Value of Anterior Band of the Inferior Glenohumeral Ligament Area as a Morphological Parameter of Adhesive Capsulitis

Bang, Yun-Sic; Park, Junbeom; Lee, Sun Young; Park, Jiyeon; Park, Sukhee; Joo, Young; Kim, Young Uk; Lee, Yoon Kyung

doi:https://doi.org/10.1155/2019/9301970

Pain Research and Management

On this page

Abstract Introduction Methods Results Discussion Conclusion Data Availability Ethical Approval Conflicts of Interest Authors’ Contributions References Copyright Related Articles

Research Article | Open Access

Volume 2019 | Article ID 9301970 | https://doi.org/10.1155/2019/9301970

Value of Anterior Band of the Inferior Glenohumeral Ligament Area as a Morphological Parameter of Adhesive Capsulitis

Yun-Sic Bang,¹Junbeom Park,¹Sun Young Lee,¹Jiyeon Park,²Sukhee Park,²Young Joo,²Young Uk Kim,²and Yoon Kyung Lee³

Academic Editor: Marina De Tommaso

Received22 Nov 2018

Revised18 Mar 2019

Accepted28 Mar 2019

Published07 May 2019

Abstract

Objective. Thickened inferior glenohumeral ligament (IGHL) is considered as one of the major morphological parameters of adhesive capsulitis (AC). Previous studies reported that the anterior band of inferior glenohumeral ligament thickness (aIGHLT) is correlated with shoulder capsular contracture, luxatio erecta humeri, and AC. However, the thickness varies from the measured angle. To reduce this measurement error, we devised a new morphological parameter, called the anterior band of inferior glenohumeral ligament area (aIGHLA). Methods. The aIGHL samples were collected from 54 patients with AC and from 50 control subjects who underwent shoulder magnetic resonance imaging (MRI) without any evidence of AC. Coronal T2-weighted MRI images were obtained at the shoulder level from each patient. We measured the aIGHLA and aIGHLT at the maximal view of the IGHL in the coronal plane using our picture archiving and communication system. The aIGHLA was measured at the whole cross-sectional area of the IGHL in the most hypertrophied segment of the coronal MR images. The aIGHLT was measured at the thickest point of the IGHL. Results. The average aIGHLA was 55.58 ± 14.16 mm² in the control group and 83.71 ± 28.45 mm² in the AC group. The average aIGHLT was 3.47 ± 0.99 mm in the control group and 4.52 ± 1.02 mm in the AC group. AC patients showed significantly greater aIGHLA () and aIGHLT () than control subjects. Receiver operating characteristic (ROC) curve analysis showed that the optimal cut-off score of the aIGHLA was 63.37 mm², with 79.6% sensitivity, 80.0% specificity, and AUC of 0.84 (95% CI, 0.76–0.92). The optimal cut-off point of the IGHLT was 3.81 mm, with 74.1% sensitivity, 74.0% specificity, and AUC of 0.77 (95% CI, 0.68–0.86). Conclusions. Although the aIGHLA and aIGHLT were both significantly associated with AC, the aIGHLA was a more sensitive diagnostic parameter.

