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What Factors Are Associated with Symptomatic Rotator Cuff Tears: A Meta-analysis

Zhao, Jinlong MD1,2; Luo, Minghui MD2,3; Liang, Guihong MD2,3; Pan, Jianke MD, PhD2,3; Han, Yanhong MD2,3; Zeng, Lingfeng MD, PhD2,3; Yang, Weiyi MD, PhD2,3; Liu, Jun MD, PhD2,3

Author Information
Clinical Orthopaedics and Related Research: January 2022 - Volume 480 - Issue 1 - p 96-105
doi: 10.1097/CORR.0000000000001949



Rotator cuff tears are one of the most common causes of shoulder pain and limited movement [30, 50]. Despite their great frequency, the pathogenesis of cuff tears is not well known [52]. In the past 15 years, the number of rotator cuff tears in Western countries has increased substantially [13]. The costs of the rotator cuff repair are substantial; the annual medical cost in the United States is between USD 1.2 and USD 1.6 billion [13]. Clarifying the factors associated with symptomatic rotator cuff tears and educating patients or the general population about how to control any modifiable factors may help to reduce the occurrence and progression of rotator cuff tears. Identifying risk factors believed to be associated with cuff tears might also help individual clinicians ascertain the likelihood of a rotator cuff injury being present in a particular patient; this could guide the utilization of screening tests.

One systematic review reported several factors associated with rotator cuff tears [54], but it included few studies and evaluated few variables. In addition, heterogeneity was a concern. These shortcomings limit the ability of clinicians to more fully understand the factors associated with symptomatic rotator cuff tears as well as to formulate prevention and treatment strategies. In addition, it would be helpful to include parameters related to shoulder anatomy, such as critical shoulder angle and glenoid version angle [63, 65]. Finally, studies have disagreed to some degree on which factors are or are not associated with rotator cuff tears [2, 7, 25, 54, 57], which suggests that a meta-analysis may be helpful.

We therefore performed a systematic review and meta-analysis, in which we asked: What (1) demographic, (2) disease, and (3) imaging factors are associated with symptomatic rotator cuff tears?

Materials and Methods

Search Strategy

We electronically searched PubMed, Embase, and Web of Science. Combinations of MeSH words and free words were used in the search. Articles published from the establishment of each database through February 2021 were considered potentially eligible. We completed the search in February 2021. The keywords included “risk factor,” “rotator cuff injury,” “rotator cuff tears,” and “"rotator cuff tendinitis” (Supplemental Digital Content 1,

Inclusion and Exclusion Criteria

We compared patients diagnosed with rotator cuff tears with a group of controls, defined as the study group. We included studies that involved patients with rotator cuff tears (regardless of rotator cuff tear type) and control groups of patients without rotator cuff tears, as well as studies in which the study and control groups were identified based on tools such as MRI. We also included prospective or retrospective studies with control groups and those that used at least one formal evaluation index that measured demographic, disease, or imaging factors. No language restrictions were implemented.

The exclusion criteria were duplicate studies, grey literature (unpublished studies, abstracts, preprint articles), studies whose data could not be converted and merged, and studies of low quality (Newcastle-Ottawa Scale score < 4 and Agency for Healthcare Research and Quality [AHRQ] score < 4).

Study Screening and Data Extraction

Two researchers (ML, JP) independently screened the studies, extracted data, and cross-checked the data. Disagreements were settled through discussion or negotiation with a third party (JL). After duplicate data were removed from the data retrieved, the abstracts and full texts were read to determine whether the study should be included. If necessary, we contacted the corresponding author of the original study by email or telephone to obtain information that was important for this study. The extracted information comprised basic study information, including the first author, publication date, and study design; baseline characteristics of the participants, including the sampling and imaging methods; key elements of the risk of bias assessment; and relevant outcome indicators and measurement data.

Search Results

We identified 987 studies, and 269 papers remained after we removed duplicates. After reading the title and abstract, we were left with 56 articles. After re-reading the full text, we excluded 30 articles that did not meet the inclusion criteria, and leaving 26 articles [1, 4, 5, 9, 10, 16, 17, 20, 24, 27, 28, 29, 31, 34, 37, 40, 41, 43, 44, 48, 49, 56, 58, 61, 62, 64] in our study (Fig. 1).

Fig. 1:
This flow diagram shows the number of studies identified and included in this meta-analysis.

Basic Characteristics of the Included Studies

Twenty-six articles from 14 countries were included; 18 were prospective comparative studies and eight were retrospective comparative studies (Table 1). A total of 9809 patients were included in this study, with 3164 in the study group and 6645 in the control group. Seventeen associated factors were identified.

