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ORIGINAL ARTICLE

Effect of root and bone morphology on the stress distribution in


the periodontal ligament

Kwangchul Choy, DDS, PhD,a Eung-Kwon Pae, DDS, MSc, PhD,b Youngchel Park, DDS, PhD,c Kyung-
Ho Kim, DDS, PhD,d and Charles J. Burstone, DDS, MSe
Seoul, Korea, and Farmington, Conn

To achieve predictable and physiologic orthodontic tooth movement, estimating the axis of rotation of a tooth
and the level and location of maximum stress distributed in the periodontal ligament is essential. An extracted
upper canine was scanned into a computer 2-dimensionally and divided into 80 nodes along the long axis of
the tooth. A mathematical formula was derived, and stress was calculated on each node. The purpose of this
study was to reveal the center of resistance, axis of rotation, and an ideal force magnitude associated with
various periodontal conditions, such as potential root resorption, alveolar bone loss, and varying anatomic root
shape by analyzing the stress distribution in the periodontal ligament. The study demonstrates that the location
of center of resistance changes significantly with variation of shape and length of the root embedded in alveolar
bone. In contrast, in response to alveolar bone loss, the relative location of the center of resistance to total root
length remains constant. Analysis of the stress distribution pattern in our 2-dimensional model reveals that the
relationship between location of force and axis of rotation is determined by s2 (that is) a constant depends on
shape and length of a root in alveolar bone. Tapered and short roots that result from alveolar bone loss or
apical root resorption are prone to tipping. The optimal orthodontic force may vary depending on the maximum
stress in the periodontal ligament. (Am J Orthod Dentofacial Orthop 2000;117:98-105)

To achieve predictable and physiologic Christiansen and Burstone2 showed the relationship
orthodontic tooth movement, the axis of rotation and between the axis of rotation and the location of force
level and location of maximum stress should be identi- relative to root length in a 2-dimensional parabolic root.
fied. Once force is applied to a tooth, stress is distrib- Nikolai3 has described the center of resistance and the
uted instantly along the periodontal ligament to achieve axis of rotation in a rhomboid root shape with a mathe-
a state of equilibrium. The axis of rotation and location matical analytical model. Davidian14 and Halazonetis15
of maximum stress level can be revealed by investigat- used a computer model to study the center of resistance
ing this stress distribution. and the axis of rotation. Despite the highly sophisticated
Because direct investigation inside the periodon- methods used in each of these studies, variable results
tium is impossible in vivo, mathematical analytical were obtained that showed that the mechanism of stress
studies,1-5 double exposure laser holographic interfer- distribution had not been clearly illustrated.
ometry or reflection studies,6-8 displacement transduc- The purpose of this study is 2-fold: (1) to better
ers,9 and finite element methods10-12 have been used to understand the location of the center of resistance, the
reveal the axis of rotation and stress distribution. relationship between the location of force, and the axis
Synge13 introduced the concept of the axis of rota- of rotation, and (2) to identify the ideal force magni-
tion when a tooth is subjected to force. Burstone1 and tude associated with various periodontal conditions,
such as root resorption, alveolar bone loss, and varying
aAssistant Professor, Department of Orthodontics, College of Dentistry, Yonsei root shape.
University.
bAssistant Professor, Department of Orthodontics, School of Dental Medicine, MATERIAL AND METHODS
University of Connecticut.
cProfessor, Department of Orthodontics, College of Dentistry, Yonsei University. The lateral view of an extracted upper canine was
dAssistant Professor, Department of Orthodontics, College of Dentistry, Yonsei scanned 2-dimensionally, and the scanned image was
University. divided into 80 nodes (Fig 1A). The width of each node
eProfessor, Department of Orthodontics, School of Dental Medicine, University

of Connecticut. became 0.2 mm along the long axis of the tooth. Fig 1
Reprint requests to: Eung-Kwon Pae, DDS, MSc, PhD, Assistant Professor, shows detailed specifications of the model used in this
Department of Orthodontics, School of Dental Medicine, University of Con- study. A canine was chosen because it is the tooth most
necticut, Farmington, Conn 06030-1725; e-mail, pae@up.uchc.edu
Copyright © 2000 by the American Association of Orthodontists. often translated a long distance. A computer program,
0889-5406/2000/$12.00 + 0 8/1/102179 Visual Basic 4.0, was used to calculate the geometry of
98
American Journal of Orthodontics and Dentofacial Orthopedics Choy et al 99
Volume 117, Number 1

