Punnath Kishore, Dayanand Kiran K, Chandrashekhar Valleesha N, Achur Rajeshwara N, Kakkilaya Srinivasa B, Ghosh Susanta K, Kumari Suchetha N, Gowda D Channe
Department of Biochemistry, Kuvempu University, Shivamogga, Karnataka, India.
Light House Polyclinic, K. S. Hegde Medical Academy, Nitte (Deemed to be University), Mangalore, Karnataka, India.
Trop Parasitol. 2019 Jul-Dec;9(2):98-107. doi: 10.4103/tp.TP_66_18. Epub 2019 Sep 18.
Dysregulated production of inflammatory cytokines might play important role in anemia during malaria infection. The objective of this study was to assess the extent of anemia due to malaria, associated complications, and inflammatory cytokines (tumor necrosis factor alpha [TNF-α], interleukin [IL]-6, and IL-10) across varying anemic intensity during malaria infections.
A hospital-based cross-sectional study was conducted at District Wenlock hospital in Mangaluru city. Samples from 627 patients and 168 healthy controls (HC) were analyzed for level of hemoglobin (Hb), red blood cells (RBCs), and inflammatory cytokines. The blood cell parameters and inflammatory cytokines levels across varying intensity of anemia were analyzed using Kruskal-Wallis test and pair-wise comparison between two groups were by Mann-Whitney U-test. Correlations were calculated by Pearson's and Spearman rank correlations.
Compared to HC, Hb, and RBC levels were significantly lower in infected patients. On comparison with mild anemia patients (Hb 8-10.9 g/dL), the levels of TNF-α and IL-6 were significantly elevated, whereas IL-10 levels were lower during severe anemia (SA) (Hb <5 g/dL). In this endemic setting, we found a strong negative association between Hb levels and parasitemia, Hb and TNF-α, and positive relationship with IL-10; anemic patients also had significantly high TNF-α/IL-10 ratios. SA was associated with complications such as acute renal failure (16.0%), jaundice (16.0%), metabolic acidosis (24.0%), hypoglycemia (12.0%), hyperparasitemia (4.0%), and hepatic dysfunction (16.0%).
Contrary to its benign reputation, (Pv) infections can also result in severe malarial anemia (SMA) and its associated severe complications similar to infections. Dysregulated inflammatory cytokine responses play an important role in the pathogenesis of SMA, especially during Pv infections.
炎症细胞因子产生失调可能在疟疾感染期间的贫血中起重要作用。本研究的目的是评估疟疾所致贫血的程度、相关并发症以及疟疾感染期间不同贫血严重程度下的炎症细胞因子(肿瘤坏死因子α [TNF-α]、白细胞介素 [IL]-6 和 IL-10)情况。
在芒格洛尔市的温洛克地区医院开展了一项基于医院的横断面研究。对627例患者和168例健康对照(HC)的样本进行血红蛋白(Hb)、红细胞(RBC)和炎症细胞因子水平分析。使用Kruskal-Wallis检验分析不同贫血严重程度下的血细胞参数和炎症细胞因子水平,两组之间的两两比较采用Mann-Whitney U检验。通过Pearson和Spearman等级相关性计算相关性。
与健康对照相比,感染患者的Hb和RBC水平显著降低。与轻度贫血患者(Hb 8 - 10.9 g/dL)相比,TNF-α和IL-6水平显著升高,而在重度贫血(SA)(Hb <5 g/dL)期间IL-10水平较低。在这种地方病环境中,我们发现Hb水平与疟原虫血症、Hb与TNF-α之间存在强烈的负相关,与IL-10呈正相关;贫血患者的TNF-α/IL-10比值也显著较高。SA与急性肾衰竭(16.0%)、黄疸(16.0%)、代谢性酸中毒(24.0%)、低血糖(12.0%)、高疟原虫血症(4.0%)和肝功能障碍(16.0%)等并发症相关。
与通常认为的良性情况相反,间日疟原虫(Pv)感染也可导致严重的疟疾贫血(SMA)及其相关的严重并发症,类似于恶性疟原虫感染。炎症细胞因子反应失调在SMA的发病机制中起重要作用,尤其是在Pv感染期间。