The Effects of a Remote-based Weight Loss Program on Adipocytokines, Metabolic Markers, and Telomere Length in Breast Cancer Survivors: the POWER-Remote Trial
We initiated a clinical trial to determine the proportion of breast cancer survivors achieving ≥5% weight loss using a remotely delivered weight loss intervention (POWER-remote) or a self-directed approach, and to determine the effects of the intervention on biomarkers of cancer risk including metab...
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creator | Santa-Maria, Cesar A Coughlin, Janelle W Sharma, Dipali Armanios, Mary Blackford, Amanda L Schreyer, Colleen Dalcin, Arlene Carpenter, Ashley Jerome, Gerald J Armstrong, Deborah K Chaudhry, Madhu Cohen, Gary I Connolly, Roisin M Fetting, John Miller, Robert S Smith, Karen L Snyder, Claire Wolfe, Andrew Wolff, Antonio C Huang, Chiung-Yu Appel, Lawrence J Stearns, Vered |
description | We initiated a clinical trial to determine the proportion of breast cancer survivors achieving ≥5% weight loss using a remotely delivered weight loss intervention (POWER-remote) or a self-directed approach, and to determine the effects of the intervention on biomarkers of cancer risk including metabolism, inflammation, and telomere length.
Women with stage 0-III breast cancer, who completed local therapy and chemotherapy, with a body mass index ≥25 kg/m
were randomized to a 12-month intervention (POWER-remote) versus a self-directed approach. The primary objective was to determine the number of women who achieved at least 5% weight loss at 6 months. We assessed baseline and 6-month change in a panel of adipocytokines (adiponectin, leptin, resistin, HGF, NGF, PAI1, TNFα, MCP1, IL1β, IL6, and IL8), metabolic factors (insulin, glucose, lipids, hs-CRP), and telomere length in peripheral blood mononuclear cells.
From 2013 to 2015, 96 women were enrolled, and 87 were evaluable for the primary analysis; 45 to POWER-remote and 42 to self-directed. At 6 months, 51% of women randomized to POWER-remote lost ≥5% of their baseline body weight, compared with 12% in the self-directed arm [OR, 7.9; 95% confidence interval (CI), 2.6-23.9;
= 0.0003]; proportion were similar at 12 months (51% vs 17%, respectively,
= 0.003). Weight loss correlated with significant decreases in leptin, and favorable modulation of inflammatory cytokines and lipid profiles. There was no significant change in telomere length at 6 months.
A remotely delivered weight loss intervention resulted in significant weight loss in breast cancer survivors, and favorable effects on several biomarkers. |
doi_str_mv | 10.1158/1078-0432.CCR-19-2935 |
format | Article |
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Women with stage 0-III breast cancer, who completed local therapy and chemotherapy, with a body mass index ≥25 kg/m
were randomized to a 12-month intervention (POWER-remote) versus a self-directed approach. The primary objective was to determine the number of women who achieved at least 5% weight loss at 6 months. We assessed baseline and 6-month change in a panel of adipocytokines (adiponectin, leptin, resistin, HGF, NGF, PAI1, TNFα, MCP1, IL1β, IL6, and IL8), metabolic factors (insulin, glucose, lipids, hs-CRP), and telomere length in peripheral blood mononuclear cells.
From 2013 to 2015, 96 women were enrolled, and 87 were evaluable for the primary analysis; 45 to POWER-remote and 42 to self-directed. At 6 months, 51% of women randomized to POWER-remote lost ≥5% of their baseline body weight, compared with 12% in the self-directed arm [OR, 7.9; 95% confidence interval (CI), 2.6-23.9;
= 0.0003]; proportion were similar at 12 months (51% vs 17%, respectively,
= 0.003). Weight loss correlated with significant decreases in leptin, and favorable modulation of inflammatory cytokines and lipid profiles. There was no significant change in telomere length at 6 months.
