Original ResearchFree Access

Long Biceps Tendon: Normal Position, Shape, and Orientation in Its Groove in Neutral Position and External and Internal Rotation

Published Online:https://doi.org/10.1148/radiol.11110914

Abstract

Purpose

To characterize the position, shape, and orientation of the long biceps tendon (LBT) on transverse magnetic resonance (MR) images acquired in neutral position and in maximal external and internal rotation of the shoulder in asymptomatic volunteers.

Materials and Methods

Informed consent was obtained from all volunteers for this institutional review board–approved study. Fifty-three asymptomatic volunteers (mean age, 33 years; age range, 21–58 years) were included. The position of the LBT with respect to the bicipital groove was measured by two musculoskeletal radiologists on three levels along the bicipital groove on axial MR images in neutral position and in external and internal rotation of the shoulder. The shape of the LBT was classified as round, oval, flat, or comma shaped, and the orientation of the LBT was measured.

Results

The position of the LBT changed significantly at the entrance into the bicipital groove in the mediolateral and anteroposterior directions (P < .01). The changes of LBT position in external rotation and internal rotation compared with the neutral position were markedly small (< 1.5 mm). Medial eccentricity of the LBT was greatest in the neutral shoulder position at all measurement levels. Differences in LBT shape and orientation were found between the neutral position and external or internal rotation and between the three measurement levels.

Conclusion

The position of the LBT is only slightly dependent on shoulder rotation. LBT eccentricity is maximal in the neutral position. Rotational misplacement during image acquisition does not increase LBT eccentricity.

© RSNA, 2011

Introduction

The tendon of the long head of the biceps brachii muscle—the long biceps tendon (LBT)—attaches at its anchor to the superior glenoid tubercle (1). From this position, it courses intraarticularly to the entrance of the bicipital groove between the major and lesser tubercles of the proximal humerus, runs caudally inside the groove, and eventually leaves the groove to end in the proximal musculotendinous junction (2,3). Along its intraarticular course, the LBT is suspended by the coracohumeral ligament, the superior glenohumeral ligament, and the pulley fibers, which arise from the aforementioned ligaments and the subscapularis tendon (410). Additionally, it may be stabilized by a variety of sporadic developmental interconnections with the joint capsule, ranging from pulleylike slings to complete adherence of the LBT to the joint capsule (11,12). This suspension, especially by the pulley fibers, is thought to keep the LBT in place and centered at the entrance to the bicipital groove (35,1315).

Instability of the LBT can be observed arthroscopically in about 45% of patients with rotator cuff tears, and injury to the pulley fibers has an incidence of about 7% at diagnostic arthroscopy (16). These lesions are thought to be responsible for medial dislocation of the LBT and could possibly lead to a subset of partial LBT tears at the entrance to the bicipital groove (1721). In addition to abnormalities in the ligamentous suspension of the LBT, there are abnormalities in the subscapularis tendon in most patients with LBT dislocation. Typically, partial tears at the superior margin of the subscapularis tendon are present (9,21).

An eccentric position of the LBT, especially at the level of the entrance to the bicipital groove, has been proposed as a diagnostic criterion for the detection of pulley lesions that may not be otherwise apparent (2224). So far, eccentricity of the LBT at the entrance to the groove has not been measured but merely described qualitatively. Furthermore, the criteria for LBT instability, dislocation, and subluxation are not uniform, and these terms are used differently (16,2527).

Thus, the purpose of this study was to characterize the position, shape, and orientation of the LBT on transverse magnetic resonance (MR) images acquired in the neutral position and in maximal external and internal rotation of the shoulder in asymptomatic volunteers.

Materials and Methods

The institutional review board of the University of Zurich approved this study, and informed consent was obtained from all volunteers.

Volunteers

Fifty-three asymptomatic volunteers (mean age, 33 years; age range, 21–58 years) were included in the study. There were 23 men (mean age, 34 years; age range, 21–56 years) and 30 women (mean age, 33 years; age range, 21–58 years). The volunteers had never experienced shoulder pain, could not recollect any shoulder trauma, had not undergone shoulder surgery of any kind, and reported no limitation in range of motion in the shoulder joint during daily activity. Twenty-nine right and 24 left shoulders were examined. Twenty-four shoulders were of the dominant side, and 29 were of the nondominant side. For the first volunteer, the shoulder to image was determined randomly. For the following volunteers, the shoulder to image was chosen so that we could obtain the same amount of right and left shoulders and the same amount of shoulders of the dominant and nondominant sides, if possible. Because of a preponderance of right-handed volunteers, however, this was not entirely possible.

MR Imaging

Two 1.5-T MR imaging systems (Avanto or Espree; Siemens Medical Solutions, Erlangen, Germany) were used with a dedicated four-element shoulder array coil.