Table 1. - Characteristics of studies included in this review
Author Publication year Country Design Ethical approval Number of patients Imaging modality NOS or AHRQ score
Rotator cuff tear No Tear
Abate et al. [1] 2014 Italy Prospective, comparative study Yes 27 205 Ultrasound 7a
Watanabe et al. [62] 2018 Japan Retrospective, comparative study Yes 54 54 MRI 6b
Applegate et al. [4] 2016 USA Prospective, comparative study Yes 156 1070 MRI 7a
Atala et al. [5] 2020 Argentina Prospective, comparative study Yes 52 53 MRI 8a
Bjarnison et al. [9] 2017 Denmark Retrospective, comparative study Yes 95 285 MRI 9b
Blonna et al. [10] 2015 Italy Prospective, comparative study Yes 40 80 MRI 8a
Cunningham et al. [16] 2018 Switzerland Prospective, comparative study Yes 33 38 MRI 7a
Dogan et al. [17] 2012 Turkey Retrospective, comparative study Yes 62 60 MRI 7b
Figueiredo et al. [20] 2020 Brazil Prospective, comparative study Yes 211 567 MRI 6a
Gumina et al. [24] 2013 Italy Retrospective, comparative study Yes 215 201 MRI 5b
Haveri et al. [27] 2020 India Prospective, comparative study Yes 69 31 MRI 8a
İncesoy et al. [28] 2020 Turkey Retrospective, comparative study Yes 437 433 MRI 8b
Jeong et al. [31] 2016 Korea Prospective, comparative study Yes 23 355 Ultrasound 6a
Jeong et al. [29] 2020 Korea Retrospective, comparative study Yes 40 160 MRI 7b
van Kampen et al. [61] 2014 Netherlands Prospective, comparative study Yes 38 62 MRA 9a
Kim et al. [34] 2018 Korea Prospective, comparative study Yes 214 109 MRI 7a
Lee et al. [37] 2015 China Prospective, comparative study Yes 140 176 Ultrasound 6a
Longo et al. [40] 2009 UK Retrospective, comparative study NR 97 97 Imaging 5b
Mehta et al. [41] 2020 USA Prospective, comparative study Yes 49 305 Ultrasound 9a
Mohamed et al [43] 2014 Egypt Prospective, comparative study Yes 56 30 MRI 6a
Motta et al. [44] 2014 USA Prospective, comparative study Yes 203 207 MRI 6a
Park et al. [48] 2018 Korea Prospective, comparative study Yes 199 435 MRI 7a
Passaretti et al. [49] 2016 Italy Prospective, comparative study Yes 249 356 MRI 6a
Shinagawa et al. [56] 2018 Japan Prospective, comparative study Yes 112 183 MRI or ultrasound 8a
Spiegl et al. [58] 2015 USA Retrospective, comparative study Yes 10 10 MRI 4b
Yamamoto et al. [64] 2010 Japan Prospective, comparative study Yes 283 1083 Ultrasound 8a
aAHRQ = American Agency for Healthcare Research and Quality (0-11 points).
bNOS = Newcastle-Ottawa Scale (0-9 points); for both scales, the higher the score, the better the quality of the study; RCT = rotator cuff tear; NR = not reported.

Assessment of Study Quality

The Newcastle-Ottawa Scale was used to evaluate the risk of bias of the retrospective comparative studies included in our review [59]. The following three aspects were assessed: the research participant selection process, level of intergroup comparability, and data measurement process. The total possible score was 9 points, with higher scores indicating better study quality. The prospective comparative studies were evaluated using the risk of bias evaluation standards recommended by the AHRQ [14], with 11 items in total. The response options for each item were yes, no, or not clear. The higher the score, the higher the quality of the study.

In total, eight retrospective comparative studies had quality scores of 4 to 9 (Table 1). The quality score of the 18 prospective comparative studies ranged from 6 to 9. These results suggest that the included studies had a low risk of bias and high methodological quality (Supplemental Digital Content 2,

This meta-analysis was performed in strict accordance with the requirements of the Meta-analysis of Observational Studies in Epidemiology statement [60] and was registered with the PROSPERO International Prospective Register of Systematic Reviews (registration number: CRD42021239990).

