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Published in: Osteoporosis International 2/2012

Open Access 01-02-2012 | Original Article

‘Sink or swim’: an evaluation of the clinical characteristics of individuals with high bone mass

Authors: C. L. Gregson, S. A. Steel, K. P. O’Rourke, K. Allan, J. Ayuk, A. Bhalla, G. Clunie, N. Crabtree, I. Fogelman, A. Goodby, C. M. Langman, S. Linton, E. Marriott, E. McCloskey, K. E. Moss, T. Palferman, S. Panthakalam, K. E. S. Poole, M. D. Stone, J. Turton, D. Wallis, S. Warburton, J. Wass, E. L. Duncan, M. A. Brown, G. Davey-Smith, J. H. Tobias

Published in: Osteoporosis International | Issue 2/2012

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Abstract

Summary

High bone mineral density on routine dual energy X-ray absorptiometry (DXA) may indicate an underlying skeletal dysplasia. Two hundred fifty-eight individuals with unexplained high bone mass (HBM), 236 relatives (41% with HBM) and 58 spouses were studied. Cases could not float, had mandible enlargement, extra bone, broad frames, larger shoe sizes and increased body mass index (BMI). HBM cases may harbour an underlying genetic disorder.

Introduction

High bone mineral density is a sporadic incidental finding on routine DXA scanning of apparently asymptomatic individuals. Such individuals may have an underlying skeletal dysplasia, as seen in LRP5 mutations. We aimed to characterize unexplained HBM and determine the potential for an underlying skeletal dysplasia.

Methods

Two hundred fifty-eight individuals with unexplained HBM (defined as L1 Z-score ≥ +3.2 plus total hip Z-score ≥ +1.2, or total hip Z-score ≥ +3.2) were recruited from 15 UK centres, by screening 335,115 DXA scans. Unexplained HBM affected 0.181% of DXA scans. Next 236 relatives were recruited of whom 94 (41%) had HBM (defined as L1 Z-score + total hip Z-score ≥ +3.2). Fifty-eight spouses were also recruited together with the unaffected relatives as controls. Phenotypes of cases and controls, obtained from clinical assessment, were compared using random-effects linear and logistic regression models, clustered by family, adjusted for confounders, including age and sex.

Results

Individuals with unexplained HBM had an excess of sinking when swimming (7.11 [3.65, 13.84], p < 0.001; adjusted odds ratio with 95% confidence interval shown), mandible enlargement (4.16 [2.34, 7.39], p < 0.001), extra bone at tendon/ligament insertions (2.07 [1.13, 3.78], p = 0.018) and broad frame (3.55 [2.12, 5.95], p < 0.001). HBM cases also had a larger shoe size (mean difference 0.4 [0.1, 0.7] UK sizes, p = 0.009) and increased BMI (mean difference 2.2 [1.3, 3.1] kg/m2, p < 0.001).

