Distal Insertional Footprint of the Brachialis Muscle: 3D Morphometric Study
Objective. The purpose of this study is to describe the three-dimensional morphometry of the brachialis muscle at its distal attachment to the ulna. Methods. Fifty cadaveric elbows were dissected and the brachialis distal insertion was isolated on the ulna bone and probed with a three-dimensional digitizer, to create a three-dimensional model of the footprint. Measurements and analysis of each footprint shape were recorded and compared based on gender and size. Results. There was significant gender difference in the surface length () and projected length () of the brachialis footprint. The shapes of the footprint also differed among the specimens. Conclusion. The shape of the brachialis muscle insertion differed among all the specimens without significant variation in gender or sides. There was also a significant difference in muscle length between males and females with little difference in the width and surface area. Significance. The information obtained from this study is important for kinematic understanding and surgical procedures around the elbow joint as well as the understanding of the natural age related anatomy of the brachialis footprint morphology.
The brachialis muscle is the major elbow flexor. The brachialis tendon inserts distally to the coronoid process at the tuberosity of the ulna. This distal attachment has been described by previous studies as fibers of the brachialis muscle converging to a thick, broad tendon which is attached to the tuberosity of the ulna and to a rough impression on the anterior aspect of the coronoid process [1–3]. It is innervated by branches of the musculocutaneous and radial nerves [4, 5].
Injury to the brachialis is uncommon and reports are often limited to small case series or case reports [6, 7]. As a result, there has been little anatomical characterization of the distal attachment of the brachialis muscle . According to Cage et al. , the brachialis muscle is injured during type III coronoid fractures that involve disruption of more than 50% of the height of the coronoid process, affecting the brachialis distal tendinous insertion at the more proximal aspect of the ulnar tuberosity.
Previous research on the muscle footprints took measurements with calipers and MRI as illustrated in Table 1. Three-dimensional characterization allows for a more objective morphometric analysis of the muscle footprint. This study provides information on the qualitative and quantitative morphometry of the distal brachialis muscle insertion on the ulna. The knowledge obtained from the study contributes to our understanding of the functional and anatomic characteristics of the brachialis muscle.
A better understanding of the muscle footprint could be used to improve the current anterior and anterolateral surgical approaches to repair fractures around the elbow joint with ulnar bony involvement . Although injury to the brachialis muscle or tendon is rare, information from this study could serve as a guide for orthopedic surgeons considering the use of the brachialis tendon as a treatment option in cases like brachialis tendon injuries, biceps brachii tendon ruptures, brachial plexus injury, and coronoid process fractures [2, 9].
2. Materials and Methods
Fifty cadaveric upper limbs from twenty-eight formalin preserved cadavers (University of Kentucky) were dissected from the proximal segment of the humerus distally to the wrist, leaving the distal insertions of the brachialis intact. The muscle was stripped off the distal humerus and scissor dissection was used to free the brachialis from its surrounding soft tissue attachments on the anterior capsule and in the antecubital region. The limbs of twenty-one cadavers were dissected bilaterally, while eight were dissected unilaterally. Next, each dissected elbow was secured in a customized jig and the data was acquired by tracing the footprints of the brachialis insertion and the proximal ulna using a three-dimensional digitizer (FARO, Faro Technologies, Lake Mary, FL, USA) mounted with a 2 mm ball probe (Renishaw, Gloucestershire, UK).
The digitized specimens were registered on a three-dimensional inspection computer software, Geomagic Qualify version 12 (Geomagic, Research Triangle Park, NC). The established muscle footprints on the intact elbow bones produced a model to obtain accurate measurements of the muscles with respect to the length, width, and area at their distal insertions. The muscles were then characterized based on their shape and relative locations (Figure 1).
Due to the irregularity and variability of the shapes , they were classified as being proximal or distal in relation to the widest point of the footprint; top and bottom halves of the footprints were described as narrow or wide relative to each other as illustrated in Figure 2. The length and width of the footprint projection were measured as lines connecting the distal most points of the projection lengthwise and widthwise; the second measurement, the surface length and width, were taken using the same points on the bone surface with the contours of the bone taken into consideration (Figure 3). The width measured was the maximum width of the footprint anywhere along its length. The area of the muscle insertion was derived directly using the computer software.
A one-way ANOVA test was used to determine the presence of any statistical difference between males and females and between the left and right sides. The statistics package SPSS version 20 was used (SPSS, IBM corporations, Somers, NY). A value of less than 0.05 was considered significant.
The data obtained for this study were divided into two components. The first component entailed the qualitative analysis of the shape of all 50 specimens. The second component of the study involved a quantitative description of the length, width, and area of the muscle insertion on 23 specimens. All of the data presented here was acquired using a ball probe.