The shoulder was imaged in neutral position with the arm flanking the body and the thumb pointing up. First, the standard protocol for shoulder examinations at our institution was performed. This protocol consisted of a coronal fat-saturated intermediate-weighted turbo spin-echo sequence (repetition time msec/echo time msec, 3000/13; field of view, 16 × 16 cm; matrix, 512 × 512 pixels; number of signals acquired, one; section thickness, 4 mm; and echo train length, seven), a coronal fat-saturated T2-weighted turbo spin-echo sequence (3130/72; field of view, 16 × 16 cm; matrix, 512 × 512 pixels; number of signals acquired, one; section thickness, 4 mm; and echo train length, 11), a sagittal non–fat-saturated T1-weighted turbo spin-echo sequence (525/12; field of view, 16 × 16 cm; matrix, 512 × 512 pixels; number of signals acquired, one; and section thickness, 4 mm), a sagittal short inversion time inversion-recovery sequence (5500/18; inversion time, 150 msec; field of view, 16 × 16 cm; matrix, 512 × 512 pixels; number of signals acquired, one; section thickness, 4 mm; and echo train length, seven), and an axial fat-suppressed steady-state gradient-echo (true fast imaging with steady-state precession) sequence (12.43/5.31; field of view, 18 × 18 cm; matrix, 512 × 512 pixels; number of signals acquired, one; and section thickness, 1.7 mm). Additionally, the last sequence (the axial steady-state gradient-echo sequence) was repeated with the shoulder in positions of maximal external and maximal internal rotation. External rotation of the shoulder was achieved by maximal external rotation of the shoulder joint and forearm, resulting in the palm of the hand facing upward; this position was stabilized by placing a heavy 2-kg bag filled with sand over the wrist. The whole arm was then externally rotated once again until a soft “stop” was felt; the arm was stabilized in this position. Maximal internal rotation was achieved by placing the volunteer’s hand palm-backward on the back of his or her lumbar spine with the elbow flexed 90°.

Measurements and Evaluations on MR Images

All MR images were evaluated by a musculoskeletal radiologist (F.M.B., with 5 years of experience in musculoskeletal radiology) before the measurements. Volunteers with lesions or any kind of degenerative changes to the rotator cuff tendons, coracohumeral ligament, superior glenohumeral ligament, and/or pulley fibers would have been excluded from the study. However, no volunteers had to be excluded.

The LBT was evaluated by two independent musculoskeletal radiologists (F.M.B. [reader 1] and T.J.D. [reader 2, with 2 years of experience in musculoskeletal radiology]) at three levels of the bicipital groove (superior, middle, and inferior) with the shoulder in neutral position, in external rotation, and in internal rotation. The superior level, at the entrance of the LBT into the bicipital groove, was defined as being shown on the most superior image that included the subscapularis tendon; the inferior level, where the LBT exited from the bicipital groove, was defined as being shown on the most inferior image that included the subscapularis tendon; and the middle level represented the midway point between those levels (Fig 1). All three levels and all three positions were evaluated at the same time in a standardized order: first, on the images obtained in neutral position, then, on the images obtained in maximal external rotation, and finally, on the images obtained in maximal internal rotation.

Figure 1a:

Figure 1a: (a) Schematic diagram of right shoulder joint shows the three measurement levels. (b–d) Axial fat-suppressed steady-state gradient-echo MR images. (b) The superior level, at the entrance of the LBT into the bicipital groove, was defined as being shown on the most superior image that included the subscapularis tendon (arrowheads). (c) The middle level represented the midway point between the inferior level and the superior level. Arrowheads = subscapularis tendon. (d) The inferior level, where the LBT exits from the bicipital groove (white arrowheads), was defined as being shown on the most inferior image that included the subscapularis tendon (black arrowheads).

Figure 1b:

Figure 1b: (a) Schematic diagram of right shoulder joint shows the three measurement levels. (b–d) Axial fat-suppressed steady-state gradient-echo MR images. (b) The superior level, at the entrance of the LBT into the bicipital groove, was defined as being shown on the most superior image that included the subscapularis tendon (arrowheads). (c) The middle level represented the midway point between the inferior level and the superior level. Arrowheads = subscapularis tendon. (d) The inferior level, where the LBT exits from the bicipital groove (white arrowheads), was defined as being shown on the most inferior image that included the subscapularis tendon (black arrowheads).

Figure 1c:

Figure 1c: (a) Schematic diagram of right shoulder joint shows the three measurement levels. (b–d) Axial fat-suppressed steady-state gradient-echo MR images. (b) The superior level, at the entrance of the LBT into the bicipital groove, was defined as being shown on the most superior image that included the subscapularis tendon (arrowheads). (c) The middle level represented the midway point between the inferior level and the superior level. Arrowheads = subscapularis tendon. (d) The inferior level, where the LBT exits from the bicipital groove (white arrowheads), was defined as being shown on the most inferior image that included the subscapularis tendon (black arrowheads).

Figure 1d:

Figure 1d: (a) Schematic diagram of right shoulder joint shows the three measurement levels. (b–d) Axial fat-suppressed steady-state gradient-echo MR images. (b) The superior level, at the entrance of the LBT into the bicipital groove, was defined as being shown on the most superior image that included the subscapularis tendon (arrowheads). (c) The middle level represented the midway point between the inferior level and the superior level. Arrowheads = subscapularis tendon. (d) The inferior level, where the LBT exits from the bicipital groove (white arrowheads), was defined as being shown on the most inferior image that included the subscapularis tendon (black arrowheads).

Position.—The position of the center of the LBT was evaluated with respect to the bicipital groove. The center of the LBT was defined as the point in the middle of the LBT (Fig 2). In flat or comma-shaped tendons, the center of the LBT was defined as the point in the middle of the LBT on a line drawn perpendicular to the greatest tendon diameter (Fig 1). The distance from the center of the LBT to a reference line connecting the anterior contours of the greater and lesser tubercles was measured (Fig 2). This measurement quantified the LBT position in the anteroposterior direction; a positive measurement indicated that the LBT was located outside the bicipital groove, and a negative measurement indicated how deep the LBT was located in the bicipital groove.

