progressed to end-stage renal disease (ESRD) including 98(17.7%) in non-B antigen group and 26(7.1%) in B antigen group. Kaplan-Meier analysis showed the median ESRD-free survival time of patients in non-B antigen group was significantly shorter than patients in B antigen group [143.09±6.38 159.05±4.94months, < 0.001]. Furthermore, non-B antigen blood group was associated with an independently increased risk of ESRD (HR=2.21, 95%CI 1.35-3.62, = 0.002) after fully adjusted by age, sex, SBP, eGFR, blood urea nitrogen, hypoalbuminemia, uric acid, triglycerides, hemoglobin, serum C3, urine protein, Oxford classification and glucocorticoid treatment. In conclusion, our study suggests that ABO blood type is a new risk factor for IgAN progression. IgAN patients with blood type O or A have an independent increased risk for renal function deterioration which might be explained by an increased level of inflammatory status.
据报道,ABO血型抗原与炎症和感染有关,而炎症和感染在很大程度上与免疫介导疾病的发生和发展有关。本研究旨在评估ABO血型与IgA肾病(IgAN)进展之间的关联。我们回顾性纳入了919例经活检证实的IgAN患者,这些患者在肾活检时至少随访1年且估算肾小球滤过率(eGFR)≥15ml/min/1.73m²。与B抗原组(B型/AB型)患者相比,非B抗原组(O型/A型)患者的基线eGFR较低,收缩压(SBP)、尿酸、乳酸脱氢酶、高敏C反应蛋白和肿瘤坏死因子-α较高。中位随访57.46个月后,124例(13.5%)患者进展为终末期肾病(ESRD),其中非B抗原组98例(17.7%),B抗原组26例(7.1%)。Kaplan-Meier分析显示,非B抗原组患者的无ESRD中位生存时间显著短于B抗原组患者[143.09±6.38对159.05±4.94个月,P<0.001]。此外,在对年龄、性别、SBP、eGFR、血尿素氮、低白蛋白血症、尿酸、甘油三酯、血红蛋白、血清C3、尿蛋白、牛津分类和糖皮质激素治疗进行全面调整后,非B抗原血型与ESRD风险独立增加相关(风险比[HR]=2.21,95%置信区间[CI]1.35 - 3.62,P=0.002)。总之,我们的研究表明ABO血型是IgAN进展的一个新危险因素。O型或A型血的IgAN患者肾功能恶化的风险独立增加,这可能是由于炎症状态升高所致。