Associations of Albumin and BMI with Colorectal Cancer Risk in the Southern Community Cohort Study: a Prospective Cohort Study.

IF 3.2 3区 医学 Q2 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Journal of Racial and Ethnic Health Disparities Pub Date : 2024-12-01 Epub Date: 2023-09-21 DOI:10.1007/s40615-023-01797-x
Zoe Walts, Lisa Parlato, Ronni Brent, Qiuyin Cai, Mark Steinwandel, Wei Zheng, Shaneda Warren Andersen
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Abstract

Background: Obesity may increase colorectal cancer (CRC) risk through mechanisms of increased inflammation. Although BMI is the most used adiposity indicator, it may less accurately measure adiposity in Black populations. Herein, we investigate associations between BMI, low albumin as an inflammation biomarker, and CRC risk in a racially diverse cohort.

Methods: Participant data arise from 71,141 participants of the Southern Community Cohort Study, including 724 incident CRC cases. Within the cohort, 69% are Black. Blood serum albumin concentrations, from samples taken at enrollment, were available for 235 cases and 567 controls. Controls matched by age, sex, and race were selected through incidence density sampling. Cox proportional hazards calculated BMI and CRC risk associations (hazard ratios [HRs]; 95% confidence intervals [CIs]. Conditional logistic regression calculated albumin and CRC risk associations (odds ratios [ORs]; 95%CIs).

Results: Underweight, but not overweight or obese, compared to normal BMI was associated with increased CRC risk (HR:1.75, 95%CI:1.00-3.09). Each standard deviation increase of albumin was associated with decreased CRC risk, particularly for those who self-identified as non-Hispanic Black (OR: 0.56, 95%CI:0.34-0.91), or female (OR:0.54, 95%CI:0.30-0.98), but there was no evidence for interaction by these variables (p-interactions > 0.05). Moreover, albumin concentration was lower in Black than White participants. Mediation analysis suggested that the relation between albumin and CRC was not mediated by BMI.

Conclusions: Null associations of overweight/obesity with CRC risk demonstrates limited utility of BMI, especially among Black populations. Low albumin may indicate CRC risk. In Black individuals, albumin may better predict adiposity related risks than BMI.

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南部社区队列研究中白蛋白和BMI与结直肠癌癌症风险的相关性:一项前瞻性队列研究。
背景:肥胖可能通过增加炎症的机制增加癌症(CRC)的风险。尽管BMI是最常用的肥胖指标,但它可能不太准确地衡量黑人人群的肥胖程度。在此,我们在一个种族多样的队列中研究了BMI、作为炎症生物标志物的低白蛋白和CRC风险之间的关系。方法:参与者数据来自71141名南方社区队列研究参与者,包括724例CRC事件。在这一群体中,69%是黑人。235例病例和567例对照组的血清白蛋白浓度来自入组时采集的样本。通过发病率密度抽样选择按年龄、性别和种族匹配的对照组。Cox比例风险计算BMI和CRC风险相关性(风险比[HRs];95%置信区间[CI]。条件logistic回归计算白蛋白和CRC风险关联(比值比[ORs];95%CI)。结果:体重不足,但不超重或肥胖,与正常BMI相比,与CRC风险增加相关(HR:1.75,95%CI:1.00-3.09)。白蛋白的每一个标准差增加都与CRC风险降低相关,特别是对于那些自称为非西班牙裔黑人(OR:0.56,95%CI:0.34-0.91)或女性(OR:0.54,95%CI:0.30-0.98)的人,但没有证据表明这些变量之间存在相互作用(p相互作用 > 0.05)。此外,黑人参与者的白蛋白浓度低于白人参与者。中介分析表明,白蛋白和CRC之间的关系不是由BMI介导的。结论:超重/肥胖与CRC风险的零关联表明BMI的效用有限,尤其是在黑人人群中。低白蛋白可能提示CRC风险。在黑人个体中,白蛋白可能比BMI更好地预测与肥胖相关的风险。
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来源期刊
Journal of Racial and Ethnic Health Disparities
Journal of Racial and Ethnic Health Disparities PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH-
CiteScore
7.30
自引率
5.10%
发文量
263
期刊介绍: Journal of Racial and Ethnic Health Disparities reports on the scholarly progress of work to understand, address, and ultimately eliminate health disparities based on race and ethnicity. Efforts to explore underlying causes of health disparities and to describe interventions that have been undertaken to address racial and ethnic health disparities are featured. Promising studies that are ongoing or studies that have longer term data are welcome, as are studies that serve as lessons for best practices in eliminating health disparities. Original research, systematic reviews, and commentaries presenting the state-of-the-art thinking on problems centered on health disparities will be considered for publication. We particularly encourage review articles that generate innovative and testable ideas, and constructive discussions and/or critiques of health disparities.Because the Journal of Racial and Ethnic Health Disparities receives a large number of submissions, about 30% of submissions to the Journal are sent out for full peer review.
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