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DOI: 10.1055/s-0045-1804493
Assessment of the Pennation Angle of the Medial Gastrocnemius Muscle in Road Runners and Non-runners
Article in several languages: português | EnglishAbstract
Objective To evaluate the pennation angle (PA) of the medial gastrocnemius muscle (MGM) in orthostasis and bilateral maximum plantar flexion (BMPF) in road runners and non-runners.
Methods We assessed 31 runners and 31 non-runners from both genders between January and April 2019. We measured the MGM's PA on both sides by ultrasound during orthostasis and BMPF.
Results The groups were homogeneous regarding the dominant side, gender, and age. During orthostasis, the mean right-sided PA was 19.46° in runners and 22.5° in non-runners (p < 0.004). On the left side, the mean PA was 20.79° in runners and 22.83° in non-runners (p < 0.029). During BMPF, the right-side PA was 40.06° in runners and 40.89° in non-runners, and, on the left side, the mean PA was 40.01° in runners and 40.52° in non-runners. The MGM's PA of the right limb from male runners was statistically significantly higher in orthostasis (p < 0.029) and BMPF (p < 0.045). The correlation between MGM in orthostasis and BMPF in the leg in each group was statistically significant in the right lower limb of non-runners.
Conclusion Road runners presented a significantly lower MGM's PA than non-runners in orthostasis.
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Keywords
motor activity - muscle contraction - muscle, skeletal - sedentary behavior - ultrasonographyIntroduction
Running started in prehistoric times when humans needed to move quickly to hunt or escape predators. Running, even for 5 to 10 minutes per day and at slow speeds (< 9.65 km/h), is associated with significantly reduced risk of death from all causes and, specifically, from cardiovascular disease. The present study may motivate healthy but sedentary subjects to start and continue running to achieve substantial mortality reduction benefits.[1]
Human muscle architecture has been studied in cadaveric specimens. However, scarce data are available on living human muscles.[2] [3] [4] Skeletal muscle tissue has properties that determine its characteristics and performance, such as excitability, contractility, extensibility, and elasticity.[5] The mechanical properties of skeletal muscle account for its performance, such as strength, length, speed, work, and power.[6]
The pennation angle (PA) of the muscle fiber is the angle between the muscle fascicle and the intramuscular tendon, that is, the vertical inclination of the muscle fibers from the long muscle-tendon axis.[5] [7] [8] The fiber PA is a crucial functional feature of the muscle and varies according to the muscle contraction intensity and fiber length.[9] Muscle contraction causes fibers to shorten, increasing the PA.[9] [10] Ultrasound allows accurate measurements of the length or PA of a muscle fascicle.[10] [11] [12]
Muscle pain in the posterior region of the lower limb is a common complaint among runners.[13] [14] Of all calf muscle injuries, 58 to 65% involve the medial gastrocnemius muscle (MGM), 8 to 38% affect the lateral head of the gastrocnemius, and 58 to 66% involve the soleus.[14] We believe that ultrasonographic studies of muscle architecture can support further research on the treatment and prevention of muscle injuries.
The objective of the current study was to compare the PA differences in the MGM in orthostasis and bilateral maximum plantar flexion (BMPF) in runners and non-runners.
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Materials and Methods
The Research Ethics Committee approved the present study under CAAE 02582718.0.0000.5505, opinion number 3.115.229. This study was clinical, observational, cross-sectional, and comparative.
The study included volunteers aged 18 to 60 years old. The non-runner group included subjects who had not practiced physical activity for over a year. The road runner group included those who ran for more than a year at least twice a week and five kilometers per week. We did not include subjects with musculoskeletal injuries, neuromuscular diseases, prostheses, acute or chronic pain in the lower extremities, cognitive disabilities, malignant diseases, or pregnancy.
The study participants completed a questionnaire, and their body mass index (BMI) was calculated as the ratio between weight (in kilograms) and the square of their height (in meters).
A physician specialized in musculoskeletal imaging and an orthopedist supervised the ultrasound examinations.
Images were obtained with a real-time ultrasound, model HD 11(Philips Medical Systems, Amsterdam, Netherlands), with a 9-MHz linear transducer and an acoustic coupling gel.
