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dc.contributor.authorMartinaityte, Ieva
dc.contributor.authorJorde, Rolf
dc.contributor.authorEmaus, Nina
dc.contributor.authorEggen, Anne Elise
dc.contributor.authorJoakimsen, Ragnar Martin
dc.contributor.authorKamycheva, Elena
dc.date.accessioned2018-02-14T10:03:11Z
dc.date.available2018-02-14T10:03:11Z
dc.date.issued2017-03-02
dc.description.abstractBackground:<br>Bone mineral density (BMD) is determined by bone remodeling processes regulated by endocrine, autocrine and genetic mechanisms. Thus, some studies have reported that BMD is associated with single nucleotide polymorphisms (SNPs) associated with vitamin D receptor (VDR), serum 25(OH)D levels and estrogen receptor 1 (ESR1), but without consensus. Therefore, we aimed to map and compare the risk genotypes for forearm and total hip low BMD.<br>Methods and findings:<br>Data were derived from a population-based study in northern Norway; the Tromsø Study. Distal forearm BMD was measured with a single x-ray absorptiometric device, while total hip BMD was measured with a dual-energy x-ray absorptiometric device. There were 7,317 and 4,082 successful analyses of distal forearm and total hip BMD, respectively, and at least one SNP of interest. We evaluated plausible BMD modulating factors and associations of BMD and SNPs related to vitamin D metabolism (FokI, Cdx2, BsmI, rs2298850, rs10741657, rs3794060, rs6013897), ApaI-BsmI-TaqI haplotypes and ESR1 SNP rs4870044.<br>Results:<br>Age, BMI, physical activity and smoking were significantly associated with BMD. In a linear regression model with adjustment for age and gender and with the major homozygote as reference, rs6013897 had a standardized beta coefficient (β) of –0.031 (P = 0.024) for total hip BMD. β for ESR1 SNP rs4870044 was –0.016 (P = 0.036) for forearm BMD and –0.034 (P = 0.015) for total hip BMD. The other SNPs nor serum 25(OH)D were significantly associated with BMD.<br>Conclusions:<br>Both forearm and total hip BMD were associated with ESR1 SNP rs4870044. Of the vitamin D–related genes, only CYP24A1 gene rs6013897 was associated with total hip BMD, but the association was weak and needs confirmation in other studies. Serum 25(OH)D was not associated with BMD in our population, probably due to the generally sufficient vitamin D levels in the population.en_US
dc.descriptionSource at <a href=http://doi.org/10.1371/journal.pone.0173045>http://doi.org/10.1371/journal.pone.0173045</a>en_US
dc.identifier.citationMartinaityte, I., Jorde, R., Emaus, N., Eggen, A.E., Joakimsen, R.M., Kamycheva, E. Bone mineral density is associated with Vitamin D related rs6013897 and estrogen receptor polymorphism rs4870044: The Tromsø study. PLoS ONE. 2017;12:e0173045(3):1-12en_US
dc.identifier.cristinIDFRIDAID 1488393
dc.identifier.doi10.1371/journal.pone.0173045
dc.identifier.issn1932-6203
dc.identifier.urihttps://hdl.handle.net/10037/12164
dc.language.isoengen_US
dc.publisherPublic Library of Scienceen_US
dc.relation.journalPLoS ONE
dc.rights.accessRightsopenAccessen_US
dc.subjectVDP::Medisinske Fag: 700::Klinisk medisinske fag: 750::Endokrinologi: 774en_US
dc.subjectVDP::Medical disciplines: 700::Clinical medical disciplines: 750::Endocrinology: 774en_US
dc.titleBone mineral density is associated with Vitamin D related rs6013897 and estrogen receptor polymorphism rs4870044: The Tromsø studyen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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