Antioxidant Supplements Block the Response of HDL to Simvastatin-Niacin Therapy in Patients With Coronary Artery Disease and Low HDL
One strategy for treating coronary artery disease (CAD) patients with low HDL cholesterol (HDL-C) is to maximally increase the HDL-C to LDL-C ratio by combining lifestyle changes with niacin (N) plus a statin. Because HDL can prevent LDL oxidation, the low-HDL state also may benefit clinically from...
Gespeichert in:
Veröffentlicht in: | Arteriosclerosis, thrombosis, and vascular biology thrombosis, and vascular biology, 2001-08, Vol.21 (8), p.1320-1326 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1326 |
---|---|
container_issue | 8 |
container_start_page | 1320 |
container_title | Arteriosclerosis, thrombosis, and vascular biology |
container_volume | 21 |
creator | Cheung, Marian C Zhao, Xue-Qiao Chait, Alan Albers, John J Brown, B Greg |
description | One strategy for treating coronary artery disease (CAD) patients with low HDL cholesterol (HDL-C) is to maximally increase the HDL-C to LDL-C ratio by combining lifestyle changes with niacin (N) plus a statin. Because HDL can prevent LDL oxidation, the low-HDL state also may benefit clinically from supplemental antioxidants. Lipoprotein changes over 12 months were studied in 153 CAD subjects with low HDL-C randomized to take simvastatin and niacin (S-N), antioxidants (vitamins E and C, β-carotene, and selenium), S-N plus antioxidants (S-N+A), or placebo. Mean baseline plasma cholesterol, triglyceride, LDL-C, and HDL-C levels of the 153 subjects were 196, 207, 127, and 32 mg/dL, respectively. Without S-N, lipid changes were minor. The S-N and S-N+A groups had comparably significant reductions (P ≤0.001) in plasma cholesterol, triglyceride, and LDL-C. However, increases in HDL-C, especially HDL2-C, were consistently higher in the S-N group than in the S-N+A group (25% vs 18% and 42% vs 0%, respectively). With S-N, but not with S-N+A, there was a selective increase in apolipoprotein (apo) A-I (64%) in HDL particles containing apo A-I but not A-II [Lp(A-I)] and their particle size. Thus, in CAD patients with low HDL-C, S-N substantially increased HDL2-C, Lp(A-I), and HDL particle size. These favorable responses were blunted by the antioxidants used owing to a striking selective effect on Lp(A-I). This unexpected adverse interaction between antioxidants and lipid therapy may have important implications for the management of CAD. |
doi_str_mv | 10.1161/hq0801.095151 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_204302237</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>78995559</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4345-4004f1907b2817618f443c2144c5999f542f55852fa0a7a85f1f7bc09705855d3</originalsourceid><addsrcrecordid>eNpFkc9vFCEUx4nR2Fo9ejXEO_U9BubHcd2qNdmosTUeCTsLGdpZmALj2rt_uKyziQfyXl4--fD4QshrhEvEGt8ND9ACXkInUeITco6SCybqqn5aemg6JmvBz8iLlO4AQHAOz8kZouhaUcM5-bPy2YXfbqd9pjfzNI1mb3xO9P0Y-nuaB0O_mzQFnwwNll5fbWgO9Mbtf-mUdXaefXG6d57eDibq6ZGW9luZ_3P8dHmg6xCD1_GRrmI2pVy5ZHSxab-jm3A4Kl-SZ1aPybw61Qvy4-OH2_U123z99Hm92rBeVEIyUfa32EGz5S02NbZWiKrnKEQvu66zUnArZSu51aAb3UqLttn20DVQpnJXXZC3i3eK4WE2Kau7MEdfrlQcRAWcV02B2AL1MaQUjVVTdPvyAIWgjpGrJXK1RF74NyfpvN2b3X_6lHEBxAIcwlgSSPfjfDBRDUaPeVDHT6lqkIwDYPECsHJQVn8BVIeKMA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>204302237</pqid></control><display><type>article</type><title>Antioxidant Supplements Block the Response of HDL to Simvastatin-Niacin Therapy in Patients With Coronary Artery Disease and Low HDL</title><source>MEDLINE</source><source>Journals@Ovid Complete</source><source>Alma/SFX Local Collection</source><creator>Cheung, Marian C ; Zhao, Xue-Qiao ; Chait, Alan ; Albers, John J ; Brown, B Greg</creator><creatorcontrib>Cheung, Marian C ; Zhao, Xue-Qiao ; Chait, Alan ; Albers, John J ; Brown, B Greg</creatorcontrib><description>One strategy for treating coronary artery disease (CAD) patients with low HDL cholesterol (HDL-C) is to maximally increase the HDL-C to LDL-C ratio by combining lifestyle changes with niacin (N) plus a statin. Because HDL can prevent LDL oxidation, the low-HDL state also may benefit clinically