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Schistosoma haematobium infection is associated with lower serum cholesterol levels and improved lipid profile in overweight/obese individuals

Infection with parasitic helminths has been reported to improve insulin sensitivity and glucose homeostasis, lowering the risk for type 2 diabetes. However, little is known about its impact on whole-body lipid homeostasis, especially in obese individuals. For this purpose, a cross-sectional study wa...

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Published in:PLoS neglected tropical diseases 2020-07, Vol.14 (7), p.e0008464-e0008464
Main Authors: Zinsou, Jeannot F., Janse, Jacqueline J., Honpkehedji, Yabo Y., Dejon-Agobé, Jean Claude, García-Tardón, Noemí, Hoekstra, Pytsje T., Massinga-Loembe, Marguerite, Corstjens, Paul L. A. M., van Dam, Govert J., Giera, Martin, Kremsner, Peter G., Yazdanbakhsh, Maria, Adegnika, Ayola A., Guigas, Bruno
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Language:English
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Summary:Infection with parasitic helminths has been reported to improve insulin sensitivity and glucose homeostasis, lowering the risk for type 2 diabetes. However, little is known about its impact on whole-body lipid homeostasis, especially in obese individuals. For this purpose, a cross-sectional study was carried out in lean and overweight/obese adults residing in the Lambaréné region of Gabon, an area endemic for Schistosoma haematobium. Helminth infection status, peripheral blood immune cell counts, and serum metabolic and lipid/lipoprotein levels were analyzed. We found that urine S. haematobium egg-positive individuals exhibited lower serum total cholesterol (TC; 4.42 vs 4.01 mmol/L, adjusted mean difference [95%CI] -0.30 [-0.68,-0.06]; P = 0.109), high-density lipoprotein (HDL)-C (1.44 vs 1.12 mmol/L, -0.24 [-0.43,-0.06]; P = 0.009) and triglyceride (TG; 0.93 vs 0.72 mmol/L, -0.20 [-0.39,-0.03]; P = 0.022) levels than egg-negative individuals. However, when stratified according to body mass index, these effects were only observed in overweight/obese infected individuals. Similarly, significant negative correlations between the intensity of infection, assessed by serum circulating anodic antigen (CAA) concentrations, and TC (r = -0.555; P
ISSN:1935-2735
1935-2727
1935-2735
DOI:10.1371/journal.pntd.0008464