Cargando…

Can Biomarkers Identify Women at Increased Stroke Risk? The Women's Health Initiative Hormone Trials

OBJECTIVE: The Women's Health Initiative hormone trials identified a 44% increase in ischemic stroke risk with combination estrogen plus progestin and a 39% increase with estrogen alone. We undertook a case-control biomarker study to elucidate underlying mechanisms, and to potentially identify...

Descripción completa

Detalles Bibliográficos
Autores principales: Kooperberg, Charles, Cushman, Mary, Hsia, Judith, Robinson, Jennifer G, Aragaki, Aaron K, Lynch, John K, Baird, Alison E, Johnson, Karen C, Kuller, Lewis H, Beresford, Shirley A. A, Rodriguez, Beatriz
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1891725/
https://www.ncbi.nlm.nih.gov/pubmed/17571161
http://dx.doi.org/10.1371/journal.pctr.0020028
_version_ 1782133785647644672
author Kooperberg, Charles
Cushman, Mary
Hsia, Judith
Robinson, Jennifer G
Aragaki, Aaron K
Lynch, John K
Baird, Alison E
Johnson, Karen C
Kuller, Lewis H
Beresford, Shirley A. A
Rodriguez, Beatriz
author_facet Kooperberg, Charles
Cushman, Mary
Hsia, Judith
Robinson, Jennifer G
Aragaki, Aaron K
Lynch, John K
Baird, Alison E
Johnson, Karen C
Kuller, Lewis H
Beresford, Shirley A. A
Rodriguez, Beatriz
author_sort Kooperberg, Charles
collection PubMed
description OBJECTIVE: The Women's Health Initiative hormone trials identified a 44% increase in ischemic stroke risk with combination estrogen plus progestin and a 39% increase with estrogen alone. We undertook a case-control biomarker study to elucidate underlying mechanisms, and to potentially identify women who would be at lower or higher risk for stroke with postmenopausal hormone therapy (HT). DESIGN: The hormone trials were randomized, double-blind, and placebo controlled. SETTING: The Women's Health Initiative trials were conducted at 40 clinical centers in the United States. PARTICIPANTS: The trials enrolled 27,347 postmenopausal women, aged 50–79 y. INTERVENTIONS: We randomized 16,608 women with intact uterus to conjugated estrogens 0.625 mg with medroxyprogesterone acetate 2.5 mg daily or placebo, and 10,739 women with prior hysterectomy to conjugated estrogens 0.625 mg daily or placebo. OUTCOME MEASURES: Stroke was ascertained during 5.6 y of follow-up in the estrogen plus progestin trial and 6.8 y of follow-up in the estrogen alone trial. RESULTS: No baseline clinical characteristics, including gene polymorphisms, identified women for whom the stroke risk from HT was higher. Paradoxically, women with higher baseline levels of some stroke-associated biomarkers had a lower risk of stroke when assigned to estrogen plus progestin compared to placebo. For example, those with higher IL-6 were not at increased stroke risk when assigned to estrogen plus progestin (odds ratio 1.28) but were when assigned to placebo (odds ratio 3.47; p for difference = 0.02). Similar findings occurred for high baseline PAP, leukocyte count, and D-dimer. However, only an interaction of D-dimer during follow-up interaction with HT and stroke was marginally significant (p = 0.03). CONCLUSIONS: Biomarkers did not identify women at higher stroke risk with postmenopausal HT. Some biomarkers appeared to identify women at lower stroke risk with estrogen plus progestin, but these findings may be due to chance.
format Text
id pubmed-1891725
institution National Center for Biotechnology Information
language English
publishDate 2007
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-18917252007-06-14 Can Biomarkers Identify Women at Increased Stroke Risk? The Women's Health Initiative Hormone Trials Kooperberg, Charles Cushman, Mary Hsia, Judith Robinson, Jennifer G Aragaki, Aaron K Lynch, John K Baird, Alison E Johnson, Karen C Kuller, Lewis H Beresford, Shirley A. A Rodriguez, Beatriz PLoS Clin Trials Research Article OBJECTIVE: The Women's Health Initiative hormone trials identified a 44% increase in ischemic stroke risk with combination estrogen plus progestin and a 39% increase with estrogen alone. We undertook a case-control biomarker study to elucidate underlying mechanisms, and to potentially identify women who would be