Alcohol and cannabis use associated with cardiometabolic biomarkers among "All of Us" cancer survivors.

IF 3.7 3区 医学 Q2 ONCOLOGY
Angel Arizpe, Tiffany M Chapman, Claudia Rodriguez, Alberto Carvajal, Katelyn J Queen, Stephanie Navarro, Carol Y Ochoa-Dominguez, Sue E Kim, Claudia M Toledo-Corral, Albert J Farias
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引用次数: 0

Abstract

Background: Cancer survivors are at increased risk for cardiometabolic comorbidities following cancer treatment which may be further exacerbated by cannabis and alcohol use. We aimed to examine the direct relationships of cannabis, alcohol, and the co-use of both substances with cardiometabolic risk factors and to explore disparities by race/ethnicity and sex.

Methods: Cross-sectional data were extracted from adult cancer survivors in the "All of Us" from 2018-2022. Cannabis use was defined as occasional or frequent/regular cannabis use (vs never) in the past three months and hazardous alcohol intake (AUDIT-C >3 for females, AUDIT-C >4 for males) vs non-hazardous in the past year, respectively. Co-use was defined as participants who engaged in regular cannabis and hazardous alcohol intake. We identified binary cardiovascular, immune, and metabolic systems biomarkers, with high values defined by clinically established cutoffs or >75th percentile. We used multivariable logistic regression adjusting for socio-demographic and clinical factors.

Results: In our sample (N=7,054), 7.6% were Hispanic, 6.2% were Black, and 86.2% were White cancer survivors. Less than 5% of Hispanic and White survivors reported substance co-use compared to 7% of Black survivors. Compared to never users, co-users were 1.58(95% CI=1.14-2.19) more likely to have high blood pressure. No significant associations were found between co-use and immune biomarkers or sex differences.

Conclusion: Co-use of cannabis and hazardous alcohol may worsen high blood pressure in survivors, who are at higher risk for cardiometabolic comorbidities.

Impact: The study investigates substance use and cardiometabolic biomarkers, urging more research on their effects on cancer survivors.

酒精和大麻的使用与 "我们所有人 "癌症幸存者的心脏代谢生物标志物有关。
背景:癌症幸存者在接受癌症治疗后出现心脏代谢合并症的风险增加,而使用大麻和酒精可能会进一步加剧这种风险。我们旨在研究大麻、酒精以及同时使用这两种物质与心脏代谢风险因素之间的直接关系,并探讨不同种族/民族和性别之间的差异:从 2018-2022 年 "我们所有人 "的成年癌症幸存者中提取横截面数据。大麻使用分别定义为过去三个月偶尔或经常/定期使用大麻(vs 从未),以及过去一年有害酒精摄入量(女性 AUDIT-C >3,男性 AUDIT-C >4)vs 非有害酒精摄入量。共同使用被定义为经常吸食大麻和摄入有害酒精的参与者。我们确定了二元心血管、免疫和代谢系统生物标志物,高值由临床确定的临界值或大于 75 百分位数定义。我们使用多变量逻辑回归法对社会人口学和临床因素进行了调整:在我们的样本(N=7054)中,7.6% 为西班牙裔癌症幸存者,6.2% 为黑人癌症幸存者,86.2% 为白人癌症幸存者。在西班牙裔和白人癌症幸存者中,共同使用药物的比例不到 5%,而在黑人癌症幸存者中,这一比例为 7%。与从不使用药物者相比,共同使用药物者患高血压的几率要高出 1.58(95% CI=1.14-2.19)。在共同使用与免疫生物标志物或性别差异之间没有发现明显的关联:结论:共同使用大麻和有害酒精可能会加重幸存者的高血压,而幸存者患心脏代谢合并症的风险较高:该研究对药物使用和心脏代谢生物标志物进行了调查,敦促对它们对癌症幸存者的影响开展更多研究。
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来源期刊
Cancer Epidemiology Biomarkers & Prevention
Cancer Epidemiology Biomarkers & Prevention 医学-公共卫生、环境卫生与职业卫生
CiteScore
6.50
自引率
2.60%
发文量
538
审稿时长
1.6 months
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.
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