Professional Documents
Culture Documents
com/
The Three-dimensional Active Envelope of Jaw Border Movement and its Determinants
J.H. Koolstra, M. Naeije and T.M.G.J. Van Eijden J DENT RES 2001 80: 1908 DOI: 10.1177/00220345010800100901 The online version of this article can be found at: http://jdr.sagepub.com/content/80/10/1908
Published by:
http://www.sagepublications.com
On behalf of:
International and American Associations for Dental Research
Additional services and information for Journal of Dental Research can be found at: Email Alerts: http://jdr.sagepub.com/cgi/alerts Subscriptions: http://jdr.sagepub.com/subscriptions Reprints: http://www.sagepub.com/journalsReprints.nav Permissions: http://www.sagepub.com/journalsPermissions.nav Citations: http://jdr.sagepub.com/content/80/10/1908.refs.html
Downloaded from jdr.sagepub.com by guest on July 10, 2011 For personal use only. No other uses without permission.
The Three-dimensional Active Envelope of Jaw Border Movement and its Determinants
INTRODUCTION
The excursions of the human lower jaw with respect to the skull are limited by constraints within the masticatory system. These limitations are considered to be a fundamental portion of the functional performance of the masticatory system, while all its separate functional contributions are related to these limitations (Heners, 1977). In the sagittal plane, these limits have a banana-like shape (Posselt, 1952) which is known as the socalled "Posselt figure". Such a figure can be constructed by tracing the path of the lower central incisors during a maximum open-close movement while keeping the jaw as far as possible in a forward or backward direction. Such so-called "border movements" can also be made while keeping the lower jaw to one side as far as possible. In this way, the envelope of border movement in a more or less frontal plane can be constructed (Nishigawa et al., 1991). Jaw movements are not restricted to the frontal and sagittal plane only. Border movements, therefore, can also be performed in directions oblique to these planes. The area that can be reached by the lower central incisors will have a three-dimensional shape. Presently, three-dimensional jaw movement analysis systems (e.g., Naeije et al., 1995) can be applied to trace the path of the lower incisor point during three-dimensional border movements (Fig. 1). The constraints that determine the envelope of border movement may be passive (articular surfaces, temporomandibular ligaments, passive forces of the muscles) and/or active (reflexes of muscles to protect the articular capsule) (Posselt, 1962; Lauer, 1985). At present, it is not known in what way the shape of the envelope of border movement is influenced by these factors. Therefore, although shape characteristics of the envelope may be correlated to masticatory function characteristics, no unambiguous causal relationships can be established. Unfortunately, it is not possible to study the determinants for the active envelope of border movement experimentally. Therefore, a biomechanical modeling approach has to be applied. This approach allows one to study the influence of one of the structures on the behavior of the complete system by adapting its mechanical or morphological characteristics. If model predictions can be validated experimentally, this has proved to be a powerful tool in masticatory function analysis (Koolstra and van Eijden, 1992). The purpose of the present study was to determine the influence of passive structures on the active three-dimensional envelope of border movement. This was accomplished by simulation of border movements with a three-dimensional dynamic model of the human masticatory system (Koolstra and van Eijden, 1995, 2001). Similar simulations were performed after removal of the temporomandibular ligaments or adaptation of the passive tensions of the masticatory muscles. While the masticatory muscles have a limited range of active shortening, it was hypothesized that they are the predominant factor for the shape of the envelope of border movement and that the influence of the passive constraints is much less.
ABSTRACT
The sagittal and frontal active envelope of border movement is applied regularly as a clinical tool in functional examinations of the human masticatory system. In contrast, the three-dimensional movement area has hardly been examined. Furthermore, the determinants of this area are not established unambiguously. In the present study, the three-dimensional envelope of incisor movement was predicted with a three-dimensional mathematical model of the human masticatory system, which included the morphology of the system and the fine architecture of its muscles. With this model, the influence of the temporomandibular ligaments and the passive muscle tensions on the envelope were estimated. The predicted threedimensional active envelope of border movements was limited in horizontal directions, predominantly by the temporomandibular ligaments. The passive tensions of the masticatory muscles influenced, although marginally, its vertical extension. It appeared unlikely that, in a normal situation, active muscle tensions (casu quo muscle reflexes) contribute to the shape of the envelope.