Quantitative Analysis

RevMan 5.3 software (Cochrane Collaboration) was used for the meta-analysis. The weighted mean difference was used to determine the effect size of the measurement data, and the risk ratio (RR) was used to determine the effect size for categorical variables. The 95% confidence interval for each effect size was calculated. A heterogeneity test was used to evaluate the heterogeneity of the included studies. If there was no heterogeneity (I2 ≤ 50%), a fixed-effects model was used to determine the overall effect size; if there was heterogeneity (I2 > 50%), a random-effects model was used to merge the effect values [11]. According to the heterogeneity test results, the heterogeneity levels of BMI (I2 = 11%), male sex (I2 = 50%), smoking (I2 = 49%), dominant arm (I2 = 18%), height (I2 = 0%), weight (I2 = 0%), traumatic events (I2 = 35%), hypertension (I2 = 0%), thyroid disease (I2 = 0%), critical shoulder angle (I2 = 23%), and glenoid version angle (I2 = 0%) were low. The heterogeneity values of age (I2 = 94%), female sex (I2 = 51%), diabetes mellitus (I2 = 86%), acromion index (I2 = 83%), lateral acromion angle (I2 = 88%), and acromiohumeral distance (I2 = 92%) were high (Supplemental Digital Content 3, For the outcome indicators included in three or more articles, Stata 15.1 software (StataCorp LLC) was used to conduct an Egger test to evaluate publication bias.

The results of the Egger test showed that there was no publication bias related to the outcome indicators of this study with combined data from three or more articles (p > 0.05) (Supplemental Digital Content 4,


Demographic Factors

The results of the meta-analysis showed that older age (mean difference 3.1 [95% CI 1.4 to 4.8]; p < 0.001), BMI (mean difference 0.77 [95% CI 0.37 to 1.17]; p < 0.001), smoking (RR 1.32 [95% CI 1.17 to 1.49]; p < 0.001), injured dominant arm (RR 1.15 [95% CI 1.06 to 1.24]; p < 0.001), height (mean difference 0.9 [95% CI 0.4 to 1.4]; p < 0.001), and weight (mean difference 2.24 [95% CI 0.82 to 3.66]; p = 0.002) were factors associated with rotator cuff tears. In addition, our results suggest that sex (RR 0.98 [95% CI 0.92 to 1.05]; p = 0.64 for female versus male) was not a factor associated with rotator cuff tears (Table 2).

Table 2. - Outcomes of the meta-analysis
Risk factor Number of studies RR or WMD (95% CI) p value I2, % Analysis model
Demographic factors
 Age in years 24 WMD 3.1 (1.4-4.8) < 0.001 94 IV, random
 BMI in kg/m2 5 WMD 0.77 (0.37-1.17) < 0.001 11 IV, fixed
 Female sex 23 RR 0.98 (0.92-1.05) 0.64 51 M-H, random
 Male sex 22 RR 1.03 (0.97-1.08) 0.31 50 M-H, fixed
 Smoking, yes versus no 9 RR 1.32 (1.17-1.49) < 0.001 49 M-H, fixed
 Dominant arm 7 RR 1.15 (1.06-1.24) < 0.001 18 M-H, fixed
 Height in cm 2 WMD 0.9 (0.4-1.4) < 0.001 0 IV, fixed
 Weight in kg 2 WMD 2.24 (0.82-3.66) 0.002 0 IV, fixed
Underlying disease
 Traumatic events, yes versus no 3 RR 1.91 (1.40-2.54) < 0.001 35 M-H, fixed
 Diabetes mellitus, yes versus no 7 RR 1.22 (0.72-2.07) 0.47 86 M-H, random
 Hypertension, yes versus no 5 RR 1.50 (1.32-1.70) < 0.001 0 M-H, fixed
 Thyroid disease, yes versus no 4 RR 0.88 (0.45-1.73) 0.71 0 M-H, fixed
Morphologic parameters
 AI 3 WMD 0.11 (0.06-0.16) < 0.001 83 IV, random
 LAA in ° 2 WMD -3.7 (-8.2 to 0.9) 0.11 88 IV, random
 CSA in ° 6 WMD 1.9 (1.5-2.3) < 0.001 23 IV, fixed
 GVA in ° 2 WMD -1.3 (-1.9 to -0.8) < 0.001 0 IV, fixed
 AD in mm 2 WMD -0.8 (-2.4 to 0.8) 0.32 92 IV, random
A forest plot of all risk factors is shown in Supplementary Material 3 (Supplemental Digital Content 3, RR = relative risk; WMD = weighted mean difference; IV = inverse variance; M-H = Mantel Haenszel test; AI = acromion index; LAA = lateral acromion angle; CSA = critical shoulder angle; GVA = glenoid version angle; AD = acromiohumeral distance.

Disease Factors

Our meta-analysis revealed that traumatic events (RR 1.91 [95% CI 1.40 to 2.54]; p < 0.001) and hypertension (RR 1.50 [95% CI 1.32 to 1.70]; p < 0.001) were associated with rotator cuff tears; however, diabetes mellitus (RR 1.22 [95% CI 0.72 to 2.07]; p = 0.47) was not. In addition, we found no association between the presence of thyroid disease and the likelihood of a rotator cuff tear being present (RR 0.88 [95% CI 0.45 to 1.73]; p = 0.71) (Table 2).

