Difference in Articular Degeneration Depending on the Type of Sport*

 

ABSTRACT:

OBJECTIVE To determine whether type-II collagen degradation is determined by the type of sport. Carboxy-terminal telepoptide of type-II collagen (CTX-II), a serum biomarker of collagen degradation, was measured in athletes who play different sports, and was compared with matched controls.
METHODS The sample size consisted of 70 female participants aged between 18 and 25 years, 15 of whom were members of a soccer team, 10 of a futsal (a variant of association football played on a hard court) team, 10 of a handball team, 18 of a volleyball team, and 7 of a swimming team. A total of 9 age- and sex-matched individuals with sedentary lifestyles were included in the control group. 3-mL blood samples were collected from each participant, and they were analyzed using an enzyme-linked immunosorbent assay (ELISA).
RESULTS A comparison of the CTX-II concentrations of the players of different sports with those of the control group resulted in the following p-values: volleyball (p = 0.21); soccer (p = 0.91); handball (p = 0.13); futsal (p = 0.02); and swimming (p = 0.0015). Therefore, in the investigated population, futsal represented the highest risk for type-II collagen degradation and, consequently, for articular cartilage degradation, whereas swimming was a protective factor for the articular cartilage. No statistically significant difference was found in the body mass index among the groups.
CONCLUSION Futsal players are exposed to greater articular degradation, while swimmers exhibited less cartilage degradation compared with the control group in the study population, suggesting that strengthening the periarticular muscles and aerobic exercise in low-load environments has a positive effect on the articular cartilage.

Keywords: cartilage; biomarkers; arthrosis; athletes.

RESUMO:

OBJETIVO Determinar se a degradação de colágeno tipo II é determinada pelo tipo de esporte. O telopeptídeo carboxiterminal do colágeno tipo II (CTX-II), biomarcador de soro de degradação de colágeno, foi medido em atletas de esportes diferentes e comparado aos controles correspondentes.
MÉTODOS A amostra consistiu em 70 participantes do sexo feminino com idade entre 18 a 25 anos, das quais 15 eram membros de uma equipe de futebol, 10 de uma equipe de futebol de salão, 10 de uma equipe de handebol, 18 de uma equipe de voleibol, e 7 de uma equipe de natação. Foram incluídos no grupo de controle 9 indivíduos sedentários, pareados por idade e sexo. Uma amostra de sangue de 3 ml foi coletada de cada participante e analisada usando um ensaio imunossorvente ligado a enzima (ELISA, do inglês enzyme-linked immunosorbent assay).
RESULTADOS Uma comparação das concentrações de CTX-II das praticantes de diferentes esportes em comparação com o grupo de controle apresentou os seguintes valores de p: voleibol (p = 0,21); futebol (p = 0,91); handebol (p = 0,13); futebol de salão (p = 0,02) e natação (p = 0,0015). Portanto, na população investigada, o futebol de salão apresentou o maior risco de degradação do colágeno tipo II, e, consequentemente, de degradação da cartilagem articular, enquanto a prática de natação foi um fator protetor para a cartilagem articular. Não foi observada diferença estatisticamente significativa no índice de massa corporal entre os grupos.
CONCLUSÃO As jogadoras de futebol de salão estão expostas a uma maior degradação articular, enquanto as nadadoras apresentam menor degradação da cartilagem em comparação com o grupo de controle na população estudada, o que sugere que o fortalecimento dos músculos periarticulares e o exercício aeróbico em ambientes de baixa carga têm um efeito positivo na cartilagem articular.

Palavras-chave: cartilagem; biomarcadores; artrose; atletas.

FIGURES

Citation: Jorge PB, Sprey JWC, Runco GM, Lima MV, Severino NR, Santili C. Difference in Articular Degeneration Depending on the Type of Sport*. 54(5):509. doi:10.1016/j.rboe.2018.02.012

Note: * Published Originally by Elsevier Editora Ltda.

Received: October 31 2017; Accepted: February 21 2018

 

INTRODUCTION

The articular cartilage is a specialized avascular, aneural tissue that covers the bony parts of the diarthrodial joints. Its function is to facilitate smooth motion via its low frictional coefficient, in addition to absorbing shock and supporting load in several planes.^1,2

The preservation of the articular cartilage depends on maintaining the integrity of its molecular structure.¹ The main macromolecules that comprise cartilage are collagen and proteoglycans; during the course of life, the activity of the chondral cells is determined by several autocrine and non-autocrine factors that result in the maintenance or destruction of articular homeostasis. Osteoarthrosis is a common condition in the elderly, but it can also affect young people who are subjected to excessive articular loads.^1-17