Received October 11, 2000; Last revision September 10, 2001; Accepted September 20, 2001
A supplemental appendix to this article is published electronically only at http://www.dentalresearch.org.
1908
Downloaded from jdr.sagepub.com by guest on July 10, 2011 For personal use only. No other uses without permission.
1909
acbvanon dynDacs
..... .....r
ooz oon
,,-C-I
ni-m (pm!
-1-1.
]el.
im
1910
Koolstra et a/.
reference .....,..." ,,
no
ligaments
-
+44-U'Sis
dimesioa
A:
cosrce
',,
~ -i3wwm
11
d-*
W v
1,
enelp
ofbre
oeet
+thrug
these
tJDe
Jugi'"s
b
;
,9
S dii .E
+t
,4.
IZ
e$
Figure 3. Border points as predicted by the model and the active threedimensional envelope of border movement constructed through these points. + = border points predicted for all maximally retruded positions. o = border points predicted for all maximally protruded positions. (A) Postero-lateral view. (B) Lateral view. (C) Antero-lateral view.
We explored the iniluence of the temporomilandibular ligaments on the active envelope of' border movxemeit by pertorminig a series of border movemenlt simulationis with a model lfrom whicih they werc rcmovcd. Thc iniluence ol' the passive elastic tension of the masticatory muscles was studicd by similar simulations while thc tension was dccreased or increased by a factor oft2.
.ZI
'I
ft,
ft
7,
-
-0
iI~
A
n
D
v
Figure 4. Active three-dimensional envelopes of border movement as predicted by the model. (A) Normal model. (B) Model without temporomandibular ligaments. (C) Model with reduced passive muscle tensions. (D) Model with increased muscle tensions. Left panels: crosssectional frontal view. Bars: 1 cm. Upper right panels: sagittal view. Lower right panels: frontal view.
(artilicially cxtended) temporal surtheCC, to retrude the inicisor as much as possible (data not shown). The applied chaniges in passive elastic properties of' the muscles had much less inIluelice on the cnxvclope of movexilemit. Reductioll ot' this property (Fig. 4C) led to a slightly larger rnaxilmti jaw openinig (3.6 cm). The moveminciit possibilities in the sagittal and fronital planes in the extended part of the envelope were small. The other maxilulIL exCursions wxere not aflfected. A doublinig of the passive elastic muscle forces (Fig. 4D) reduced maximlium jaw openinig to 3.1 cm. Also, maxilmlumIL protrusion, retrLisioni, and laterodeviation were slightly reduced to 7.7, 2.6, and II mim, respectively. Chaniges in this parameter did not affect the amount of'terimlinal hinige movemilenit. The condylar excursions were almost similar to those obtained with the norimial model. There was one exception: To reach the anterior border wheln the passive muscIe tensiolIs were reduced, the antero-posterior excursionl of' the ipsilateral condyle increased 6.6 mm, to about 19 mmll (data not shox n).
