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Title

Increased thioredoxin levels are related to insulin resistance in familial combined hyperlipidaemia.

Authors

Martinez‐Hervas, Sergio; Artero, Ana; Martinez‐Ibañez, Juncal; Tormos, Mari C.; Gonzalez‐Navarro, Herminia; Priego, Antonia; Martinez‐Valls, Jose F.; Saez, Guillermo T.; Real, Jose T.; Carmena, Rafael; Ascaso, Juan F.

Abstract

Background Thioredoxins ( TRX) are major cellular protein disulphide reductases that are critical for redox regulation. Oxidative stress and inflammation play promoting roles in the genesis and progression of atherosclerosis, but until now scarce data are available considering the influence of TRX activity in familial combined hyperlipidaemia ( FCH). Since FCH is associated with high risk of cardiovascular disease, the objective of the present study was to assess oxidative stress status in FCH patients, and evaluate the influence of insulin resistance ( IR). Materials and methods A cohort of 35 control subjects and 35 non-related FCH patients were included, all of them nondiabetic, normotensive and nonsmokers. We measured lipid profile, glucose and insulin levels in plasma, and markers of oxidative stress and inflammation such as oxidized glutathione ( GSSG), reduced glutathione ( GSH) and TRX. Results Familial combined hyperlipidaemia subjects showed significantly higher levels of GSSG, GSSG/ GSH ratio and TRX than controls. In addition, FCH individuals with IR showed the worst profile of oxidative stress status compared to controls and FCH patients without IR ( P < 0·01). TRX levels correlated with higher insulin resistance. Conclusion Familial combined hyperlipidaemia patients showed increased TRX levels. TRX was positively correlated with IR. These data could partially explain the increased risk of cardiovascular events in primary dyslipidemic patients.

Subjects

THIOREDOXIN; INSULIN resistance; FAMILIAL hypercholesterolemia; OXIDATIVE stress; CARDIOVASCULAR diseases; THERAPEUTICS

Publication

European Journal of Clinical Investigation, 2016, Vol 46, Issue 7, p636

ISSN

0014-2972

Publication type

Academic Journal

DOI

10.1111/eci.12642

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