The Effects of Tamoxifen on Plasma Lipoprotein(a) Concentrations: Systematic Review and Meta-Analysis

Introduction Tamoxifen is a selective estrogen receptor modulator widely used in the treatment of breast cancer. Tamoxifen therapy is associated with lower circulating low-density lipoprotein cholesterol and increased triglycerides, but its effects on other lipids are less well studied. Aims We aime...

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Veröffentlicht in:Drugs (New York, N.Y.) N.Y.), 2017-07, Vol.77 (11), p.1187-1197
Hauptverfasser: Sahebkar, Amirhossein, Serban, Maria-Corina, Penson, Peter, Gurban, Camelia, Ursoniu, Sorin, Toth, Peter P., Jones, Steven R., Lippi, Giuseppe, Kotani, Kazuhiko, Kostner, Karam, Rizzo, Manfredi, Rysz, Jacek, Banach, Maciej
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container_end_page 1197
container_issue 11
container_start_page 1187
container_title Drugs (New York, N.Y.)
container_volume 77
creator Sahebkar, Amirhossein
Serban, Maria-Corina
Penson, Peter
Gurban, Camelia
Ursoniu, Sorin
Toth, Peter P.
Jones, Steven R.
Lippi, Giuseppe
Kotani, Kazuhiko
Kostner, Karam
Rizzo, Manfredi
Rysz, Jacek
Banach, Maciej
description Introduction Tamoxifen is a selective estrogen receptor modulator widely used in the treatment of breast cancer. Tamoxifen therapy is associated with lower circulating low-density lipoprotein cholesterol and increased triglycerides, but its effects on other lipids are less well studied. Aims We aimed to investigate the effect of tamoxifen on circulating concentrations of lipoprotein(a) [Lp(a)] through a meta-analysis of available randomized controlled trials (RCTs) and observational studies. Methods This study was registered in the PROSPERO database (CRD42016036890). Scopus, MEDLINE and EMBASE were searched from inception until 22 March 2016 to identify studies investigating the effect of tamoxifen on Lp(a) values in humans. Meta-analysis was performed using an inverse variance-weighted, random-effects model with standardized mean difference (SMD) as the effect size estimate. Results Meta-analysis of five studies with 215 participants suggested a statistically significant reduction of Lp(a) levels following tamoxifen treatment (SMD −0.41, 95% confidence interval −0.68 to −0.14, p  = 0.003). This effect was robust in the sensitivity analysis. Conclusions Meta-analysis suggested a statistically significant reduction of Lp(a) levels following tamoxifen treatment. Further well-designed trials are required to validate these results.
doi_str_mv 10.1007/s40265-017-0767-4
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Tamoxifen therapy is associated with lower circulating low-density lipoprotein cholesterol and increased triglycerides, but its effects on other lipids are less well studied. Aims We aimed to investigate the effect of tamoxifen on circulating concentrations of lipoprotein(a) [Lp(a)] through a meta-analysis of available randomized controlled trials (RCTs) and observational studies. Methods This study was registered in the PROSPERO database (CRD42016036890). Scopus, MEDLINE and EMBASE were searched from inception until 22 March 2016 to identify studies investigating the effect of tamoxifen on Lp(a) values in humans. Meta-analysis was performed using an inverse variance-weighted, random-effects model with standardized mean difference (SMD) as the effect size estimate. Results Meta-analysis of five studies with 215 participants suggested a statistically significant reduction of Lp(a) levels following tamoxifen treatment (SMD −0.41, 95% confidence interval −0.68 to −0.14, p  = 0.003). This effect was robust in the sensitivity analysis. Conclusions Meta-analysis suggested a statistically significant reduction of Lp(a) levels following tamoxifen treatment. Further well-designed trials are required to validate these results.</description><identifier>ISSN: 0012-6667</identifier><identifier>EISSN: 1179-1950</identifier><identifier>DOI: 10.1007/s40265-017-0767-4</identifier><identifier>PMID: 28573436</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Breast cancer ; Breast Neoplasms - drug therapy ; Breast Neoplasms - metabolism ; Cardiovascular disease ; Cell Line, Tumor ; Cholesterol ; Confidence intervals ; Disease prevention ; Estrogens ; Female ; Humans ; Internal Medicine ; Lipids ; Lipoprotein(a) - blood ; Medicine ; Medicine &amp; Public Health ; Meta-analysis ; Pharmacology/Toxicology ; Pharmacotherapy ; Randomized Controlled Trials as Topic ; Reduction ; Selective Estrogen Receptor Modulators ; Sensitivity analysis ; Statistical analysis ; Statistical significance ; Studies ; Systematic Review ; Tamoxifen ; Tamoxifen - pharmacology ; Tamoxifen - therapeutic use ; Triglycerides ; Womens health</subject><ispartof>Drugs (New York, N.Y.), 2017-07, Vol.77 (11), p.1187-1197</ispartof><rights>The Author(s) 2017</rights><rights>Copyright Springer Science &amp; Business Media Jul 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c470t-c0b2d3eb729dc2d8ae4fa78cdf4664c1114c16c6d0d66e5a25e2b3400da916903</citedby><cites>FETCH-LOGICAL-c470t-c0b2d3eb729dc2d8ae4fa78cdf4664c1114c16c6d0d66e5a25e2b3400da916903</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s40265-017-0767-4$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s40265-017-0767-4$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,27903,27904,41467,42536,51297</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28573436$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sahebkar, Amirhossein</creatorcontrib><creatorcontrib>Serban, Maria-Corina</creatorcontrib><creatorcontrib>Penson, Peter</creatorcontrib><creatorcontrib>Gurban, Camelia</creatorcontrib><creatorcontrib>Ursoniu, Sorin</creatorcontrib><creatorcontrib>Toth, Peter P.