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• Ackermann, P.W., Renstrom, P., Tendinopathy in sport. Sports Health 2 (2012), 193–201.
• Kaux, J.F., Forthomme, B., Le Goff, et al. Current opinions on tendinopathy. J Sports Sci Med 10 (2011), 238–253.
• Kaux, J.F., Crielaard, J.M., Tendon et tendinopathie. J Traumatol Sport 31 (2014), 235–240.
• Meeuwisse, W.H., Assessing causation in sport injury: a multifactorial model. Clin J Sport Med 4 (1994), 166–170.
• Dakin, S.G., Dudhia, J., Werling, N.J., et al. Inflamm-aging and arachadonic acid metabolite differences with stage of tendon disease. PLoS One, 2012, 10.1371/journal.pone.0048978.
• Kohler, J., Popov, C., Klotz, B., et al. Uncovering the cellular and molecular changes in tendon stem/progenitor cells attributed to tendon aging and degeneration. Aging Cell 12 (2013), 988–999.
• Thorpe, C.T., Streeter, I., Pinchbeck, G.L., et al. Aspartic acid racemization and collagen degradation markers reveal an accumulation of damage in tendon collagen that is enhanced with aging. J Biol Chem 285 (2010), 15674–15681.
• Strocchi, R., De Pasquale, V., Guizzardi, S., et al. Human Achilles tendon: morphological and morphometric variations as a function of age. Foot Ankle 12 (1991), 100–104.
• Tuite, D.J., Renström, P.A., O'Brien, M., The aging tendon. Scand J Med Sci Sports 7 (1997), 72–77.
• Teunis, T., Lubberts, B., Reilly, B.T., et al. A systematic review and pooled analysis of the prevalence of rotator cuff disease with increasing age. J Shoulder Elb Surg 23 (2014), 1913–1921.
• Renstrom, P., Ljungqvist, A., Arendt, E., et al. Non-contact ACL injuries in female athletes: an International Olympic Committee current concepts statement. Br J Sports Med 42 (2008), 394–412.
• Maffulli, N., Waterston, W., Squair, J., et al. Changing incidence Achilles tendon rupture in Scotland: a 15 year study. Clin J Sports Med 9 (1999), 157–160.
• Sullivan, B.E., Caroll, C.C., Jemiolo, B., et al. Effet of acute resistance exercise and sex on human patellar tendon structural and regulatory mRNA expression. J Appl Physiol 106 (2009), 468–475.
• Miller, B.F., Hansen, M., Olesen, J.L., et al. Tendon collagen synthesis at rest and after exercise in women. J Appl Physiol 102 (2006), 541–546.
• Westh, E., Kongsgraad, M., Bojsen-Moller, J., et al. Effect of habitual exercise on the structural and mechanical properties of human tendon, in vivo, in men and women. Scand J Med Sci Sports 18 (2008), 23–30.
• Cook, J.L., Bass, S.L., Black, J.E., Hormone therapy associated with smaller Achilles tendon diameter in active post-menopausal women. Scand J Med Sci Sports 17 (2007), 128–132.
• Jozsa, L., Balint, J.B., Kannus, P., et al. Distribution of blood groups in patients with tendon rupture. An analysis of 832 cases. J Bone Joint Surg Br 71 (1989), 272–274.
• Witschew, N., Tantschew, P., Gertschew, A., Beziechungen zwichen Blutgruppenzugehörigkeit und Knochenbruchheilung. Beitr Orthop Traumatol 34 (1987), 515–522.
• Kujala, U.M., Järvinen, M., Natri, A., et al. ABO blood groups and musculoskeletal injuries. Injury 23 (1992), 131–133.
• Maffulli, N., Reaper, J.A., Waterston, S.W., et al. ABO blood groups and achilles tendon rupture in the Grampian Region of Scotland. Clin J Sport Med 10 (2000), 269–271.
• Hakim, A.J., Cherkas, L.F., Spector, T.D., et al. Genetic associations between frozen shoulder and tennis elbow: a female twin study. Rheumatology (Oxford) 42 (2003), 739–742.
• Saunders, C.J., Jalali Sefid Dashti, M., Gamieldien, J., Semantic interrogation of a multi knowledge domain ontological model of tendinopathy identifies four strong candidate risk genes. Sci Rep, 2016, 10.1038/srep19820.
• Del Rosso, A., Cerinic, M.M., De Giorgio, et al. Rheumatological manifestations in diabetes mellitus. Curr Diabetes Rev 2 (2006), 455–466.
