Relapsing-remitting multiple sclerosis patients display an altered lipoprotein profile with dysfunctional HDL

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作者
Winde Jorissen
Elien Wouters
Jeroen F. Bogie
Tim Vanmierlo
Jean-Paul Noben
Denis Sviridov
Niels Hellings
Veerle Somers
Roland Valcke
Bart Vanwijmeersch
Piet Stinissen
Monique T. Mulder
Alan T. Remaley
Jerome J. A. Hendriks
机构
[1] Hasselt University,
[2] Dept. of Immunology and Biochemistry,undefined
[3] NIH,undefined
[4] Dept. of Laboratory Medicine,undefined
[5] Clinical Center,undefined
[6] Hasselt University,undefined
[7] Faculty of Sciences,undefined
[8] Molecular and Physical Plant Physiology,undefined
[9] Revalidation and MS Center,undefined
[10] Erasmus MC,undefined
[11] Dept. of Vasc. and Met. diseases,undefined
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摘要
Lipoproteins modulate innate and adaptive immune responses. In the chronic inflammatory disease multiple sclerosis (MS), reports on lipoprotein level alterations are inconsistent and it is unclear whether lipoprotein function is affected. Using nuclear magnetic resonance (NMR) spectroscopy, we analysed the lipoprotein profile of relapsing-remitting (RR) MS patients, progressive MS patients and healthy controls (HC). We observed smaller LDL in RRMS patients compared to healthy controls and to progressive MS patients. Furthermore, low-BMI (BMI ≤ 23 kg/m2) RRMS patients show increased levels of small HDL (sHDL), accompanied by larger, triglyceride (TG)-rich VLDL, and a higher lipoprotein insulin resistance (LP-IR) index. These alterations coincide with a reduced serum capacity to accept cholesterol via ATP-binding cassette (ABC) transporter G1, an impaired ability of HDL3 to suppress inflammatory activity of human monocytes, and modifications of HDL3’s main protein component ApoA-I. In summary, lipoprotein levels and function are altered in RRMS patients, especially in low-BMI patients, which may contribute to disease progression in these patients.
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