Peak vertical jump power predicts radial bone strength better than hand grip strength in healthy individuals. | Communications in Kinesiology

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Published: Mar 9, 2021

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2021-11-21 (3)

2021-03-14 (2)

2021-03-09 (1)

DOI: https://doi.org/10.51224/cik.v1i2.13

Keywords:

pQCT, strength-strain index, bone strength index, vertical jump, grip strength, bone strength

Vanessa Yingling

California State University, East Bay

https://orcid.org/0000-0002-7775-6223

Rebekkah Reichert

California State University, East Bay

Andrew Denys

California State University, East Bay

Priscilla Franson

California State University, East Bay

Kimberly Espartero

California State University, East Bay

Maria Alvarez

California State University, East Bay

Kirstie Huynh

California State University, East Bay

Karen Serrano Vides

California State University, East Bay

Arianna Mazzarini

California State University, East Bay

Abstract

Osteoporosis is considered a pediatric disease with geriatric consequences. However, measuring bone strength in children is complex and creates a practical problem for health professionals, teachers and parents. A non-invasive measure of muscle fitness that correlates to bone strength may provide a means to monitor bone strength throughout the lifespan. Therefore, the purpose of this study was to investigate the relationship between common muscle function tests (relative grip strength (RGS), peak vertical jump power (PP)) and bone strength in the radial diaphysis and epiphysis of a healthy population. Healthy participants (n=147 (81 female)) performed a bilateral grip strength test using a hand dynamometer, and a maximal vertical jump test. Peak vertical jump power was calculated from maximal jump height using the Sayer’s equation. Moment of inertia (MoI), cortical area (CoA), cortical bone mineral density (cBMD), and polar strength-strain index (SSIp) were measured using peripheral Quantitative Computed Tomography (pQCT) to determine bone strength parameters at the 66% radial site (predominantly cortical bone). At the 4% site (trabecular bone site), bone mineral content (vBMC.tb), bone mineral density (vBMD.tb), total area (ToA.tb) and bone strength index (BSIc) were measured. Hierarchical multiple regression analyses determined the relationship of each muscle function test for each bone envelope (cortical and trabecular). For the cortical bone measurements: RGS, and PP were both significantly correlated with CoA, MoI, and SSIp. Peak vertical jump power predicted bone strength parameters to a greater extent compared to RGS. For the trabecular bone envelope, RGS was not a predictor of bone strength however peak power was a significant predictor of bone strength parameters. Peak vertical jump power was a significant predictor of bone strength at both trabecular and cortical radial sites. Interestingly PP, a lower limb measurement explained the most variance in the bone strength of the upper limb.

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Yingling, V., Reichert, R., Denys, A., Franson, P., Espartero, K., Alvarez, M. ., … Mazzarini, A. (2021). Peak vertical jump power predicts radial bone strength better than hand grip strength in healthy individuals . Communications in Kinesiology, 1(2). https://doi.org/10.51224/cik.v1i2.13

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Vol. 1 No. 2 (2021)

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Articles

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This work is licensed under a Creative Commons Attribution 4.0 International License.

Authors retain the copyright of their manuscripts, and all Open Access articles are distributed under the terms of the Creative Commons Attribution License (CC-BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.

Author Biographies

Vanessa Yingling, California State University, East Bay

Department of Kinesiology Associate Professor California State University, East Bay