from supplemental antioxidants. Lipoprotein changes over 12 months were studied in 153 CAD subjects with low HDL-C randomized to take simvastatin and niacin (S-N), antioxidants (vitamins E and C, β-carotene, and selenium), S-N plus antioxidants (S-N+A), or placebo. Mean baseline plasma cholesterol, triglyceride, LDL-C, and HDL-C levels of the 153 subjects were 196, 207, 127, and 32 mg/dL, respectively. Without S-N, lipid changes were minor. The S-N and S-N+A groups had comparably significant reductions (P ≤0.001) in plasma cholesterol, triglyceride, and LDL-C. However, increases in HDL-C, especially HDL2-C, were consistently higher in the S-N group than in the S-N+A group (25% vs 18% and 42% vs 0%, respectively). With S-N, but not with S-N+A, there was a selective increase in apolipoprotein (apo) A-I (64%) in HDL particles containing apo A-I but not A-II [Lp(A-I)] and their particle size. Thus, in CAD patients with low HDL-C, S-N substantially increased HDL2-C, Lp(A-I), and HDL particle size. These favorable responses were blunted by the antioxidants used owing to a striking selective effect on Lp(A-I). This unexpected adverse interaction between antioxidants and lipid therapy may have important implications for the management of CAD.</description><identifier>ISSN: 1079-5642</identifier><identifier>EISSN: 1524-4636</identifier><identifier>DOI: 10.1161/hq0801.095151</identifier><identifier>PMID: 11498460</identifier><language>eng</language><publisher>United States: American Heart Association, Inc</publisher><subject>Adult ; Aged ; Antioxidants - pharmacology ; Ascorbic Acid - pharmacology ; beta Carotene - pharmacology ; Cholesterol, HDL - chemistry ; Cholesterol, HDL - metabolism ; Cholesterol, LDL - metabolism ; Coronary Disease - drug therapy ; Coronary Disease - metabolism ; Dietary Supplements ; Drug Interactions ; Female ; Humans ; Hypolipidemic Agents - pharmacology ; Hypolipidemic Agents - therapeutic use ; Male ; Middle Aged ; Niacin - pharmacology ; Niacin - therapeutic use ; Particle Size ; Selenium - pharmacology ; Simvastatin - pharmacology ; Simvastatin - therapeutic use ; Vitamin E - pharmacology</subject><ispartof>Arteriosclerosis, thrombosis, and vascular biology, 2001-08, Vol.21 (8), p.1320-1326</ispartof><rights>2001 American Heart Association, Inc.</rights><rights>Copyright American Heart Association, Inc. Aug 2001</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4345-4004f1907b2817618f443c2144c5999f542f55852fa0a7a85f1f7bc09705855d3</citedby><cites>FETCH-LOGICAL-c4345-4004f1907b2817618f443c2144c5999f542f55852fa0a7a85f1f7bc09705855d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11498460$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cheung, Marian C</creatorcontrib><creatorcontrib>Zhao, Xue-Qiao</creatorcontrib><creatorcontrib>Chait, Alan</creatorcontrib><creatorcontrib>Albers, John J</creatorcontrib><creatorcontrib>Brown, B Greg</creatorcontrib><title>Antioxidant Supplements Block the Response of HDL to Simvastatin-Niacin Therapy in Patients With Coronary Artery Disease and Low HDL</title><title>Arteriosclerosis, thrombosis, and vascular biology</title><addtitle>Arterioscler Thromb Vasc Biol</addtitle><description>One strategy for treating coronary artery disease (CAD) patients with low HDL cholesterol (HDL-C) is to maximally increase the HDL-C to LDL-C ratio by combining lifestyle changes with niacin (N) plus a statin. Because HDL can prevent LDL oxidation, the low-HDL state also may benefit clinically from supplemental antioxidants. Lipoprotein changes over 12 months were studied in 153 CAD subjects with low HDL-C randomized to take simvastatin and niacin (S-N), antioxidants (vitamins E and C, β-carotene, and selenium), S-N plus antioxidants (S-N+A), or placebo. Mean baseline plasma cholesterol, triglyceride, LDL-C, and HDL-C levels of the 153 subjects were 196, 207, 127, and 32 mg/dL, respectively. Without S-N, lipid changes were minor. The S-N and S-N+A groups had comparably significant reductions (P ≤0.001) in plasma cholesterol, triglyceride, and LDL-C. However, increases in HDL-C, especially HDL2-C, were consistently higher in the S-N group than in the S-N+A group (25% vs 18% and 42% vs 0%, respectively). With S-N, but not with S-N+A, there was a selective increase in apolipoprotein (apo) A-I (64%) in HDL particles containing apo A-I but not A-II [Lp(A-I)] and their particle size. Thus, in CAD patients with low HDL-C, S-N substantially increased HDL2-C, Lp(A-I), and HDL particle size. These favorable responses were blunted by the antioxidants used owing to a striking selective effect on Lp(A-I). This unexpected adverse interaction between antioxidants and lipid therapy may have important implications for the management of CAD.