Loosening and periprosthetic osteolysis of articular prostheses;Uvolnění a periprotetická osteoýza kloubních nh́rad

Ceska Revmatologie

Volumn 10, Issue 4, 2002, Pages 157-164

  Vavrik P ^a   Veigl, D ^a  

^a CHARLES UNIVERSITY   (Czech Republic)

Author keywords

Abrasion granuloma; Periprosthetic osteolysis; Polyethylene abrasion; Receptor activator of nuclear factor B ligand (RANKL)

Indexed keywords

AUTACOID; METAL; POLY(METHYL METHACRYLATE); POLYETHYLENE;

ABRASION; ARTICLE; BIOCOMPATIBILITY; CELL ACTIVATION; CERAMIC PROSTHESIS; CLINICAL FEATURE; ENDOPROSTHESIS LOOSENING; FOREIGN BODY REACTION; GRANULOMA; HUMAN; JOINT PROSTHESIS; MACROPHAGE; OSSIFICATION; OSTEOLYSIS; PHAGOCYTOSIS; PROSTHESIS FAILURE; THEORY;

EID: 0036449147     PISSN: 12107905     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (47)

1. Willert HG, Buchhorn G, Semlitsch M. Tissue reaction to abrasion of upper extremityjoint endoprostheses. Orthopade 1980; 9: 94-107.
2. Schmalzried TP, Jasty M, Harris W-H. Periprosthetic bone loss in total hip arthroplasty. Polyethylene wear debris and the concept of the effective joint space. J Bone Joint Surg Am 1992; 74: 849-63.
3. Kirschenbaum IH. Basic principles of hydroxyapatite in joint replacement surgery. Semin Arthroplasty 1991; 2: 252-9.
4. Overgaard S, Lind M, Glerup H, Grundvig S, Bunger C, Soballe K. Hydroxyapatite and fluorapatite coatings for fixation of weight loaded implants. Clin Orthop 1997; 336: 286-96.
5. Heinert K. Computergesteuerte Langzeitauswertungen zementierter Hüftendoprothesen, Primär-und Revisions-Alloarthroplastik Hüft-und Kniegelenk. Berlin, Heidelberg, 1987; 93-102.
6. Thabe H. Total Hip Replacement Using Bone cement, The Rheumatoid Hip. Berlin, Springer Verlag, 1990; 114-21.
7. Barrack RL. Early Failure of Modern Cemented Stems. J Arthroplasty 2000; 15: 1036-50.
8. Murray DV, Rushton N. Macrophages stimulate bone resorption when they phagocytose particles. J Bone Joint Surg 1990; 72: 988-92.
9. Jochanan HB, Misselevich I, Behar J, Mendes D. Histologic Analysis of the Periprosthetic Tissues of Long-Term Surviving Cemented Total Hip Arthroplaties, Journal of Long-Term Effects of Medical Implants 1996; 6: 73-90.
10. Athanasou NA, Path FRC. Cellular biology of bone-resorbing cells. J Bone Joint Surg Am 1996; 78: 1096-112.
11. Kadoya Y, Revell PA, Al-Saffar N, Kobayashi A, Scott G, Freeman MAR. BOne formation and bone resorption in failed total joint replacements arthroplaties: histomorphometric analysis with histochemical and immunohistochemical technique. J Ortho Res 1997; 14: 473-82.
12. Harris WH. Wear and periprosthetic osteolysis: the problem. Clin Orthop 2001; 393: 66-70.
13. Howling GI, Barnettn PI, Tipper JL, Stone MH, Fisher J, Ingham E. Quantitative characterization of polyethylene debris isolated from periprosthetic tissue in early failure knee implants and early and late failure Charnley hip implants. J Biomed Mater Res 2001; 58: 415-20.
14. McKellop HA, Campbell P, Park SH, et al. The origin of submicron polyethylene wear debris in total hip arthroplasty. Clin Orthop 1995; 311: 3-20.
15. Landy MM, Walker PS. Wear of ultra-high-molecular-weight polyethylene components of 90 retrieved knee prostheses. J Arthroplasty 1988; 3: 73-85.
16. Mathias PB, Bennet AP, Rimmac CM, Wright TM. The Natural History of Ultra High Molecular Weight Polyethylene, Clinical Orthopaedics and Related Research. 1994; 309: 20-8.
17. Horowitz SM, Gonzales JB. Effects of polyethylene on macrophages. J Orthop Res 1997; 15: 50-6.
18. Green TR, Fisher J, Stone M, Wroblewski BM, Ingham E. Polyethylene particles of a 'critical size' are necessary for the induction of cytokines by macrophages in vitro. Biomaterials 1998; 19: 297-302.
19. Green TR, Fisher J, Matthews JB, Stone MH, Ingham E. Effect of size and dose on bone resorption activity of macrophages by in vitro clinically relevant ultra high molecular weight polyethylene particles. J Biomed Mater Res 2000;53:490-7.
20. Benz EB, Federman M, Godleski JJ, Bierbaum BE, Thornhill TS, Spector M. Transmission electron microscopy of intracellular particles of polyethylene from joint replacement prostheses: size distribution and cellular response. Biomaterials 2001; 22: 2835-42.
21. Kadoya Y, Kobayashi A, Ohashi H. Wear and osteolysis in total joint replacements. Acta Orthopaedica Scandinavica 1998; 69: (Suppl) 278.
22. Lennox DW, Schofield BH, McDonald DF, Riley LH. A histologic comparison of aseptic loosening of cemented, press-fit and biologic ingrowth prostheses. Clin Ortop 1987; 225:171-91.
