PMID- 30123046 OWN - NLM STAT- MEDLINE DCOM- 20181211 LR - 20230928 IS - 1449-1907 (Electronic) IS - 1449-1907 (Linking) VI - 15 IP - 11 DP - 2018 TI - The Relationship of Serum Antigen-Specific and Total Immunoglobulin E with Adult Cardiovascular Diseases. PG - 1098-1104 LID - 10.7150/ijms.25857 [doi] AB - Background: The relationship of serum antigen-specific immunoglobulin E (IgE) with cardiovascular diseases (CVDs) remains poorly understood. This study aimed to explore the association of antigen-specific and total IgE with CVDs using data derived from the National Health and Nutrition Examination Survey (NHANES) 2005-2006. Methods and Results: The association of serum total or antigen-specific IgE levels with CVDs was analyzed by survey-weighted logistic regression modeling, adjusted by age, sex, race, education, body mass index, blood pressure, total cholesterol, C-reactive protein, homocysteine, diabetes, smoking, and alcohol consumption. 4953 subjects were included. Coronary heart disease was significantly related to serum total IgE levels. The association of serum total IgE levels with coronary heart disease was further validated by negative, >/=1 and 1-6 positive antigen-specific IgE. Myocardial infarction was positively associated with serum total IgE levels only when all antigen-specific IgE were negative, but inversely associated with serum total IgE when plant-specific IgE test results were positive. More specifically, myocardial infarction was also inversely related to positive oak, birch, or peanut-specific IgE. In addition, serum total IgE are positively associated with angina when at least one specific IgE were positive. Conclusions: Serum antigen-specific IgE, as well as total IgE, is significantly associated with CVDs independently of a long list of established cardiovascular risk factors, which is more informative than total IgE per se. FAU - Xu, Zhiyan AU - Xu Z AD - Department of Pathophysiology, State Key Laboratory of Medical Molecular Biology, Peking Union Medical College, Beijing, China. AD - Department of Anatomy, Histology and Embryology; Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing, China. FAU - Wang, Tao AU - Wang T AD - Department of Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China. FAU - Guo, Xiaoxiao AU - Guo X AD - Department of Cardiology, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, China. FAU - Li, Yao AU - Li Y AD - Department of Pathophysiology, State Key Laboratory of Medical Molecular Biology, Peking Union Medical College, Beijing, China. FAU - Hu, Yi AU - Hu Y AD - CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety, Multi-disciplinary Research Division, Institute of High Energy Physics, Chinese Academy of Sciences (CAS), Beijing, China. FAU - Ma, Chao AU - Ma C AD - Department of Anatomy, Histology and Embryology; Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing, China. FAU - Wang, Jing AU - Wang J AD - Department of Pathophysiology, State Key Laboratory of Medical Molecular Biology, Peking Union Medical College, Beijing, China. LA - eng PT - Journal Article DEP - 20180701 PL - Australia TA - Int J Med Sci JT - International journal of medical sciences JID - 101213954 RN - 0 (Allergens) RN - 37341-29-0 (Immunoglobulin E) SB - IM MH - Adolescent MH - Adult MH - Aged MH - Allergens MH - Cardiovascular Diseases/*blood MH - Child MH - Cross-Sectional Studies MH - Humans MH - Immunoglobulin E/*blood/immunology MH - Logistic Models MH - Male MH - Middle Aged MH - Nutrition Surveys MH - Young Adult PMC - PMC6097256 OTO - NOTNLM OT - Antigen-specific IgE OT - Cardiovascular diseases OT - Immune system OT - Immunoglobulin E COIS- Competing Interests: The authors have declared that no competing interest exists. EDAT- 2018/08/21 06:00 MHDA- 2018/12/12 06:00 PMCR- 2018/01/01 CRDT- 2018/08/21 06:00 PHST- 2018/03/04 00:00 [received] PHST- 2018/05/22 00:00 [accepted] PHST- 2018/08/21 06:00 [entrez] PHST- 2018/08/21 06:00 [pubmed] PHST- 2018/12/12 06:00 [medline] PHST- 2018/01/01 00:00 [pmc-release] AID - ijmsv15p1098 [pii] AID - 10.7150/ijms.25857 [doi] PST - epublish SO - Int J Med Sci. 2018 Jul 1;15(11):1098-1104. doi: 10.7150/ijms.25857. eCollection 2018.