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Acta veterinaria Scandinavica2012; 54(1); 41; doi: 10.1186/1751-0147-54-41

The analysis of densitometric and geometric parameters of bilateral proximal phalanges in horses with the use of peripheral quantitative computed tompgraphy.

Abstract: Proximal phalanges in horses are among bones that are most prone to injuries. So far, the detailed analysis of densitometric and geometric parameters of both front legs proximal phalanges in horses has not been investigated. The aim of this study was to compare the densitometric and geometric parameters between proximal phalanges in equine both front legs with the use of peripheral quantitative computed tomography (pQCT). Methods: The study material comprised isolated both front legs proximal phalanges derived from 22 horses. The structure analysis of the proximal phalanges was conducted with the pQCT. The following bone parameters were determined: bone mineral content, volumetric bone mineral density, total bone area, trabecular area, cortical area, cortical thickness, periosteal circumference, endocortical circumference, Strength Strain Index. Tomographic analysis of proximal phalanges was conducted at three levels: at 15%, 50% and 85% of the bone length. Results: The statistical analysis showed that both the densitometric and geometric parameters of the bone at 50% and 85% of its length, did not present any statistically significant differences for the left or right proximal phalanges of the forelimb. At the same time, all examined parameters measured at 15% of the bone length, in the vicinity of the proximal metaphysis revealed significant statistical differences between both front legs proximal phalanges. Conclusions: The proximal phalanx parameters in the forelimbs are significantly different for the left and right proximal phalanx at 15% of the length and they indicate higher Strength Strain Index of the left bone in this location. The densitometric and geometric parameters of the bone at 50% and 85% of its length, did not present any statistically significant differences for the left or right proximal phalanges of the left and right forelimbs. The most serious changes caused by asymmetrical load of the thoracic limbs in horses occur near the proximal metaphysis, where the spongious substance is most abundant. This may happen because the metabolism of the spongious bone tissue is eight times faster compared to the compact bone tissue. Thus, any changes, including those caused by asymmetrical strain exerted on the right and left thoracic limbs, are the earliest to be observed.
Publication Date: 2012-07-13 PubMed ID: 22794083PubMed Central: PMC3408367DOI: 10.1186/1751-0147-54-41Google Scholar: Lookup
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  • Journal Article

Summary

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The research studied the geometric and densitometric parameters of proximal phalanges in horse’s front legs using peripheral quantitative computed tomography. The study found significant variations in these parameters at 15% of bone length and indicated higher strength strain index for the left bone in this area.

Objectives and Methods

  • The study sought to examine the densitometric and geometric parameters of the proximal phalanges in both front legs of horses, which have not been significantly studied in the past.
  • The researchers used peripheral quantitative computed tomography (pQCT) as their tool for analyzing the bone structure.
  • The sample comprised isolated proximal phalanges from the front legs of 22 horses and was analysed at three levels of bone length: 15%, 50%, and 85%.

Measurements Observed

  • Various parameters of the bone were determined in the study including bone mineral content, volumetric bone mineral density, total bone area, trabecular area, cortical area, cortical thickness, periosteal circumference, endocortical circumference, and Strength Strain Index.

Findings

  • The statistical analysis showed that both the densitometric and geometric parameters did not show any significant difference for the left or right proximal phalanges at 50% and 85% of its length.
  • However, all parameters measured at 15% of the bone length revealed significant statistical differences between the proximal phalanges of both front legs. Specifically, the left bone indicated a higher Strength Strain Index in this location.

Conclusions and Implications

  • The difference in parameters in forelimbs at 15% of the length may be due to asymmetrical load on the thoracic limbs in horses. This change is most visible at the proximal metaphysis, where the spongious substance (a younger and less dense form of bone tissue) is most abundant.
  • Because the metabolism of spongious bone tissue is eight times faster than compact bone tissue, alterations due to asymmetrical strain exerted on the right and left limbs can be detected early. This discovery could be instrumental in early detection and prevention of horse-limb-related issues.

Cite This Article

APA
Dzierzęcka M, Charuta A. (2012). The analysis of densitometric and geometric parameters of bilateral proximal phalanges in horses with the use of peripheral quantitative computed tompgraphy. Acta Vet Scand, 54(1), 41. https://doi.org/10.1186/1751-0147-54-41

Publication

ISSN: 1751-0147
NlmUniqueID: 0370400
Country: England
Language: English
Volume: 54
Issue: 1
Pages: 41

Researcher Affiliations

Dzierzęcka, Małgorzata
  • Department of Morphological Science, Faculty of Veterinary Medicine, Warsaw University of Life Sciences, Nowoursynowska 166, Warsaw 02-776, Poland. malgorzatadzierzecka@wp.pl
Charuta, Anna

    MeSH Terms

    • Animals
    • Bone Density
    • Densitometry / veterinary
    • Female
    • Forelimb / anatomy & histology
    • Forelimb / physiology
    • Horses / anatomy & histology
    • Horses / physiology
    • Male
    • Toes / anatomy & histology
    • Toes / physiology
    • Tomography, X-Ray Computed / veterinary

