Gray, M., Wallace, A. & Aldridge, S. Assessment of shoulder pain for non-specialists. BMJ 355, i5783 (2016).
Rugg, C. M., Gallo, R. A., Craig, E. V. & Feeley, B. T. The pathogenesis and management of cuff tear arthropathy. J. Shoulder Elbow Surg. 27, 2271–2283 (2018).
Millar, N. L. et al. Tendinopathy. Nat. Rev. Dis. Primers 7, 1 (2021).
Keener, J. D. et al. Patterns of tear progression for asymptomatic degenerative rotator cuff tears. J. Shoulder Elbow Surg. 24, 1845–1851 (2015).
Article PubMed PubMed Central Google Scholar
Keener, J. D. et al. A prospective evaluation of survivorship of asymptomatic degenerative rotator cuff tears. J. Bone Joint Surg. Am. 97, 89–98 (2015).
Article PubMed PubMed Central Google Scholar
Nie, D., Zhou, Y., Wang, W., Zhang, J. & Wang, J. H. Mechanical overloading induced-activation of mTOR signaling in tendon stem/progenitor cells contributes to tendinopathy development. Front. Cell Dev. Biol. 9, 687856 (2021).
Article PubMed PubMed Central Google Scholar
Gladstone, J. N., Bishop, J. Y., Lo, I. K. & Flatow, E. L. Fatty infiltration and atrophy of the rotator cuff do not improve after rotator cuff repair and correlate with poor functional outcome. Am. J. Sports Med. 35, 719–728 (2007).
Davies, M. R. et al. Rotator cuff tear size regulates fibroadipogenic progenitor number and gene expression profile in the supraspinatus independent of patient age. Am. J. Sports Med. 50, 208–215 (2022).
Feeley, B. T. et al. Human rotator cuff tears have an endogenous, inducible stem cell source capable of improving muscle quality and function after rotator cuff repair. Am. J. Sports Med. 48, 2660–2668 (2020).
Article PubMed PubMed Central Google Scholar
Yanik, E. L., Chamberlain, A. M. & Keener, J. D. Trends in rotator cuff repair rates and comorbidity burden among commercially insured patients younger than the age of 65 years, United States 2007-2016. JSES Rev. Rep. Tech. 1, 309–316 (2021).
PubMed PubMed Central Google Scholar
Keener, J. D., Steger-May, K., Stobbs, G. & Yamaguchi, K. Asymptomatic rotator cuff tears: patient demographics and baseline shoulder function. J. Shoulder Elbow Surg. 19, 1191–1198 (2010).
Article PubMed PubMed Central Google Scholar
Hinsley, H., Ganderton, C., Arden, N. K. & Carr, A. J. Prevalence of rotator cuff tendon tears and symptoms in a Chingford general population cohort, and the resultant impact on UK health services: a cross-sectional observational study. BMJ Open 12, e059175 (2022).
Article PubMed PubMed Central Google Scholar
Yamamoto, A. et al. Prevalence and risk factors of a rotator cuff tear in the general population. J. Shoulder Elbow Surg. 19, 116–120 (2010).
Minagawa, H. et al. Prevalence of symptomatic and asymptomatic rotator cuff tears in the general population: from mass-screening in one village. J. Orthop. 10, 8–12 (2013).
Article PubMed PubMed Central Google Scholar
Keener, J. D., Patterson, B. M., Orvets, N. & Chamberlain, A. M. Degenerative rotator cuff tears: refining surgical indications based on natural history data. J. Am. Acad. Orthop. Surg. 27, 156–165 (2019).
Article PubMed PubMed Central Google Scholar
Kim, H. M. et al. Relationship of tear size and location to fatty degeneration of the rotator cuff. J. Bone Joint Surg. Am. 92, 829 (2010).
Article PubMed PubMed Central Google Scholar
Yamaguchi, K. et al. The demographic and morphological features of rotator cuff disease. A comparison of asymptomatic and symptomatic shoulders. J. Bone Joint Surg. Am. 88, 1699–1704 (2006).
Mall, N. A. et al. Symptomatic progression of asymptomatic rotator cuff tears: a prospective study of clinical and sonographic variables. J. Bone Joint Surg. Am. 92, 2623–2633 (2010).
Article PubMed PubMed Central Google Scholar
Yamaguchi, K. et al. Natural history of asymptomatic rotator cuff tears: a longitudinal analysis of asymptomatic tears detected sonographically. J. Shoulder Elbow Surg. 10, 199–203 (2001).