Imaging Factors

The meta-analysis showed that a greater acromion index (mean difference 0.11 [95% CI 0.06 to 0.16]; p < 0.001), a larger critical shoulder angle (mean difference 1.9 [95% CI 1.5 to 2.3]; p < 0.001), and a smaller glenoid version angle (mean difference -1.3 [95% CI -1.9 to -0.8]; p < 0.001) were factors associated with rotator cuff tears. The lateral acromion angle and acromiohumeral distance had no correlation with symptomatic rotator cuff tears (Table 2).


Rotator cuff tears are common, they substantially reduce patients’ quality of life, and they impose a heavy economic burden on patients and healthcare systems. Although many studies have evaluated the factors associated with rotator cuff tears, there is a lack of high-quality systematic review articles; such sources can help aggregate data and focus clinicians’ attention on the factors that matter most. We collected and assessed the best-available evidence about factors associated with rotator cuff tears, including demographic factors, disease factors, and imaging parameters, and we identified a number of potentially modifiable factors associated with symptomatic rotator cuff tears, including blood glucose control, blood pressure, weight, and cigarette smoking. These findings may help clinicians to intervene to the benefit of patients who have symptoms but who have not yet developed a cuff tear. Future research can further assess whether controlling these associated factors can delay the progression and size of rotator cuff tears.


There are some limitations to this study. First, the study population was mainly patients with symptomatic shoulder pain or dyskinesia, so the conclusion of this study is only applicable to patients with symptomatic rotator cuff tears. In addition, our study is about factors associated with rotator cuff tears; the papers included in our analysis could not prove causation. Whether the factors identified in this study can, in fact, influence the progression of rotator cuff tears in patients with shoulder symptoms who are not diagnosed with rotator cuff tears is worthy of further study. Another limitation is the heterogeneity of the included studies, which were of various designs, came from different countries, included patients of a variety of races, and were performed in diverse medical economic environments. In particular, the factors of age, diabetes, acromion index, lateral acromion angle, and acromiohumeral distance were associated with greater heterogeneity, and they should be interpreted accordingly. Future studies including larger sample sizes and less heterogeneity should be considered. However, the fact that the source studies came from diverse environments and included patients of different races and were performed in different settings may offer a measure of generalizability, which may be perceived as advantageous. Finally, the low level of evidence and lack of prospective cohort studies is concerning; however, we restricted inclusion to papers with a Newcastle-Ottawa Scale assessment or AHRQ score of four or more (Supplemental Digital Content 2,, which generally suggests intermediate or better study quality.

Demographic Factors

Older age, greater BMI, smoking, dominant hand, and greater height and weight were factors associated with symptomatic rotator cuff tears; by contrast, sex (male or female) was not associated with symptomatic rotator cuff tears. With increasing age, the incidence of symptomatic rotator cuff tears is higher, which has been recognized by many studies [44, 46, 55]. In older people, the number of microvessels in the tendon is substantially reduced, which makes the rotator cuff tissue more prone to fibrovascular hyperplasia, adiposis, atrophy, and calcification, which may be more likely to be associated with rotator cuff tears [44, 53]. One study found the risk of rotator cuff injury in people older than 60 years was 5.07 times that in people younger than 60 years [54]. Although obviously age is a continuous variable (that is, the difference probably will not be so dramatic between a patient who is 59 and a patient who is 61), the evidence suggests that surgeons certainly can consider older patients as being at higher risk. Increases in BMI are closely related to rotator cuff tendinitis and rotator cuff tears [23]. There is a theory that with increasing BMI, there is more serious microvascular damage after a slight rotator cuff injury, which impairs rotator cuff repair and potentiates further subsequent tearing of the rotator cuff [23]. An increase in BMI can also promote inflammation, which may have a negative influence on disease progression and decompensation of rotator cuff tears [33]. Patients with shoulder pain or movement disorders should try to maintain weight control, which may help to prevent the pathological progression of symptomatic rotator cuff tears. Family doctors and surgeons also can provide dietary advice for high-risk groups. We also found cigarette smoking to be associated with rotator cuff tear. Hatta et al. [26] found that nicotine-exposed tendons showed a decrease in gene expression and enzyme activity in a dose-dependent manner. Studies have shown that some components of cigarettes can produce negative influences on the generation, apoptosis, and metabolism of muscle cells in vitro [12, 26]. Smoking cessation is important for many reasons; its effect on the rotator cuff is just one more.

