Oxidized LDL is associated with metabolic syndrome traits independently of central obesity and insulin resistance
- ,
- Hector Bueno,
- Antonio Fernandez-Ortiz,
- Jose Maria Ordovas,
- Borja Ibañez,
- Valentin Fuster
- ,
- Boca Raton Clinical Research Global Peru,
- Universidad Autonoma de Madrid/Idipaz,
- Centro Nacional de Investigaciones Cardiovasculares Carlos III,
- Hospital 12 de Octubre,
- Universidad Complutense de Madrid
Publication Information
Output type
Original language
EnglishPages from-to (Number of pages)
Pages 474-482 (9 pages)Journal (Volume, Issue Number)
Diabetes (Volume 66, Issue 2)Publication milestones
- Published - 01/02/2017
Publication status
ISSN
0012-1797Publication IDs
- Scopus: 85011673019
- PubMed: 27993926
Abstract
This study assesses whether oxidative stress, using oxidized LDL (ox-LDL) as a proxy, is associated with metabolic syndrome (MS), whether ox-LDL mediates the association between central obesity andMS, and whether insulin resistance mediates the association between ox-LDL and MS. We examined baseline data from 3,987 subjects without diabetes in the Progression of Early Subclinical Atherosclerosis (PESA) Study. For the second, third, and fourth ox-LDL quartiles versus the first, the odds ratios (95% CI) for MS were 0.84 (0.52, 1.36), 1.47 (0.95, 2.32), and 2.57 (1.66, 4.04) (P < 0.001 for trend) once adjusted for age, sex, smoking, LDL-cholesterol, BMI, waist circumference, and HOMA-insulin resistance (HOMA-IR). Results showing the same trend were found for all MS components except glucose concentration. Ox-LDL mediated 13.9% of the association of waist circumference with triglycerides and only 1-3% of the association with HDL-cholesterol, blood pressure, and insulin concentration. HOMA-IR did not mediate the association between ox-LDL and MS components. This study found higher ox-LDL concentrations were associated with MS and its components independently of central obesity and insulin resistance. Ox-LDL may reflect core mechanisms through which MS components develop and progress in parallel with insulin resistance and could be a clinically relevant predictor of MS development.
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