To capture the image in the maximum cross-section area of MGM, the transducer was in a longitudinal position to the tibia, parallel to the muscle fascicles, and perpendicular to the skin in the upper third of an imaginary line from the flexion crease of the popliteal fossa to the center of the medial malleolus.[10] [15] As described by Narici et al.,[11] for the orthostatic examination, the volunteers remained in orthostasis with their feet parallel to the sagittal axis and the hip and knee in maximum extension ([Fig. 1A]).


We asked the study participants to stand up and actively and gradually increase the force until BMPF for image capture on one leg ([Fig. 1B]), followed by a gradual relaxation for five seconds. Next, we instructed them to perform the same maneuver for image capture of the contralateral leg. Images were satisfactory when they allowed the delineation of multiple fascicles across the entire image without interruption.[10] [16] Stored images underwent a subsequent analysis with the free open-source medical image viewer Horos (version 3.1.1) distributed under a Lesser General Public License (LGPL) at Horosproject.org. Pennation angle was the angle between the deep intramuscular aponeurosis and a visible muscle fascicle in orthostasis ([Fig. 2A]) and BMPF ([Fig. 2B]).[9] [11] [17] [18] The same orthopedist obtained three PA measurements from each image, using different fibers. The data underwent statistical analysis.


Statistical analysis
The Kolmogorov-Smirnov test assessed the normality of quantitative variables. The Student's t-test, Chi-squared test, and Pearson's correlation were used for data evaluation. The result of each comparison presented a p-value, defined as a statistical significance, at 0.05 (5%). Statistical analysis employed the following software: IBM SPSS Statistics for Windows, version 20.0 (IBM Corp., Armonk, NY, USA), Minitab version 16 (Minitab LLC, State College, PA, USA), and MS Excel 2010 (Microsoft Corp., Redmond, WA, USA).
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Results
The present study consisted of 62 volunteers, including 31 runners and 31 non-runners. The runner group had 14 (45.2%) females and 17 (54.8%) males. The non-runner group had 18 (58.1%) females and 13 (41.9%) males.
The runner group had 25 (80.6%) subjects with right-side dominance and 6 (19.4%) participants with left-side dominance. The non-runner group had 28 participants (90.3%) with right-side dominance and 3 (9.7%) with left-side dominance.
The age in the runner group ranged from 23 to 51 years, with a mean age of 35.6 years, and a coefficient of variation (CV) of 19%. The age in the non-runner group ranged from 18 to 59 years, with a mean value of 34.5 years, and a CV of 24%. According to the Chi-squared test, the groups were homogeneous regarding the dominant side, gender, and age.
The mean BMI was higher in the non-runner group (26.6) than in the runner group (22.40) (p < 0.001).
[Table 1] shows the descriptive statistical analysis of PA in orthostasis and BMPF of the right or left lower limbs from runners and non-runners.
Inferior limb |
Condition |
Group |
PA (mean) |
PA (median) |
SD |
CV |
Min. |
Max. |
N |
95%CI |
p |
---|---|---|---|---|---|---|---|---|---|---|---|
Right |
Orthostasis |
Runners |
19.46 |
19.12 |
3.57 |
18 |
11.36 |
26.79 |
31 |
10.26 |
00.004 |
Non-runners |
22.25 |
22.04 |
3.77 |
17 |
13.23 |
30.23 |
31 |
10.33 |
|||
BMPF |
Runners |
40.06 |
39.44 |
7.78 |
19 |
26.10 |
55.72 |
31 |
20.74 |
00.680 |
|
Non-runners |
40.89 |
40.47 |
8.07 |
20 |
25.42 |
56.25 |
31 |
20.84 |
|||
Left |
Orthostasis |
Runners |
20.79 |
20.88 |
3.58 |
17 |
14.75 |
28.04 |
31 |
10.26 |
00.029 |
Non-runners |
22.83 |
22.45 |
3.61 |
16 |
15.12 |
29.45 |
31 |
10.27 |
|||
BMPF |
Runners |
40.01 |
39.99 |
7.48 |
19 |
24.54 |
56.75 |
31 |
20.63 |
00.774 |
|
Non-runners |
40.52 |
39.95 |
6.38 |
16 |
27.56 |
59.26 |
31 |
20.25 |
The Pearson's correlation was used to assess the correlation between MGM in orthostasis and BMPF of each leg in each group ([Table 2]). We found a positive correlation (higher than 0) in all comparisons, which was greater in the right lower limb of the non-runner group.