Karen Serrano Vides, California State University, East Bay

Osteoporosis is considered a pediatric disease with geriatric consequences. However, measuring bone strength in children is complex and creates a practical problem for health professionals, teachers and parents. A non-invasive measure of muscle fitness that correlates to bone strength may provide a means to monitor bone strength throughout the lifespan. Therefore, the purpose of this study was to investigate the relationship between common muscle function tests (relative grip strength (RGS), peak vertical jump power (PP)) and bone strength in the radial diaphysis and epiphysis of a healthy population. Healthy participants (n=147 (81 female)) performed a bilateral grip strength test using a hand dynamometer, and a maximal vertical jump test. Peak vertical jump power was calculated from maximal jump height using the Sayer’s equation. Moment of inertia (MoI), cortical area (CoA), cortical bone mineral density (cBMD), and polar strength-strain index (SSIp) were measured using peripheral Quantitative Computed Tomography (pQCT) to determine bone strength parameters at the 66% radial site (predominantly cortical bone). At the 4% site (trabecular bone site), bone mineral content (vBMC.tb), bone mineral density (vBMD.tb), total area (ToA.tb) and bone strength index (BSIc) were measured. Hierarchical multiple regression analyses determined the relationship of each muscle function test for each bone envelope (cortical and trabecular). For the cortical bone measurements: RGS, and PP were both significantly correlated with CoA, MoI, and SSIp. Peak vertical jump power predicted bone strength parameters to a greater extent compared to RGS. For the trabecular bone envelope, RGS was not a predictor of bone strength however peak power was a significant predictor of bone strength parameters. Peak vertical jump power was a significant predictor of bone strength at both trabecular and cortical radial sites. Interestingly PP, a lower limb measurement explained the most variance in the bone strength of the upper limb.

References

Ashe, M. C., Liu-Ambrose, T. Y. L., Cooper, D. M. L., Khan, K. M., & McKay, H. A. (2008). Muscle power is related to tibial bone strength in older women. Osteoporosis International, 19(12), 1725–1732. https://doi.org/10.1007/s00198-008-0655-6

Augat, P., Iida, H., Jiang, Y., Diao, E., & Genant, H. K. (1998). Distal radius fractures: mechanisms of injury and strength prediction by bone mineral assessment. Journal of Orthopaedic Research: Official Publication of the Orthopaedic Research Society, 16(5), 629–635. https://doi.org/10.1002/jor.1100160517

Baptista, F., Mil-Homens, P., Carita, A., Janz, K., & Sardinha, L. (2016). Peak vertical jump power as a marker of bone health in children. International Journal of Sports Medicine, 37(08), 653–658. https://doi.org/10.1055/s-0042-105290

Best, A., Holt, B., Troy, K., & Hamill, J. (2017). Trabecular bone in the calcaneus of runners. PLOS ONE, 12(11), e0188200. https://doi.org/10.1371/journal.pone.0188200

Boonen, S., Cheng, X. G., Nijs, J., Nicholson, P. H. F., Verbeke, G., Lesaffre, E., … Dequeker, J. (1997). Factors associated with cortical and trabecular bone loss as quantified by peripheral computed tomography (pQCT) at the ultradistal radius in aging women. Calcified Tissue International, 60(2), 164–170. https://doi.org/10.1007/s002239900208

Canadian Society for Exercise Physiology, Canada, & Health Canada. (2003). The Canadian physical activity, fitness & lifestyle approach: CSEP health & fitness program’s health-related appraisal & counselling strategy. Ottawa, Ont.: Canadian Society for Exercise Physiology.

Cointry, G., Ferretti, J. L., Reina, P. S., Nocciolono, L. M., Rittweger, J., & Capozza, R. F. (2014). The pQCT “Bone Strength Indices”(BSIs, SSI). Relative mechanical impact and diagnostic value of the indicators of bone tissue and design quality employed in their calculation in healthy men and pre-and post-menopausal women. Journal of Musculoskeletal and Neuronal Interactions, 14(1), 29–40.

Cooper, C., Campion, G., & Melton, L. J. (1992). Hip fractures in the elderly: A world-wide projection. Osteoporosis International: A Journal Established as Result of Cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA, 2(6), 285–289. https://doi.org/10.1007/bf01623184

Dequeker, J., & Van Tendeloo, G. (1982). Metacarpal bone mass and upper-extremity strength in 18-year-old boys. Investigative Radiology, 17(4), 427–429. https://doi.org/10.1097/00004424-198207000-00026

Ferretti, J. L., Cointry, G. R., Capozza, R. F., Capiglioni, R., & Chiappe, M. A. (2001). Analysis of biomechanical effects on bone and on the muscle-bone interactions in small animal models. Journal of Musculoskeletal & Neuronal Interactions, 1(3), 263–274.

