scholarly journals Coronary calcification is associated with elevated serum lipoprotein (a) levels in asymptomatic men over the age of 45 years

Medicine ◽  
2021 ◽  
Vol 100 (9) ◽  
pp. e24962
Author(s):  
Young Hak Chung ◽  
Byoung-Kwon Lee ◽  
Hyuck Moon Kwon ◽  
Pil-Ki Min ◽  
Eui-Young Choi ◽  
...  
Circulation ◽  
1995 ◽  
Vol 91 (5) ◽  
pp. 1403-1409 ◽  
Author(s):  
Rene L. Desmarais ◽  
Ian J. Sarembock ◽  
Carlos R. Ayers ◽  
Sarah M. Vernon ◽  
Eric R. Powers ◽  
...  

2019 ◽  
Vol 104 (10) ◽  
pp. 4793-4803 ◽  
Author(s):  
Hagai Tavori ◽  
Alexandra M Fenton ◽  
Deanna L Plubell ◽  
Sara Rosario ◽  
Elisabeth Yerkes ◽  
...  

Abstract Context Elevated serum lipoprotein(a) [Lp(a)] levels are associated with increased cardiovascular disease risk. ABCA1-mediated cholesterol efflux from macrophages may be an antiatherogenic process. Plasminogen (PLG) is a driver of ABCA1-mediated cholesterol efflux, and its action is inhibited by purified human Lp(a). Objective To determine the effects of Lp(a) in human serum on ABCA1 cholesterol efflux. Methods Cholesterol efflux capacity (CEC) was measured with two different cell-culture models using serum from 76 patients with either low (<50 mg/dL) or high (>50 mg/dL) Lp(a) levels. Results Using cAMP-stimulated J774 macrophages or baby hamster kidney fibroblasts overexpressing human ABCA1, we show that CEC was lower in patients with high Lp(a) levels compared with patients with low levels (−30.6%, P = 0.002 vs −24.1%, P < 0.001, respectively). Total-serum CEC negatively correlated with Lp(a) levels (r = −0.433, P = 0.0007 vs r = −0.505, P = 0.0011, respectively). These negative associations persisted after adjusting for serum cholesterol, age, sex, and statin use in a multiple linear regression model (adjusted R2 = 0.413 or 0.405, respectively) and were strengthened when further adjusting for the interaction between Lp(a) and PLG levels (adjusted R2 = 0.465 and 0.409, respectively). Total-serum and isolated Lp(a) from patients with high Lp(a) inhibited PLG-mediated ABCA1 cholesterol efflux. Conclusion Total-serum CEC is reduced in patients with high Lp(a) levels. This is in part due to the inhibition of PLG-mediated ABCA1 cholesterol efflux by Lp(a). Our findings suggest an atherogenic role for Lp(a) through its ability to inhibit CEC.


1995 ◽  
Vol 43 (4) ◽  
pp. 445-449 ◽  
Author(s):  
A. W. C. Kung ◽  
R. W. C. Pang ◽  
E. D. Janus

Metabolism ◽  
1997 ◽  
Vol 46 (7) ◽  
pp. 735-739 ◽  
Author(s):  
David Crook ◽  
Rosemary Howell ◽  
Mandeep Sidhu ◽  
D.Keith Edmonds ◽  
John C. Stevenson

Metabolism ◽  
2007 ◽  
Vol 56 (9) ◽  
pp. 1187-1191 ◽  
Author(s):  
Toshio Murase ◽  
Minoru Okubo ◽  
Michiyo Amemiya-Kudo ◽  
Takaki Hiraga ◽  
Junko Oka ◽  
...  

Blood ◽  
2018 ◽  
Vol 132 (Supplement 1) ◽  
pp. 5055-5055
Author(s):  
Sonha Nguyen ◽  
Lynette Ilano ◽  
Nneka Oluoha ◽  
Zahra Pakbaz

Abstract Introduction: Despite convincing evidence toward causal role of Lipoprotein(a) in occlusive arterial disease, the data is conflicting when it comes to venous thromboembolism (VTE) and pulmonary embolism (PE). Also it is not known if intervention to normalize Lipoprotein(a) will decrease risk of recurrent VTE and PE eliminating the need for life long anticoagulation. To our knowledge this isfirst data set report focusing on evaluating association between Lipoprotein(a) and VTE in patients younger than 50 years old. Methods: Inthis retrospective study, chart review was completed for twenty-six consecutive patients referred to hematology clinic with diagnosis of deep vein thrombosis (DVT) or PE in year 2017-2018 . Four patients older than 50 years old at the time of acute events were excluded. Lipoprotein(a) had only been measured in patients who had negative hypercoagulable work up with normal lipid panel but had obesity . Protein C, S and anti-thrombin were not measured if patients were already on anticoagulation. Serum level of Lipoprotein(a) greater than 75 nmol/L was considered to be elevated. Results: Total of 22 patients (18 females) were included in the data analysis. Nine patients had DVT, 5 patients had PE, and 8 patients had both DVT and PE. Median age was 34 (12-47). Lipoprotein(a) level was not checked on eight patients who had SLE (n=1), surgery (n=1), Factor V Leiden mutation (n=1), protein S deficiency (n=1), anti-phospholipid syndrome (n=2), prothrombin gene mutation (n=1), and one patient who had lost follow up. The median Lipoprotein(a) level was 107 (8-276). Serum Lipoprotein(a) was elevated in 8 out of the 14 screened patients (57%) with the median of 135 (107-276). Out of 8 patients with elevated Lipoprotein(a), only 1 patient had additional clinical risk factors for thrombosis (history of smoking, alcohol abuse, hypertriglyceridemia and elevated LDL). In an attempt to normalize Lipoprotein(a) level, 3 patients were started on niacin but only one tolerated maximum 1000 mg niacin daily which resulted in decrease in level but did not achieve normalization. Conclusion: This data suggests that elevated serum Lipoprotein(a) in females younger than 50 years old is associated with DVT/PE events. Further investigation is required to confirm this finding. At this time it is not known if attempt to normalize Lipoprotein(a) will prevent recurrent PE/DVT and eliminate need for long life anticoagulation in patients with unprovoked VTE who have elevated lipoprotein(a). Disclosures Pakbaz: Novartis: Membership on an entity's Board of Directors or advisory committees, Speakers Bureau.


2017 ◽  
Vol 263 ◽  
pp. e60
Author(s):  
Radzi Rahmat ◽  
Yung -An Chua ◽  
Zaliha Ismail ◽  
Noor Alicezah Mohd Kasim ◽  
Thuhairah Abdul Rahman ◽  
...  

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