Abstract
Bone loss is more common in Parkinson’s disease (PD) than in the general population. Several factors may be involved in the development of bone loss, including malnutrition, immobilization, low body mass index, decreased muscle strength, vitamin D deficiency and medication use. This study investigates the prevalence of osteoporosis and possible risk factors associated with bone loss in early stage PD. In 186 PD patients (Hoehn and Yahr stage 1–2.5, mean age 64.1 years, 71 % men) bone mineral density (BMD) measurements were performed with DEXA. T- and Z-scores were calculated. Univariate linear regression analysis was performed to identify variables that contributed to BMD. 25-OH-vitamin D status of PD patients was compared with 802 controls (mean age 63.3 years, 50 % men) using linear regression analysis. Osteoporosis (11.8 %) and osteopenia (41.4 %) were common in PD patients. Mean Z-score for the hip was 0.24 (SD 0.93), and for the lumbar spine 0.72 (SD 1.91). Female gender, low weight, and low 25-OH-vitamin D were significantly correlated with BMD of the hip and lumbar spine. PD patients had lower 25(OH)D serum levels than controls (B = −10, p = 0.000). More than half of the patients with early stage PD had an abnormal BMD. Female gender, low weight, and low vitamin D concentration were associated with bone loss. Furthermore, vitamin D concentrations were reduced in PD patients. These results underscore the importance of proactive screening for bone loss and vitamin D deficiency, even in early stages of PD.
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Abou-Raya S, Helmii M, Abou-Raya A (2009) Bone and mineral metabolism in older adults with Parkinson’s disease. Age Ageing 38:675–680
Allen NE, Sherrington C, Paul SS, Canning CG (2011) Balance and falls in Parkinson’s disease: a meta-analysis of the effect of exercise and motor training. Mov Disord 26:1605–1615
Ashburn A, Fazakarley L, Ballinger C, Pickering R, McLellan LD, Fitton C (2007) A randomised controlled trial of a home based exercise programme to reduce the risk of falling among people with Parkinson’s disease. J Neurol Neurosurg Psychiatry 78:678–684
Bachmann CG, Trenkwalder C (2006) Body weight in patients with Parkinson’s disease. Mov Disord 21:1824–1830
Bezza A, Ouzzif Z, Naji H, Achemlal L, Mounach A, Nouijai M, Bourazza A, Mossadeq R, El MA (2008) Prevalence and risk factors of osteoporosis in patients with Parkinson’s disease. RheumatolInt 28:1205–1209
Bloem BR, Geurts AC, Hassin-Baer S, Giladi N (2008) Treatment of gait and balance disorders. In: Hallett M, Poewe W (eds) Therapeutics of Parkinson’s disease and other movement disorders. Wiley, Chichester, pp 417–443
Canning CG, Allen NE, Dean CM, Goh L, Fung VS (2012) Home-based treadmill training for individuals with Parkinson’s disease: a randomized controlled pilot trial. Clin Rehabil 26(9):817–826
Cruise KE, Bucks RS, Loftus AM, Newton RU, Pegoraro R, Thomas MG (2010) Exercise and Parkinson’s: benefits for cognition and quality of life. Acta NeurolScand 123(1):13–19
Evatt ML, Delong MR, Khazai N, Rosen A, Triche S, Tangpricha V (2008) Prevalence of vitamin d insufficiency in patients with Parkinson disease and Alzheimer disease. Arch Neurol 65:1348–1352
Evatt ML, DeLong MR, Kumari M, Auinger P, McDermott MP, Tangpricha V (2011) High prevalence of hypovitaminosis D status in patients with early Parkinson disease. Arch Neurol 68:314–319
Fink HA, Kuskowski MA, Orwoll ES, Cauley JA, Ensrud KE (2005) Association between Parkinson’s disease and low bone density and falls in older men: the osteoporotic fractures in men study. J Am Geriatr Soc 53:1559–1564
Gelb DJ, Oliver E, Gilman S (1999) Diagnostic criteria for Parkinson disease. Arch Neurol 56:33–39
Goetz CG, Poewe W, Rascol O, Sampaio C, Stebbins GT, Counsell C, Giladi N, Holloway RG, Moore CG, Wenning GK, Yahr MD, Seidl L (2004) Movement disorder society task force report on the Hoehn and Yahr staging scale: status and recommendations. Mov Disord 19:1020–1028
Goetz CG, Tilley BC, Shaftman SR, Stebbins GT, Fahn S, Martinez-Martin P, Poewe W, Sampaio C, Stern MB, Dodel R, Dubois B, Holloway R, Jankovic J, Kulisevsky J, Lang AE, Lees A, Leurgans S, LeWitt PA, Nyenhuis D, Olanow CW, Rascol O, Schrag A, Teresi JA, van Hilten JJ, LaPelle N (2008) Movement Disorder Society-sponsored revision of the Unified Parkinson’s Disease Rating Scale (MDS-UPDRS): scale presentation and clinimetric testing results. Mov Disord 23:2129–2170
Hyattsville M (2007) Dual-energy X-ray absorptiometry (DXA) procedure manual. In: US Department of Health and Human Services CfDCaP (ed) Centers for Disease Control and Prevention, National Center for Health Statistics, National Health and Nutrition Examination Survey
Idjadi JA, Aharonoff GB, Su H, Richmond J, Egol KA, Zuckerman JD, Koval KJ (2005) Hip fracture outcomes in patients with Parkinson’s disease. Am J Orthop (Belle Mead, NJ) 34:341–346
