Impact of Paradoxical Decrease in High-Density Lipoprotein Cholesterol Levels After Statin Therapy on Major Adverse Cardiovascular Events in Patients with Stable Angina Pectoris
Abstract Purpose Statin therapy usually increases HDL-C levels. However, a paradoxical decrease in HDL-C levels after statin therapy is often seen in clinical settings. The relationship between a paradoxical decrease in HDL-C levels after statin therapy and adverse cardiovascular events in patients...
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Veröffentlicht in: | Clinical therapeutics 2017-02, Vol.39 (2), p.279-287 |
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creator | Hirayama, Kenshi, MD Ota, Tomoyuki, MD, PhD Harada, Kazuhiro, MD Shibata, Yohei, MD Tatami, Yosuke, MD Harata, Shingo, MD Kawashima, Kazuhiro, MD Kunimura, Ayako, MD Shimbo, Yusaku, MD Takayama, Yohei, MD Kawamiya, Toshiki, MD Yamamoto, Dai, MD Osugi, Naohiro, MD Suzuki, Susumu, MD Ishii, Hideki, MD, PhD Murohara, Toyoaki, MD, PhD |
description | Abstract Purpose Statin therapy usually increases HDL-C levels. However, a paradoxical decrease in HDL-C levels after statin therapy is often seen in clinical settings. The relationship between a paradoxical decrease in HDL-C levels after statin therapy and adverse cardiovascular events in patients with stable angina pectoris (SAP) is not well understood. The purpose of this study was to analyze the relationship between paradoxical HDL-C decreases after statin therapy and major adverse cardiovascular events (MACEs) in patients undergoing percutaneous coronary intervention (PCI) for SAP. Methods Between January 2006 and March 2015, 867 patients underwent PCI for SAP. Of them, we enrolled 209 patients who were newly started on statin therapy before PCI. We excluded patients who had started statin therapy earlier than 6 months before PCI, patients who had not started statin therapy after PCI, and patients who were diagnosed with acute coronary syndrome. They were divided into 2 groups according to the change in their HDL-C levels between baseline and 6 to 9 months after the index PCI: decreased HDL group after statin treatment (80 patients) and increased HDL group (129 patients). The primary end points were MACEs defined as a composite of all-cause death, nonfatal acute myocardial infarction, and target vessel revascularization (TVR). Findings Using Kaplan-Meier analysis, the 7-year event rate for composite MACEs in the decreased HDL group was found to be higher than that for the increased HDL group (38% versus 24%, log-rank P = 0.02). TVR occurred more frequently in the decreased HDL group than in the increased HDL group (32% versus 12%, log-rank P = 0.01). With the use of multivariate analysis, changes in HDL-C levels after statin therapy indicated a significant inverse association with the increased risk of MACEs, (hazard ratio [HR] = 0.94; 95% CI, 0.92–0.97; P < 0.01). The incidence of MACEs was more strongly associated with ΔHDL than with ΔLDL. Moreover, BMS usage also independently predicted MACEs (HR = 2.18; 95% CI, 1.14–4.17; P < 0.01). Implications A paradoxical decrease in HDL-C levels after statin therapy might be a risk factor for MACEs, especially TVR, in patients with SAP. |
doi_str_mv | 10.1016/j.clinthera.2016.12.006 |
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However, a paradoxical decrease in HDL-C levels after statin therapy is often seen in clinical settings. The relationship between a paradoxical decrease in HDL-C levels after statin therapy and adverse cardiovascular events in patients with stable angina pectoris (SAP) is not well understood. The purpose of this study was to analyze the relationship between paradoxical HDL-C decreases after statin therapy and major adverse cardiovascular events (MACEs) in patients undergoing percutaneous coronary intervention (PCI) for SAP. Methods Between January 2006 and March 2015, 867 patients underwent PCI for SAP. Of them, we enrolled 209 patients who were newly started on statin therapy before PCI. We excluded patients who had started statin therapy earlier than 6 months before PCI, patients who had not started statin therapy after PCI, and patients who were diagnosed with