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Race/ethnicity, genetic ancestry, and breast cancer-related lymphedema in the Pathways Study.

Identifieur interne : 000683 ( PubMed/Checkpoint ); précédent : 000682; suivant : 000684

Race/ethnicity, genetic ancestry, and breast cancer-related lymphedema in the Pathways Study.

Auteurs : Marilyn L. Kwan [États-Unis] ; Song Yao [États-Unis] ; Valerie S. Lee [États-Unis] ; Janise M. Roh [États-Unis] ; Qianqian Zhu [États-Unis] ; Isaac J. Ergas [États-Unis] ; Qian Liu [États-Unis] ; Yali Zhang [États-Unis] ; Susan E. Kutner [États-Unis] ; Charles P. Quesenberry [États-Unis] ; Christine B. Ambrosone [États-Unis] ; Lawrence H. Kushi [États-Unis]

Source :

RBID : pubmed:27449493

Abstract

Breast cancer-related lymphedema (BCRL) is a serious chronic condition after breast cancer (BC) surgery and treatment. It is unclear if BCRL risk varies by race/ethnicity. In a multiethnic prospective cohort study of 2953 BC patients, we examined the association of self-reported BCRL status with self-reported race/ethnicity and estimated genetic ancestry. Hazard ratios (HR) and 95 % confidence intervals (CI) were calculated by multivariable Cox proportional hazards models, with follow-up starting 6 months post-BC diagnosis. Estimates were further stratified by body mass index (BMI). By 48 months of follow-up, 342 (11.6 %) women reported having BCRL. Younger age at BC diagnosis, higher BMI at baseline, and lower physical activity were associated with greater BCRL risk. African American (AA) women had a 2-fold increased risk of BCRL compared with White women (HR = 2.04; 95 % CI 1.35-3.08). African genetic ancestry was also associated with an increased risk (HR = 2.50; 95 % CI 1.43, 4.36). Both risks were attenuated but remained elevated after adjusting for known risk factors and became more pronounced when restricted to the nonobese women (adjusted HR = 2.31 for AA and HR = 3.70 for African ancestry, both p < 0.05). There was also evidence of increased BCRL risk with Hispanic ethnicity in the nonobese women. Nonobese AA women had a higher risk of BCRL than White women, which cannot be fully explained by known risk factors. This is the first large-scale, prospective study demonstrating differences in BCRL risk according to race/ethnicity as assessed by both self-report and genetic ancestry data, with a potential ancestry-obesity interaction.

