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Family cancer history and pedigrees as a public health intervention for promoting health and preventing prostate cancer in African-Americans.

机译:家庭癌症史和血统书作为一种公共卫生干预措施,旨在促进非裔美国人的健康和预防前列腺癌。

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摘要

Prostate cancer is the most common cancer diagnosed in men and the second leading cause of cancer death among men in the United States. African-American men have substantially higher prostate cancer incidence and mortality than European-American men. It is unclear whether this incidence is due to acquired DNA changes (sporadic cancer) or if germline Mendelian genetics/genomics (inherited cancer) is the source of this health disparity. To explore this cause, the focus of this dissertation paper is family health history and hereditary prostate cancer. A family history tool is the most commonly used predictive instrument for hereditary prostate cancer. The identification of men with hereditary prostate cancer allows healthcare providers to identify high-risk relatives who are more likely to benefit from targeted health promotion and cancer prevention programs. Use of non-validated family history tools may prevent healthcare providers from collecting information needed to identify hereditary prostate cancer and ascertaining accurate risk assessment in unaffected African-American men. This pilot study was conducted to validate the effectiveness of a family cancer history tool and pedigree analysis in the identification of hereditary prostate cancer in a community based sample of African-American men. While small sample size limited the power of the analysis, the family history tool and pedigree analysis appears to have analytical validity as a public health instrument for identifying hereditary prostate cancer. Twenty-two percent (11 of 49) of consultands reported a personal history of prostate cancer with one hereditary prostate cancer family observed. Age was significantly related to a personal history of prostate cancer (p= 0.05) but other known predictors of prostate cancer were statistically undetectable. The pilot study demonstrated that though the family cancer history tool appears to have clinical validity a larger sample is needed to prove clinical validity. Additional research is needed to examine analytical validity, clinical utility and ethical, legal and social issues surrounding the use of family cancer history and pedigree analysis as a public health intervention for addressing the health disparity of prostate cancer in African-American men.
机译:前列腺癌是男性中最常见的癌症,在美国男性中,其是导致癌症死亡的第二大原因。非裔美国人的男性前列腺癌的发病率和死亡率远高于欧美男性。目前尚不清楚该发病率是由于获得性DNA改变(散发性癌症)还是由于孟德尔遗传学/基因组学(遗传性癌症)是这种健康差异的根源。为了探究这一原因,本论文的重点是家族健康史和遗传性前列腺癌。家族史工具是遗传性前列腺癌最常用的预测工具。患有遗传性前列腺癌的男性的识别使医疗保健提供者可以识别出更有可能从针对性的健康促进和癌症预防计划中受益的高风险亲戚。使用未经验证的家族史工具可能会阻止医疗保健提供者收集识别遗传性前列腺癌所需的信息,并确定未受影响的非裔美国人的准确风险评估。进行了该初步研究,以验证家族癌症史工具和血统分析在基于社区的非洲裔美国人样本中识别遗传性前列腺癌中的有效性。虽然小样本量限制了分析的能力,但家族史工具和血统分析似乎具有分析性,可作为鉴定遗传性前列腺癌的公共卫生工具。 22%的被咨询者(49名中的11名)报告了前列腺癌的个人病史,并观察到一个遗传性前列腺癌家族。年龄与前列腺癌的个人病史显着相关(p = 0.05),但其他已知的前列腺癌预测因子在统计学上不可检测。初步研究表明,尽管家族癌症史工具似乎具有临床有效性,但仍需要更大的样本量来证明临床有效性。还需要进行其他研究,以检验围绕家族癌症史和血统分析作为治疗非裔美国人男性前列腺癌健康差异的公共卫生干预措施的分析有效性,临床效用以及伦理,法律和社会问题。

著录项

  • 作者

    Wharton, Holisa Coleman.;

  • 作者单位

    Clemson University.;

  • 授予单位 Clemson University.;
  • 学科 Genetics.;Oncology.;African American studies.;Nursing.;Health sciences.
  • 学位 Ph.D.
  • 年度 2012
  • 页码 130 p.
  • 总页数 130
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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