Group |
Inferior limb |
r |
p |
---|---|---|---|
Runners |
Right |
34.4 |
0.058 |
Left |
37.8 |
0.036 |
|
Non-runners |
Right |
60.7 |
0.001 |
Left |
26.3 |
0.152 |
[Table 3] shows the descriptive statistical analysis of MGM's PA in orthostasis and BMPF of both lower limbs and gender.
Inferior limb |
Condition |
Gender |
PA (mean) |
PA (median) |
SD |
CV |
Min. |
Max. |
N |
95%CI |
p |
---|---|---|---|---|---|---|---|---|---|---|---|
Right |
Orthostasis |
F |
17.94 |
17.33 |
3.92 |
22 |
11.36 |
26.79 |
14 |
2.05 |
0.029 |
M |
20.71 |
21.64 |
2.78 |
13 |
13.60 |
24.24 |
17 |
1.32 |
|||
BMPF |
F |
37.00 |
36.73 |
7.02 |
19 |
27.20 |
53.49 |
14 |
3.68 |
0.045 |
|
M |
42.57 |
43.21 |
7.66 |
18 |
26.10 |
55.72 |
17 |
3.64 |
|||
Left |
Orthostasis |
F |
19.49 |
19.42 |
2.74 |
14 |
14.75 |
24.40 |
14 |
1.43 |
0.067 |
M |
21.85 |
21.10 |
3.90 |
18 |
16.93 |
28.04 |
17 |
1.85 |
|||
BMPF |
F |
38.28 |
38.23 |
6.71 |
18 |
26.07 |
49.16 |
14 |
3.51 |
0.247 |
|
M |
41.45 |
42.36 |
7.98 |
19 |
24.54 |
56.75 |
17 |
3.79 |
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Discussion
Scientific research has demonstrated that muscle architecture, including PA, fascicle length, and fiber composition and arrangement, affects muscle functions.[17] [18] [19] [20]
The first authors to describe PA were Gans and de Vree, in 1987,[21] when studying the external adductor muscle of a lizard's jaw. In 1992, Henriksson-Larsen et al.[22] evaluated the vastus lateralis muscle PA of 15 female volunteers. This was the first in vivo assessment of contraction and relaxation using an ultrasound device. The authors photographed the images for later PA analysis, being the first to demonstrate the feasibility of in vivo measurements and observing that the fiber angle in the relaxed position was smaller than in contraction. These results showed that the methodology for PA measurement using ultrasound images had high reliability. Our study evaluated PA in road runners compared with non-runners. We did not find any studies with this comparison in the literature.
The ultrasound method for capturing PA measurements from the MGM effectively determined muscle architecture parameters.[23] Its advantages included low relative cost, easy handling, portability, tissue contrast, good reproducibility, no radiation exposure, and real-time image analysis.[11] [18] [24] [25] [26]
Our sample consisted of 62 participants. Only four studies (Binzoni et al.,[27] Kubo et al.,[15] [28] and Kawakami et al.[29]) presented a larger sample than ours. However, unlike us, these authors did not evaluate the PA during BMPF.
Regarding gender, the current study had a slight female predominance (51.61%; 32 out of 62), but without statistical significance. A paper on injuries in amateur runners demonstrated a male predominance.[30]
In the present study, the mean PA in males was higher compared with females, consistent with the findings of other authors.[16] [28] [29]
The mean age in years was 35.6 in runners and 34.5 in non-runners, contrasting with other authors, such as 22, according to Chow et al.,[16] 28.3, per Maganaris et al.,[12] 24, per Manal et al.,[31] and 38.8, per Narici et al.[11] The mean age in our study was higher than in some studies in the literature. Kubo et al.[15] noted a significant difference in PA between young and elderly subjects only in the vastus lateralis muscle of the thigh. The same authors described that MGM did not present a statistically significant value regarding PA and age. We did not analyze whether age was a factor in MGM's PA range.
There are different methods for assessing muscle strength, including isometric, isokinetic, variable resistance, and free weight tests. The selection of a strength testing method involves specificities, ease of acquisition, cost, and safety.[32] Although runners perform monopodial support during their practice, we measured the PA during BMPF with the volunteer's body weight, as it is safe and easy to perform and analyze the data. We did not find any PA measurements in the literature using this method.