In adults, the activation of the articular function within the physiological limits of load and work frequency is crucial to maintain joint health;^3-6,9,13 therefore, joints working below the required levels are also at risk of degenerating.¹⁰

Work frequency and articular overload are important factors in articular destruction, which is characterized by damage to cartilaginous tissue.² Indeed, excessive exposure to overload leads to early articular wear,^2-6,9,10,13 which is then perpetuated by an inflammatory cascade that affects all of the articular tissue.¹⁶ Therefore, high-performance athletes subjected to excessive training loads over a short period of time are at a higher risk of developing articular damage; the knees, in particular, tend to be overexposed in most sports. As a function of the constant demand for maximal performance, early articular wear and functional disabilities might result in the end of an athletic career.

Most patients are diagnosed in the advanced stages of arthrosis, when a series of metabolic events has already occurred, and the process is likely past the point at which pharmacological and surgical interventions are truly effective.¹⁸

The products of collagen matrix degradation might serve as useful markers of the severity and progression of arthrosis. Such products might be measured in the synovial fluid, blood or urine, and thus supply important information for the early diagnosis of arthrosis.

Regarding Articular Collagen

Collagen represents 50 to 60% of the dry weight of the cartilage. Its fibers form a dense network that gives shape to this tissue. The most important mechanical properties of collagen are resistance and resilience, which are transmitted to the cartilage.¹

Type-II collagen is specific to cartilage, and represents nearly 98% of the total collagen content in this tissue.¹

Type-II collagen is the largest macromolecule that composes the cartilage, and it consists of three identical polypeptide chains arranged in a triple helix. Each such chain is synthesized as a pro-chain that contains large pro-peptides at its ends, which are separated from the central part by telopeptides. During the maturation of type-II collagen molecules, proteases cleave the pro-peptides; thus, the mature structure consists of the central part of the triple helix and telopeptides.

When the articular components degrade, they are expelled from their source tissue and are measured most accurately in the articular fluid. However, when studying osteoarthritis, the measurement of biomarkers in the blood and urine is made using less aggressive methods that are still effective and precise.¹

The carboxy-terminal telopeptide of type-II collagen (CTX-II) is a biomarker of articular degradation. The use of CTX-II as a biomarker, in addition to its direct relationship with the radiological grade of disease, clinical scores and severity of cartilaginous lesions, is well established in the literature.^2,18-28 Thus, the measurement of CTX-II appears to be an effective method to investigate the turnover of type-II collagen.

The present study aimed to detect the early degradation of articular type-II collagen by measuring CTX-II levels in the blood of athletes performing different sports and comparing them with those of a control group. We sought to establish whether sport participation is a risk factor for early articular degradation in our country, and which sport was the most harmful to articular type-II collagen in the investigated population.

 

MATERIALS AND METHODS

The present study was performed at the Sports Trauma Group of the Department of Orthopedics and Traumatology of our institution. The study was approved by the institutional ethics committee (number 244/11), and signed informed consent was obtained from every participant.

The study population consisted only of females aged between 18 and 25 years, who were members of competitive sports teams, including soccer, futsal (a variant of association football played on a hard court), handball, volleyball and swimming, at Clube Atlético São José, which is a partner of the Sports Trauma Group of our institution. The participants had to have between 5 and 8 years of training in the sport, and none of the athletes participated in other sports.

Patients with articular pain undergoing treatment, history of articular orthopedic surgery or of untreated articular pain due to any cause were excluded from the study, and all individuals in this group were female.

A total of 9 individuals with sedentary lifestyles who met the inclusion criteria formed the control group. None of them had ever participated in sports in a competitive way.

A total of 70 female participants aged between 18 and 25 years were included: soccer (n = 15), futsal (n = 10), handball (n = 10), volleyball (n = 18) and swimming (n = 7); 9 individuals with sedentary lifestyles were included in the control group.

A total of 3 mL of blood was collected from each participant by simple venous puncture of the non-dominant upper limb using a vacuum collection kit, in which there is contact of the sample with ethylenediaminetetraacetic acid (EDTA), which does not affect the result, and the body mass index (BMI) was calculated as the weight divided by the height squared of each person.

The blood was centrifuged, and the plasma was stored at - 80ºC until all of the blood samples were ready for analysis, in a total of 23 days, because the test was performed in the same day. The samples were analyzed to detect human CTX-II using enzyme-linked immunosorbent assays (ELISAs; Hu CTX-II kit, Cusabio Biotech, Houston, TX, US). This test has 100% of specificity for human CTX-II without any cross-reactions, and a minimum level of detection of 0.2 ng/mL, which is informed by the manufacturer.

