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Hyperinsulinemia, abnormal glucose tolerance and subsequent risk of cancer.

机译:高胰岛素血症,异常的葡萄糖耐量和随后的癌症风险。

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摘要

Although many risk factors for cancer have been established, the causes of many cancers remain unexplained and the mechanisms underlying metabolic risk factors, such as physical activity, obesity and diet, are uncertain. It is hypothesized that hyperinsulinemia and associated abnormal glucose tolerance links these metabolic risk factors and may be associated with an increased risk of cancer. Increased insulin levels may lead to increased cancer, particularly colorectal cancer, through a decrease in insulin-like growth factor binding proteins and an increase in insulin-like growth factors. Few studies have examined the joint role of insulin, abnormal glucose tolerance and insulin-like growth-factor binding proteins on development of subsequent cancers. To test this hypothesis two studies were conducted.;The first study was a prospective cohort study using data from the NHANES II Mortality Study, a prospective study of adults examined in the Second National Health and Nutrition Examination Survey (NHANES II) to determine the association of abnormal glucose tolerance and cancer mortality. This analysis focused upon a nationally representative sample of 3,174 adults aged 30--74 years who underwent an oral glucose tolerance test at baseline (1976--1980), whose deaths were identified by searching national mortality files through 1992. These data suggest that in the general U.S. population, impaired glucose tolerance is a strong predictor of cancer mortality, particularly colon cancer.;The second study was a case-control study nested within the CLUE II cohort to determine the association of hyperinsulinemia, IGFBP-1 and subsequent colorectal cancer. CLUE II participants that were diagnosed with colorectal cancer from 1989 to 2001 (n = 173) were matched to 2 controls on age, sex, race, time of last meal and date of blood draw. At baseline, participants provided a blood sample and this stored serum was analyzed for insulin, IGBPP-1, triglycerides, and HDL cholesterol levels. Neither increasing insulin levels nor decreasing IGBP-1 levels were associated with an increased risk of colorectal cancer.;From these studies it can be concluded that impaired glucose tolerance is an independent predictor for cancer mortality, but that it is still uncertain whether this relationship is acting through increased insulin levels and/or decreased IGFBP-1 or another unknown mechanism.
机译:尽管已经确定了许多癌症的危险因素,但许多癌症的原因仍无法解释,而代谢危险因素(例如体力活动,肥胖和饮食)的机制尚不确定。假设高胰岛素血症和相关的异常葡萄糖耐量将这些代谢风险因素联系在一起,并且可能与癌症风险增加有关。胰岛素水平的升高可通过减少胰岛素样生长因子结合蛋白和增加胰岛素样生长因子而导致癌症增加,特别是结直肠癌。很少有研究检查胰岛素,异常葡萄糖耐量和胰岛素样生长因子结合蛋白在随后癌症发展中的联合作用。为了验证这一假设,进行了两项研究。第一项研究是使用NHANES II死亡率研究的数据进行的前瞻性队列研究,NHANES II死亡率研究是在第二次全国健康与营养检查调查(NHANES II)中检查的成年人的前瞻性研究,以确定关联性。糖耐量异常和癌症死亡率。这项分析的重点是全国代表性的3,174名30-74岁成年人,他们在基线时(1976--1980年)接受了口服葡萄糖耐量测试,这些人的死亡是通过搜索1992年以前的国家死亡率档案来确定的。这些数据表明,在美国普通人群中,糖耐量降低是癌症死亡率(特别是结肠癌)的有力预测指标;第二项研究是一项病例对照研究,嵌套在CLUE II队列中,以确定高胰岛素血症,IGFBP-1与随后的大肠癌的相关性。在1989年至2001年期间诊断为大肠癌的CLUE II参与者(n = 173)与年龄,性别,种族,最后进餐时间和抽血日期的两个对照组相匹配。在基线时,参与者提供了血液样本,并对该存储的血清进行了胰岛素,IGBPP-1,甘油三酸酯和HDL胆固醇水平的分析。胰岛素水平的升高或IGBP-1水平的降低均与结直肠癌的风险增加无关。从这些研究可以得出结论,糖耐量降低是癌症死亡率的独立预测因子,但仍不确定这种关系是否通过增加胰岛素水平和/或降低IGFBP-1或其他未知机制发挥作用。

著录项

  • 作者

    Saydah, Sharon Hope.;

  • 作者单位

    The Johns Hopkins University.;

  • 授予单位 The Johns Hopkins University.;
  • 学科 Health Sciences Public Health.
  • 学位 Ph.D.
  • 年度 2002
  • 页码 128 p.
  • 总页数 128
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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