When comparing our PA data in the standing position with the literature,[11] [12] [15] we noted a non-significant difference of one or two degrees. Comparing road runners and non-runners, we found statistically significant values in the standing position and the BMPF.
Pearson's correlation was used to measure the degree of variable interconnection. We found a positive correlation of 60.7% when analyzing contraction in orthostasis and BMPF, indicating that the greater the angle in orthostasis, the greater the muscle contraction, consistent with the literature.[10] [11] [12] [31]
The present study had some limitations, such as considering road runners' answers as reliable regarding the time spent running and the distance covered per week. In addition, some runners may perform other types of physical exercise, such as weight training, swimming, and ballet, potentially changing the leg muscles.
Another limiting factor of our study was measuring a single variable from the muscle architecture, the PA, hindering the comparison with other muscle components. Muscle architecture presents several parameters for analysis, such as muscle thickness, fiber length, physiological cross-sectional area, and PA, which impact a muscle's force production capacity. Although ultrasound quality depends on the operator and is subject to interpretation errors, measurements of muscle structure following a protocol performed by sonographers with different training and experience can achieve objective image measurements with few differences and little variation in results.[33]
Considering the great plasticity of the muscular system and the ability of skeletal muscles to adapt to different stimuli, such as disuse or training types, studies to elucidate the mechanisms by which muscle tissues adapt to these changes are relevant. For instance, we know that children with cerebral palsy have spastic muscles. We can evaluate the PA in contractures after surgical treatment for muscle stretching. In tendon transfers, we can choose muscles with similar PAs. In muscle injuries, we can monitor healing with serial PA assessments.
In sports medicine, we can study training variability by evaluating the PA in structural and functional muscle changes, especially in the force production capacity. A meta-analysis of Brazilian studies investigating the prevalence and risk factors for injury in amateur road runners detected a higher prevalence of injuries in men, most frequently muscle injuries (27.9%, 95% confidence interval [CI] 18.2–40.1%).[34] Timmins et al.[35] described a PA increase in the injured biceps femoris compared with the unaffected side. These findings encourage studies to help treat and prevent injuries early in road runners and other athletes.
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Conclusion
Road runners presented a significantly lower PA in MGM than non-runners in orthostasis.
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Conflito de Interesses
Os autores não possuem conflito de interesses a declarar.
Acknowledgments
The authors would like to thank radiologist Dr. Giovanni Bessa Pereira Lima for his availability and promptness in collecting data and for his friendship during so many journeys. The present work is dedicated to the volunteers who provided their time and patience to perform the imaging exams; without them, this project would not have happened.
Study developed at the Sports Medicine and Physical Activity Course, Sports Traumatology Center, Department of Orthopedics and Traumatology, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
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Referências
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- 2 Fukunaga T, Kawakami Y, Kuno S, Funato K, Fukashiro S. Muscle architecture and function in humans. J Biomech 1997; 30 (05) 457-463