23. Holowitz SM, Doty SB, Lane JM, Burstain AH. Studies of the mechanism by which the mechanical failure of polymethylmethacrylate leads to bone resorption. J Bone Joint Surg (Am) 1993; 75: 802-13.
24. Salvati EA, Betts F, Doty SB. Particulate metallic debris in cemented total hip arthroplasty. Clin Orthop 1993; 293: 160-73.
25. Lalor PA, Revell PA, Gray AB, et al. Sensitivity to titanium. A cause of implant failure? J Bone Joint Surg (Br) 1991;73:25-8.
26. Liu HC, Chang WH, Lin FH, Lu Y.H, Tsuang YH, Sun JS. Cytokine and prostaglandin E2 release from leukocytes in response to metal ions derived from different prosthetic materials: an in vitro study. Artif Organs 1999; 23: 1099-106.
27. Davidson JA, Poggie RA, Mishra AK. Abrasive wear of ceramic, metal, and UHMWPE bearing surfaces from third-body bone, PMMA bone cement, and titanium debris. Biomed Mater Eng 1994; 4: 213-29.
28. Lennox DW, Schofield BA, McDonald DF, Riley JLH. A histologic comparison of aseptic loosening of cemented, press-fit and biologic ingrowth prostheses. Clin Orthop 1987;225:171-91.
29. Kim KJ, Rubash HE, Wilson SC, Dantonio JA, McClain EJ. A histologic and biochemical comparison of the interface tissues in cementless and cemented hip prostheses. Clin Orthop 1993; 287: 142-52.
30. Goldring MB, Goldring SR. Skeletal tissue response to cytokine. Clin Orthop 1990; 258: 245-78.
31. Jiranek WA, Machado M, Jasty M, et al. Production of Cytokines around Loosened Cemented Acetabular Components J Bone Joint Surg 1993; 6: 863-79.
32. Xu JW, Konttinen YT, Waris V, et al. Macrophage-colony stimulating factor is increased in the synovial-like membrane of the periprosthetic tissues in the loosening of total hip replacement. Clin Rheumatol 1997; 16: 243-8.
33. Goodman SB, Huie P, Song Y, et al. Cellular profile and cytokine production at prosthetic interfaces. J Bone Joint Surg 1998; 3: 531-9.
34. Neale SD, Sabokbar A, Howie DW, Murray DW, Athanasou NA. Macrophage Colony-Stimulating Factor and Interleukin-6 Release by Periprosthetic Cells Stimulates Osteoclast Formation and Bone Resorption. J Orthopaedic Research 1999; 17: 686-94.
35. Takei I, Takagi M, Ida H, Ogino T, Santavirta S. High Macrophage-Colony Stimulating Factor Levels in Synovial Fluid of Loose Artificial Hip Joints. J Revmatology 2000; 27: 894-9.
36. Hirashima Y, Ishiguro N, Kondo S, lwata H. Osteoclast induction from bone marrow cells is due to pro-inflammatory mediators from macrophages exposed to polyethylene particles: a possible mechanism of osteolysis in failed THA. J Biomed Mater Res 2001; 56: 177-83.
37. Quinn JM, Itoh K, Udagawa N, et al. Transforming growth factor beta affects osteoclast differentiation via direct and indirect actions. J Bone Miner Res 2001; 16: 1787-94.
38. Suda T, Takahashi N, Udagawa N, Jimi E, Gillespie MT, Martin J. Modulation of Osteoclast Differentiation and Function by the New Members of the Tumor Necrosis Factor Receptor and Ligand Families. Endocrine Reviews 1999;20:345-357.
39. Takayanagi H, lizuka H, Juji T, et al. Involment of Receptor Activator of Nuclear Factor kapaB Ligand/Osteoclast Differentiation Factor in Osteoclastogenesis from Synoviocytes in Rheumatoid Arthritis. Arthritis Rheum 2000; 43: 259-69.
40. Kong Y, Yoshida H, Sarosi I, et al. OPGL is a key regulator of osteoclastogenesis, lymphocyte development and lymph-node organogenesis. Nature 397, 1999; 315-323.
41. Itonaga I, Fujikawa Y, Sabokbar A, Murray DW, Athanasou NA. Rheumatoid arthritis synovial marcophage - osteoclast diferentiation is osteoprotegerin ligand - dependent. J Pathol 2000; 192: 97-104.
42. Horwood NJ, Kartsogiannis V, Quinn JAW, et al. Activated T lymphocytes Support Osteoclast Formation in Vitro. 1999; 265: 144-50.
43. Takayanagi H, Ogasawara K, Hida S, et al. T-cell-mediated, regulation of osteoclastogenesis by signalling cross-talk between RANKL and IFN-gamma. Nature 408, 2000; 600-605.
44. Kong Y, Feige U, Sarosi I, et al. Activated T cells regulate bone loss and joint destruction in adjuvant arthritis through osteoprotegerin ligand. Nature 402, 1999; 304-9.
45. Goodman S, Wang JS, Regula D, Aspenherg P. T-lymfocytes are not necessary for particulate polyethylane-induced macrophage recritment. Acts. orthop Scand 1994; 65: 157-160.
46. Goodmen SB, Huie P, Song Y, et al. Loosening and Osteolysis of Cemented Joint Arthroplasties. Clinical Orthopaedics Related Research 1997; 337: 149-63.
47. Pollice PF, Rosier RN, Looney RJ, Puzas JE, Schwarz EM, OKeefe RJ. Oral pentoxifylline inhibits release of tumor necrosis factor-alpha from human peripheral blood monocytes: a potential treatment for aseptic loosening of total joint components. J Bone Joint Surg Am 2001; 83: 1057-61.