Figure 2a:

Figure 2a: (a, b) Measurement of LBT is illustrated (a) schematically and (b) on an axial MR image. The position of the LBT (∗) was evaluated with respect to the bicipital groove. Two auxiliary reference lines were needed. The first (A) was drawn between the anterior contours of the greater and lesser tubercles. The second (B) was drawn perpendicular to the first reference line through the deepest point of the bicipital groove (C). The distances from the center of the LBT (D) to the two reference lines were measured. The distance to A quantified the LBT position in the anteroposterior direction. A positive measurement (+) indicated that the LBT was located outside the bicipital groove, and a negative measurement (−) indicated how deep the LBT was located in the bicipital groove. The distance of the center of the LBT to B indicated the LBT position in the mediolateral direction. A positive measurement (+) indicated an LBT position medial to the deepest point of the bicipital groove, and a negative measurement (−) indicated an LBT position lateral to the deepest point of the bicipital groove.

Figure 2b:

Figure 2b: (a, b) Measurement of LBT is illustrated (a) schematically and (b) on an axial MR image. The position of the LBT (∗) was evaluated with respect to the bicipital groove. Two auxiliary reference lines were needed. The first (A) was drawn between the anterior contours of the greater and lesser tubercles. The second (B) was drawn perpendicular to the first reference line through the deepest point of the bicipital groove (C). The distances from the center of the LBT (D) to the two reference lines were measured. The distance to A quantified the LBT position in the anteroposterior direction. A positive measurement (+) indicated that the LBT was located outside the bicipital groove, and a negative measurement (−) indicated how deep the LBT was located in the bicipital groove. The distance of the center of the LBT to B indicated the LBT position in the mediolateral direction. A positive measurement (+) indicated an LBT position medial to the deepest point of the bicipital groove, and a negative measurement (−) indicated an LBT position lateral to the deepest point of the bicipital groove.

So that we could evaluate the position of the LBT in the mediolateral direction, a perpendicular line to the above-mentioned reference line (Fig 2) was drawn through the deepest point of the bicipital groove. The distance of the center of the LBT to this line was determined (Fig 2); a positive measurement indicated a position of the LBT medial to the deepest point of the bicipital groove, and a negative measurement indicated a position of the LBT lateral to the deepest point of the bicipital groove.

Any changes in the position of the LBT in the neutral position and in external and internal rotation of the shoulder were then determined at the three measurement levels.

Shape.—The cross-sectional shape of the LBT was categorized as round, oval, flat, or comma shaped (Fig 3). For a round LBT, the cross-sectional area was a circle with equal perpendicular diameters. For an oval LBT, the dimension of the smallest cross-sectional tendon diameter was greater than (but not equal to) half of the greatest tendon diameter. For a flat LBT, the smallest cross-sectional tendon diameter was smaller than half of the greatest diameter, and the lateral and medial contours of the tendon were roundish and obtusely angled. For a comma-shaped LBT, the same criteria applied as for a flat LBT, but the medial contour of the tendon was pointed and acutely angled.

Figure 3a:

Figure 3a: (a–d) On axial MR images, the cross-sectional shape of the LBT was classified as (a) round, (b) oval, (c) flat, or (d) comma shaped. In a round LBT, the cross-sectional area was a circle. In an oval LBT, the dimension of the smallest cross-sectional tendon diameter was greater than (but not equal to) half of the greatest tendon diameter. In (c) a flat LBT, the smallest cross-sectional tendon diameter was smaller than half of the greatest diameter, and the lateral and medial tendon contours were roundish and obtusely angled (white arrowhead). Black arrowhead = subscapularis tendon insertion. In (d) a comma-shaped LBT, the same criteria applied as for a flat LBT, but the medial contour of the tendon was pointed and acutely angled (arrow). At the superior evaluation level, the medial contour of the LBT was often located superficial to the most lateral aspect of the subscapularis tendon insertion (arrowhead), which sometimes reached far into the depth of the intertubercular groove.

Figure 3b:

Figure 3b: (a–d) On axial MR images, the cross-sectional shape of the LBT was classified as (a) round, (b) oval, (c) flat, or (d) comma shaped. In a round LBT, the cross-sectional area was a circle. In an oval LBT, the dimension of the smallest cross-sectional tendon diameter was greater than (but not equal to) half of the greatest tendon diameter. In (c) a flat LBT, the smallest cross-sectional tendon diameter was smaller than half of the greatest diameter, and the lateral and medial tendon contours were roundish and obtusely angled (white arrowhead). Black arrowhead = subscapularis tendon insertion. In (d) a comma-shaped LBT, the same criteria applied as for a flat LBT, but the medial contour of the tendon was pointed and acutely angled (arrow). At the superior evaluation level, the medial contour of the LBT was often located superficial to the most lateral aspect of the subscapularis tendon insertion (arrowhead), which sometimes reached far into the depth of the intertubercular groove.

Figure 3c:

Figure 3c: (a–d) On axial MR images, the cross-sectional shape of the LBT was classified as (a) round, (b) oval, (c) flat, or (d) comma shaped. In a round LBT, the cross-sectional area was a circle. In an oval LBT, the dimension of the smallest cross-sectional tendon diameter was greater than (but not equal to) half of the greatest tendon diameter. In (c) a flat LBT, the smallest cross-sectional tendon diameter was smaller than half of the greatest diameter, and the lateral and medial tendon contours were roundish and obtusely angled (white arrowhead). Black arrowhead = subscapularis tendon insertion. In (d) a comma-shaped LBT, the same criteria applied as for a flat LBT, but the medial contour of the tendon was pointed and acutely angled (arrow). At the superior evaluation level, the medial contour of the LBT was often located superficial to the most lateral aspect of the subscapularis tendon insertion (arrowhead), which sometimes reached far into the depth of the intertubercular groove.