DOI: 10.1007/s10549-016-3913-x
PubMed: 27449493


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<div type="abstract" xml:lang="en">Breast cancer-related lymphedema (BCRL) is a serious chronic condition after breast cancer (BC) surgery and treatment. It is unclear if BCRL risk varies by race/ethnicity. In a multiethnic prospective cohort study of 2953 BC patients, we examined the association of self-reported BCRL status with self-reported race/ethnicity and estimated genetic ancestry. Hazard ratios (HR) and 95 % confidence intervals (CI) were calculated by multivariable Cox proportional hazards models, with follow-up starting 6 months post-BC diagnosis. Estimates were further stratified by body mass index (BMI). By 48 months of follow-up, 342 (11.6 %) women reported having BCRL. Younger age at BC diagnosis, higher BMI at baseline, and lower physical activity were associated with greater BCRL risk. African American (AA) women had a 2-fold increased risk of BCRL compared with White women (HR = 2.04; 95 % CI 1.35-3.08). African genetic ancestry was also associated with an increased risk (HR = 2.50; 95 % CI 1.43, 4.36). Both risks were attenuated but remained elevated after adjusting for known risk factors and became more pronounced when restricted to the nonobese women (adjusted HR = 2.31 for AA and HR = 3.70 for African ancestry, both p < 0.05). There was also evidence of increased BCRL risk with Hispanic ethnicity in the nonobese women. Nonobese AA women had a higher risk of BCRL than White women, which cannot be fully explained by known risk factors. This is the first large-scale, prospective study demonstrating differences in BCRL risk according to race/ethnicity as assessed by both self-report and genetic ancestry data, with a potential ancestry-obesity interaction.</div>
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<LastName>Ambrosone</LastName>
<ForeName>Christine B</ForeName>
<Initials>CB</Initials>
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<Affiliation>Department of Cancer Prevention and Control, Roswell Park Cancer Institute, Buffalo, 14263, NY, USA.</Affiliation>
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<LastName>Kushi</LastName>
<ForeName>Lawrence H</ForeName>
<Initials>LH</Initials>
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<Affiliation>Division of Research, Kaiser Permanente Northern California, Oakland, CA, 94612, USA.</Affiliation>
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<OtherID Source="NLM">NIHMS805457 [Available on 08/01/17]</OtherID>
<OtherID Source="NLM">PMC5010992 [Available on 08/01/17]</OtherID>
<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="N">Ancestry</Keyword>
<Keyword MajorTopicYN="N">Breast cancer-related lymphedema</Keyword>
<Keyword MajorTopicYN="N">Genetics</Keyword>
<Keyword MajorTopicYN="N">Interaction</Keyword>
<Keyword MajorTopicYN="N">Obesity</Keyword>
<Keyword MajorTopicYN="N">Racial disparity</Keyword>
</KeywordList>
<CoiStatement>Compliance with ethical standards: Conflict of Interest The authors declare that they have no conflict of interest.</CoiStatement>
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<Month>03</Month>
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<PubMedPubDate PubStatus="accepted">
<Year>2016</Year>
<Month>07</Month>
<Day>14</Day>
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<Year>2016</Year>
<Month>7</Month>
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<ArticleId IdType="pubmed">27449493</ArticleId>
<ArticleId IdType="doi">10.1007/s10549-016-3913-x</ArticleId>
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<list>
<country>
<li>États-Unis</li>
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<li>Californie</li>
<li>État de New York</li>
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<name sortKey="Kwan, Marilyn L" sort="Kwan, Marilyn L" uniqKey="Kwan M" first="Marilyn L" last="Kwan">Marilyn L. Kwan</name>
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<name sortKey="Ambrosone, Christine B" sort="Ambrosone, Christine B" uniqKey="Ambrosone C" first="Christine B" last="Ambrosone">Christine B. Ambrosone</name>
<name sortKey="Ergas, Isaac J" sort="Ergas, Isaac J" uniqKey="Ergas I" first="Isaac J" last="Ergas">Isaac J. Ergas</name>
<name sortKey="Kushi, Lawrence H" sort="Kushi, Lawrence H" uniqKey="Kushi L" first="Lawrence H" last="Kushi">Lawrence H. Kushi</name>
<name sortKey="Kutner, Susan E" sort="Kutner, Susan E" uniqKey="Kutner S" first="Susan E" last="Kutner">Susan E. Kutner</name>
<name sortKey="Lee, Valerie S" sort="Lee, Valerie S" uniqKey="Lee V" first="Valerie S" last="Lee">Valerie S. Lee</name>
<name sortKey="Liu, Qian" sort="Liu, Qian" uniqKey="Liu Q" first="Qian" last="Liu">Qian Liu</name>
<name sortKey="Quesenberry, Charles P" sort="Quesenberry, Charles P" uniqKey="Quesenberry C" first="Charles P" last="Quesenberry">Charles P. Quesenberry</name>
<name sortKey="Roh, Janise M" sort="Roh, Janise M" uniqKey="Roh J" first="Janise M" last="Roh">Janise M. Roh</name>
<name sortKey="Yao, Song" sort="Yao, Song" uniqKey="Yao S" first="Song" last="Yao">Song Yao</name>
<name sortKey="Zhang, Yali" sort="Zhang, Yali" uniqKey="Zhang Y" first="Yali" last="Zhang">Yali Zhang</name>
<name sortKey="Zhu, Qianqian" sort="Zhu, Qianqian" uniqKey="Zhu Q" first="Qianqian" last="Zhu">Qianqian Zhu</name>
</country>
</tree>
</affiliations>
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