Increased serum APOC3 in patients with syphilis can predict the absence of Jarisch-Herxheimer reaction after benzathine penicillin treatment.

Hung-Chin Tsai, Pei-Yun Chou, Hui-Min Chang, Susan Shin-Jung Lee, Yao-Shen Chen
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Abstract

Background: Apolipoprotein C3 (APOC3) was found to induce inflammation in human monocytes. Jarisch-Herxheimer reaction (JHR) was perceived to be caused by immune reactions of dividing spirochaetes to penicillin treatment. The aim of this study was to investigate the role of APOC3 in patients with syphilis and JHR.

Methods: This prospective cohort study enrolled adult patients with active syphilis with/without JHR. Serum samples were collected before and after administration of the first dose of benzathine penicillin and the serum levels of APOC3 were determined by enzyme-linked immunosorbent assay (ELISA). The APOC3 level and changes in APOC3 level before and after benzathine penicillin treatment in different groups were compared with the Mann-Whitney U test or Kruskal-Wallis test.

Results: Forty adult patients with syphilis and 32 controls were enrolled. All 40 patients with syphilis were men who have sex with men, and 30 (75%) were people living with human immunodeficiency virus (HIV). Overall, 19 patients (47%) developed JHR. The active syphilis group had a significantly higher serum APOC3 level (median 38.3 µg/mL, interquartile range [IQR]: 34.5-48.0 µg/mL) than the controls ( p = 0.020). The serum levels of APOC3 were higher in the 21 patients without JHR before and after benzathine penicillin treatment compared with the controls (38.9 µg/mL [IQR: 34.5-66.7 µg/mL] and 39.4 µg/mL [IQR: 33.7-62.9] µg/mL vs 31.8 µg/mL [IQR: 27.5-42.2 µg/mL]). Receiving operating characteristic curve analysis showed that the best cutoff value of APOC3 to predict the absence of JHR before benzathine penicillin therapy compared to the controls was 34.2 µg/mL (area under the curve 0.695, p = 0.017, CI = 0.544-0.846, sensitivity = 0.81, specificity = 0.406).

Conclusion: A high baseline serum APOC3 level can predict the absence of JHR in patients with syphilis treated with the first dose of benzathine penicillin.

梅毒患者血清APOC3升高可预测苄星青霉素治疗后是否无Jarisch-Herxheimer反应。
背景:载脂蛋白C3 (APOC3)被发现在人单核细胞中诱导炎症。Jarisch-Herxheimer反应(JHR)被认为是由分裂螺旋体对青霉素治疗的免疫反应引起的。本研究的目的是探讨APOC3在梅毒和JHR患者中的作用。方法:本前瞻性队列研究纳入了伴有/不伴有JHR的成年活动性梅毒患者。采用酶联免疫吸附法(ELISA)测定首次给药前和给药后血清APOC3水平。采用Mann-Whitney U检验和Kruskal-Wallis检验比较不同组间苄星星青霉素治疗前后APOC3水平及变化。结果:纳入40例成年梅毒患者和32例对照。所有40例梅毒患者均为男男性行为者,其中30例(75%)为艾滋病毒感染者。总体而言,19名患者(47%)发展为JHR。活动性梅毒组血清APOC3水平(中位数38.3 ug/ml,四分位数范围34.5 ~ 48.0 ug/ml)显著高于对照组(p =0.020)。21例无JHR患者在苄星青霉素治疗前后血清APOC3水平均高于对照组(38.9 ug/ml [IQR 34.5-66.7 ug/ml]和39.4 ug/ml [IQR 33.7-62.9] ug/ml vs.31.8 ug/ml [IQR 27.5-42.2 ug/ml])。接受工作特征曲线分析显示,与对照组相比,APOC3预测苄星青霉素治疗前JHR缺失的最佳截止值为34.2µg/ml(曲线下面积0.695,p =0.017, CI 0.544 ~ 0.846,敏感性0.81,特异性0.406)。结论:高基线血清APOC3水平可预测首次使用苄星青霉素治疗的梅毒患者不存在JHR。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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