Conclusion

Individuals with unexplained HBM have an excess of clinical characteristics associated with skeletal dysplasia and their relatives are commonly affected, suggesting many may harbour an underlying genetic disorder affecting bone mass.
Appendix
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Literature
1.
go back to reference Cherian RA, Haddaway MJ, Davie MW, McCall IW, Cassar-Pullicino VN (2000) Effect of Paget’s disease of bone on areal lumbar spine bone mineral density measured by DXA, and density of cortical and trabecular bone measured by quantitative CT. Br J Radiol 73:720–726PubMed Cherian RA, Haddaway MJ, Davie MW, McCall IW, Cassar-Pullicino VN (2000) Effect of Paget’s disease of bone on areal lumbar spine bone mineral density measured by DXA, and density of cortical and trabecular bone measured by quantitative CT. Br J Radiol 73:720–726PubMed
2.
go back to reference Gregson CL, Tobias JH (2007) Interpretation of high bone mineral density measurements. Osteoporos Rev 15:2–6 Gregson CL, Tobias JH (2007) Interpretation of high bone mineral density measurements. Osteoporos Rev 15:2–6
3.
go back to reference Diamond T, Smith A, Schnier R, Manoharan A (2002) Syndrome of myelofibrosis and osteosclerosis: a series of case reports and review of the literature. Bone 30:498–501PubMedCrossRef Diamond T, Smith A, Schnier R, Manoharan A (2002) Syndrome of myelofibrosis and osteosclerosis: a series of case reports and review of the literature. Bone 30:498–501PubMedCrossRef
4.
go back to reference Manganelli P, Giuliani N, Fietta P, Mancini C, Lazzaretti M, Pollini A, Quaini F, Pedrazzoni M (2005) OPG/RANKL system imbalance in a case of hepatitis C-associated osteosclerosis: the pathogenetic key? Clin Rheumatol 24:296–300PubMedCrossRef Manganelli P, Giuliani N, Fietta P, Mancini C, Lazzaretti M, Pollini A, Quaini F, Pedrazzoni M (2005) OPG/RANKL system imbalance in a case of hepatitis C-associated osteosclerosis: the pathogenetic key? Clin Rheumatol 24:296–300PubMedCrossRef
5.
6.
go back to reference Balemans W, Patel N, Ebeling M, Van Hul E, Wuyts W, Lacza C, Dioszegi M, Dikkers FG, Hildering P, Willems PJ, Verheij JBGM, Lindpaintner K, Vickery B, Foernzler D, Van Hul W (2002) Identification of a 52 kb deletion downstream of the SOST gene in patients with van Buchem disease. J Med Genet 39:91–97PubMedCrossRef Balemans W, Patel N, Ebeling M, Van Hul E, Wuyts W, Lacza C, Dioszegi M, Dikkers FG, Hildering P, Willems PJ, Verheij JBGM, Lindpaintner K, Vickery B, Foernzler D, Van Hul W (2002) Identification of a 52 kb deletion downstream of the SOST gene in patients with van Buchem disease. J Med Genet 39:91–97PubMedCrossRef
7.
go back to reference Balemans W, Van WL, Van HW (2005) A clinical and molecular overview of the human osteopetroses. Calcif Tissue Int 77:263–274PubMedCrossRef Balemans W, Van WL, Van HW (2005) A clinical and molecular overview of the human osteopetroses. Calcif Tissue Int 77:263–274PubMedCrossRef
8.
go back to reference Hamersma H, Gardner J, Beighton P (2003) The natural history of sclerosteosis. Clin Genet 63:192–197PubMedCrossRef Hamersma H, Gardner J, Beighton P (2003) The natural history of sclerosteosis. Clin Genet 63:192–197PubMedCrossRef
9.