The qualitative results combined the first study of 27 cadaveric elbows and the second study of 23 cadaveric elbows. Fifty brachialis footprints were described in total: 27 of those footprints were located on the right side and 23 were located on the left side. The mean donor age was 81.3 years (range: 68–92 years). Due to the shape variation of the 50 brachialis footprints (Figure 3), the shapes of 30 were described as proximally narrow and distally wide, 15 were described as proximally wide and distally narrow, and 5 footprints were irregularly shaped and classified as miscellaneous (Figure 4).
The measurements of the brachialis footprint were based on the data collected from 23 elbows, 12 on the right side and 11 on the left side (Table 2). When considering the length of the footprints, the measurements were divided based on projected length and surface length (with the contours of the ulnar bone taken into consideration) (Figure 3). The mean projected length of the footprint was mm (range, 22.2–38.2 mm), mean surface length was mm (range, 22.6–40.1 mm), mean projected width was mm (range, 4.9–13.2 mm), mean surface width was mm (range, 5.3–13.6 mm), and mean surface area was mm (range, 128.3–398.3 mm).
When the results were compared by gender, only the surface length was found to be significantly larger in males compared to females, (Table 3). When the results were compared by side, no significant difference existed between any of the measurements (Table 4).
We set out to describe the three-dimensional morphometry of the brachialis muscle at its distal attachment on the ulna. The results from this study indicate that the projected and surface lengths of the brachialis footprint are significantly longer in males compared to females. The projected and surface width and the surface area, however, were not found to be significantly different between males and females. The lengths, widths, and surface area of the left distal footprint were consistently larger than the footprints on the right side, but these results were not statistically significant. The shapes were described as proximal narrow and distal wide, proximally wide and distal narrow, or miscellaneous, which may represent true geometric variation or different stages of age related degenerative change.
According to Cage et al. , Leonello et al. , and Sanal et al. , the insertion has been described as a thick, broad tendon or as having two heads, one with a tendinous and the other with an aponeurotic attachment. The superficial head is more distal to the ulnar tuberosity and is in the form of a thick tendinous structure, while the deep head is more proximal to the ulnar tuberosity and is musculoaponeurotic, fan shaped, and broad at its site of attachment. Although they differ at their distal ends, the two heads attach to the ulnar tuberosity as a single blended structure, which was consistent with our observations. This allows the brachialis muscle to be the primary flexor of the elbow joint regardless of whether the forearm is in pronation or supination . Most of the brachialis insertion was medial to the line of olecranon-coronoid tip, which was consistent with results from Ma and Chang .
Some reports indicated that fibers of the brachialis muscle had no direct attachment to the anterior capsule of the elbow joint  but rather a connection between the muscle and anterior capsule that existed via connective tissue [2, 10, 11]. According to Leonello et al. and Morrey [1, 14], a small collection of fibers, articularis cubitus, extend from the deep aspect of the deep head of the brachialis muscle and attach directly to the anterior capsule of the elbow joint. Other reports found both a combination of muscle fibers and connective tissue that connected the brachialis muscle to the anterior elbow capsule . Deep aspect brachialis muscle fibers were observed to attach directly to the capsule in 19 of our specimens (Figure 5).
When the brachialis footprints were compared among different studies (Table 1), the measurements from our study were in between the range from all the studies listed. These variations could be attributed to several reasons such as the differences in patient demographics, data measurement techniques, data acquisition and analysis, and age and number of specimens utilized in each study.
With regard to the limitations of the study, firstly, the anatomic study was conducted with cadaveric specimens derived from elderly donors, without a younger age spectrum for comparison. Secondly, no histological analysis was carried out to determine the nature of the insertion of the muscle on the ulnar tuberosity. This made our qualitative analysis purely observational. Therefore, the presence of tears (due to dissection) and removal (during the disarticulation of the elbow joint) of the muscle fibers that connected to the elbow capsule  might have contributed to some sampling errors during data collection and analysis. Thirdly, the total number of samples was relatively small, potentially inadequate to achieve high statistical power. Finally, not all of the footprints were quantitatively analyzed because of mismatch errors that occurred when using the laser scanner and ball probe in combination. Hence quantitative analysis was confined to those specimens with matching laser and ball probe data.
This study provides information on the qualitative and quantitative morphometry of the distal brachialis muscle insertion on the ulna, in an older population. The knowledge of the anatomic description of the distal insertion of the brachialis muscle aids in comprehending the functional and anatomic characteristics of the muscle, without automatically inferring the existence of pathological changes when the morphology has age related alterations. This information would not only greatly enhance the understanding of the natural history and kinematics of the brachialis but could be used to vastly improve the current anterior and anterolateral surgical approaches used to repair fractures around the elbow joint.