at lower or higher risk for stroke with postmenopausal hormone therapy (HT). DESIGN: The hormone trials were randomized, double-blind, and placebo controlled. SETTING: The Women's Health Initiative trials were conducted at 40 clinical centers in the United States. PARTICIPANTS: The trials enrolled 27,347 postmenopausal women, aged 50–79 y. INTERVENTIONS: We randomized 16,608 women with intact uterus to conjugated estrogens 0.625 mg with medroxyprogesterone acetate 2.5 mg daily or placebo, and 10,739 women with prior hysterectomy to conjugated estrogens 0.625 mg daily or placebo. OUTCOME MEASURES: Stroke was ascertained during 5.6 y of follow-up in the estrogen plus progestin trial and 6.8 y of follow-up in the estrogen alone trial. RESULTS: No baseline clinical characteristics, including gene polymorphisms, identified women for whom the stroke risk from HT was higher. Paradoxically, women with higher baseline levels of some stroke-associated biomarkers had a lower risk of stroke when assigned to estrogen plus progestin compared to placebo. For example, those with higher IL-6 were not at increased stroke risk when assigned to estrogen plus progestin (odds ratio 1.28) but were when assigned to placebo (odds ratio 3.47; p for difference = 0.02). Similar findings occurred for high baseline PAP, leukocyte count, and D-dimer. However, only an interaction of D-dimer during follow-up interaction with HT and stroke was marginally significant (p = 0.03). CONCLUSIONS: Biomarkers did not identify women at higher stroke risk with postmenopausal HT. Some biomarkers appeared to identify women at lower stroke risk with estrogen plus progestin, but these findings may be due to chance. Public Library of Science 2007-06-15 /pmc/articles/PMC1891725/ /pubmed/17571161 http://dx.doi.org/10.1371/journal.pctr.0020028 Text en This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Kooperberg, Charles
Cushman, Mary
Hsia, Judith
Robinson, Jennifer G
Aragaki, Aaron K
Lynch, John K
Baird, Alison E
Johnson, Karen C
Kuller, Lewis H
Beresford, Shirley A. A
Rodriguez, Beatriz
Can Biomarkers Identify Women at Increased Stroke Risk? The Women's Health Initiative Hormone Trials
title Can Biomarkers Identify Women at Increased Stroke Risk? The Women's Health Initiative Hormone Trials
title_full Can Biomarkers Identify Women at Increased Stroke Risk? The Women's Health Initiative Hormone Trials
title_fullStr Can Biomarkers Identify Women at Increased Stroke Risk? The Women's Health Initiative Hormone Trials
title_full_unstemmed Can Biomarkers Identify Women at Increased Stroke Risk? The Women's Health Initiative Hormone Trials
title_short Can Biomarkers Identify Women at Increased Stroke Risk? The Women's Health Initiative Hormone Trials
title_sort can biomarkers identify women at increased stroke risk? the women's health initiative hormone trials
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1891725/
https://www.ncbi.nlm.nih.gov/pubmed/17571161
http://dx.doi.org/10.1371/journal.pctr.0020028
work_keys_str_mv AT kooperbergcharles canbiomarkersidentifywomenatincreasedstrokeriskthewomenshealthinitiativehormonetrials
AT cushmanmary canbiomarkersidentifywomenatincreasedstrokeriskthewomenshealthinitiativehormonetrials
AT hsiajudith canbiomarkersidentifywomenatincreasedstrokeriskthewomenshealthinitiativehormonetrials
AT robinsonjenniferg canbiomarkersidentifywomenatincreasedstrokeriskthewomenshealthinitiativehormonetrials
AT aragakiaaronk canbiomarkersidentifywomenatincreasedstrokeriskthewomenshealthinitiativehormonetrials
AT lynchjohnk canbiomarkersidentifywomenatincreasedstrokeriskthewomenshealthinitiativehormonetrials
AT bairdalisone canbiomarkersidentifywomenatincreasedstrokeriskthewomenshealthinitiativehormonetrials
AT johnsonkarenc canbiomarkersidentifywomenatincreasedstrokeriskthewomenshealthinitiativehormonetrials
AT kullerlewish canbiomarkersidentifywomenatincreasedstrokeriskthewomenshealthinitiativehormonetrials
AT beresfordshirleyaa canbiomarkersidentifywomenatincreasedstrokeriskthewomenshealthinitiativehormonetrials
AT rodriguezbeatriz canbiomarkersidentifywomenatincreasedstrokeriskthewomenshealthinitiativehormonetrials