Main morbidities recorded in the women's international study of long duration oestrogen after menopause (WISDOM): a randomised controlled trial of hormone replacement therapy in postmenopausal women

Objective To assess the long term risks and benefits of hormone replacement therapy (combined hormone therapy versus placebo, and oestrogen alone versus combined hormone therapy). Design Multicentre, randomised, placebo controlled, double blind trial. Setting General practices in UK (384), Australia...

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Veröffentlicht in:BMJ 2007-08, Vol.335 (7613), p.239-244
Hauptverfasser: Vickers, Madge R, MacLennan, Alastair H, Lawton, Beverley, Ford, Deborah, Martin, Jeannett, Meredith, Sarah K, DeStavola, Bianca L, Rose, Sally, Dowell, Anthony, Wilkes, Helen C, Darbyshire, Janet H, Meade, Tom W
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container_end_page 244
container_issue 7613
container_start_page 239
container_title BMJ
container_volume 335
creator Vickers, Madge R
MacLennan, Alastair H
Lawton, Beverley
Ford, Deborah
Martin, Jeannett
Meredith, Sarah K
DeStavola, Bianca L
Rose, Sally
Dowell, Anthony
Wilkes, Helen C
Darbyshire, Janet H
Meade, Tom W
description Objective To assess the long term risks and benefits of hormone replacement therapy (combined hormone therapy versus placebo, and oestrogen alone versus combined hormone therapy). Design Multicentre, randomised, placebo controlled, double blind trial. Setting General practices in UK (384), Australia (91), and New Zealand (24). Participants Postmenopausal women aged 50-69 years at randomisation. At early closure of the trial, 56 583 had been screened, 8980 entered run-in, and 5692 (26% of target of 22 300) started treatment. Interventions Oestrogen only therapy (conjugated equine oestrogens 0.625 mg orally daily) or combined hormone therapy (conjugated equine oestrogens plus medroxyprogesterone acetate 2.5/5.0 mg orally daily). Ten years of treatment planned. Main outcome measures Primary outcomes: major cardiovascular disease, osteoporotic fractures, and breast cancer. Secondary outcomes: other cancers, death from all causes, venous thromboembolism, cerebrovascular disease, dementia, and quality of life. Results The trial was prematurely closed during recruitment, after a median follow-up of 11.9 months (interquartile range 7.1-19.6, total 6498 women years) in those enrolled, after the publication of early results from the women's health initiative study. The mean age of randomised women was 62.8 (SD 4.8) years. When combined hormone therapy (n=2196) was compared with placebo (n=2189), there was a significant increase in the number of major cardiovascular events (7 v 0, P=0.016) and venous thromboembolisms (22 v 3, hazard ratio 7.36 (95% CI 2.20 to 24.60)). There were no statistically significant differences in numbers of breast or other cancers (22 v 25, hazard ratio 0.88 (0.49 to 1.56)), cerebrovascular events (14 v 19, 0.73 (0.37 to 1.46)), fractures (40 v 58, 0.69 (0.46 to 1.03)), and overall deaths (8 v 5, 1.60 (0.52 to 4.89)). Comparison of combined hormone therapy (n=815) versus oestrogen therapy (n=826) outcomes revealed no significant differences. Conclusions Hormone replacement therapy increases cardiovascular and thromboembolic risk when started many years after the menopause. The results are consistent with the findings of the women's health initiative study and secondary prevention studies. Research is needed to assess the long term risks and benefits of starting hormone replacement therapy near the menopause, when the effect may be different. Trial registration Current Controlled Trials ISRCTN 63718836
doi_str_mv 10.1136/bmj.39266.425069.AD
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Design Multicentre, randomised, placebo controlled, double blind trial. Setting General practices in UK (384), Australia (91), and New Zealand (24). Participants Postmenopausal women aged 50-69 years at randomisation. At early closure of the trial, 56 583 had been screened, 8980 entered run-in, and 5692 (26% of target of 22 300) started treatment. Interventions Oestrogen only therapy (conjugated equine oestrogens 0.625 mg orally daily) or combined hormone therapy (conjugated equine oestrogens plus medroxyprogesterone acetate 2.5/5.0 mg orally daily). Ten years of treatment planned. Main outcome measures Primary outcomes: major cardiovascular disease, osteoporotic fractures, and breast cancer. Secondary outcomes: other cancers, death from all causes, venous thromboembolism, cerebrovascular disease, dementia, and quality of life. Results The trial was prematurely closed during recruitment, after a median follow-up of 11.9 months (interquartile range 7.1-19.6, total 6498 women years) in those enrolled, after the publication of early results