- 3 Aagaard P, Andersen JL, Dyhre-Poulsen P. et al. A mechanism for increased contractile strength of human pennate muscle in response to strength training: changes in muscle architecture. J Physiol 2001; 534 (Pt. 2): 613-623
- 4 Azizi E, Brainerd EL, Roberts TJ. Variable gearing in pennate muscles. Proc Natl Acad Sci U S A 2008; 105 (05) 1745-1750
- 5 Hamill J, Knutzen M, Derrick R. Bases biomecânicas do movimento humano. São Paulo: Manole; 2016
- 6 Zatsiorsky M. Biomecânica no esporte. Rio de Janeiro: Guanabara; 2016
- 7 Ikegawa S, Funato K, Tsunoda N, Kanehisa H, Fukunaga T, Kawakami Y. Muscle force per cross-sectional area is inversely related with pennation angle in strength trained athletes. J Strength Cond Res 2008; 22 (01) 128-131
- 8 McArdle D, Katch IF, Katch VL. Fisiologia do exercício: nutrição, energia e desempenho humano. 8ª ed. Rio de Janeiro: Guanabara; 2016
- 9 Fukunaga T, Ichinose Y, Ito M, Kawakami Y, Fukashiro S. Determination of fascicle length and pennation in a contracting human muscle in vivo. J Appl Physiol 1997; 82 (01) 354-358
- 10 Kawakami Y, Ichinose Y, Fukunaga T. Architectural and functional features of human triceps surae muscles during contraction. J Appl Physiol 1998; 85 (02) 398-404
- 11 Narici MV, Binzoni T, Hiltbrand E, Fasel J, Terrier F, Cerretelli P. In vivo human gastrocnemius architecture with changing joint angle at rest and during graded isometric contraction. J Physiol 1996; 496 (Pt 1): 287-297
- 12 Maganaris CN, Baltzopoulos V, Sargeant AJ. In vivo measurements of the triceps surae complex architecture in man: implications for muscle function. J Physiol 1998; 512 (Pt 2): 603-614
- 13 Marti B, Vader JP, Minder CE, Abelin T. On the epidemiology of running injuries. The 1984 Bern Grand-Prix study. Am J Sports Med 1988; 16 (03) 285-294
- 14 Fields KB, Rigby MD. Muscular Calf Injuries in Runners. Curr Sports Med Rep 2016; 15 (05) 320-324
- 15 Kubo K, Kanehisa H, Azuma K. et al. Muscle architectural characteristics in young and elderly men and women. Int J Sports Med 2003; 24 (02) 125-130
- 16 Chow RS, Medri MK, Martin DC, Leekam RN, Agur AM, McKee NH. Sonographic studies of human soleus and gastrocnemius muscle architecture: gender variability. Eur J Appl Physiol 2000; 82 (03) 236-244
- 17 Rutherford OM, Jones DA. Measurement of fibre pennation using ultrasound in the human quadriceps in vivo. Eur J Appl Physiol Occup Physiol 1992; 65 (05) 433-437
- 18 Kawakami Y, Abe T, Fukunaga T. Muscle-fiber pennation angles are greater in hypertrophied than in normal muscles. J Appl Physiol 1993; 74 (06) 2740-2744
- 19 Ichinose Y, Kanehisa H, Ito M, Kawakami Y, Fukunaga T. Relationship between muscle fiber pennation and force generation capability in Olympic athletes. Int J Sports Med 1998; 19 (08) 541-546
- 20 Kumagai K, Abe T, Brechue WF, Ryushi T, Takano S, Mizuno M. Sprint performance is related to muscle fascicle length in male 100-m sprinters. J Appl Physiol 2000; 88 (03) 811-816
- 21 Gans C, de Vree F. Functional bases of fiber length and angulation in muscle. J Morphol 1987; 192 (01) 63-85
- 22 Henriksson-Larsén K, Wretling ML, Lorentzon R, Oberg L. Do muscle fibre size and fibre angulation correlate in pennated human muscles?. Eur J Appl Physiol Occup Physiol 1992; 64 (01) 68-72
- 23 Martins Nda F, Peixinho CC, Oliveira Lde. Confiabilidade de medidas de arquitetura muscular do tríceps sural por ultrassonografia de imagem. Rev Bras Cineantropom Desempenho Hum 2012; 14 (02) 212-220
- 24 Maganaris CN, Baltzopoulos V. Predictability of in vivo changes in pennation angle of human tibialis anterior muscle from rest to maximum isometric dorsiflexion. Eur J Appl Physiol Occup Physiol 1999; 79 (03) 294-297
- 25 Zhou Y, Li JZ, Zhou G, Zheng YP. Dynamic measurement of pennation angle of gastrocnemius muscles during contractions based on ultrasound imaging. Biomed Eng Online 2012; 11: 63