Table II. Changes in location of the center of resistance


in relation to varying root shape, amount of alveolar
bone loss, and amount of apical root resorption
Percentage of total Distance from
Tooth length of the root bracket slot (mm)

Rectangular root 50.0 13.4


Blunt root 43.9 12.4
Standard root 41.8 12.1
Tapered root 39.0 11.6
Triangular root 33.0 10.8
A Amount of alveolar bone
loss in standard root
2 mm 41.2 13.2
4 mm 40.9 14.3
6 mm 40.7 15.5
8 mm 40.4 16.6
10 mm 40.1 17.8
12 mm 40.1 19.0
14 mm 41.0 20.2
Amount of apical root
resorption in standard root
2 mm 44.8 11.7
B 4 mm 46.7 11.0
6 mm 47.9 10.2
Fig 1. A, Specifications of standard model used in this 8 mm 48.8 9.3
study: a is distance between applied force and center of 10 mm 49.7 8.4
resistance; b is distance between center of resistance 12 mm 50.3 7.4
and axis of rotation. B, Schematic drawing of various
root shapes and location of center of resistance.

Table I. Typical results on location of the center of resis- program was encoded to calculate area of root surface,
tance1,3,7,9,10 the level of stress at each node, moment, and moment of
inertia. The center of resistance and the axis of rotation
Model used in study (method) Percentage of root length*
were obtained in each case.
2D parabola of Burstone (calculation) 40 When a line of action of force perpendicular to
3D parabola of Burstone (experiment) 33 the long axis of a restrained object varies the appli-
2D Rhomboid of Nikolai (calculation) 55 cation point at which stress is uniformly distributed,
Tooth of Burstone (experiment) 27 - 42
the center of resistance can be calculated similar to
3D of Tanne (calculation) 24
2D standard model in this study (calculation) 41.8 obtaining a centroid.16 When the line of action does
not pass through the center of resistance, this force
*Measured from the alveolar crest
can be relocated to the center of resistance with the
addition of a moment; this is the concept of equiva-
lent force systems. Therefore, the stress at an arbi-
the scanned canine. All data were manipulated with trary point in the periodontal ligament is the sum of
Microsoft Excel 97. the stress of the force applied at the center of resis-
This standard model is not an exact parabola, but tance and its accompanying moment.
approximates Burstone’s parabola.1,2 With this as a
M F
standard model, conditions were varied according to σ = –   + 
root shape and alveolar bone quantity. First, the shape of I A
the root was varied (triangular, tapered, blunt, and rec- can be derived (M, moment; y, distance from center of
tangular), while keeping the root length constant (Fig resistance to the node; I, moment of inertia; F, applied
1B). Second, the amount of alveolar bone loss and root force; A, area of root).16
resorption at the apex was gradually changed at 2-mm The node where stress is zero would be the axis of
increments. It was assumed that the tooth is a rigid rotation. As the stress is linearly increased from this
body, the periodontal ligament is homogenous isotropic, point, maximum stress (σmax) should be found at the
and stress and strain are linearly related. A computer most distant node from the axis of rotation where y = c
100 Choy et al American Journal of Orthodontics and Dentofacial Orthopedics
January 2000

A A

B B
Fig 2. Position of center of resistance (Cr) in response Fig 3. Position of center of resistance (Cr) in response
to the amount of alveolar bone loss in relation to the to apical root resorption in relation to the bracket slot (A)
bracket (A) and in relation to the root length (B). and in relation to the root length (B).

RESULTS
(c is distance from center of resistance to apex of the
Change of the Center of Resistance in Accordance
root). Maximum stress was obtained using
with the Variation in Root Shape
M F
σmax = –   + . The location of the center of resistance was
I A reported to be between 24% and 55% of root length
The relationship between the location of applied measured from alveolar crest to root apex depending
force and the axis of rotation was determined with a on boundary conditions. Typical results of previous
× b = s2, where a is the distance between the applied investigations are summarized in Table I. The center of
force and the center of resistance, b is the distance resistance of the standard model used in this study was
between the center of resistance and the axis of rota- 41.8% of total root length measured from alveolar
tion, and s2 indicates the variance of distribution of crest. Assuming that the bracket is placed at the center
stress (Fig 1A). of the crown, the center of the resistance would be 12.1
Based on these formulas, the location of the center mm from the bracket slot (Table II). In other words, a
of resistance, s2, and a location and level of maximum M/F ratio of 12.1 is required at the bracket to translate
stress was determined for that of varying root form, this standard model. This value was very similar to that
amount of loss of the alveolar bone, and amount of root of the 2-dimensional model of Burstone1 and Chris-
resorption. Physiologic optimal magnitude of ortho- tiansen and Burstone2 with a parabolic-shaped root
dontic force was also estimated with respect to the (40%). The evaluation of root shape on location of the
maximum stress level. center of resistance showed that as the shape of the root
American Journal of Orthodontics and Dentofacial Orthopedics Choy et al 101
Volume 117, Number 1

