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PTHR1 polymorphisms influence BMD variation through effects on the growing skeleton

PTHR1 polymorphisms influence BMD variation through effects on the growing skeleton
PTHR1 polymorphisms influence BMD variation through effects on the growing skeleton
We investigated whether polymorphisms in PTHR1 are associated with bone mineral density (BMD), to determine whether the association of this gene with BMD was due to effects on attainment of peak bone mass or effects on subsequent bone loss. The PTHR1 gene, including its 14 exons, their exon-intron boundaries, and 1,500 bp of its promoter region, was screened for polymorphisms by denaturing high-performance liquid chromatography (dHPLC) and sequencing in 36 osteoporotic cases. Eleven single-nucleotide polymorphisms (SNPs), one tetranucleotide repeat, and one tetranucleotide deletion were identified. A cohort of 634 families, including 1,236 men (39%) and 1,926 women (61%) ascertained with probands with low BMD (Z5%) and the tetranucleotide repeat. In our osteoporosis families, association was noted between lumbar spine BMD and alleles of a known functional tetranucleotide repeat (U4) in the PTHR1 promoter region (P = 0.042) and between two and three marker haplotypes of PTHR1 polymorphisms with lumbar spine, femoral neck, and total hip BMD (P = 0.021-0.047). This association was restricted to the youngest tertile of the population (age 16-39 years, P = 0.013-0.048). A similar association was found for the ALSPAC cohort: two marker haplotypes of SNPs A48609T and C52813T were associated with height (P = 0.006) and total body less head BMD (P = 0.02), corrected for age and gender, confirming the family findings. These findings suggest a role for PTHR1 variation in determining peak BMD.
protein, parents, hip, bone density, alleles, parathyroid hormone, neck, cohort studies, dna primers, gene deletion, single nucleotide, sequence analysis, research, dna, bone and bones, adult, women, type 1, cohort, adolescent, polymerase chain reaction, longitudinal studies, exons, linkage disequilibrium, polymorphism, genetic markers, head, osteoporosis, physiology, height, bone, receptor, introns, haplotypes, genetics, nucleic acid amplification techniques, human, promoter regions (genetics), humans, tandem repeat sequences, bone mass
0171-967X
270-278
Vilarino-Guell, Carles
b1c252b6-7a01-4acf-b27e-7bdfe8482de5
Miles, Lisa J.
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Duncan, Emma L.
881b5a19-428d-4a07-97c0-59492e814f56
Ralston, Stuart H.
1edc2a3a-ef8d-459d-a9a2-d7ef14462d2b
Compston, Juliet E.
1038f0cb-dd36-49e5-8609-9091266faf67
Cooper, Cyrus
e05f5612-b493-4273-9b71-9e0ce32bdad6
Langdahl, Bente L.
b733a5be-1f14-421c-ac50-5f5fd81b26ec
MacLelland, Alasdair
bd07fd83-8bab-4dde-8e50-7d727653c3a7
Pols, Huibert A.
a0e72ed7-b9f7-4845-86fd-c7ae43e72637
Reid, David M.
2e17f1fd-d47a-4ba2-88db-1b25731224c8
Uitterlinden, Andre G.
845d72ec-de5a-4d53-9678-7469af317b29
Steer, Colin D.
d96b32bc-cac4-4c4f-9117-225edc148624
Tobias, Jon H.
b41958fb-62c0-4d28-a93e-008a78681817
Wass, John A.
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Brown, Matthew A.
2e7de455-bcc3-4b8b-a7b9-96b6e0367c1d
Vilarino-Guell, Carles
b1c252b6-7a01-4acf-b27e-7bdfe8482de5
Miles, Lisa J.
5b19b905-0b41-4de8-b507-c2c8ca5ccd20
Duncan, Emma L.
881b5a19-428d-4a07-97c0-59492e814f56
Ralston, Stuart H.
1edc2a3a-ef8d-459d-a9a2-d7ef14462d2b
Compston, Juliet E.
1038f0cb-dd36-49e5-8609-9091266faf67
Cooper, Cyrus
e05f5612-b493-4273-9b71-9e0ce32bdad6
Langdahl, Bente L.
b733a5be-1f14-421c-ac50-5f5fd81b26ec
MacLelland, Alasdair
bd07fd83-8bab-4dde-8e50-7d727653c3a7
Pols, Huibert A.
a0e72ed7-b9f7-4845-86fd-c7ae43e72637
Reid, David M.
2e17f1fd-d47a-4ba2-88db-1b25731224c8
Uitterlinden, Andre G.
845d72ec-de5a-4d53-9678-7469af317b29
Steer, Colin D.
d96b32bc-cac4-4c4f-9117-225edc148624
Tobias, Jon H.
b41958fb-62c0-4d28-a93e-008a78681817
Wass, John A.
c3cea4d1-6256-4f31-86ee-6e86409f95ad
Brown, Matthew A.
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Vilarino-Guell, Carles, Miles, Lisa J., Duncan, Emma L., Ralston, Stuart H., Compston, Juliet E., Cooper, Cyrus, Langdahl, Bente L., MacLelland, Alasdair, Pols, Huibert A., Reid, David M., Uitterlinden, Andre G., Steer, Colin D., Tobias, Jon H., Wass, John A. and Brown, Matthew A. (2007) PTHR1 polymorphisms influence BMD variation through effects on the growing skeleton. Calcified Tissue International, 81 (4), 270-278. (doi:10.1007/s00223-007-9072-7).

