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Osteopathien und Knochenstoffwechselerkrankungen

Klinische Bedeutung für die Frakturbehandlung

Pathological and metabolic bone diseases

Clinical importance for fracture treatment

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Zusammenfassung

Osteopathien und Knochenstoffwechselerkrankungen sind insgesamt häufig, werden aber im orthopädischen/unfallchirurgischen Alltag meist unzureichend adressiert! Das Symptom „Fraktur“ sollte Anlass sein, eine ursächliche Knochenstoffwechselstörung zu diagnostizieren und ggf. zu therapieren, um eine optimale Frakturheilung zu gewährleisten und Folgefrakturen zu verhindern. Im vorliegenden Artikel werden die Osteoporose, Osteopetrose, Hypophosphatasie und der Morbus Paget beispielhaft besprochen.Bei osteoporotischer Wirbelkörper- bzw. proximaler Femurfraktur muss neben der operativen Therapie auch die medikamentöse Behandlung der Grunderkrankung erfolgen. Da der Osteopetrose Defekte der osteoklastären Resorption zugrunde liegen, ist trotz pathologisch erhöhter Knochenmasse die Basistherapie mit Vitamin D3 und ggf. Kalzium entscheidend, um Hypokalzämien zu vermeiden. Diffuse muskuloskelettale Beschwerden – vor allem in Kombination mit Stressfrakturen – sollten an das Vorliegen einer Hypophosphatasie denken lassen und eine Bestimmung der alkalischen Phosphatase (AP) nach sich ziehen. Für den Morbus Paget, der oft durch eine erhöhte AP auffällt, stellen Bisphosphonate weiterhin die Therapie der Wahl dar.

Abstract

Pathological and metabolic bone diseases are common and relevant occurrences in orthopedics and trauma surgery; however, fractures are often treated as being the illness itself and not seen as the symptom of an underlying bone disease. This is why further diagnostics and systemic treatment options are often insufficiently considered in the routine treatment of fractures. This review focuses on osteoporosis, osteopetrosis, hypophosphatasia and Paget’s disease of bone.In patients with osteoporotic vertebral or proximal femur fractures, pharmaceutical treatment to prevent subsequent fractures is an integral part of fracture therapy together with surgical treatment. Osteopetrosis is caused by compromised osteoclastic bone resorption; therefore, even in the face of an elevated bone mass, vitamin D3 supplementation is crucial to avoid clinically relevant hypocalcemia. Unspecific symptoms of the musculoskeletal system, especially together with stress fractures, are typically found in patients suffering from hypophosphatasia. In these patients measurement of alkaline phosphatase shows reduced enzyme activity. Elevated levels of alkaline phosphatase are found in Paget’s disease of bone where bisphosphonates are still the treatment of choice.

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Literatur

  1. Barvencik F, Beil FT, Gebauer M, Busse B, Koehne T, Seitz S, Zustin J, Pogoda P, Schinke T, Amling M (2011) Skeletal mineralization defects in adult hypophosphatasia–a clinical and histological analysis. Osteoporos Int 22(10):2667–2675

    Article  CAS  PubMed  Google Scholar 

  2. Barvencik F, Gebauer M, Schinke T, Amling M (2008) Case report: multiple fractures in a patient with mutations of TWIST1 and TNSALP. Clin Orthop Relat Res 466(4):990–996

    Article  PubMed Central  PubMed  Google Scholar 

  3. Bollerslev J, Andersen PE Jr (1988) Radiological, biochemical and hereditary evidence of two types of autosomal dominant osteopetrosis. Bone 9:7–13

    Article  CAS  PubMed  Google Scholar 

  4. Bollerslev J, Henriksen K, Nielsen MF, Brixen K, Van Hul W (2013) Autosomal dominant osteopetrosis revisited: lessons from recent studies. Eur J Endocrinol 169(2):R39–R57

    Article  CAS  PubMed  Google Scholar 

  5. Breer S, Krause M, Marshall RP, Oheim R, Amling M, Barvencik F (2012) Stress fractures in elderly patients. Int Orthop 36(12):2581–2587

    Article  PubMed Central  PubMed  Google Scholar 

  6. Cameron HU, Fornasier VL, Van Zyl DV (2000) Strut allograft invasion by Paget’s disease of bone: a case report. Can J Surg 43(2):140–141

    PubMed Central  CAS  PubMed  Google Scholar 

  7. Coe JD, Murphy WA, Whyte MP (1986) Management of femoral fractures and pseudofractures in adult hypophosphatasia. J Bone Joint Surg Am 68:981–990

    CAS  PubMed  Google Scholar 

  8. Cole DE, Salisbury SR, Stinson RA, Coburn SP, Ryan LM, Whyte MP (1986) Increased serum pyridoxal-5’-phosphate in pseudohypophosphatasia. N Engl J Med 314(15):992–993

