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Vitamin D Binding Protein Genotype and Osteoporosis

Overview of attention for article published in Calcified Tissue International, June 2009
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About this Attention Score

  • Good Attention Score compared to outputs of the same age (65th percentile)

Mentioned by

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5 patents
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1 Facebook page

Citations

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98 Dimensions

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99 Mendeley
Title
Vitamin D Binding Protein Genotype and Osteoporosis
Published in
Calcified Tissue International, June 2009
DOI 10.1007/s00223-009-9251-9
Pubmed ID
Authors

Yue Fang, Joyce B. J. van Meurs, Pascal Arp, Johannes P. T. van Leeuwen, Albert Hofman, Huibert A. P. Pols, André G. Uitterlinden

Abstract

Osteoporosis is a bone disease leading to an increased fracture risk. It is considered a complex multifactorial genetic disorder with interaction of environmental and genetic factors. As a candidate gene for osteoporosis, we studied vitamin D binding protein (DBP, or group-specific component, Gc), which binds to and transports vitamin D to target tissues to maintain calcium homeostasis through the vitamin D endocrine system. DBP can also be converted to DBP-macrophage activating factor (DBP-MAF), which mediates bone resorption by directly activating osteoclasts. We summarized the genetic linkage structure of the DBP gene. We genotyped two single-nucleotide polymorphisms (SNPs, rs7041 = Glu416Asp and rs4588 = Thr420Lys) in 6,181 elderly Caucasians and investigated interactions of the DBP genotype with vitamin D receptor (VDR) genotype and dietary calcium intake in relation to fracture risk. Haplotypes of the DBP SNPs correspond to protein variations referred to as Gc1s (haplotype 1), Gc2 (haplotype 2), and Gc1f (haplotype3). In a subgroup of 1,312 subjects, DBP genotype was found to be associated with increased and decreased serum 25-(OH)D(3) for haplotype 1 (P = 3 x 10(-4)) and haplotype 2 (P = 3 x 10(-6)), respectively. Similar associations were observed for 1,25-(OH)(2)D(3). The DBP genotype was not significantly associated with fracture risk in the entire study population. Yet, we observed interaction between DBP and VDR haplotypes in determining fracture risk. In the DBP haplotype 1-carrier group, subjects of homozygous VDR block 5-haplotype 1 had 33% increased fracture risk compared to noncarriers (P = 0.005). In a subgroup with dietary calcium intake <1.09 g/day, the hazard ratio (95% confidence interval) for fracture risk of DBP hap1-homozygote versus noncarrier was 1.47 (1.06-2.05). All associations were independent of age and gender. Our study demonstrated that the genetic effect of the DBP gene on fracture risk appears only in combination with other genetic and environmental risk factors for bone metabolism.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 99 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Spain 1 1%
Netherlands 1 1%
Sweden 1 1%
Italy 1 1%
Unknown 95 96%

Demographic breakdown

Readers by professional status Count As %
Researcher 17 17%
Student > Bachelor 17 17%
Student > Ph. D. Student 13 13%
Student > Doctoral Student 10 10%
Other 9 9%
Other 20 20%
Unknown 13 13%
Readers by discipline Count As %
Medicine and Dentistry 35 35%
Biochemistry, Genetics and Molecular Biology 15 15%
Agricultural and Biological Sciences 13 13%
Nursing and Health Professions 9 9%
Pharmacology, Toxicology and Pharmaceutical Science 2 2%
Other 7 7%
Unknown 18 18%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 4. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 06 June 2017.
All research outputs
#8,577,479
of 25,837,817 outputs
Outputs from Calcified Tissue International
#596
of 1,909 outputs
Outputs of similar age
#43,948
of 130,040 outputs
Outputs of similar age from Calcified Tissue International
#2
of 3 outputs
Altmetric has tracked 25,837,817 research outputs across all sources so far. This one has received more attention than most of these and is in the 66th percentile.
So far Altmetric has tracked 1,909 research outputs from this source. They typically receive a little more attention than average, with a mean Attention Score of 7.2. This one has gotten more attention than average, scoring higher than 68% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 130,040 tracked outputs that were published within six weeks on either side of this one in any source. This one has gotten more attention than average, scoring higher than 65% of its contemporaries.
We're also able to compare this research output to 3 others from the same source and published within six weeks on either side of this one.