Figure 3d:

Figure 3d: (a–d) On axial MR images, the cross-sectional shape of the LBT was classified as (a) round, (b) oval, (c) flat, or (d) comma shaped. In a round LBT, the cross-sectional area was a circle. In an oval LBT, the dimension of the smallest cross-sectional tendon diameter was greater than (but not equal to) half of the greatest tendon diameter. In (c) a flat LBT, the smallest cross-sectional tendon diameter was smaller than half of the greatest diameter, and the lateral and medial tendon contours were roundish and obtusely angled (white arrowhead). Black arrowhead = subscapularis tendon insertion. In (d) a comma-shaped LBT, the same criteria applied as for a flat LBT, but the medial contour of the tendon was pointed and acutely angled (arrow). At the superior evaluation level, the medial contour of the LBT was often located superficial to the most lateral aspect of the subscapularis tendon insertion (arrowhead), which sometimes reached far into the depth of the intertubercular groove.

Orientation.—The angle of the direction of the greatest LBT diameter with respect to the previously described reference line drawn between the anterior contour of the major and lesser tubercles was defined as the LBT orientation (Figs 4, 5). The orientation of the LBT along its course in the bicipital groove, as well as any changes in its orientation during external and internal rotation of the shoulder, were then described at the three measurement levels.

Figure 4a:

Figure 4a: (a, b) Measurement of LBT orientation at the superior level in a right shoulder on axial MR images. Typically, the lateral contour of the LBT lies on the level of the deepest point of the bicipital groove (arrow). The superior edge of the subscapularis tendon (arrowheads) is seen. The angle of the direction of the greatest LBT diameter with respect to the previously described reference line drawn between the anterior contours of the major and lesser tubercles (see Fig 1b) was defined as the LBT orientation.

Figure 4b:

Figure 4b: (a, b) Measurement of LBT orientation at the superior level in a right shoulder on axial MR images. Typically, the lateral contour of the LBT lies on the level of the deepest point of the bicipital groove (arrow). The superior edge of the subscapularis tendon (arrowheads) is seen. The angle of the direction of the greatest LBT diameter with respect to the previously described reference line drawn between the anterior contours of the major and lesser tubercles (see Fig 1b) was defined as the LBT orientation.

Figure 5a:

Figure 5a: (a–f) Axial fat-suppressed steady-state gradient-echo MR images in 38-year-old male volunteer at the superior evaluation level in (a, d) external rotation, (b, e) neutral position, and (c, f) internal rotation show (a–c) LBT shape and (d–f) LBT orientation. The LBT shape was flat in the neutral position and in external rotation. In internal rotation, the shape changed to oval. Compared with the neutral position, the LBT was 5° internally rotated in external rotation of the shoulder and 4° externally rotated in internal rotation of the shoulder. Arrowheads = subscapularis tendon.

Figure 5b:

Figure 5b: (a–f) Axial fat-suppressed steady-state gradient-echo MR images in 38-year-old male volunteer at the superior evaluation level in (a, d) external rotation, (b, e) neutral position, and (c, f) internal rotation show (a–c) LBT shape and (d–f) LBT orientation. The LBT shape was flat in the neutral position and in external rotation. In internal rotation, the shape changed to oval. Compared with the neutral position, the LBT was 5° internally rotated in external rotation of the shoulder and 4° externally rotated in internal rotation of the shoulder. Arrowheads = subscapularis tendon.

Figure 5c:

Figure 5c: (a–f) Axial fat-suppressed steady-state gradient-echo MR images in 38-year-old male volunteer at the superior evaluation level in (a, d) external rotation, (b, e) neutral position, and (c, f) internal rotation show (a–c) LBT shape and (d–f) LBT orientation. The LBT shape was flat in the neutral position and in external rotation. In internal rotation, the shape changed to oval. Compared with the neutral position, the LBT was 5° internally rotated in external rotation of the shoulder and 4° externally rotated in internal rotation of the shoulder. Arrowheads = subscapularis tendon.

Figure 5d:

Figure 5d: (a–f) Axial fat-suppressed steady-state gradient-echo MR images in 38-year-old male volunteer at the superior evaluation level in (a, d) external rotation, (b, e) neutral position, and (c, f) internal rotation show (a–c) LBT shape and (d–f) LBT orientation. The LBT shape was flat in the neutral position and in external rotation. In internal rotation, the shape changed to oval. Compared with the neutral position, the LBT was 5° internally rotated in external rotation of the shoulder and 4° externally rotated in internal rotation of the shoulder. Arrowheads = subscapularis tendon.

Figure 5e:

Figure 5e: (a–f) Axial fat-suppressed steady-state gradient-echo MR images in 38-year-old male volunteer at the superior evaluation level in (a, d) external rotation, (b, e) neutral position, and (c, f) internal rotation show (a–c) LBT shape and (d–f) LBT orientation. The LBT shape was flat in the neutral position and in external rotation. In internal rotation, the shape changed to oval. Compared with the neutral position, the LBT was 5° internally rotated in external rotation of the shoulder and 4° externally rotated in internal rotation of the shoulder. Arrowheads = subscapularis tendon.

Figure 5f:

Figure 5f: (a–f) Axial fat-suppressed steady-state gradient-echo MR images in 38-year-old male volunteer at the superior evaluation level in (a, d) external rotation, (b, e) neutral position, and (c, f) internal rotation show (a–c) LBT shape and (d–f) LBT orientation. The LBT shape was flat in the neutral position and in external rotation. In internal rotation, the shape changed to oval. Compared with the neutral position, the LBT was 5° internally rotated in external rotation of the shoulder and 4° externally rotated in internal rotation of the shoulder. Arrowheads = subscapularis tendon.

