<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>5(11)</volume><submitter>Lee J</submitter><pubmed_abstract>&lt;h4>Importance&lt;/h4>Body mass index (BMI) may affect the 21-gene recurrence score (RS) in patients with ER-positive, ERBB2-negative breast cancer. If high BMI increases genomic risk in ER-positive, ERBB2-negative breast cancer, weight control will become more important.&lt;h4>Objective&lt;/h4>To assess the association between RS and BMI according to age groups and address BMI as a factor associated with high RS.&lt;h4>Design, setting, and participants&lt;/h4>This cohort study included 2295 patients with ER-positive, ERBB2-negative breast cancer who had undergone a multigene assay between March 29, 2010, and December 31, 2020, in 2 hospitals. All of the study patients were Korean women, and the median follow-up period was 45 months (range, 1-40 months). The correlations between continuous RS and BMI were investigated. A high BMI was defined as a body mass index greater than or equal to 25. In the younger age group (age ≤45 years), a high RS was defined as an RS of greater than 20.&lt;h4>Exposures&lt;/h4>Body mass index.&lt;h4>Main outcomes and measures&lt;/h4>The Pearson correlation coefficient was used to estimate the association between RS and BMI. A multivariable binary logistic model was used to identify high RS.&lt;h4>Results&lt;/h4>Among the 2295 women included (mean [SD] age, 49.8 [4.00] years; range, 22-81 years), 776 were aged 45 years or younger; RS and BMI were weakly correlated (correlation coefficient, 0.119; P &lt; .001) in this younger group. Among them, the proportion of patients with an RS greater than 20 was significantly higher in the high BMI group than in the normal BMI group (45.5% [46 of 101] vs 27.3% [184 of 675]; P &lt; .001). In the multivariable analysis, high BMI was an associated factor for high RS (odds ratio, 2.06; 95% CI, 1.28-3.32; P = .003). The 21-gene multigene assay-guided chemotherapy rate was significantly higher in patients with high BMI (30.7% [31 of 101] vs 20.2% [136 of 674]; P = .02).&lt;h4>Conclusions and relevance&lt;/h4>In this cohort study of women aged 45 years or younger, high BMI was associated with higher RS in those with ER-positive, ERBB2-negative breast cancer; further studies are necessary to examine the underlying mechanisms.</pubmed_abstract><journal>JAMA network open</journal><pagination>e2243935</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9706366</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Association of Body Mass Index With 21-Gene Recurrence Score Among Women With Estrogen Receptor-Positive, ERBB2-Negative Breast Cancer.</pubmed_title><pmcid>PMC9706366</pmcid><pubmed_authors>Jeong J</pubmed_authors><pubmed_authors>Bae SJ</pubmed_authors><pubmed_authors>Son BH</pubmed_authors><pubmed_authors>Kim H</pubmed_authors><pubmed_authors>Lee J</pubmed_authors><pubmed_authors>Ahn SH</pubmed_authors><pubmed_authors>Ahn SG</pubmed_authors><pubmed_authors>Ji JH</pubmed_authors><pubmed_authors>Lee SB</pubmed_authors><pubmed_authors>Lee JW</pubmed_authors></additional><is_claimable>false</is_claimable><name>Association of Body Mass Index With 21-Gene Recurrence Score Among Women With Estrogen Receptor-Positive, ERBB2-Negative Breast Cancer.</name><description>&lt;h4>Importance&lt;/h4>Body mass index (BMI) may affect the 21-gene recurrence score (RS) in patients with ER-positive, ERBB2-negative breast cancer. If high BMI increases genomic risk in ER-positive, ERBB2-negative breast cancer, weight control will become more important.&lt;h4>Objective&lt;/h4>To assess the association between RS and BMI according to age groups and address BMI as a factor associated with high RS.&lt;h4>Design, setting, and participants&lt;/h4>This cohort study included 2295 patients with ER-positive, ERBB2-negative breast cancer who had undergone a multigene assay between March 29, 2010, and December 31, 2020, in 2 hospitals. All of the study patients were Korean women, and the median follow-up period was 45 months (range, 1-40 months). The correlations between continuous RS and BMI were investigated. A high BMI was defined as a body mass index greater than or equal to 25. In the younger age group (age ≤45 years), a high RS was defined as an RS of greater than 20.&lt;h4>Exposures&lt;/h4>Body mass index.&lt;h4>Main outcomes and measures&lt;/h4>The Pearson correlation coefficient was used to estimate the association between RS and BMI. A multivariable binary logistic model was used to identify high RS.&lt;h4>Results&lt;/h4>Among the 2295 women included (mean [SD] age, 49.8 [4.00] years; range, 22-81 years), 776 were aged 45 years or younger; RS and BMI were weakly correlated (correlation coefficient, 0.119; P &lt; .001) in this younger group. Among them, the proportion of patients with an RS greater than 20 was significantly higher in the high BMI group than in the normal BMI group (45.5% [46 of 101] vs 27.3% [184 of 675]; P &lt; .001). In the multivariable analysis, high BMI was an associated factor for high RS (odds ratio, 2.06; 95% CI, 1.28-3.32; P = .003). The 21-gene multigene assay-guided chemotherapy rate was significantly higher in patients with high BMI (30.7% [31 of 101] vs 20.2% [136 of 674]; P = .02).&lt;h4>Conclusions and relevance&lt;/h4>In this cohort study of women aged 45 years or younger, high BMI was associated with higher RS in those with ER-positive, ERBB2-negative breast cancer; further studies are necessary to examine the underlying mechanisms.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-29T11:05:28.245Z</modification><creation>2025-04-06T19:50:48.882Z</creation></dates><accession>S-EPMC9706366</accession><cross_references><pubmed>36441548</pubmed><doi>10.1001/jamanetworkopen.2022.43935</doi></cross_references></HashMap>