Visser Benjamin J, de Vries Sophia G, Vingerling Rieke, Gritter Martin, Kroon Danielle, Aguilar Lídia Ciudad, Kraan Rik B J, Wieten Rosanne W, Danion François, Sjouke Barbara, Adegnika Akim A, Agnandji Selidji T, Kremsner Peter G, Hänscheid Thomas, Mens Petra F, van Vugt Michèle, Grobusch Martin P
Institute of Tropical Medicine, University of Tübingen, Tübingen, Germany.
Department of Infectious Diseases, Division of Internal Medicine, Center of Tropical Medicine and Travel Medicine, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Am J Trop Med Hyg. 2017 May;96(5):1205-1214. doi: 10.4269/ajtmh.16-0721.
AbstractThe serum lipid profile in malaria patients has been found to differ from that of healthy controls. We investigated serum lipid profile changes in malaria patients over time compared with patients with other febrile diseases. In total, 217 patients were included in the study (111 malaria patients and 106 symptomatic controls, defined as malaria-negative febrile patients). Serum lipid levels (mmol/L) were significantly lower in malaria patients compared with those with other febrile diseases (total cholesterol [TC] = 3.26 [standard deviation = 0.94] versus 3.97 [1.22; < 0.001]; high-density lipoprotein cholesterol [HDL-C] = 0.43 [0.47] versus 1.05 [0.67; < 0.001], low-density lipoprotein cholesterol [LDL-C] = 2.05 [0.76] versus 2.42 [0.90; < 0.001]. Triglycerides (TGs) levels were higher in malaria patients (1.81 [1.02] versus 1.11 [0.82; < 0.001]). No significant differences were found for apolipoprotein A1, apolipoprotein B, and lipoprotein(a). Cholesterol levels increased toward reference values on day 28 (TC = 3.26-3.98, < 0.001; HDL-C = 0.43-0.96, < 0.001; LDL-C = 2.05-2.60, < 0.001). TG levels decreased from 1.81 on admission to 1.76 (day 3) and 0.88 (day 28; = 0.130). Lipid profile changes were not correlated with parasitemia or histidine-rich protein 2 levels. This study confirms characteristic temporary lipid profile changes in malaria. Lipid profile changes demonstrated a good accuracy to discriminate between malaria and other febrile diseases (area under the curve = 0.80 (95% confidence interval = 0.742-0.863, < 0.001). Several plausible hypotheses exist regarding the pathophysiology of lipid profile changes in malaria. Further studies to elucidate the precise pathways may lead to improved understanding of the underlying pathophysiology.
已发现疟疾患者的血清脂质谱与健康对照者不同。我们调查了与其他发热性疾病患者相比,疟疾患者血清脂质谱随时间的变化情况。本研究共纳入217例患者(111例疟疾患者和106例有症状对照者,定义为疟疾阴性的发热患者)。与其他发热性疾病患者相比,疟疾患者的血清脂质水平(mmol/L)显著较低(总胆固醇[TC]=3.26[标准差=0.94]对3.97[1.22];P<0.001];高密度脂蛋白胆固醇[HDL-C]=0.43[0.47]对1.05[0.67];P<0.001],低密度脂蛋白胆固醇[LDL-C]=2.05[0.76]对2.42[0.90];P<0.001]。疟疾患者的甘油三酯(TGs)水平较高(1.81[1.02]对1.11[0.82];P<0.001])。载脂蛋白A1、载脂蛋白B和脂蛋白(a)未发现显著差异。胆固醇水平在第28天趋向于参考值(TC=3.26 - 3.98;P<0.001];HDL-C=0.43 - 0.96;P<0.001];LDL-C=2.05 - 2.60;P<0.001])。TG水平从入院时的1.81降至第3天的1.76和第28天的0.88(P=0.130)。脂质谱变化与疟原虫血症或富含组氨酸蛋白2水平无关。本研究证实了疟疾患者特征性的暂时性脂质谱变化。脂质谱变化在区分疟疾和其他发热性疾病方面具有良好的准确性(曲线下面积=0.80[95%置信区间=0.742 - 0.863];P<0.001])。关于疟疾脂质谱变化的病理生理学存在几种合理的假设。进一步研究以阐明确切途径可能有助于更好地理解潜在的病理生理学。