1. Introduction

Adhesive capsulitis (AC) of shoulder describes a pathological process, in which the body forms adhesions or excessive scar tissue across the glenohumeral (GH) joint, leading to stiffness, dysfunction, and pain. It is a debilitating condition that occurs spontaneously (idiopathic or primary AC) or following shoulder trauma during surgery (secondary AC) [1]. Although most AC patients are successfully treated with nonoperative care, years can ensue (mean, 1.5–3 years) before recovering normal range of motion (ROM) [2, 3]. Prompt diagnosis of AC and effective treatment with intra-articular corticosteroid injection or physical therapy shortens the duration of joint pain and stiffness and significantly reduces patient morbidity [2, 4]. The diagnosis of AC still remains clinical [5, 6]. The diagnostic criteria for AC include shoulder stiffness lasting more than one month, shoulder pain, and absence of other abnormalities [2, 3]. In the presence of established physical signs and typical symptoms, the clinical evaluation of AC has high diagnostic sensitivity and specificity [1, 7, 8]. However, the early phases of AC are characterized by variable symptoms and diagnostic challenges [3]. Imaging modalities play an important role in the diagnosis of AC in the presence of atypical clinical symptoms. The inferior glenohumeral ligament (IGHL) complex comprises three components supporting the inferior aspect of the shoulder. It consists of an anterior band, a posterior band, and an interposed axillary pouch [9]. The IGHL complex stabilizes the shoulder, and its function depends on the position of the shoulder. With the arm in a 90° abduction and external rotation, the anterior band of the IGHL is the main glenohumeral joint stabilizer [9, 10]. An abnormal anterior band of IGHL (aIGHL) is a major finding of AC [11]. Magnetic resonance imaging (MRI) facilitates the pathological evaluation of the aIGHL and other associated pathological findings associated with the shoulder joint [12]. Previous studies investigated the aIGHL based on a single measurement at the approximate “middle” or “halfway” of the aIGHL [11]. However, partial tear and asymmetrical thickening of the aIGHL may be detected widely, suggesting the scope for measurement error(s). In contrast to aIGHLT, the anterior band of inferior glenohumeral cross-sectional area (aIGHLA) measures the whole cross-sectional area of the aIGHL without the possibility of measurement error. Thus, for evaluation of hypertrophy of the whole IGHL, we developed a new morphological parameter, called the aIGHLA. We hypothesized that the aIGHLA is a key morphological parameter in AC diagnosis. Therefore, we compared the aIGHLA and aIGHLT between AC patients and normal controls using shoulder MRI.

2. Methods

2.1. Patients

This study was registered at the University of Catholic Kwandong, Republic of Korea, Incheon (IS18RISI0014). The Institutional Review Board (IRB) reviewed and approved the research protocol. We retrospectively reviewed patients who visited our pain clinic from November 2015 to November 2017 and who were diagnosed with AC.

The inclusion criteria were as follows: (1) ache or dull pain in the outer shoulder area; (2) available shoulder MRI image(s); (3) severe restriction in shoulder movement; (4) progressive loss of both passive and active range of motion (ROM); (5) symptoms present for at least 3 months; and (6) medical charts containing follow-up data of AC patients were analyzed for confirmation. We excluded patients if they had any of the following conditions: (1) history of shoulder surgery; (2) history of rheumatoid arthritis; (3) calcific tendinitis; (4) full-thickness rotator cuff tear; and (4) any neuromuscular disease.

A total of 54 patients who met the inclusion criteria were enrolled after an experienced board-certified musculoskeletal radiologist confirmed the diagnosis of AC.

There were 20 (37.0%) men and 34 (63.0%) women with a mean age of 56.98 ± 7.16 years (range, 41 to 74 years) (Table 1). All patients underwent shoulder MRI. To compare the aIGHLA and aIGHLT between patients with and without AC, we also enrolled a control group of subjects who underwent shoulder MRI, without any evidence of AC from November 2015 to November 2017. We only enrolled patients in the control group who did not have AC-related symptoms. The control group included 50 individuals (19 men and 31 women) with a mean age of 56.44 ± 5.52 years (range, 44 to 65 years).

2.2. Imaging Parameters

MRI analyses were performed with 3.0T Magnetom Skyra MRI system (Siemens Healthcare, Erlangen, Germany) and 3T Ingina (Philips, Eindhoven, Netherlands) scanners. For all MRI examinations, we obtained sagittal and coronal T2-weighted images with <3 mm slice thickness, 0.9-mm intersection gap, 4010-ms/76-ms repetition time (TR)/echo time (TE), 150 × 150 field of view, 512 × 256 matrix, and >3 echo train length (ETL).

2.3. Image Analysis

The aIGHLT and aIGHLA measurements were performed by the same physician, who was blinded to the diagnosis of the AC. T2-weighted turbo-spin-echo coronal MR images were obtained at the thickest visualization of aIGHL. We measured the aIGHLA and aIGHLT on MRI using a picture archiving and communication system (INFINITT; Infinitt Healthcare, Seoul, Korea). INFINITT system offers an enterprise imaging solution with exact diagnostic viewer. The aIGHLA was measured as the whole cross-sectional area of the IGHL at the thickest point. The aIGHLT was measured at the thickest point between the origin and insertion (Figures 1(a)–1(d)).