</description><subject>Adult</subject><subject>Aged</subject><subject>Antioxidants - pharmacology</subject><subject>Ascorbic Acid - pharmacology</subject><subject>beta Carotene - pharmacology</subject><subject>Cholesterol, HDL - chemistry</subject><subject>Cholesterol, HDL - metabolism</subject><subject>Cholesterol, LDL - metabolism</subject><subject>Coronary Disease - drug therapy</subject><subject>Coronary Disease - metabolism</subject><subject>Dietary Supplements</subject><subject>Drug Interactions</subject><subject>Female</subject><subject>Humans</subject><subject>Hypolipidemic Agents - pharmacology</subject><subject>Hypolipidemic Agents - therapeutic use</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Niacin - pharmacology</subject><subject>Niacin - therapeutic use</subject><subject>Particle Size</subject><subject>Selenium - pharmacology</subject><subject>Simvastatin - pharmacology</subject><subject>Simvastatin - therapeutic use</subject><subject>Vitamin E - pharmacology</subject><issn>1079-5642</issn><issn>1524-4636</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkc9vFCEUx4nR2Fo9ejXEO_U9BubHcd2qNdmosTUeCTsLGdpZmALj2rt_uKyziQfyXl4--fD4QshrhEvEGt8ND9ACXkInUeITco6SCybqqn5aemg6JmvBz8iLlO4AQHAOz8kZouhaUcM5-bPy2YXfbqd9pjfzNI1mb3xO9P0Y-nuaB0O_mzQFnwwNll5fbWgO9Mbtf-mUdXaefXG6d57eDibq6ZGW9luZ_3P8dHmg6xCD1_GRrmI2pVy5ZHSxab-jm3A4Kl-SZ1aPybw61Qvy4-OH2_U123z99Hm92rBeVEIyUfa32EGz5S02NbZWiKrnKEQvu66zUnArZSu51aAb3UqLttn20DVQpnJXXZC3i3eK4WE2Kau7MEdfrlQcRAWcV02B2AL1MaQUjVVTdPvyAIWgjpGrJXK1RF74NyfpvN2b3X_6lHEBxAIcwlgSSPfjfDBRDUaPeVDHT6lqkIwDYPECsHJQVn8BVIeKMA</recordid><startdate>200108</startdate><enddate>200108</enddate><creator>Cheung, Marian C</creator><creator>Zhao, Xue-Qiao</creator><creator>Chait, Alan</creator><creator>Albers, John J</creator><creator>Brown, B Greg</creator><general>American Heart Association, Inc</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>K9.</scope></search><sort><creationdate>200108</creationdate><title>Antioxidant Supplements Block the Response of HDL to Simvastatin-Niacin Therapy in Patients With Coronary Artery Disease and Low HDL</title><author>Cheung, Marian C ; Zhao, Xue-Qiao ; Chait, Alan ; Albers, John J ; Brown, B Greg</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4345-4004f1907b2817618f443c2144c5999f542f55852fa0a7a85f1f7bc09705855d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antioxidants - pharmacology</topic><topic>Ascorbic Acid - pharmacology</topic><topic>beta Carotene - pharmacology</topic><topic>Cholesterol, HDL - chemistry</topic><topic>Cholesterol, HDL - metabolism</topic><topic>Cholesterol, LDL - metabolism</topic><topic>Coronary Disease - drug therapy</topic><topic>Coronary Disease - metabolism</topic><topic>Dietary Supplements</topic><topic>Drug Interactions</topic><topic>Female</topic><topic>Humans</topic><topic>Hypolipidemic Agents - pharmacology</topic><topic>Hypolipidemic Agents - therapeutic use</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Niacin - pharmacology</topic><topic>Niacin - therapeutic use</topic><topic>Particle Size</topic><topic>Selenium - pharmacology</topic><topic>Simvastatin - pharmacology</topic><topic>Simvastatin - therapeutic use</topic><topic>Vitamin E - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cheung, Marian C</creatorcontrib><creatorcontrib>Zhao, Xue-Qiao</creatorcontrib><creatorcontrib>Chait, Alan</creatorcontrib><creatorcontrib>Albers, John J</creatorcontrib><creatorcontrib>Brown, B Greg</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 Health & Medical Complete (Alumni)</collection><jtitle>Arteriosclerosis, thrombosis, and vascular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cheung, Marian C</au><au>Zhao, Xue-Qiao</au><au>Chait, Alan</au><au>Albers, John J</au><au>Brown, B Greg</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antioxidant Supplements Block the Response of HDL to Simvastatin-Niacin Therapy in Patients With Coronary Artery Disease and Low HDL</atitle><jtitle>Arteriosclerosis, thrombosis, and vascular biology</jtitle><addtitle>Arterioscler Thromb Vasc Biol</addtitle><date>2001-08</date><risdate>2001</risdate><volume>21</volume><issue>8</issue><spage>1320</spage><epage>1326</epage><pages>1320-1326</pages><issn>1079-5642</issn><eissn>1524-4636</eissn><abstract>One strategy for treating coronary artery disease (CAD) patients with low HDL cholesterol (HDL-C) is to maximally increase the HDL-C to LDL-C ratio by combining lifestyle changes with niacin (N) plus a statin. Because HDL can prevent LDL oxidation, the low-HDL state also may benefit clinically from supplemental antioxidants. Lipoprotein changes over 12 months were studied in 153 CAD subjects with low HDL-C randomized to take simvastatin and niacin (S-N), antioxidants (vitamins E and C, β-carotene, and selenium), S-N plus antioxidants (S-N+A), or placebo. Mean baseline plasma cholesterol, triglyceride, LDL-C, and HDL-C levels of the 153 subjects were 196, 207, 127, and 32 mg/dL, respectively. Without S-N, lipid changes were minor. The S-N and S-N+A groups had comparably significant reductions (P ≤0.001) in plasma cholesterol, triglyceride, and LDL-C. However, increases in HDL-C, especially HDL2-C, were consistently higher in the S-N group than in the S-N+A group (25% vs 18% and 42% vs 0%, respectively). With S-N, but not with S-N+A, there was a selective increase in apolipoprotein (apo) A-I (64%) in HDL particles containing apo A-I but not A-II [Lp(A-I)] and their particle size. Thus, in CAD patients with low HDL-C, S-N substantially increased HDL2-C, Lp(A-I), and HDL particle size. These favorable responses were blunted by the antioxidants used owing to a striking selective effect on Lp(A-I). This unexpected adverse interaction between antioxidants and lipid therapy may have important implications for the management of CAD.</abstract><cop>United States</cop><pub>American Heart Association, Inc</pub><pmid>11498460</pmid><doi>10.1161/hq0801.095151</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1079-5642 |
ispartof | Arteriosclerosis, thrombosis, and vascular biology, 2001-08, Vol.21 (8), p.1320-1326 |
issn | 1079-5642 1524-4636 |
language | eng |
recordid | cdi_proquest_journals_204302237 |
source | MEDLINE; Journals@Ovid Complete; Alma/SFX Local Collection |
subjects | Adult Aged Antioxidants - pharmacology Ascorbic Acid - pharmacology beta Carotene - pharmacology Cholesterol, HDL - chemistry Cholesterol, HDL - metabolism Cholesterol, LDL - metabolism Coronary Disease - drug therapy Coronary Disease - metabolism Dietary Supplements Drug Interactions Female Humans Hypolipidemic Agents - pharmacology Hypolipidemic Agents - therapeutic use Male Middle Aged Niacin - pharmacology Niacin - therapeutic use Particle Size Selenium - pharmacology Simvastatin - pharmacology Simvastatin - therapeutic use Vitamin E - pharmacology |
title | Antioxidant Supplements Block the Response of HDL to Simvastatin-Niacin Therapy in Patients With Coronary Artery Disease and Low HDL |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-24T01%3A32%3A45IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Antioxidant%20Supplements%20Block%20the%20Response%20of%20HDL%20to%20Simvastatin-Niacin%20Therapy%20in%20Patients%20With%20Coronary%20Artery%20Disease%20and%20Low%20HDL&rft.jtitle=Arteriosclerosis,%20thrombosis,%20and%20vascular%20biology&rft.au=Cheung,%20Marian%20C&rft.date=2001-08&rft.volume=21&rft.issue=8&rft.spage=1320&rft.epage=1326&rft.pages=1320-1326&rft.issn=1079-5642&rft.eissn=1524-4636&rft_id=info:doi/10.1161/hq0801.095151&rft_dat=%3Cproquest_cross%3E78995559%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=204302237&rft_id=info:pmid/11498460&rfr_iscdi=true |