Abstract

Obesity associates with reduced life expectancy, type 2 diabetes, hypertension and cardiovascular disease, and is characterized by chronic inflammation. Phosphorylcholine (PC) is an epitope on oxidized low-density lipoprotein, dead cells and some microorganisms. Antibodies against PC (anti-PC) have anti-inflammatory properties. Here, we explored the role of anti-PC in hospitalized versus non-hospitalized obese. One-hundred-and-twenty-eight obese (BMI ≥ 30 kg/m2) individuals (59.8 (± 5.5) years, 53.9% women) from the Malmö Diet and Cancer Cardiovascular Cohort were examined and IgM, IgG1 and IgG2 anti-PC were analyzed by ELISA. Individuals with at least one recorded history of hospitalization prior to study baseline were considered hospitalized obese (HO). Associations between IgM, IgG1 and IgG2 anti-PC and HO (n = 32)/non-hospitalized obese (NHO) (n = 96), but also with metabolic syndrome and diabetes were analysed using logistic regressions. Both IgM and IgG1 anti-PC were inversely associated with HO, also after controlling for age and sex. When further adjusted for waist circumference, systolic blood pressure, glucose levels and smoking status, only IgG1 anti-PC remained significantly associated with HO. In multivariate models, each 1 standard deviation of increment in anti-PC IgG1 levels was inversely associated with prevalence of HO (odds ratio 0.57; CI 95% 0.33–0.98; p = 0.044). IgG2 anti-PC did not show any associations with HO. Low levels of IgM and IgG1 anti-PC are associated with higher risk of being a HO individual independent of sex and age, IgG1 anti-PC also independently of diabetes and metabolic syndrome. The anti-inflammatory properties of these antibodies may be related to inflammation in obesity and its complications.

Details

Title
Antibodies against phosphorylcholine in hospitalized versus non-hospitalized obese subjects
Author
Jujić Amra 1 ; Korduner, J 2 ; Holm, H 3 ; Engström, G 3 ; Bachus, E 3 ; Bhattacharya, P 4 ; Nilsson, P M 2 ; Frostegård Johan 4 ; Magnusson, M 5 

 Lund University, Department of Clinical Sciences, Clinical Research Centre, Malmö, Sweden (GRID:grid.4514.4) (ISNI:0000 0001 0930 2361); Skåne University Hospital, Department of Cardiology, Malmö, Sweden (GRID:grid.411843.b) (ISNI:0000 0004 0623 9987); Lund University, Lund University Diabetes Centre, Malmö, Sweden (GRID:grid.4514.4) (ISNI:0000 0001 0930 2361) 
 Lund University, Department of Clinical Sciences, Clinical Research Centre, Malmö, Sweden (GRID:grid.4514.4) (ISNI:0000 0001 0930 2361); Skåne University Hospital, Department of Internal Medicine, Malmö, Sweden (GRID:grid.411843.b) (ISNI:0000 0004 0623 9987) 
 Lund University, Department of Clinical Sciences, Clinical Research Centre, Malmö, Sweden (GRID:grid.4514.4) (ISNI:0000 0001 0930 2361) 
 Karolinska Institutet, IMM, Institute of Environmental Medicine, Stockholm, Sweden (GRID:grid.4714.6) (ISNI:0000 0004 1937 0626) 
 Lund University, Department of Clinical Sciences, Clinical Research Centre, Malmö, Sweden (GRID:grid.4514.4) (ISNI:0000 0001 0930 2361); Skåne University Hospital, Department of Cardiology, Malmö, Sweden (GRID:grid.411843.b) (ISNI:0000 0004 0623 9987); Lund University, Wallenberg Center for Molecular Medicine, Lund, Sweden (GRID:grid.4514.4) (ISNI:0000 0001 0930 2361); North-West University, Hypertension in Africa Research Team (HART), Potchefstroom, South Africa (GRID:grid.25881.36) (ISNI:0000 0000 9769 2525) 
Publication year
2021
Publication date
2021
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2581099845
Copyright
© The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.