go back to reference Van Hul W, Balemans W, Van Hul E, Dikkers FG, Obee H, Stokroos RJ, Hildering P, Vanhoenacker F, Van Camp G, Willems PJ (1998) Van Buchem disease (hyperostosis corticalis generalisata) maps to chromosome 17q12–q21. Am J Hum Genet 62:391–399PubMedCrossRef Van Hul W, Balemans W, Van Hul E, Dikkers FG, Obee H, Stokroos RJ, Hildering P, Vanhoenacker F, Van Camp G, Willems PJ (1998) Van Buchem disease (hyperostosis corticalis generalisata) maps to chromosome 17q12–q21. Am J Hum Genet 62:391–399PubMedCrossRef
10.
go back to reference Benichou OD, Laredo JD, de Vernejoul MC (2000) Type II autosomal dominant osteopetrosis (Albers–Schonberg disease): clinical and radiological manifestations in 42 patients. Bone 26:87–93PubMedCrossRef Benichou OD, Laredo JD, de Vernejoul MC (2000) Type II autosomal dominant osteopetrosis (Albers–Schonberg disease): clinical and radiological manifestations in 42 patients. Bone 26:87–93PubMedCrossRef
11.
go back to reference Nurnberg P, Thiele H, Chandler D, Hohne W, Cunningham ML, Ritter H, Leschik G, Uhlmann K, Mischung C, Harrop K, Goldblatt J, Borochowitz ZU, Kotzot D, Westermann F, Mundlos S, Braun HS, Laing N, Tinschert S (2001) Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia. Nat Genet 28:37–41PubMed Nurnberg P, Thiele H, Chandler D, Hohne W, Cunningham ML, Ritter H, Leschik G, Uhlmann K, Mischung C, Harrop K, Goldblatt J, Borochowitz ZU, Kotzot D, Westermann F, Mundlos S, Braun HS, Laing N, Tinschert S (2001) Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia. Nat Genet 28:37–41PubMed
12.
go back to reference Johnson ML, Gong G, Kimberling W, Recker SM, Kimmel DB, Recker RB (1997) Linkage of a gene causing high bone mass to human chromosome 11 (11q12–13). Am J Hum Genet 60:1326–1332PubMedCrossRef Johnson ML, Gong G, Kimberling W, Recker SM, Kimmel DB, Recker RB (1997) Linkage of a gene causing high bone mass to human chromosome 11 (11q12–13). Am J Hum Genet 60:1326–1332PubMedCrossRef
13.
go back to reference Little RD, Carulli JP, Del Mastro RG, Dupuis J, Osborne M, Folz C, Manning SP, Swain PM, Zhao SC, Eustace B, Lappe MM, Spitzer L, Zweier S, Braunschweiger K, Benchekroun Y, Hu X, Adair R, Chee L, FitzGerald MG, Tulig C, Caruso A, Tzellas N, Bawa A, Franklin B, McGuire S, Nogues X, Gong G, Allen KM, Anisowicz A, Morales AJ, Lomedico PT, Recker SM, Van Eerdewegh P, Recker RR, Johnson ML (2002) A mutation in the LDL receptor-related protein 5 gene results in the autosomal dominant high-bone-mass trait. Am J Hum Genet 70:11–19PubMedCrossRef Little RD, Carulli JP, Del Mastro RG, Dupuis J, Osborne M, Folz C, Manning SP, Swain PM, Zhao SC, Eustace B, Lappe MM, Spitzer L, Zweier S, Braunschweiger K, Benchekroun Y, Hu X, Adair R, Chee L, FitzGerald MG, Tulig C, Caruso A, Tzellas N, Bawa A, Franklin B, McGuire S, Nogues X, Gong G, Allen KM, Anisowicz A, Morales AJ, Lomedico PT, Recker SM, Van Eerdewegh P, Recker RR, Johnson ML (2002) A mutation in the LDL receptor-related protein 5 gene results in the autosomal dominant high-bone-mass trait. Am J Hum Genet 70:11–19PubMedCrossRef
14.
go back to reference Van WL, Cleiren E, Gram J, Beals RK, Benichou O, Scopelliti D, Key L, Renton T, Bartels C, Gong Y, Warman ML, de Vernejoul MC, Bollerslev J, Van HW (2003) Six novel missense mutations in the LDL receptor-related protein 5 (LRP5) gene in different conditions with an increased bone density. Am J Hum Genet 72:763–771CrossRef Van WL, Cleiren E, Gram J, Beals RK, Benichou O, Scopelliti D, Key L, Renton T, Bartels C, Gong Y, Warman ML, de Vernejoul MC, Bollerslev J, Van HW (2003) Six novel missense mutations in the LDL receptor-related protein 5 (LRP5) gene in different conditions with an increased bone density. Am J Hum Genet 72:763–771CrossRef