No patients participated in this study; therefore IRB approval was not obtained.
Conflict of Interests
None of the authors have any financial conflict of interests.
The authors would like to thank Dr. Bruce Maley and Mr. Gary Ginn for their assistance in specimen acquisition from the University of Kentucky Anatomy Laboratory and thank Dr. Timothy Uhl for statistical assistance.
D. T. Leonello, I. J. Galley, G. I. Bain, and C. D. Carter, “Brachialis muscle anatomy: a study in cadavers,” The Journal of Bone & Joint Surgery—American Volume, vol. 89, no. 6, pp. 1293–1297, 2007.View at: Publisher Site | Google Scholar
H. T. Sanal, L. Chen, P. Negrao, P. Haghighi, D. J. Trudell, and D. L. Resnick, “Distal attachment of the brachialis muscle: anatomic and MRI study in cadavers,” American Journal of Roentgenology, vol. 192, no. 2, pp. 468–472, 2009.View at: Publisher Site | Google Scholar
S. Standring, Ed., Gray's Anatomy, Reviewed by P. Driscoll, Churchill Livingstone, New York, NY, USA, 39th edition, 2004.
E. A. Frazer, M. Hobson, and S. W. McDonald, “The distribution of the radial and musculocutaneous nerves in the brachialis muscle,” Clinical Anatomy, vol. 20, no. 7, pp. 785–789, 2007.View at: Publisher Site | Google Scholar
P. Mahakkanukrauh and V. Somsarp, “Dual innervation of the brachialis muscle,” Clinical Anatomy, vol. 15, no. 3, pp. 206–209, 2002.View at: Publisher Site | Google Scholar
J. B. Winblad, E. Escobedo, and J. C. Hunter, “Brachialis muscle rupture and hematoma,” Radiol Case Reports, vol. 3, no. 4, 2008.View at: Publisher Site | Google Scholar
A. J. Krych, R. B. Kohen, S. A. Rodeo, R. P. Barnes, R. F. Warren, and R. N. Hotchkiss, “Acute brachialis muscle rupture caused by closed elbow dislocation in a professional American football player,” Journal of Shoulder and Elbow Surgery, vol. 21, no. 7, pp. e1–e5, 2012.View at: Publisher Site | Google Scholar
D. J. N. Cage, R. A. Abrams, J. J. Callahan, and M. J. Botte, “Soft tissue attachments of the ulnar coronoid process: an anatomic study with radiographic correlation,” Clinical Orthopaedics and Related Research, vol. 320, pp. 154–158, 1995.View at: Google Scholar
V. Mehta, R. K. Suri, J. Arora, G. Rath, and S. Das, “Peculiar tendinous origin of the brachialis muscle: anatomic and clinical insight,” Romanian Journal of Morphology and Embryology, vol. 50, no. 1, pp. 141–143, 2009.View at: Google Scholar
J.-F. Ma and S.-M. Chang, “Brachialis insertion measurement: an anatomic cadaver study for plate fixation of the coronoid process fracture,” Clinical Anatomy, vol. 24, no. 2, pp. 179–182, 2011.View at: Publisher Site | Google Scholar
R. S. Tubbs, M. W. Yablick, M. Loukas, M. M. Shoja, M. Ardalan, and W. J. Oakes, “Capsular attachment of the brachialis muscle (Portal's muscle): an anatomical and functional study,” Surgical and Radiologic Anatomy, vol. 30, no. 3, pp. 229–232, 2008.View at: Publisher Site | Google Scholar
K. L. Moore and A. F. Dalley, Clinically Oriented Anatomy, Lippincott Williams & Wilkins, Philadelphia, Pa, USA, 4th edition, 1999.
M. Benjamin, R. L. M. Newell, E. J. Evans, J. R. Ralphs, and D. J. Pemberton, “The structure of the insertions of the tendons of biceps brachii, triceps and brachialis in elderly dissecting room cadavers,” Journal of Anatomy, vol. 180, no. 2, pp. 327–332, 1992.View at: Google Scholar
B. F. Morrey, “Anatomy of the elbow joint,” in The Elbow and Its Disorders, B. F. Morrey, Ed., p. 34, Saunders, Philadelphia, Pa, USA, 2nd edition, 2000.View at: Google Scholar
R. Vadgaonkar, R. Rai, S. R. Nayak, S. D'Costa, V. Saralaya, and Dhanya, “An anatomical and clinical insight on brachialis with emphasis on portal's muscle,” Romanian Journal of Morphology and Embryology, vol. 51, no. 3, pp. 551–553, 2010.View at: Google Scholar