was gradually tapered from a rectangular to a triangu- Table III.The value of s2 in response to anatomic root
lar shape with the root length and maximum width kept shape, amount of alveolar bone loss, and amount of api-
cal root resorption; s2 decreases as the root becomes
constant, the location of the center of resistance was tapered and as alveolar bone loss and root resorption
50.0% in rectangular, 43.9% in blunt, 41.8% in stan- increase. A decrease of s2 is associated with greater sen-
dard, 39.0% in tapered, and 33.0% in triangular shape, sitivity to tooth tipping.
respectively (Fig 1B, Table II). It was found that the Tooth s2
location of the center of resistance is not constant even
though the width and length of the root is kept constant, Rectangular root 27.929
Blunt root 23.215
but it was affected by the anatomic shape of the root.
Standard root 17.520
The more the root tapers, the more coronal the location Tapered root 16.349
of the center of resistance moved. Triangular root 9.540
Amount of alveolar bone loss in standard root
Change of Center of Resistance in Relation to the 2 mm 13.505
Amount of Alveolar Bone Loss 4 mm 9.921
6 mm 7.451
As the amount of alveolar bone loss increased, the 8 mm 4.393
center of resistance gradually moved apically. For 10 mm 2.490
instance, the center of resistance moved 1.1 mm api- 12 mm 1.131
cally when 2 mm of alveolar bone was lost. In an 14 mm 0.292
Amount of apical root resorption in standard root
extreme example, loss of 14 mm of alveolar bone
2 mm 14.873
would cause the center of resistance to move apically 4 mm 11.397
8.1 mm. It was noted that the relationship between 6 mm 8.055
alveolar bone loss and changes in the center of resis- 8 mm 5.191
tance was almost linear when measured from the 10 mm 2.958
12 mm 1.332
bracket. The relative location of the center of resistance
to the total root length is quite constant from 40.1% to
41.8% (Table II, Fig 2).
bracket slot. With a rectangular root with a large s2,
Change of Center of Resistance in Relation to changes in the axis of rotation were much smaller than
Root Resorption those in a triangular root (Table IV, Fig 4).
When the apical part of the root is resorbed, the shape
and length of the root change simultaneously. As the root Pattern of Stress Distribution in the Periodontal
was shortened, the center of resistance moved coronally. Ligament in Relation to the Amount of Alveolar
The center of resistance moved 0.4 mm coronally when Bone Loss and Root Resorption
root was resorbed 2 mm; 12 mm of root resorption Length of the root embedded in alveolar bone
resulted in the center of resistance moving 4.7 mm coro- decreased as the amount of alveolar bone loss or root
nally. The relative location of the center of resistance to resorption increased. The value of s2 was affected
total root length varied from 41.8% to 50.3% as the greatly by the amount of alveolar bone loss and root
amount of root resorption increased (Table II, Fig 3B). resorption (Table III). Location of the axis of rotation
in relation to amount of alveolar bone loss and root
Pattern of Stress Distribution in the Periodontal resorption is shown in Fig 4. The data suggested that a
Ligament in Relation to Root Shape very exact placement of force is required for the given
Table III showed changes in the value of s2 accord- axis of rotation as s2 decreases.
ing to various root shapes. The relationship between
the location of force and the axis of rotation based on Optimal Magnitude of Orthodontic Force
the formula is shown in Table IV. The value of s2 The optimal magnitude of orthodontic force was
decreases as the shape of the root tapered. Fig 4 determined based on the pattern of stress distribution in
demonstrates that a minor change in positioning a force the periodontal ligament. For practical reasons, we con-
around the center of resistance results in a large change sidered maximum stress (σmax) in the periodontal liga-
in the axis of rotation depending on the root shape. For ment only. It was postulated that a stress greater than
example, in a triangular root that had a smaller s2, a blood pressure could make the capillary blood vessel in
clinically insignificant error such as ±1 mm in posi- the periodontal ligament collapse and can in turn cause
tioning of a horizontal force to the center of resistance a blocking of the blood supply. Conversely, if maximum
moves the axis of rotation from the root apex to the stress is less than the blood pressure, the capillary
102 Choy et al American Journal of Orthodontics and Dentofacial Orthopedics
January 2000