• Lui, P.P.Y., Tendinopathy in diabetes mellitus patients-Epidemiology, pathogenesis, and management. Scand J Med Sci Sports 27 (2017), 776–787.
• Grant, W.P., Sullivan, R., Sonenshine, D.E., et al. Electron microscopic investigation of the effects of diabetes mellitus on the Achilles tendon. J Foot Ankle Surg 36 (1997), 272–278.
• Goldin, A., Beckman, J.A., Schmidt, A.M., et al. Advanced glycation end products: sparking the development of diabetic vascular injury. Circulation 114 (2006), 597–605.
• Ansari, N.A., Ali, R., Glycated lysine residues: a marker for non-enzymatic protein glycation in age-related diseases. Dis Markers 30 (2011), 317–324.
• Sugiyama, N., Marcovina, S., Grown, A.M., et al. Immunohistochemical distribution of lipoprotein epitopes in xanthomas from patients with familial hypercholesterolemia. Am J Pathol 141 (1992), 99–106.
• Abate, M., Schiavone, C., Salini, V., et al. Occurrence of tendon pathologies in metabolic disorders. Rheumatology 52 (2013), 599–608.
• Chhana, A., Callon, K.E., Dray, M., et al. Interactions between tenocytes and monosodium urate monohydrate crystals: implications for tendon involvement in gout. Ann Rheum Dis 73 (2014), 1737–1741.
• Naredo, E., Uson, J., Jiménez-Palop, M., et al. Ultrasound detected musculoskeletal urate crystal deposition: which joints and what findings should be assessed for diagnosing gout?. Ann Rheum Dis 73 (2014), 1522–1528.
• Pineda, C., Amezcua-Guerra, L.M., Solano, C., et al. Joint and tendon subclinical involvement suggestive of gouty arthritis in asymptomatic hyperuricemia: an ultrasound controlled study. Arthritis Res Ther, 13, 2011, R4.
• Oliva, F., Berardi, A.C., Misiti, S., et al. Thyroid hormones enhance growth and counteract apoptosis in human tenocytes isolated from rotator cuff tendons. Cell Death Dis, 2013, 10.1038/cddis.2013.229.
• Oliva, F., Misiti, S., Maffulli, N., Metabolic diseases and tendinopathies: the missing link. Muscles Ligaments Tendons J 4 (2014), 273–274.
• Harvie, P., Pollards, T.C., Carr, A.J., Calcific tendinitis: natural history and association with endocrine disorders. J Shoulder Elbow Surg 16 (2007), 169–173.
• Jarvinen, T.A., Kannus, P., Paavola, M., et al. Achilles tendon injuries. Curr Opin Rheumatol 13 (2001), 150–155.
• Kipgen, L., Kaux, J.F., Rompen, E., et al. Impact of oral hygiene on sport. Review of the literature. J Traumatol Sport 32 (2015), 41–45.
• Kipgen, L., Kaux, J.F., Rompen, E., et al. Relationship between oral hygiene and tendinopathy in sportsmen. Science Sports 31 (2016), 227–229.
• Solleveld, H., Goedhart, A., Vanden Bossche, L., Associations between poor oral health and reinjuries in male elite soccer players: a cross-sectional self-report stud. BMC Sports Sci Med Rehabil, 2015, 10.1186/s13102-015-0004-y.
• Ackermann, P.W., Tendinopathy: understanding epidemiology, pathology, healing, and treatment. Gomes, M.E., Reis, R.L., Rodrigues, M.T., (eds.) Tendon regeneration, 2015, Academic Press, Boston, 113–147.
• Lago, R., Gomez, R., Otero, M., et al. A new player in cartilage homeostasis: adiponectin induces nitric oxide synthase type II and pro-inflammatory cytokines in chondrocytes. Osteoarthritis Cartilage 16 (2008), 1101–1109.
• Robson-Ansley, P.J., de Milander, L., Collins, M., Noakes, T.D., Acute interleukin-6 administration impairs athletic performance in healthy, trained male runners. Can J Appl Physiol 29 (2004), 411–418.
• Tsai, W.C., Liang, F.C., Cheng, J.W., et al. High glucose concentration up-regulates the expression of matrix metalloproteinase-9 and -13 in tendon cells. BMC Musculoskelet Disord, 14, 2013, 255.
• Benito, J.R., Martinez, I., Monner, J., et al. Primary amyloidosis presenting as extensor tenosynovitis. Plast Reconstr Surg 103 (1999), 556–558.