The extension oh the active envelope of border movement became about 63% larger in the antero-posterior direction and about 27% in the rnedio-lateral direction after the temporomandibular ligaments were removed (Fig. 4B). The increasc was not found in the vertical direction; the maximum DISCUSSION amount of jaw opening remained the same. The amount of' Border Movement Simulations opening by rotation about the intercondylar axis was less (about x In the present study. we were able to explore the thiee1.7 cm), whereas the posterior prominence in the posterior dimensionial active envelope ol' border movemilenit. F urthermore, border of the envelope had almost disappeared. Maximum the inifluenice of the temporomanidibular ligamenits and the protrusion, retrusion, and laterodeviation were increased to 10, passive muscle tensionis On this envelope could be predicted. 9.4, and 16 mmr, respectively. The active envelope of' border movemilenit predicted by our Alter removal of the ligaments, the condyle was able to unmodified model (Fig. 4A) displayed featul-es similar- to those move beyond the natural borders of the area of articular obtained experimentally (Fig. I ). The vertical ranige ol' the the contralateral contact. The largest excursions were found for predicted movements, however, was smaller. A possible condyle, wliich moved 1.5 cm medially wheni the incisors explanation for this fact is an overestimationi of the passive moved to their most lateral position. Both condyles moved Downloaded from jdr.sagepub.com along the muscle only. No other (Langenbacih maximally about 3 cm in the posterior direction by guest on July 10, 2011 For personal use tensionisuses without permission. and llainiaii, 1999) (but Vide
1911
infra). Furthermore, the incorporated jaw-opening muscles could have been relatively weak. Their properties were estimated from cadaveric specimens. Although these specimens had a reasonable dentition, they were relatively old (van Eijden et al., 1995), and it can be assumed that their muscle strength was less than the average. One of the most likely explanations relates to head movements during jaw opening. It has been demonstrated that the upper jaw may move up to 50% of jaw opening (Eriksson et al., 1998; Kohno et al., 2001), herewith stretching the contracted jaw openers toward their optimum lengths. This mechanism presumably enables the jaw openers to produce enough force to counteract the stretching jaw closers to open the jaw much further than in the present simulations. Despite similar features between the simulated and measured envelopes of border movement, there were also differences. The differences were not larger than those observed in border movements from different subjects (Brown, 1975; Lewin, 1985; Nishigawa et al., 1991). The morphology of the relevant subject was not incorporated into the model (Koolstra and van Eijden, 1992), while such is possible only for macroscopic features such as overall muscle direction and cross-section. The fine muscle architecture incorporating sarcomere length and fiber length, which are assumed to play a dominant role for the active envelope of border movement, cannot be obtained in vivo without disturbing the integrity of the muscle tissue. The endpoints of the border movements were not distributed regularly over the simulated envelope of border movement (Fig. 3), although a 5 x 5 mm grid was applied for the putative destinations. This is a consequence of the applied procedure for generating muscle recruitment patterns (Koolstra and van Eijden, 2001), which attempted to move the incisors across, but not along, the border to get closer to a putative destination.
of the envelope, however, was much smaller than generally assumed. By postulation of optimum length or 150% optimum length for all muscles at a jaw opening of 12 mm or 50 mm, respectively, wide-open jaw positions could be simulated (Langenbach and Hannam, 1999; Peck et al., 2000). However, human masticatory muscles do not reach optimum sarcomere length simultaneously (Koolstra and van Eijden, 1997a). The model applied optimum sarcomere length obtained from related animal masticatory muscles (Muhl et al., 1978), while this parameter has not been experimentally established in humans. We were reluctant to adapt optimum sarcomere length, without a physiological or experimental basis, only to reach a larger jaw opening. At the present maximum amount of jaw opening, the jaw closers apparently do not become stretched beyond the length where their passive forces become dominant. In the present study, the influence of active muscle forces on the active envelope of border movement was not examined separately. Since the simulated envelope was not larger than the measured one, it is unlikely that the maximum excursions of the lower jaw are limited actively by muscle reflexes (Posselt, 1962; Lauer, 1985). The differences in the active envelope of border movement predicted by the models with and without the presence of the temporomandibular ligament suggest that the articular capsule is loaded during extreme laterodeviation, protrusion, or retrusion. Extreme wide jaw opening without head movement presumably does not load these capsules. The difference between the model predictions as a function of the implemented amount of passive muscle tensions suggests that if the position of the hyoid bone with respect to the skull remains stationary, the jaw muscles are not stretched to the point where their passive forces become the dominant limiting factor for movement possibilities. The mechanism that renders the muscles insufficient for force production is suggested to be the dominant factor for vertical movement limitations.
ACKNOWLEDGMENTS
We gratefully thank Academic Computing Services Amsterdam (SARA) for technical support. This research was institutionally supported by the Interuniversity Research School of Dentistry, through the Academic Centre of Dentistry Amsterdam.
