کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1968505 1059723 2016 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Paraoxonase-1 arylesterase activity is an independent predictor of myeloperoxidase levels in overweight patients with or without cardiovascular complications
ترجمه فارسی عنوان
فعالیت پاراکسوناز-1 آریلستراز یک پیش بینی کننده مستقل از میزان میلورپسیداز در بیماران دارای اضافه وزن با یا بدون عوارض قلبی عروقی است
کلمات کلیدی
ApoB، آپوليپوپروتئين B؛ ApoA1، apolipoprotein A1؛ BMI، شاخص توده بدنی؛ ELISA، آنزیم وابسته به ایمنی اسیدهای ارگانیک؛ HbA1C، هموگلوبین A1C؛ HDL، لیپوپروتئین با چگالی بالا؛ HDL-C، HDL-کلسترول؛ HsCRP، پروتئین واکنش پذیر با حساسیت بالا؛ LDL، کم چگالی لی
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شیمی
چکیده انگلیسی


• Hyperlipidemic patients with vascular complications had higher MPO levels.
• MPO levels showed a negative correlation with PON1 arylesterase activity.
• MPO levels showed positive correlations with MMP-9 and TIMP-1 levels.
• PON1 arylesterase activity was found to be an independent predictor of MPO levels.
• MPO, MMP-9 levels and PON1 activity may be useful atherosclerosis markers.

ObjectivesMyeloperoxidase (MPO), matrix metalloproteinase-9 (MMP-9) and tissue inhibitor of matrix metalloproteinase-1 (TIMP-1) were shown to contribute to atherogenesis, while human paraoxonase-1 (PON1) protects against oxidative stress. Although several studies investigated these biomarkers, their associations have not been completely clarified yet. We aimed to investigate these parameters in overweight hyperlipidemic, lipid-lowering therapy-naive patients (n = 167) with and without vascular complications.Design and methodsMPO, MMP-9 and TIMP-1 levels were measured by ELISA. PON1 activities were detected spectrophotometrically. PON1 phenotype was calculated by using a dual substrate method.ResultsPatients with vascular complications (VC) had significantly higher MPO and TIMP-1 levels compared to those without (patients with no vascular complications; NVC) (728 (367.25–1177.90) mg/ml vs. 315.9 (176.05–687.40) mg/ml; p < 0.001; and 172.7 (157.7–197.7) ng/ml vs. 152.6 (129.3–172.3) ng/ml; p < 0.0001; respectively). MPO levels showed a significant negative correlation with PON1 arylesterase activity (whole patient group (W): r = 0.42, p < 0.0001; VC: r = 0.44, p = 0.01; NVC: r = 0.39, p < 0.0001) and positive correlations with MMP-9 (W: r = 0.37, p < 0.0001; VC: r = 0.29, p = 0.07; NVC: r = 0.42, p < 0.0001) and TIMP-1 (W: r = 0.42, p < 0.0001; VC: r = 0.33, p < 0.05; NVC: r = 0.41, p < 0.0001), respectively. PON1 arylesterase activity was found to be an independent predictor of MPO levels in the whole patient group (β = − 0.350, p < 0.0001) or when studied separately in the subgroups with or without cardiovascular complications (VC: β = − 0.57, p < 0.05; NVC: β = − 0.33, p < 0.0001).ConclusionsOur results suggest that parallel investigation of MPO, MMP-9 and TIMP-1 levels and PON1 arylesterase activity may be a more accurate indicator of atherosclerosis, which may allow earlier treatment and therefore, improvement of treatment efficacy.

Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Clinical Biochemistry - Volume 49, Issue 12, August 2016, Pages 862–867
نویسندگان
, , , , , , , , , ,