Centre for Safe Medication Practice and Research, Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
Laboratory of Data Discovery for Health (D24H), Hong Kong Science and Technology Park, Sha Tin, Hong Kong SAR, China.
Nephrol Dial Transplant. 2023 Jan 23;38(1):129-137. doi: 10.1093/ndt/gfac292.
With accruing case reports on de novo or relapsing glomerular diseases (GD) following different severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines, we evaluated the risk of GD following BNT162b2 and CoronaVac vaccines.
A modified self-controlled case series analysis was conducted using anonymized, territory-wide SARS-CoV-2 vaccination records in Hong Kong. All Hong Kong residents aged 18 years or above with outcomes of interest were included. Outcomes of interest were GD, proteinuria or hematuria within 42 days following each dose of SARS-CoV-2 vaccines. Incidence per 100 000 doses of SARS-CoV-2 vaccines administered was calculated, and incidence rate ratios (IRRs) were estimated using conditional Poisson regression with seasonality adjustment.
Between 23 February 2021 and 31 March 2022, 4062 patients had an incident diagnosis of GD, proteinuria or hematuria, with 2873 of them being vaccinated during the observation period. The incidences of the composite events 1-41 days after vaccination were 3.7 (95% CI 3.1-4.4) per 100 000 doses of BNT162b2 administered, and 6.5 (95% CI 5.7-7.5) per 100 000 doses CoronaVac administered. There was no significant increase in the risks of composite events following the first (BNT162b2: IRR = 0.76, 95% CI 0.56-1.03; CoronaVac: IRR = 0.92, 95% CI 0.72-1.19), second (BNT162b2: IRR = 0.92, 95% CI 0.72-1.17; CoronaVac: IRR = 0.88. 95% CI 0.68-1.14) or third (BNT162b2: IRR = 0.39. 95% CI 0.15-1.03; CoronaVac: IRR = 1.18. 95% CI 0.53-2.63) dose of SARS-CoV-2 vaccines.
There was no evidence of increased risks of de novo or relapsing GD with either BNT162b2 or CoronaVac vaccines.
随着越来越多关于新型或复发肾小球疾病(GD)的病例报告在不同的严重急性呼吸综合征冠状病毒 2 (SARS-CoV-2)疫苗接种后出现,我们评估了 BNT162b2 和科兴疫苗接种后 GD 的风险。
使用香港匿名、全港范围的 SARS-CoV-2 疫苗接种记录,对改良的自身对照病例系列分析进行了评估。所有年龄在 18 岁及以上、有兴趣的结局的香港居民均被纳入研究。有兴趣的结局是指在 SARS-CoV-2 疫苗接种后 42 天内出现 GD、蛋白尿或血尿。每接种 100000 剂 SARS-CoV-2 疫苗的发病率计算,并使用带有季节性调整的条件泊松回归估计发病率比(IRR)。
2021 年 2 月 23 日至 2022 年 3 月 31 日期间,4062 例患者发生 GD、蛋白尿或血尿的首发诊断,其中 2873 例患者在观察期间接种了疫苗。接种后 1-41 天复合事件的发生率分别为 BNT162b2 每 100000 剂 3.7(95%CI 3.1-4.4)和科兴每 100000 剂 6.5(95%CI 5.7-7.5)。首次接种(BNT162b2:IRR=0.76,95%CI 0.56-1.03;科兴:IRR=0.92,95%CI 0.72-1.19)、第二次接种(BNT162b2:IRR=0.92,95%CI 0.72-1.17;科兴:IRR=0.88,95%CI 0.68-1.14)或第三次接种(BNT162b2:IRR=0.39,95%CI 0.15-1.03;科兴:IRR=1.18,95%CI 0.53-2.63)SARS-CoV-2 疫苗后,复合事件的风险均无显著增加。
BNT162b2 或科兴疫苗接种均未发现新发或复发 GD 风险增加的证据。