EVALUATION OF ELEVATED SERUM UPOPROTEIN (a) AS A RISK FACTOR FOR LEFT ATRIAL THROMBUS IN PATIENTS WITH CHRONIC ATRIAL FIBRILLATION
• 1970
معلومات البحث
المؤلفون
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الكلمات المفتاحية
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المجلة العلمية
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الناشر
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العدد
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publication.type
Local
رابط البحث
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المواد المرفقة
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الملخص
The aim of the study was to determine the role of Lp(a) level on left atrial thrombus formation and plasminogen activity in patients with chronic atrial fibrillation.
Materials and Methods: Clinical, laboratory and transoesophageal echocardiographic data were collected from fifty consecutive non anticoagulated patients with chronic atrial fibrillation. They were divided into two groups according to Lp(a) level: Thirty patients were with Lp(a) level> 30mgldl (group I) and twenty patients had Lp(a) level < 30mgldl (group II).
Results: There was no significant difference in left atrial size between the two groups (5.53 vs 5.08cm) (P > 0.05). group I showed a significant decrease of left atrial appendage (LAA) flow velocity (15.93vs 27.42cm/s) (p< 0.01) and a significant increase of spontaneous echo contrast (SEC) (2.0 vs 0.3%) (p < 0.01) A significant increase in fibrinogen level (480.7 vs 387.55mg/dl) (p< 0.01) and total cholesterol (193.17vs 143.3mgldl) (P< 0.01) were observed in group I. There was no significant difference in plasminogen activity and D-dimers level between the two groups I & II (p > 0.05). multiple regression analysis showed a positive correlation between Lp (a) > 30 mg/dl and high fibrinogen level. A negative correlation was observed between Lp(a» 30mg/dl and both left atrial appendage flow velocity and plasminogen activity.
Conclusion: Elevated Lp(a) in chronic AF patients can be considered as a predictor for left atrial thrombus formation and thromboembolic risk. Long term anticoagulation should be considered in those patients.
Key words: AF, Lp (a), plasminogen
Materials and Methods: Clinical, laboratory and transoesophageal echocardiographic data were collected from fifty consecutive non anticoagulated patients with chronic atrial fibrillation. They were divided into two groups according to Lp(a) level: Thirty patients were with Lp(a) level> 30mgldl (group I) and twenty patients had Lp(a) level < 30mgldl (group II).
Results: There was no significant difference in left atrial size between the two groups (5.53 vs 5.08cm) (P > 0.05). group I showed a significant decrease of left atrial appendage (LAA) flow velocity (15.93vs 27.42cm/s) (p< 0.01) and a significant increase of spontaneous echo contrast (SEC) (2.0 vs 0.3%) (p < 0.01) A significant increase in fibrinogen level (480.7 vs 387.55mg/dl) (p< 0.01) and total cholesterol (193.17vs 143.3mgldl) (P< 0.01) were observed in group I. There was no significant difference in plasminogen activity and D-dimers level between the two groups I & II (p > 0.05). multiple regression analysis showed a positive correlation between Lp (a) > 30 mg/dl and high fibrinogen level. A negative correlation was observed between Lp(a» 30mg/dl and both left atrial appendage flow velocity and plasminogen activity.
Conclusion: Elevated Lp(a) in chronic AF patients can be considered as a predictor for left atrial thrombus formation and thromboembolic risk. Long term anticoagulation should be considered in those patients.
Key words: AF, Lp (a), plasminogen
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