Abstract
This chapter introduces the readers of this volume to arthritic diseases including osteoarthritis (OA) and rheumatoid arthritis (RA) before focusing on collagenous and non-collagenous biomarkers of these joint diseases. The main objective of this chapter is to focus on reactive oxygen species and in vivo biomarkers of oxidative stress. Such biomarkers may be early indicators of oxidative stress-induced tissue damage and could be used to identify patients at increased risk of developing joint disease.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Notes
- 1.
- 2.
- 3.
- 4.
- 5.
- 6.
- 7.
- 8.
Abbreviations
- ACCP:
-
Anti-cyclic citrullinated protein antibodies
- ACPA:
-
Anti-citrullinated protein antibodies
- AGE:
-
Advanced glycation end product
- BMD:
-
Bone mineral density
- CDC:
-
Centers for Disease Control and Prevention
- CML:
-
Carboxymethyl lysine
- COMO:
-
Cartilage oligomeric matrix protein
- CRP:
-
C-reactive protein
- CTX-I:
-
Carboxy-terminal cross-linked telopeptide of type I collagen
- CTX-II:
-
Carboxy-terminal cross-linked telopeptide of type II collagen
- DNA:
-
Deoxyribonucleic acid
- DTPA:
-
Diethylene triamine penta-acetate
- ECM:
-
Extracellular matrix
- EFSA:
-
European Food Safety Authority
- EGR-1:
-
Early growth response protein 1
- ELISA:
-
Enzyme-linked immunosorbent assays
- eNOS:
-
Endothelial NOS
- ESR:
-
Erythrocyte sedimentation rate
- ESR:
-
Electron spin resonance
- GC:
-
Gas chromatography
- GSH:
-
Glutathione or gamma-l-glutamyl-l-cysteinylglycine
- H2O2 :
-
Hydrogen peroxide
- HA:
-
Hyaluronic acid
- HPLC:
-
High-performance liquid chromatography
- HRT:
-
Hormone replacement therapy
- IFN-γ:
-
Interferon gamma
- IGF-I:
-
Insulin-like growth factor I
- IGF-IR:
-
Insulin-like growth factor I receptor
- IL-1β:
-
Interleukin 1 beta
- IL-6:
-
Interleukin-6
- iNOS:
-
Inducible NOS
- JSW:
-
Joint space width
- LC:
-
Liquid chromatography
- MMP-13:
-
Matrix metalloproteinase 13
- MPO:
-
Peroxynitrite
- MRI:
-
Magnetic resonance imaging
- MS:
-
Mass spectrometry
- NADPH:
-
Nicotinamide adenine dinucleotide phosphate
- NALP:
-
Pyrin-like protein containing a pyrin domain
- NEN:
-
Nonenzymatic nitrite
- NF-κB:
-
Nuclear factor kappa B
- NIAMS:
-
National Institute of Arthritis and Musculoskeletal and Skin Diseases
- NO:
-
Nitric oxide
- NTX-I:
-
Amino-terminal cross-linked telopeptide of type I collagen
- OA:
-
Osteoarthritis
- PAS:
-
Patient Activity Scale
- PGE2 :
-
Prostaglandin E2
- PKC:
-
Protein kinase C
- PMN:
-
Polymorphonuclear leukocytes
- PYCARD:
-
Apoptosis-associated speck-like protein containing a caspase recruitment domain (CARD)
- RA:
-
Rheumatoid arthritis
- RAGE:
-
AGE receptor
- RF:
-
Rheumatoid factor
- ROS:
-
Reactive oxygen species
- SOD:
-
Superoxide dismutase
- TBAR:
-
Thiobarbituric acid reactants
- TIINE:
-
Collagen type II neoepitope
- uPA:
-
Urokinase or urokinase-type plasminogen activator
- WHO:
-
World Health Organization
- WOMAC:
-
Western Ontario and McMaster University Osteoarthritis Index
- WT:
-
Wild type
- YKL-40:
-
Cartilage glycoprotein-39
References
Oeppen J, Vaupel JW (2002) Demography. Broken limits to life expectancy. Science 296(5570):1029–1031
Woolf AD, Pfleger B (2003) Burden of major musculoskeletal conditions. Bull World Health Organ 81(9):646–656
Di Paola R, Cuzzocrea S (2008) Predictivity and sensitivity of animal models of arthritis. Autoimmun Rev 8(1):73–75
Aigner T, Rose J, Martin J, Buckwalter J (2004) Aging theories of primary osteoarthritis: from epidemiology to molecular biology. Rejuvenation Res 7(2):134–145
Abramson SB, Attur M (2009) Developments in the scientific understanding of osteoarthritis. Arthritis Res Ther 11(3):227