</creatorcontrib><creatorcontrib>Jones, Steven R.</creatorcontrib><creatorcontrib>Lippi, Giuseppe</creatorcontrib><creatorcontrib>Kotani, Kazuhiko</creatorcontrib><creatorcontrib>Kostner, Karam</creatorcontrib><creatorcontrib>Rizzo, Manfredi</creatorcontrib><creatorcontrib>Rysz, Jacek</creatorcontrib><creatorcontrib>Banach, Maciej</creatorcontrib><creatorcontrib>Lipid and Blood Pressure Meta-analysis Collaboration (LBPMC) Group</creatorcontrib><creatorcontrib>for the Lipid and Blood Pressure Meta-analysis Collaboration (LBPMC) Group</creatorcontrib><title>The Effects of Tamoxifen on Plasma Lipoprotein(a) Concentrations: Systematic Review and Meta-Analysis</title><title>Drugs (New York, N.Y.)</title><addtitle>Drugs</addtitle><addtitle>Drugs</addtitle><description>Introduction Tamoxifen is a selective estrogen receptor modulator widely used in the treatment of breast cancer. Tamoxifen therapy is associated with lower circulating low-density lipoprotein cholesterol and increased triglycerides, but its effects on other lipids are less well studied. Aims We aimed to investigate the effect of tamoxifen on circulating concentrations of lipoprotein(a) [Lp(a)] through a meta-analysis of available randomized controlled trials (RCTs) and observational studies. Methods This study was registered in the PROSPERO database (CRD42016036890). Scopus, MEDLINE and EMBASE were searched from inception until 22 March 2016 to identify studies investigating the effect of tamoxifen on Lp(a) values in humans. Meta-analysis was performed using an inverse variance-weighted, random-effects model with standardized mean difference (SMD) as the effect size estimate. Results Meta-analysis of five studies with 215 participants suggested a statistically significant reduction of Lp(a) levels following tamoxifen treatment (SMD −0.41, 95% confidence interval −0.68 to −0.14, p  = 0.003). This effect was robust in the sensitivity analysis. Conclusions Meta-analysis suggested a statistically significant reduction of Lp(a) levels following tamoxifen treatment. 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Tamoxifen therapy is associated with lower circulating low-density lipoprotein cholesterol and increased triglycerides, but its effects on other lipids are less well studied. Aims We aimed to investigate the effect of tamoxifen on circulating concentrations of lipoprotein(a) [Lp(a)] through a meta-analysis of available randomized controlled trials (RCTs) and observational studies. Methods This study was registered in the PROSPERO database (CRD42016036890). Scopus, MEDLINE and EMBASE were searched from inception until 22 March 2016 to identify studies investigating the effect of tamoxifen on Lp(a) values in humans. Meta-analysis was performed using an inverse variance-weighted, random-effects model with standardized mean difference (SMD) as the effect size estimate. Results Meta-analysis of five studies with 215 participants suggested a statistically significant reduction of Lp(a) levels following tamoxifen treatment (SMD −0.41, 95% confidence interval −0.68 to −0.14, p  = 0.003). This effect was robust in the sensitivity analysis. Conclusions Meta-analysis suggested a statistically significant reduction of Lp(a) levels following tamoxifen treatment. Further well-designed trials are required to validate these results.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>28573436</pmid><doi>10.1007/s40265-017-0767-4</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
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subjects Breast cancer
Breast Neoplasms - drug therapy
Breast Neoplasms - metabolism
Cardiovascular disease
Cell Line, Tumor
Cholesterol
Confidence intervals
Disease prevention
Estrogens
Female
Humans
Internal Medicine
Lipids
Lipoprotein(a) - blood
Medicine
Medicine & Public Health
Meta-analysis
Pharmacology/Toxicology
Pharmacotherapy
Randomized Controlled Trials as Topic
Reduction
Selective Estrogen Receptor Modulators
Sensitivity analysis
Statistical analysis
Statistical significance
Studies
Systematic Review
Tamoxifen
Tamoxifen - pharmacology
Tamoxifen - therapeutic use
Triglycerides
Womens health
title The Effects of Tamoxifen on Plasma Lipoprotein(a) Concentrations: Systematic Review and Meta-Analysis
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