Record type: Article

Abstract

We investigated whether polymorphisms in PTHR1 are associated with bone mineral density (BMD), to determine whether the association of this gene with BMD was due to effects on attainment of peak bone mass or effects on subsequent bone loss. The PTHR1 gene, including its 14 exons, their exon-intron boundaries, and 1,500 bp of its promoter region, was screened for polymorphisms by denaturing high-performance liquid chromatography (dHPLC) and sequencing in 36 osteoporotic cases. Eleven single-nucleotide polymorphisms (SNPs), one tetranucleotide repeat, and one tetranucleotide deletion were identified. A cohort of 634 families, including 1,236 men (39%) and 1,926 women (61%) ascertained with probands with low BMD (Z5%) and the tetranucleotide repeat. In our osteoporosis families, association was noted between lumbar spine BMD and alleles of a known functional tetranucleotide repeat (U4) in the PTHR1 promoter region (P = 0.042) and between two and three marker haplotypes of PTHR1 polymorphisms with lumbar spine, femoral neck, and total hip BMD (P = 0.021-0.047). This association was restricted to the youngest tertile of the population (age 16-39 years, P = 0.013-0.048). A similar association was found for the ALSPAC cohort: two marker haplotypes of SNPs A48609T and C52813T were associated with height (P = 0.006) and total body less head BMD (P = 0.02), corrected for age and gender, confirming the family findings. These findings suggest a role for PTHR1 variation in determining peak BMD.

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More information

Published date: 2007
Keywords: protein, parents, hip, bone density, alleles, parathyroid hormone, neck, cohort studies, dna primers, gene deletion, single nucleotide, sequence analysis, research, dna, bone and bones, adult, women, type 1, cohort, adolescent, polymerase chain reaction, longitudinal studies, exons, linkage disequilibrium, polymorphism, genetic markers, head, osteoporosis, physiology, height, bone, receptor, introns, haplotypes, genetics, nucleic acid amplification techniques, human, promoter regions (genetics), humans, tandem repeat sequences, bone mass

Identifiers

Local EPrints ID: 61588
URI: http://eprints.soton.ac.uk/id/eprint/61588
ISSN: 0171-967X
PURE UUID: e28a0e43-709a-4d12-a03c-621f44049e7d
ORCID for Cyrus Cooper: ORCID iD orcid.org/0000-0003-3510-0709

Catalogue record

Date deposited: 10 Sep 2008
Last modified: 18 Mar 2024 02:44

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Contributors

Author: Carles Vilarino-Guell
Author: Lisa J. Miles
Author: Emma L. Duncan
Author: Stuart H. Ralston
Author: Juliet E. Compston
Author: Cyrus Cooper ORCID iD
Author: Bente L. Langdahl
Author: Alasdair MacLelland
Author: Huibert A. Pols
Author: David M. Reid
Author: Andre G. Uitterlinden
Author: Colin D. Steer
Author: Jon H. Tobias
Author: John A. Wass
Author: Matthew A. Brown

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