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
Hauptverfasser: 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
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container_end_page 287
container_issue 2
container_start_page 279
container_title Clinical therapeutics
container_volume 39
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 &lt; 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 &lt; 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 &lt; 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 &lt; 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 &amp; 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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 &lt; 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 &lt; 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
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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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