- 26 Narici M. Human skeletal muscle architecture studied in vivo by non-invasive imaging techniques: functional significance and applications. J Electromyogr Kinesiol 1999; 9 (02) 97-103
- 27 Binzoni T, Bianchi S, Hanquinet S. et al. Human gastrocnemius medialis pennation angle as a function of age: from newborn to the elderly. J Physiol Anthropol Appl Human Sci 2001; 20 (05) 293-298
- 28 Kubo K, Kanehisa H, Azuma K. et al. Muscle architectural characteristics in women aged 20-79 years. Med Sci Sports Exerc 2003; 35 (01) 39-44
- 29 Kawakami Y, Abe T, Kanehisa H, Fukunaga T. Human skeletal muscle size and architecture: variability and interdependence. Am J Hum Biol 2006; 18 (06) 845-848
- 30 de Araujo MK, Baeza RM, Zalada SRB, Alves PBR, de Mattos CA. Injuries among amateur runners. Rev Bras Ortop 2015; 50 (05) 537-540
- 31 Manal K, Roberts DP, Buchanan TS. Optimal pennation angle of the primary ankle plantar and dorsiflexors: variations with sex, contraction intensity, and limb. J Appl Biomech 2006; 22 (04) 255-263
- 32 Powers S. Fisiologia do exercício: teoria e aplicação ao condicionamento e ao desempenho. 8ª e ed. São Paulo: Manole; 2014
- 33 Chiaramonte R, Bonfiglio M, Castorina EG, Antoci SAM. The primacy of ultrasound in the assessment of muscle architecture: precision, accuracy, reliability of ultrasonography. Physiatrist, radiologist, general internist, and family practitioner's experiences. Rev Assoc Med Bras 2019; 65 (02) 165-170
- 34 Borel WP, Elias Filho J, Diz JBM. et al. Prevalence of Injuries in Brazilian Recreational Street Runners: Meta-Analysis. Rev Bras Med Esporte 2019; 25 (02) 161-167
- 35 Timmins RG, Shield AJ, Williams MD, Opar DA. Is There Evidence to Support the Use of the Angle of Peak Torque as a Marker of Hamstring Injury and Re-Injury Risk?. Sports Med 2016; 46 (01) 7-13
Endereço para correspondência
Publication History
Received: 18 April 2021
Accepted: 25 October 2024
Article published online:
15 April 2025
© 2025. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution 4.0 International License, permitting copying and reproduction so long as the original work is given appropriate credit (https://creativecommons.org/licenses/by/4.0/)
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Lara Barros Cecílio Mendes, Carlos Henrique Fernandes, Paulo Santoro Bellangero, Benno Ejnisman, Moisés Cohen. Avaliação do ângulo de penação do músculo gastrocnêmio medial em corredores de rua e não corredores. Rev Bras Ortop (Sao Paulo) 2025; 60: s00451804493.
DOI: 10.1055/s-0045-1804493
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Referências
- 1 Lee DC, Pate RR, Lavie CJ, Sui X, Church TS, Blair SN. Leisure-time running reduces all-cause and cardiovascular mortality risk. J Am Coll Cardiol 2014; 64 (05) 472-481
- 2 Fukunaga T, Kawakami Y, Kuno S, Funato K, Fukashiro S. Muscle architecture and function in humans. J Biomech 1997; 30 (05) 457-463
- 3 Aagaard P, Andersen JL, Dyhre-Poulsen P. et al. A mechanism for increased contractile strength of human pennate muscle in response to strength training: changes in muscle architecture. J Physiol 2001; 534 (Pt. 2): 613-623
- 4 Azizi E, Brainerd EL, Roberts TJ. Variable gearing in pennate muscles. Proc Natl Acad Sci U S A 2008; 105 (05) 1745-1750
- 5 Hamill J, Knutzen M, Derrick R. Bases biomecânicas do movimento humano. São Paulo: Manole; 2016
- 6 Zatsiorsky M. Biomecânica no esporte. Rio de Janeiro: Guanabara; 2016
- 7 Ikegawa S, Funato K, Tsunoda N, Kanehisa H, Fukunaga T, Kawakami Y. Muscle force per cross-sectional area is inversely related with pennation angle in strength trained athletes. J Strength Cond Res 2008; 22 (01) 128-131
- 8 McArdle D, Katch IF, Katch VL. Fisiologia do exercício: nutrição, energia e desempenho humano. 8ª ed. Rio de Janeiro: Guanabara; 2016
