Nishimoto Inês Nobuko, Pinheiro Nidia A, Rogatto Silvia R, Carvalho André Lopes, de Moura Ricardo Pereira, Caballero Otavia L, Simpson Andrew, Kowalski Luiz Paulo
Department of Head and Neck Surgery and Otorhinolaryngology, Centro de Tratamento e Pesquisa Hospital do Câncer A. C. Camargo, São Paulo, Brazil.
Arch Otolaryngol Head Neck Surg. 2004 Jan;130(1):78-82. doi: 10.1001/archotol.130.1.78.
To assess alcohol dehydrogenase 3 (ADH3) polymorphism at position Ile349Val as indicator of risk factor for upper aerodigestive tract (UADT) cancer to verify its association with UADT cancer in nonalcoholic or nonsmoking individuals.
Cross-sectional study.
Primary care or referral center.
The study group consisted of 141 consecutive patients with newly diagnosed squamous cell carcinoma of the oral cavity, oropharynx, hypopharynx, or larynx admitted for surgical treatment. The comparison group consisted of 94 inpatients without cancer from the A. C. Camargo or other São Paulo (Brazil) hospital and 40 healthy individuals.
All participants were interviewed and data were collected using a structured questionnaire. After written informed consent was obtained, 20 mL of blood was collected in heparinized tubes.
Odds ratio for ADH3 genotypes using logistic regression models.
After adjustment for sex, age, tobacco use, and history of cancer in first-degree family relatives, a significantly higher odds ratio for UADT cancer was observed among individuals with AA genotype and low cumulative alcohol consumption (< or =100 kg of ethanol) (odds ratio = 3.8 [95% confidence interval, 1.5-9.7]). A 4-fold increase in odds ratio for UADT cancer among individuals with AA genotype and low tobacco consumption (< or =25 pack-years) was also found in the adjusted model.
These results suggest that genotype AA may be a risk factor for UADT cancer, especially in individuals with low alcohol or tobacco consumption. However, further epidemiological case-control or cohort studies, preferably prospective, are needed to establish the exact role of ADH3 polymorphism and its association with the development of UADT cancers.
评估位于Ile349Val位置的乙醇脱氢酶3(ADH3)多态性,作为上呼吸消化道(UADT)癌症危险因素的指标,以验证其与非酒精或非吸烟个体UADT癌症的关联。
横断面研究。
初级保健或转诊中心。
研究组由141例连续收治接受手术治疗的新诊断口腔、口咽、下咽或喉鳞状细胞癌患者组成。对照组由来自A.C.卡马戈或巴西圣保罗其他医院的94例无癌症住院患者和40例健康个体组成。
对所有参与者进行访谈,并使用结构化问卷收集数据。在获得书面知情同意后,用肝素化管采集20毫升血液。
使用逻辑回归模型计算ADH3基因型的比值比。
在对性别、年龄、烟草使用和一级家族亲属癌症病史进行调整后,AA基因型且累积酒精摄入量低(≤100千克乙醇)的个体中,UADT癌症的比值比显著更高(比值比 = 3.8 [95%置信区间,1.5 - 9.7])。在调整模型中还发现,AA基因型且烟草消费量低(≤25包年)的个体中,UADT癌症的比值比增加了4倍。
这些结果表明,基因型AA可能是UADT癌症的危险因素,尤其是在酒精或烟草消费量低的个体中。然而,需要进一步进行流行病学病例对照或队列研究,最好是前瞻性研究,以确定ADH3多态性的确切作用及其与UADT癌症发生的关联。