The results were compared using the Student t-test with a 95% confidence interval (95%CI), and values of p < 0.05 were considered statistically significant.

 

RESULTS

A total of 70 female participants aged between 18 and 25 years were included: soccer (n = 15), futsal (n = 10), handball (n = 10), volleyball (n = 18) and swimming (n = 7); 9 individuals with sedentary lifestyles were included in the control group.

The average age for the control group was of 22.6 years, the mean BMI was of 22.3, and the mean concentration of CTX-II was of 0.453 ng/mL (Table 1).

Among the 18 volleyball players, the average age was of 18.3 years, the mean BMI was of 22.33, and the mean CTX-II was of 0.429 ng/mL; this team trained 36 hours per week (Table 2).

Among the 15 soccer players, the average age was of 22.36 years, the mean BMI was of 22.06, and the mean CTX-II was of 0.456 ng/mL; this team trained 15 hours per week (Table 3).

Among the futsal players, the average age was of 18.5 years, the mean BMI was of 22.21, and the mean CTX-II was of 0.542 ng/mL; this team trained 15 hours per week (Table 4).

Among the handball players, the average age was of 18.9 years, the mean BMI was of 22.88, and the mean CTX-II was of 0.416 ng/mL; this team trained 25 hours per week (Table 5).

Among the swimmers, the average age was of 18.9 years, the mean BMI was of 20.71, and the mean CTX-II was of 0.373; this team trained 12 hours per week (Table 6).

The following p-values were obtained by comparing the different sports to the control group using the Student t-test: volleyball, p = 0.21 (Fig. 1); soccer, p = 0.91 (Fig. 2); handball, p = 0.13 (Fig. 3); futsal, p = 0.02 (Fig. 4); and swimming, p = 0.0015 (Fig. 5).

Thus, futsal represented the highest risk for type-II collagen degradation and consequently for articular cartilage degradation, whereas swimming was a protective factor for the articular cartilage in the investigated population.

 

DISCUSSION

Currently, prevention is emphasized over treatment; thus, the early diagnosis of osteoarthrosis is of paramount importance. In the case of athletes, early diagnosis is even more important because their occupation depends directly on the health of their joints.

Because the first cleavage of articular type-II collagen catalyzed by collagenases releases the CTX-II epitope, which can be measured in the blood, urine and synovial fluid, it is a powerful tool for the early diagnosis of articular wear.

Type-II collagen is present in every synovial joint; however, the concentration of CTX-II is higher in patients with knee and hip arthrosis compared with the overall population.²⁷ CTX-II is a biomarker for cartilage destruction, and an increased level is a positive predictor for articular space reduction.^27,28

When we measured the concentration of CTX-II in athletes who play different sports, we sought to detect whether the risk of overload and early articular destruction would be higher for any particular sport. Although the sample size for each sport might appear small, these are closed teams subjected to the same training load and, in theory, to the same articular overload.

In our study population, the volleyball, handball and soccer players did not exhibit higher type-II collagen degradation, although they participated intensively in high-impact activities. Perhaps this finding is explained by the fact that the study population was very young, and, for these three modalities, either the terrain or the shoes are able to absorb the shock.

Type-II collagen degradation was highest among the futsal players, and was significantly different than that of the control group (Fig. 4) using a 95%CI. This discrepancy was likely because this sport is played on a rigid floor, requires shoes that do not absorb shock, and has frequent shifts in direction overload on the joints, especially the knees (repeated pivot movements).

Another remarkable finding is that the swimming team had significantly lower CTX-II concentrations compared with the control group (Fig. 5). In other words, swimming was a protective factor for the articular collagen in the investigated population. This finding is likely due to a combination of factors known to protect the joints, including aerobic exercise, low-impact activity and strengthening of the periarticular muscles.¹⁷

 

CONCLUSION

Therefore, we conclude that, in the investigated population, professional futsal training is a risk factor for type-II collagen degradation and, thus, for articular cartilage degradation. In contrast, swimming is a protective factor for the joints in this same population, resulting in less articular collagen degradation.

Such data suggests that some sports can indeed lead to early articular degradation. Sports trauma physicians must consider this fact, and clinical protocols aimed at joint protection must be studied and applied.

However, the findings of the present study indicate that some sports may provide joint protection, suggesting an important tool to prevent joint erosion, and mixed training may be highly beneficial for professional teams.

Further studies on this subject must be performed with larger samples, and they should be aimed at controlling articular destruction using pharmacological and non-pharmacological means.

In addition, the use of biomarkers of joint destruction is an important tool for the early detection of joint overload. Those working in sports trauma need to diagnose joint lesions early to improve the lives of athletes.

 

REFERENCES