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Pigment cell & melanoma research · 2013

An inherited variant in the gene coding for vitamin D-binding protein and survival from cutaneous melanoma: a BioGenoMEL study.

СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
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Davies John R, Field Sinead, Randerson-Moor Juliette, Harland Mark, Kumar Rajiv, Anic Gabriella M, Nagore Eduardo, Hansson Johan, Höiom Veronica, Jönsson Göran, Gruis Nelleke A, Park Jong Y, Guan Jian, Sivaramakrishna Rachakonda P, Wendt Judith, Pjanova Dace, Puig Susana, Schadendorf Dirk, Okamoto Ichiro, Olsson Håkan, Affleck Paul, García-Casado Zaida, Puig-Butille Joan Anton, Stratigos Alexander J, Kodela Elizabeth, Donina Simona, Sucker Antje, Hosen Ismail, Egan Kathleen M, Barrett Jennifer H, van Doorn Remco, Bishop D Timothy, Newton-Bishop Julia

Аннотация

An association between low serum vitamin D levels and poorer melanoma survival has been reported. We have studied inheritance of a polymorphism of the GC gene, rs2282679, coding for the vitamin D-binding protein, which is associated with lower serum levels of vitamin D, in a meta-analysis of 3137 melanoma patients. The aim was to investigate evidence for a causal relationship between vitamin D and outcome (Mendelian randomization). The variant was not associated with reduced overall survival (OS) in the UK cohort, per-allele hazard ratio (HR) for death 1.23 (95% confidence interval (CI) 0.93, 1.64). In the smaller cohorts, HR in OS analysis was 1.07 (95% CI 0.88, 1.3) and for all cohorts combined, HR for OS was 1.09 (95% CI 0.93, 1.29). There was evidence of increased melanoma-specific deaths in the seven cohorts for which these data were available. The lack of unequivocal findings despite the large sample size illustrates the difficulties of implementing Mendelian randomization.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты