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人类白细胞抗原II类DR-DQ与塞内加尔女性宫颈癌风险增加

HLA class II DR-DQ and increased risk of cervical cancer among Senegalese women.

作者信息

Lin P, Koutsky L A, Critchlow C W, Apple R J, Hawes S E, Hughes J P, Touré P, Dembele A, Kiviat N B

机构信息

Department of Epidemiology, University of Washington, Seattle, 98195, USA.

出版信息

Cancer Epidemiol Biomarkers Prev. 2001 Oct;10(10):1037-45.

Abstract

To examine Senegalese women to confirm and extend associations between HLA class II types and cervical cancer previously observed among African-American, Caucasian, Hispanic, and Japanese ethnic populations, 55 Senegalese women with invasive cervical carcinoma were compared with age-matched (human papillomavirus) HPV-positive (n = 83) and HPV-negative (n = 107) control women. PCR-based HPV and HLA typing methods were used. Data were analyzed using a global randomization test and conditional logistic regression. Although this study failed to confirm a previously reported association between cervical cancer and DQB103 alleles, the DRB11101-DQB10301 haplotype was detected more frequently among cervical carcinoma cases than among controls (adjusted odds ratio, 2.6; 95% confidence interval, 1.0-7.1). Furthermore, as reported by others, we observed a negative association of borderline statistical significance between DRB113 and cervical carcinoma (adjusted odds ratio, 0.5; 95% confidence interval, 0.2-1.1). Observations from this study confirm earlier findings of a negative association between DRB113 and cervical cancer and suggest that specific DRB1-DQB1 haplotype combinations, rather than individual DQB103 alleles, increase the risk for cervical cancer.

摘要

为了对塞内加尔女性进行检测,以确认并拓展先前在非裔美国人、高加索人、西班牙裔和日本族裔人群中观察到的HLA II类基因分型与宫颈癌之间的关联,研究人员将55名患有浸润性宫颈癌的塞内加尔女性与年龄匹配的(人乳头瘤病毒)HPV阳性(n = 83)和HPV阴性(n = 107)对照女性进行了比较。采用了基于PCR的HPV和HLA基因分型方法。数据通过全局随机化检验和条件逻辑回归进行分析。尽管本研究未能证实先前报道的宫颈癌与DQB103等位基因之间的关联,但在宫颈癌病例中检测到的DRB11101-DQB10301单倍型比对照组更为频繁(校正比值比,2.6;95%置信区间,1.0 - 7.1)。此外,正如其他人所报道的,我们观察到DRB113与宫颈癌之间存在边缘统计学意义的负相关(校正比值比,0.5;95%置信区间,0.2 - 1.1)。本研究的观察结果证实了DRB113与宫颈癌之间负相关的早期发现,并表明特定的DRB1 - DQB1单倍型组合,而非单个DQB103等位基因,会增加患宫颈癌的风险。

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