from the women's health initiative study. The mean age of randomised women was 62.8 (SD 4.8) years. When combined hormone therapy (n=2196) was compared with placebo (n=2189), there was a significant increase in the number of major cardiovascular events (7 v 0, P=0.016) and venous thromboembolisms (22 v 3, hazard ratio 7.36 (95% CI 2.20 to 24.60)). There were no statistically significant differences in numbers of breast or other cancers (22 v 25, hazard ratio 0.88 (0.49 to 1.56)), cerebrovascular events (14 v 19, 0.73 (0.37 to 1.46)), fractures (40 v 58, 0.69 (0.46 to 1.03)), and overall deaths (8 v 5, 1.60 (0.52 to 4.89)). Comparison of combined hormone therapy (n=815) versus oestrogen therapy (n=826) outcomes revealed no significant differences. Conclusions Hormone replacement therapy increases cardiovascular and thromboembolic risk when started many years after the menopause. The results are consistent with the findings of the women's health initiative study and secondary prevention studies. Research is needed to assess the long term risks and benefits of starting hormone replacement therapy near the menopause, when the effect may be different. Trial registration Current Controlled Trials ISRCTN 63718836</description><edition>International edition</edition><identifier>ISSN: 0959-8138</identifier><identifier>ISSN: 0959-8146</identifier><identifier>ISSN: 0959-535X</identifier><identifier>EISSN: 1468-5833</identifier><identifier>EISSN: 1756-1833</identifier><identifier>DOI: 10.1136/bmj.39266.425069.AD</identifier><identifier>PMID: 17626056</identifier><identifier>CODEN: BMJOAE</identifier><language>eng</language><publisher>London: British Medical Journal Publishing Group</publisher><subject>Aged ; Biological and medical sciences ; Breast cancer ; Breast Neoplasms - chemically induced ; Cardiovascular diseases ; Cardiovascular Diseases - chemically induced ; Double-Blind Method ; Epidemiology ; Estrogen Replacement Therapy - adverse effects ; Estrogens ; Ethics committees ; Experimentation ; Female ; Fractures ; Fractures, Bone - chemically induced ; General aspects ; Hormone replacement therapy ; Humans ; Medical research ; Medical sciences ; Menopause ; Middle Aged ; Osteoporosis ; Osteoporosis - chemically induced ; Placebos ; Postmenopausal women ; Postmenopause ; Public health. Hygiene ; Public health. Hygiene-occupational medicine ; Quality of Life ; Risk Factors ; Treatment Outcome ; Wisdom ; Womens health</subject><ispartof>BMJ, 2007-08, Vol.335 (7613), p.239-244</ispartof><rights>BMJ Publishing Group Ltd 2007</rights><rights>2007 BMJ Publishing Group Ltd</rights><rights>2007 INIST-CNRS</rights><rights>Copyright: 2007 (c) BMJ Publishing Group Ltd 2007</rights><rights>Copyright BMJ Publishing Group Aug 4, 2007</rights><rights>BMJ Publishing Group Ltd 2007 2007 BMJ Publishing Group Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b650t-a397ec35753350971535f3f9b7ecd442b8a6612646c9a3327e0c246f9e16b3573</citedby><cites>FETCH-LOGICAL-b650t-a397ec35753350971535f3f9b7ecd442b8a6612646c9a3327e0c246f9e16b3573</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttp://bmj.com/content/335/7613/239.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://bmj.com/content/335/7613/239.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,230,314,776,780,799,881,3183,23550,27901,27902,30976,30977,57992,58225,77343,77374</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=18961982$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17626056$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vickers, Madge R</creatorcontrib><creatorcontrib>MacLennan, Alastair H</creatorcontrib><creatorcontrib>Lawton, Beverley</creatorcontrib><creatorcontrib>Ford, Deborah</creatorcontrib><creatorcontrib>Martin, Jeannett</creatorcontrib><creatorcontrib>Meredith, Sarah K</creatorcontrib><creatorcontrib>DeStavola, Bianca L</creatorcontrib><creatorcontrib>Rose, Sally</creatorcontrib><creatorcontrib>Dowell, Anthony</creatorcontrib><creatorcontrib>Wilkes, Helen C</creatorcontrib><creatorcontrib>Darbyshire, Janet H</creatorcontrib><creatorcontrib>Meade, Tom W</creatorcontrib><creatorcontrib>WISDOM group</creatorcontrib><title>Main morbidities recorded in the women's international study of long duration oestrogen after menopause (WISDOM): a randomised controlled trial of hormone replacement therapy in postmenopausal women</title><title>BMJ</title><addtitle>BMJ</addtitle><description>Objective To assess the long term risks and benefits of hormone replacement therapy (combined hormone therapy versus placebo, and oestrogen alone versus combined hormone therapy). Design Multicentre, randomised, placebo controlled, double blind trial. Setting General practices in UK (384), Australia (91), and New Zealand (24). Participants Postmenopausal women aged 50-69 years at randomisation. At