Table IV. Relationship between the axis of rotation and M/F ratio with varying root shapes
Location of the axis of rotation (Type of tooth movement)
Between Cr and apex Apex Infinity Bracket
M/F ratio at bracket (uncontrolled tipping) (controlled tipping) (bodily movement) (root movement)

Standard model 0 10.2 12.1 13.6


Rectangular root 0 9.9 13.4 15.5
Triangular root 0 9.8 10.7 11.6

would not be collapsed in any part of the periodontal contrast, during alveolar bone loss, the root anatomy
ligament. If we assume that a rate of tooth movement is remained unchanged. This may explain why the rela-
proportional to the magnitude of force, the optimum tive location of the center of resistance remained con-
force level would exist when the force producing the stant (40.1% to 41.8%) during alveolar bone loss.
maximum stress was equal to the blood pressure. The results of this study demonstrate the importance
Because normal systolic blood pressure is 120 mm of s2 a concept developed by Nägerl et al.9 If we imag-
Hg (1.56 g/mm2) and the surface area of the root of our ine a tooth as a stick and periodontal ligament fibers as
standard model is 94.1 mm2, more than 147 g of force small springs, the center of resistance is a mean value of
for translation would result in a collapse of all capillar- the distribution of the spring constant. The schematic
ies at the compression site (147 g/94.1 mm2 = 1.56 drawing (Fig 5) shows that continuous distribution of
g/mm2); 74 g of force for tipping at the apex, 20 g for the springs can be substituted with 2 large and more
uncontrolled tipping, and 83 g for root movement with rigid springs per side with the distance s apart from cen-
the center of rotation at the tip of a bracket would ren- ter of resistance (Fig 5A). The value s may be consid-
der 1.56 g/mm2 of stress in maximum. ered as a standard deviation of the distribution of spring
constant (Fig 5B). In the formula developed by Chris-
DISCUSSION tiansen and Burstone2 and Nägerl et al,9 y × (M/F) =
When orthodontic force is applied to a tooth, stress 0.068h2, 0.068h2 is a special case of s2 when root shape
is distributed throughout the periodontal ligament and is exactly a parabola. Fig 5C shows zero s. Force
reaches a state of equilibrium within 2 minutes.8,17 applied to other than the center of resistance will rotate
Biologic responses such as bone resorption and apposi- the tooth around the center of resistance regardless of
tion follow in response to strain in the periodontal lig- the location of the force and the magnitude of force.
ament. An instant tooth movement within the peri- Translating the tooth is almost impossible in such a
odontal ligament is called a primary displacement, case. In Fig 5D, the force is applied at a = s. Although
whereas the movement followed by a biologic response the force application point is same as in Fig 5C, the
is called a secondary displacement. The exact relation- tooth will rotate around the point b, and less tipping will
ship between these 2 types of tooth movement is com- be developed. Therefore, s2 or s may be a constant that
pounded by biologic variation. For instance, tissue represents the distribution of stress when translation
response to orthodontic force in older patients is much occurs. Clinically, the greater the s2, the less the tooth
slower than that in younger patients. Thus, the sec- will tip. Thus, s2 can be considered as an index for sen-
ondary displacement would occur at a slower pace.18 sitivity of tipping. The center of resistance and s appear
Nevertheless, secondary displacement can be predicted to be analogous to the mean and standard deviation in
by the primary tooth movement that, in turn, can be statistics. As s becomes smaller, the location of force
determined by analyzing the stress distribution pattern should be more precisely located for a given axis of
in the periodontal ligament.1,19,20 In our idealized rotation. An s2 is influenced by shape and length of the
model, uniform strain should be found along the com- root embedded in alveolar bone. The axis of rotation
pression site to allow the teeth to be translated. The was influenced only by the constant s and the location
location of force at which the tooth is translated is of applied force, yet it was independent from a modulus
defined as the center of resistance. The position of the of elasticity (E) of the periodontal ligament or the mag-
center of resistance is influenced not only by alveolar nitude of force. It may be a common misunderstanding
bone loss or apical root resorption, but also by the vari- that less tipping will occur with a lighter force.
able shape of the root. When apical root resorption Clinicians are interested in an optimal magnitude of
occurs, the root shape becomes more rectangular with orthodontic force. The optimal force magnitude should
the center of resistance at 50% of total root length. In be modified depending on the type of tooth movement.
American Journal of Orthodontics and Dentofacial Orthopedics Choy et al 103
Volume 117, Number 1

