Source:http://linkedlifedata.com/resource/pubmed/id/15193550
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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0002085,
umls-concept:C0043210,
umls-concept:C0177804,
umls-concept:C0240966,
umls-concept:C0332281,
umls-concept:C0339510,
umls-concept:C0917713,
umls-concept:C1305855,
umls-concept:C1414083,
umls-concept:C1419771,
umls-concept:C1513126,
umls-concept:C1704675,
umls-concept:C1826421,
umls-concept:C2699549
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pubmed:issue |
6
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pubmed:dateCreated |
2004-6-14
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pubmed:abstractText |
Bone mineral density (BMD) is influenced by both environmental and genetic factors. We previously reported the association of the RUNX2 A allele with increased bone mineral density (BMD) and protection against a common form of osteoporotic fracture within a Geelong population. We genotyped 991 women from a Scottish cohort to decipher the role of RUNX2 alleles in regulating BMD. The alleles of RUNX2 within the glutamine-alanine repeat were determined by MspA1I restriction digest. Allele frequencies estimated from Scottish cohort were G allele, 0.87 +/- 0.01; A allele, 0.08 +/- 0.01; and 11Ala alanine deletion allele, 0.05 +/- 0.01. Analysis of covariance (ANCOVA) was used to adjust for the covariates weight and age for BMD at the femoral neck (FN). The A allele was associated with higher FN BMD (P = 0.035) within a postmenopausal subgroup of the population (n = 312). The effect of RUNX2 A alleles increased with increasing weight; A alleles were associated with FN BMD in those above the median BMI (BMI > 25), while no association was observed in thin/normal (BMI </= 25) postmenopausal women. Glutamine variants and an alanine insertion were identified within the group. These data suggest that the RUNX2 alleles are associated with BMD in a menopause- and weight-dependent manner.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Core Binding Factor Alpha 1 Subunit,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/RUNX2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factor AP-2,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
8756-3282
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
34
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1029-36
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15193550-Analysis of Variance,
pubmed-meshheading:15193550-Base Sequence,
pubmed-meshheading:15193550-Body Mass Index,
pubmed-meshheading:15193550-Bone Density,
pubmed-meshheading:15193550-Cohort Studies,
pubmed-meshheading:15193550-Core Binding Factor Alpha 1 Subunit,
pubmed-meshheading:15193550-DNA-Binding Proteins,
pubmed-meshheading:15193550-Female,
pubmed-meshheading:15193550-Gene Frequency,
pubmed-meshheading:15193550-Genotype,
pubmed-meshheading:15193550-Humans,
pubmed-meshheading:15193550-Menopause,
pubmed-meshheading:15193550-Middle Aged,
pubmed-meshheading:15193550-Molecular Sequence Data,
pubmed-meshheading:15193550-Scotland,
pubmed-meshheading:15193550-Transcription Factor AP-2,
pubmed-meshheading:15193550-Transcription Factors
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pubmed:year |
2004
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pubmed:articleTitle |
RUNX2 alleles associated with BMD in Scottish women; interaction of RUNX2 alleles with menopausal status and body mass index.
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pubmed:affiliation |
School of Health Science, Griffith University Gold Coast Campus, 4215 Queensland, Australia.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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