acute coronary syndrome. They were divided into 2 groups according to the change in their HDL-C levels between baseline and 6 to 9 months after the index PCI: decreased HDL group after statin treatment (80 patients) and increased HDL group (129 patients). The primary end points were MACEs defined as a composite of all-cause death, nonfatal acute myocardial infarction, and target vessel revascularization (TVR). Findings Using Kaplan-Meier analysis, the 7-year event rate for composite MACEs in the decreased HDL group was found to be higher than that for the increased HDL group (38% versus 24%, log-rank P = 0.02). TVR occurred more frequently in the decreased HDL group than in the increased HDL group (32% versus 12%, log-rank P = 0.01). With the use of multivariate analysis, changes in HDL-C levels after statin therapy indicated a significant inverse association with the increased risk of MACEs, (hazard ratio [HR] = 0.94; 95% CI, 0.92–0.97; P < 0.01). The incidence of MACEs was more strongly associated with ΔHDL than with ΔLDL. Moreover, BMS usage also independently predicted MACEs (HR = 2.18; 95% CI, 1.14–4.17; P < 0.01). Implications A paradoxical decrease in HDL-C levels after statin therapy might be a risk factor for MACEs, especially TVR, in patients with SAP.</description><identifier>ISSN: 0149-2918</identifier><identifier>EISSN: 1879-114X</identifier><identifier>DOI: 10.1016/j.clinthera.2016.12.006</identifier><identifier>PMID: 28034517</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Acute Coronary Syndrome - drug therapy ; Acute coronary syndromes ; Aged ; Angina pectoris ; Angina, Stable - drug therapy ; Cardiovascular disease ; Cholesterol ; Cholesterol, HDL - blood ; Clinical outcomes ; Diabetes ; Female ; Health risk assessment ; Heart attacks ; high-density lipoprotein cholesterol ; Humans ; Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use ; Hypertension ; Internal Medicine ; Kaplan-Meier Estimate ; Lipids ; Male ; Medical Education ; Middle Aged ; Multivariate analysis ; Myocardial Infarction - epidemiology ; Percutaneous Coronary Intervention - methods ; Proportional Hazards Models ; Risk Factors ; Smoking cessation ; stable angina pectoris ; statin ; Statins ; Statistical analysis ; Stents ; Studies ; Values ; Variables</subject><ispartof>Clinical therapeutics, 2017-02, Vol.39 (2), p.279-287</ispartof><rights>Elsevier HS Journals, Inc.</rights><rights>2017 Elsevier HS Journals, Inc.</rights><rights>Copyright © 2017 Elsevier HS Journals, Inc. All rights reserved.</rights><rights>Copyright Elsevier Limited Feb 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c487t-8bdfa45325c8448dadaba1428af8c0a3546869a7280e95a5853531c857593a003</citedby><cites>FETCH-LOGICAL-c487t-8bdfa45325c8448dadaba1428af8c0a3546869a7280e95a5853531c857593a003</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/1873405197?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995,64385,64387,64389,72469</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28034517$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hirayama, Kenshi, MD</creatorcontrib><creatorcontrib>Ota, Tomoyuki, MD, PhD</creatorcontrib><creatorcontrib>Harada, Kazuhiro, MD</creatorcontrib><creatorcontrib>Shibata, Yohei, MD</creatorcontrib><creatorcontrib>Tatami, Yosuke, MD</creatorcontrib><creatorcontrib>Harata, Shingo, MD</creatorcontrib><creatorcontrib>Kawashima, Kazuhiro, MD</creatorcontrib><creatorcontrib>Kunimura, Ayako, MD</creatorcontrib><creatorcontrib>Shimbo, Yusaku, MD</creatorcontrib><creatorcontrib>Takayama, Yohei, MD</creatorcontrib><creatorcontrib>Kawamiya, Toshiki, MD</creatorcontrib><creatorcontrib>Yamamoto, Dai, MD</creatorcontrib><creatorcontrib>Osugi, Naohiro, MD</creatorcontrib><creatorcontrib>Suzuki, Susumu, MD</creatorcontrib><creatorcontrib>Ishii, Hideki, MD, PhD</creatorcontrib><creatorcontrib>Murohara, Toyoaki, MD, PhD</creatorcontrib><title>Impact of Paradoxical Decrease in High-Density Lipoprotein Cholesterol Levels After Statin Therapy on Major Adverse Cardiovascular Events in Patients with Stable Angina Pectoris</title><title>Clinical therapeutics</title><addtitle>Clin Ther</addtitle><description>Abstract Purpose Statin therapy usually increases HDL-C