A B

C D
Fig 5. Stick diagrams of tooth; springs represent peri-
odontal fibers. A, Continuous periodontal fibers are rep-
resented by a series of small springs. B, Continuous
periodontal fibers are represented by 2 stiff springs per
side. C, When s = 0, force acting on any point other than
Cr will produce a rotation around Cr. D, When s = a, the
axis of location lies at distance b from Cr. Note that the
stick shows less tendency to tip in D compared with C.

movement. The actual force that the tooth felt should


have been much lower because friction was not consid-
ered in the study. In the present study, an optimal ortho-
dontic force was derived based on the assumption that the
stress does not exceed the capillary blood pressure.
Approximately 222 g (= 74 g × 3) per side would be opti-
B mal for a controlled tipping (center of rotation at apex) of
6 anterior teeth retraction. This approximates the value
Fig 4. A, Relationship between the location of force and
the axis of rotation (Arot) in response to alveolar bone Burstone et al22 suggested. Considering the result of
loss. B, Relationship between the location of force and Weinstein23 (2 g) and this study (20 g), it is noted that
the axis of rotation (Arot) in response to apical root even a very light force could result in an uncontrolled tip-
resorption. The value in parentheses of the graph inset ping produced by a horizontal force on the crown of the
indicates s2. Some lines in the graphs are omitted pur- tooth. A single force applied at the crown, such as retrac-
posely for better visualization. tion of anterior teeth with round wires or by a removable
appliance, can cause uncontrolled tipping. If heavier
forces are used, there may be a higher risk of root resorp-
Smith and Storey21 studied clinically optimal orthodontic tion. The force level should also be reduced in cases of
forces. Unfortunately, a tipping occurred with an appli- alveolar bone resorption or root resorption, not only
ance designed to produce translation. Their results illus- because the total root area is small, but also because, with
trated that 150 to 200 g was optimal for single canine a smaller s2, these teeth tip more easily.
104 Choy et al American Journal of Orthodontics and Dentofacial Orthopedics
January 2000