Földhazy, Z., Arndt, A., Milgrom, C., Finestone, A., & Ekenman, I. (2005). Exercise-induced strain and strain rate in the distal radius. The Journal of Bone and Joint Surgery. British Volume, 87-B(2), 261–266. https://doi.org/10.1302/0301-620X.87B2.14857

Frank, A. W., Lorbergs, A. L., Chilibeck, P. D., Farthing, J. P., & Kontulainen, S. A. (2010). Muscle cross sectional area and grip torque contraction types are similarly related to pQCT derived bone strength indices in the radii of older healthy adults. Journal of musculoskeletal & neuronal interactions. 10. 136-41.

Frank, A. W., Labas, M. C., Johnston, J. D., & Kontulainen, S. A. (2012). Site-specific variance in radius and tibia bone strength as determined by muscle size and body mass. Physiotherapy Canada, 64(3), 292–301. https://doi.org/10.3138/ptc.2010-40BH

Glüer, C.-C., Blake, G., Lu, Y., Blunt, B. A., Jergas, M., & Genant, H. K. (1995). Accurate assessment of precision errors: how to measure the reproducibility of bone densitometry techniques. Osteoporosis International, 5(4), 262–270. https://doi.org/10.1007/BF01774016

Golden, N. H. (2000). Osteoporosis prevention: A pediatric challenge. Archives of Pediatrics & Adolescent Medicine, 154(6), 542–543.

Greene, D. A., Naughton, G. A., Bradshaw, E., Moresi, M., & Ducher, G. (2012). Mechanical loading with or without weight-bearing activity: Influence on bone strength index in elite female adolescent athletes engaged in water polo, gymnastics, and track-and-field. Journal of Bone and Mineral Metabolism, 30(5), 580–587. https://doi.org/10.1007/s00774-012-0360-6

Haapasalo, H., Kontulainen, S., Sievänen, H., Kannus, P., Järvinen, M., & Vuori, I. (2000). Exercise-induced bone gain is due to enlargement in bone size without a change in volumetric bone density: A peripheral quantitative computed tomography study of the upper arms of male tennis players. Bone, 27(3), 351–357. https://doi.org/10.1016/s8756-3282(00)00331-8

Hasegawa, Y., Schneider, P., & Reiners, C. (2001). Age, sex, and grip strength determine architectural bone parameters assessed by peripheral quantitative computed tomography (pQCT) at the human radius. Journal of Biomechanics, 34(4), 497–503. https://doi.org/10.1016/s0021-9290(00)00211-6

Hsieh, Y.-F., Robling, A. G., Ambrosius, W. T., Burr, D. B., & Turner, C. H. (2001). Mechanical loading of diaphyseal bone in vivo: The strain threshold for an osteogenic response varies with location. Journal of Bone and Mineral Research, 16(12), 2291–2297. https://doi.org/10.1359/jbmr.2001.16.12.2291

Innes, E. (1999). Handgrip strength testing: A review of the literature. Australian Occupational Therapy Journal, 46(3), 120–140. https://doi.org/10.1046/j.1440-1630.1999.00182.x

Janz, K. (2002). Physical activity and bone development during childhood and adolescence. Implications for the prevention of osteoporosis. Minerva Pediatrica, 54(2), 93–104.