Sutton S, Clutterbuck A, Harris P et al (2009) The contribution of the synovium, synovial derived inflammatory cytokines and neuropeptides to the pathogenesis of osteoarthritis. Vet J 179(1):10–24
Lotz MK, Kraus VB (2010) New developments in osteoarthritis. Posttraumatic osteoarthritis: pathogenesis and pharmacological treatment options. Arthritis Res Ther 12(3):211
Yusuf E, Nelissen RG, Ioan-Facsinay A et al (2010) Association between weight or body mass index and hand osteoarthritis: a systematic review. Ann Rheum Dis 69(4):761–765
Buckwalter JA, Mankin HJ, Grodzinsky AJ (2005) Articular cartilage and osteoarthritis. Instr Course Lect 54:465–480
Goldring MB, Goldring SR (2007) Osteoarthritis. J Cell Physiol 213(3):626–634
Sellam J, Berenbaum F (2010) The role of synovitis in pathophysiology and clinical symptoms of osteoarthritis. Nat Rev Rheumatol 6(11):625–635
Wolfe F, Michaud K (2007) The effect of methotrexate and anti-tumor necrosis factor therapy on the risk of lymphoma in rheumatoid arthritis in 19,562 patients during 89,710 person-years of observation. Arthritis Rheum 56(5):1433–1439
Wolfe F, Michaud K (2004) Lymphoma in rheumatoid arthritis: the effect of methotrexate and anti-tumor necrosis factor therapy in 18,572 patients. Arthritis Rheum 50(6):1740–1751
Pinals RS (1987) Survival in rheumatoid arthritis. Arthritis Rheum 30(4):473–475
Reilly PA, Cosh JA, Maddison PJ, Rasker JJ, Silman AJ (1990) Mortality and survival in rheumatoid arthritis: a 25 year prospective study of 100 patients. Ann Rheum Dis 49(6): 363–369
Mitchell DM, Spitz PW, Young DY, Bloch DA, McShane DJ, Fries JF (1986) Survival, prognosis, and causes of death in rheumatoid arthritis. Arthritis Rheum 29(6):706–714
Goemaere S, Ackerman C, Goethals K et al (1990) Onset of symptoms of rheumatoid arthritis in relation to age, sex and menopausal transition. J Rheumatol 17(12):1620–1622
D’Elia HF, Larsen A, Mattsson LA et al (2003) Influence of hormone replacement therapy on disease progression and bone mineral density in rheumatoid arthritis. J Rheumatol 30(7): 1456–1463
D’Elia HF, Mattsson LA, Ohlsson C, Nordborg E, Carlsten H (2003) Hormone replacement therapy in rheumatoid arthritis is associated with lower serum levels of soluble IL-6 receptor and higher insulin-like growth factor 1. Arthritis Res Ther 5(4):R202–R209
Biomarkers Definitions Working Group (2001) Biomarkers and surrogate endpoints: preferred definitions and conceptual framework. Clin Pharmacol Ther 69(3):89–95
Eyre DR (2004) Collagens and cartilage matrix homeostasis. Clin Orthop Relat Res 427(Suppl):S118–S122
Todhunter RJ (1996) Anatomy and physiology of synovial joints. In: McIllwraith CW, Trotter GW (eds) Joint disease in the horse. WB Saunders, Philadelphia, pp 1–28
Henrotin Y, Addison S, Kraus V, Deberg M (2007) Type II collagen markers in osteoarthritis: what do they indicate? Curr Opin Rheumatol 19(5):444–450
Elsaid KA, Chichester CO (2006) Review: collagen markers in early arthritic diseases. Clin Chim Acta 365(1–2):68–77
Lohmander LS, Eyre D (2008) Biochemical markers as surrogate end points of joint disease. In: Reid D, Miller C (eds) Clinical trials in rheumatoid arthritis and osteoarthritis. Springer, New York, pp 249–274
Garvican ER, Vaughan-Thomas A, Innes JF, Clegg PD (2010) Biomarkers of cartilage turnover. Part 1: Markers of collagen degradation and synthesis. Vet J 185(1):36–42
Garvican ER, Vaughan-Thomas A, Clegg PD, Innes JF (2010) Biomarkers of cartilage turnover. Part 2: Non-collagenous markers. Vet J 185(1):43–49
Tseng S, Reddi AH, Di Cesare PE (2009) Cartilage oligomeric matrix protein (COMP): a biomarker of arthritis. Biomark Insights 4:33–44
Jordan JM (2004) Cartilage oligomeric matrix protein as a marker of osteoarthritis. J Rheumatol Suppl 70:45–49