- 9 Fukunaga T, Ichinose Y, Ito M, Kawakami Y, Fukashiro S. Determination of fascicle length and pennation in a contracting human muscle in vivo. J Appl Physiol 1997; 82 (01) 354-358
- 10 Kawakami Y, Ichinose Y, Fukunaga T. Architectural and functional features of human triceps surae muscles during contraction. J Appl Physiol 1998; 85 (02) 398-404
- 11 Narici MV, Binzoni T, Hiltbrand E, Fasel J, Terrier F, Cerretelli P. In vivo human gastrocnemius architecture with changing joint angle at rest and during graded isometric contraction. J Physiol 1996; 496 (Pt 1): 287-297
- 12 Maganaris CN, Baltzopoulos V, Sargeant AJ. In vivo measurements of the triceps surae complex architecture in man: implications for muscle function. J Physiol 1998; 512 (Pt 2): 603-614
- 13 Marti B, Vader JP, Minder CE, Abelin T. On the epidemiology of running injuries. The 1984 Bern Grand-Prix study. Am J Sports Med 1988; 16 (03) 285-294
- 14 Fields KB, Rigby MD. Muscular Calf Injuries in Runners. Curr Sports Med Rep 2016; 15 (05) 320-324
- 15 Kubo K, Kanehisa H, Azuma K. et al. Muscle architectural characteristics in young and elderly men and women. Int J Sports Med 2003; 24 (02) 125-130
- 16 Chow RS, Medri MK, Martin DC, Leekam RN, Agur AM, McKee NH. Sonographic studies of human soleus and gastrocnemius muscle architecture: gender variability. Eur J Appl Physiol 2000; 82 (03) 236-244
- 17 Rutherford OM, Jones DA. Measurement of fibre pennation using ultrasound in the human quadriceps in vivo. Eur J Appl Physiol Occup Physiol 1992; 65 (05) 433-437
- 18 Kawakami Y, Abe T, Fukunaga T. Muscle-fiber pennation angles are greater in hypertrophied than in normal muscles. J Appl Physiol 1993; 74 (06) 2740-2744
- 19 Ichinose Y, Kanehisa H, Ito M, Kawakami Y, Fukunaga T. Relationship between muscle fiber pennation and force generation capability in Olympic athletes. Int J Sports Med 1998; 19 (08) 541-546
- 20 Kumagai K, Abe T, Brechue WF, Ryushi T, Takano S, Mizuno M. Sprint performance is related to muscle fascicle length in male 100-m sprinters. J Appl Physiol 2000; 88 (03) 811-816
- 21 Gans C, de Vree F. Functional bases of fiber length and angulation in muscle. J Morphol 1987; 192 (01) 63-85
- 22 Henriksson-Larsén K, Wretling ML, Lorentzon R, Oberg L. Do muscle fibre size and fibre angulation correlate in pennated human muscles?. Eur J Appl Physiol Occup Physiol 1992; 64 (01) 68-72
- 23 Martins Nda F, Peixinho CC, Oliveira Lde. Confiabilidade de medidas de arquitetura muscular do tríceps sural por ultrassonografia de imagem. Rev Bras Cineantropom Desempenho Hum 2012; 14 (02) 212-220
- 24 Maganaris CN, Baltzopoulos V. Predictability of in vivo changes in pennation angle of human tibialis anterior muscle from rest to maximum isometric dorsiflexion. Eur J Appl Physiol Occup Physiol 1999; 79 (03) 294-297
- 25 Zhou Y, Li JZ, Zhou G, Zheng YP. Dynamic measurement of pennation angle of gastrocnemius muscles during contractions based on ultrasound imaging. Biomed Eng Online 2012; 11: 63
- 26 Narici M. Human skeletal muscle architecture studied in vivo by non-invasive imaging techniques: functional significance and applications. J Electromyogr Kinesiol 1999; 9 (02) 97-103
- 27 Binzoni T, Bianchi S, Hanquinet S. et al. Human gastrocnemius medialis pennation angle as a function of age: from newborn to the elderly. J Physiol Anthropol Appl Human Sci 2001; 20 (05) 293-298
- 28 Kubo K, Kanehisa H, Azuma K. et al. Muscle architectural characteristics in women aged 20-79 years. Med Sci Sports Exerc 2003; 35 (01) 39-44
- 29 Kawakami Y, Abe T, Kanehisa H, Fukunaga T. Human skeletal muscle size and architecture: variability and interdependence. Am J Hum Biol 2006; 18 (06) 845-848
- 30 de Araujo MK, Baeza RM, Zalada SRB, Alves PBR, de Mattos CA. Injuries among amateur runners. Rev Bras Ortop 2015; 50 (05) 537-540
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