(a)

(b)

(c)

(d)

2.4. Statistical Analysis

Data were presented as mean ± standard deviation (SD). We compared the aIGHLA and aIGHLT between the AC and control groups using unpaired t-tests. The validity of the aIGHLA and aIGHLT for diagnosis of AC was estimated by receiver operator characteristic (ROC) curves, area under the curve (AUC), cut-off values, sensitivity, and specificity with 95% confidence intervals (CIs). values less than 0.05 were considered statistically significantly different. SPSS for Windows version 22 (IBM SPSS Inc., Chicago, IL) was used for the statistical analysis.

3. Results

AC affected 29 right shoulders and 25 left shoulders of patients. The average aIGHLA was 55.58 ± 14.16 mm² in the control group and 83.71 ± 28.45 mm² in the AC group. The average aIGHLT was 3.47 ± 0.99 mm in the control group and 4.52 ± 1.02 mm in the AC group. AC patients had significantly greater aIGHLA () and aIGHLT () than control subjects (Table 1). The ROC curve analysis (Figure 2) showed that the optimal cut-off point of the IGHLT was 3.81 mm, with 74.1% sensitivity, 74.0% specificity, and AUC of 0.77 (95% CI, 0.68–0.86) (Table 2). The optimal cut-off score of the aIGHLA was 63.37 mm², with 79.6% sensitivity, 80.0% specificity, and AUC of 0.84 (95% CI, 0.76–0.92) (Table 3).

Figure 2

Receiver operating characteristic (ROC) curve of anterior band of inferior glenohumeral ligament thickness (aIGHLT) and anterior band of inferior glenohumeral ligament area (aIGHLA) for prediction of adhesive capsulitis. The best cut off point of aIGHLA was 63.37 mm² versus 3.81 mm of aIGHLT, with sensitivity 79.6% versus 74.1%, specificity 80.0% versus 74.0% and AUC 0.84 versus 0.77, respectively. aIGHLT AUC (95% CI) = 0.77 (0.68–0.86). aIGHLA AUC (95% CI) = 0.84 (0.76–0.92). AUC = area under the curve.

4. Discussion

AC is a common clinical condition characterized by global limitation of passive and active ROM and pain in the affected shoulder [7, 13]. AC was challenging in previous histological studies without evidence of significant inflammatory focus [14]. Several types of conservative management at primary care facilities have not proven effective in most AC patients [14]. The primary objective of the management of AC associated with stiffness is to restore or improve the shoulder ROM. Various imaging modalities, such as arthrogram, ultrasonography, and Doppler ultrasound, facilitate precise diagnosis [12, 15]. MRI is also commonly used to investigate shoulder disorders and exclude concomitant conditions [13]. It has been used to identify morphological changes in the joint capsule at the axillary pouch level with variable results and the joint capsule and periarticular tissues (obliteration of adjacent fat planes, contrast enhancement, and thickening) at the rotator interval [16, 17].

However, diagnosis is still a challenge, especially due to the lack of reliable diagnostic standards for AC. Based on clinical and experimental investigations, the contracture of the aIGHL restricting flexion and internal rotation was confirmed [18]. The aIGHL is the main glenohumeral joint stabilizer [9]. Thus, aIGHL injury is associated with clinically evident instability [19]. The aIGHL arises from the anterior inferior labrum. It is important clinically for AC diagnosis [20]. The normal aIGHL appears as low-signal intensity bands, stretching from the inferior labrum to the humeral neck on MR coronal view [9, 19]. The anterior band is best seen on anterior coronal image through the glenohumeral joint. Gondim Teixeira et al. demonstrated that changes in signal intensity at the aIGHL are the key parameters in the diagnosis of AC on conventional MRI [3]. Passanante et al. insisted that aIGHL injuries are the most important cause of shoulder pain [9]. Michelin et al. reported that the aIGHL is thickened in AC patients, and ultrasound enables the measurement of aIGHL thickness in the axilla [11]. The average thickness of aIGHL using ultrasound was 4.0 mm in an AC shoulder compared with 1.3 mm in the asymptomatic contralateral shoulder. However, these studies did not compare normal subjects and AC. Our results demonstrated that the aIGHLT of normal subjects was 3.47 ± 0.99 mm and in patients with AC, it was 4.52 ± 1.02 mm.