Petersson IF, Sandqvist L, Svensson B, Saxne T (1997) Cartilage markers in synovial fluid in symptomatic knee osteoarthritis. Ann Rheum Dis 56(1):64–67
Petersson IF, Boegard T, Svensson B, Heinegard D, Saxne T (1998) Changes in cartilage and bone metabolism identified by serum markers in early osteoarthritis of the knee joint. Br J Rheumatol 37(1):46–50
Conrozier T, Saxne T, Fan CS et al (1998) Serum concentrations of cartilage oligomeric matrix protein and bone sialoprotein in hip osteoarthritis: a one year prospective study. Ann Rheum Dis 57(9):527–532
Saxne T, Heinegard D (1992) Cartilage oligomeric matrix protein: a novel marker of cartilage turnover detectable in synovial fluid and blood. Br J Rheumatol 31(9):583–591
Neidhart M, Hauser N, Paulsson M, DiCesare PE, Michel BA, Hauselmann HJ (1997) Small fragments of cartilage oligomeric matrix protein in synovial fluid and serum as markers for cartilage degradation. Br J Rheumatol 36(11):1151–1160
Kuhne SA, Neidhart M, Everson MP et al (1998) Persistent high serum levels of cartilage oligomeric matrix protein in a subgroup of patients with traumatic knee injury. Rheumatol Int 18(1):21–25
Lohmander LS, Ionescu M, Jugessur H, Poole AR (1999) Changes in joint cartilage aggrecan after knee injury and in osteoarthritis. Arthritis Rheum 42(3):534–544
Clark AG, Jordan JM, Vilim V et al (1999) Serum cartilage oligomeric matrix protein reflects osteoarthritis presence and severity: the Johnston County Osteoarthritis Project. Arthritis Rheum 42(11):2356–2364
Dodge GR, Hawkins D, Boesler E, Sakai L, Jimenez SA (1998) Production of cartilage oligomeric matrix protein (COMP) by cultured human dermal and synovial fibroblasts. Osteoarthritis Cartilage 6(6):435–440
Goldberg RL, Huff JP, Lenz ME, Glickman P, Katz R, Thonar EJ (1991) Elevated plasma levels of hyaluronate in patients with osteoarthritis and rheumatoid arthritis. Arthritis Rheum 34(7):799–807
Sharif M, George E, Shepstone L, Knudson W, Thonar EJ, Cushnaghan J et al (1995) Serum hyaluronic acid level as a predictor of disease progression in osteoarthritis of the knee. Arthritis Rheum 38(6):760–767
Pavelka K, Forejtova S, Olejarova M et al (2004) Hyaluronic acid levels may have predictive value for the progression of knee osteoarthritis. Osteoarthritis Cartilage 12(4):277–283
Iwase T, Hasegawa Y, Ishiguro N et al (1998) Synovial fluid cartilage metabolism marker concentrations in osteonecrosis of the femoral head compared with osteoarthrosis of the hip. J Rheumatol 25(3):527–531
Bruyere O, Collette JH, Ethgen O et al (2003) Biochemical markers of bone and cartilage remodeling in prediction of longterm progression of knee osteoarthritis. J Rheumatol 30(5):1043–1050
Taylor SE, Weaver MP, Pitsillides AA et al (2006) Cartilage oligomeric matrix protein and hyaluronan levels in synovial fluid from horses with osteoarthritis of the tarsometatarsal joint compared to a control population. Equine Vet J 38(6):502–507
Budsberg SC, Lenz ME, Thonar EJ (2006) Serum and synovial fluid concentrations of keratan sulfate and hyaluronan in dogs with induced stifle joint osteoarthritis following cranial cruciate ligament transection. Am J Vet Res 67(3):429–432
Nganvongpanit K, Itthiarbha A, Ong-Chai S, Kongtawelert P (2008) Evaluation of serum chondroitin sulfate and hyaluronan: biomarkers for osteoarthritis in canine hip dysplasia. J Vet Sci 9(3):317–325
Chichibu K, Matsuura T, Shichijo S, Yokoyama MM (1989) Assay of serum hyaluronic acid in clinical application. Clin Chim Acta 181(3):317–323
Kongtawelert P, Ghosh P (1990) A method for the quantitation of hyaluronan (hyaluronic acid) in biological fluids using a labeled avidin-biotin technique. Anal Biochem 185(2):313–318
Wakitani S, Nawata M, Kawaguchi A et al (2007) Serum keratan sulfate is a promising marker of early articular cartilage breakdown. Rheumatology (Oxford) 46(11): 1652–1656