Statistical Analysis

Because LBT position and orientation are continuous variables and LBT shape is categoric, interreader agreement was quantified by calculating the intraclass correlation coefficient (ICC) for the evaluation of the biceps tendon position and orientation, and the weighted κ statistic was used to determine interreader agreement of the evaluation of the biceps tendon shape. The Wilcoxon signed-rank test was used to find significant differences in LBT position, shape, and orientation at the different measurement levels and in the different positions of the shoulder. Statistical software (PASW, version 18; SPSS, Chicago, Ill) was used. P < .05 was considered to indicate a significant difference.

Results

Position

The position of the LBT changed significantly in both directions (anteroposterior and mediolateral) from the neutral position to external rotation and from the neutral position to internal rotation at all measurement levels, except for some measurements in the anteroposterior direction on the middle and inferior levels. Detailed measurement and statistical results are provided in Table 1.

Table 1 Position and Orientation of LBT in Different Rotational Positions of the Humerus

Table 1

Note.—Data are means ± standard deviations, with ranges in parentheses. P values were calculated with the Wilcoxon signed-rank test.

However, the changes in LBT position in external rotation and internal rotation compared with its position at neutral were markedly small (Fig 6). On the superior and middle measurement levels, these differences were all less than 1 mm for both readers; on the inferior measurement level, they were less than 1.5 mm.

Figure 6a:

Figure 6a: (a–i) Axial fat-suppressed steady-state gradient-echo MR images in 35-year-old female volunteer show LBT (arrow) shape and orientation in (a, d, g) external rotation, (b, e, h) the neutral position, and (c, f, i) internal rotation at (a–c) the superior level, (d–f) the middle level, and (g–i) the inferior level. Arrowheads = subscapularis tendon.

Figure 6b:

Figure 6b: (a–i) Axial fat-suppressed steady-state gradient-echo MR images in 35-year-old female volunteer show LBT (arrow) shape and orientation in (a, d, g) external rotation, (b, e, h) the neutral position, and (c, f, i) internal rotation at (a–c) the superior level, (d–f) the middle level, and (g–i) the inferior level. Arrowheads = subscapularis tendon.

Figure 6c:

Figure 6c: (a–i) Axial fat-suppressed steady-state gradient-echo MR images in 35-year-old female volunteer show LBT (arrow) shape and orientation in (a, d, g) external rotation, (b, e, h) the neutral position, and (c, f, i) internal rotation at (a–c) the superior level, (d–f) the middle level, and (g–i) the inferior level. Arrowheads = subscapularis tendon.

Figure 6d:

Figure 6d: (a–i) Axial fat-suppressed steady-state gradient-echo MR images in 35-year-old female volunteer show LBT (arrow) shape and orientation in (a, d, g) external rotation, (b, e, h) the neutral position, and (c, f, i) internal rotation at (a–c) the superior level, (d–f) the middle level, and (g–i) the inferior level. Arrowheads = subscapularis tendon.

Figure 6e:

Figure 6e: (a–i) Axial fat-suppressed steady-state gradient-echo MR images in 35-year-old female volunteer show LBT (arrow) shape and orientation in (a, d, g) external rotation, (b, e, h) the neutral position, and (c, f, i) internal rotation at (a–c) the superior level, (d–f) the middle level, and (g–i) the inferior level. Arrowheads = subscapularis tendon.

Figure 6f:

Figure 6f: (a–i) Axial fat-suppressed steady-state gradient-echo MR images in 35-year-old female volunteer show LBT (arrow) shape and orientation in (a, d, g) external rotation, (b, e, h) the neutral position, and (c, f, i) internal rotation at (a–c) the superior level, (d–f) the middle level, and (g–i) the inferior level. Arrowheads = subscapularis tendon.

Figure 6g:

Figure 6g: (a–i) Axial fat-suppressed steady-state gradient-echo MR images in 35-year-old female volunteer show LBT (arrow) shape and orientation in (a, d, g) external rotation, (b, e, h) the neutral position, and (c, f, i) internal rotation at (a–c) the superior level, (d–f) the middle level, and (g–i) the inferior level. Arrowheads = subscapularis tendon.

Figure 6h:

Figure 6h: (a–i) Axial fat-suppressed steady-state gradient-echo MR images in 35-year-old female volunteer show LBT (arrow) shape and orientation in (a, d, g) external rotation, (b, e, h) the neutral position, and (c, f, i) internal rotation at (a–c) the superior level, (d–f) the middle level, and (g–i) the inferior level. Arrowheads = subscapularis tendon.

Figure 6i:

Figure 6i: (a–i) Axial fat-suppressed steady-state gradient-echo MR images in 35-year-old female volunteer show LBT (arrow) shape and orientation in (a, d, g) external rotation, (b, e, h) the neutral position, and (c, f, i) internal rotation at (a–c) the superior level, (d–f) the middle level, and (g–i) the inferior level. Arrowheads = subscapularis tendon.

In neutral position of the shoulder joint, the averaged (between readers 1 and 2) position of the LBT was 2 mm medial to the deepest point of the bicipital groove at the superior level, 1.7 mm medial to the deepest point of the bicipital groove at the middle level, and 1.4 mm medial to the deepest point of the bicipital groove at the inferior level.

Interreader agreement was substantial (ICC > 0.6) to almost perfect (ICC > 0.8) and highly significant (P < .005), except for those measurements at the superior level in internal rotation and at the inferior level in the neutral position in the anteroposterior direction. Detailed results are provided in Table 2.

