Solange Parra-Soto PhD, Jirapitcha Boonpor MSc, Nathan Lynskey MSc, Carolina Araya MSc, Frederick Ho PhD, Jill P. Pell PhD, Carlos Celis-Morales PhD
{"title":"英国生物库队列中内脏脂肪指数与癌症风险之间的关系。","authors":"Solange Parra-Soto PhD, Jirapitcha Boonpor MSc, Nathan Lynskey MSc, Carolina Araya MSc, Frederick Ho PhD, Jill P. Pell PhD, Carlos Celis-Morales PhD","doi":"10.1002/cncr.35576","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background</h3>\n \n <p>The visceral adiposity index (VAI) is a marker of visceral fat accumulation and metabolic dysfunction, but there is limited evidence of its association with cancer. The objective of this study was to investigate associations between the VAI and both incident cancer at 23 sites and all-cause cancer.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>In total, 385,477 participants (53.3% women; mean age, 56.3 years) from the UK Biobank prospective cohort were included in this study. The median follow-up was 8.2 years (interquartile range, 7.3–8.9 years). The VAI was calculated using formula the published by Amato et al. and was categorized into sex-specific tertiles. Twenty-four incident cancers were the outcomes. Cox proportional hazard models were adjusted for sociodemographics, lifestyle factors, and multimorbidity counts.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Over the follow-up period, 47,882 individuals developed cancer. In the fully adjusted models, the VAI was associated with a higher risk of six cancer sites. Individuals in the highest tertile, compared with those in the lowest tertile, had higher risks of uterine (hazard ratio [HR], 2.09; 95% confidence interval [CI], 1.76–2.49), gallbladder (HR, 1.83; 95% CI, 1.26–2.66), kidney (HR, 1.39; 95% CI, 1.18–1.64), liver (HR, 1.25; 95% CI, 1.00–1.56), colorectal (HR, 1.14; 95% CI, 1.05–1.24), and breast (HR, 1.11; 95% CI, 1.03–1.19) cancers and of all-cause cancer (HR, 1.05). There was no evidence of a nonlinear association between the VAI and cancer risk.</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>The VAI was associated with six cancer sites and with all-cause cancer. The prognostic and etiologic roles of visceral fat accumulation and dysfunction in cancer warrant further research.</p>\n </section>\n </div>","PeriodicalId":138,"journal":{"name":"Cancer","volume":"131 1","pages":""},"PeriodicalIF":6.1000,"publicationDate":"2024-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11694164/pdf/","citationCount":"0","resultStr":"{\"title\":\"Association between visceral adiposity index and cancer risk in the UK Biobank cohort\",\"authors\":\"Solange Parra-Soto PhD, Jirapitcha Boonpor MSc, Nathan Lynskey MSc, Carolina Araya MSc, Frederick Ho PhD, Jill P. Pell PhD, Carlos Celis-Morales PhD\",\"doi\":\"10.1002/cncr.35576\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background</h3>\\n \\n <p>The visceral adiposity index (VAI) is a marker of visceral fat accumulation and metabolic dysfunction, but there is limited evidence of its association with cancer. The objective of this study was to investigate associations between the VAI and both incident cancer at 23 sites and all-cause cancer.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>In total, 385,477 participants (53.3% women; mean age, 56.3 years) from the UK Biobank prospective cohort were included in this study. The median follow-up was 8.2 years (interquartile range, 7.3–8.9 years). The VAI was calculated using formula the published by Amato et al. and was categorized into sex-specific tertiles. Twenty-four incident cancers were the outcomes. Cox proportional hazard models were adjusted for sociodemographics, lifestyle factors, and multimorbidity counts.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>Over the follow-up period, 47,882 individuals developed cancer. In the fully adjusted models, the VAI was associated with a higher risk of six cancer sites. Individuals in the highest tertile, compared with those in the lowest tertile, had higher risks of uterine (hazard ratio [HR], 2.09; 95% confidence interval [CI], 1.76–2.49), gallbladder (HR, 1.83; 95% CI, 1.26–2.66), kidney (HR, 1.39; 95% CI, 1.18–1.64), liver (HR, 1.25; 95% CI, 1.00–1.56), colorectal (HR, 1.14; 95% CI, 1.05–1.24), and breast (HR, 1.11; 95% CI, 1.03–1.19) cancers and of all-cause cancer (HR, 1.05). There was no evidence of a nonlinear association between the VAI and cancer risk.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusions</h3>\\n \\n <p>The VAI was associated with six cancer sites and with all-cause cancer. 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Association between visceral adiposity index and cancer risk in the UK Biobank cohort
Background
The visceral adiposity index (VAI) is a marker of visceral fat accumulation and metabolic dysfunction, but there is limited evidence of its association with cancer. The objective of this study was to investigate associations between the VAI and both incident cancer at 23 sites and all-cause cancer.
Methods
In total, 385,477 participants (53.3% women; mean age, 56.3 years) from the UK Biobank prospective cohort were included in this study. The median follow-up was 8.2 years (interquartile range, 7.3–8.9 years). The VAI was calculated using formula the published by Amato et al. and was categorized into sex-specific tertiles. Twenty-four incident cancers were the outcomes. Cox proportional hazard models were adjusted for sociodemographics, lifestyle factors, and multimorbidity counts.
Results
Over the follow-up period, 47,882 individuals developed cancer. In the fully adjusted models, the VAI was associated with a higher risk of six cancer sites. Individuals in the highest tertile, compared with those in the lowest tertile, had higher risks of uterine (hazard ratio [HR], 2.09; 95% confidence interval [CI], 1.76–2.49), gallbladder (HR, 1.83; 95% CI, 1.26–2.66), kidney (HR, 1.39; 95% CI, 1.18–1.64), liver (HR, 1.25; 95% CI, 1.00–1.56), colorectal (HR, 1.14; 95% CI, 1.05–1.24), and breast (HR, 1.11; 95% CI, 1.03–1.19) cancers and of all-cause cancer (HR, 1.05). There was no evidence of a nonlinear association between the VAI and cancer risk.
Conclusions
The VAI was associated with six cancer sites and with all-cause cancer. The prognostic and etiologic roles of visceral fat accumulation and dysfunction in cancer warrant further research.
期刊介绍:
The CANCER site is a full-text, electronic implementation of CANCER, an Interdisciplinary International Journal of the American Cancer Society, and CANCER CYTOPATHOLOGY, a Journal of the American Cancer Society.
CANCER publishes interdisciplinary oncologic information according to, but not limited to, the following disease sites and disciplines: blood/bone marrow; breast disease; endocrine disorders; epidemiology; gastrointestinal tract; genitourinary disease; gynecologic oncology; head and neck disease; hepatobiliary tract; integrated medicine; lung disease; medical oncology; neuro-oncology; pathology radiation oncology; translational research