As discussed above, previous studies focused only on the aIGHLT [11]. However, the wide range of locations of partial tear and asymmetrical thickening of the aIGHL leads to measurement errors. By contrast, the aIGHLA is not associated with such error as it measures the whole cross-sectional area of the IGHL.

We hypothesized that the coronal cross-sectional area of the aIGHLA may predict AC. Due to the absence of measurement errors, the aIGHLA is better than the aIGHLT as a morphological parameter of AC. In the current study, we found that the aIGHLA had 79.6% sensitivity, 80.0% specificity, and AUC of 0.84 (95% CI, 0.76–0.92) to predict AC. By contrast, the aIGHLT had 74.1% sensitivity, 74.0% specificity, and AUC of 0.77 (95% CI of 0.68–0.86). These findings suggest that the aIGHLA is a better predictor of AC than the aIGHLT.

Our present study has several limitations. The IGHL consists of an anterior band, a posterior band, and an interposed axillary pouch. However, we focused only on aIGHL because of its prime importance in the stability of the shoulder joint [12].

Second, there are several morphological abnormalities of AC, such as coracohumeral ligament contracture, changes in the appearance of the shoulder joint capsule, or thickened periarticular tissues, which are effective in discriminating AC [3, 14, 21–25]. However, we only assessed the measurement of aIGHLA and aIGHLT on MRI. Third, errors may be associated with the shoulder MRI measurement of aIGHLA and aIGHLT. Although we measured these morphological parameters in the coronal plane that best showed the ATFL, the coronal images used for the analysis of the variables may be inhomogeneous because of differences in the cutting angle or MRI level due to technical reasons and individual anatomic variation. In addition, a 3 mm slice of axial T2-weighted TRE MR image is thicker than the ideal slice. Thus, small lesions are frequently difficult to detect. Fourth, the principal methodological limitation was the retrospective evaluation of the medical records for data analysis [26–28]. Despite these weaknesses, this is the first study to document that the aIGHLA is associated with AC.

5. Conclusion

Although aIGHLA and aIGHLT are both significantly associated with AC, the aIGHLA is a more sensitive diagnostic parameter for AC than aIGHLT. We identified the optimal cut-off point of the aIGHLA as 63.37 mm², with 79.6% sensitivity and 80.0% specificity. The best cut-off point of the aIGHLT was 3.81 mm, with 74.1% sensitivity and 74.0% specificity. When evaluating patients with AC, physicians should carefully assess the aIGHLA rather than the aIGHLT.

Data Availability

The data used to support the findings of this study are available from the corresponding author upon request.

Ethical Approval

The ethical approval was obtained (IRB number: IS18RISI0014).

Conflicts of Interest

All authors declare that they have no conflicts of interest.

Authors’ Contributions

Young Uk Kim and Yoon Kyung Lee contributed equally to this article as co-corresponding authors. Young Uk Kim and Yoon Kyung Lee contributed to the interpretation of the data and revising and drafting the article, gave final approval of the version to be published, and agree to be accountable for all aspects of the work.