The model used for the current study has been pur- 11. Tanne K, Nagataki T, Inoue Y, Sakuda M, Burstone CJ. Patterns of initial tooth dis-
placements associated with various root length and alveolar bone height. Am J Orthod
posely oversimplified. It is 2-dimensional and assumes Dentofacial Orthop 1991;100:66-71.
the periodontal ligament to be homogenous and 12. Yettram AL, Wright KWJ, Houston WJB. Center of rotation of a maxillary central
incisor under orthodontic loading. Br J Orthod 1977;4:23-7.
isotropic with a linear stress-strain relationship. It also 13. Synge JL. The tightness of teeth, considered as a problem concerning the equilibrium
ignores variation in periodontal ligament thickness, as of a thin incompressible elastic membrane. Philos Trans R Soc Lond, Series A 231,
1933;435-70.
well as irregularity in the bone and tooth. Nevertheless, 14. Davidian EJ. Use of a computer model to study the force distribution on the root of
it has been useful in delineating some fundamental rela- the maxillary central incisor. Am J Orthod Dentofacial Orthop 1971;59:581-8.
15. Halazonetis DJ. Computer experiments using a two-dimensional model of tooth sup-
tionships between applied force and tooth movement. port. Am J Orthod Dentofacial Orthop 1996;109:598-606.
16. Popov EP. Mechanics of materials. Englewood Cliffs, NJ: Prentice-Hall 2nd Ed., 1978.
CONCLUSIONS 17. Pryputniewicz RJ, Burstone CJ. The effect of time and force magnitude on orthodon-
tic tooth movement. J Dent Res 1979;58:1754-64.
The distribution of stress in the periodontal liga- 18. Reitan K, Rygh P. Biomechanical principles and reactions. In: Graber TM, Vanarsdall
RL Jr, eds. Orthodontics, current principles and techniques. St Louis: CV Mosby;
ment during tooth movement was investigated to find 1994. p. 96-192.
the location of center of resistance and to elucidate the 19. Burstone CJ. The biomechanics of tooth movement. In: Kraus BS, Reidel RS, editors.
Vistas in orthodontics. Philadelphia: Lea & Febiger; 1962. p. 197-213.
relationship between force and the axis of rotation. In 20. Burstone CJ. Application of bioengineering to clinical orthodontics. In: Graber TM,
addition, optimal magnitude of orthodontic forces in Swain BF, eds. Orthodontics, current principles and techniques. St Louis: CV Mosby;
1985. p. 194-227.
various simulated conditions were examined. Signifi- 21. Storey E, Smith R. Force in orthodontics and its relation to tooth movement. Aus J
cant findings are the following: Orthod 1952;56:11-8.
22. Burstone CJ, Steenbergen EV, Hanley K. Modern edgewise mechanics and the seg-
1. The location of the center of resistance in the upper canine mented arch technique. Glendora, CA: Ormco Co; 1995.
is found at 42% of the root length measured from the alve- 23. Weinstein S. Minimal forces in tooth movement. Am J Orthod Dentofacial Orthop
1967;53:881-903.
olar crest. The more a root tapers, the more the center of
resistance moves coronally.
2. As the amount of alveolar bone loss increases, the center
of resistance moves apically proportionally, but its per-
centage of total root length remains unchanged. APPENDIX
3. As the amount of apical root resorption increases, the center
of resistance moves coronally with a nonlinear relationship. 1. Tooth translates when force passes through center of
4. The value s2, which explains the distribution of stress, resistance. Stress is evenly distributed along the peri-
decreases with increased root taper, increased alveolar odontal ligament for a tooth to be translated (Appendix
bone loss, and increased apical root resorption. A tooth Fig 1A). Sum of all forces should be zero to satisfy the
with a small s2 may therefore be more prone to tipping as first condition of state of equilibrium.
it is difficult to manage its axis of rotation.
5. Optimal orthodontic force for tooth movement may be  – F = 0
defined by maximal limit of stress that capillary blood
vessels in the periodontal ligament can withstand. The Sum of all moments measured from the X axis should be
optimal orthodontic force varies with the location of axis zero to satisfy the second condition of state of equilibrium.
of rotation. Optimal forces increase in tooth movement
approaching translation. F × d – y = 0
y
REFERENCES d = 
A
1. Burstone CJ. The biophysics of bone remodeling during orthodontics-optimal force con-
sideration. In: Biology of tooth movement. Boca Raton, FL: CRC Press; 1989. p. 321-33. if d = 0 then y = 0
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Orthod Dentofacial Orthop 1969;55:353-69. 2. Tooth rotates around center of resistance when a couple is
3. Nikolai RJ. Periodontal ligament reaction and displacements of a maxillary central applied. When a couple is applied to a tooth, maximum
incisor loading. J Biomech 1974;7:93-9.
4. Steyn CL, Verwoerd WS, Merwe EJ, Fourie OL. Calculation of the position of the axis stress(σmax) is found at the most distant node from the
of rotation when single rooted teeth are orthodontically tipped. Br J Orthod axis of rotation (z axis) (Appendix Fig 1B). Stress at arbi-
1978;5:153-6.
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extrusion. Am J Orthod 1982;82:1-9.
7. Burstone CJ, Pryputniewicz RJ. Holographic determination of center of rotation pro-
y
duced by orthodontic forces. Am J Orthod Dentofacial Orthop 1980;77:396-409. –  σmax
8. Burstone CJ, Pryputniewicz RJ, Bowley WW. Holographic measurement of tooth c
mobility in three-dimensions. J Periodont Res 1978;13:283-94.
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forces acting at each node along the periodontal ligament
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J Orthod Dentofacial Orthop 1988;94:426-31. should be zero.
American Journal of Orthodontics and Dentofacial Orthopedics Choy et al 105
Volume 117, Number 1

A B
F Force
M Moment
a Distance between center of resistance and force
b Distance between center of resistance and axis of rotation
y Distance between node and center of resistance
c Distance between center of resistance and apex
A Total area of root
A Area of a node
I Moment of inertia
σ Stress
σmax Maximum stress

Appendix Fig 1

As force and moment is applied simultaneously at the cen-


y
 (–   max)  = 0 ter of resistance, a total stress is
c
My F
As c or σmax is not zero, y = 0 =– —+—
A A
In y = yA, as A is not zero, y = 0
3. The relationship between location of force and axis of As b = y, and M/F = a
rotation is a × b = s2 where a is the distance between the
I (Appendix Fig 1B)
force and the center of resistance, b is the distance ab = —
between the center of resistance and the axis of rotation. A
As a tooth is in equilibrium,
I y2
As — =  resembles the variance
Mz = 0 A 
 = s2

y σ ax A
M =  (–   max)  = – m y2
c c ab = s2
Mc
σmax = –  (I = y2A) As maximum stress (σmax) occurs where y = c,
I
My Mc F
 = –  σmax = – — + —
I I A

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