REFERENCES AQ
Brown T (1975). Mandibular movements. Monogr Oral Sci 4:126-150. Eriksson PO, Zafar H, Nordh E (1998). Concomitant mandibular and head-neck movements during jaw opening-closing in man. J Oral Rehabil 25:859-870. Heners M (1977). Elektronische Untersuchungen zur dreidimensionalen Bewegung des Unterkiefers. Dtsch Zahndrztl Z 32:104-107. Kohno S, Matsuyama T, Medina RU, Arai Y (2001). Functionalrhythmical coupling of head and mandibular movements. J Oral Rehabil 28:161-167. Koolstra JH, van Eijden TMGJ (1992). Application and validation of a three-dimensional mathematical model of the human masticatory system in vivo. JBiomech 25:175-187. Koolstra JH, van Eijden TMGJ (1995). Biomechanical analysis of jaw closing movements. JDent Res 74:1564-1570. Koolstra JH, van Eijden TMGJ (1996). Influence of the dynamical properties of the human masticatory muscles on jaw closing movements. Eur J Morphol 34:11-18.
Downloaded from jdr.sagepub.com by guest on July 10, 2011 For personal use only. No other uses without permission.
1912
Koolstra et al.
Koolstra JH, van Eijden TMGJ (1997a). Dynamics of the human masticatory muscles during a jaw open-close movement. J Biomech 30:883-889. Koolstra JH, van Eijden TMGJ (1997b). The jaw open-close movements predicted by biomechanical modelling. J Biomech 30:943950. Koolstra JH, van Eijden TMGJ (1999). Three-dimensional dynamical capabilities of the human masticatory muscles. J Biomech 32:145-152. Koolstra JH, van Eijden TMGJ (2001). A method to predict muscle control in the kinematically and dynamically indeterminate human masticatory system. JBiomech 34:1179-1188. Langenbach GEJ, Hannam AG (1999). The role of passive muscle tensions in a three-dimensional dynamic model of the human jaw. Arch Oral Biol 44:557-573. Lauer HC (1985). Uber die Abhangigkeit der Unterkiefergrenzbewegung von der Okklusionshohe. Dtsch Zahndrztl Z40:1016-1019. Lewin A (1985). Electrognathographics. Atlas of diagnostic procedures and interpretation. Chicago: Quintessence Publishing Co., Inc. Muhl ZF, Grimm AF, Glick PL (1978). Physiologic and histologic measurements of the rabbit digastric muscle. Arch Oral Biol 23:1051-1059. Naeije M, van der Weijden JJ, Megens CCEJ (1995). OKAS-3D: opto-
electronic movement recording system with six degrees of freedom. Med Biol Eng Comput 33:683-688. Nishigawa K, Nakano M, Bando E, Clark GT (1991). The relationship between lateral border movements of the mandible and the determinants of occlusion. JProsthet Dent 66:486-492. Peck CC, Langenbach GEJ, Hannam AG (2000). Dynamic simulation of muscle and articular properties during human wide jaw opening. Arch Oral Biol 45:963-982. Posselt U (1952). Studies in the mobility of the human mandible. Acta Odontol Scand 10(Suppl 10): 19-160. Posselt U (1962). Physiology of occlusion and rehabilitation. Oxford: Blackwell Scientific Publications. van Eijden TMGJ, Koolstra JH, Brugman P (1995). Architecture of the human pterygoid muscles. JDent Res 74:1489-1495. van Eijden TMGJ, Koolstra JH, Brugman P (1996). Three-dimensional structure of the human temporalis muscle. Anat Rec 246:565-572. van Eijden TMGJ, Korfage JAM, Brugman P (1997). Architecture of the human jaw-closing and jaw-opening muscles. Anat Rec 248:464-474. van Ruijven LJ, Weijs WA (1990). A new model for calculating muscle forces from electromyograms. Eur JAppl Physiol 61:479-485. Winters JM, Stark L (1987). Muscle models: what is gained and what is lost by varying model complexity. Biol Cybern 55:403-420.
Downloaded from jdr.sagepub.com by guest on July 10, 2011 For personal use only. No other uses without permission.