A remotely delivered weight loss intervention resulted in significant weight loss in breast cancer survivors, and favorable effects on several biomarkers.</description><identifier>ISSN: 1078-0432</identifier><identifier>EISSN: 1557-3265</identifier><identifier>DOI: 10.1158/1078-0432.CCR-19-2935</identifier><identifier>PMID: 32071117</identifier><language>eng</language><publisher>United States</publisher><ispartof>Clinical cancer research, 2020-06, Vol.26 (12), p.3024-3034</ispartof><rights>2020 American Association for Cancer Research.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c411t-5b5d76e5b279da863a555dbbdad7530059d828f68d25868a91d7467e79e82ef73</citedby><cites>FETCH-LOGICAL-c411t-5b5d76e5b279da863a555dbbdad7530059d828f68d25868a91d7467e79e82ef73</cites><orcidid>0000-0003-0869-6316 ; 0000-0003-2313-3562 ; 0000-0002-6519-4833 ; 0000-0003-3734-1063 ; 0000-0002-0673-6823 ; 0000-0003-0979-8787 ; 0000-0003-1120-1679</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,3343,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32071117$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Santa-Maria, Cesar A</creatorcontrib><creatorcontrib>Coughlin, Janelle W</creatorcontrib><creatorcontrib>Sharma, Dipali</creatorcontrib><creatorcontrib>Armanios, Mary</creatorcontrib><creatorcontrib>Blackford, Amanda L</creatorcontrib><creatorcontrib>Schreyer, Colleen</creatorcontrib><creatorcontrib>Dalcin, Arlene</creatorcontrib><creatorcontrib>Carpenter, Ashley</creatorcontrib><creatorcontrib>Jerome, Gerald J</creatorcontrib><creatorcontrib>Armstrong, Deborah K</creatorcontrib><creatorcontrib>Chaudhry, Madhu</creatorcontrib><creatorcontrib>Cohen, Gary I</creatorcontrib><creatorcontrib>Connolly, Roisin M</creatorcontrib><creatorcontrib>Fetting, John</creatorcontrib><creatorcontrib>Miller, Robert S</creatorcontrib><creatorcontrib>Smith, Karen L</creatorcontrib><creatorcontrib>Snyder, Claire</creatorcontrib><creatorcontrib>Wolfe, Andrew</creatorcontrib><creatorcontrib>Wolff, Antonio C</creatorcontrib><creatorcontrib>Huang, Chiung-Yu</creatorcontrib><creatorcontrib>Appel, Lawrence J</creatorcontrib><creatorcontrib>Stearns, Vered</creatorcontrib><title>The Effects of a Remote-based Weight Loss Program on Adipocytokines, Metabolic Markers, and Telomere Length in Breast Cancer Survivors: the POWER-Remote Trial</title><title>Clinical cancer research</title><addtitle>Clin Cancer Res</addtitle><description>We initiated a clinical trial to determine the proportion of breast cancer survivors achieving ≥5% weight loss using a remotely delivered weight loss intervention (POWER-remote) or a self-directed approach, and to determine the effects of the intervention on biomarkers of cancer risk including metabolism, inflammation, and telomere length.
Women with stage 0-III breast cancer, who completed local therapy and chemotherapy, with a body mass index ≥25 kg/m
were randomized to a 12-month intervention (POWER-remote) versus a self-directed approach. The primary objective was to determine the number of women who achieved at least 5% weight loss at 6 months. We assessed baseline and 6-month change in a panel of adipocytokines (adiponectin, leptin, resistin, HGF, NGF, PAI1, TNFα, MCP1, IL1β, IL6, and IL8), metabolic factors (insulin, glucose, lipids, hs-CRP), and telomere length in peripheral blood mononuclear cells.
From 2013 to 2015, 96 women were enrolled, and 87 were evaluable for the primary analysis; 45 to POWER-remote and 42 to self-directed. At 6 months, 51% of women randomized to POWER-remote lost ≥5% of their baseline body weight, compared with 12% in the self-directed arm [OR, 7.9; 95% confidence interval (CI), 2.6-23.9;
= 0.0003]; proportion were similar at 12 months (51% vs 17%, respectively,
= 0.003). Weight loss correlated with significant decreases in leptin, and favorable modulation of inflammatory cytokines and lipid profiles. There was no significant change in telomere length at 6 months.