Janz, K. F., Letuchy, E. M., Burns, T. L., Francis, S. L., & Levy, S. M. (2015). Muscle power predicts adolescent bone strength: Iowa Bone Development Study. Medicine & Science in Sports & Exercise, 47(10), 2201–2206. https://doi.org/10.1249/MSS.0000000000000648

Kaji, H., Kosaka, R., Yamauchi, M., Kuno, K., Chihara, K., & Sugimoto, T. (2005). Effects of age, grip strength and smoking on forearm volumetric bone mineral density and bone geometry by peripheral quantitative computed tomography: Comparisons between Female and Male. Endocrine Journal, 52(6), 659–666. https://doi.org/10.1507/endocrj.52.659

Kannus, P., Haapasalo, H., Sankelo, M., Sievänen, H., Pasanen, M., Heinonen, A., … Vuori, I. (1995). Effect of starting age of physical activity on bone mass in the dominant arm of tennis and squash players. Annals of Internal Medicine, 123(1), 27–31. https://doi.org/10.7326/0003-4819-123-1-199507010-00003

Kontulainen, S. A., Johnston, J. D., Liu, D., Leung, C., Oxland, T. R., & McKay, H. A. (2008). Strength indices from pQCT imaging predict up to 85% of variance in bone failure properties at tibial epiphysis and diaphysis. Journal of Musculoskeletal & Neuronal Interactions, 8(4), 401–409.

Kontulainen, S., Sievänen, H., Kannus, P., Pasanen, M., & Vuori, I. (2003). Effect of long-term impact-loading on mass, size, and estimated strength of humerus and radius of female racquet-sports players: A Peripheral quantitative computed tomography study between young and old starters and controls. Journal of Bone and Mineral Research, 18(2), 352–359. https://doi.org/10.1359/jbmr.2003.18.2.352

Lambert, C., Beck, B. R., Harding, A. T., Watson, S. L., & Weeks, B. K. (2019). Impact versus resistance training for bone in young women: Preliminary Findings Of The OPTIMA-Ex Trial: 3067 Board #113 May 31 3:30 PM - 5:00 PM. Medicine & Science in Sports & Exercise, 51(Supplement), 845. https://doi.org/10.1249/01.mss.0000563025.70640.3b

Lanyon, L. E. (1996). Using functional loading to influence bone mass and architecture: Objectives, mechanisms, and relationship with estrogen of the mechanically adaptive process in bone. Bone, 18(1 Suppl), 37S-43S. https://doi.org/10.1016/8756-3282(95)00378-9

Lorbergs, A. L., Farthing, J. P., Baxter-Jones, A. D. G., & Kontulainen, S. A. (2011). Forearm muscle size, strength, force, and power in relation to pQCT-derived bone strength at the radius in adults. Applied Physiology, Nutrition, and Metabolism = Physiologie Appliquée, Nutrition Et Métabolisme, 36(5), 618–625. https://doi.org/10.1139/h11-065

Macdonald, H., Kontulainen, S., Petit, M., Janssen, P., & McKay, H. (2006). Bone strength and its determinants in pre- and early pubertal boys and girls. Bone, 39(3), 598–608. https://doi.org/10.1016/j.bone.2006.02.057

Marks, R. (2009). Hip fracture epidemiological trends, outcomes, and risk factors, 1970–2009. International Journal of General Medicine, 1. https://doi.org/10.2147/IJGM.S5906

Mathiowetz, V., Weber, K., Volland, G., & Kashman, N. (1984). Reliability and validity of grip and pinch strength evaluations. The Journal of Hand Surgery, 9(2), 222–226. https://doi.org/10.1016/s0363-5023(84)80146-x

Mosley, J. R., & Lanyon, L. E. (1998). Strain rate as a controlling influence on adaptive modeling in response to dynamic loading of the ulna in growing male rats. Bone, 23(4), 313–318. https://doi.org/10.1016/s8756-3282(98)00113-6

Nellans, K. W., Kowalski, E., & Chung, K. C. (2012). The epidemiology of distal radius fractures. Hand Clinics, 28(2), 113–125. https://doi.org/10.1016/j.hcl.2012.02.001