Pothacharoen P, Teekachunhatean S, Louthrenoo W et al (2006) Raised chondroitin sulfate epitopes and hyaluronan in serum from rheumatoid arthritis and osteoarthritis patients. Osteoarthritis Cartilage 14(3):299–301
Itokazu M, Shinozaki M, Ohno T (1998) Quantitative analysis of hyaluronan in the synovial tissues of patients with joint disorders. Clin Rheumatol 17(3):261–262
Elliott AL, Kraus VB, Luta G et al (2005) Serum hyaluronan levels and radiographic knee and hip osteoarthritis in African Americans and Caucasians in the Johnston County Osteoarthritis Project. Arthritis Rheum 52(1):105–111
Chen HC, Shah S, Stabler TV, Li YJ, Kraus VB (2008) Biomarkers associated with clinical phenotypes of hand osteoarthritis in a large multigenerational family: the CARRIAGE family study. Osteoarthritis Cartilage 16(9):1054–1059
Filkova M, Senolt L, Braun M et al (2009) Serum hyaluronic acid as a potential marker with a predictive value for further radiographic progression of hand osteoarthritis. Osteoarthritis Cartilage 17(12):1615–1619
Kong SY, Stabler TV, Criscione LG, Elliott AL, Jordan JM, Kraus VB (2006) Diurnal variation of serum and urine biomarkers in patients with radiographic knee osteoarthritis. Arthritis Rheum 54(8):2496–2504
Criscione LG, Elliott AL, Stabler T, Jordan JM, Pieper CF, Kraus VB (2005) Variation of serum hyaluronan with activity in individuals with knee osteoarthritis. Osteoarthritis Cartilage 13(9):837–840
Chua SD Jr, Messier SP, Legault C, Lenz ME, Thonar EJ, Loeser RF (2008) Effect of an exercise and dietary intervention on serum biomarkers in overweight and obese adults with osteoarthritis of the knee. Osteoarthritis Cartilage 16(9):1047–1053
Nagaya H, Ymagata T, Ymagata S et al (1999) Examination of synovial fluid and serum hyaluronidase activity as a joint marker in rheumatoid arthritis and osteoarthritis patients (by zymography). Ann Rheum Dis 58(3):186–188
Punzi L, Oliviero F, Ramonda R, Valvason C, Sfriso P, Todesco S (2003) Laboratory investigations in osteoarthritis. Aging Clin Exp Res 15(5):373–379
Huang K, Wu LD (2009) YKL-40: a potential biomarker for osteoarthritis. J Int Med Res 37(1):18–24
Johansen JS, Hvolris J, Hansen M, Backer V, Lorenzen I, Price PA (1996) Serum YKL-40 levels in healthy children and adults. Comparison with serum and synovial fluid levels of YKL-40 in patients with osteoarthritis or trauma of the knee joint. Br J Rheumatol 35(6):553–559
Clancy R (1999) Nitric oxide alters chondrocyte function by disrupting cytoskeletal signaling complexes. Osteoarthritis Cartilage 7(4):399–400
Conrozier T, Carlier MC, Mathieu P et al (2000) Serum levels of YKL-40 and C reactive protein in patients with hip osteoarthritis and healthy subjects: a cross sectional study. Ann Rheum Dis 59(10):828–831
Kawasaki M, Hasegawa Y, Kondo S, Iwata H (2001) Concentration and localization of YKL-40 in hip joint diseases. J Rheumatol 28(2):341–345
Volck B, Johansen JS, Stoltenberg M et al (2001) Studies on YKL-40 in knee joints of patients with rheumatoid arthritis and osteoarthritis. Involvement of YKL-40 in the joint pathology. Osteoarthritis Cartilage 9(3):203–214
Volck B, Ostergaard K, Johansen JS, Garbarsch C, Price PA (1999) The distribution of YKL-40 in osteoarthritic and normal human articular cartilage. Scand J Rheumatol 28(3): 171–179
Vos K, Steenbakkers P, Miltenburg AM et al (2000) Raised human cartilage glycoprotein-39 plasma levels in patients with rheumatoid arthritis and other inflammatory conditions. Ann Rheum Dis 59(7):544–548
Farng E, Friedrich JB (2011) Laboratory diagnosis of rheumatoid arthritis. J Hand Surg Am 36(5):926–927, quiz 8
Waits JB (2010) Rational use of laboratory testing in the initial evaluation of soft tissue and joint complaints. Prim Care 37(4):673–689, v
