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1
Serum vitamin D and risk of prostate cancer in a case-control analysis nested within the European Prospective Investigation into Cancer and Nutrition (EPIC).在欧洲癌症与营养前瞻性调查(EPIC)中的一项病例对照分析中,血清维生素D与前列腺癌风险的关系
Am J Epidemiol. 2009 May 15;169(10):1223-32. doi: 10.1093/aje/kwp022. Epub 2009 Apr 9.
2
Serum 25-hydroxyvitamin D status of the US population: 1988-1994 compared with 2000-2004.美国人群血清25-羟维生素D状况:1988 - 1994年与2000 - 2004年的比较
Am J Clin Nutr. 2008 Dec;88(6):1519-27. doi: 10.3945/ajcn.2008.26182.
3
Circulating fatty acids and prostate cancer risk in a nested case-control study: the Multiethnic Cohort.巢式病例对照研究中循环脂肪酸与前列腺癌风险:多民族队列研究
Cancer Causes Control. 2009 Mar;20(2):211-23. doi: 10.1007/s10552-008-9236-4. Epub 2008 Sep 27.
4
Assessing the vitamin D status of the US population.评估美国人群的维生素D状况。
Am J Clin Nutr. 2008 Aug;88(2):558S-564S. doi: 10.1093/ajcn/88.2.558S.
5
Serum vitamin D concentration and prostate cancer risk: a nested case-control study.血清维生素D浓度与前列腺癌风险:一项巢式病例对照研究。
J Natl Cancer Inst. 2008 Jun 4;100(11):796-804. doi: 10.1093/jnci/djn152. Epub 2008 May 27.
6
Blood biomarkers of vitamin D status.维生素D状态的血液生物标志物。
Am J Clin Nutr. 2008 Apr;87(4):1087S-91S. doi: 10.1093/ajcn/87.4.1087S.
7
Lack of association between serum levels of 25-hydroxyvitamin D and the subsequent risk of prostate cancer in Finnish men.芬兰男性血清25-羟基维生素D水平与前列腺癌后续发病风险之间无关联。
Cancer Epidemiol Biomarkers Prev. 2007 Dec;16(12):2784-6. doi: 10.1158/1055-9965.EPI-07-0672.
8
Vitamin D deficiency.维生素D缺乏症
N Engl J Med. 2007 Jul 19;357(3):266-81. doi: 10.1056/NEJMra070553.
9
Vitamin D receptor (VDR) gene polymorphisms and haplotypes, interactions with plasma 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D, and prostate cancer risk.维生素D受体(VDR)基因多态性与单倍型、与血浆25-羟基维生素D和1,25-二羟基维生素D的相互作用以及前列腺癌风险
Prostate. 2007 Jun 15;67(9):911-23. doi: 10.1002/pros.20570.
10
UV, latitude, and spatial trends in prostate cancer mortality: all sunlight is not the same (United States).紫外线、纬度与前列腺癌死亡率的空间趋势:并非所有阳光都一样(美国)
Cancer Causes Control. 2006 Oct;17(8):1091-101. doi: 10.1007/s10552-006-0050-6.

血浆 25-羟维生素 D 与前列腺癌风险:多民族队列研究。

Plasma 25-hydroxyvitamin D and prostate cancer risk: the multiethnic cohort.

机构信息

Epidemiology Program, Cancer Research Center of Hawaii, University of Hawaii, 1236 Lauhala Street, Honolulu, HI 96813, USA.

出版信息

Eur J Cancer. 2010 Mar;46(5):932-6. doi: 10.1016/j.ejca.2009.12.030. Epub 2010 Feb 8.

DOI:10.1016/j.ejca.2009.12.030
PMID:20064705
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2834847/
Abstract

The purpose of this study was to examine the relationship of plasma 25-hydroxyvitamin D (25(OH)D) concentrations to prostate cancer within a large multiethnic cohort in Hawaii and California using a nested case-control design. The study included 329 incidents of prostate cancer of African American, Native Hawaiian, Japanese, Latino and White ancestry, and 656 controls matched on age, race/ethnicity, date/time of blood collection and fasting status. Conditional logistic regression was used to estimate odds ratios (ORs) and 95% confidence intervals (95% CI). No association with prostate cancer risk was found in an analysis based on quartiles of 25(OH)D. When clinically defined cutpoints were used, there was no increased risk for the lowest 25(OH)D concentration (OR for <20 versus 30-<50ng/ml=1.10, 95% CI=0.68-1.78), while there was a suggestive increased risk for higher concentrations (OR for 50ng/ml=1.52, 95% CI=0.92-2.51). The findings from this prospective study of men in the Multiethnic Cohort do not support the hypothesis that vitamin D lowers the risk of prostate cancer. Further follow-up is warranted to determine whether the findings are consistent across ethnic groups.

摘要

本研究旨在通过巢式病例对照设计,在夏威夷和加利福尼亚的大型多民族队列中,研究血浆 25-羟维生素 D(25(OH)D)浓度与前列腺癌之间的关系。该研究包括 329 例非裔美国人、夏威夷原住民、日本裔、拉丁裔和白人后裔的前列腺癌病例,以及 656 例按年龄、种族/民族、采血日期/时间和禁食状态匹配的对照。条件逻辑回归用于估计比值比(OR)和 95%置信区间(95%CI)。基于 25(OH)D 的四分位数分析,未发现与前列腺癌风险相关。当使用临床定义的切点时,最低 25(OH)D 浓度(<20 与 30-<50ng/ml 相比的 OR=1.10,95%CI=0.68-1.78)没有增加风险,而较高浓度(50ng/ml 的 OR=1.52,95%CI=0.92-2.51)则提示有增加的风险。这项对多民族队列中男性进行的前瞻性研究的结果不支持维生素 D 降低前列腺癌风险的假设。需要进一步随访以确定这些发现是否在不同种族群体中一致。