Study of Prediagnostic Selenium Level in Toenails and the Risk of Advanced Prostate Cancer

Background: In a recent randomized intervention trial, the risk of prostate cancer for men receiving a daily supplement of 200 µg selenium was one third of that for men receiving placebo. By use of a nested case-control design within a prospective study, i.e., the Health Professionals Follow-Up Stud...

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Veröffentlicht in:JNCI : Journal of the National Cancer Institute 1998-08, Vol.90 (16), p.1219-1224
Hauptverfasser: Yoshizawa, Kazuko, Willett, Walter C., Morris, Steven J., Stampfer, Meir J., Spiegelman, Donna, Rimm, Eric B., Giovannucci, Edward
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container_end_page 1224
container_issue 16
container_start_page 1219
container_title JNCI : Journal of the National Cancer Institute
container_volume 90
creator Yoshizawa, Kazuko
Willett, Walter C.
Morris, Steven J.
Stampfer, Meir J.
Spiegelman, Donna
Rimm, Eric B.
Giovannucci, Edward
description Background: In a recent randomized intervention trial, the risk of prostate cancer for men receiving a daily supplement of 200 µg selenium was one third of that for men receiving placebo. By use of a nested case-control design within a prospective study, i.e., the Health Professionals Follow-Up Study, we investigated the association between risk of prostate cancer and prediagnostic level of selenium in toenails, a measure of long-term selenium intake. Methods: In 1986, 51 529 male health professionals aged 40–75 years responded to a mailed questionnaire to form the prospective study. In 1987, 33 737 cohort members provided toenail clippings. In 1988, 1990, 1992, and 1994, follow-up questionnaires were mailed. From 1989 through 1994, 181 new cases of advanced prostate cancer were reported. Case and control subjects were matched by age, smoking status, and month of toenail return. Selenium levels were determined by neutron activation. All P values are twosided. Results: The selenium level in toenails varied substantially among men, with quintile medians ranging from 0.66 to 1.14 µg/g for control subjects. When matched case-control data were analyzed, higher selenium levels were associated with a reduced risk of advanced prostate cancer (odds ratio [OR] for comparison of highest to lowest quintile = 0.49; 95% confidence interval [CI] = 0.25–0.96; P for trend = .11). After additionally controlling for family history of prostate cancer, body mass index, calcium intake, lycopene intake, saturated fat intake, vasectomy, and geographical region, the OR was 0.35 (95% CI = 0.16–0.78; P for trend = .03). Conclusions: Our results support earlier findings that higher selenium intakes may reduce the risk of prostate cancer. Further prospective studies and randomized trials of this relationship should be conducted. [J Natl Cancer Inst 1998;90:1219–24]
doi_str_mv 10.1093/jnci/90.16.1219
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By use of a nested case-control design within a prospective study, i.e., the Health Professionals Follow-Up Study, we investigated the association between risk of prostate cancer and prediagnostic level of selenium in toenails, a measure of long-term selenium intake. Methods: In 1986, 51 529 male health professionals aged 40–75 years responded to a mailed questionnaire to form the prospective study. In 1987, 33 737 cohort members provided toenail clippings. In 1988, 1990, 1992, and 1994, follow-up questionnaires were mailed. From 1989 through 1994, 181 new cases of advanced prostate cancer were reported. Case and control subjects were matched by age, smoking status, and month of toenail return. Selenium levels were determined by neutron activation. All P values are twosided. Results: The selenium level in toenails varied substantially among men, with quintile medians ranging from 0.66 to 1.14 µg/g for control subjects. When matched case-control data were analyzed, higher selenium levels were associated with a reduced risk of advanced prostate cancer (odds ratio [OR] for comparison of highest to lowest quintile = 0.49; 95% confidence interval [CI] = 0.25–0.96; P for trend = .11). After additionally controlling for family history of prostate cancer, body mass index, calcium intake, lycopene intake, saturated fat intake, vasectomy, and geographical region, the OR was 0.35 (95% CI = 0.16–0.78; P for trend = .03). Conclusions: Our results support earlier findings that higher selenium intakes may reduce the risk of prostate cancer. Further prospective studies and randomized trials of this relationship should be conducted. 