Table 2 Interreader Agreement for Position and Orientation of LBT

Table 2

Surprisingly, LBT eccentricity in the mediolateral direction was most pronounced in the neutral position and was less pronounced in external rotation and internal rotation at all measurement levels.

Shape

At the superior level, the LBT was flat to comma shaped in almost all volunteers independent of the shoulder position. At the middle level, the LBT was flat to comma shaped, whereas in external rotation, the tendon had an oval shape at times. At the inferior level, the LBT was predominantly oval to flat, except in internal rotation, when there was a tendency for it to be round or oval in shape.

In all joint positions (neutral, external rotation, and internal rotation), there was a significant difference in LBT shape between the superior and middle levels (Table 3). For readers 1 and 2, respectively, for the neutral position, P = .002 and .002; for external rotation, P = .003 and < .001; and for internal rotation, P = .010 and .003. The same applied to the difference in LBT shape between the middle and inferior levels. For readers 1 and 2, respectively, for the neutral position, P = .001 and .009; for external rotation, P = .001 and .002; and for internal rotation, P < .001 and < .001. More results of LBT shape classification are provided in Table 3.

Table 3 Shape of 52 LBTs in Different Rotational Positions of the Humerus

Table 3

Note.—Data are numbers of tendons, with percentages in parentheses and P values (calculated with the Wilcoxon signed-rank test) in brackets. Change = numbers of tendons that changed their shape between the position to the left and the position to the right (external rotation vs neutral, neutral vs internal rotation).

Interreader agreement was moderate (weighted κ > 0.5) to substantial (weighted κ > 0.6). Specifically, weighted κ values were as follows: 0.72 for external rotation, 0.72 for the neutral position, and 0.71 for internal rotation at the superior level; 0.81 for external rotation, 0.73 for the neutral position, and 0.62 for internal rotation at the middle level; and 0.68 for external rotation, 0.55 for the neutral position, and 0.59 for internal rotation at the inferior level.

Orientation

In all shoulder joint positions, the differences in LBT orientation between the measurements at the superior and middle levels and between the middle and inferior levels were both highly significant (P < .001), except for the comparison of measurements in external rotation between the superior and middle levels (reader 1: P = .192; reader 2: P = .167) and for the comparison of measurements in internal rotation between the middle and inferior levels (reader 1: P = .206; reader 2: P = .920).

Compared with the orientation of the LBT in neutral position, the orientation of the LBT changed significantly (P < .001) in external and internal rotation of the shoulder at the middle and inferior levels but not at the superior measurement level (Table 1).

Results concerning the interreader agreement of the LBT orientation measurements are provided in Table 4. Interreader agreement was mostly statistically significant (P < .05) and was substantial to almost perfect. Except at the superior level, there was no significant interreader agreement in internal rotation.

Table 4 Interreader Agreement for Evaluation of LBT Orientation

Table 4

Discussion

Our data describe the physiologic position, shape, and orientation of the LBT in the neutral position, in external rotation, and in internal rotation of the shoulder.

In our volunteers, the position of the LBT in the bicipital groove was slightly dependent on the rotation of the shoulder. The changes in LBT position in external and internal rotation compared with the neutral position were less than 1.5 mm at all measurements levels. Surprisingly, medial eccentricity of the LBT was greatest in the neutral position of the shoulder joint at all measurement levels. Therefore, rotational misplacement in the shoulder joint at the time of image acquisition does not increase LBT eccentricity to the medial side and should not lead to erroneously diagnosed LBT subluxation or dislocation.

Superiorly, the LBT was situated eccentrically in the mediolateral direction with respect to the bicipital groove, irrespective of the shoulder joint position. With regard to the normal LBT position in the mediolateral direction at the entrance of the bicipital groove, physiologic values were found to be −1.0 to 7.5 mm medial to the deepest point of the bicipital groove. Because of this wide variability, a far medial LBT position of 8 mm medial to the deepest point of the bicipital groove would be required if the diagnosis of LBT subluxation was being considered. However, because our data are based on measurements in healthy volunteers, we cannot provide criteria to diagnose LBT instability but emphasize the variability of the LBT position in physiologic conditions.

The shape and orientation of the LBT changed depending on the level of evaluation and the position of the shoulder. Superiorly, the tendon was almost exclusively flat or comma shaped. In the middle of the bicipital groove, the tendon was generally flat to comma shaped, with a tendency to be more oval in external rotation. Inferiorly, the tendon was generally oval to flat, with a tendency to be more rounded in internal rotation.

Interreader agreement of the LBT orientation was considerably weaker at the inferior evaluation level. This may relate to a preponderance of round to oval tendon shapes and, hence, greater difficulty in the precise identification of the greatest tendon diameter at this level. Also, interreader agreement of the evaluation of images acquired in internal rotation was poorer compared with the interreader agreement of measurements on images acquired in the neutral position or in external rotation. We believe that this may relate to the crowding of the subscapularis tendon, LBT, and joint capsule between the humeral head, coracoid process, and anterior rim of the glenoid in maximal internal rotation. As a consequence, these structures were much more difficult to identify. Despite the fact that there is a change of shape and orientation of the LBT depending on the level of evaluation and the position of the shoulder, we have no evidence of any direct correlation between the shape of the LBT and its position with respect to the intertubercular groove.