early closure of the trial, 56 583 had been screened, 8980 entered run-in, and 5692 (26% of target of 22 300) started treatment. Interventions Oestrogen only therapy (conjugated equine oestrogens 0.625 mg orally daily) or combined hormone therapy (conjugated equine oestrogens plus medroxyprogesterone acetate 2.5/5.0 mg orally daily). Ten years of treatment planned. Main outcome measures Primary outcomes: major cardiovascular disease, osteoporotic fractures, and breast cancer. Secondary outcomes: other cancers, death from all causes, venous thromboembolism, cerebrovascular disease, dementia, and quality of life. Results The trial was prematurely closed during recruitment, after a median follow-up of 11.9 months (interquartile range 7.1-19.6, total 6498 women years) in those enrolled, after the publication of early results from the women's health initiative study. The mean age of randomised women was 62.8 (SD 4.8) years. When combined hormone therapy (n=2196) was compared with placebo (n=2189), there was a significant increase in the number of major cardiovascular events (7 v 0, P=0.016) and venous thromboembolisms (22 v 3, hazard ratio 7.36 (95% CI 2.20 to 24.60)). There were no statistically significant differences in numbers of breast or other cancers (22 v 25, hazard ratio 0.88 (0.49 to 1.56)), cerebrovascular events (14 v 19, 0.73 (0.37 to 1.46)), fractures (40 v 58, 0.69 (0.46 to 1.03)), and overall deaths (8 v 5, 1.60 (0.52 to 4.89)). Comparison of combined hormone therapy (n=815) versus oestrogen therapy (n=826) outcomes revealed no significant differences. Conclusions Hormone replacement therapy increases cardiovascular and thromboembolic risk when started many years after the menopause. The results are consistent with the findings of the women's health initiative study and secondary prevention studies. Research is needed to assess the long term risks and benefits of starting hormone replacement therapy near the menopause, when the effect may be different. Trial registration Current Controlled Trials ISRCTN 63718836</description><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - chemically induced</subject><subject>Cardiovascular diseases</subject><subject>Cardiovascular Diseases - chemically induced</subject><subject>Double-Blind Method</subject><subject>Epidemiology</subject><subject>Estrogen Replacement Therapy - adverse effects</subject><subject>Estrogens</subject><subject>Ethics committees</subject><subject>Experimentation</subject><subject>Female</subject><subject>Fractures</subject><subject>Fractures, Bone - chemically induced</subject><subject>General aspects</subject><subject>Hormone replacement therapy</subject><subject>Humans</subject><subject>Medical research</subject><subject>Medical sciences</subject><subject>Menopause</subject><subject>Middle Aged</subject><subject>Osteoporosis</subject><subject>Osteoporosis - chemically induced</subject><subject>Placebos</subject><subject>Postmenopausal women</subject><subject>Postmenopause</subject><subject>Public health. Hygiene</subject><subject>Public health. 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Hygiene</topic><topic>Public health. Hygiene-occupational medicine</topic><topic>Quality of Life</topic><topic>Risk Factors</topic><topic>Treatment Outcome</topic><topic>Wisdom</topic><topic>Womens health</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vickers, Madge R</creatorcontrib><creatorcontrib>MacLennan, Alastair H</creatorcontrib><creatorcontrib>Lawton, Beverley</creatorcontrib><creatorcontrib>Ford, Deborah</creatorcontrib><creatorcontrib>Martin, Jeannett</creatorcontrib><creatorcontrib>Meredith, Sarah K</creatorcontrib><creatorcontrib>DeStavola, Bianca L</creatorcontrib><creatorcontrib>Rose, Sally</creatorcontrib><creatorcontrib>Dowell, Anthony</creatorcontrib><creatorcontrib>Wilkes, Helen C</creatorcontrib><creatorcontrib>Darbyshire, Janet H</creatorcontrib><creatorcontrib>Meade, Tom W</creatorcontrib><creatorcontrib>WISDOM group</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><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>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science 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>British Nursing Index</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>British Nursing Index (BNI) (1985 to Present)</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>SciTech Premium Collection</collection><collection>British Nursing Index</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</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>Applied Social Sciences Index &amp; Abstracts (ASSIA)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMJ</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vickers, Madge R</au><au>MacLennan, Alastair