Anderson J, Caplan L, Yazdany J et al (2012) Rheumatoid arthritis disease activity measures: American College of Rheumatology recommendations for use in clinical practice. Arthritis Care Res (Hoboken) 64(5):640–647
Parke DV, Sapota A (1996) Chemical toxicity and reactive oxygen species. Int J Occup Med Environ Health 9(4):331–340
Gloire G, Legrand-Poels S, Piette J (2006) NF-kappaB activation by reactive oxygen species: fifteen years later. Biochem Pharmacol 72(11):1493–1505
Schreck R, Rieber P, Baeuerle PA (1991) Reactive oxygen intermediates as apparently widely used messengers in the activation of the NF-kappa B transcription factor and HIV-1. EMBO J 10(8):2247–2258
Meister A (1994) Glutathione-ascorbic acid antioxidant system in animals. J Biol Chem 269(13):9397–9400
Meister A (1994) Glutathione, ascorbate, and cellular protection. Cancer Res 54(7 Suppl): 1969s–1975s
Schalkwijk J, van den Berg WB, van de Putte LB, Joosten LA (1986) An experimental model for hydrogen peroxide-induced tissue damage. Effects of a single inflammatory mediator on (peri)articular tissues. Arthritis Rheum 29(4):532–538
Tiku ML, Liesch JB, Robertson FM (1990) Production of hydrogen peroxide by rabbit articular chondrocytes. Enhancement by cytokines. J Immunol 145(2):690–696
Baker MS, Feigan J, Lowther DA (1988) Chondrocyte antioxidant defences: the roles of catalase and glutathione peroxidase in protection against H2O2 dependent inhibition of proteoglycan biosynthesis. J Rheumatol 15(4):670–677
Saura R, Matsubara T, Hirohata K, Itoh H (1992) Damage of cultured chondrocytes by hydrogen peroxide derived from polymorphonuclear leukocytes: a possible mechanism of cartilage degradation. Rheumatol Int 12(4):141–146
Tschan T, Hoerler I, Houze Y, Winterhalter KH, Richter C, Bruckner P (1990) Resting chondrocytes in culture survive without growth factors, but are sensitive to toxic oxygen metabolites. J Cell Biol 111(1):257–260
Deahl ST 2nd, Oberley LW, Oberley TD, Elwell JH (1992) Immunohistochemical identification of superoxide dismutases, catalase, and glutathione-S-transferases in rat femora. J Bone Miner Res 7(2):187–198
Schalkwijk J, van den Berg WB, van de Putte LB, Joosten LA (1985) Hydrogen peroxide suppresses the proteoglycan synthesis of intact articular cartilage. J Rheumatol 12(2): 205–210
Carlo MD Jr, Loeser RF (2003) Increased oxidative stress with aging reduces chondrocyte survival: correlation with intracellular glutathione levels. Arthritis Rheum 48(12): 3419–3430
He SJ, Hou JF, Dai YY, Zhou ZL, Deng YF (2011) N-acetyl-cysteine protects chicken growth plate chondrocytes from T-2 toxin-induced oxidative stress. J Appl Toxicol 28:111–134
Ueno T, Yamada M, Sugita Y, Ogawa T (2011) N-acetyl cysteine protects TMJ chondrocytes from oxidative stress. J Dent Res 90(3):353–359
Nakagawa S, Arai Y, Mazda O et al (2010) N-acetylcysteine prevents nitric oxide-induced chondrocyte apoptosis and cartilage degeneration in an experimental model of osteoarthritis. J Orthop Res 28(2):156–163
Li WQ, Dehnade F, Zafarullah M (2000) Thiol antioxidant, N-acetylcysteine, activates extracellular signal-regulated kinase signaling pathway in articular chondrocytes. Biochem Biophys Res Commun 275(3):789–794
Vaillancourt F, Fahmi H, Shi Q et al (2008) 4-Hydroxynonenal induces apoptosis in human osteoarthritic chondrocytes: the protective role of glutathione-S-transferase. Arthritis Res Ther 10(5):R107
Studer RK (2004) Nitric oxide decreases IGF-1 receptor function in vitro; glutathione depletion enhances this effect in vivo. Osteoarthritis Cartilage 12(11):863–869
Chakravarthi S, Jessop CE, Bulleid NJ (2006) The role of glutathione in disulphide bond formation and endoplasmic-reticulum-generated oxidative stress. EMBO Rep 7(3):271–275