Disease Factors

Our results showed that hypertension and traumatic shoulder events were associated with symptomatic rotator cuff tears but diabetes and thyroid disease were not. There is a lack of research on the relationship between hypertension and the pathogenesis of symptomatic rotator cuff tears; we believe this could be a productive area of future research. Of course, surgeons (and internists) should continue to help patients achieve good blood pressure control, and future studies can explore whether blood pressure control can delay the pathological progression of rotator cuff tears. A history of shoulder trauma has been considered a risk factor for rotator cuff tears [19, 51], as confirmed by our meta-analysis. The number of rotator cuff tears in patients younger than 45 years is increasing because of trauma [6, 38]. Biomechanically, various external forces can lead to overload and overstretching of the rotator cuff tendon, leading to traumatic rotator cuff tears [39]. Diabetes has long been considered an independent risk factor for rotator cuff tears [3, 15], which is not in accordance with our findings. There is a big difference between the susceptible group of diabetes and the susceptible population of rotator cuff tear, so diabetes may not be associated with the rotator cuff tear. Another possible explanation is that the studies we included involved patients who were of different races and from different countries, which could have blunted the apparent association; it is possible that diabetes may have a differential effect on the rotator cuff among people of different races. Future studies might investigate this.

Imaging Factors

Our study showed that a greater critical shoulder angle, a lower glenoid version angle, and a greater acromion index were factors independently associated with rotator cuff tears. The compressive and shear forces of the joint depend on the critical shoulder angle [22, 42]. With an increasing critical shoulder angle, the shear force of the joint increases, which may increase the load on the rotator cuff. A high critical shoulder angle can induce supraspinatus overload and may explain why some rotator cuff tears are associated with a high critical shoulder angle [8, 21]. The critical shoulder angle can be measured on radiographs instead of MRI, and if a patient has shoulder pain and a high critical shoulder angle, one should have a high index of suspicion that the patient may have a rotator cuff tear. Prior studies have disagreed on whether greater glenoid retroversion is associated with rotator cuff tears [18, 28, 32, 36]; our meta-analysis found that it is. Based on this, surgeons might further study the biomechanical effect of glenoid version angle on rotator cuff. Our meta-analysis confirmed that a higher acromion index is associated with the risk of rotator cuff tear. And surgeons might maintain a high index of suspicion for rotator cuff tear in patients with shoulder pain who have a high acromion index (as well as an abnormal critical shoulder angle or excessive glenoid retroversion); this could help guide the judicious use of advanced diagnostic imaging, like MRI and ultrasound, particularly in resource-constrained countries. Previous studies found that patients with a critical shoulder angle greater than 30° to 35° [35, 45], an acromion index greater than 0.6 to 0.64 [28, 47], and abnormal glenoid version angle (less than -2.2°) [28] were at greater risk of developing rotator cuff tears. The critical shoulder angle, glenoid version angle, and the acromion index are anatomical parameters of the shoulder that are nonmodifiable other than, perhaps, with surgery. When a patient is diagnosed with a rotator cuff tear and surgical treatment is considered, in addition to repairing the rotator cuff tear, the surgeon may consider addressing the above three factors in the hope of reducing the risk of retear. Further research might seek to evaluate approaches to addressing those anatomic factors through surgery, to determine whether this will have a protective effect on the rotator cuff after surgery.


This study identified a number of potentially modifiable factors associated with symptomatic rotator cuff tears, including blood glucose, blood pressure, weight, and smoking. Clinicians may help patients with shoulder pain who do not yet have a cuff tear to modify these factors, as such interventions may help prevent a tear; furthermore, there is no risk to modifying those factors because doing so would also improve patients’ overall health. The radiographic factors we identified, including the acromion index, critical shoulder angle, and glenoid version angle, may help surgeons determine which patients with symptoms suggestive of a cuff tear are more or less likely to actually have a tear. Future research can further study whether controlling these factors may delay the progression and size of rotator cuff tears. In addition, future studies can continue to explore whether changing the anatomical parameters of the shoulder during surgery, such as the critical shoulder angle, glenoid version angle, and the acromion index, will help to protect the rotator cuff from retear after surgery. Finally, we should further explore whether there are differences in risk factors for rotator cuff tears among patients of different ages and ethnic groups.


We thank American Journal Experts for linguistic assistance during the preparation of this manuscript.


