Emory University and Children's Healthcare of Atlanta, Atlanta, Georgia.
University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Am J Kidney Dis. 2024 Jan;83(1):37-46. doi: 10.1053/j.ajkd.2023.07.008. Epub 2023 Aug 31.
RATIONALE & OBJECTIVE: Patients with glomerular disease (GN) may be at increased risk of severe COVID-19, yet concerns over vaccines causing disease relapse may lead to vaccine hesitancy. We examined the associations of COVID-19 with longitudinal kidney function and proteinuria and compared these with similar associations with COVID-19 vaccination.
Observational cohort study from July 1, 2021, to January 1, 2023.
SETTING & PARTICIPANTS: A prospective observational study network of 71 centers from North America and Europe (CureGN) with children and adults with primary minimal change disease, focal segmental glomerulosclerosis, membranous nephropathy, or IgA nephropathy.
COVID-19 and COVID-19 vaccination.
Repeated measure of estimated glomerular filtration rate (eGFR); recurrent time-to-event outcome of GN disease worsening as defined by doubling of the urinary protein-creatinine ratio (UPCR) to at least 1.5g/g or increase in dipstick urine protein by 2 ordinal levels to 3+(300mg/dL) or above.
Interrupted time series analysis for eGFR. Prognostic matched sequential stratification recurrent event analysis for GN disease worsening.
Among 2,055 participants, 722 (35%) reported COVID-19 infection; of these, 92 (13%) were hospitalized, and 3 died (<1%). The eGFR slope before COVID-19 infection was-1.40mL/min/1.73m (± 0.29 SD); within 6 months after COVID-19 infection, the eGFR slope was-4.26mL/min/1.73m (± 3.02 SD), which was not significantly different (P=0.34). COVID-19 was associated with increased risk of worsening GN disease activity (HR, 1.35 [95% CI, 1.01-1.80]). Vaccination was not associated with a change in eGFR (-1.34mL/min/1.73m±0.15 SD vs-2.16mL/min/1.73m±1.74 SD; P=0.6) or subsequent GN disease worsening (HR 1.02 [95% CI, 0.79-1.33]) in this cohort.
Infrequent or short follow-up.
Among patients with primary GN, COVID-19 infection was severe for 1 in 8 cases and was associated with subsequent worsening of GN disease activity, as defined by proteinuria. By contrast, vaccination against COVID-19 was not associated with change in disease activity or kidney function decline. These results support COVID-19 vaccination for patients with GN.
PLAIN-LANGUAGE SUMMARY: In this cohort study of 2,055 patients with minimal change disease, focal segmental glomerulosclerosis, membranous nephropathy, or IgA nephropathy, COVID-19 resulted in hospitalization or death for 1 in 8 cases and was associated with a 35% increase in risk for worsening proteinuria. By contrast, vaccination did not appear to adversely affect kidney function or proteinuria. Our data support vaccination for COVID-19 in patients with glomerular disease.
患有肾小球疾病 (GN) 的患者可能面临罹患严重 COVID-19 的风险增加,但对疫苗导致疾病复发的担忧可能导致疫苗犹豫。我们研究了 COVID-19 与纵向肾功能和蛋白尿的关联,并将其与 COVID-19 疫苗接种的类似关联进行了比较。
这是一项从 2021 年 7 月 1 日至 2023 年 1 月 1 日进行的观察性队列研究。
来自北美和欧洲的 71 个中心的前瞻性观察性研究网络(CureGN),纳入了原发性微小病变肾病、局灶节段性肾小球硬化症、膜性肾病或 IgA 肾病的儿童和成人患者。
COVID-19 和 COVID-19 疫苗接种。
估计肾小球滤过率(eGFR)的重复测量值;根据尿蛋白/肌酐比(UPCR)翻倍(至少 1.5g/g)或尿蛋白试纸条尿蛋白增加 2 个等级至 3+(300mg/dL)或以上定义的 GN 疾病恶化的复发性时间事件结局。
eGFR 的中断时间序列分析。GN 疾病恶化的预后匹配序贯分层复发性事件分析。
在 2055 名参与者中,722 名(35%)报告了 COVID-19 感染;其中 92 名(13%)住院,3 名死亡(<1%)。COVID-19 感染前 eGFR 斜率为-1.40mL/min/1.73m(±0.29 SD);在 COVID-19 感染后 6 个月内,eGFR 斜率为-4.26mL/min/1.73m(±3.02 SD),两者无显著差异(P=0.34)。COVID-19 与 GN 疾病活动恶化的风险增加相关(HR,1.35 [95% CI,1.01-1.80])。在该队列中,疫苗接种与 eGFR 变化(-1.34mL/min/1.73m±0.15 SD 与-2.16mL/min/1.73m±1.74 SD;P=0.6)或随后的 GN 疾病恶化(HR 1.02 [95% CI,0.79-1.33])无关。
随访时间不频繁或较短。
在原发性 GN 患者中,每 8 例 COVID-19 感染中就有 1 例为重症,并且与蛋白尿定义的 GN 疾病活动恶化相关。相比之下,COVID-19 疫苗接种与疾病活动或肾功能下降无关。这些结果支持对 GN 患者进行 COVID-19 疫苗接种。
在这项针对 2055 名微小病变肾病、局灶节段性肾小球硬化症、膜性肾病或 IgA 肾病患者的队列研究中,COVID-19 导致 1/8 的患者住院或死亡,并使蛋白尿恶化的风险增加 35%。相比之下,疫苗接种似乎对肾功能或蛋白尿没有不利影响。我们的数据支持对肾小球疾病患者进行 COVID-19 疫苗接种。