Centre of Tropical Medicine and Travel Medicine, Department of Infectious Diseases, Academic Medical Centre, University of Amsterdam, Meibergdreef 9, PO Box 226601100 DD, Amsterdam, The Netherlands.
Malar J. 2013 Dec 7;12:442. doi: 10.1186/1475-2875-12-442.
Serum lipid profile changes have been observed during malaria infection. The underlying biological mechanisms remain unclear. The aim of this paper is to provide an overview on those serum lipid profile changes, and to discuss possible underlying biological mechanisms and the role of lipids in malaria pathogenesis.
A systematic review and meta-analysis to determine lipid profile changes during malaria was conducted, following PRISMA guidelines. Without language restrictions, Medline/PubMed, Embase, Cochrane Central Register of Controlled Trials, Web of Science, LILACS, Biosis Previews and the African Index Medicus were searched for studies published up to 11 July, 2013, that measured serum lipid parameters in malaria patients. Also, major trial registries were searched. Mean differences in lipid profile parameters were combined in fixed and random effects meta-analysis, with a separate analysis for different groups of controls (healthy, other febrile illnesses or very low parasitaemia). These parameters were also compared between severe malaria and uncomplicated malaria. Funnel plots were used to test for publication bias.
Of 2,518 studies reviewed, 42 met the criteria for inclusion in the qualitative analysis, and of these, 15 reported the necessary data for inclusion in the meta-analysis for cholesterol; nine for high-density lipoprotein (HDL), eight for low-density lipoprotein (LDL), and nine for triglycerides, respectively. Total cholesterol, HDL and LDL concentrations were lower in malaria and other febrile diseases compared to healthy controls. The decline was more pronounced and statistically significant during malaria compared to other febrile diseases. These results were consistent across included studies. Triglycerides were raised compared to healthy controls, but not statistically significant when compared to symptomatic controls.
This meta-analysis suggests that the observed lipid profile changes are characteristic for malaria. Although a definite link with the pathogenesis of malaria cannot yet be demonstrated, plausible hypotheses of biological mechanisms involving host lipid alterations and the pathogenesis of malaria exist. An increased research effort to elucidate the precise pathways is warranted, since this could lead to better understanding of malaria pathophysiology and consequently to novel treatment approaches.
在疟疾感染期间,血清脂质谱发生了变化。其潜在的生物学机制尚不清楚。本文旨在综述这些血清脂质谱的变化,并讨论可能的潜在生物学机制以及脂质在疟疾发病机制中的作用。
按照 PRISMA 指南,进行了系统综述和荟萃分析,以确定疟疾期间的脂质谱变化。无语言限制,检索了 Medline/PubMed、Embase、Cochrane 中心对照试验注册库、Web of Science、LILACS、Biosis Previews 和非洲医学索引中截至 2013 年 7 月 11 日发表的测量疟疾患者血清脂质参数的研究。此外,还检索了主要的试验注册库。采用固定效应和随机效应荟萃分析综合了脂质谱参数的均值差异,并对不同对照组(健康人群、其他发热性疾病或极低疟原虫血症)进行了单独分析。还比较了重症疟疾和无并发症疟疾之间的这些参数。使用漏斗图来检验发表偏倚。
在综述的 2518 项研究中,有 42 项符合纳入定性分析的标准,其中 15 项报告了纳入胆固醇荟萃分析的必要数据;9 项报告高密度脂蛋白(HDL),8 项报告低密度脂蛋白(LDL),9 项报告甘油三酯。与健康对照组相比,总胆固醇、HDL 和 LDL 浓度在疟疾和其他发热性疾病中较低。与其他发热性疾病相比,疟疾期间的下降更为明显且具有统计学意义。这些结果在纳入的研究中是一致的。与健康对照组相比,甘油三酯升高,但与症状对照组相比无统计学意义。
这项荟萃分析表明,观察到的脂质谱变化是疟疾的特征。虽然还不能确定与疟疾发病机制之间存在明确的联系,但存在涉及宿主脂质改变和疟疾发病机制的合理生物学机制假说。需要加强研究力度以阐明确切的途径,因为这可能有助于更好地了解疟疾病理生理学,并因此开发新的治疗方法。