High-density lipoprotein dysfunction in carotid artery stenosis
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作者:
Senat, Almila
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Ankara Yildirim Beyazit Univ, Dept Biochem, Fac Med, Ankara City Hosp, Ankara, TurkiyeAnkara Yildirim Beyazit Univ, Dept Biochem, Fac Med, Ankara City Hosp, Ankara, Turkiye
Senat, Almila
[1
]
Yon, Mehmet Ilker
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Ankara Yildirim Beyazit Univ, Dept Neurol, Fac Med, Ankara City Hosp, Ankara, TurkiyeAnkara Yildirim Beyazit Univ, Dept Biochem, Fac Med, Ankara City Hosp, Ankara, Turkiye
Yon, Mehmet Ilker
[2
]
Yuce, Gokhan
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Ankara City Hosp, Dept Radiol, Ankara, TurkiyeAnkara Yildirim Beyazit Univ, Dept Biochem, Fac Med, Ankara City Hosp, Ankara, Turkiye
Yuce, Gokhan
[3
]
Deniz, Orhan
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Ankara Yildirim Beyazit Univ, Dept Neurol, Fac Med, Ankara City Hosp, Ankara, TurkiyeAnkara Yildirim Beyazit Univ, Dept Biochem, Fac Med, Ankara City Hosp, Ankara, Turkiye
Deniz, Orhan
[2
]
Erel, Ozcan
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Ankara Yildirim Beyazit Univ, Dept Biochem, Fac Med, Ankara City Hosp, Ankara, TurkiyeAnkara Yildirim Beyazit Univ, Dept Biochem, Fac Med, Ankara City Hosp, Ankara, Turkiye
Erel, Ozcan
[1
]
机构:
[1] Ankara Yildirim Beyazit Univ, Dept Biochem, Fac Med, Ankara City Hosp, Ankara, Turkiye
[2] Ankara Yildirim Beyazit Univ, Dept Neurol, Fac Med, Ankara City Hosp, Ankara, Turkiye
[3] Ankara City Hosp, Dept Radiol, Ankara, Turkiye
Background: High density lipoprotein (HDL) is well established to have an athero-protective role under normal conditions; however, pro-inflammatory alteration of HDL proteins may transform the HDL particle into a dysfunctional molecule. Our aim was to investigate HDL dysfunction by measuring enzyme-based markers in carotid artery stenosis (CAS). Patients and methods: All participants underwent duplex ultrasound and 52 subjects diagnosed with CAS and 51 subjects who had no significant stenosis (as controls) were enrolled in this study. Serum lipid profiles and serum parameters associated with dysfunctional HDL including myeloperoxidase (MPO), paraoxonase 1 (PON1), arylesterase (ARE) activity, and lipid hydroperoxide (LOOH) levels were measured. Results: It was found that the patients with CAS had increased levels of MPO and LOOH while PON1 activity was decreased. There was no significant difference between the CAS and non-CAS groups in terms of HDL levels. MPO/PON1, MPO/ARE, and LOOH/PON1 ratios were significantly increased in the CAS group. MPO/ PON1 and MPO/ARE ratios both demonstrated significant correlations with degree of stenosis (%). Conclusions: The MPO/ PON1 and MPO/ARE ratios may be potential serum markers that can enable the monitoring of HDL functionality and the assessment of atherosclerotic disease risks. Additionally, monitoring the oxidative balance of lipids on HDL molecules by LOOH/PON1 ratio may have value in the early detection of pro-atherosclerotic transformation of the HDL particle.
机构:
Sidney Kimmel Lab. Prev. Cardiology, Thomas Jefferson University, Jefferson Heart Institute, Philadelphia, PA 19107Sidney Kimmel Lab. Prev. Cardiology, Thomas Jefferson University, Jefferson Heart Institute, Philadelphia, PA 19107
Morgan J.
Carey C.
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Sidney Kimmel Lab. Prev. Cardiology, Thomas Jefferson University, Jefferson Heart Institute, Philadelphia, PA 19107Sidney Kimmel Lab. Prev. Cardiology, Thomas Jefferson University, Jefferson Heart Institute, Philadelphia, PA 19107
Carey C.
Lincoff A.
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Sidney Kimmel Lab. Prev. Cardiology, Thomas Jefferson University, Jefferson Heart Institute, Philadelphia, PA 19107Sidney Kimmel Lab. Prev. Cardiology, Thomas Jefferson University, Jefferson Heart Institute, Philadelphia, PA 19107
Lincoff A.
Capuzzi D.
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机构:
Sidney Kimmel Lab. Prev. Cardiology, Thomas Jefferson University, Jefferson Heart Institute, Philadelphia, PA 19107Sidney Kimmel Lab. Prev. Cardiology, Thomas Jefferson University, Jefferson Heart Institute, Philadelphia, PA 19107
机构:
Univ Penn Hlth Syst, Div Cardiovasc Med, Philadelphia, PA USAUniv Penn, Translat Res Ctr 11 125, Div Translat Med & Human Genet, Inst Translat Med & Therapeut,Perelman Sch Med, Philadelphia, PA 19104 USA
deGoma, Emil M.
Rader, Daniel J.
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Univ Penn, Translat Res Ctr 11 125, Div Translat Med & Human Genet, Inst Translat Med & Therapeut,Perelman Sch Med, Philadelphia, PA 19104 USAUniv Penn, Translat Res Ctr 11 125, Div Translat Med & Human Genet, Inst Translat Med & Therapeut,Perelman Sch Med, Philadelphia, PA 19104 USA