Lafosse et al (16) observed LBT instability, defined as subluxation or dislocation of the LBT, in 45% of 200 consecutive patients undergoing arthroscopic rotator cuff repair. In these patients, LBT instability was anterior in 16%, posterior in 19%, and both in 10%. However, frank dislocation was observed only in the anterior direction. To the best of our knowledge, there have been no criteria published that allow for the diagnosis of posterior LBT instability on MR images. Our results describe the physiologic variation of LBT position in asymptomatic volunteers. It remains unanswered if there is a reasonable threshold that enables the identification of a pathologically eccentric LBT.

Spritzer et al (28) examined a small group of nine patients with arthroscopically proven LBT instability (average age, 42 years) and compared MR imaging findings with those in a small control group of 10 patients (average age, 47 years) with shoulder disease that was different from LBT instability. The authors concluded that “in the clinical setting of pain or symptoms referable to the biceps, the presence of a flat, degenerated biceps tendon perched on the lesser tubercle with an obtusely angled bicipital groove should raise the suspicion of instability of the long head of the biceps tendon.” Our data, although partly in agreement with these findings, indicate that a flat LBT perched on the lesser tubercle can also be seen in the neutral position or with external rotation of the shoulder in asymptomatic persons, suggesting that this position and shape of the LBT can be physiologic (Fig 7).

Figure 7a:

Figure 7a: (a, b) Axial MR images in (a) 27-year-old female volunteer and (b) 26-year-old female volunteer show flat LBT perched on the lesser tuberosity with an obtusely angled intertubercular sulcus that may simulate instability of the long head of the biceps tendon.

Figure 7b:

Figure 7b: (a, b) Axial MR images in (a) 27-year-old female volunteer and (b) 26-year-old female volunteer show flat LBT perched on the lesser tuberosity with an obtusely angled intertubercular sulcus that may simulate instability of the long head of the biceps tendon.

Surprisingly, the LBT was more centered in external rotation of the shoulder joint. The data acquired for this study do not allow for an explanation of this finding. It seems that an uninjured pulley system and rotator cuff tendons center the LBT better in external rotation of the shoulder joint than in the neutral position.

There were some limitations of this study. The position, shape, and orientation of the LBT in asymptomatic volunteers with no degenerative changes on MR images are described. Despite the evaluation of the suspension of the LBT to the best of our knowledge, it is still possible that a volunteer had minor degeneration of these structures. Because there was no control group consisting of patients with proven LBT instability, it was not possible to identify reliable criteria for LBT instability.

In conclusion, the position of the LBT is only slightly dependent on shoulder rotation. LBT eccentricity is maximal in the neutral position. Rotational misplacement during image acquisition does not increase LBT eccentricity and should not lead to erroneously diagnosed LBT subluxation or dislocation.

Advances in Knowledge
•. 

• The position of the long biceps tendon (LBT) in the intertubercular groove is only slightly dependent on rotation in the shoulder joint.

•. 

• The eccentricity of the LBT in the intertubercular groove is maximal in the neutral position.

Implication for Patient Care
•. 

• The external or internal rotation position of the humerus does not increase LBT eccentricity and should not lead to false-positive diagnosis of an LBT subluxation or dislocation.

Disclosures of Potential Conflicts of Interest: F.M.B. No potential conflicts of interest to disclose. T.J.D. No potential conflicts of interest to disclose. D.R. No potential conflicts of interest to disclose. B.J. Financial activities related to the present article: none to disclose. Financial activities not related to the present article: is a consultant with Zimmer and with Karl Storz Endoscopy. Other relationships: none to disclose. C.W.A.P. No potential conflicts of interest to disclose.

Author Contributions

Author contributions: Guarantor of integrity of entire study, F.M.B.; study concepts/study design or data acquisition or data analysis/interpretation, all authors; manuscript drafting or manuscript revision for important intellectual content, all authors; manuscript final version approval, all authors; literature research, F.M.B., T.J.D., C.W.A.P.; clinical studies, F.M.B., T.J.D., B.J., C.W.A.P.; statistical analysis, F.M.B., C.W.A.P.; and manuscript editing, all authors