Invernizzi M, Carda S, Viscontini GS, Cisari C (2009) Osteoporosis in Parkinson’s disease. Parkinsonism Relat Disord 15:339–346
Lam K, Li M, Mok V, Hui A, Woo J (2010) A case control study on bone mineral density in Chinese patients with Parkinson’s disease. Parkinsonism Relat Disord 16:471–474
Lebrun CE, van der Schouw YT, de Jong FH, Pols HA, Grobbee DE, Lamberts SW (2005) Endogenous oestrogens are related to cognition in healthy elderly women. Clin Endocrinol (Oxf) 63:50–55
Lorefalt B, Ganowiak W, Palhagen S, Toss G, Unosson M, Granerus AK (2004) Factors of importance for weight loss in elderly patients with Parkinson’s disease. Acta Neurol Scand 110:180–187
Muller M, Aleman A, Grobbee DE, de Haan EH, van der Schouw YT (2005) Endogenous sex hormone levels and cognitive function in aging men: is there an optimal level? Neurology 64:866–871
Pang MY, Mak MK (2009) Muscle strength is significantly associated with hip bone mineral density in women with Parkinson’s disease: a cross-sectional study. J Rehabil Med 41:223–230
Pang MY, Mak MK (2009) Trunk muscle strength, but not trunk rigidity, is independently associated with bone mineral density of the lumbar spine in patients with Parkinson’s disease. Mov Disord 24:1176–1182
Pickering RM, Grimbergen YA, Rigney U, Ashburn A, Mazibrada G, Wood B, Gray P, Kerr G, Bloem BR (2007) A meta-analysis of six prospective studies of falling in Parkinson’s disease. Mov Disord 22:1892–1900
Sato Y, Iwamoto J, Honda Y (2011) Amelioration of osteoporosis and hypovitaminosis D by sunlight exposure in Parkinson’s disease. Parkinsonism Relat Disord 17:22–26
Schneider JL, Fink HA, Ewing SK, Ensrud KE, Cummings SR (2008) The association of Parkinson’s disease with bone mineral density and fracture in older women. Osteoporos Int 19:1093–1097
Song IU, Kim JS, Lee SB, Ryu SY, An JY, Jeong DS, Kim YI, Lee KS (2009) The relationship between low bone mineral density and Parkinson’s disease in a Korean population. J Clin Neurosci 16:807–809
Stel VS, Smit JH, Pluijm SM, Visser M, Deeg DJ, Lips P (2004) Comparison of the LASA physical activity questionnaire with a 7-day diary and pedometer. J Clin Epidemiol 57:252–258
Taggart H, Crawford V (1995) Reduced bone density of the hip in elderly patients with Parkinson’s disease. Age Ageing 24:326–328
van der Marck MA, Dicke HC, Uc EY, Kentin ZH, Borm GF, Bloem BR, Overeem S, Munneke M (2012) Body mass index in Parkinson’s disease: a meta-analysis. Parkinsonism Relat Disord 18:263–267
van Nimwegen M, Speelman AD, Hofman-van Rossum EJ, Overeem S, Deeg DJ, Borm GF, van der Horst MH, Bloem BR, Munneke M (2011) Physical inactivity in Parkinson’s disease. J Neurol 258:2214–2221
van Nimwegen M, Speelman AD, Smulders K, Overeem S, Borm GF, Backx FJ, Bloem BR, Munneke M (2010) Design and baseline characteristics of the ParkFit study, a randomized controlled trial evaluating the effectiveness of a multifaceted behavioral program to increase physical activity in Parkinson patients. BMC Neurol 10:70–79
Vaserman N (2005) Parkinson’s disease and osteoporosis. Joint Bone Spine 72:484–488
Wood B, Walker R (2005) Osteoporosis in Parkinson’s disease. Mov Disord 20:1636–1640
Acknowledgments
This study is funded by ZonMw (The Netherlands Organization for Health Research and Development (75020012)); The Michael J Fox Foundation for Parkinson’s research; VGZ; Glaxo Smith Kline; the Dutch Parkinson’s disease society; and the National Parkinson Foundation.
Conflicts of interest
FB, ADS, MvN, YTvdS and HJJV reported no conflicts of interest. FJGB received grants from ZonMw and the Dutch Diabetes Fund. BRB has served as an editorial board member of Movement Disorders, currently serves as an editorial board member of Physiotherapy Canada, and is Associate Editor for the Journal of Parkinson’s disease. He received honoraria from serving on the scientific advisory board for Boehringer Ingelheim, Teva, Glaxo-Smith-Kline and Novartis and research support from the Netherlands Organization for Scientific Research (016.076.352), the Michael J Fox Foundation, the Prinses Beatrix Foundation, the Stichting Internationaal Parkinson Fonds and the Alkemade Keuls fonds. MM received grants from ZonMw, the Michael J Fox Foundation, the National Parkinson Foundation, the Dutch Parkinson’s Disease Society, and the Prinses Beatrix Fonds.
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All human studies must state that they have been approved by the appropriate ethics committee and have therefore been performed in accordance with the ethical standards laid down in 1964 Declaration of Helsinki.
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van den Bos, F., Speelman, A.D., van Nimwegen, M. et al. Bone mineral density and vitamin D status in Parkinson’s disease patients. J Neurol 260, 754–760 (2013). https://doi.org/10.1007/s00415-012-6697-x
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DOI: https://doi.org/10.1007/s00415-012-6697-x