Institute of Cardiometabolism and Nutrition (ICAN), Centre de Recherche Saint-Antoine (CRSA), INSERM, Sorbonne Université, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
BioPredictive, Research, Paris, France.
PLoS One. 2020 Nov 20;15(11):e0242306. doi: 10.1371/journal.pone.0242306. eCollection 2020.
Since 1920, a decrease in serum cholesterol has been identified as a marker of severe pneumonia. We have assessed the performance of serum apolipoprotein-A1, the main transporter of HDL-cholesterol, to identify the early spread of coronavirus disease 2019 (Covid-19) in the general population and its diagnostic performance for the Covid-19.
We compared the daily mean serum apolipoprotein-A1 during the first 34 weeks of 2020 in a population that is routinely followed for a risk of liver fibrosis risk in the USA (212,297 serum) and in France (20,652 serum) in relation to a local increase in confirmed cases, and in comparison to the same period in 2019 (266,976 and 28,452 serum, respectively). We prospectively assessed the sensitivity of this marker in an observational study of 136 consecutive hospitalized cases and retrospectively evaluated its specificity in 7,481 controls representing the general population.
The mean serum apolipoprotein-A1 levels in the survey populations began decreasing in January 2020, compared to the same period in 2019. This decrease was highly correlated with the daily increase in confirmed Covid-19 cases in the following 34 weeks, both in France and USA, including the June and mid-July recovery periods in France. Apolipoprotein-A1 at the 1.25 g/L cutoff had a sensitivity of 90.6% (95%CI84.2-95.1) and a specificity of 96.1% (95.7-96.6%) for the diagnosis of Covid-19. The area under the characteristics curve was 0.978 (0.957-0.988), and outperformed haptoglobin and liver function tests. The adjusted risk ratio of apolipoprotein-A1 for survival without transfer to intensive care unit was 5.61 (95%CI 1.02-31.0; P = 0.04).
Apolipoprotein-A1 could be a sentinel of the pandemic in existing routine surveillance of the general population. NCT01927133, CER-2020-14.
自 1920 年以来,血清胆固醇的降低已被确定为严重肺炎的标志物。我们评估了血清载脂蛋白-A1(HDL-胆固醇的主要转运蛋白)的性能,以确定其在普通人群中对 2019 年冠状病毒病(Covid-19)的早期传播及其对 Covid-19 的诊断性能。
我们比较了 2020 年前 34 周内美国(212,297 例血清)和法国(20,652 例血清)常规随访肝脏纤维化风险人群的每日平均血清载脂蛋白-A1水平,与当地确诊病例增加有关,并与 2019 年同期进行了比较(分别为 266,976 和 28,452 例血清)。我们前瞻性评估了该标志物在 136 例连续住院病例的观察性研究中的敏感性,并回顾性评估了该标志物在代表普通人群的 7,481 例对照中的特异性。
与 2019 年同期相比,调查人群的血清载脂蛋白-A1 水平在 2020 年 1 月开始下降。这种下降与随后 34 周内确诊的 Covid-19 病例的每日增加高度相关,包括法国的 6 月和 7 月中旬恢复期。在 1.25g/L 截止值时,载脂蛋白-A1 对 Covid-19 的诊断具有 90.6%(95%CI84.2-95.1)的敏感性和 96.1%(95.7-96.6%)的特异性。特征曲线下面积为 0.978(0.957-0.988),优于结合珠蛋白和肝功能检查。载脂蛋白-A1 用于预测无转入重症监护病房生存的调整风险比为 5.61(95%CI 1.02-31.0;P = 0.04)。
载脂蛋白-A1 可能是普通人群常规监测大流行的哨兵。NCT01927133,CER-2020-14。