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社会人口统计学指标与脑肿瘤风险

Sociodemographic indicators and risk of brain tumours.

作者信息

Inskip Peter D, Tarone Robert E, Hatch Elizabeth E, Wilcosky Timothy C, Fine Howard A, Black Peter M, Loeffler Jay S, Shapiro William R, Selker Robert G, Linet Martha S

机构信息

Epidemiology and Biostatistics Program, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Int J Epidemiol. 2003 Apr;32(2):225-33. doi: 10.1093/ije/dyg051.

Abstract

BACKGROUND

To better understand patterns of occurrence or diagnosis of brain tumours in different segments of the population, we evaluated associations between sociodemographic variables and the relative incidence of brain tumours as part of a multi-faceted case-control study.

METHODS

The study was conducted at hospitals in three US cities between 1994 and 1998. In all, 489 glioma cases (354 high-grade, 135 low-grade), 197 meningioma cases, 96 acoustic neuroma cases, and 799 controls admitted to the same hospitals for any of a variety of non-neoplastic diseases or conditions were enrolled and interviewed. Logistic regression was used to estimate odds ratios (OR), calculate 95% CI, and test for trends.

RESULTS

The OR showed significant positive associations with household income for low-grade glioma, meningioma, and acoustic neuroma, but not for high-grade glioma. Positive associations were observed with level of education for low-grade glioma and acoustic neuroma, but not for high-grade glioma or meningioma. Jewish religion was associated with a significantly elevated risk for meningioma (OR = 4.3; 95% CI: 2.0-9.0). Being single at the time of tumour diagnosis or enrolment was associated with significantly reduced risks for meningioma (OR = 0.4; 95% CI: 0.3-0.6) and low- or high-grade glioma (OR = 0.6; 95% CI: 0.5-0.8), but not for acoustic neuroma.

CONCLUSIONS

Associations with sociodemographic variables varied considerably among the different subtypes of brain tumour, including between low-grade and high-grade glioma. The general pattern was for associations with indicators of affluence and education to be stronger for tumours that tend to grow more slowly and have less catastrophic effects, although the evidence was mixed for meningioma. We cannot isolate the specific factors underlying the observed associations, but intrapopulation differences in the completeness or timing of diagnosis may have played a role. There is less opportunity for such influences to operate for the rapidly progressing, high-grade gliomas than for more slowly growing tumours.

摘要

背景

为了更好地了解不同人群中脑肿瘤的发生或诊断模式,作为一项多方面病例对照研究的一部分,我们评估了社会人口统计学变量与脑肿瘤相对发病率之间的关联。

方法

该研究于1994年至1998年在美国三个城市的医院进行。总共招募并访谈了489例胶质瘤患者(354例高级别、135例低级别)、197例脑膜瘤患者、96例听神经瘤患者以及799名因各种非肿瘤性疾病或病症入住同一医院的对照者。采用逻辑回归来估计比值比(OR)、计算95%置信区间(CI)并进行趋势检验。

结果

OR显示,低级别胶质瘤、脑膜瘤和听神经瘤与家庭收入呈显著正相关,但高级别胶质瘤并非如此。低级别胶质瘤和听神经瘤与教育程度呈正相关,但高级别胶质瘤或脑膜瘤并非如此。犹太教与脑膜瘤风险显著升高相关(OR = 4.3;95% CI:2.0 - 9.0)。在肿瘤诊断或入组时单身与脑膜瘤(OR = 0.4;95% CI:0.3 - 0.6)以及低级别或高级别胶质瘤(OR = 0.6;95% CI:0.5 - 0.8)风险显著降低相关,但与听神经瘤无关。

结论

脑肿瘤不同亚型与社会人口统计学变量之间的关联差异很大,包括低级别和高级别胶质瘤之间。总体模式是,对于生长较慢且灾难性影响较小的肿瘤,与富裕和教育指标的关联更强,尽管脑膜瘤的证据不一。我们无法确定所观察到的关联背后的具体因素,但人群内部诊断的完整性或时间差异可能起到了一定作用。对于快速进展的高级别胶质瘤,这种影响发挥作用的机会比生长较慢的肿瘤要少。

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