Previous studies investigated the role of vitamin D intake and cancer risk. The kidney is a major organ for vitamin D metabolism, activity, and calcium homeostasis; therefore, it was hypothesized that dietary vitamin D intake and polymorphisms in the vitamin D receptor (VDR) gene may modify renal cell carcinoma (RCC) risk. Three common VDR gene polymorphisms (BsmI, FokI, TaqI) were evaluated among 925 RCC cases and 1192 controls enrolled in a hospital-based case-control study conducted in Central and Eastern Europe. Overall associations with RCC risk were not observed; however, subgroup analyses revealed associations after stratification by median age of diagnosis and family history of cancer. Among subjects over 60 yr, reduced risks were observed among carriers of the f alleles in the FokI single-nuceotide polymorphism (SNP) (odds ratio [OR] = 0.61 for Ff and OR = 0.74 for ff genotypes) compared to subjects with the FF genotype (P trend = 0.04; P interaction = 0.004). Subjects with the BB BsmI genotype and a positive family history of cancer had lower risk compared to subjects with the bb allele (OR = 0.60; 95% CI: 0.33-1.1; P trend = 0.05). Genotype associations with these subgroups were not modified when dietary sources of vitamin D or calcium were considered. Additional studies of genetic variation in the VDR gene are warranted. Copyright © Taylor & Francis Group, LLC.

Vitamin D receptor polymorphisms and renal cancer risk in Central and Eastern Europe / Karami, S.; Brennan, P.; Hung, R.J.; Boffetta, P.; Toro, J.; Wilson, R.T.; Zaridze, D.; Navratilova, M.; Chatterjee, N.; Mates, D.; Janout, V.; Kollarova, H.; Bencko, V.; Szeszenia-Dabrowska, N.; Holcatova, I.; Moukeria, A.; Welch, R.; Chanock, S.; Rothman, N.; Chow, W.-H.; Moore, L.E.. - In: JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH. PART A. - ISSN 1528-7394. - ELETTRONICO. - 71:6(2008), pp. 367-372. [10.1080/15287390701798685]

Vitamin D receptor polymorphisms and renal cancer risk in Central and Eastern Europe

Boffetta, P.;
2008

Abstract

Previous studies investigated the role of vitamin D intake and cancer risk. The kidney is a major organ for vitamin D metabolism, activity, and calcium homeostasis; therefore, it was hypothesized that dietary vitamin D intake and polymorphisms in the vitamin D receptor (VDR) gene may modify renal cell carcinoma (RCC) risk. Three common VDR gene polymorphisms (BsmI, FokI, TaqI) were evaluated among 925 RCC cases and 1192 controls enrolled in a hospital-based case-control study conducted in Central and Eastern Europe. Overall associations with RCC risk were not observed; however, subgroup analyses revealed associations after stratification by median age of diagnosis and family history of cancer. Among subjects over 60 yr, reduced risks were observed among carriers of the f alleles in the FokI single-nuceotide polymorphism (SNP) (odds ratio [OR] = 0.61 for Ff and OR = 0.74 for ff genotypes) compared to subjects with the FF genotype (P trend = 0.04; P interaction = 0.004). Subjects with the BB BsmI genotype and a positive family history of cancer had lower risk compared to subjects with the bb allele (OR = 0.60; 95% CI: 0.33-1.1; P trend = 0.05). Genotype associations with these subgroups were not modified when dietary sources of vitamin D or calcium were considered. Additional studies of genetic variation in the VDR gene are warranted. Copyright © Taylor & Francis Group, LLC.
2008
Vitamin D receptor polymorphisms and renal cancer risk in Central and Eastern Europe / Karami, S.; Brennan, P.; Hung, R.J.; Boffetta, P.; Toro, J.; Wilson, R.T.; Zaridze, D.; Navratilova, M.; Chatterjee, N.; Mates, D.; Janout, V.; Kollarova, H.; Bencko, V.; Szeszenia-Dabrowska, N.; Holcatova, I.; Moukeria, A.; Welch, R.; Chanock, S.; Rothman, N.; Chow, W.-H.; Moore, L.E.. - In: JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH. PART A. - ISSN 1528-7394. - ELETTRONICO. - 71:6(2008), pp. 367-372. [10.1080/15287390701798685]
Karami, S.; Brennan, P.; Hung, R.J.; Boffetta, P.; Toro, J.; Wilson, R.T.; Zaridze, D.; Navratilova, M.; Chatterjee, N.; Mates, D.; Janout, V.; Kollarova, H.; Bencko, V.; Szeszenia-Dabrowska, N.; Holcatova, I.; Moukeria, A.; Welch, R.; Chanock, S.; Rothman, N.; Chow, W.-H.; Moore, L.E.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/669491
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