H</au><au>Lawton, Beverley</au><au>Ford, Deborah</au><au>Martin, Jeannett</au><au>Meredith, Sarah K</au><au>DeStavola, Bianca L</au><au>Rose, Sally</au><au>Dowell, Anthony</au><au>Wilkes, Helen C</au><au>Darbyshire, Janet H</au><au>Meade, Tom W</au><aucorp>WISDOM group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Main morbidities recorded in the women's international study of long duration oestrogen after menopause (WISDOM): a randomised controlled trial of hormone replacement therapy in postmenopausal women</atitle><jtitle>BMJ</jtitle><addtitle>BMJ</addtitle><date>2007-08-04</date><risdate>2007</risdate><volume>335</volume><issue>7613</issue><spage>239</spage><epage>244</epage><pages>239-244</pages><issn>0959-8138</issn><issn>0959-8146</issn><issn>0959-535X</issn><eissn>1468-5833</eissn><eissn>1756-1833</eissn><coden>BMJOAE</coden><abstract>Objective To assess the long term risks and benefits of hormone replacement therapy (combined hormone therapy versus placebo, and oestrogen alone versus combined hormone therapy). Design Multicentre, randomised, placebo controlled, double blind trial. Setting General practices in UK (384), Australia (91), and New Zealand (24). Participants Postmenopausal women aged 50-69 years at randomisation. At early closure of the trial, 56 583 had been screened, 8980 entered run-in, and 5692 (26% of target of 22 300) started treatment. Interventions Oestrogen only therapy (conjugated equine oestrogens 0.625 mg orally daily) or combined hormone therapy (conjugated equine oestrogens plus medroxyprogesterone acetate 2.5/5.0 mg orally daily). Ten years of treatment planned. Main outcome measures Primary outcomes: major cardiovascular disease, osteoporotic fractures, and breast cancer. Secondary outcomes: other cancers, death from all causes, venous thromboembolism, cerebrovascular disease, dementia, and quality of life. Results The trial was prematurely closed during recruitment, after a median follow-up of 11.9 months (interquartile range 7.1-19.6, total 6498 women years) in those enrolled, after the publication of early results from the women's health initiative study. The mean age of randomised women was 62.8 (SD 4.8) years. When combined hormone therapy (n=2196) was compared with placebo (n=2189), there was a significant increase in the number of major cardiovascular events (7 v 0, P=0.016) and venous thromboembolisms (22 v 3, hazard ratio 7.36 (95% CI 2.20 to 24.60)). There were no statistically significant differences in numbers of breast or other cancers (22 v 25, hazard ratio 0.88 (0.49 to 1.56)), cerebrovascular events (14 v 19, 0.73 (0.37 to 1.46)), fractures (40 v 58, 0.69 (0.46 to 1.03)), and overall deaths (8 v 5, 1.60 (0.52 to 4.89)). Comparison of combined hormone therapy (n=815) versus oestrogen therapy (n=826) outcomes revealed no significant differences. Conclusions Hormone replacement therapy increases cardiovascular and thromboembolic risk when started many years after the menopause. The results are consistent with the findings of the women's health initiative study and secondary prevention studies. Research is needed to assess the long term risks and benefits of starting hormone replacement therapy near the menopause, when the effect may be different. Trial registration Current Controlled Trials ISRCTN 63718836</abstract><cop>London</cop><pub>British Medical Journal Publishing Group</pub><pmid>17626056</pmid><doi>10.1136/bmj.39266.425069.AD</doi><tpages>6</tpages><edition>International edition</edition><oa>free_for_read</oa></addata></record>
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identifier ISSN: 0959-8138
ispartof BMJ, 2007-08, Vol.335 (7613), p.239-244
issn 0959-8138
0959-8146
0959-535X
1468-5833
1756-1833
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1939792
source Applied Social Sciences Index & Abstracts (ASSIA); Jstor Complete Legacy; MEDLINE; BMJ Journals - NESLi2; Alma/SFX Local Collection
subjects Aged
Biological and medical sciences
Breast cancer
Breast Neoplasms - chemically induced
Cardiovascular diseases
Cardiovascular Diseases - chemically induced
Double-Blind Method
Epidemiology
Estrogen Replacement Therapy - adverse effects
Estrogens
Ethics committees
Experimentation
Female
Fractures
Fractures, Bone - chemically induced
General aspects
Hormone replacement therapy
Humans
Medical research
Medical sciences
Menopause
Middle Aged
Osteoporosis
Osteoporosis - chemically induced
Placebos
Postmenopausal women
Postmenopause
Public health. Hygiene
Public health. Hygiene-occupational medicine
Quality of Life
Risk Factors
Treatment Outcome
Wisdom
Womens health
title Main morbidities recorded in the women's international study of long duration oestrogen after menopause (WISDOM): a randomised controlled trial of hormone replacement therapy in postmenopausal women
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