levels. However, a paradoxical decrease in HDL-C levels after statin therapy is often seen in clinical settings. The relationship between a paradoxical decrease in HDL-C levels after statin therapy and adverse cardiovascular events in patients with stable angina pectoris (SAP) is not well understood. The purpose of this study was to analyze the relationship between paradoxical HDL-C decreases after statin therapy and major adverse cardiovascular events (MACEs) in patients undergoing percutaneous coronary intervention (PCI) for SAP. Methods Between January 2006 and March 2015, 867 patients underwent PCI for SAP. Of them, we enrolled 209 patients who were newly started on statin therapy before PCI. We excluded patients who had started statin therapy earlier than 6 months before PCI, patients who had not started statin therapy after PCI, and patients who were diagnosed with acute coronary syndrome. They were divided into 2 groups according to the change in their HDL-C levels between baseline and 6 to 9 months after the index PCI: decreased HDL group after statin treatment (80 patients) and increased HDL group (129 patients). The primary end points were MACEs defined as a composite of all-cause death, nonfatal acute myocardial infarction, and target vessel revascularization (TVR). Findings Using Kaplan-Meier analysis, the 7-year event rate for composite MACEs in the decreased HDL group was found to be higher than that for the increased HDL group (38% versus 24%, log-rank P = 0.02). TVR occurred more frequently in the decreased HDL group than in the increased HDL group (32% versus 12%, log-rank P = 0.01). With the use of multivariate analysis, changes in HDL-C levels after statin therapy indicated a significant inverse association with the increased risk of MACEs, (hazard ratio [HR] = 0.94; 95% CI, 0.92–0.97; P < 0.01). The incidence of MACEs was more strongly associated with ΔHDL than with ΔLDL. Moreover, BMS usage also independently predicted MACEs (HR = 2.18; 95% CI, 1.14–4.17; P < 0.01). Implications A paradoxical decrease in HDL-C levels after statin therapy might be a risk factor for MACEs, especially TVR, in patients with SAP.</description><subject>Acute Coronary Syndrome - drug therapy</subject><subject>Acute coronary syndromes</subject><subject>Aged</subject><subject>Angina pectoris</subject><subject>Angina, Stable - drug therapy</subject><subject>Cardiovascular disease</subject><subject>Cholesterol</subject><subject>Cholesterol, HDL - blood</subject><subject>Clinical outcomes</subject><subject>Diabetes</subject><subject>Female</subject><subject>Health risk assessment</subject><subject>Heart attacks</subject><subject>high-density lipoprotein cholesterol</subject><subject>Humans</subject><subject>Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use</subject><subject>Hypertension</subject><subject>Internal Medicine</subject><subject>Kaplan-Meier Estimate</subject><subject>Lipids</subject><subject>Male</subject><subject>Medical Education</subject><subject>Middle Aged</subject><subject>Multivariate analysis</subject><subject>Myocardial Infarction - epidemiology</subject><subject>Percutaneous Coronary Intervention - methods</subject><subject>Proportional Hazards Models</subject><subject>Risk Factors</subject><subject>Smoking cessation</subject><subject>stable angina pectoris</subject><subject>statin</subject><subject>Statins</subject><subject>Statistical analysis</subject><subject>Stents</subject><subject>Studies</subject><subject>Values</subject><subject>Variables</subject><issn>0149-2918</issn><issn>1879-114X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqNUk1vEzEUXCEQLYW_AJa4cNlgr-1d7wUpSgutFESkFomb9eJ92zhs1sF2AvlZ_ENsUorUC5z88Wbm-Y2nKF4xOmGU1W_XEzPYMa7Qw6RKFxNWTSitHxWnTDVtyZj48rg4pUy0ZdUydVI8C2FNKeWtrJ4WJ5WiXEjWnBY_rzZbMJG4nizAQ-d-WAMDOUfjEQISO5JLe7sqz3EMNh7I3G7d1ruIqTBbuQFDRO8GMsc9DoFM-3Qk1xFiqt_k520PxI3kI6ydJ9Nujz6JzsB31u0hmN0AnlzscYwht1ok3u_9dxtXWWY5IJmOt3YEskATnbfhefGkhyHgi7v1rPj8_uJmdlnOP324mk3npRGqiaVadj0IyStplBCqgw6WwESloFeGApeiVnULTbICWwlSSS45M0o2suWQnDor3hx107jfdmlOvbHB4DDAiG4XdDK6UYKpRPs3NHVjvK6aBH39ALp2Oz-mQbIgF1SyNqOaI8p4F4LHXm-93YA_aEZ1DoBe6_sA6BwAzSqdApCYL-_0d8sNdve8Pz-eANMjIH0X7i16HUzy3GBnfXJYd87-R5N3DzQyLgfnKx4w_J1Ih