    References

    This article includes 34 references
    1. Dzierzęcka M, Wąsowski AJ, Kobryń H. Leg bones injuries during race training in two- year-old thoroughbred horses.. Med Wet 2007;63:574–577.
    2. Yovich JV, McIlwraith CW. Arthroscopic surgery for osteochondral fractures of the proximal phalanx of the metacarpophalangeal and metatarsophalangeal (fetlock) joints in horses.. J Am Vet Med Assoc 1986 Feb 1;188(3):273-9.
      pubmed: 2869018
    3. Ellis DR, Simpson DJ, Greenwood RE, Crowhurst JS. Observations and management of fractures of the proximal phalanx in young Thoroughbreds.. Equine Vet J 1987 Jan;19(1):43-9.
    4. Parkin TD, Clegg PD, French NP, Proudman CJ, Riggs CM, Singer ER, Webbon PM, Morgan KL. Risk of fatal distal limb fractures among Thoroughbreds involved in the five types of racing in the United Kingdom.. Vet Rec 2004 Apr 17;154(16):493-7.
      doi: 10.1136/vr.154.16.493pubmed: 15130054google scholar: lookup
    5. Tóth P, Horváth C, Ferencz V, Nagy K, Gligor N, Szenci O, Bodó G. Assessment of the mineral density and mineral content of the equine third metacarpal and first phalanx bone by dual energy x-ray absorptiometry.. Acta Vet Hung 2010 Sep;58(3):317-29.
      doi: 10.1556/AVet.58.2010.3.5pubmed: 20713323google scholar: lookup
    6. Firth EC, Rogers CW, van Weeren PR, Barneveld A, McIlwraith CW, Kawcak CE, Goodship AE, Smith RK. Mild exercise early in life produces changes in bone size and strength but not density in proximal phalangeal, third metacarpal and third carpal bones of foals.. Vet J 2011 Dec;190(3):383-9.
      doi: 10.1016/j.tvjl.2010.11.016pubmed: 21186128google scholar: lookup
    7. Alho A. Mineral and mechanics of bone fragility fractures. A review of fixation methods.. Acta Orthop Scand 1993 Apr;64(2):227-32.
      doi: 10.3109/17453679308994578pubmed: 8498193google scholar: lookup
    8. Czerwiński E. [Radiologic diagnosis and densitometry of osteoporosis].. Przegl Lek 1997;54(4):220-5.
      pubmed: 9333870
    9. Claes LE, Wilke HJ, Kiefer H. Osteonal structure better predicts tensile strength of healing bone than volume fraction.. J Biomech 1995 Nov;28(11):1377-90.
      doi: 10.1016/0021-9290(95)00006-4pubmed: 8522550google scholar: lookup
    10. Chappard D, Legrand E, Basle MF, Audran M. Measuring trabecular bone architecture by image analysis of histological sections.. Eur Microsc Anal 1997;11:13–15.
    11. Walters J, Koo WW, Bush A, Hammami M. Effect of hand dominance on bone mass measurement in sedentary individuals.. J Clin Densitom 1998 Winter;1(4):359-67.
      doi: 10.1385/JCD:1:4:359pubmed: 15304882google scholar: lookup
    12. Akar S, Sivrikaya H, Canikli A, Varoğlu E. Lateralized mineral content and density in distal forearm bones in right-handed men and women: relation of structure to function.. Int J Neurosci 2002 Mar;112(3):301-11.
      pubmed: 12187781doi: 10.1080/00207450212034google scholar: lookup
    13. Sanchis-Moysi J, Dorado C, Olmedillas H, Serrano-Sanchez JA, Calbet JA. Bone mass in prepubertal tennis players.. Int J Sports Med 2010 Jun;31(6):416-20.
      doi: 10.1055/s-0030-1248331pubmed: 20301044google scholar: lookup
    14. Gümüştekin K, Akar S, Dane S, Yildirim M, Seven B, Varoglu E. Handedness and bilateral femoral bone densities in men and women.. Int J Neurosci 2004 Dec;114(12):1533-47.
      doi: 10.1080/00207450490509186pubmed: 15512837google scholar: lookup
    15. Llorente M, Riba D, Palou L, Carrasco L, Mosquera M, Colell M, Feliu O. Population-level right-handedness for a coordinated bimanual task in naturalistic housed chimpanzees: replication and extension in 114 animals from Zambia and Spain.. Am J Primatol 2011 Mar;73(3):281-90.
      doi: 10.1002/ajp.20895pubmed: 20954250google scholar: lookup
    16. Smith HM, Thompson CL. Observations of hand preference in wild groups of white-faced sakis (Pithecia pithecia) in Suriname.. Am J Primatol 2011 Jul;73(7):655-64.
      doi: 10.1002/ajp.20942pubmed: 21425315google scholar: lookup
    17. Blendinger W. Psychologie und Verhaltenweisen des Pferdes.. .
