Cecily A Byrne, Sage J Kim, Greg Kopetsky, Evgenia Karayeva, Vanessa M Oddo
{"title":"在我们所有人的研究计划中,癌症幸存者的食物不安全和炎症的临床生物标志物。","authors":"Cecily A Byrne, Sage J Kim, Greg Kopetsky, Evgenia Karayeva, Vanessa M Oddo","doi":"10.1158/1055-9965.EPI-24-1757","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Food insecurity is associated with a 40% increase in the prevalence of chronic conditions, including cancer. Stress-evoked inflammation is a hypothesized mechanism driving these associations. This study tested the association between food insecurity and inflammation in cancer survivors.</p><p><strong>Methods: </strong>Our sample included individuals with a history of lung, breast, prostate, and colorectal cancer from the All of Us Research Program. Food insecurity was measured using validated questions, and inflammatory biomarkers were obtained from electronic health records (EHR). Our primary analysis tested the association between food insecurity and c-reactive protein (CRP; n=413) using multivariable regression models, controlling for sociodemographics and current cancer treatment.</p><p><strong>Results: </strong>The primary cohort was 69.8 ± 9.5 years in age, 61.0% female, 89.3% non-Hispanic White, and 9.9% had food insecurity. A higher proportion of racial/ethnic minorities (40.8%) and individuals with lower annual household income (33.3%) and education (29.4%) had food insecurity. Mean CRP was higher among those with food insecurity (14.5 ± 18.5) than food secure individuals (10.4 ± 17.8), but it was not significantly associated with CRP in our fully adjusted models.</p><p><strong>Conclusion: </strong>Lung, breast, prostate, and colorectal cancer survivors had moderate levels of inflammation measured by CRP; however, food insecurity was not associated with CRP in fully adjusted models.</p><p><strong>Impact: </strong>In this cohort, there was no association between food insecurity and CRP; however, given that food insecurity and inflammation are plausible contributors to chronic disease, future studies should include underrepresented survivors with EHR data and a broader range of cancers.</p>","PeriodicalId":9458,"journal":{"name":"Cancer Epidemiology Biomarkers & Prevention","volume":" ","pages":""},"PeriodicalIF":3.7000,"publicationDate":"2025-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Food Insecurity and Clinical Biomarkers of Inflammation among Cancer Survivors in the All of Us Research Program.\",\"authors\":\"Cecily A Byrne, Sage J Kim, Greg Kopetsky, Evgenia Karayeva, Vanessa M Oddo\",\"doi\":\"10.1158/1055-9965.EPI-24-1757\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Food insecurity is associated with a 40% increase in the prevalence of chronic conditions, including cancer. Stress-evoked inflammation is a hypothesized mechanism driving these associations. This study tested the association between food insecurity and inflammation in cancer survivors.</p><p><strong>Methods: </strong>Our sample included individuals with a history of lung, breast, prostate, and colorectal cancer from the All of Us Research Program. Food insecurity was measured using validated questions, and inflammatory biomarkers were obtained from electronic health records (EHR). Our primary analysis tested the association between food insecurity and c-reactive protein (CRP; n=413) using multivariable regression models, controlling for sociodemographics and current cancer treatment.</p><p><strong>Results: </strong>The primary cohort was 69.8 ± 9.5 years in age, 61.0% female, 89.3% non-Hispanic White, and 9.9% had food insecurity. A higher proportion of racial/ethnic minorities (40.8%) and individuals with lower annual household income (33.3%) and education (29.4%) had food insecurity. Mean CRP was higher among those with food insecurity (14.5 ± 18.5) than food secure individuals (10.4 ± 17.8), but it was not significantly associated with CRP in our fully adjusted models.</p><p><strong>Conclusion: </strong>Lung, breast, prostate, and colorectal cancer survivors had moderate levels of inflammation measured by CRP; however, food insecurity was not associated with CRP in fully adjusted models.</p><p><strong>Impact: </strong>In this cohort, there was no association between food insecurity and CRP; however, given that food insecurity and inflammation are plausible contributors to chronic disease, future studies should include underrepresented survivors with EHR data and a broader range of cancers.</p>\",\"PeriodicalId\":9458,\"journal\":{\"name\":\"Cancer Epidemiology Biomarkers & Prevention\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2025-05-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cancer Epidemiology Biomarkers & Prevention\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1158/1055-9965.EPI-24-1757\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cancer Epidemiology Biomarkers & Prevention","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1158/1055-9965.EPI-24-1757","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ONCOLOGY","Score":null,"Total":0}
Food Insecurity and Clinical Biomarkers of Inflammation among Cancer Survivors in the All of Us Research Program.
Background: Food insecurity is associated with a 40% increase in the prevalence of chronic conditions, including cancer. Stress-evoked inflammation is a hypothesized mechanism driving these associations. This study tested the association between food insecurity and inflammation in cancer survivors.
Methods: Our sample included individuals with a history of lung, breast, prostate, and colorectal cancer from the All of Us Research Program. Food insecurity was measured using validated questions, and inflammatory biomarkers were obtained from electronic health records (EHR). Our primary analysis tested the association between food insecurity and c-reactive protein (CRP; n=413) using multivariable regression models, controlling for sociodemographics and current cancer treatment.
Results: The primary cohort was 69.8 ± 9.5 years in age, 61.0% female, 89.3% non-Hispanic White, and 9.9% had food insecurity. A higher proportion of racial/ethnic minorities (40.8%) and individuals with lower annual household income (33.3%) and education (29.4%) had food insecurity. Mean CRP was higher among those with food insecurity (14.5 ± 18.5) than food secure individuals (10.4 ± 17.8), but it was not significantly associated with CRP in our fully adjusted models.
Conclusion: Lung, breast, prostate, and colorectal cancer survivors had moderate levels of inflammation measured by CRP; however, food insecurity was not associated with CRP in fully adjusted models.
Impact: In this cohort, there was no association between food insecurity and CRP; however, given that food insecurity and inflammation are plausible contributors to chronic disease, future studies should include underrepresented survivors with EHR data and a broader range of cancers.
期刊介绍:
Cancer Epidemiology, Biomarkers & Prevention publishes original peer-reviewed, population-based research on cancer etiology, prevention, surveillance, and survivorship. The following topics are of special interest: descriptive, analytical, and molecular epidemiology; biomarkers including assay development, validation, and application; chemoprevention and other types of prevention research in the context of descriptive and observational studies; the role of behavioral factors in cancer etiology and prevention; survivorship studies; risk factors; implementation science and cancer care delivery; and the science of cancer health disparities. Besides welcoming manuscripts that address individual subjects in any of the relevant disciplines, CEBP editors encourage the submission of manuscripts with a transdisciplinary approach.