15.
go back to reference Rickels MR, Zhang X, Mumm S, Whyte MP (2005) Oropharyngeal skeletal disease accompanying high bone mass and novel LRP5 mutation. J Bone Miner Res 20:878–885PubMedCrossRef Rickels MR, Zhang X, Mumm S, Whyte MP (2005) Oropharyngeal skeletal disease accompanying high bone mass and novel LRP5 mutation. J Bone Miner Res 20:878–885PubMedCrossRef
16.
go back to reference Boyden LM, Mao J, Belsky J, Mitzner L, Farhi A, Mitnick MA, Wu D, Insogna K, Lifton RP (2002) High bone density due to a mutation in LDL-receptor-related protein 5. N Engl J Med 346:1513–1521PubMedCrossRef Boyden LM, Mao J, Belsky J, Mitzner L, Farhi A, Mitnick MA, Wu D, Insogna K, Lifton RP (2002) High bone density due to a mutation in LDL-receptor-related protein 5. N Engl J Med 346:1513–1521PubMedCrossRef
17.
go back to reference Kellgren J, Lawrence J (1957) Radiological assessment of osteo-arthrosis. Ann Rheum Dis 16:494–502PubMedCrossRef Kellgren J, Lawrence J (1957) Radiological assessment of osteo-arthrosis. Ann Rheum Dis 16:494–502PubMedCrossRef
18.
go back to reference Gregson C, Steel S, Yoshida K, Reid D, Tobias J (2008) An investigation into the impact of osteoarthritic changes on bone mineral density measurements in patients with high bone mass. In: ASBMR 30th annual meeting, Montreal, SA257 ed. Gregson C, Steel S, Yoshida K, Reid D, Tobias J (2008) An investigation into the impact of osteoarthritic changes on bone mineral density measurements in patients with high bone mass. In: ASBMR 30th annual meeting, Montreal, SA257 ed.
19.
go back to reference Hansen KE, Binkley N, Christian R, Vallarta-Ast N, Krueger D, Drezner MK, Blank RD (2005) Interobserver reproducibility of criteria for vertebral body exclusion. J Bone Miner Res 20:501–508PubMedCrossRef Hansen KE, Binkley N, Christian R, Vallarta-Ast N, Krueger D, Drezner MK, Blank RD (2005) Interobserver reproducibility of criteria for vertebral body exclusion. J Bone Miner Res 20:501–508PubMedCrossRef
20.
go back to reference White J, Yeats A, Skipworth G (1979) Tables for statisticians, 3rd edn. Stanley Thornes, Cheltenham White J, Yeats A, Skipworth G (1979) Tables for statisticians, 3rd edn. Stanley Thornes, Cheltenham
21.
go back to reference World Medical Association (2008) WMA Declaration of Helsinki—ethical principles for medical research involving human subjects. In: 59th WMA general assembly, Seoul World Medical Association (2008) WMA Declaration of Helsinki—ethical principles for medical research involving human subjects. In: 59th WMA general assembly, Seoul
22.
go back to reference Hanson J (1997) Standardization of femur BMD. J BoneMiner Res 12:1316–1317CrossRef Hanson J (1997) Standardization of femur BMD. J BoneMiner Res 12:1316–1317CrossRef
23.
go back to reference Hui SL, Gao S, Zhou XH, Johnston CC, Lu Y, Gluer CC, Grampp S, Genant H (1997) Universal standardization of bone density measurements: a method with optimal properties for calibration among several instruments. J Bone Miner Res 12:1463–1470PubMedCrossRef Hui SL, Gao S, Zhou XH, Johnston CC, Lu Y, Gluer CC, Grampp S, Genant H (1997) Universal standardization of bone density measurements: a method with optimal properties for calibration among several instruments. J Bone Miner Res 12:1463–1470PubMedCrossRef
24.
