Impact of high lipoprotein(a) levels on in‐stent restenosis and long‐term clinical outcomes of angina pectoris patients undergoing percutaneous coronary intervention with drug‐eluting stents in Asian population. (June 2015)
- Record Type:
- Journal Article
- Title:
- Impact of high lipoprotein(a) levels on in‐stent restenosis and long‐term clinical outcomes of angina pectoris patients undergoing percutaneous coronary intervention with drug‐eluting stents in Asian population. (June 2015)
- Main Title:
- Impact of high lipoprotein(a) levels on in‐stent restenosis and long‐term clinical outcomes of angina pectoris patients undergoing percutaneous coronary intervention with drug‐eluting stents in Asian population
- Authors:
- Park, Sang‐Ho
Rha, Seung‐Woon
Choi, Byoung‐Geol
Park, Ji‐Young
Jeon, Ung
Seo, Hong‐Seog
Kim, Eung‐Ju
Na, Jin‐Oh
Choi, Cheol‐Ung
Kim, Jin‐Won
Lim, Hong‐Euy
Park, Chang‐Gyu
Oh, Dong‐Joo - Abstract:
- <abstract abstract-type="main" id="cep12396-abs-0001"> <title>Summary</title> <p>Lipoprotein(a) (Lp(a)) is known to be associated with cardiovascular complications and atherothrombotic properties in general populations. However, it has not been examined whether Lp(a) levels are able to predict adverse cardiovascular outcomes in patients undergoing percutaneous coronary intervention (PCI) with drug‐eluting stents (DES). A total of 595 consecutive patients with angina pectoris who underwent elective PCI with DES were enrolled from 2004 to 2010. The patients were divided into two groups according to the levels of Lp(a): Lp(a) &lt; 50 mg/dL (<italic>n</italic> = 485 patients), and Lp(a) ≥ 50 mg/dL (<italic>n</italic> = 111 patients). The 6–9‐month angiographic outcomes and 3‐year cumulative major clinical outcomes were compared between the two groups. Binary restenosis occurred in 26 of 133 lesions (19.8%) in the high Lp(a) group and 43 of 550 lesions (7.9%) in the low Lp(a) group (<italic>P</italic> = 0.001). In multivariate analysis, the reference vessel diameter, low density lipoprotein cholesterol, total lesion length, and Lp(a) ≥ 50 mg/dL were predictors of binary restenosis. In the Cox proportional hazards regression analysis, Lp(a) &gt; 50 mg/dL was significantly associated with the 3‐year adverse clinical outcomes including any myocardial infarction, revascularization (target lesion revascularization (TLR) and target vessel revascularization (TVR)), TLR‐major adverse<abstract abstract-type="main" id="cep12396-abs-0001"> <title>Summary</title> <p>Lipoprotein(a) (Lp(a)) is known to be associated with cardiovascular complications and atherothrombotic properties in general populations. However, it has not been examined whether Lp(a) levels are able to predict adverse cardiovascular outcomes in patients undergoing percutaneous coronary intervention (PCI) with drug‐eluting stents (DES). A total of 595 consecutive patients with angina pectoris who underwent elective PCI with DES were enrolled from 2004 to 2010. The patients were divided into two groups according to the levels of Lp(a): Lp(a) &lt; 50 mg/dL (<italic>n</italic> = 485 patients), and Lp(a) ≥ 50 mg/dL (<italic>n</italic> = 111 patients). The 6–9‐month angiographic outcomes and 3‐year cumulative major clinical outcomes were compared between the two groups. Binary restenosis occurred in 26 of 133 lesions (19.8%) in the high Lp(a) group and 43 of 550 lesions (7.9%) in the low Lp(a) group (<italic>P</italic> = 0.001). In multivariate analysis, the reference vessel diameter, low density lipoprotein cholesterol, total lesion length, and Lp(a) ≥ 50 mg/dL were predictors of binary restenosis. In the Cox proportional hazards regression analysis, Lp(a) &gt; 50 mg/dL was significantly associated with the 3‐year adverse clinical outcomes including any myocardial infarction, revascularization (target lesion revascularization (TLR) and target vessel revascularization (TVR)), TLR‐major adverse cardiac events (MACEs), TVR‐MACE, and All‐MACEs. In our study, high Lp(a) level ≥ 50 mg/dL in angina pectoris patients undergoing elective PCI with DES was significantly associated with binary restenosis and 3‐year adverse clinical outcomes in an Asian population.</p> </abstract> … (more)
- Is Part Of:
- Clinical and experimental pharmacology and physiology. Volume 42:Number 6(2015:Jun.)
- Journal:
- Clinical and experimental pharmacology and physiology
- Issue:
- Volume 42:Number 6(2015:Jun.)
- Issue Display:
- Volume 42, Issue 6 (2015)
- Year:
- 2015
- Volume:
- 42
- Issue:
- 6
- Issue Sort Value:
- 2015-0042-0006-0000
- Page Start:
- 588
- Page End:
- 595
- Publication Date:
- 2015-06
- Subjects:
- Clinical pharmacology -- Periodicals
Pharmacology, Experimental -- Periodicals
Physiology, Experimental -- Periodicals
Physiology, Pathological -- Periodicals
615.1 - Journal URLs:
- http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=cep ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/1440-1681.12396 ↗
- Languages:
- English
- ISSNs:
- 0305-1870
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.252000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3088.xml