Afonso V, Champy R, Mitrovic D, Collin P, Lomri A (2007) Reactive oxygen species and superoxide dismutases: role in joint diseases. Joint Bone Spine 74(4):324–329
Michiels C, Raes M, Zachary MD, Delaive E, Remacle J (1988) Microinjection of antibodies against superoxide dismutase and glutathione peroxidase. Exp Cell Res 179(2):581–589
Zhou R, Yazdi AS, Menu P, Tschopp J (2011) A role for mitochondria in NLRP3 inflammasome activation. Nature 469(7329):221–225
Ogura Y, Sutterwala FS, Flavell RA (2006) The inflammasome: first line of the immune response to cell stress. Cell 126(4):659–662
Tschopp J (2011) Mitochondria: Sovereign of inflammation? Eur J Immunol 41(5): 1196–1202
Blanco FJ, Lopez-Armada MJ, Maneiro E (2004) Mitochondrial dysfunction in osteoarthritis. Mitochondrion 4(5–6):715–728
Terkeltaub R, Johnson K, Murphy A, Ghosh S (2002) Invited review: the mitochondrion in osteoarthritis. Mitochondrion 1(4):301–319
Blanco FJ, Rego I, Ruiz-Romero C (2011) The role of mitochondria in osteoarthritis. Nat Rev Rheumatol 7(3):161–169
Carames B, Taniguchi N, Otsuki S, Blanco FJ, Lotz M (2010) Autophagy is a protective mechanism in normal cartilage, and its aging-related loss is linked with cell death and osteoarthritis. Arthritis Rheum 62(3):791–801
Loeser RF (2011) Aging and osteoarthritis. Curr Opin Rheumatol 23(5):492–496
Valgimigli M, Valgimigli L, Trere D et al (2002) Oxidative stress EPR measurement in human liver by radical-probe technique. Correlation with etiology, histology and cell proliferation. Free Radic Res 36(9):939–948
Pratico D, Reilly M, Lawson J, Delanty N, FitzGerald GA (1995) Formation of 8-iso-prostaglandin F2 alpha by human platelets. Agents Actions Suppl 45:27–31
Henrotin Y, Deberg M, Mathy-Hartert M, Deby-Dupont G (2009) Biochemical biomarkers of oxidative collagen damage. Adv Clin Chem 49:31–55
Morrow JD, Roberts LJ 2nd (1996) The isoprostanes. Current knowledge and directions for future research. Biochem Pharmacol 51(1):1–9
Draper HH, Hadley M (1990) Malondialdehyde determination as index of lipid peroxidation. Methods Enzymol 186:421–431
Esterbauer H, Cheeseman KH (1990) Determination of aldehydic lipid peroxidation products: malonaldehyde and 4-hydroxynonenal. Methods Enzymol 186:407–421
Cowley HC, Bacon PJ, Goode HF, Webster NR, Jones JG, Menon DK (1996) Plasma antioxidant potential in severe sepsis: a comparison of survivors and nonsurvivors. Crit Care Med 24(7):1179–1183
Chuang CC, Shiesh SC, Chi CH et al (2006) Serum total antioxidant capacity reflects severity of illness in patients with severe sepsis. Crit Care 10(1):R36
Bauer DC, Hunter DJ, Abramson SB et al (2006) Classification of osteoarthritis biomarkers: a proposed approach. Osteoarthritis Cartilage 14(8):723–727
Garnero P (2006) Biochemical markers in osteoarthritis: will they measure up? Nat Clin Pract 2(3):116–117
Garnero P (2006) Use of biochemical markers to study and follow patients with osteoarthritis. Curr Rheumatol Rep 8(1):37–44
Kraus VB (2006) Do biochemical markers have a role in osteoarthritis diagnosis and treatment? Best Pract Res Clin Rheumatol 20(1):69–80
Lichtman MA (1975) Does ATP, decrease exponentially during red cell aging? Nouv Rev Fr Hematol 15(6):625–632
Monboisse JC, Braquet P, Randoux A, Borel JP (1983) Non-enzymatic degradation of acid-soluble calf skin collagen by superoxide ion: protective effect of flavonoids. Biochem Pharmacol 32(1):53–58
Monboisse JC, Poulin G, Braquet P, Randoux A, Ferradini C, Borel JP (1984) Effect of oxy radicals on several types of collagen. Int J Tissue React 6(5):385–390
Monboisse V, Monboisse JC, Borel JP, Randoux A (1989) Nonisotopic evaluation of collagen in fibroblasts cultures. Anal Biochem 176(2):395–399
