Department of Cardiology (P.L.M., T.O.), Akershus University Hospital, Lørenskog, Norway.
Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Norway (P.L.M., C.P., R.R., S.S., H.R., M.S., J.E.B., T.O.).
Circulation. 2020 Dec;142(22):2128-2137. doi: 10.1161/CIRCULATIONAHA.120.050360. Epub 2020 Oct 15.
Growth differentiation factor 15 (GDF-15) is a strong prognostic marker in sepsis and cardiovascular disease (CVD). The prognostic value of GDF-15 in coronavirus disease 2019 (COVID-19) is unknown.
Consecutive, hospitalized patients with laboratory-confirmed infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and symptoms of COVID-19 were enrolled in the prospective, observational COVID Mechanisms Study. Biobank samples were collected at baseline, day 3 and day 9. The primary end point was admission to the intensive care unit or death during hospitalization, and the prognostic performance of baseline and serial GDF-15 concentrations were compared with that of established infectious disease and cardiovascular biomarkers.
Of the 123 patients enrolled, 35 (28%) reached the primary end point; these patients were older, more often had diabetes, and had lower oxygen saturations and higher National Early Warning Scores on baseline. Baseline GDF-15 concentrations were elevated (>95th percentile in age-stratified healthy individuals) in 97 (79%), and higher concentrations were associated with detectable SARS-CoV-2 viremia and hypoxemia (both <0.001). Patients reaching the primary end point had higher concentrations of GDF-15 (median, 4225 [IQR, 3197-5972] pg/mL versus median, 2187 [IQR, 1344-3620] pg/mL, <0.001). The area under the receiver operating curve was 0.78 (95% CI, 0.70-0.86). The association between GDF-15 and the primary end point persisted after adjusting for age, sex, race, body mass index, estimated glomerular filtration rate, previous myocardial infarction, heart failure, and atrial fibrillation (<0.001) and was superior and incremental to interleukin-6, C-reactive protein, procalcitonin, ferritin, D-dimer, cardiac troponin T, and N-terminal pro-B-type natriuretic peptide. Increase in GDF-15 from baseline to day 3 was also greater in patients reaching the primary end point (median, 1208 [IQR, 0-4305] pg/mL versus median, -86 [IQR, -322 to 491] pg/mL, <0.001).
GDF-15 is elevated in the majority of patients hospitalized with COVID-19, and higher concentrations are associated with SARS-CoV-2 viremia, hypoxemia, and worse outcome. The prognostic value of GDF-15 was additional and superior to established cardiovascular and inflammatory biomarkers. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT04314232.
生长分化因子 15(GDF-15)是脓毒症和心血管疾病(CVD)的强有力预后标志物。GDF-15 在 2019 年冠状病毒病(COVID-19)中的预后价值尚不清楚。
连续纳入了患有经实验室证实的严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染并伴有 COVID-19 症状的住院患者,进行前瞻性观察性 COVID 机制研究。在基线、第 3 天和第 9 天采集生物样本。主要终点是住院期间入住重症监护病房或死亡,比较基线和连续 GDF-15 浓度的预后性能与既定的传染病和心血管生物标志物。
在纳入的 123 例患者中,35 例(28%)达到了主要终点;这些患者年龄较大,更常患有糖尿病,且基线时血氧饱和度较低,国家早期预警评分较高。97 例(79%)患者的基线 GDF-15 浓度升高(>按年龄分层的健康个体的第 95 百分位),且更高的浓度与可检测到的 SARS-CoV-2 病毒血症和低氧血症相关(均<0.001)。达到主要终点的患者 GDF-15 浓度更高(中位数,4225[四分位距,3197-5972]pg/mL 与中位数,2187[四分位距,1344-3620]pg/mL,<0.001)。接受者操作特征曲线下面积为 0.78(95%置信区间,0.70-0.86)。调整年龄、性别、种族、体重指数、估计肾小球滤过率、既往心肌梗死、心力衰竭和心房颤动后,GDF-15 与主要终点之间的关联仍然存在(<0.001),并且优于白细胞介素-6、C 反应蛋白、降钙素原、铁蛋白、D-二聚体、心肌肌钙蛋白 T 和 N 端脑钠肽前体。达到主要终点的患者从基线到第 3 天的 GDF-15 升高也更大(中位数,1208[四分位距,0-4305]pg/mL 与中位数,-86[四分位距,-322 至 491]pg/mL,<0.001)。
大多数 COVID-19 住院患者的 GDF-15 升高,且浓度较高与 SARS-CoV-2 病毒血症、低氧血症和预后不良相关。GDF-15 的预后价值优于既定的心血管和炎症生物标志物。注册:网址:https://www.clinicaltrials.gov;唯一标识符:NCT04314232。