1. Abate M, Schiavone C, Di Carlo L, Salini V. Prevalence of and risk factors for asymptomatic rotator cuff tears in postmenopausal women. Menopause. 2014;21:275-280.
2. Abboud JA, Abboud JA, Kim JS, Kim JS. The effect of hypercholesterolemia on rotator cuff disease. Clin Orthop Relat Res. 2010;468:1493-1497.
3. Acar B, Köse Ö, Aytaç G, et al. Diabetes mellitus accelerates fatty degeneration of the supraspinatus muscle after tendon tear: an experimental study in rats. Eklem Hastalik Cerrahisi. 2018;29:176-183.
4. Applegate KA, Thiese MS, Merryweather AS, et al. Association between cardiovascular disease risk factors and rotator cuff tendinopathy: a cross-sectional study. J Occup Environ Med. 2017;59:154-160.
5. Atala NA, Bongiovanni SL, Galich AM, et al. Is sarcopenia a risk factor for rotator cuff tears? J Shoulder Elbow Surg. 2021;30:1851-1855.
6. Azzam MG, Dugas JR, Andrews JR, Goldstein SR, Emblom BA, Cain EL. Rotator cuff repair in adolescent athletes. Am J Sports Med. 2018;46:1084-1090.
7. Baumgarten KM, Gerlach D, Galatz LM, et al. Cigarette smoking increases the risk for rotator cuff tears. Clin Orthop Relat Res. 2010;468:1534-1541.
8. Bhatia DN, DeBeer JF, Toit DFD. Association of a large lateral extension of the acromion with rotator cuff tears. J Bone Joint Surg Am. 2006;88:1889.
9. Bjarnison AO, Sørensen TJ, Kallemose T, Barfod KW. The critical shoulder angle is associated with osteoarthritis in the shoulder but not rotator cuff tears: a retrospective case-control study. J Shoulder Elbow Surg. 2017;26:2097-2102.
10. Blonna D, Giani A, Bellato E, et al. Predominance of the critical shoulder angle in the pathogenesis of degenerative diseases of the shoulder. J Shoulder Elbow Surg. 2016;25:1328-1336.
11. Borenstein M, Hedges LV, Higgins JP, Rothstein HR. Introduction to Meta-analysis. John Wiley & Sons; 2011.
12. Carbone SM, Gumina SMP, Arceri VM, Campagna VM, Fagnani CM, Postacchini FMP. The impact of preoperative smoking habit on rotator cuff tear: cigarette smoking influences rotator cuff tear sizes. J Shoulder Elbow Surg. 2012;21:56-60.
13. Chalmers PN, Granger E, Nelson R, Yoo M, Tashjian RZ. Factors affecting cost, outcomes, and tendon healing after arthroscopic rotator cuff repair. Arthroscopy. 2018;34:1393-1400.
14. Chou R, Baker WL, Bañez LL, et al. Agency for Healthcare Research and Quality evidence-based practice center methods provide guidance on prioritization and selection of harms in systematic reviews. J Clin Epidemiol. 2018;98:98-104.
15. Cronin NJ, Peltonen J, Ishikawa M, et al. Achilles tendon length changes during walking in long-term diabetes patients. Clin Biomech. 2010;25:476-482.
16. Cunningham G, Nicodème-Paulin E, Smith MM, Holzer N, Cass B, Young AA. The greater tuberosity angle: a new predictor for rotator cuff tear. J Shoulder Elbow Surg. 2018;27:1415-1421.
17. Dogan M, Cay N, Tosun O, Karaoglanoglu M, Bozkurt M. Glenoid axis is not related with rotator cuff tears-a magnetic resonance imaging comparative study. Int Orthop. 2012;36:595-598.
18. Dyrna F, Berthold DP, Muench LN, et al. Graft tensioning in superior capsular reconstruction improves glenohumeral joint kinematics in massive irreparable rotator cuff tears: a biomechanical study of the influence of superior capsular reconstruction on dynamic shoulder abduction. Orthop J Sports Med. 2020;8:2325967120957424.
19. Dornan GJ, Katthagen JC, Tahal DS, et al. Cost-effectiveness of arthroscopic rotator cuff repair versus reverse total shoulder arthroplasty for the treatment of massive rotator cuff tears in patients with pseudoparalysis and nonarthritic shoulders. Arthroscopy. 2017;33:716-725.
20. Figueiredo EA, Loyola LC, Belangero PS, et al. Rotator cuff tear susceptibility is associated with variants in genes involved in tendon extracellular matrix homeostasis. J Orthop Res. 2019;38:192-201.
21. Gerber C, Snedeker JG, Baumgartner D, Viehöfer AF. Supraspinatus tendon load during abduction is dependent on the size of the critical shoulder angle: a biomechanical analysis. J Orthop Res. 2014;32:952-957.
