非洲裔美国人雄激素受体基因CAG重复序列长度与前列腺癌风险相关性的缺失

Timothy Gilligan , Judith Manola , Oliver Sartor , Sally P. Weinrich , Judd W. Moul , Philip W. Kantoff
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引用次数: 39

摘要

较短的雄激素受体基因CAG重复长度与前列腺癌风险增加、发病年龄较早和疾病进展较晚有关。比较不同人群中CAG重复序列长度分布的研究报道,前列腺癌发病率较高的种族群体CAG重复序列长度也较短。我们评估了路易斯安那州、南卡罗来纳州和哥伦比亚特区参加前列腺癌筛查的685名黑人男性的CAG重复序列长度,将118名诊断为前列腺癌的男性与567名血清前列腺特异性抗原水平正常且直肠指检无癌症证据的男性进行比较。病例CAG重复长度中位数为21,对照组为19 (P = 0.11)。病例明显大于对照组,中位年龄为68岁,而对照组为54岁(P <0.0001)。在调整年龄后,我们发现前列腺癌风险与CAG重复序列长度没有关联(优势比,1.05;95% ci, 0.98-1.13;P = 0.16)。将CAG重复序列长度分成九段,并计算每段的优势比,结果显示没有特定的重复序列长度范围与前列腺癌风险显著升高或降低有关,但趋势检验显示较长的CAG重复序列长度与前列腺癌风险升高之间存在显著关联(P = 0.02)。分级和分期与CAG重复长度无关。这项研究证实了先前的报道,即黑人男性CAG重复序列长度比白人和亚洲人短。我们没有发现CAG重复数较少的黑人男性患前列腺癌的风险增加。
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Absence of a Correlation of Androgen Receptor Gene CAG Repeat Length and Prostate Cancer Risk in an African-American Population

Shorter androgen receptor gene CAG repeat length has been associated with an increased risk of prostate cancer, an earlier age of onset, and more advanced stage of disease. Studies comparing the distribution of CAG repeat lengths within different populations have reported that racial groups with higher prostate cancer incidence also have shorter CAG repeat lengths. We evaluated CAG repeat length in 685 black men in Louisiana, South Carolina, and the District of Columbia who were participating in prostate cancer screening, comparing the 118 who were diagnosed with prostate cancer with 567 who had normal serum prostate-specific antigen levels and no evidence of cancer on digital rectal examination. The median CAG repeat length was 21 among cases and 19 among controls (P = 0.11). Cases were significantly older than controls, with a median age of 68 years compared with 54 years (P < 0.0001). After adjusting for age, we found no association between prostate cancer risk and CAG repeat length (odds ratio, 1.05; 95% CI, 0.98-1.13; P = 0.16). Dividing CAG repeat lengths into septiles and calculating the odds ratio for each revealed no specific repeat-length range with a significantly elevated or depressed risk of prostate cancer, but a trend test showed a significant association between longer CAG repeat lengths and an elevated risk of prostate cancer (P = 0.02). Neither grade nor stage was associated with CAG repeat length. This study confirms earlier reports that black men have shorter CAG repeat lengths than reported white and Asian populations. We did not find an increased risk of prostate cancer among black men with fewer CAG repeats.

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