go back to reference Vedi S, Purdie DW, Ballard P, Bord S, Cooper AC, Compston JE (1999) Bone remodeling and structure in postmenopausal women treated with long-term, high-dose estrogen therapy. Osteoporos Int 10:52–58PubMedCrossRef Vedi S, Purdie DW, Ballard P, Bord S, Cooper AC, Compston JE (1999) Bone remodeling and structure in postmenopausal women treated with long-term, high-dose estrogen therapy. Osteoporos Int 10:52–58PubMedCrossRef
25.
go back to reference Clement-Lacroix P, Ai M, Morvan F, Roman-Roman S, Vayssiere B, Belleville C, Estrera K, Warman ML, Baron R, Rawadi G (2005) Lrp5-independent activation of Wnt signaling by lithium chloride increases bone formation and bone mass in mice. Proc Natl Acad Sci USA 102:17406–17411PubMedCrossRef Clement-Lacroix P, Ai M, Morvan F, Roman-Roman S, Vayssiere B, Belleville C, Estrera K, Warman ML, Baron R, Rawadi G (2005) Lrp5-independent activation of Wnt signaling by lithium chloride increases bone formation and bone mass in mice. Proc Natl Acad Sci USA 102:17406–17411PubMedCrossRef
26.
go back to reference Liang G, Katz LD, Insogna KL, Carpenter TO, Macica CM (2009) Survey of the enthesopathy of X-linked hypophosphatemia and its characterization in Hyp mice. Calcif Tissue Int 85:235–246PubMedCrossRef Liang G, Katz LD, Insogna KL, Carpenter TO, Macica CM (2009) Survey of the enthesopathy of X-linked hypophosphatemia and its characterization in Hyp mice. Calcif Tissue Int 85:235–246PubMedCrossRef
27.
go back to reference Mclean SP, Hinrichs RN (2000) Buoyancy, gender, and swimming performance. J Appl Biomech 16:248–263 Mclean SP, Hinrichs RN (2000) Buoyancy, gender, and swimming performance. J Appl Biomech 16:248–263
28.
go back to reference Gardner JC, van Bezooijen RL, Mervis B, Hamdy NAT, Lowik CWGM, Hamersma H, Beighton P, Papapoulos SE (2005) Bone mineral density in sclerosteosis; affected individuals and gene carriers. J Clin Endocrinol Metab 90:6392–6395PubMedCrossRef Gardner JC, van Bezooijen RL, Mervis B, Hamdy NAT, Lowik CWGM, Hamersma H, Beighton P, Papapoulos SE (2005) Bone mineral density in sclerosteosis; affected individuals and gene carriers. J Clin Endocrinol Metab 90:6392–6395PubMedCrossRef
29.
go back to reference Duncan EL, Gregson CL, Addison K, Brugmans M, Pointon JJ, Appleton LH, Tobias JH, Brown MA (2009) Mutations in LRP5 and SOST are a rare cause of high bone mass in the general population. Bone 44:S340–S341CrossRef Duncan EL, Gregson CL, Addison K, Brugmans M, Pointon JJ, Appleton LH, Tobias JH, Brown MA (2009) Mutations in LRP5 and SOST are a rare cause of high bone mass in the general population. Bone 44:S340–S341CrossRef
30.
go back to reference Genevieve D, Proulle V, Isidor B, Bellais S, Serre V, Djouadi F, Picard C, Vignon-Savoye C, Bader-Meunier B, Blanche S, de Vernejoul MC, Legeai-Mallet L, Fischer AM, Le Merrer M, Dreyfus M, Gaussem P, Munnich A, Cormier-Daire V (2008) Thromboxane synthase mutations in an increased bone density disorder (Ghosal syndrome). Nat Genet 40:284–286PubMedCrossRef Genevieve D, Proulle V, Isidor B, Bellais S, Serre V, Djouadi F, Picard C, Vignon-Savoye C, Bader-Meunier B, Blanche S, de Vernejoul MC, Legeai-Mallet L, Fischer AM, Le Merrer M, Dreyfus M, Gaussem P, Munnich A, Cormier-Daire V (2008) Thromboxane synthase mutations in an increased bone density disorder (Ghosal syndrome). Nat Genet 40:284–286PubMedCrossRef
31.