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By use of a nested case-control design within a prospective study, i.e., the Health Professionals Follow-Up Study, we investigated the association between risk of prostate cancer and prediagnostic level of selenium in toenails, a measure of long-term selenium intake. Methods: In 1986, 51 529 male health professionals aged 40–75 years responded to a mailed questionnaire to form the prospective study. In 1987, 33 737 cohort members provided toenail clippings. In 1988, 1990, 1992, and 1994, follow-up questionnaires were mailed. From 1989 through 1994, 181 new cases of advanced prostate cancer were reported. Case and control subjects were matched by age, smoking status, and month of toenail return. Selenium levels were determined by neutron activation. All P values are twosided. Results: The selenium level in toenails varied substantially among men, with quintile medians ranging from 0.66 to 1.14 µg/g for control subjects. When matched case-control data were analyzed, higher selenium levels were associated with a reduced risk of advanced prostate cancer (odds ratio [OR] for comparison of highest to lowest quintile = 0.49; 95% confidence interval [CI] = 0.25–0.96; P for trend = .11). After additionally controlling for family history of prostate cancer, body mass index, calcium intake, lycopene intake, saturated fat intake, vasectomy, and geographical region, the OR was 0.35 (95% CI = 0.16–0.78; P for trend = .03). Conclusions: Our results support earlier findings that higher selenium intakes may reduce the risk of prostate cancer. Further prospective studies and randomized trials of this relationship should be conducted. [J Natl Cancer Inst 1998;90:1219–24]</description><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Case-Control Studies</subject><subject>Dietary supplements</subject><subject>Humans</subject><subject>Male</subject><subject>Medical research</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>Nails - chemistry</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Odds Ratio</subject><subject>Prostate cancer</subject><subject>Prostatic Neoplasms - chemistry</subject><subject>Prostatic Neoplasms - diagnosis</subject><subject>Risk</subject><subject>Selenium - administration &amp; dosage</subject><subject>Selenium - analysis</subject><subject>Surveys and Questionnaires</subject><subject>Toes</subject><subject>Tumors of the urinary system</subject><subject>Urinary tract. 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By use of a nested case-control design within a prospective study, i.e., the Health Professionals Follow-Up Study, we investigated the association between risk of prostate cancer and prediagnostic level of selenium in toenails, a measure of long-term selenium intake. Methods: In 1986, 51 529 male health professionals aged 40–75 years responded to a mailed questionnaire to form the prospective study. In 1987, 33 737 cohort members provided toenail clippings. In 1988, 1990, 1992, and 1994, follow-up questionnaires were mailed. From 1989 through 1994, 181 new cases of advanced prostate cancer were reported. Case and control subjects were matched by age, smoking status, and month of toenail return. Selenium levels were determined by neutron activation. All P values are twosided. Results: The selenium level in toenails varied substantially among men, with quintile medians ranging from 0.66 to 1.14 µg/g for control subjects. When matched case-control data were analyzed, higher selenium levels were associated with a reduced risk of advanced prostate cancer (odds ratio [OR] for comparison of highest to lowest quintile = 0.49; 95% confidence interval [CI] = 0.25–0.96; P for trend = .11). After additionally controlling for family history of prostate cancer, body mass index, calcium intake, lycopene intake, saturated fat intake, vasectomy, and geographical region, the OR was 0.35 (95% CI = 0.16–0.78; P for trend = .03). Conclusions: Our results support earlier findings that higher selenium intakes may reduce the risk of prostate cancer. Further prospective studies and randomized trials of this relationship should be conducted. [J Natl Cancer Inst 1998;90:1219–24]</abstract><cop>Cary, NC</cop><pub>Oxford University Press</pub><pmid>9719083</pmid><doi>10.1093/jnci/90.16.1219</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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source Oxford University Press Journals All Titles (1996-Current); MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Adult
Aged
Biological and medical sciences
Case-Control Studies
Dietary supplements
Humans
Male
Medical research
Medical sciences
Middle Aged
Multivariate Analysis
Nails - chemistry
Nephrology. Urinary tract diseases
Odds Ratio
Prostate cancer
Prostatic Neoplasms - chemistry
Prostatic Neoplasms - diagnosis
Risk
Selenium - administration & dosage
Selenium - analysis
Surveys and Questionnaires
Toes
Tumors of the urinary system
Urinary tract. Prostate gland
title Study of Prediagnostic Selenium Level in Toenails and the Risk of Advanced Prostate Cancer
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