Jorde Rolf, Schirmer Henrik, Wilsgaard Tom, Bøgeberg Mathiesen Ellisiv, Njølstad Inger, Løchen Maja-Lisa, Joakimsen Ragnar Martin, Grimnes Guri
Tromsø Endocrine Research Group, Department of Clinical Medicine, UiT The Arctic University of Norway, Tromsø, Norway; Division of Internal Medicine, University Hospital of North Norway, Tromsø, Norway; The School of Population Health, University of Auckland, Auckland, New Zealand.
Department of Clinical Medicine, UiT The Arctic University of Norway, Tromsø, Norway.
PLoS One. 2015 May 18;10(5):e0126359. doi: 10.1371/journal.pone.0126359. eCollection 2015.
In addition to its role as a transport protein, the vitamin D binding protein (DBP) may also affect lipid metabolism, inflammation and carcinogenesis. There are three common variants of the DBP, Gc1s (1s), Gc1f (1f), Gc2 (2) that result in six common phenotypes (1s/1s, 1s/1f, 1s/2, 1f/1f, 1f/2, and 2/2). These phenotypes can be identified by genotyping for the two single nucleotide polymorphisms rs7041 and rs4588 in the GC gene. The DBP variants have different binding coefficients for the vitamin D metabolites, and accordingly there may be important relations between DBP phenotypes and health.
DNA was prepared from subjects who participated in the fourth survey of the Tromsø Study in 1994-1995 and who were registered with the endpoints myocardial infarction (MI), type 2 diabetes (T2DM), cancer or death as well as a randomly selected control group. The endpoint registers were complete up to 2010- 2013. Genotyping was performed for rs7041 and rs4588 and serum 25-hydroxyvitamin D (25(OH)D) was measured.
Genotyping for rs7041 and rs4588 was performed successfully in 11 704 subjects. Among these, 1660 were registered with incident MI, 958 with T2DM, 2410 with cancer and 4318 had died. Subjects with the DBP phenotype 1f/1f had 23 - 26 % reduced risk of incident cancer compared to the 1s/1s and 2/2 phenotypes (P < 0.02, Cox regression with gender as covariate). Differences in serum 25(OH)D levels could not explain the apparent cancer protective effect of the DBP variant 1f. In addition to cancer and 25(OH)D, there were significant associations between DBP phenotype and body height, hip circumference and serum calcium.
There are important biological differences between the common DBP phenotypes. If the relation between the DBP variant 1f and cancer is confirmed in other studies, determination of DBP phenotype may have clinical importance.
维生素D结合蛋白(DBP)除了作为一种转运蛋白发挥作用外,还可能影响脂质代谢、炎症和致癌作用。DBP有三种常见变体,即Gc1s(1s)、Gc1f(1f)、Gc2(2),它们导致六种常见表型(1s/1s、1s/1f、1s/2、1f/1f、1f/2和2/2)。这些表型可通过对GC基因中的两个单核苷酸多态性rs7041和rs4588进行基因分型来识别。DBP变体对维生素D代谢产物具有不同的结合系数,因此DBP表型与健康之间可能存在重要关系。
从参与1994 - 1995年特罗姆瑟研究第四次调查且登记有心肌梗死(MI)、2型糖尿病(T2DM)、癌症或死亡终点以及随机选择的对照组的受试者中提取DNA。终点登记截至2010 - 2013年。对rs7041和rs4588进行基因分型,并测量血清25 - 羟基维生素D(25(OH)D)。
对11704名受试者成功进行了rs7041和rs4588的基因分型。其中,1660人登记有新发MI,958人患有T2DM,2410人患有癌症,4318人已死亡。与1s/1s和2/2表型相比,DBP表型为1f/1f的受试者患新发癌症的风险降低了23 - 26%(P < 0.02,以性别作为协变量的Cox回归)。血清25(OH)D水平的差异无法解释DBP变体1f对癌症的明显保护作用。除了癌症和25(OH)D外,DBP表型与身高、臀围和血清钙之间也存在显著关联。
常见DBP表型之间存在重要的生物学差异。如果DBP变体1f与癌症之间的关系在其他研究中得到证实,那么DBP表型的测定可能具有临床重要性。