22. Gomide LC, Carmo TCD, Bergo GHM, Oliveira GA, Macedo IS. Relationship between the critical shoulder angle and the development of rotator cuff lesions: a retrospective epidemiological study. Rev Bras Ortop. 2017;52:423-427.
23. Gumina S, Candela V, Passaretti D, et al. The association between body fat and rotator cuff tear: the influence on rotator cuff tear sizes. J Shoulder Elbow Surg. 2014;23:1669-1674.
24. Gumina SMP, Arceri VM, Carbone SM, et al. The association between arterial hypertension and rotator cuff tear: the influence on rotator cuff tear sizes. J Shoulder Elbow Surg. 2013;22:229-232.
25. Harvie P, Ostlere SJ, Teh J, et al. Genetic influences in the aetiology of tears of the rotator cuff. J Bone Joint Surg Br. 2004;86:696-700.
26. Hatta T, Sano H, Sakamoto N, Kishimoto KN, Sato M, Itoi E. Nicotine reduced MMP-9 expression in the primary porcine tenocytes exposed to cyclic stretch. J Orthop Res. 2013;31:645-650.
27. Haveri S, Patil KS, Uppin RB, Patil S, Putti BB. A cross-sectional study on novel-risk factors associated with supraspinatus tendon tear. Indian J Orthop. 2020;55:457-463.
28. İncesoy MA, Yıldız Kİ, Türk Öİ, et al. The critical shoulder angle, the acromial index, the glenoid version angle and the acromial angulation are associated with rotator cuff tears. Knee Surg Sports Traumatol Arthrosc. 2021;29:2257-2263.
29. Jeong HJ, Kim HS, Rhee S, Oh JH. Risk factors for and prognosis of folded rotator cuff tears: a comparative study using propensity score matching. J Shoulder Elbow Surg. 2021;30:826-835.
30. Jeong J, Park S, Ji J, Lee H, Jung S, Choi B. Trans-tendon suture bridge rotator cuff repair with tenotomized pathologic biceps tendon augmentation in high-grade PASTA lesions. Arch Orthop Traum Surg. 2020;140:67-76.
31. Jeong J, Shin D, Kim T, Kim K. Prevalence of asymptomatic rotator cuff tear and their related factors in the Korean population. J Shoulder Elbow Surg. 2017;26:30-35.
32. Kandemir U, Allaire RB, Jolly JT, Debski RE, McMahon PJ. The relationship between the orientation of the glenoid and tears of the rotator cuff. J Bone Joint Surg Br. 2006;88:1105-1109.
33. Kessler KE, Robbins CB, Bedi A, Carpenter JE, Gagnier JJ, Miller BS. Does increased body mass index influence outcomes after rotator cuff repair? Arthroscopy. 2018;34:754-761.
34. Kim J, Min Y, Gwak H, Kim C, Lee C, Lee S. Rotator cuff tear incidence association with critical shoulder angle and subacromial osteophytes. J Shoulder Elbow Surg. 2019;28:470-475.
35. Kim JR, Ryu KJ, Hong IT, Kim BK, Kim JH. Can a high acromion index predict rotator cuff tears? Int Orthop. 2012;36:1019-1024.
36. Kum DH, Kim JH, Park KM, Lee ES, Park YB, Yoo JC. Acromion index in Korean population and Its relationship with rotator cuff tears. Clin Orthop Surg. 2017;9:218-222.
37. Lee DM, Lee HM, Yoon SMP. Relationship of ABO blood type on rotator cuff tears. PM R. 2015;7:1137-1141.
38. Lin EC, Mall NA, Dhawan A, et al. Arthroscopic primary rotator cuff repairs in patients aged younger than 45 years. Arthroscopy. 2013;29:811-817.
39. Loew M, Habermeyer P, Wiedemann E, Rickert M, Gohlke F. Recommendations for diagnosis and expert assessment of traumatic rotator cuff lesions Unfallchirurg. 2000;103:417-426.
40. Longo UG, Franceschi F, Ruzzini L, Spiezia F, Maffulli N, Denaro V. Higher fasting plasma glucose levels within the normoglycaemic range and rotator cuff tears. Brit J Sport Med. 2009;43:284-287.
41. Mehta SK, Teefey SA, Middleton W, Steger-May K, Sefko JA, Keener JD. Prevalence and risk factors for development of subscapularis and biceps pathology in shoulders with degenerative rotator cuff disease: a prospective cohort evaluation. J Shoulder Elbow Surg. 2020;29:451-458.
42. Miyazaki AN, Itoi E, Sano H, et al. Comparison between the acromion index and rotator cuff tears in the Brazilian and Japanese populations. J Shoulder Elbow Surg. 2011;20:1082-1086.
43. Mohamed RE, Abo-Sheisha DM. Assessment of acromial morphology in association with rotator cuff tear using magnetic resonance imaging. The Egyptian Journal of Radiology and Nuclear Medicine. 2014;45:169-180.