0TQ1zmHOYas5rRlreS_ABjA3CQ</recordid><startdate>20170201</startdate><enddate>20170201</enddate><creator>Hirayama, Kenshi, MD</creator><creator>Ota, Tomoyuki, MD, PhD</creator><creator>Harada, Kazuhiro, MD</creator><creator>Shibata, Yohei, MD</creator><creator>Tatami, Yosuke, MD</creator><creator>Harata, Shingo, MD</creator><creator>Kawashima, Kazuhiro, MD</creator><creator>Kunimura, Ayako, MD</creator><creator>Shimbo, Yusaku, MD</creator><creator>Takayama, Yohei, MD</creator><creator>Kawamiya, Toshiki, MD</creator><creator>Yamamoto, Dai, MD</creator><creator>Osugi, Naohiro, MD</creator><creator>Suzuki, Susumu, MD</creator><creator>Ishii, Hideki, MD, PhD</creator><creator>Murohara, Toyoaki, MD, PhD</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88C</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>M2O</scope><scope>M7N</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>20170201</creationdate><title>Impact of Paradoxical Decrease in High-Density Lipoprotein Cholesterol Levels After Statin Therapy on Major Adverse Cardiovascular Events in Patients with Stable Angina Pectoris</title><author>Hirayama, Kenshi, MD ; Ota, Tomoyuki, MD, PhD ; Harada, Kazuhiro, MD ; Shibata, Yohei, MD ; Tatami, Yosuke, MD ; Harata, Shingo, MD ; Kawashima, Kazuhiro, MD ; Kunimura, Ayako, MD ; Shimbo, Yusaku, MD ; Takayama, Yohei, MD ; Kawamiya, Toshiki, MD ; Yamamoto, Dai, MD ; Osugi, Naohiro, MD ; Suzuki, Susumu, MD ; Ishii, Hideki, MD, PhD ; Murohara, Toyoaki, MD, PhD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c487t-8bdfa45325c8448dadaba1428af8c0a3546869a7280e95a5853531c857593a003</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Acute Coronary Syndrome - drug therapy</topic><topic>Acute coronary syndromes</topic><topic>Aged</topic><topic>Angina pectoris</topic><topic>Angina, Stable - drug therapy</topic><topic>Cardiovascular disease</topic><topic>Cholesterol</topic><topic>Cholesterol, HDL - blood</topic><topic>Clinical outcomes</topic><topic>Diabetes</topic><topic>Female</topic><topic>Health risk assessment</topic><topic>Heart attacks</topic><topic>high-density lipoprotein cholesterol</topic><topic>Humans</topic><topic>Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use</topic><topic>Hypertension</topic><topic>Internal Medicine</topic><topic>Kaplan-Meier Estimate</topic><topic>Lipids</topic><topic>Male</topic><topic>Medical Education</topic><topic>Middle Aged</topic><topic>Multivariate analysis</topic><topic>Myocardial Infarction - epidemiology</topic><topic>Percutaneous Coronary Intervention - methods</topic><topic>Proportional Hazards Models</topic><topic>Risk Factors</topic><topic>Smoking cessation</topic><topic>stable angina pectoris</topic><topic>statin</topic><topic>Statins</topic><topic>Statistical analysis</topic><topic>Stents</topic><topic>Studies</topic><topic>Values</topic><topic>Variables</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hirayama, Kenshi, MD</creatorcontrib><creatorcontrib>Ota, Tomoyuki, MD, PhD</creatorcontrib><creatorcontrib>Harada, Kazuhiro, MD</creatorcontrib><creatorcontrib>Shibata, Yohei, MD</creatorcontrib><creatorcontrib>Tatami, Yosuke, MD</creatorcontrib><creatorcontrib>Harata, Shingo, MD</creatorcontrib><creatorcontrib>Kawashima, Kazuhiro, MD</creatorcontrib><creatorcontrib>Kunimura, Ayako, MD</creatorcontrib><creatorcontrib>Shimbo, Yusaku, MD</creatorcontrib><creatorcontrib>Takayama, Yohei, MD</creatorcontrib><creatorcontrib>Kawamiya, Toshiki, MD</creatorcontrib><creatorcontrib>Yamamoto, Dai, MD</creatorcontrib><creatorcontrib>Osugi, Naohiro, MD</creatorcontrib><creatorcontrib>Suzuki, Susumu, MD</creatorcontrib><creatorcontrib>Ishii, Hideki, MD, PhD</creatorcontrib><creatorcontrib>Murohara, Toyoaki, MD, PhD</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Clinical therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hirayama, Kenshi, MD</au><au>Ota, Tomoyuki, MD, PhD</au><au>Harada, Kazuhiro, MD</au><au>Shibata, Yohei, MD</au><au>Tatami, Yosuke, MD</au><au>Harata, Shingo, MD</au><au>Kawashima, Kazuhiro, MD</au><au>Kunimura, Ayako, MD</au><au>Shimbo, Yusaku, MD</au><au>Takayama, Yohei, MD</au><au>Kawamiya, Toshiki, MD</au><au>Yamamoto, Dai, MD</au><au>Osugi, Naohiro, MD</au><au>Suzuki, Susumu, MD</au><au>Ishii, Hideki, MD, PhD</au><au>Murohara, Toyoaki, MD, PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of