    Article  CAS  PubMed  Google Scholar 

  9. Cooper C, Harvey NC, Dennison EM, van Staa TP (2006) Update on the epidemiology of Paget’s disease of bone. J Bone Miner Res 21(Suppl 2):3–8

    Article  Google Scholar 

  10. Cortis K, Micallef K, Mizzi A (2011) Imaging Paget’s disease of bone – from head to toe. Clin Radiol 66:662–672

    Article  CAS  PubMed  Google Scholar 

  11. Dove J (1980) Complete fractures of the femur in Paget’s disease of bone. J Bone Joint Surg Br 62-B(1):12–17

    CAS  PubMed  Google Scholar 

  12. Fraser D (1957) Hypophosphatasia. Am J Med 22:730–746

    Article  CAS  PubMed  Google Scholar 

  13. Gauthier A, Kanis JA, Jiang Y, Dreinhöfer K, Martin M, Compston J, Borgström F, Cooper C, McCloskey E (2012) Burden of postmenopausal osteoporosis in Germany: estimations from a disease model. Arch Osteoporos 7:209–218

    Article  CAS  PubMed  Google Scholar 

  14. Girschick HJ, Schneider P, Haubitz I, Hiort O, Collmann H, Beer M, Shin JS, Seyberth HW (2006) Effective NSAID treatment indicates that hyperprostaglandinism is affecting the clinical severity of childhood hypophosphatasia. Orphanet J Rare Dis 1:24

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  15. Gonçalves MJ, Romão VC (2014) Images in clinical medicine. Saber tibia in Paget’s disease of bone. N Engl J Med 371(25):2417

    Article  PubMed  Google Scholar 

  16. Griz L, Fontan D, Mesquita P, Lazaretti-Castro M, Borba VZ, Borges JL, Fontenele T, Maia J, Bandeira F (2014) Diagnosis and management of Paget’s disease of bone. Arq Bras Endocrinol Metabol 58(6):587–599

    Article  PubMed  Google Scholar 

  17. Häussler B, Gothe H, Göl D, Glaeske G, Pientka L, Felsenberg D (2007) Epidemiology, treatment and costs of osteoporosis in Germany-the BoneEVA Study. Osteoporos Int 18(1):77–84

    Article  PubMed  Google Scholar 

  18. Hosking D, Meunier PJ, Ringe JD, Reginster JY, Gennari C (1996) Fortnightly review: Paget’s disease of bone: diagnosis and management. BMJ 312:491–494

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  19. van Hove RP, de Jong T, Nolte PA (2014) Autosomal dominant type I osteopetrosis is related with iatrogenic fractures in arthroplasty. Clin Orthop Surg 6(4):484–488

    Article  PubMed Central  PubMed  Google Scholar 

  20. Johnell O, Kanis JA (2006) An estimate of the worldwide prevalence and disability associated with osteoporotic fractures. Osteoporos Int 17(12):1726–1733

    Article  CAS  PubMed  Google Scholar 

  21. Langston AL, Campbell MK, Fraser WD, Maclennan G, Selby P, Ralston SH (2007) Clinical determinants of quality of life in Paget’s disease of bone. Calcif Tissue Int 80:1–9

    Article  CAS  PubMed  Google Scholar 

  22. Langston AL, Campbell MK, Fraser WD, MacLennan GS, Selby PL, Ralston SH et al (2010) Randomized trial of intensive bisphosphonate treatment versus symptomatic management in Paget’s disease of bone. J Bone Miner Res 25:20–31

    Article  CAS  PubMed  Google Scholar 

  23. Lucas GJ, Daroszewska A, Ralston SH (2006) Contribution of genetic factors to the pathogenesis of Paget’s disease of bone and related disorders. J Bone Miner Res 21(Suppl 2):31–37

    Article  Google Scholar 

  24. Mentrup B, Marschall C, Barvencik F, Amling M, Plendl H, Jakob F, Beck C (2011) Functional characterization of a novel mutation localized in the start codon of the tissue-nonspecific alkaline phosphatase gene. Bone 48(6):1401–1408

    Article  CAS  PubMed  Google Scholar 

  25. Mornet E (2007) Hypophosphatasia. Orphanet J Rare Dis 2:40

    Article  PubMed Central  PubMed  Google Scholar 

  26. Oliveira L, Torrijos EA (2012) Treatment of Paget’s disease of bone. Reumatol Clin 8(4):220–224

    Article  Google Scholar 

  27. Priemel M, von Domarus C, Klatte TO, Kessler S, Schlie J, Meier S, Proksch N, Pastor F, Netter C, Streichert T, Püschel K, Amling M (2010) Bone mineralization defects and vitamin D deficiency: histomorphometric analysis of iliac crest bone biopsies and circulating 25-hydroxyvitamin D in 675 patients. J Bone Miner Res 25(2):305–312