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Coughlin, Janelle W ; Sharma, Dipali ; Armanios, Mary ; Blackford, Amanda L ; Schreyer, Colleen ; Dalcin, Arlene ; Carpenter, Ashley ; Jerome, Gerald J ; Armstrong, Deborah K ; Chaudhry, Madhu ; Cohen, Gary I ; Connolly, Roisin M ; Fetting, John ; Miller, Robert S ; Smith, Karen L ; Snyder, Claire ; Wolfe, Andrew ; Wolff, Antonio C ; Huang, Chiung-Yu ; Appel, Lawrence J ; Stearns, Vered</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c411t-5b5d76e5b279da863a555dbbdad7530059d828f68d25868a91d7467e79e82ef73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Santa-Maria, Cesar A</creatorcontrib><creatorcontrib>Coughlin, Janelle W</creatorcontrib><creatorcontrib>Sharma, Dipali</creatorcontrib><creatorcontrib>Armanios, Mary</creatorcontrib><creatorcontrib>Blackford, Amanda L</creatorcontrib><creatorcontrib>Schreyer, Colleen</creatorcontrib><creatorcontrib>Dalcin, Arlene</creatorcontrib><creatorcontrib>Carpenter, Ashley</creatorcontrib><creatorcontrib>Jerome, Gerald J</creatorcontrib><creatorcontrib>Armstrong, Deborah K</creatorcontrib><creatorcontrib>Chaudhry, Madhu</creatorcontrib><creatorcontrib>Cohen, Gary I</creatorcontrib><creatorcontrib>Connolly, Roisin M</creatorcontrib><creatorcontrib>Fetting, John</creatorcontrib><creatorcontrib>Miller, Robert S</creatorcontrib><creatorcontrib>Smith, Karen L</creatorcontrib><creatorcontrib>Snyder, Claire</creatorcontrib><creatorcontrib>Wolfe, Andrew</creatorcontrib><creatorcontrib>Wolff, Antonio C</creatorcontrib><creatorcontrib>Huang, Chiung-Yu</creatorcontrib><creatorcontrib>Appel, Lawrence J</creatorcontrib><creatorcontrib>Stearns, Vered</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical cancer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Santa-Maria, Cesar A</au><au>Coughlin, Janelle W</au><au>Sharma, Dipali</au><au>Armanios, Mary</au><au>Blackford, Amanda L</au><au>Schreyer, Colleen</au><au>Dalcin, Arlene</au><au>Carpenter, Ashley</au><au>Jerome, Gerald J</au><au>Armstrong, Deborah K</au><au>Chaudhry, Madhu</au><au>Cohen, Gary I</au><au>Connolly, Roisin M</au><au>Fetting, John</au><au>Miller, Robert S</au><au>Smith, Karen L</au><au>Snyder, Claire</au><au>Wolfe, Andrew</au><au>Wolff, Antonio C</au><au>Huang, Chiung-Yu</au><au>Appel, Lawrence J</au><au>Stearns, Vered</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Effects of a Remote-based Weight Loss Program on Adipocytokines, Metabolic Markers, and Telomere Length in Breast Cancer Survivors: the POWER-Remote Trial</atitle><jtitle>Clinical cancer research</jtitle><addtitle>Clin Cancer Res</addtitle><date>2020-06-15</date><risdate>2020</risdate><volume>26</volume><issue>12</issue><spage>3024</spage><epage>3034</epage><pages>3024-3034</pages><issn>1078-0432</issn><eissn>1557-3265</eissn><abstract>We initiated a clinical trial to determine the proportion of breast cancer survivors achieving ≥5% weight loss using a remotely delivered weight loss intervention (POWER-remote) or a self-directed approach, and to determine the effects of the intervention on biomarkers of cancer risk including metabolism, inflammation, and telomere length.
Women with stage 0-III breast cancer, who completed local therapy and chemotherapy, with a body mass index ≥25 kg/m
were randomized to a 12-month intervention (POWER-remote) versus a self-directed approach. The primary objective was to determine the number of women who achieved at least 5% weight loss at 6 months. We assessed baseline and 6-month change in a panel of adipocytokines (adiponectin, leptin, resistin, HGF, NGF, PAI1, TNFα, MCP1, IL1β, IL6, and IL8), metabolic factors (insulin, glucose, lipids, hs-CRP), and telomere length in peripheral blood mononuclear cells.
From 2013 to 2015, 96 women were enrolled, and 87 were evaluable for the primary analysis; 45 to POWER-remote and 42 to self-directed. At 6 months, 51% of women randomized to POWER-remote lost ≥5% of their baseline body weight, compared with 12% in the self-directed arm [OR, 7.9; 95% confidence interval (CI), 2.6-23.9;
= 0.0003]; proportion were similar at 12 months (51% vs 17%, respectively,
= 0.003). Weight loss correlated with significant decreases in leptin, and favorable modulation of inflammatory cytokines and lipid profiles. There was no significant change in telomere length at 6 months.
A remotely delivered weight loss intervention resulted in significant weight loss in breast cancer survivors, and favorable effects on several biomarkers.</abstract><cop>United States</cop><pmid>32071117</pmid><doi>10.1158/1078-0432.CCR-19-2935</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-0869-6316</orcidid><orcidid>https://orcid.org/0000-0003-2313-3562</orcidid><orcidid>https://orcid.org/0000-0002-6519-4833</orcidid><orcidid>https://orcid.org/0000-0003-3734-1063</orcidid><orcidid>https://orcid.org/0000-0002-0673-6823</orcidid><orcidid>https://orcid.org/0000-0003-0979-8787</orcidid><orcidid>https://orcid.org/0000-0003-1120-1679</orcidid><oa>free_for_read</oa></addata></record> |
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source | American Association for Cancer Research; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
title | The Effects of a Remote-based Weight Loss Program on Adipocytokines, Metabolic Markers, and Telomere Length in Breast Cancer Survivors: the POWER-Remote Trial |
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