Paradoxical Decrease in High-Density Lipoprotein Cholesterol Levels After Statin Therapy on Major Adverse Cardiovascular Events in Patients with Stable Angina Pectoris</atitle><jtitle>Clinical therapeutics</jtitle><addtitle>Clin Ther</addtitle><date>2017-02-01</date><risdate>2017</risdate><volume>39</volume><issue>2</issue><spage>279</spage><epage>287</epage><pages>279-287</pages><issn>0149-2918</issn><eissn>1879-114X</eissn><abstract>Abstract Purpose Statin therapy usually increases HDL-C levels. However, a paradoxical decrease in HDL-C levels after statin therapy is often seen in clinical settings. The relationship between a paradoxical decrease in HDL-C levels after statin therapy and adverse cardiovascular events in patients with stable angina pectoris (SAP) is not well understood. The purpose of this study was to analyze the relationship between paradoxical HDL-C decreases after statin therapy and major adverse cardiovascular events (MACEs) in patients undergoing percutaneous coronary intervention (PCI) for SAP. Methods Between January 2006 and March 2015, 867 patients underwent PCI for SAP. Of them, we enrolled 209 patients who were newly started on statin therapy before PCI. We excluded patients who had started statin therapy earlier than 6 months before PCI, patients who had not started statin therapy after PCI, and patients who were diagnosed with acute coronary syndrome. They were divided into 2 groups according to the change in their HDL-C levels between baseline and 6 to 9 months after the index PCI: decreased HDL group after statin treatment (80 patients) and increased HDL group (129 patients). The primary end points were MACEs defined as a composite of all-cause death, nonfatal acute myocardial infarction, and target vessel revascularization (TVR). Findings Using Kaplan-Meier analysis, the 7-year event rate for composite MACEs in the decreased HDL group was found to be higher than that for the increased HDL group (38% versus 24%, log-rank P = 0.02). TVR occurred more frequently in the decreased HDL group than in the increased HDL group (32% versus 12%, log-rank P = 0.01). With the use of multivariate analysis, changes in HDL-C levels after statin therapy indicated a significant inverse association with the increased risk of MACEs, (hazard ratio [HR] = 0.94; 95% CI, 0.92–0.97; P < 0.01). The incidence of MACEs was more strongly associated with ΔHDL than with ΔLDL. Moreover, BMS usage also independently predicted MACEs (HR = 2.18; 95% CI, 1.14–4.17; P < 0.01). Implications A paradoxical decrease in HDL-C levels after statin therapy might be a risk factor for MACEs, especially TVR, in patients with SAP.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>28034517</pmid><doi>10.1016/j.clinthera.2016.12.006</doi><tpages>9</tpages></addata></record> |
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identifier | ISSN: 0149-2918 |
ispartof | Clinical therapeutics, 2017-02, Vol.39 (2), p.279-287 |
issn | 0149-2918 1879-114X |
language | eng |
recordid | cdi_proquest_miscellaneous_1877841835 |
source | MEDLINE; Access via ScienceDirect (Elsevier); ProQuest Central UK/Ireland |
subjects | Acute Coronary Syndrome - drug therapy Acute coronary syndromes Aged Angina pectoris Angina, Stable - drug therapy Cardiovascular disease Cholesterol Cholesterol, HDL - blood Clinical outcomes Diabetes Female Health risk assessment Heart attacks high-density lipoprotein cholesterol Humans Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use Hypertension Internal Medicine Kaplan-Meier Estimate Lipids Male Medical Education Middle Aged Multivariate analysis Myocardial Infarction - epidemiology Percutaneous Coronary Intervention - methods Proportional Hazards Models Risk Factors Smoking cessation stable angina pectoris statin Statins Statistical analysis Stents Studies Values Variables |
title | Impact of Paradoxical Decrease in High-Density Lipoprotein Cholesterol Levels After Statin Therapy on Major Adverse Cardiovascular Events in Patients with Stable Angina Pectoris |
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