Article CAS PubMed Google Scholar
Teunis, T., Lubberts, B., Reilly, B. T. & Ring, D. A systematic review and pooled analysis of the prevalence of rotator cuff disease with increasing age. J. Shoulder Elbow Surg. 23, 1913–1921 (2014).
Harvie, P. et al. Genetic influences in the aetiology of tears of the rotator cuff. Sibling risk of a full-thickness tear. J. Bone Joint Surg. Br. 86, 696–700 (2004).
Article CAS PubMed Google Scholar
Gwilym, S. E. et al. Genetic influences in the progression of tears of the rotator cuff. J. Bone Joint Surg. Br. 91, 915–917 (2009).
Article CAS PubMed Google Scholar
Zhao, J. et al. Risk factors for supraspinatus tears: a meta-analysis of observational studies. Orthop. J. Sports Med. 9, 23259671211042826 (2021).
Article PubMed PubMed Central Google Scholar
Tashjian, R. Z., Granger, E. K., Farnham, J. M., Cannon-Albright, L. A. & Teerlink, C. C. Genome-wide association study for rotator cuff tears identifies two significant single-nucleotide polymorphisms. J. Shoulder Elbow Surg. 25, 174–179 (2016).
Tashjian, R. Z., Kim, S. K., Roche, M. D., Jones, K. B. & Teerlink, C. C. Genetic variants associated with rotator cuff tearing utilizing multiple population-based genetic resources. J. Shoulder Elbow Surg. 30, 520–531 (2021).
Yanik, E. L. et al. Identification of a novel genetic marker for risk of degenerative rotator cuff disease surgery in the UK biobank. J. Bone Joint Surg. Am. 103, 1259–1267 (2021).
Kim, S. K., Nguyen, C., Jones, K. B. & Tashjian, R. Z. A genome-wide association study for shoulder impingement and rotator cuff disease. J. Shoulder Elbow Surg. 30, 2134–2145 (2021).
Yoshida, K. et al. Association of superoxide-induced oxidative stress with rotator cuff tears in human patients. J. Orthop. Res. 38, 212–218 (2020).
Article CAS PubMed Google Scholar
Zhao, J. et al. What factors are associated with symptomatic rotator cuff tears: a meta-analysis. Clin. Orthop. Relat. Res. 480, 96–105 (2022).
Huang, S. W. et al. Autoimmune connective tissue diseases and the risk of rotator cuff repair surgery: a population-based retrospective cohort study. BMJ Open 9, e023848 (2019).
Article PubMed PubMed Central Google Scholar
Huang, S. W. et al. Diabetes mellitus increases the risk of rotator cuff tear repair surgery: a population-based cohort study. J. Diabetes Complications 30, 1473–1477 (2016).
Huang, S. W., Wu, C. W., Lin, L. F., Liou, T. H. & Lin, H. W. Gout can increase the risk of receiving rotator cuff tear repair surgery. Am. J. Sports Med. 45, 2355–2363 (2017).
Mandalia, K. et al. Social determinants of health influence clinical outcomes of patients undergoing rotator cuff repair: a systematic review. J. Shoulder Elbow Surg. 32, 419–434 (2023).
Chung, S. W. et al. Altered gene and protein expressions in torn rotator cuff tendon tissues in diabetic patients. Arthroscopy 33, 518–526 e1 (2017).
Yeom, J. W. et al. Postoperative HbA1c level as a predictor of rotator cuff integrity after arthroscopic rotator cuff repair in patients with type 2 diabetes. Orthop. J. Sports Med. 11, 23259671221145987 (2023).
Article PubMed PubMed Central Google Scholar
Kim, M. S., Rhee, S. M. & Cho, N. S. Increased HbA1c levels in diabetics during the postoperative 3-6 months after rotator cuff repair correlated with increased retear rates. Arthroscopy 39, 176–182 (2023).
Wilde, B. et al. Abnormal laboratory values for metabolic and hormonal syndromes are prevalent among patients undergoing rotator cuff repair. Arthrosc. Sports Med. Rehabil. 5, e695–e701 (2023).
Article PubMed PubMed Central Google Scholar
Smith, K. M. et al. The effect of sex hormone deficiency on the incidence of rotator cuff repair: analysis of a large insurance database. J. Bone Joint Surg. Am. 104, 774–779 (2022).
Soslowsky, L. J. et al. Neer Award 1999. Overuse activity injures the supraspinatus tendon in an animal model: a histologic and biomechanical study. J. Shoulder Elbow Surg. 9, 79–84 (2000).
留言 (0)