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基于林县发育异常营养干预试验(NIT)队列的上消化道癌家族史与上消化道癌死亡风险之间的关联

The Association Between Family History of Upper Gastrointestinal Cancer and the Risk of Death from Upper Gastrointestinal Cancer-based on Linxian Dysplasia Nutrition Intervention Trial (NIT) Cohort.

作者信息

Sun Wan-Yi, Yang Huan, Wang Xiao-Kun, Fan Jin-Hu, Qiao You-Lin, Taylor Philip R

机构信息

Department of Cancer Epidemiology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

Metabolic Epidemiology Branch, Division of Cancer Epidemiology & Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, United States.

出版信息

Front Oncol. 2022 Jun 8;12:897534. doi: 10.3389/fonc.2022.897534. eCollection 2022.

Abstract

OBJECTIVE

Explore the influence of family history of upper gastrointestinal (UGI) cancer on UGI cancer death, based on the Linxian Dysplasia Nutrition Intervention Trial (NIT) cohort.

METHODS

Family history of UGI cancer was defined as at least one first-degree relative (parent, child, or sibling) had a history of esophageal or gastric cancer. Cancer death was carried out by ICD-10 code. Family history information was collected at baseline and cancer deaths were assessed at each annual follow-up. The COX proportional risk model was used to estimate the hazard ratio (HR) and 95% confidence interval (95% CI). We compared the positive family history group with the negative to determine the risk of family history on UGI cancer death. The effect of category of relatives, number of relatives with UGI cancer, and diagnosis age of relatives on the UGI death risk were further analyzed. Interaction and stratification analyses were done to see the subgroup effects. Sensitivity analyses were also conducted by exclusion of individuals who were followed up less than three years. We considered controlling of covariates including: gender, age (continuity), community, education level, number of siblings (continuity), BMI (continuity), smoking, alcohol use, fresh fruit intake, fresh vegetable intake, hot beverage intake, edible oil intake, meat intake, and moldy staple food intake. All food intake variables were converted into categorical variables.

RESULTS

From1985 to2015, we followed up total 3,318 individuals with 898 UGI cancer deaths (537 from ESCC, 77 from GNCC, and 284 from GCC). In a single factor analysis, family history of UGI cancer increased the risk of death of esophageal squamous cell carcinoma (ESCC) by 27% (HR=1.270, 95%CI1.072-1.504). No associations were observed in gastric cardia carcinoma (GCC) and gastric non-cardia carcinoma (GNCC). After adjusting for multi-factor, a family history of UGI cancer risk of death increased by 31.9% from ESCC (HR=1.319,95%CI:1.110-1.567). Subgroup analysis of different types of relatives with UGI cancers, UGI cancers in the mother (HR=1.457,95%CI:1.200-1.768), brother (HR=1.522,95%CI:1.117-2.073), and sister (HR=1.999,95%CI:1.419-2.817) were independent risk factors for ESCC death, while the father was not. In addition, 2 relatives with UGI cancer (HR=1.495, 95%, CI:1.110-2.013) and ≥3 relatives with UGI cancer (HR=2.836, 95%CI:1.842-4.367) significantly increased the risk of ESCC death, and the trend test was statistically significant (P<0.001). Relatives' diagnostic age of 51-60 years (HR=1.322, 95%CI:1.046-1.672) and 41-50 years (HR=1.442, 95%CI:1.078-1.930) were the risk factors for ESCC death, with statistical significance in the trend test (P=0.010). No statistically significant result of the family history effect on the risk of death from GCC or GNCC was found. Sensitivity analysis of 80% of subjects, randomly selected, did not change the results.

CONCLUSION

A family history of UGI cancer may predict the risk of death from ESCC but not from GCC or GNCC. UGI cancer in the mother may predict the risk of death from ESCC, but not father, which indicates gender differences. Gender and smoking are the interaction items with family history in a similar extent. In the subgroup, the risk of ESCC death is more distinct by family history in younger, female, and better-lifestyle individuals, which indicates the unique role of genetic factors.

摘要

目的

基于林县发育异常营养干预试验(NIT)队列,探讨上消化道(UGI)癌家族史对上消化道癌死亡的影响。

方法

上消化道癌家族史定义为至少有一位一级亲属(父母、子女或兄弟姐妹)有食管癌或胃癌病史。癌症死亡情况通过国际疾病分类第十版(ICD - 10)编码确定。家族史信息在基线时收集,每年随访时评估癌症死亡情况。采用COX比例风险模型估计风险比(HR)和95%置信区间(95%CI)。我们将阳性家族史组与阴性家族史组进行比较,以确定家族史对上消化道癌死亡的风险。进一步分析亲属类别、患有上消化道癌的亲属数量以及亲属的诊断年龄对上消化道癌死亡风险的影响。进行交互作用和分层分析以观察亚组效应。还通过排除随访时间少于三年的个体进行敏感性分析。我们考虑控制协变量,包括:性别、年龄(连续性变量)、社区、教育水平、兄弟姐妹数量(连续性变量)、体重指数(BMI,连续性变量)、吸烟、饮酒、新鲜水果摄入量、新鲜蔬菜摄入量、热饮摄入量、食用油摄入量、肉类摄入量和霉变主食摄入量。所有食物摄入量变量均转换为分类变量。

结果

1985年至2015年,我们共随访了3318名个体,其中898例上消化道癌死亡(537例来自食管鳞状细胞癌(ESCC),77例来自贲门癌(GNCC),284例来自胃非贲门癌(GCC))。在单因素分析中,上消化道癌家族史使食管鳞状细胞癌(ESCC)死亡风险增加27%(HR = 1.270,95%CI 1.072 - 1.504)。在贲门癌(GCC)和胃非贲门癌(GNCC)中未观察到关联。多因素调整后,上消化道癌家族史使ESCC死亡风险增加31.9%(HR = 1.319,95%CI:1.110 - 1.567)。对上消化道癌不同类型亲属的亚组分析显示,母亲患UGI癌(HR = 1.457,95%CI:1.200 - 1.768)、兄弟患UGI癌(HR = 1.522,95%CI:1.117 - 2.073)和姐妹患UGI癌(HR = 1.999,95%CI:1.419 - 2.817)是ESCC死亡的独立危险因素,而父亲患UGI癌不是。此外,有2名亲属患UGI癌(HR = 1.495,95%,CI:1.110 - 2.013)和≥3名亲属患UGI癌(HR = 2.836,95%CI:1.842 - 4.367)显著增加了ESCC死亡风险,趋势检验具有统计学意义(P < 0.001)。亲属诊断年龄在51 - 60岁(HR = 1.322,95%CI:1.046 - 1.672)和41 - 50岁(HR = 1.442,95%CI:1.078 - 1.930)是ESCC死亡的危险因素,趋势检验具有统计学意义(P = 0.010)。未发现家族史对GCC或GNCC死亡风险影响的统计学显著结果。对随机选择的80%受试者进行的敏感性分析未改变结果。

结论

上消化道癌家族史可能预测ESCC死亡风险,但不能预测GCC或GNCC死亡风险。母亲患UGI癌可能预测ESCC死亡风险,但父亲患UGI癌则不能,这表明存在性别差异。性别和吸烟与家族史在相似程度上存在交互作用。在亚组中,ESCC死亡风险在年轻、女性和生活方式较好的个体中受家族史影响更为明显,这表明遗传因素的独特作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22b0/9213690/800007b2be46/fonc-12-897534-g001.jpg

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