Serum 25-hydroxyvitamin D and risk of post-menopausal breast cancer--results of a large case-control study.

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Serum 25-hydroxyvitamin D and risk of post-menopausal breast cancer--results of a large case-control study. / Abbas, Sascha; Linseisen, Jakob; Slanger, Tracy; Kropp, Silke; Mutschelknauss, Elke; Flesch-Janys, Dieter; Chang-Claude, Jenny.

In: CARCINOGENESIS, Vol. 29, No. 1, 1, 2008, p. 93-99.

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@article{151c235840be4197a647e35cc4cdb6f2,
title = "Serum 25-hydroxyvitamin D and risk of post-menopausal breast cancer--results of a large case-control study.",
abstract = "Various studies suggest that vitamin D may reduce breast cancer risk. Most studies assessed the effects of dietary intake only, although endogenous production is an important source of vitamin D. Therefore, the measurement of serum 25-hydroxyvitamin D [25(OH)D] better indicates overall vitamin D status. To assess the association of 25(OH)D serum concentrations with post-menopausal breast cancer risk, we used a population-based case-control study in Germany, which recruited incident breast cancer patients aged 50-74 between 2002 and 2005. Information on sociodemographic and breast cancer risk factors was collected by personal interview. For this analysis, we included 1394 cases and 1365 controls, matched on year of birth and time of blood collection. Conditional logistic regression was used to calculate odds ratios (ORs) for breast cancer adjusted for potential confounders. Serum 25(OH)D concentration was significantly inversely associated with post-menopausal breast cancer risk. Compared with the lowest category (/=75 nM) were 0.57 (0.45-0.73), 0.49 (0.38-0.64), 0.43 (0.32-0.57) and 0.31 (0.24-0.42), respectively (P(trend) <0.0001). Analysis using fractional polynomials indicated a non-linear association. The association was stronger in women never using menopausal hormone therapy (HT) compared with past and current users (P(interaction) <0.0001). Our findings strongly suggest a protective effect for post-menopausal breast cancer through a better vitamin D supply as characterized by serum 25(OH)D measurement, with a stronger inverse association in women with low serum 25(OH)D concentrations (",
author = "Sascha Abbas and Jakob Linseisen and Tracy Slanger and Silke Kropp and Elke Mutschelknauss and Dieter Flesch-Janys and Jenny Chang-Claude",
year = "2008",
language = "Deutsch",
volume = "29",
pages = "93--99",
journal = "CARCINOGENESIS",
issn = "0143-3334",
publisher = "Oxford University Press",
number = "1",

}

RIS

TY - JOUR

T1 - Serum 25-hydroxyvitamin D and risk of post-menopausal breast cancer--results of a large case-control study.

AU - Abbas, Sascha

AU - Linseisen, Jakob

AU - Slanger, Tracy

AU - Kropp, Silke

AU - Mutschelknauss, Elke

AU - Flesch-Janys, Dieter

AU - Chang-Claude, Jenny

PY - 2008

Y1 - 2008

N2 - Various studies suggest that vitamin D may reduce breast cancer risk. Most studies assessed the effects of dietary intake only, although endogenous production is an important source of vitamin D. Therefore, the measurement of serum 25-hydroxyvitamin D [25(OH)D] better indicates overall vitamin D status. To assess the association of 25(OH)D serum concentrations with post-menopausal breast cancer risk, we used a population-based case-control study in Germany, which recruited incident breast cancer patients aged 50-74 between 2002 and 2005. Information on sociodemographic and breast cancer risk factors was collected by personal interview. For this analysis, we included 1394 cases and 1365 controls, matched on year of birth and time of blood collection. Conditional logistic regression was used to calculate odds ratios (ORs) for breast cancer adjusted for potential confounders. Serum 25(OH)D concentration was significantly inversely associated with post-menopausal breast cancer risk. Compared with the lowest category (/=75 nM) were 0.57 (0.45-0.73), 0.49 (0.38-0.64), 0.43 (0.32-0.57) and 0.31 (0.24-0.42), respectively (P(trend) <0.0001). Analysis using fractional polynomials indicated a non-linear association. The association was stronger in women never using menopausal hormone therapy (HT) compared with past and current users (P(interaction) <0.0001). Our findings strongly suggest a protective effect for post-menopausal breast cancer through a better vitamin D supply as characterized by serum 25(OH)D measurement, with a stronger inverse association in women with low serum 25(OH)D concentrations (

AB - Various studies suggest that vitamin D may reduce breast cancer risk. Most studies assessed the effects of dietary intake only, although endogenous production is an important source of vitamin D. Therefore, the measurement of serum 25-hydroxyvitamin D [25(OH)D] better indicates overall vitamin D status. To assess the association of 25(OH)D serum concentrations with post-menopausal breast cancer risk, we used a population-based case-control study in Germany, which recruited incident breast cancer patients aged 50-74 between 2002 and 2005. Information on sociodemographic and breast cancer risk factors was collected by personal interview. For this analysis, we included 1394 cases and 1365 controls, matched on year of birth and time of blood collection. Conditional logistic regression was used to calculate odds ratios (ORs) for breast cancer adjusted for potential confounders. Serum 25(OH)D concentration was significantly inversely associated with post-menopausal breast cancer risk. Compared with the lowest category (/=75 nM) were 0.57 (0.45-0.73), 0.49 (0.38-0.64), 0.43 (0.32-0.57) and 0.31 (0.24-0.42), respectively (P(trend) <0.0001). Analysis using fractional polynomials indicated a non-linear association. The association was stronger in women never using menopausal hormone therapy (HT) compared with past and current users (P(interaction) <0.0001). Our findings strongly suggest a protective effect for post-menopausal breast cancer through a better vitamin D supply as characterized by serum 25(OH)D measurement, with a stronger inverse association in women with low serum 25(OH)D concentrations (

M3 - SCORING: Zeitschriftenaufsatz

VL - 29

SP - 93

EP - 99

JO - CARCINOGENESIS

JF - CARCINOGENESIS

SN - 0143-3334

IS - 1

M1 - 1

ER -