• Hart, L., Corticosteroid and other injections in the management of tendinopathies: a review. Clin J Sport Med 21 (2011), 540–541.
• Roche, A.J., Calder, J.D., Achilles tendinopathy: a review of the current concepts of treatment. Bone Joint J 95 (2013), 1299–1307.
• Lundblad, R.L., Bradshaw, R.A., Gabriel, D., et al. A review of the therapeutic uses of thrombin. Thromb Haemost 91 (2004), 851–860.
• Knobloch, K., Tendinopathy and drugs–potential implications for beneficial and detrimental effects on painful tendons. J Sci Med Sport, 12, 2009, 423.
• Virchenko, O., Aspenberg, P., Lindahl, T.L., Low molecular weight heparin impairs tendon repair. J Bone Joint Surg Br 90 (2008), 388–392.
• Tanne, J.H., FDA adds “black box” warning to fuoroquinolone antibiotics. BMJ, 2008, 10.1136/bmj.a816.
• Kaleagasioglu, F., Olcay, E., Fluoroquinolone-induced tendinopathy: etiology and preventive measures. Tohoku J Exp Med 226 (2012), 251–258.
• Gotoh, M., Mitsui, Y., Shibata, H., et al. Increased matrix metalloprotease-3 gene expression in ruptured rotator cuff tendons is associated with postoperative tendon retear. Knee Surg Sports Traumatol Arthrosc 12 (2013), 1807–1812.
• Pasternak, B., Fellenius, M., Aspenberg, P., Doxycycline impairs tendon repair in rats. Acta Orthop Belg 72 (2006), 756–760.
• Pasternak, B., Missios, A., Askendal, A., et al. Doxycycline-coated sutures improve the suture-holding capacity of the rat Achilles tendon. Acta Orthop 78 (2007), 680–686.
• Bedi, A., Fox, A.J., Kovacevic, D., et al. Doxycycline-mediated inhibition of matrix metalloproteinases improves healing after rotator cuff repair. Am J Sports Med 38 (2010), 308–317.
• Kessler, M.W., Barr, J., Greenwald, R., et al. Enhancement of Achilles tendon repair mediated by matrix metalloproteinase inhibition via systemic administration of doxycycline. J Orthop Res 32 (2014), 500–506.
• Marie, I., Noblet, C., Tendinopathies induites par les statines. John Libbey Euronext 16 (2010), 238–243.
• Kamio, K., Liu, X.D., Sugiura, H., et al. Statins inhibit matrix metalloproteinase release from human lung fibroblasts. Eur Respir J 35 (2010), 637–646.
• Marie, I., Delafenêtre, H., Massy, N., et al. Complications tendineuses des statines : à propos de 96 observations. J Mal Vasc 33 (2008), 34–35.
• Kaleagasioglu, F., Olcay, E., Olgac, V., Statin-induced calcific Achilles tendinopathy in rats: comparison of biomechanical and histopathological effects of simvastatin, atorvastatin and rosuvastatin. Knee Surg Sports Traumatol Arthrosc 25 (2015), 1884–1891.
• Davis, M.E., Korn, M.A., Gumucio, J.P., et al. Simvastatin reduces fibrosis and protects against muscle weakness after massive rotator cuff tear. J Shoulder Elbow Surg 24 (2015), 280–287.
• Knobloch, K., Drug-Induced Tendon Disorders. Ackermann, P., Hart, D., (eds.) Metabolic Influences on Risk for Tendon Disorders. Advances in Experimental Medicine and Biology, 2016, Springer, 229–238.
• Marsolais, D., Frenette, J., Inflammation et réparation tendineuse. Med Sci 21 (2005), 181–186.
• Dahners, L.E., Gilbert, J.A., Lester, G.E., et al. The effect of a nonsteroidal antiinflammatory drug on the healing of ligaments. Am J Sports Med 16 (1988), 641–646.
• Elder, C.L., Dahners, L.E., Weinhold, P.S., A cyclooxygenase-2 inhibitor impairs ligament healing in the rat. Am J Sports Med 29 (2001), 801–805.
• Marsolais, D., Côté, C.H., Frenette, J., Nonsteroidal anti-inflammatory drug reduces neutrophil and macrophage accumulation but does not improve tendon regeneration. Lab Invest 83 (2003), 991–999.
• Lapointe, B.M., Frément, P., Côté, C.H., Adaptation to lengthening contractions is independent of voluntary muscle recruitment but relies on inflammation. Am J Physiol 282 (2002), 323–329.
