State-Level Prevalence of Obesity/overweight and Pancreatic Cancer Incidence in the United States: An Ecological Analysis Using BRFSS, CDC WONDER and ACS for the Year 2021.

IF 2.2 Q4 ONCOLOGY
Sanchit Mehta, Sai Sushrutha Mudupula Vemula, Abdul Aleem, Maria Khakwani, Ahsan Wahab, Karine Tawagi
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引用次数: 0

Abstract

Purpose: While obesity is established as an individual-level risk factor for pancreatic cancer (PC), population-level associations remain unclear. This study examines whether state-level overweight/obesity (O/OV) prevalence corresponds with age-adjusted PC incidence across the United States.

Methods: We conducted an ecological, cross-sectional analysis using 2021 data from the Behavioral Risk Factor Surveillance System (BRFSS) for state-level O/OV prevalence (BMI ≥ 25 kg/m²) and CDC WONDER for age-adjusted incidence rates (AAIR) of PC per 100,000 population. Demographic covariates such as percentage of non-Hispanic Black (NHB) population and population ≥ 65 years old were extracted from American Community Survey (ACS) data. Prevalence of current smokers and diabetes were also extracted from BRFSS. As a descriptive exploratory approach, incidence rate ratios (IRR) were calculated relative to West Virginia (WV) which had the highest O/OV prevalence, 73.6%. For inferential analysis, a univariable ordinary least square (OLS) linear regression was used to determine the association between O/OV prevalence and PC incidence. Multivariable linear regression model was fitted to adjust for prevalence of age ≥ 65, NHB race/ethnicity, current smokers and diabetes prevalence.

Results: Across 50 US jurisdictions, including DC, the mean O/OV prevalence was 67.72%, ranging from 55.4% in DC to 73.6% in WV. Florida was excluded from the complete-case analysis and OLS due to missing BRFSS values for O/OV. Twenty-nine states with O/OV prevalence lower than WV also had lower PC incidence (concordance) whereas 20 states including DC exhibited lower O/OV prevalence yet higher PC incidence (discordance). Univariable OLS model showed no statistically significant association between O/OV and AAIR (slope: -0.035, p = 0.56; R²=0.007). Multivariable OLS well fitted model showed no significant association between O/OV and AAIR. Only Black population proportion was significantly associated with PC incidence across the states.

Conclusions: In this study, state-level O/OV prevalence failed to demonstrate a statistically significant association with PC incidence. Proportion of Black population was significantly associated with increased PC incidence. These findings suggest that population-level PC risk is likely influenced by multiple interacting metabolic, behavioral, sociodemographic, environmental, and healthcare-related factors beyond obesity alone. Further longitudinal and multivariable studies are needed to better delineate the complex relationship between obesity and PC at the population level.

美国各州肥胖/超重患病率和胰腺癌发病率:2021年使用BRFSS、CDC WONDER和ACS进行的生态分析
目的:虽然肥胖已被确定为胰腺癌(PC)的个体水平危险因素,但人群水平的相关性尚不清楚。本研究探讨了美国各州超重/肥胖(O/OV)患病率是否与年龄调整后的PC发病率相对应。方法:我们利用行为风险因素监测系统(BRFSS)的2021年国家级O/OV患病率(BMI≥25 kg/m²)和CDC WONDER的每10万人中PC的年龄调整发病率(AAIR)数据进行了生态横断面分析。从美国社区调查(ACS)数据中提取人口统计学协变量,如非西班牙裔黑人(NHB)人口比例和≥65岁人口比例。从BRFSS中还提取了当前吸烟者和糖尿病的患病率。作为一种描述性的探索性方法,计算了相对于O/OV患病率最高的西弗吉尼亚州(WV)的发病率比(IRR),为73.6%。为了进行推断分析,采用单变量普通最小二乘(OLS)线性回归来确定O/OV患病率与PC发病率之间的关系。拟合多变量线性回归模型,调整年龄≥65岁、NHB种族/民族、当前吸烟者和糖尿病患病率。结果:在包括DC在内的50个美国司法管辖区,O/OV的平均患病率为67.72%,从DC的55.4%到WV的73.6%不等。由于缺少O/OV的BRFSS值,佛罗里达被排除在完整病例分析和OLS之外。29个O/OV患病率低于WV的州PC发病率也较低(一致性),而包括DC在内的20个州O/OV患病率较低,但PC发病率较高(不一致性)。单变量OLS模型显示,O/OV与AAIR之间无统计学意义相关(斜率:-0.035,p = 0.56; R²=0.007)。多变量OLS拟合模型显示,O/OV与AAIR之间无显著相关性。只有黑人人口比例与各州PC发病率显著相关。结论:在本研究中,州级O/OV患病率未能证明与PC发病率有统计学意义的关联。黑人人口比例与PC发病率增加显著相关。这些发现表明,人群水平的PC风险可能受多种相互作用的代谢、行为、社会人口、环境和医疗保健相关因素的影响,而不仅仅是肥胖。需要进一步的纵向和多变量研究来更好地描述人群水平上肥胖和PC之间的复杂关系。
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来源期刊
CiteScore
3.80
自引率
0.00%
发文量
121
期刊介绍: The Journal of Gastrointestinal Cancer is a multidisciplinary medium for the publication of novel research pertaining to cancers arising from the gastrointestinal tract.The journal is dedicated to the most rapid publication possible.The journal publishes papers in all relevant fields, emphasizing those studies that are helpful in understanding and treating cancers affecting the esophagus, stomach, liver, gallbladder and biliary tree, pancreas, small bowel, large bowel, rectum, and anus. In addition, the Journal of Gastrointestinal Cancer publishes basic and translational scientific information from studies providing insight into the etiology and progression of cancers affecting these organs. New insights are provided from diverse areas of research such as studies exploring pre-neoplastic states, risk factors, epidemiology, genetics, preclinical therapeutics, surgery, radiation therapy, novel medical therapeutics, clinical trials, and outcome studies.In addition to reports of original clinical and experimental studies, the journal also publishes: case reports, state-of-the-art reviews on topics of immediate interest or importance; invited articles analyzing particular areas of pancreatic research and knowledge; perspectives in which critical evaluation and conflicting opinions about current topics may be expressed; meeting highlights that summarize important points presented at recent meetings; abstracts of symposia and conferences; book reviews; hypotheses; Letters to the Editors; and other items of special interest, including:Complex Cases in GI Oncology:  This is a new initiative to provide a forum to review and discuss the history and management of complex and involved gastrointestinal oncology cases. The format will be similar to a teaching case conference where a case vignette is presented and is followed by a series of questions and discussion points. A brief reference list supporting the points made in discussion would be expected.
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