Daumer KM, Khan AU, Steinbeck MJ (2000) Chlorination of pyridinium compounds. Possible role of hypochlorite, N-chloramines, and chlorine in the oxidation of pyridinoline cross-links of articular cartilage collagen type II during acute inflammation. J Biol Chem 275(44):34681–34692
Olszowski S, Mak P, Olszowska E, Marcinkiewicz J (2003) Collagen type II modification by hypochlorite. Acta Biochim Pol 50(2):471–479
Davies JM, Horwitz DA, Davies KJ (1993) Potential roles of hypochlorous acid and N-chloroamines in collagen breakdown by phagocytic cells in synovitis. Free Radic Biol Med 15(6):637–643
Uchida K, Kato Y, Kawakishi S (1990) A novel mechanism for oxidative cleavage of prolyl peptides induced by the hydroxyl radical. Biochem Biophys Res Commun 169(1):265–271
Wang K, Xu SJ, Zhang FH et al (1991) Free radicals-induced abnormal chondrocytes, matrix and mineralization. A new concept of Kaschin–Beck’s disease. Chin Med J (Engl) 104(4):307–312
Sajithlal GB, Chithra P, Chandrakasan G (1999) An in vitro study on the role of metal catalyzed oxidation in glycation and crosslinking of collagen. Mol Cell Biochem 194(1–2): 257–263
Sulochana KN, Ramprasad S, Coral K et al (2003) Glycation and glycoxidation studies in vitro on isolated human vitreous collagen. Med Sci Monit 9(6):BR220-4
Fu MX, Wells-Knecht KJ, Blackledge JA, Lyons TJ, Thorpe SR, Baynes JW (1994) Glycation, glycoxidation, and cross-linking of collagen by glucose. Kinetics, mechanisms, and inhibition of late stages of the Maillard reaction. Diabetes 43(5):676–683
Verzijl N, DeGroot J, Oldehinkel E et al (2000) Age-related accumulation of Maillard reaction products in human articular cartilage collagen. Biochem J 350(Pt 2):381–387
Sell DR, Nagaraj RH, Grandhee SK et al (1991) Pentosidine: a molecular marker for the cumulative damage to proteins in diabetes, aging, and uremia. Diabetes Metab Rev 7(4):239–251
Hernandez CJ, Tang SY, Baumbach BM, Hwu PB et al (2005) Trabecular microfracture and the influence of pyridinium and non-enzymatic glycation-mediated collagen cross-links. Bone 37(6):825–832
Verzijl N, DeGroot J, Bank RA et al (2001) Age-related accumulation of the advanced glycation endproduct pentosidine in human articular cartilage aggrecan: the use of pentosidine levels as a quantitative measure of protein turnover. Matrix Biol 20(7):409–417
Wang X, Shen X, Li X, Agrawal CM (2002) Age-related changes in the collagen network and toughness of bone. Bone 31(1):1–7
Monboisse JC, Rittie L, Lamfarraj H, Garnotel R, Gillery P (2000) In vitro glycoxidation alters the interactions between collagens and human polymorphonuclear leucocytes. Biochem J 350(Pt 3):777–783
Horiuchi S, Sano H, Higashi T et al (1996) Extra- and intracellular localization of advanced glycation end-products in human atherosclerotic lesions. Nephrol Dial Transplant 11(Suppl 5): 81–86
Lander HM, Tauras JM, Ogiste JS, Hori O, Moss RA, Schmidt AM (1997) Activation of the receptor for advanced glycation end products triggers a p21(ras)-dependent mitogen-activated protein kinase pathway regulated by oxidant stress. J Biol Chem 272(28):17810–17814
Paik DC, Saito LY, Sugirtharaj DD, Holmes JW (2006) Nitrite-induced cross-linking alters remodeling and mechanical properties of collagenous engineered tissues. Connect Tissue Res 47(3):163–176
Bank RA, Bayliss MT, Lafeber FP, Maroudas A, Tekoppele JM (1998) Ageing and zonal variation in post-translational modification of collagen in normal human articular cartilage. The age-related increase in non-enzymatic glycation affects biomechanical properties of cartilage. Biochem J 330(Pt 1):345–351
Maroudas A, Palla G, Gilav E (1992) Racemization of aspartic acid in human articular cartilage. Connect Tissue Res 28(3):161–169