References

H. V. Le, S. J. Lee, A. Nazarian, and E. K. Rodriguez, “Adhesive capsulitis of the shoulder: review of pathophysiology and current clinical treatments,” Shoulder & Elbow, vol. 9, no. 2, pp. 75–84, 2017.
View at: Publisher Site | Google Scholar
S. Brue, A. Valentin, M. Forssblad, S. Werner, C. Mikkelsen, and G. Cerulli, “Idiopathic adhesive capsulitis of the shoulder: a review,” Knee Surgery, Sports Traumatology, Arthroscopy, vol. 15, no. 8, pp. 1048–1054, 2007.
View at: Publisher Site | Google Scholar
P. A. Gondim Teixeira, C. Balaj, A. Chanson, S. Lecocq, M. Louis, and A. Blum, “Adhesive capsulitis of the shoulder: value of inferior glenohumeral ligament signal changes on T2-weighted fat-saturated images,” American Journal of Roentgenology, vol. 198, no. 6, pp. W589–W596, 2012.
View at: Publisher Site | Google Scholar
S. Bell, J. Coghlan, and M. Richardson, “Hydrodilatation in the management of shoulder capsulitis,” Australasian Radiology, vol. 47, no. 3, pp. 247–251, 2003.
View at: Publisher Site | Google Scholar
K.-S. Ahn, C. H. Kang, Y.-W. Oh, and W.-K. Jeong, “Correlation between magnetic resonance imaging and clinical impairment in patients with adhesive capsulitis,” Skeletal Radiology, vol. 41, no. 10, pp. 1301–1308, 2012.
View at: Publisher Site | Google Scholar
C. M. Sofka, G. A. Ciavarra, J. A. Hannafin, F. A. Cordasco, and H. G. Potter, “Magnetic resonance imaging of adhesive capsulitis: correlation with clinical staging,” HSS Journal, vol. 4, no. 2, pp. 164–169, 2008.
View at: Publisher Site | Google Scholar
J. E. Hsu, O. A. Anakwenze, W. J. Warrender, and J. A. Abboud, “Current review of adhesive capsulitis,” Journal of Shoulder and Elbow Surgery, vol. 20, no. 3, pp. 502–514, 2011.
View at: Publisher Site | Google Scholar
A. S. Neviaser and J. A. Hannafin, “Adhesive capsulitis,” American Journal of Sports Medicine, vol. 38, no. 11, pp. 2346–2356, 2010.
View at: Publisher Site | Google Scholar
G. J. Passanante, M. R. Skalski, D. B. Patel et al., “Inferior glenohumeral ligament (IGHL) complex: anatomy, injuries, imaging features, and treatment options,” Emergency Radiology, vol. 24, no. 1, pp. 65–71, 2017.
View at: Publisher Site | Google Scholar
S. J. Turkel, M. W. Panio, J. L. Marshall, and F. G. Girgis, “Stabilizing mechanisms preventing anterior dislocation of the glenohumeral joint,” Journal of Bone & Joint Surgery, vol. 63, no. 8, pp. 1208–1217, 1981.
View at: Publisher Site | Google Scholar
P. Michelin, Y. Delarue, F. Duparc, and J. N. Dacher, “Thickening of the inferior glenohumeral capsule: an ultrasound sign for shoulder capsular contracture,” European Radiology, vol. 23, no. 10, pp. 2802–2806, 2013.
View at: Publisher Site | Google Scholar
M. Jana and S. Gamanagatti, “Magnetic resonance imaging in glenohumeral instability,” World Journal of Radiology, vol. 3, no. 9, pp. 224–232, 2011.
View at: Publisher Site | Google Scholar
Y. T. Lee, K. S. Chun, K. J. Yoon et al., “Correlation of joint volume and passive range of motion with capsulo-synovial thickness measured by contrast-enhanced magnetic resonance imaging in adhesive capsulitis,” PM&R, vol. 10, no. 2, pp. 137–145, 2018.
View at: Publisher Site | Google Scholar
J. Chen, S. Chen, Y. Li, Y. Hua, and H. Li, “Is the extended release of the inferior glenohumeral ligament necessary for frozen shoulder?” Arthroscopy: The Journal of Arthroscopic & Related Surgery, vol. 26, no. 4, pp. 529–535, 2010.
View at: Publisher Site | Google Scholar
M. Cerny, P. Omoumi, A. Larbi et al., “CT arthrography of adhesive capsulitis of the shoulder: are MR signs applicable?” European Journal of Radiology Open, vol. 4, pp. 40–44, 2017.
View at: Publisher Site | Google Scholar
M.-M. Lefevre-Colau, J.-L. Drapé, F. Fayad et al., “Magnetic resonance imaging of shoulders with idiopathic adhesive capsulitis: reliability of measures,” European Radiology, vol. 15, no. 12, pp. 2415–2422, 2005.