44. Motta GDR, Amaral MV, Rezende E, et al. Evidence of genetic variations associated with rotator cuff disease. J Shoulder Elbow Surg. 2014;23:227-235.
45. Moor BK, Bouaicha S, Rothenfluh DA, Sukthankar A, Gerber C. Is there an association between the individual anatomy of the scapula and the development of rotator cuff tears or osteoarthritis of the glenohumeral joint? A radiological study of the critical shoulder angle. Bone Joint J. 2013; 95:935-941.
46. Moorthy V, Chen JY, Lee M, Lie DTT. Arthroscopic rotator cuff repair results in similar postoperative functional outcomes in patients with only rotator cuff tears and those with concomitant cervical radiculopathy. Knee Surg Sports Traumatol Arthrosc. 2021;29:2564-2569.
47. Nyffeler RW, Werner CM, Sukthankar A, Schmid MR, Gerber C. Association of a large lateral extension of the acromion with rotator cuff tears. J Bone Joint Surg Am. 2006;88:800-805.
48. Park HB, Gwark J, Im J, Jung J, Na J, Yoon CH. Factors associated with atraumatic posterosuperior rotator cuff tears. J Bone Joint Surg Am. 2018;100:1397-1405.
49. Passaretti D, Candela V, Venditto T, Giannicola G, Gumina S. Association between alcohol consumption and rotator cuff tear. Acta Orthop. 2016;87:165-168.
50. Patel S, Gualtieri AP, Lu HH, Levine WN. Advances in biologic augmentation for rotator cuff repair. Ann N Y Acad Sci. 2016;1383:97-114.
51. Pogorzelski J, Erber B, Themessl A, et al. Definition of the terms “acute” and “traumatic” in rotator cuff injuries: a systematic review and call for standardization in nomenclature. Arch Orthop Traum Surg. 2021;141:75-91.
52. Roos TR, Roos AK, Avins AL, et al. Genome-wide association study identifies a locus associated with rotator cuff injury. Plos One. 2017;12:e189317.
53. Santago AC, Vidt ME, Li X, et al. Shoulder strength requirements for upper limb functional tasks: do age and rotator cuff tear status matter? J Appl Biomech. 2017;33:446-452.
54. Sayampanathan AA, Andrew THC. Systematic review on risk factors of rotator cuff tears. J Orthop Surg (Hong Kong). 2017;25:920227919.
55. Shim SB, Jeong JY, Yum TH, Yoo JC. A comparative study to evaluate the risk factors for medium-sized rotator cuff tear in patients younger than 50 years of age. Arthroscopy. 2018;34:2971-2979.
56. Shinagawa K, Hatta T, Yamamoto N, et al. Critical shoulder angle in an East Asian population: correlation to the incidence of rotator cuff tear and glenohumeral osteoarthritis. J Shoulder Elbow Surg. 2018;27:1602-1606.
57. Spargoli G. Supraspinatus tendon pathomechanics: a current concepts review. Int J Sports Phys Ther. 2018;13:1083-1094.
58. Spiegl UJ, Horan MP, Smith SW, Ho CP, Millett PJ. The critical shoulder angle is associated with rotator cuff tears and shoulder osteoarthritis and is better assessed with radiographs over MRI. Knee Surg Sports Traumatol Arthrosc. 2016;24:2244-2251.
59. Stang A. Critical evaluation of the Newcastle-Ottawa scale for the assessment of the quality of nonrandomized studies in meta-analyses. Eur J Epidemiol. 2010;25:603-605.
60. Stroup DF, Berlin JA, Morton SC, et al. Meta-analysis of observational studies in epidemiology: a proposal for reporting. JAMA. 2000;283:2008-2012.
61. van Kampen DA, van den Berg T, van der Woude HJ, et al. The diagnostic value of the combination of patient characteristics, history, and clinical shoulder tests for the diagnosis of rotator cuff tear. J Orthop Surg Res. 2014;9:70.
62. Watanabe A, Ono Q, Nishigami T, Hirooka T, Machida H. Association between the critical shoulder angle and rotator cuff tears in Japan. Acta Med Okayama. 2018;72:547-551.
63. Wolf BR, Dunn WR, Wright RW. Indications for repair of full-thickness rotator cuff tears. Am J Sports Med. 2007;35:1007-1016.
64. Yamamoto A, Takagishi K, Osawa T, et al. Prevalence and risk factors of a rotator cuff tear in the general population. J Shoulder Elbow Surg. 2010;19:116-120.
65. Yoon J, Kim S, Choi Y, Kim S, Chun Y. Arthroscopic repair of the isolated subscapularis full-thickness tear: single- versus double-row suture-bridge technique. Am J Sports Med. 2019;47:1427-1433.

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