DeGroot J, Verzijl N, Wenting-van Wijk MJ et al (2004) Accumulation of advanced glycation end products as a molecular mechanism for aging as a risk factor in osteoarthritis. Arthritis Rheum 50(4):1207–1215
Henrotin Y, Deberg M, Dubuc JE, Quettier E, Christgau S, Reginster JY (2004) Type II collagen peptides for measuring cartilage degradation. Biorheology 41(3–4):543–547
Ameye LG, Deberg M, Oliveira M, Labasse A, Aeschlimann JM, Henrotin Y (2007) The chemical biomarkers C2C, Coll2-1, and Coll2-1NO2 provide complementary information on type II collagen catabolism in healthy and osteoarthritic mice. Arthritis Rheum 56(10):3336–3346
Henrotin Y, Martel-Pelletier J, Msika P, Guillou GB, Deberg M (2012) Usefulness of specific OA biomarkers, Coll2-1 and Coll2-1NO(2), in the anterior cruciate ligament OA canine model. Osteoarthritis Cartilage 20(7):787–790
Gangl M, Serteyn D, Lejeune JP, Schneider N, Grulke S, Peters F et al (2007) A type II-collagen derived peptide and its nitrated form as new markers of inflammation and cartilage degradation in equine osteochondral lesions. Res Vet Sci 82(1):68–75
Verwilghen DR, Enzerink E, Martens A et al (2011) Relationship between arthroscopic joint evaluation and the levels of Coll2-1, Coll2-1NO(2), and myeloperoxidase in the blood and synovial fluid of horses affected with osteochondrosis of the tarsocrural joint. Osteoarthritis Cartilage 19(11):1323–1329
Deberg M, Labasse A, Christgau S et al (2005) New serum biochemical markers (Coll 2-1 and Coll 2-1 NO2) for studying oxidative-related type II collagen network degradation in patients with osteoarthritis and rheumatoid arthritis. Osteoarthritis Cartilage 13(3):258–265
Deberg MA, Labasse AH, Collette J, Seidel L, Reginster JY, Henrotin YE (2005) One-year increase of Coll 2-1, a new marker of type II collagen degradation, in urine is highly predictive of radiological OA progression. Osteoarthritis Cartilage 13(12):1059–1065
Reginster JY, Deroisy R, Rovati LC et al (2001) Long-term effects of glucosamine sulphate on osteoarthritis progression: a randomised, placebo-controlled clinical trial. Lancet 357(9252):251–256
Glick ID, Janowsky D, Zisook S (2001) On using the ASCP model curriculum for psychopharmacology: comments and an update. Acad Psychiatry 25(4):237–238
Acknowledgments
A. Mobasheri wishes to acknowledge the financial support of the Wellcome Trust, the National Centre for the Replacement, Refinement and Reduction of Animals in Research (NC3Rs) (grant number: Mobasheri.A.28102007), the Biotechnology and Biological Sciences Research Council (BBSRC) (grants BBSRC/S/M/2006/13141 and BB/G018030/1), and the Engineering and Physical Sciences Research Council (EPSRC).
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Additional information
Conflict of Interest
This chapter was written by the authors within the scope of their academic and research positions at their host institutions. None of the authors has a financial or personal relationship with other people or organizations that could inappropriately influence or bias the content of this chapter.
Rights and permissions
Copyright information
© 2013 Springer Science+Business Media, LLC
About this chapter
Cite this chapter
Henrotin, Y., Mobasheri, A. (2013). Soluble Proteomic Biomakers in the Management of Arthritis. In: Alcaraz, M., Gualillo, O., Sánchez-Pernaute, O. (eds) Studies on Arthritis and Joint Disorders. Oxidative Stress in Applied Basic Research and Clinical Practice. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4614-6166-1_1
Download citation
DOI: https://doi.org/10.1007/978-1-4614-6166-1_1
Published:
Publisher Name: Humana Press, New York, NY
Print ISBN: 978-1-4614-6165-4
Online ISBN: 978-1-4614-6166-1
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)