References

  • 1 Nakata W, Katou S, Fujita A, Nakata M, Lefor AT, Sugimoto H. Biceps pulley: normal anatomy and associated lesions at MR arthrography. RadioGraphics 2011;31(3):791–810. LinkGoogle Scholar
  • 2 Wafae N, Atencio Santamaría LE, Vitor L, Pereira LA, Ruiz CR, Wafae GC. Morphometry of the human bicipital groove (sulcus intertubercularis). J Shoulder Elbow Surg 2010;19(1):65–68. Crossref, MedlineGoogle Scholar
  • 3 Boileau P, Maynou C, Balestro JCet al.. Long head of the biceps pathology. [in French]. Rev Chir Orthop Reparatrice Appar Mot 2007;93(8 Suppl):5S19–5S53. MedlineGoogle Scholar
  • 4 Morag Y, Jacobson JA, Shields Get al.. MR arthrography of rotator interval, long head of the biceps brachii, and biceps pulley of the shoulder. Radiology 2005;235(1):21–30. LinkGoogle Scholar
  • 5 Lee JC, Guy S, Connell D, Saifuddin A, Lambert S. MRI of the rotator interval of the shoulder. Clin Radiol 2007;62(5):416–423. Crossref, MedlineGoogle Scholar
  • 6 Yang HF, Tang KL, Chen Wet al.. An anatomic and histologic study of the coracohumeral ligament. J Shoulder Elbow Surg 2009;18(2):305–310. Crossref, MedlineGoogle Scholar
  • 7 Kask K, Põldoja E, Lont Tet al.. Anatomy of the superior glenohumeral ligament. J Shoulder Elbow Surg 2010;19(6):908–916. Crossref, MedlineGoogle Scholar
  • 8 Arai R, Mochizuki T, Yamaguchi Ket al.. Functional anatomy of the superior glenohumeral and coracohumeral ligaments and the subscapularis tendon in view of stabilization of the long head of the biceps tendon. J Shoulder Elbow Surg 2010;19(1):58–64. Crossref, MedlineGoogle Scholar
  • 9 Arai R, Sugaya H, Mochizuki T, Nimura A, Moriishi J, Akita K. Subscapularis tendon tear: an anatomic and clinical investigation. Arthroscopy 2008;24(9):997–1004. Crossref, MedlineGoogle Scholar
  • 10 Harryman DT, Sidles JA, Harris SL, Matsen FA. The role of the rotator interval capsule in passive motion and stability of the shoulder. J Bone Joint Surg Am 1992;74(1):53–66. Crossref, MedlineGoogle Scholar
  • 11 Dierickx C, Ceccarelli E, Conti M, Vanlommel J, Castagna A. Variations of the intra-articular portion of the long head of the biceps tendon: a classification of embryologically explained variations. J Shoulder Elbow Surg 2009;18(4):556–565. Crossref, MedlineGoogle Scholar
  • 12 Pouliart N, Somers K, Eid S, Gagey O. Variations in the superior capsuloligamentous complex and description of a new ligament. J Shoulder Elbow Surg 2007;16(6):821–836. Crossref, MedlineGoogle Scholar
  • 13 Patton WC, McCluskey GM. Biceps tendinitis and subluxation. Clin Sports Med 2001;20(3):505–529. Crossref, MedlineGoogle Scholar
  • 14 Werner A, Mueller T, Boehm D, Gohlke F. The stabilizing sling for the long head of the biceps tendon in the rotator cuff interval: a histoanatomic study. Am J Sports Med 2000;28(1):28–31. Crossref, MedlineGoogle Scholar
  • 15 Jost B, Koch PP, Gerber C. Anatomy and functional aspects of the rotator interval. J Shoulder Elbow Surg 2000;9(4):336–341. Crossref, MedlineGoogle Scholar
  • 16 Lafosse L, Reiland Y, Baier GP, Toussaint B, Jost B. Anterior and posterior instability of the long head of the biceps tendon in rotator cuff tears: a new classification based on arthroscopic observations. Arthroscopy 2007;23(1):73–80. Crossref, MedlineGoogle Scholar
  • 17 Pfirrmann CW, Zanetti M, Weishaupt D, Gerber C, Hodler J. Subscapularis tendon tears: detection and grading at MR arthrography. Radiology 1999;213(3):709–714. LinkGoogle Scholar
  • 18 Zanetti M, Weishaupt D, Jost B, Gerber C, Hodler J. MR imaging for traumatic tears of the rotator cuff: high prevalence of greater tuberosity fractures and subscapularis tendon tears. AJR Am J Roentgenol 1999;172(2):463–467. Crossref, MedlineGoogle Scholar
  • 19 Baumann B, Genning K, Böhm D, Rolf O, Gohlke F. Arthroscopic prevalence of pulley lesions in 1007 consecutive patients. J Shoulder Elbow Surg 2008;17(1):14–20. Crossref, MedlineGoogle Scholar
  • 20 Gaskin CM, Anderson MW, Choudhri A, Diduch DR. Focal partial tears of the long head of the biceps brachii tendon at the entrance to the bicipital groove: MR imaging findings, surgical correlation, and clinical significance. Skeletal Radiol 2009;38(10):959–965. Crossref, MedlineGoogle Scholar
  • 21 Chan TW, Dalinka MK, Kneeland JB, Chervrot A. Biceps tendon dislocation: evaluation with MR imaging. Radiology 1991;179(3):649–652. LinkGoogle Scholar
  • 22 Bennett WF. Correlation of the SLAP lesion with lesions of the medial sheath of the biceps tendon and intra-articular subscapularis tendon. Indian J Orthop 2009;43(4):342–346. Crossref, MedlineGoogle Scholar
  • 23 Weishaupt D, Zanetti M, Tanner A, Gerber C, Hodler J. Lesions of the reflection pulley of the long biceps tendon: MR arthrographic findings. Invest Radiol 1999;34(7):463–469. Crossref, MedlineGoogle Scholar
  • 24 Tung GA, Yoo DC, Levine SM, Brody JM, Green A. Subscapularis tendon tear: primary and associated signs on MRI. J Comput Assist Tomogr 2001;25(3):417–424. Crossref, MedlineGoogle Scholar
  • 25 Walch G, Nové-Josserand L, Boileau P, Levigne C. Subluxations and dislocations of the tendon of the long head of the biceps. J Shoulder Elbow Surg 1998;7(2):100–108. Crossref, MedlineGoogle Scholar
  • 26 Dines D, Warren RF, Inglis AE. Surgical treatment of lesions of the long head of the biceps. Clin Orthop Relat Res 1982(164):165–171. MedlineGoogle Scholar
  • 27 Petersson CJ. Spontaneous medial dislocation of the tendon of the long biceps brachii: an anatomic study of prevalence and pathomechanics. Clin Orthop Relat Res 1986(211):224–227. MedlineGoogle Scholar
  • 28 Spritzer CE, Collins AJ, Cooperman A, Speer KP. Assessment of instability of the long head of the biceps tendon by MRI. Skeletal Radiol 2001;30(4):199–207. Crossref, MedlineGoogle Scholar

Article History

Received May 4, 2011; revision requested June 6; revision received June 27; accepted July 3; final version accepted July 8.
Published online: Dec 2011
Published in print: Dec 2011