go back to reference Morgan EA, Schneider JG, Baroni TE, Uluckan O, Heller E, Hurchla MA, Deng H, Floyd D, Berdy A, Prior JL, Piwnica-Worms D, Teitelbaum SL, Ross FP, Weilbaecher KN (2010) Dissection of platelet and myeloid cell defects by conditional targeting of the beta 3-integrin subunit. FASEB J 24:1117–1127PubMedCrossRef Morgan EA, Schneider JG, Baroni TE, Uluckan O, Heller E, Hurchla MA, Deng H, Floyd D, Berdy A, Prior JL, Piwnica-Worms D, Teitelbaum SL, Ross FP, Weilbaecher KN (2010) Dissection of platelet and myeloid cell defects by conditional targeting of the beta 3-integrin subunit. FASEB J 24:1117–1127PubMedCrossRef
32.
go back to reference Yarali N, Fisgin T, Duru F, Kara A (2003) Osteopetrosis and Glanzmann’s thrombasthenia in a child. Ann Hematol 82:254–256PubMed Yarali N, Fisgin T, Duru F, Kara A (2003) Osteopetrosis and Glanzmann’s thrombasthenia in a child. Ann Hematol 82:254–256PubMed
33.
go back to reference Tothill P, Laskey MA, Orphanidou CI, van WM (1999) Anomalies in dual energy X-ray absorptiometry measurements of total-body bone mineral during weight change using Lunar, Hologic and Norland instruments. Br J Radiol 72:661–669PubMed Tothill P, Laskey MA, Orphanidou CI, van WM (1999) Anomalies in dual energy X-ray absorptiometry measurements of total-body bone mineral during weight change using Lunar, Hologic and Norland instruments. Br J Radiol 72:661–669PubMed
34.
go back to reference Weigert J, Cann C (1999) Dual-energy X-ray absorpitometry (DXA) in obese patients. Are normal values really normal? J Womens Imaging 1:11–17 Weigert J, Cann C (1999) Dual-energy X-ray absorpitometry (DXA) in obese patients. Are normal values really normal? J Womens Imaging 1:11–17
35.
go back to reference Department of Health (1999) Health survey for England: cardiovascular disease. Stationery Office, London Department of Health (1999) Health survey for England: cardiovascular disease. Stationery Office, London
36.
go back to reference Lawlor DA, Bedford C, Taylor M, Ebrahim S (2003) Geographical variation in cardiovascular disease, risk factors, and their control in older women: British Women’s Heart and Health Study. J Epidemiol Community Health 57:134–140PubMedCrossRef Lawlor DA, Bedford C, Taylor M, Ebrahim S (2003) Geographical variation in cardiovascular disease, risk factors, and their control in older women: British Women’s Heart and Health Study. J Epidemiol Community Health 57:134–140PubMedCrossRef
37.
go back to reference Mascie-Taylor CG (1987) Assortative mating in a contemporary British population. Ann Hum Biol 14:59–68PubMedCrossRef Mascie-Taylor CG (1987) Assortative mating in a contemporary British population. Ann Hum Biol 14:59–68PubMedCrossRef
38.
go back to reference Blake GM, Parker JC, Buxton FM, Fogelman I (1993) Dual X-ray absorptiometry: a comparison between fan beam and pencil beam scans. Br J Radiol 66:902–906PubMedCrossRef Blake GM, Parker JC, Buxton FM, Fogelman I (1993) Dual X-ray absorptiometry: a comparison between fan beam and pencil beam scans. Br J Radiol 66:902–906PubMedCrossRef
Metadata
Title
‘Sink or swim’: an evaluation of the clinical characteristics of individuals with high bone mass
Authors
C. L. Gregson
S. A. Steel
K. P. O’Rourke
K. Allan
J. Ayuk
A. Bhalla
G. Clunie
N. Crabtree
I. Fogelman
A. Goodby
C. M. Langman
S. Linton
E. Marriott
E. McCloskey
K. E. Moss
T. Palferman
S. Panthakalam
K. E. S. Poole
M. D. Stone
J. Turton
D. Wallis
S. Warburton
J. Wass
E. L. Duncan
M. A. Brown
G. Davey-Smith
J. H. Tobias
Publication date
01-02-2012
Publisher
Springer-Verlag
Published in
Osteoporosis International / Issue 2/2012
Print ISSN: 0937-941X
Electronic ISSN: 1433-2965
DOI
https://doi.org/10.1007/s00198-011-1603-4

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