• Galatz, L.M., Silva, M.J., Rothermich, S.Y., et al. Nicotine delays tendon-to-bone healing in a rat shoulder model. J Bone Joint Surg Am 88 (2006), 2027–2034.
• Baumgarten, K.M., Gerlach, D., Galatz, L.M., et al. Cigarette smoking increases the risk for rotator cuff tears. Clin Orthop Relat Res 468 (2010), 1534–1541.
• Carbon, S., Gumina, S., Arceri, V., et al. The impact of preoperative smoking habit on rotator cuff tear: cigarette smoking influences rotator cuff tear sizes. J Shoulder Elbow Surg 21 (2012), 56–60.
• Titchener, A.G., White, J.J., Hinchliffe, et al. Comorbidities in rotator cuff disease: a case-control study. J Shoulder Elbow Surg 23 (2014), 1282–1288.
• Godic, A., Poljšak, B., Adamic, M., et al. The role of antioxidants in skin cancer prevention and treatment. Oxid Med Cell Longev, 2014, 10.1155/2014/860479.
• Kannus, P., Paavola, M., Józsa, L., Aging and degeneration of tendons. Maffulli, N., Renström, P., Leadbetter, W.B., (eds.) Tendon Injuries, 2015, Springer, London, 25–31.
• Galera, O., Gleizes-Cervera, S., Pillard, F., et al. Prevalence of injuries in triathletes from a French league. Apunts Med Esport 47 (2012), 9–15.
• Fusini, F., Bisicchia, S., Bottegoni, et al. Nutraceutical supplement in the management of tendinopathies: a systematic review. Muscles Ligaments Tendons J 6 (2016), 48–57.
• Poulsen, R.C., Zarei, A., Sabokbar, A., et al. Tendon, a vitamin D-responsive tissue – why the British weather may not just be bad for your bones!. Int J Exp Pathol, 94, 2013, 20.
• Buhrmann, C., Mobasheri, A., Busch, F., et al. Curcumin modulates nuclear factor kappaB (NF-kappaB)-mediated inflammation in human tenocytes in vitro: role of the phosphatidylinositol 3-kinase/Akt pathway. J Biol Chem 286 (2011), 28556–28566.
• Subhashini, Chauhan, P.S., Kumari, S., et al. Intranasal curcumin and its evaluation in murine model of asthma. Int Immunopharmacol 17 (2013), 733–743.
• Fredberg, U., Bolvig, L., Significance of ultrasonographically detected asymptomatic tendinosis in the patellar and achilles tendons of elite soccer players: a longitudinal study. Am J Sports Med 30 (2002), 488–491.
• Fredberg, U., Bolvig, L., Andersen, N., Prophylactic training in asymptomatic soccer players with ultrasonographic abnormalities in Achilles and patellar tendons. Am J Sports Med 36 (2008), 451–460.
• Cook, J., Plazsnik, R., Kiss, Z.S., Malliars, P., Morris, M.E., Luca, J.D., High reproducibility of patellar tendon vascularity assessed by colour Doppler ultrasonography: a reliable measurement tool for quantifying tendon pathology. Br J Sports Med 39 (2005), 700–703.
• Gisslen, K., Alfredson, H., Neovascularisation and pain in jumper's knee: a prospective clinical and sonographic study in elite volleyball players. Br J Sports Med 37 (2005), 423–428.
• Turk, Z., Misur, I., Turk, N., et al. Rat tissue collagen modified by advanced glycation: correlation with duration of diabetes and glycemic control. Clin Chem Lab Med 37 (1999), 813–820.
• Perez-Ruiz, F., Dalbeth, N., Bardin, T., A review of uric acid, crystal deposition disease, and gout. Adv Ther 32 (2015), 31–41.
• Lowes, D.A., Wallace, C., Murphy, M.P., et al. The mitochondria targeted antioxidant MitoQ protects against fluoroquinolone-induced oxidative stress and mitochondrial membrane damage in human Achilles tendon cells. Free Radic Res 43 (2009), 323–328.
• Jauslin, M.L., Meier, T., Smith, R.A.J., Murphy, M.P., Mitochondria targeted antioxidants protect Friedreich ataxia fibroblasts from endogenous oxidative stress more effectively than untargeted antioxidants. FASEB J 17 (2003), 1972–1974.
• Nagai, R., Murray, D.B., Metz, T.O., et al. Chelation: a fundamental mechanism of action of AGE inhibitors, AGE breakers, and other inhibitors of diabetes complications. Diabetes 61 (2012), 549–559.