    Article  CAS  PubMed  Google Scholar 

  28. Ralston SH, Langston AL, Reid IR (2008) Pathogenesis and management of Paget’s disease of bone. Lancet 372(9633):155

    Article  CAS  PubMed  Google Scholar 

  29. Rapp K, Cameron ID, Kurrle S, Klenk J, Kleiner A, Heinrich S, König HH, Becker C (2010) Excess mortality after pelvic fractures in institutionalized older people. Osteoporos Int 21(11):1835–1839

    Article  CAS  PubMed  Google Scholar 

  30. Richter M, Droste P, Goesling T, Zech S, Krettek C (2006) Polyaxially-locked plate screws increase stability of fracture fixation in an experimental model of calcaneal fracture. J Bone Joint Surg Br 88(9):1257–1263

    Article  CAS  PubMed  Google Scholar 

  31. Röderer G, AbouElsoud M, Gebhard F, Claes L, Aschoff AJ, Kinzl L (2010) Biomechanical investigation of fixed-angle plate osteosynthesis of the proximal humerus. Unfallchirurg 113(2):133–138

    Article  PubMed  Google Scholar 

  32. Rousiere M, Michou L, Cornelis F, Orcel P (2003) Paget’s disease of bone. Best Pract Res Clin Rheumatol 17:1019–1041

    Article  CAS  PubMed  Google Scholar 

  33. S3-Leitlinie des Dachverbands der Deutschsprachigen Wissenschaftlichen Osteologischen Gesellschaften e. V. (2014) Prophylaxe, Diagnostik und Therapie der OSTEOPOROSE bei Männern ab dem 60. Lebensjahr und bei postmenopausalen Frauen

  34. Salpakoski A, Kallinen M, Kiviranta I, Alen M, Portegijs E, Jämsen E, Ylinen J, Rantanen T, Sipilä S (2015) Type of surgery is associated with pain and walking difficulties among older people with previous hip fracture. Geriatr Gerontol. doi:10.1111/ggi.12552

  35. Schulz AS, Komak U (2008) Osteopetrose – aktuelle Diagnostik und Therapie. J Mineralstoffwechsel 15(4):174–182

    Google Scholar 

  36. Seitz S, Priemel M, Zustin J, Beil FT, Semler J, Minne H, Schinke T, Amling M (2009) Paget’s disease of bone: histologic analysis of 754 patients. J Bone Miner Res 24(1):62–69

    Article  PubMed  Google Scholar 

  37. Shardlow DL, Giannoudis PV, Matthews SJ, Smith RM (1999) Stabilisation of acute femoral fractures in Paget’s disease. Int Orthop 23(5):283–285

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  38. Siris ES, Lyles KW, Singer FR, Meunier PJ (2006) Medical management of Paget’s disease of bone: indications for treatment and review of current therapies. J Bone Miner Res 21(2):P94

    Article  CAS  PubMed  Google Scholar 

  39. Stark Z, Savarirayan R (2009) Osteopetrosis. Orphanet J Rare Dis 4:5

    Article  PubMed Central  PubMed  Google Scholar 

  40. Sutton RA, Mumm S, Coburn SP, Ericson KL, Whyte MP (2012) „Atypical femoral fractures“ during bisphosphonate exposure in adult hypophosphatasia. J Bone Miner Res 27(5):987–994

    Article  CAS  PubMed  Google Scholar 

  41. Teitelbaum SL (2007) Osteoclasts: what do they do and how do they do it? Am J Pathol 170:427–435

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  42. Wähnert D, Stolarczyk Y, Hoffmeier KL, Raschke MJ, Hofmann GO, Mückley T (2012) The primary stability of angle-stable versus conventional locked intramedullary nails. Int Orthop 36(5):1059–1064

    Article  PubMed Central  PubMed  Google Scholar 

  43. Wermers RA, Tiegs RD, Atkinson EJ, Achenbach SJ, Melton LJ 3rd (2008) Morbidity and mortality associated with Paget’s disease of bone: a population-based study. J Bone Miner Res 23(6):819–825

    Article  PubMed Central  PubMed  Google Scholar 

  44. Whyte MP, Mumm S, Deal C (2007) Adult hypophosphatasia treated with teriparatide. J Clin Endocrinol Metab 92:1203–1208

    Article  CAS  PubMed  Google Scholar 

  45. Zurutuza L, Muller F, Gibrat JF, Taillandier A, Simon-Bouy B, Serre JL, Mornet E (1999) Correlations of genotype and phenotype in hypophosphatasia. Hum Mol Genet 8:1039–1046

    Article  CAS  PubMed  Google Scholar 

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M. Amling, Hamburg

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Oheim, R. Osteopathien und Knochenstoffwechselerkrankungen. Unfallchirurg 118, 1007–1016 (2015). https://doi.org/10.1007/s00113-015-0094-8

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