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Published on: October 12, 2017
High- density lipoprotein function is abnormal in idiopathic inflammatory myopathies
Sangmae Sharon Bae1, Yuen Yin Lee1, Ani Shahbazian1
1Division of Rheumatology.
Insights
High-density lipoprotein (HDL) antioxidant function is impaired in idiopathic inflammatory myopathies (IIM) patients, contributing to vascular damage. This dysfunction is linked to disease activity and specific autoantibodies, suggesting a role in IIM pathogenesis.
Area of Science:
- Cardiovascular Medicine
- Immunology
- Rheumatology
Background:
- Idiopathic inflammatory myopathies (IIM) involve vascular endothelium damage.
- High-density lipoprotein (HDL) normally protects the vascular endothelium from oxidized phospholipids.
- Oxidative stress contributes to IIM pathogenesis.
Purpose of the Study:
- To evaluate the antioxidant function of HDL in IIM patients.
- To investigate the relationship between HDL antioxidant function and IIM characteristics.
Main Methods:
- Assessed HDL antioxidant function using a cell-free assay measuring HDL's ability to inhibit LDL oxidation (HDL inflammatory index - HII).
- Analyzed cholesterol profiles, oxidized fatty acids in HDL, and plasma MPO activity.
- Compared a subgroup of IIM patients with healthy controls.
Main Results:
- HDL antioxidant function was significantly worse in IIM patients (HII 1.12) compared to controls (HII 0.82).
- Higher HII correlated with increased plasma MPO activity and oxidized fatty acids in HDL.
- Impaired HDL function was noted in patients with anti-MDA5 or anti-synthetase antibodies, and associated with higher disease activity and DM diagnosis.
Conclusions:
- HDL antioxidant function is abnormal in IIM patients.
- This dysfunction may contribute to microvascular inflammation and damage in IIM.
- Further investigation into HDL's role in IIM pathogenesis is warranted.
Objective:
Damage to the vascular endothelium is strongly implicated in the pathogenesis of idiopathic inflammatory myopathies (IIM). Normally, high-density lipoprotein (HDL) protects the vascular endothelium from damage from oxidized phospholipids, which accumulate under conditions of oxidative stress. The current work evaluated the antioxidant function of HDL in IIM patients.
Methods:
HDL's antioxidant function was measured in IIM patients using a cell-free assay, which assesses the ability of isolated patient HDL to inhibit oxidation of low-density lipoproteins and is reported as the HDL inflammatory index (HII). Cholesterol profiles were measured for all patients, and subgroup analysis included assessment of oxidized fatty acids in HDL and plasma MPO activity. A subgroup of IIM patients was compared with healthy controls.
Results:
The antioxidant function of HDL was significantly worse in patients with IIM (n = 95) compared with healthy controls (n = 41) [mean (S.d.) HII 1.12 (0.61) vs 0.82 (0.13), P < 0.0001]. Higher HII associated with higher plasma MPO activity [mean (S.d.) 13.2 (9.1) vs 9.1 (4.6), P = 0.0006] and higher oxidized fatty acids in HDL. Higher 5-hydroxyeicosatetraenoic acid in HDL correlated with worse diffusion capacity in patients with interstitial lung disease (r = -0.58, P = 0.02), and HDL's antioxidant function was most impaired in patients with autoantibodies against melanoma differentiation-associated protein 5 (MDA5) or anti-synthetase antibodies. In multivariate analysis including 182 IIM patients, higher HII was associated with higher disease activity and DM diagnosis.
Conclusion:
The antioxidant function of HDL is abnormal in IIM patients and may warrant further investigation for its role in propagating microvascular inflammation and damage in this patient population.
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