    18. Pearce GP, May-Davis S, Greaves D. Femoral asymmetry in the Thoroughbred racehorse.. Aust Vet J 2005 Jun;83(6):367-70.
    19. Davies HM, Watson KM. Third metacarpal bone laterality asymmetry and midshaft dimensions in Thoroughbred racehorses.. Aust Vet J 2005 Apr;83(4):224-6.
    20. Ramzan PH, Palmer L. Musculoskeletal injuries in Thoroughbred racehorses: a study of three large training yards in Newmarket, UK (2005-2007).. Vet J 2011 Mar;187(3):325-9.
      doi: 10.1016/j.tvjl.2009.12.019pubmed: 20089426google scholar: lookup
    21. Laib A, Häuselmann HJ, Rüegsegger P. In vivo high resolution 3D-QCT of the human forearm.. Technol Health Care 1998 Dec;6(5-6):329-37.
      pubmed: 10100936
    22. Laib A, Rüegsegger P. Calibration of trabecular bone structure measurements of in vivo three-dimensional peripheral quantitative computed tomography with 28-microm-resolution microcomputed tomography.. Bone 1999 Jan;24(1):35-9.
      doi: 10.1016/S8756-3282(98)00159-8pubmed: 9916782google scholar: lookup
    23. Link TM, Bauer JS. Imaging of trabecular bone structure.. Semin Musculoskelet Radiol 2002 Sep;6(3):253-61.
      doi: 10.1055/s-2002-36723pubmed: 12541203google scholar: lookup
    24. Fürst A, Meier D, Michel S, Schmidlin A, Held L, Laib A. Effect of age on bone mineral density and micro architecture in the radius and tibia of horses: an Xtreme computed tomographic study.. BMC Vet Res 2008 Jan 25;4:3.
      pmc: PMC2267174pubmed: 18221526doi: 10.1186/1746-6148-4-3google scholar: lookup
    25. Nicholson CL, Firth EC. Assessment of bone response to conditioning exercise in the radius and tibia of young thoroughbred horses using pQCT.. J Musculoskelet Neuronal Interact 2010 Sep;10(3):199-206.
      pubmed: 20811144
    26. Whitton RC, Trope GD, Ghasem-Zadeh A, Anderson GA, Parkin TD, Mackie EJ, Seeman E. Third metacarpal condylar fatigue fractures in equine athletes occur within previously modelled subchondral bone.. Bone 2010 Oct;47(4):826-31.
      doi: 10.1016/j.bone.2010.07.019pubmed: 20659599google scholar: lookup
    27. Claerhoudt S, Bergman EH, van der Veen H, Vanderperren K, Raes EV, Saunders JH. Computed tomographic morphology of the synovial invaginations of the distal sesamoid bone of the horse.. Anat Histol Embryol 2011 Feb;40(1):55-60.
    28. Komosa M, Moliński K, Godynicki S. The variability of cranial morphology in modern horses.. Zoolog Sci 2006 Mar;23(3):289-98.
      doi: 10.2108/zsj.23.289pubmed: 16603822google scholar: lookup
    29. Robling AG, Hinant FM, Burr DB, Turner CH. Improved bone structure and strength after long-term mechanical loading is greatest if loading is separated into short bouts.. J Bone Miner Res 2002 Aug;17(8):1545-54.
      doi: 10.1359/jbmr.2002.17.8.1545pubmed: 12162508google scholar: lookup
    30. Dziedzic-Gocławska A. Tkanka kostna.. .
    31. Piastowska AW. Influence of biologically active substances from soybean on mineral content and mechanical properties of bones in rats.. 2005.
    32. Advani S, Wimalawansa SJ. Bones and nutrition: common sense supplementation for osteoporosis.. Curr Womens Health Rep 2003 Jun;3(3):187-92.
      pubmed: 12734028
    33. Martin RB, Ishida J. The relative effects of collagen fiber orientation, porosity, density, and mineralization on bone strength.. J Biomech 1989;22(5):419-26.
      pubmed: 2777816doi: 10.1016/0021-9290(89)90202-9google scholar: lookup
    34. Turner CH, Robling AG. Designing exercise regimens to increase bone strength.. Exerc Sport Sci Rev 2003 Jan;31(1):45-50.

    Citations

    This article has been cited 2 times.
    1. Dzierzęcka M, Jaworski M, Purzyc H, Barszcz K. Regional Differences of Densitometric and Geometric Parameters of the Third Metacarpal Bone in Coldblood Horses - pQCT Study.. J Vet Res 2017 Mar;61(1):111-120.
      doi: 10.1515/jvetres-2017-0014pubmed: 29978062google scholar: lookup
    2. Paśko S, Dzierzęcka M, Purzyc H, Charuta A, Barszcz K, Bartyzel BJ, Komosa M. The Osteometry of Equine Third Phalanx by the Use of Three-Dimensional Scanning: New Measurement Possibilities.. Scanning 2017;2017:1378947.
      doi: 10.1155/2017/1378947pubmed: 29109801google scholar: lookup