View at: Publisher Site | Google Scholar
S. Walmsley, P. G. Osmotherly, C. J. Walker, and D. A. Rivett, “Power Doppler ultrasonography in the early diagnosis of primary/idiopathic adhesive capsulitis: an exploratory study,” Journal of Manipulative and Physiological Therapeutics, vol. 36, no. 7, pp. 428–435, 2013.
View at: Publisher Site | Google Scholar
M. T. Provencher, L. E. LeClere, S. King et al., “Posterior instability of the shoulder,” American Journal of Sports Medicine, vol. 39, no. 4, pp. 874–886, 2011.
View at: Publisher Site | Google Scholar
A. C. Burkart and R. E. Debski, “Anatomy and function of the glenohumeral ligaments in anterior shoulder instability,” Clinical Orthopaedics and Related Research, vol. 400, pp. 32–39, 2002.
View at: Publisher Site | Google Scholar
F. A. Ramirez Ruiz, B. C. Baranski Kaniak, P. Haghighi, D. Trudell, and D. L. Resnick, “High origin of the anterior band of the inferior glenohumeral ligament: MR arthrography with anatomic and histologic correlation in cadavers,” Skeletal Radiology, vol. 41, no. 5, pp. 525–530, 2012.
View at: Publisher Site | Google Scholar
J. W. Choi, D. K. Kim, C. K. Cho, S. J. Park, and Y. H. Son, “Trends in medical disputes involving anesthesia in the period July 2009–June 2018: an analysis of the Korean society of anesthesiologists database,” Korean Journal of Anesthesiology, vol. 72, no. 2, pp. 156–163, 2019.
View at: Publisher Site | Google Scholar
Y. D. Kim, J. Y. Yu, J. Shim, H. J. Heo, and H. Kim, “Risk of encountering dorsal scapular and long thoracic nerves during ultrasound-guided interscalene brachial plexus block with nerve stimulator,” Korean Journal of Pain, vol. 29, no. 3, pp. 179–184, 2016.
View at: Publisher Site | Google Scholar
S. K. Park, M. H. Sung, H. J. Suh, and Y. S. Choi, “Ultrasound guided low approach interscalene brachial plexus block for upper limb surgery,” Korean Journal of Pain, vol. 29, no. 1, pp. 18–22, 2016.
View at: Publisher Site | Google Scholar
E. A. Ismail, J. A. Sayed, M. H. Bakri, and R. Z. Mahfouz, “Comparison of intrathecal versus intra-articular dexmedetomidine as an adjuvant to bupivacaine on postoperative pain following knee arthroscopy: a randomized clinical trial,” Korean Journal of Pain, vol. 30, no. 2, pp. 134–141, 2017.
View at: Publisher Site | Google Scholar
K. S. Mohamed, S. K. Abd-Elshafy, and A. M. El Saman, “The impact of magnesium sulfate as adjuvant to intrathecal bupivacaine on intra-operative surgeon satisfaction and postoperative analgesia during laparoscopic gynecological surgery: randomized clinical study,” Korean Journal of Pain, vol. 30, no. 3, pp. 207–213, 2017.
View at: Publisher Site | Google Scholar
S.-S. Kang, Y.-S. Shin, S.-Y. Lee, and H. Kim, “Simplified equation for determining proper depth of peripherally inserted central catheter in relation to anatomical landmarks,” Korean Journal of Anesthesiology, vol. 71, no. 4, pp. 300–304, 2018.
View at: Publisher Site | Google Scholar
Y. Y. Kim, I. T. Kim, S. I. Shin, and S. M. Yim, “Intradermal skin tests for rocuronium and cisatracurium in patients with a history of allergy: a retrospective study,” Korean Journal of Anesthesiology, vol. 71, no. 4, pp. 296–299, 2018.
View at: Publisher Site | Google Scholar
Y.-H. Shin, J. S. Yoon, H. J. Jeon, Y. B. Kim, Y. S. Kim, and J. Y. Park, “Postoperative delirium in elderly patients with critical limb ischemia undergoing major leg amputation: a retrospective study,” Korean Journal of Anesthesiology, vol. 71, no. 4, pp. 311–316, 2018.
View at: Publisher Site | Google Scholar

Copyright

Copyright © 2019 Yun-Sic Bang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

PDF Download Citation

Download other formats

Order printed copies

Views

10691

Downloads

1590

Citations