Rantalainen, T., Nikander, R., Heinonen, A., Multanen, J., Häkkinen, A., Jämsä, T., … Sievänen, H. (2010). Neuromuscular performance and body mass as indices of bone loading in premenopausal and postmenopausal women. Bone, 46(4), 964–969. https://doi.org/10.1016/j.bone.2010.01.002

Sayers, S. P., Harackiewicz, D. V., Harman, E. A., Frykman, P. N., & Rosenstein, M. T. (1999). Cross-validation of three jump power equations. Medicine and Science in Sports and Exercise, 31(4), 572–577. https://doi.org/10.1097/00005768-199904000-00013

Schoenau, E., Neu, C. M., Beck, B., Manz, F., & Rauch, F. (2002). Bone mineral content per muscle cross-sectional area as an index of the functional muscle-bone unit. Journal of Bone and Mineral Research: American Society for Bone and Mineral Research, 17(6), 1095–1101. https://doi.org/10.1359/jbmr.2002.17.6.1095

Stengel, S. V. (2005). Power training is more effective than strength training for maintaining bone mineral density in postmenopausal women. Journal of Applied Physiology, 99(1), 181–188. https://doi.org/10.1152/japplphysiol.01260.2004

Sugiyama, T., Price, J. S., & Lanyon, L. E. (2010). Functional adaptation to mechanical loading in both cortical and cancellous bone is controlled locally and is confined to the loaded bones. Bone, 46(2), 314–321. https://doi.org/10.1016/j.bone.2009.08.054

Sumnik, Z., Land, C., Coburger, S., Neu, C., Manz, F., Hrach, K., & Schoenau, E. (2006). The muscle-bone unit in adulthood: Influence of sex, height, age and gynecological history on the bone mineral content and muscle cross-sectional area. Journal of Musculoskeletal and Neuronal Interactions, 6(2), 195.

Turner, C. H., & Robling, A. G. (2003). Designing exercise regimens to increase bone strength. Exercise and Sport Sciences Reviews, 31(1), 45–50. https://doi.org/10.1097/00003677-200301000-00009

Van der Meulen, M. C. H., Jepsen, K. J., & Mikić, B. (2001). Understanding bone strength: Size isn’t everything. Bone, 29(2), 101–104.https://doi.org/10.1016/s8756-3282(01)00491-4

Wapniarz, M., Lehmann, R., Reincke, M., Schönau, E., Klein, K., & Allolio, B. (1997). Determinants of radial bone density as measured by PQCT in pre- and postmenopausal women: The role of bone size. Journal of Bone and Mineral Research, 12(2), 248–254. https://doi.org/10.1359/jbmr.1997.12.2.248

Warden, S. J., Mantila Roosa, S. M., Kersh, M. E., Hurd, A. L., Fleisig, G. S., Pandy, M. G., & Fuchs, R. K. (2014). Physical activity when young provides lifelong benefits to cortical bone size and strength in men. Proceedings of the National Academy of Sciences, 111(14), 5337–5342. https://doi.org/10.1073/pnas.1321605111

Warden, Stuart J., Bogenschutz, E. D., Smith, H. D., & Gutierrez, A. R. (2009). Throwing induces substantial torsional adaptation within the midshaft humerus of male baseball players. Bone, 45(5), 931–941. https://doi.org/10.1016/j.bone.2009.07.075

Warden, Stuart J., Carballido-Gamio, J., Avin, K. G., Kersh, M. E., Fuchs, R. K., Krug, R., & Bice, R. J. (2019). Adaptation of the proximal humerus to physical activity: A within-subject controlled study in baseball players. Bone, 121, 107–115. https://doi.org/10.1016/j.bone.2019.01.008

Yingling, V. R., Webb, S. L., Inouye, C., O, J., & Sherwood, J. J. (2020). Muscle Power Predicts Bone Strength in Division II Athletes. Journal of strength and conditioning research, 34(6), 1657–1665. https://doi.org/10.1519/JSC.0000000000002222